Biomarkers and Stimulation Algorithms for Adaptive Brain Stimulation
- 1Department of Neurosurgery, Duke University, Durham, NC, United States
- 2Department of Biomedical Engineering, Duke University, Durham, NC, United States
- 3Department of Neurobiology, Duke University Medical Center, Duke University, Durham, NC, United States
The goal of this review is to describe in what ways feedback or adaptive stimulation may be delivered and adjusted based on relevant biomarkers. Specific treatment mechanisms underlying therapeutic brain stimulation remain unclear, in spite of the demonstrated efficacy in a number of nervous system diseases. Brain stimulation appears to exert widespread influence over specific neural networks that are relevant to specific disease entities. In awake patients, activation or suppression of these neural networks can be assessed by either symptom alleviation (i.e., tremor, rigidity, seizures) or physiological criteria, which may be predictive of expected symptomatic treatment. Secondary verification of network activation through specific biomarkers that are linked to symptomatic disease improvement may be useful for several reasons. For example, these biomarkers could aid optimal intraoperative localization, possibly improve efficacy or efficiency (i.e., reduced power needs), and provide long-term adaptive automatic adjustment of stimulation parameters. Possible biomarkers for use in portable or implanted devices span from ongoing physiological brain activity, evoked local field potentials (LFPs), and intermittent pathological activity, to wearable devices, biochemical, blood flow, optical, or magnetic resonance imaging (MRI) changes, temperature changes, or optogenetic signals. First, however, potential biomarkers must be correlated directly with symptom or disease treatment and network activation. Although numerous biomarkers are under consideration for a variety of stimulation indications the feasibility of these approaches has yet to be fully determined. Particularly, there are critical questions whether the use of adaptive systems can improve efficacy over continuous stimulation, facilitate adjustment of stimulation interventions and improve our understanding of the role of abnormal network function in disease mechanisms.
Current evidence points to various forms of invasive brain stimulation, including stimulation for epilepsy and deep brain stimulation (DBS) for movement disorders, as exerting widespread influence over multiple brain areas through modulation of disease- and patient-specific neural networks (Zamora-Lopez et al., 2011; Henderson, 2012; Lozano and Lipsman, 2013; Fox et al., 2014; Horn et al., 2017). These dynamic networks may be partially identified by structural or axonal connectivity (i.e., as demonstrated by diffusion tensor imaging tractography) or functional and physiological connectivity [i.e., as demonstrated by positron emission tomography, functional magnetic resonance imaging (MRI)] (Oswal et al., 2016). However, clinical targeting is typically confirmed by direct electrophysiological recordings and or macrostimulation to evoke the desired symptom response. Precise placement of electrodes to interact with specific brain networks is currently initially guided by pre-operative recordings (particularly in epilepsy) and imaging, with detailed MRI to define approximate anatomical localization due to high patient to patient variability. Further, in many indications microelectrode recording to refine the optimal physiological subregion is critical, since this region may be distinct from the initial anatomical target. Finally, engagement of appropriate circuitry within the desired network can be verified by clinical assessment. During awake DBS procedures, for example, appropriate neural network engagement can be directly confirmed by symptom suppression (relief of tremor, for example). The predicted sphere of activation or influence of stimulation (Butson et al., 2011) may assist with targeting. However, clinical assessment remains the primary verification of network activation in use at this time.
Although continuous DBS has significantly improved the treatment of Parkinson's disease (Odekerken et al., 2016) and tremor, this mode of stimulation has many limitations and has had limited success in other diseases, such as depression or Alzheimer's disease. The current clinical approach to programming and adjusting stimulation parameters is time consuming and a more automated approach is desirable. Likewise, improved power efficiency and fewer side effects would improve clinical treatment. Many of these improvements will be facilitated by identification and development of biomarkers linked to both network activity and symptom relief, if these relevant biomarkers can be successfully integrated into the treatment scheme. Thus, possible improvements in care may be achieved, including definitively mapping electrode location during surgical procedures (in addition to symptom suppression or as a separate, objective marker), continuous, dynamic adjustment of stimulation in either an amplitude- or time-dependent manner (Rosa et al., 2015), improved control of disease symptoms (Tinkhauser et al., 2017), and also enhancement of device lifespan, through intermittent or reduced stimulation. Beyond the operative environment, biomarkers may also facilitate initial clinical programming to provide objective endpoints as well as facilitate long-term automatic adjustment (Heldman et al., 2016). Additionally, biomarkers may help provide insight into the treatment efficacy variability between patients with optimal electrode position and long-term disease management (Trager et al., 2016). However, such insight will require confirming a direct correlation between the biomarkers reflecting underlying neural network activity and associated clinical symptoms (Kuhn et al., 2006, 2009). Confirmation of engagement of relevant neural circuitry may also help to understand possible divergence between patient-specific anatomical targeting and physiological activation of circuits.
Additional techniques under development include novel stimulation paradigms, which may be more clinically efficacious. These include structured stimulation patterns developed from extensive modeling of Parkinson's circuitry, tested intraoperatively, now being assessed in clinical trials, which include variable stimulation pulse timing (rather than regular pulse generation) and can potentially reduce the number of pulses per second needed for effective stimulation (Brocker et al., 2017), while also potentially improving the efficiency of stimulation (Brocker et al., 2013). Further, novel electrode designs are now just coming into clinical practice, including 8 contact directional electrodes (Steigerwald et al., 2016; Volkmann et al., 2016) and a research design with additional contacts spaced around the electrode (Contarino et al., 2014), both allowing for current to be steered toward treatment areas or away from critical regions. Both of these advances could also be used in combination with various types of responsive or adaptive control systems, to implement a hybrid system with multiple improved techniques.
Possible biomarkers span multiple modalities, including external wearable devices (such as an accelerometer or step counter) that analyze a symptom and may communicate with a common controller (Graupe et al., 2010; Shull et al., 2014; Ekker et al., 2016). Further, internal markers of circuitry function have been suggested, such as beta frequency oscillatory activity (Silberstein et al., 2003) and associated phase amplitude coupling (PAC) (De Hemptinne et al., 2015). Evoked field potentials arising from the DBS stimulation pulses (Kent et al., 2015) and triggering on intermittent events could be used for initiating or adjusting stimulation (Fisher and Velasco, 2014) or Tourette's (Almeida et al., 2015). Biomarkers could also be biochemical changes detected by a sensor (i.e., dopamine) (Grahn et al., 2014), blood flow (Hill et al., 2013; Haense et al., 2016; Noor et al., 2016), temperature changes, or optogenetic signals (Bernstein et al., 2012). Identification of appropriate biomarkers will be critical in the execution of responsive on/off triggerable systems (with a fixed, preset response to a threshold input), adaptive (with adjustable duration or scalar, graded adjustments in amplitude to reach a pre-defined setpoint) or dynamic, closed-loop feedback systems with multiple inputs. All of these formats require some form of circuitry-dependent signal relevant to the disease or condition for automatic adjustment of DBS settings (Carron et al., 2013; Little et al., 2013; Rehan and Hong, 2013; Meidahl et al., 2017).
Here we review the design of responsive, adaptive and closed-loop stimulation. We then discuss how various biomarkers and devices may be useful to improve stimulation to treat selected example disease conditions, some of which have already reached the market (i.e., responsive Neuropace device for epilepsy treatment), but mostly which remain experimental or conceptual. As with any new field, the translation of biomarkers into portable or implanted devices will require more critical analysis of the clinical utility in a particular condition, stability over time, the ability to record the signal, and the correlation of the proposed biomarker with clinical symptoms relevant to the disease (Kuhn et al., 2006, 2009; Meidahl et al., 2017). However, few of the biomarkers to be discussed are at this stage of translation yet into humans or clinical trials, hence considerable skepticism remains about introducing more complexity into the already complicated field of brain stimulation (Arlotti et al., 2016). Thus, we mention a number of possible biomarker signals, but as further analysis proceeds and feasibility data are obtained, many of these may or may not prove durable for clinical translation.
Modes, Devices, and Control Approaches for Adaptive Stimulation
Stimulation for treatment of epilepsy (using the Neuropace device or anterior thalamic DBS) has just reached clinical usefulness (Fisher and Velasco, 2014), whereas DBS stimulation for movement disorders provides efficacy of ~75% in patients when applied in a continuous, open-loop fashion (for example, Activa SC/PC technology, Medtronic) (Almeida et al., 2015; Odekerken et al., 2016). However, as indications for brain stimulation in other disease processes expand with further knowledge of networks that may benefit from stimulation, additional types of stimulation will likely be needed. In contrast, several clinical trials using DBS for alternative indications (i.e., depression, Alzheimer's disease) have demonstrated less efficacy and remain experimental (Hamani et al., 2009; Dougherty et al., 2015; Lozano et al., 2016). We initially review the various modes of stimulation that have been developed and associated devices, which may be able to sense and deliver adaptive stimulation.
The idea of a time constant, well-known in control systems literature, is a measure of the time required for the system to respond after a step input, assuming the device can respond faster than the system under observation (Carron et al., 2013). For example, tremor responses to thalamic DBS may take at least 10–20 s to stabilize (Rehan and Hong, 2013; Yamamoto et al., 2013) whereas steady state responses of subthalamic DBS for bradykinesia may occur within a few seconds but require >30 min for stabilization (Waldau et al., 2011). Briefly, control models of stimulation may be broken down into five major subtypes (Figure 1, Table 1), depending on the frequency of the updating needed, the flexibility of stimulation response, and rate of responsiveness. In order of increasing control systems complexity, these include simple continuous on (Figure 1A), intermittent or scheduled with a predetermined schedule and fixed amplitude (Figure 1B), responsive with a triggered onset of a preset amplitude and width (Figure 1C), and adaptive with flexibility during either on/off of a preset amplitude (i.e., variable durations of stimulation) in response to a threshold for a single biomarker input or a variable amplitude (Figure 1D). Finally, in the brain-machine interface context, closed-loop implies a multidimensional input (i.e., multiple spike trains or other input signal denoting the brain's intent), a continuous processing of this input for output predictions, and some form of feedback signal to refine the nearly constant output (Figure 1E). However, any signal where some feedback exists in a control sense could be termed closed loop in a generic sense.
Figure 1. DBS stimulation control models: (A) continuous stimulation with evenly spaced stimulation pulses; (B) scheduled intermittent stimulation with a burst of pulses at fixed intervals; (C) responsive stimulation, with triggered output based on a threshold, but each pulse is the same, preset amplitude; (D) adaptive stimulation, with threshold-based adjustments in number of pulses or in amplitude of pulses, settling in around a fixed control point; (E) closed-loop stimulation, where the constantly changing, complex input determines an equally complex, dynamic output. For each the solid arrow depicts the output stimulation and the dashed arrow depicts an input signal that is compared to some threshold. (F) Potential stimulation and recording arrays. Depending on disease pathology, inputs may be from the DBS lead itself as well as secondary DBS, EEG, or ECoG electrodes. Output stimulation from the IPG is primarily though the DBS/parenchymal lead at this time, although potential exists for subdural and scalp intervention as well.
Neuropace and DBS Devices
Rather than constant, continuous stimulation (i.e., Figure 1A) DBS for epilepsy implements an intermittent, scheduled stimulation at a preset level, potentially being more effective than constant stimulation (Fisher and Velasco, 2014) (Figure 1B, Table 1). Additionally, phase-dependent stimulation may exert a critical dampening if the response can be sufficiently rapid (Cagnan et al., 2017). In contrast, the Neuropace IPG device implements triggered or responsive stimulation to treat specific, epileptic events detected by a threshold crossing on the input channels (Figure 1C), and this may be less intrusive than constant stimulation if the events or symptoms are uncommon (Morrell and RNS System in Epilepsy Study Group, 2011). Once a pre-determined stimulation level and threshold are set the device both records ongoing brain activity and then triggers the preset stimulation burst based upon threshold criteria, with a lockout preventing overstimulation. Newer Medtronic devices (i.e., Medtronic PC+S and RC+S) also have the capability for lock-out, phase-in timing and adjustable, contingent response to the input signal (Rouse et al., 2011; Afshar et al., 2012; Stypulkowski et al., 2013). The Medtronic RC+S is the more advanced version of the PC+S with additional sensing and stimulation channels (16 vs. 8), rechargeable, improved real-time data access, and ability to connect to 4 4-channel electrodes, available in 2018 for research testing.
Some disease processes, such as epilepsy, may have long asymptomatic periods between events when stimulation is not required. Rather than subjecting the patient to the potentially deleterious effects of constant stimulation and to avoid chronic circuitry changes that may lead to loss of efficacy, scheduled intermittent stimulation (such as anterior thalamic DBS where stimulation is applied for 20–30 s with an off-time of ~5 min) reduces the amount of unnecessary stimulation by intermittently modulating the network to a less excitable state. However, the parameters of stimulation when “on” are fixed and stimulation occurs in response to detection of a potentially ictal or hyperexcitable state (Fisher and Velasco, 2014). In contrast, the Neuropace system, a responsive system, constantly monitors a set of brain electrodes for activity and then, when intermittently triggered by a critical condition, stimulates the brain to prevent seizure propagation (Morrell and RNS System in Epilepsy Study Group, 2011). Similarly, there are plans to develop a responsive or triggered DBS epilepsy system based on cortical events (Stypulkowski et al., 2014), similar to a prototype Tourette's control system with thalamic stimulation based on occurrence of cortical events (Almeida et al., 2015). In continuous, scheduled, and responsive paradigms, manual parameter adjustments performed by a clinician can be a time intensive process as the stimulus is slowly altered and the outcome is assessed at intervals.
The responsive stimulation in Neuropace implements recording electrodes to “sense” an ictal event via complex internal algorithms in its controller, and turns stimulation on and off only as needed to interrupt a developing seizure (Durand, 2009; Morrell and RNS System in Epilepsy Study Group, 2011). In these systems, upper and lower thresholds trigger the binary on and off states of the system (analogous to the thermostat controls for furnace systems), delivering stimulation when triggered at a predetermined level and with a constant width, based on prior events. This control system would appear to be best suited for diseases with intermittent and unpredictable manifestations, such as epilepsy or Tourette's Syndrome (Morrell, 2006; Okun et al., 2013). The inputs to these control systems may be external or internal, ranging from surface electromyogram (EMG) to scalp electroencephalogram (EEG) to local field potentials (LFPs) (Basu et al., 2013; Priori et al., 2013a). For example, Graupe et al. describe the use tremor-predictive information from surface EMG and accelerometers as the input to an on-off adaptive DBS system in tremor control (Graupe et al., 2010).
Adaptive and Closed-Loop Control
The integration of more advanced control systems concepts into brain stimulation can be found in the last two types of stimulation–adaptive and closed loop systems. Adaptive stimulation has adjusted stimulation in response to either external signals or an internal or biomarker signal, which has a close relationship to an external symptom. First patented in 1996 (by Michael S John), adaptive stimulation was envisioned for maintenance of “consciousness” in traumatic brain injury patients (US Patent 6066163A, 2/2/1996).
Little et al. investigated short term (externalized) adaptive DBS of the STN for Parkinson's disease based on processing of local LFPs and using an on/off system dependent on beta frequency amplitude, but with dynamic, variable widths of stimulation, hence fitting within the definition of adaptive (Little et al., 2016a,b). Interestingly Little et al. compared continuous, scheduled intermittent (termed “random” in their study), and adaptive systems head-to-head and found statistically significant motor scores, reduction in stimulation time, decreased speech side effects and decreased energy requirements with the adaptive system when triggered by a threshold but not with random stimulation (Little et al., 2013). As noted with later analysis of these and additional data, the adaptive on/off system resulted in much improved efficiency and a modest improvement in efficacy (Tinkhauser et al., 2017). The resultant improvement in clinical motor scores was also corroborated by Rosa et al. in one patient comparing continuous DBS and adaptive DBS, which utilized a continuously varying stimulation amplitude parallel to the beta frequency content (Rosa et al., 2015). Alternatively, Priori et al. implemented recordings of internal LFPs as the input to their adaptive DBS for Parkinson's disease (Priori et al., 2013a).
A scalar adaptive system has also been proposed, using variable amplitude inputs to hone in on a control point, but only tentatively implemented by Rosa et al (Santaniello et al., 2011; Carron et al., 2013; Rehan and Hong, 2013; Rosa et al., 2015). In this concept, a scaled output is provided based on the difference between a setpoint and current state, such that a larger difference from a desired value creates a larger change in stimulation (Figure 1D). A classic control system principle outside of medicine, this slightly more sophisticated variation minimizes the amount of output variable oscillation and time to reach a desired set point, as well as large or complete on/off changes which may be disturbing to the patient.
In contrast to intermittent or adaptive stimulation, closed-loop stimulation depends upon a constant, rapidly updated feedback parameter, such as visual feedback in brain computer (or brain machine) interfaces (BCI/BMI) using constant brain sensing (i.e., as in a motor task) and direct, nearly continuous contingent output for motor control (Lebedev and Nicolelis, 2006; Leuthardt et al., 2006; Patil and Turner, 2008). The update time for BMI systems is typically on the order of ~20 Hz (i.e., ~50 ms for updating the next prediction) (Hanson et al., 2012). Additionally, whereas adaptive stimulation using a DBS device may have only a single setpoint, closed-loop stimulation may enable a wide range of trajectories with continuously adjustable setpoints in a highly dynamic sense, approaching a target and performing a task (Khobragade et al., 2015).
Although the initial work focused on motor disorders, more recently Widge and Sahay also discussed the concept of closed-loop applications in psychiatric disease (Widge and Sahay, 2016), with attention to BCIs as a better, dynamic, real-time source of input for psychiatric disease states. While largely theoretical, early work in this area suggests that closed-loop feedback can remap and alter neural network firing patterns as the BCI training proceeds, allowing the device to depict intention, which may be critical for treatment of a fluctuating disease like psychiatric illness (Widge and Sahay, 2016).
The Medtronic PC+S/RC+S was developed as an open platform for chronic, adaptive brain stimulation, and has been used in a wide range of pre-clinical and clinical applications (Stanslaski et al., 2012; Carlson et al., 2013; Stypulkowski et al., 2013). These include, for example, developing a brain-computer interface in a locked-in patient with amyotrophic lateral sclerosis (Vansteensel et al., 2016), tremor control linked to a wearable device (Herron et al., 2017), brain stimulation for epilepsy (Stypulkowski et al., 2014), and recording biomarkers while stimulating in Parkinson's disease (Quinn et al., 2015; Neumann et al., 2016; Blumenfeld et al., 2017). Further generations of this PC+S device, particularly the new RC+S IPG in development, also offer the advantage of providing full clinical stimulation when not in research mode, which is desirable for intermittent clinical research in human subjects.
Characteristics of an Ideal Biomarker
Although closed-loop brain stimulation has tremendous potential, it requires an effective biomarker to serve as the feedback parameter. A biomarker should directly correlate with the clinical symptoms, such that a system could effectively use the biomarker to control a device in lieu of the specific symptoms (i.e., beta band oscillations linked to bradykinesia in Parkinson's disease) (Kuhn et al., 2006, 2009). Thus, changes in the biomarker (i.e., beta oscillations) should clearly and accurately predict alterations in the symptoms associated with the disease. Likewise, as the brain stimulation affects the neural circuits, the biomarker should directly reflect these changes and constantly and dynamically track disease state. Biomarker signals, including beta frequency oscillations in Parkinson's disease as well as further signals under consideration, are also subject to sampling issues (i.e., which site provides optimal signals if several are available), noise from surrounding brain signals obscuring the signal, and in particular signal stability over time (Steiner et al., 2017). For example, cortical pathological signals may overlap with cortical movement signals in some contexts, requiring some form of identification of signals before being used for control. Likewise, highly variable signals may be noted in the same region from different patients, leading to a need for fine tuning and adjustment for individual patients (Kent et al., 2015).
Biomarkers by Disease Process or Pathology
We review how biomarkers are implemented by disease category, beginning with epilepsy, in which the Neuropace device is now approved and starting to be more widely used. The next category includes Parkinson's disease and Tourette's syndrome, in which ongoing experiments in humans are starting to demonstrate the potential of biomarkers. Lastly, we discuss conditions in which biomarkers under development may help improve possible brain stimulation approaches, but which have not yet shown clinical utility, including continuous stimulation. These latter conditions include depression and other psychiatric diseases, Alzheimer's disease, and dystonia, for which possible biomarkers have been defined but have not yet been implemented in clinical trials. Our discussion by disease category is tabulated in Table 2. Alternatively, biomarkers and disease states are categorized in Figure 2 by biomarker type.
Figure 2. Potential Biomarker by Type. Biomarkers divided into electrophysiological, imaging, and other categories.
Neurostimulation for medication resistant epilepsy can take the form of peripheral nerve stimulation like vagal nerve stimulation (VNS), customized electrodes using the responsive Neuropace system, and anterior thalamic DBS (Fisher and Velasco, 2014). VNS and responsive Neuropace devices are approved in the USA and thalamic DBS is approved in a number of other countries, although not the US at the time of writing (Fisher and Velasco, 2014). Neuropace stimulation in response to activity detected with a strip or depth electrode adjacent to a previously identified epileptogenic zone demonstrated an improvement in relative seizure frequency of about 21% (specifically, 38% reduction in the treatment group vs. 17% reduction in the sham group) (Morrell and RNS System in Epilepsy Study Group, 2011). Of course, the epileptogenic zone and abnormal brain networks involved with seizure origination and spread must be identified to inform electrode placement, and the fact that an event or seizure must occur for stimulation to begin are limiting factors for responsive stimulation in epilepsy. However, Halpern et al. noted a progression of EEG cortical activity up to 7 h prior to seizure onset, and these pre-ictal changes could represent a future feedback signal for responsive stimulation initiation (Halpern et al., 2008). There are many limitations to implementation of the Neuropace device, including localization as to where to specifically place both sensing and stimulation electrodes, how to detect pre-ictal events sufficiently far enough in advance of a seizure so that stimulation may be subconscious and undetected by the patient, and what stimulation paradigms may actually prevent network oscillations from building up to an ictal event.
Anterior thalamic DBS may modify overall frontal lobe networks to reduce seizure susceptibility, through scheduled intermittent stimulation (Salanova et al., 2015). The pulse repetition frequency of DBS is very important as incorrect frequency leading to EEG synchrony (rather than suppression) can lead to increased seizures rather than seizure control (Durand, 2009). The anterior nucleus of the thalamus (ANT) has shown long term significant seizure frequency reduction in the SANTE trial using intermittent scheduled stimulation (Salanova et al., 2015). DBS placement in the ANT is often guided by microelectrode recording and characteristic stimulation effects on scalp EEG in the frontal lobes (Halpern et al., 2008), which could be used as an intraoperative marker for effective location of the DBS electrodes.
These clinical studies build upon numerous pre-clinical research studies focusing on the effects of stimulation inhibiting seizures, particularly since brain stimulation can also commonly induce seizure activity (Durand, 2009). For example, a landmark pre-clinical study demonstrated the ability to control epileptic events from skull (extracranial) stimulation, using implanted brain electrodes as the closed loop feedback circuit for measuring ongoing cerebral hyperactivity (Berenyi et al., 2012). The advantages of the extracranial approach for seizure control is that excitability in a wide swath of brain can potentially be controlled, whereas the focal stimulation afforded by the Neuropace device can in some instances be insufficient for seizure control.
Parkinson's disease (PD) is a chronic, progressive movement disorder that affects ~0.9 million people in the United States (Ascherio and Schwarzschild, 2016; Lee and Gilbert, 2016). DBS for PD is commonly applied to the STN and, equivalently, to globus pallidus internus (GPi) (Benabid et al., 2009; Williams et al., 2014; Delong and Wichmann, 2015), though the three year follow-up of the NSTAPS study has recently confirmed improved efficacy for STN (Odekerken et al., 2016). Although ~75% of patients get symptom relief with DBS (Odekerken et al., 2016), there remains considerable patient to patient variation in outcomes in spite of current electrode localization and placement strategies, possibly since the pathways and pathophysiology of the disease itself are not fully understood (Whitmer et al., 2012). In some cases, insufficient treatment with a single DBS electrode may be addressed with an additional electrode. For example, instability and freezing of gait (FOG) remain significantly debilitating and causes of fatal falls, hip fractures, and pneumonia in Parkinson's patients (Aminoff et al., 2011). STN DBS leads to improvement of these axial gait symptoms but not in all patients (Chenji et al., 2017; Schlenstedt et al., 2017). Further, one study implemented the measurement of PPN evoked potentials to help guide GPi DBS stimulation in a closed loop configuration, altering the GPi input based on the PPN output (Morita et al., 2014); however, conclusions are not yet available as this is a study in progress. Another consideration for dual electrode recordings is the use of STN+GPi, which has primarily been suggested for improving persistent dyskinesias after STN DBS (Sriram et al., 2014; Cook et al., 2015; Matias et al., 2016). Dual electrodes may also facilitate stimulation on one electrode and recording on another with reduced intrinsic stimulation artifact on the sensing channels.
Beta Band Oscillations
Synchronization of cortex, basal ganglia, and thalamus results in spontaneous oscillatory activity in PD in the beta band, at around 13–30 Hz, spreading throughout the cortico-basal network (Wingeier et al., 2006; Whitmer et al., 2012), and this activity is thought to be a marker of PD state in animals and humans (Kuhn et al., 2006, 2009). Hypersynchrony declines after therapeutic doses of dopaminergic medication and likely DBS at an adequate dose (Weinberger et al., 2006; Little and Brown, 2012). Such synchrony may represent a biomarker that can be quantified to guide lead placement and to determine optimal DBS parameters (Whitmer et al., 2012; Lozano and Lipsman, 2013). These beta band responses can be recorded both from motor cortex [i.e., electrocorticography (ECoG)] (De Hemptinne et al., 2015) as well as directly from STN DBS contacts (Gmel et al., 2015; Brocker et al., 2017).
The hyperdirect pathway carries excitatory input from the motor cortex to the STN (Delong and Wichmann, 2015). Recently Whitmer et al. recorded subdural ECoG and STN LFPs (in a clinical study during DBS placement in 13 humans) from both within and adjacent (dorsal) to the STN to evaluate attenuation of hyper-synchrony following STN activation (Whitmer et al., 2012). Beta band attenuation varied positively with DBS amplitude at clinical treatment levels, suggesting that beta band measurements may provide a biomarker of PD treatment effect for bradykinesia (but not necessarily tremor). However, there was enhanced attenuation of hyper-synchrony by DBS within the central STN as opposed to leads placed dorsal to the STN (Marsden et al., 2001; Mackinnon et al., 2005). This highlights the possibility that different symptoms within the same disease process may involve different nodes within the neural network, or possibly variable neural networks. Further, the ECoG recordings confirmed that the beta synchronization was also present in the premotor and motor regions, a possible indication that the STN is a node between linked regions in the cortical basal ganglia circuit. However, a direct correlation with PD symptom improvement remains a critical requirement (Whitmer et al., 2012).
In addition to reduction in synchronization, effective DBS leads to regularization in neuronal firing patterns (Hashimoto et al., 2003; Bar-Gad et al., 2004). For example, the highly oscillatory, pathological firing patterns present in PD may be replaced by DBS-evoked action potentials with regular patterns that can act as an innocuous signal (Dorval et al., 2010). This regularity can be quantified via the firing pattern entropy, which is calculated from the inter-spike intervals of single unit recordings. In the rodent GP and substantia nigra pars reticulata (SNr), entropy increases with parkinsonism and decreases back to near healthy levels with effective DBS (Dorval et al., 2008, 2015; Dorval and Grill, 2014; Anderson et al., 2015).
Along with firing pattern entropy, directed information transfer between neurons also correlates with DBS efficacy (Dorval and Grill, 2014; Anderson et al., 2015; Dorval et al., 2015). Directed information measures the degree of influence that a recorded single neuron has on another neuron (Anderson et al., 2015). In rodents and non-human primates, directed information increases with Parkinsonism between the SNr and ventral anterior thalamus and between the GP internus and GP externus, respectively. In both cases, directed information is then reduced with effective DBS (Anderson et al., 2015; Dorval et al., 2015). Although an increase in directed information with Parkinsonism might be mistaken as beneficial, it most likely indicates the pathological hyper-synchrony observed in the basal ganglia, with each neuron passing on redundant information. A reduction in directed information with DBS could thus indicate a break in this hyper-synchronous state and a return to independence between information channels. Although based on firing of single neurons, directed information may or may not be a feasible biomarker in humans, unless the unit firing can be translated into either a spontaneous or evoked potential measurable with more stable electrodes.
Phase Amplitude Coupling
Using ECoG recorded over the motor cortex, De Hemptinne et al. observed that DBS reduces exaggerated primary motor (M1) PAC between beta oscillations and higher frequency superimposed oscillations characteristic of PD (De Hemptinne et al., 2013, 2015). Normal cortical function also involves the presence of PAC, possibly coordinating timing of neuronal activity between and within cortical areas as necessary for task performance (Canolty et al., 2006; Canolty and Knight, 2010; Yanagisawa et al., 2012). The increased PAC in PD possibly reflects neurons constrained into an inflexible pattern by PD pathophysiology, leading to rigidity and bradykinesia (Moran et al., 2008; De Hemptinne et al., 2013). DBS normalizes elevated PAC, both at rest and during a motor task (De Hemptinne et al., 2015), and PAC may be a sensitive biomarker to measure both the Parkinsonian state as well as the effectiveness of therapy for these symptoms (De Hemptinne et al., 2015). Unfortunately, the presence of PD tremor alters this measure and voluntary motion also can change PAC. However, the advantages of minimal stimulation artifact in the ECoG recording electrode could potentially be applied to other neurological or psychiatric disease states (De Hemptinne et al., 2015). Overall, whether PAC can be effectively translated into a useful and consistent biomarker, separable from normal motor function, has yet to be demonstrated.
Evoked Potentials and Oscillations
Evoked responses from stimulating and recording via the same DBS lead in patients during DBS surgery (using different contacts) can provide neural circuit-specific insight into functional activation of the basal ganglia through STN–GP synaptic interactions, particularly through a comparison of responses to stimulation at effective (i.e., ~130 Hz) and ineffective (~10–40 Hz) stimulation frequencies (Grill et al., 2015). Further, gamma band oscillations (i.e., 60–90 Hz) may indicate hyperkinetic PD symptoms, such as dyskinesias, as a biomarker separate from beta band oscillations (Swann et al., 2016). Any of these electrophysiological markers could theoretically be inputs to closed-loop systems or markers of disease-treatment response in a slowly progressive disease, such as PD.
Summary of PD
Parkinson's disease (PD) is a progressive disease with varying presentations, including motor and non-motor symptoms. Conventional DBS targets (i.e., STN, GPi) focus on symptomatic relief of motor symptoms, although STN DBS does show also consistent improvement of midline and non-motor symptoms, particularly FOG. There is also the possibility of multifocal targeting with two or more DBS electrodes within known nodes (i.e., STN+GPi, for example), but this configuration will have the added complication of how to adjust cooperatively parameters from the additional recording/stimulation contacts. It also further highlights the need for brain modeling to understand circuitry and biomarkers to assist in automatic adjustment (Butson et al., 2011; Butson and Mcintyre, 2015). The potential for both a motor target and a cognitive target to treat a single disease process could also be possible with multiple electrodes (Lozano and Lipsman, 2013). The recent progress with even short-term adaptive systems using an on/off controller shows that beta band oscillations may be a suitable biomarker, particularly for particularly rigidity and bradykinesia (Little et al., 2016a; Tinkhauser et al., 2017). There are many avenues to test these possible biomarkers in initial clinical trials, including intraoperative testing, using percutaneous wires after surgery for several days, or using one of the implanted sensing/recording devices in small clinical cohorts.
Tourette syndrome (TS) is an idiopathic neuropsychiatric disorder defined by motor and phonic tics and often associated with psychiatric disorders, such as attention deficit hyperactivity disorder (ADHD) and obsessive-compulsive disorder (OCD) (Leckman, 2002; Maling et al., 2012; Almeida et al., 2015). For the small number of patients whose symptoms do not resolve prior to adulthood, the tics can become treatment refractory and debilitating (Jankovic and Kurlan, 2011; Maling et al., 2012; Almeida et al., 2015). DBS for TS first involved bilateral lead placement in the centromedian nucleus of the thalamus (Vandewalle et al., 1999). Currently, it is theorized that dopaminergic neurons contribute to a dysfunctional circuit that leads to decreased cortical inhibition (Gilbert et al., 2004; Almeida et al., 2015) and excessive inhibition of basal ganglia output to the thalamus (Mink, 2001). Current DBS targets include the centromedian-parafascicular complex of the thalamus with the nearby anterior portion of the ventralis oralis nucleus. As well, the efficacy of intermittent / scheduled as compared to continuous stimulation is currently being evaluated (Okun et al., 2013).
Recordings from the thalamic nuclei of anesthetized TS patient undergoing DBS revealed low frequency firing in bursts (Priori et al., 2013b). Awake, these frequencies seem to match with the clinical phenotype and seem preferential for tics as opposed to the OCD manifestation of TS. Maling et al. studied 5 patients implanted with the Neuropace device using cortical ECoG strips, CT-MRI fusion and intraoperative microelectrode recordings to delineate their anatomic CM target (Maling et al., 2012). Over time, the best responders to adaptive stimulation of the thalamus following bursting in the ECoG demonstrated increased gamma activity and return to higher frequencies with the best symptom relief correlating with synchronization within a single oscillatory frequency. Furthermore, GPi low frequency oscillations preceded EMG recordings of the tic by 50–2,000 ms, a potential foreshadowing of tic activity based on the suspected anatomical circuit (Priori et al., 2013b). For patients with OCD comorbid to their TS, the anterior limb of the internal capsule and nucleus accumbens is another anatomical target. LFP recordings demonstrate high beta frequency oscillations, another possible physiological marker of OCD, and a speculative precursor to low frequency thalamic oscillations (Priori et al., 2013b). These changes in oscillatory activity could also provide an adaptive trigger for preventing motor tics through demand DBS stimulation.
Stimulation of the ventral intermediate nucleus of the thalamus [Vim] is useful for control of essential tremor, which affects ~7 million people in the United States (Deuschl et al., 2011). Spontaneous or evoked responses may be directly recorded from the DBS lead (Afshar et al., 2012). Kent et al. investigated the evoked compound action potential (ECAP) intraoperatively within Vim as a potential surrogate marker in thalamic DBS (Kent et al., 2015), with the ECAP arising from synchronously-activated neural elements (likely axons) near the lead (Kent and Grill, 2012). While recording from two non-stimulating contacts of the lead, stimulation parameters and tremor measured via accelerometer were correlated with neural activation assessed from the ECAP (Kent et al., 2015). High frequency 130 Hz DBS reduced essential tremor, while 10 Hz DBS worsened tremor. During high frequency DBS, a monotonic relationship between voltage and tremor was noted up to an optimal voltage; however, ECAP signal amplitudes varied as much as an order of magnitude between subjects. The study also suggested that cerebellar afferents were the primary determinants of the ECAP response (Kent et al., 2015). Lastly, it was noted that as more glial scar or electrode conditioning with stimulation occurred around the leads with continued chronic DBS (measured during IPG replacements), the stimulation artifact in the ECAP recording increased, potentially hampering long-term applications (Henderson et al., 2002; Kent et al., 2015). A consistent evoked response with consistency across patients has proven elusive, however.
Another concept to improve the signal to noise ratio during Vim DBS would be to record the evoked field potential within postsynaptic areas anterior to Vim, where the cerebellothalamic fibers have their synapses (in VOP particularly) (Gallay et al., 2008). This would involve recording from a more anterior DBS electrode, which has typically been placed for improved tremor control in difficult cases (Foote and Okun, 2005). The advantages of a second electrode include the possibility that all contacts on the primary electrode could be used for stimulation (as opposed to sharing stimulation and recording contacts) and that there would be improved isolation from the stimulation artifact, similar to recording from the isolated ECoG motor cortex strip electrode (Kent and Grill, 2012; Almeida et al., 2015).
External signals from wearable devices, such as accelerometers, may also provide direct and dynamic feedback on tremor intensity, and can be potentially included in closed-loop control (Herron et al., 2017). For example, Cagnan et al. (2017) developed a prototype system for phase-specific stimulation, linking the measured phase of tremor to the DBS IPG for intermittent stimulation. This worked well for tremor control in some patients and could potentially improve the efficiency of stimulation with reduced IPG output. Further, Slavin et al. developed a tremor prediction and control algorithm for on/off adaptive control of tremor based on muscle contraction and accelerometry (Shukla et al., 2012; Basu et al., 2013). Potentially, the internal accelerometer with the Medtronic PC+S device could also function to detect tremor within the upper extremities, though differentiating one arm from the other may be difficult (Afshar et al., 2012; Stanslaski et al., 2012).
Deep brain stimulation (DBS) for treatment resistant depression (TRD) has developed over the past 10 years (Crowell et al., 2015) with targeting of multiple sites, including subcallosal cingulate (SCC) white matter or Brodmann area 25 gray matter, ventral capsule/ventral striatum, nucleus accumbens, inferior thalamic peduncles, medial forebrain bundle, and the lateral habenula (Mayberg et al., 2005; Schlaepfer et al., 2013; Riva-Posse et al., 2014; Crowell et al., 2015). While small trials demonstrated efficacy even at long-term time points (Holtzheimer et al., 2012), larger industry sponsored trials, such as BROADEN (St. Jude) did not (Dougherty et al., 2015). Invasive electrophysiological recordings from reward and mood circuitry are far less common than those from movement centers (Lozano and Lipsman, 2013). However, a recent neurophysiological study combined SCC DBS in depression with (non-invasive) EEG pre- and post-operatively and observed that coherence of pre-operative frontal lobe theta EEG signal across multiple recording sites predicted a better response to DBS treatment (Broadway et al., 2012).
The SCC is the most studied site, initially chosen following imaging data showing changes in the SCC white matter in response to standard antidepressant treatment (Mayberg et al., 2000; Seminowicz et al., 2004; Mayberg, 2009). Lead placement in DBS studies of SCC was initially anatomically guided to white matter (Mayberg et al., 2000; Holtzheimer et al., 2012). However, therapeutic responses to DBS differed among those studied, and anatomical location did not predict those who would and would not respond (Hamani et al., 2009). Further PET studies, fiber tractography, DBS activation volumes and probabilistic tractography subsequently supported a theory that SCC is part of a larger circuit of multiple afferents to the frontal lobes as well as fibers of passage in this area (Hartmann et al., 2015), which may prove equally important as SCC in depression modulation (Butson et al., 2007; Hamani et al., 2009; Lujan et al., 2013). Thus, anatomical localization alone appears unable to predict which specific white matter tract is being stimulated and which frontal lobe target receives the stimulation. To overcome this limitation, Riva-Posse et al. observed that clinical response to SCC DBS was linked to proximity of the intersection of three fiber bundles: (1) bilateral forceps minor of the anterior corpus callosum, (2) bilateral cingulum bundles connecting ipsilateral SCC to rostral, dorsal anterior, and mid-cingulate cortices, and (3) medial branch of the uncinate fasciculus connecting the subcallosal cingulate and medial frontal cortex rostrally and subcallosal cingulate to the nucleus accumbens and anterior thalamus (Riva-Posse et al., 2014). Prospective trials of this intersection as well as directional steering and specific evaluation of evoked responses to DBS in the various frontal lobe areas (i.e., with ECoG) to evaluate each of the components of the fiber bundles would be helpful in understanding if indeed tractography provides a better target for depression modulation (Martens et al., 2011; Riva-Posse et al., 2014).
Intraoperative testing is challenging in DBS for TRD as patient response is highly variable and personal. Autonomic effects (tachycardia and increases in skin conductance) appear to correlate reproducibly in the OR with appropriate lead placement via tractography as described above (Riva-Posse et al., 2014) and may provide reliable biomarkers of post-operative response and efficacy (Crowell et al., 2015). As another perioperative marker of clinical efficacy, EEG frontal theta changes noted 1 month after DBS appear to predict 6 month response to DBS (Broadway et al., 2012). Further physiological biomarkers reflect subcortical limbic changes in depression (Neumann et al., 2014). Each of these quantifiable changes could be assessed as potential biomarkers with respect to depression and validated as potentially relevant biomarkers.
Primary dystonia is an uncommon movement disorder (~16–17/100,000 population) characterized by abnormal, repetitive muscle contractions and postures (Steeves et al., 2012; Williams et al., 2017). DBS to improve motor features of focal and diffuse dystonia is FDA approved in the USA, though only as a humanitarian device approval due to the low numbers and decreased efficacy, which is equivalent to an orphan drug approval. Of the dystonias, focal dystonia (i.e., cervical dystonia or torticollis and writer's cramp are examples) is the most common, followed by genetic (i.e., DYT1) generalized dystonias (Williams et al., 2017). Unlike Parkinson's disease or tremor, the time course to onset with changes in stimulation in dystonia can take beyond seconds or minutes, usually taking weeks to months to reach full effect. The onset effect of brain stimulation in dystonia is difficult to predict, suggesting possible plasticity or synaptic changes associated with stimulation, leading to slow improvement in symptoms. However, Barow detected suppression of low frequency pallidal activity during treatment of phasic, dystonic movements, and this may improve our understanding of this slow time to onset as a possible biomarker (Barow et al., 2014). The slow dynamic effect also creates difficulties with developing an adaptive or closed-loop system due to unpredictable timing and might suggest only very slow (weeks to months) adjustments (Wang et al., 2016). However, there are several studies analyzing the differences in subcortical recorded potentials between Parkinson's disease and dystonia, both as initial evidence to discover how the circuit changes underlying these diseases differ and to develop biomarkers of dystonia (Silberstein et al., 2003; Neumann et al., 2015; Wang et al., 2016). For example, Wang et al. found no difference in biomarkers between the two diseases (Wang et al., 2016) whereas Geng et al. suggested more specificity (Geng et al., 2017), indicating that biomarkers may in some instances be useful disease indicators.
As a predicted future health burden without good current treatment, Alzheimer's Disease (AD) may theoretically respond to brain stimulation (Hardenacke et al., 2013b; Hescham et al., 2013; Sharma et al., 2015). Novel techniques, such as DBS of the fornix were developed as an offshoot of hypothalamic stimulation when it was noted that fornix stimulation resulted in improved recall (Laxton et al., 2010). It should be noted that possible loss of functional integrity of the fornix in AD may limit the effectiveness of fornix stimulation (Mielke et al., 2012). However, it is difficult to test the efficacy of DBS applied to fornix stimulation intraoperatively so biomarkers may be very helpful to confirm appropriate electrode location as well as to set DBS parameters.
Although fornix stimulation in clinical trials has shown limited clinical efficacy (Ponce et al., 2015; Lozano et al., 2016) the downstream effects of stimulation of the post-commissural fornix (below the anterior commissure) on the mammillary bodies remain unknown. The post-commissural fornix antidromically stimulates the subiculum, since this is the main hippocampal output, resulting in a large hippocampal evoked potentials (Stypulkowski et al., 2014; Sweet et al., 2014). This evoked potential (as recorded from the hippocampus) could provide an excellent biomarker both to adjust fornix stimulation amplitude (currently empirically determined) and to estimate if there is indeed plasticity resulting following a period of fornix stimulation, possibly leading to an on-demand fornix stimulation system to maintain hippocampal evoked responses within a set, optimal range. Although the current clinical application of fornix stimulation does not include the medial septum (just in front of the anterior commissure), additional stimulation of the medial septum could facilitate memory and hippocampal vascular changes through cholinergic enhancement, also resulting in an evoked response within the hippocampus proper (Colgin et al., 2003; Gu and Yakel, 2011). Further, DBS of the nucleus basalis of Meynert, the primary cholinergic region for the cortex, may diffusely enhance cholinergic function and also improve AD, without direct fornix stimulation (Hardenacke et al., 2013a; Sharma et al., 2015). A cholinergic sensory or biomarker within the brain may be required to measure effectively such cholinergic enhancement and to create a dose-response curve. Thus, there are a number of clinical avenues which may enhanced the potential treatment possibilities of brain stimulation for AD.
Identifying and verifying the usefulness of biomarkers for accurate electrode placement and creating more effective adaptive brain stimulation systems will require considerable additional development, and is clearly subject to significant research and initial clinical trials. Methods for optimal electrode localization and verification of both symptom suppression and physiological efficacy are clearly needed, likely through modulation of appropriate neural networks. Placing stimulating electrodes into defined anatomical targets in the operating room without symptom suppression or intraoperative clinical testing will require better imaging with emphasis on pre-operative tractography and functional MRI as well as use of biomarkers during surgery, as they are developed and validated. Understanding pathophysiology and structural connectivity in individual disease processes will elucidate key pathways and, subsequently, the hubs of electrical activity for optimal sites of stimulation. Spontaneous and evoked potentials, phase-amplitude coupling, and other electrophysiological measures can provide intraoperative data beyond imaging to place leads in locations correlated with more reliable outcomes. Possible neurochemical or other markers may also act as biomarkers to join imaging and electrophysiological measures as suitable signals for stimulation optimization. As external, wearable devices become more widespread and available, further data on motion and tremor may also eventually be included in adaptive control on a long-term basis if these data can be communicated effectively to an internal device (Roy et al., 2013; Shull et al., 2014; Lieber et al., 2015). Further development in this area has the potential to alter significantly our understanding of the underlying circuitry and pathophysiology of neurologic disease, as well as optimize treatment approaches.
KH, IC, WG, and DT wrote this manuscript collectively, with KH contributing the initial draft and subsequent significant editing by all of the authors. All contributed to the ideas contained within the manuscript and all contributed at least one major section. All authors have reviewed and edited this final version.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
This work was supported by NIH R01 NS079312, NIH R37 NS040984, and NIH UH3 NS103468.
DBS, deep brain stimulation; VNS, vagal nerve stimulation; TBI, traumatic brain injury; aDBS, adaptive DBS; IPG, internal pulse generator; EEG, electroencephalogram; ECoG, electrocorticography; EMG, electromyogram; PAC, phase amplitude coupling; ECAP, evoked compound action potential; LFP, local field potential; MRI, magnetic resonance imaging; CT, computed tomography; BCI/BMI, brain computer/machine interface; GPi, globus pallidus internus; SNr, substantia nigra pars reticulata; STN, subthalamic nucleus; PPN, pedunculopontine nucleus; Vim, ventral intermediate nucleus of the thalamus; SCC, subcallosal cingulate; ANT, anterior nucleus of the thalamus; PD, Parkinson's disease; AD, Alzheimer's disease; TS, Tourette syndrome; TRD, treatment resistant depression; ADHD, attention deficit hyperactivity disorder; OCD, obsessive-compulsive disorder; FOG, freezing of gait.
Afshar, P., Khambhati, A., Stanslaski, S., Carlson, D., Jensen, R., Linde, D., et al. (2012). A translational platform for prototyping closed-loop neuromodulation systems. Front. Neural Circuits 6:117. doi: 10.3389/fncir.2012.00117
Almeida, L., Martinez-Ramirez, D., Rossi, P. J., Peng, Z., Gunduz, A., and Okun, M. S. (2015). Chasing tics in the human brain: development of open, scheduled and closed loop responsive approaches to deep brain stimulation for tourette syndrome. J. Clin. Neurol. 11, 122–131. doi: 10.3988/jcn.2015.11.2.122
Aminoff, M. J., Christine, C. W., Friedman, J. H., Chou, K. L., Lyons, K. E., Pahwa, R., et al. (2011). Management of the hospitalized patient with Parkinson's disease: current state of the field and need for guidelines. Parkinsonism Relat. Disord. 17, 139–145. doi: 10.1016/j.parkreldis.2010.11.009
Anderson, C. J., Sheppard, D. T., Huynh, R., Anderson, D. N., Polar, C. A., and Dorval, A. D. (2015). Subthalamic deep brain stimulation reduces pathological information transmission to the thalamus in a rat model of parkinsonism. Front. Neural Circuits 9:31. doi: 10.3389/fncir.2015.00031
Bar-Gad, I., Elias, S., Vaadia, E., and Bergman, H. (2004). Complex locking rather than complete cessation of neuronal activity in the globus pallidus of a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-treated primate in response to pallidal microstimulation. J. Neurosci. 24, 7410–7419. doi: 10.1523/JNEUROSCI.1691-04.2004
Barow, E., Neumann, W. J., Brucke, C., Huebl, J., Horn, A., Brown, P., et al. (2014). Deep brain stimulation suppresses pallidal low frequency activity in patients with phasic dystonic movements. Brain 137, 3012–3024. doi: 10.1093/brain/awu258
Basu, I., Graupe, D., Tuninetti, D., Shukla, P., Slavin, K. V., Metman, L. V., et al. (2013). Pathological tremor prediction using surface electromyogram and acceleration: potential use in 'ON-OFF' demand driven deep brain stimulator design. J. Neural Eng. 10:036019. doi: 10.1088/1741-2560/10/3/036019
Benabid, A. L., Chabardes, S., Mitrofanis, J., and Pollak, P. (2009). Deep brain stimulation of the subthalamic nucleus for the treatment of Parkinson's disease. Lancet Neurol. 8, 67–81. doi: 10.1016/S1474-4422(08)70291-6
Bernstein, J. G., Garrity, P. A., and Boyden, E. S. (2012). Optogenetics and thermogenetics: technologies for controlling the activity of targeted cells within intact neural circuits. Curr. Opin. Neurobiol. 22, 61–71. doi: 10.1016/j.conb.2011.10.023
Blumenfeld, Z., Koop, M. M., Prieto, T. E., Shreve, L. A., Velisar, A., Quinn, E. J., et al. (2017). Sixty-hertz stimulation improves bradykinesia and amplifies subthalamic low-frequency oscillations. Mov. Disord. 32, 80–88. doi: 10.1002/mds.26837
Broadway, J. M., Holtzheimer, P. E., Hilimire, M. R., Parks, N. A., Devylder, J. E., Mayberg, H. S., et al. (2012). Frontal theta cordance predicts 6-month antidepressant response to subcallosal cingulate deep brain stimulation for treatment-resistant depression: a pilot study. Neuropsychopharmacology 37, 1764–1772. doi: 10.1038/npp.2012.23
Brocker, D. T., Swan, B. D., So, R. Q., Turner, D. A., Gross, R. E., and Grill, W. M. (2017). Optimized temporal pattern of brain stimulation designed by computational evolution. Sci. Transl. Med. 9:eaah3532. doi: 10.1126/scitranslmed.aah3532
Brocker, D. T., Swan, B. D., Turner, D. A., Gross, R. E., Tatter, S. B., Koop, M. M., et al. (2013). Improved efficacy of temporally non-regular deep brain stimulation in Parkinson's disease. Exp. Neurol. 239, 60–67. doi: 10.1016/j.expneurol.2012.09.008
Butson, C. R., Cooper, S. E., Henderson, J. M., and Mcintyre, C. C. (2007). Patient-specific analysis of the volume of tissue activated during deep brain stimulation. Neuroimage 34, 661–670. doi: 10.1016/j.neuroimage.2006.09.034
Butson, C. R., Cooper, S. E., Henderson, J. M., Wolgamuth, B., and Mcintyre, C. C. (2011). Probabilistic analysis of activation volumes generated during deep brain stimulation. Neuroimage 54, 2096–2104. doi: 10.1016/j.neuroimage.2010.10.059
Cagnan, H., Pedrosa, D., Little, S., Pogosyan, A., Cheeran, B., Aziz, T., et al. (2017). Stimulating at the right time: phase-specific deep brain stimulation. Brain 140, 132–145. doi: 10.1093/brain/aww286
Canolty, R. T., Edwards, E., Dalal, S. S., Soltani, M., Nagarajan, S. S., Kirsch, H. E., et al. (2006). High gamma power is phase-locked to theta oscillations in human neocortex. Science 313, 1626–1628. doi: 10.1126/science.1128115
Carlson, D., Linde, D., Isaacson, B., Afshar, P., Bourget, D., Stanslaski, S., et al. (2013). A flexible algorithm framework for closed-loop neuromodulation research systems. Conf. Proc. IEEE Eng. Med. Biol. Soc. 2013, 6146–6150. doi: 10.1109/EMBC.2013.6610956
Chenji, G., Wright, M. L., Chou, K. L., Seidler, R. D., and Patil, P. G. (2017). Parkinsonian gait improves with bilateral subthalamic nucleus deep brain stimulation during cognitive multi-tasking. Parkinsonism Relat. Disord. 38, 72–79. doi: 10.1016/j.parkreldis.2017.02.028
Contarino, M. F., Bour, L. J., Verhagen, R., Lourens, M. A., De Bie, R. M., Van Den Munckhof, P., et al. (2014). Directional steering: a novel approach to deep brain stimulation. Neurology 83, 1163–1169. doi: 10.1212/WNL.0000000000000823
Cook, R. J., Jones, L., Fracchia, G., Anderson, N., Miu, J., Meagher, L. J., et al. (2015). Globus pallidus internus deep brain stimulation as rescue therapy for refractory dyskinesias following effective subthalamic nucleus stimulation. Stereotact. Funct. Neurosurg. 93, 25–29. doi: 10.1159/000365223
Crowell, A. L., Garlow, S. J., Riva-Posse, P., and Mayberg, H. S. (2015). Characterizing the therapeutic response to deep brain stimulation for treatment-resistant depression: a single center long-term perspective. Front. Integr. Neurosci. 9:41. doi: 10.3389/fnint.2015.00041
De Hemptinne, C., Ryapolova-Webb, E. S., Air, E. L., Garcia, P. A., Miller, K. J., Ojemann, J. G., et al. (2013). Exaggerated phase-amplitude coupling in the primary motor cortex in Parkinson disease. Proc. Natl. Acad. Sci. U.S.A. 110, 4780–4785. doi: 10.1073/pnas.1214546110
De Hemptinne, C., Swann, N. C., Ostrem, J. L., Ryapolova-Webb, E. S., San Luciano, M., Galifianakis, N. B., et al. (2015). Therapeutic deep brain stimulation reduces cortical phase-amplitude coupling in Parkinson's disease. Nat. Neurosci. 18, 779–786. doi: 10.1038/nn.3997
Dorval, A. D., and Grill, W. M. (2014). Deep brain stimulation of the subthalamic nucleus reestablishes neuronal information transmission in the 6-OHDA rat model of parkinsonism. J. Neurophysiol. 111, 1949–1959. doi: 10.1152/jn.00713.2013
Dorval, A. D., Kuncel, A. M., Birdno, M. J., Turner, D. A., and Grill, W. M. (2010). Deep brain stimulation alleviates parkinsonian bradykinesia by regularizing pallidal activity. J. Neurophysiol. 104, 911–921. doi: 10.1152/jn.00103.2010
Dorval, A. D., Muralidharan, A., Jensen, A. L., Baker, K. B., and Vitek, J. L. (2015). Information in pallidal neurons increases with parkinsonian severity. Parkinsonism Relat. Disord. 21, 1355–1361. doi: 10.1016/j.parkreldis.2015.09.045
Dorval, A. D., Russo, G. S., Hashimoto, T., Xu, W., Grill, W. M., and Vitek, J. L. (2008). Deep brain stimulation reduces neuronal entropy in the MPTP-primate model of Parkinson's disease. J. Neurophysiol. 100, 2807–2818. doi: 10.1152/jn.90763.2008
Dougherty, D. D., Rezai, A. R., Carpenter, L. L., Howland, R. H., Bhati, M. T., O'reardon, J. P., et al. (2015). A randomized sham-controlled trial of deep brain stimulation of the ventral capsule/ventral striatum for chronic treatment-resistant depression. Biol. Psychiatry 78, 240–248. doi: 10.1016/j.biopsych.2014.11.023
Ekker, M. S., Janssen, S., Nonnekes, J., Bloem, B. R., and De Vries, N. M. (2016). Neurorehabilitation for Parkinson's disease: future perspectives for behavioural adaptation. Parkinsonism Relat. Disord. 22(Suppl. 1), S73–S77. doi: 10.1016/j.parkreldis.2015.08.031
Foote, K. D., and Okun, M. S. (2005). Ventralis intermedius plus ventralis oralis anterior and posterior deep brain stimulation for posttraumatic Holmes tremor: two leads may be better than one: technical note. Neurosurgery 56, E445; discussion E445. doi: 10.1227/01.NEU.0000157104.87448.78
Fox, M. D., Buckner, R. L., Liu, H., Chakravarty, M. M., Lozano, A. M., and Pascual-Leone, A. (2014). Resting-state networks link invasive and noninvasive brain stimulation across diverse psychiatric and neurological diseases. Proc. Natl. Acad. Sci. U.S.A. 111, E4367–E4375. doi: 10.1073/pnas.1405003111
Gallay, M. N., Jeanmonod, D., Liu, J., and Morel, A. (2008). Human pallidothalamic and cerebellothalamic tracts: anatomical basis for functional stereotactic neurosurgery. Brain Struct. Funct. 212, 443–463. doi: 10.1007/s00429-007-0170-0
Geng, X., Zhang, J., Jiang, Y., Ashkan, K., Foltynie, T., Limousin, P., et al. (2017). Comparison of oscillatory activity in subthalamic nucleus in Parkinson's disease and dystonia. Neurobiol. Dis. 98, 100–107. doi: 10.1016/j.nbd.2016.12.006
Gilbert, D. L., Bansal, A. S., Sethuraman, G., Sallee, F. R., Zhang, J., Lipps, T., et al. (2004). Association of cortical disinhibition with tic, ADHD, and OCD severity in Tourette syndrome. Mov. Disord. 19, 416–425. doi: 10.1002/mds.20044
Gmel, G. E., Hamilton, T. J., Obradovic, M., Gorman, R. B., Single, P. S., Chenery, H. J., et al. (2015). A new biomarker for subthalamic deep brain stimulation for patients with advanced Parkinson's disease–a pilot study. J. Neural Eng. 12:066013. doi: 10.1088/1741-2560/12/6/066013
Grahn, P. J., Mallory, G. W., Khurram, O. U., Berry, B. M., Hachmann, J. T., Bieber, A. J., et al. (2014). A neurochemical closed-loop controller for deep brain stimulation: toward individualized smart neuromodulation therapies. Front. Neurosci. 8:169. doi: 10.3389/fnins.2014.00169
Graupe, D., Basu, I., Tuninetti, D., Vannemreddy, P., and Slavin, K. V. (2010). Adaptively controlling deep brain stimulation in essential tremor patient via surface electromyography. Neurol. Res. 32, 899–904. doi: 10.1179/016164110X12767786356354
Grill, W. M., Brocker, D. T., Swan, B. D., Kent, A. R., Turner, D. A., and Hickey, P. T. (2015). Local Evoked Potentials Recorded during Subthalamic Nuceleus Deep Brain Stimulation in Humans with Parkinson's Disease. Chicago, IL: Society for Neuroscience.
Haense, C., Muller-Vahl, K. R., Wilke, F., Schrader, C., Capelle, H. H., Geworski, L., et al. (2016). Effect of deep brain stimulation on regional cerebral blood flow in patients with medically refractory tourette syndrome. Front. Psychiatry. 7:118. doi: 10.3389/fpsyt.2016.00118
Hamani, C., Mayberg, H., Snyder, B., Giacobbe, P., Kennedy, S., and Lozano, A. M. (2009). Deep brain stimulation of the subcallosal cingulate gyrus for depression: anatomical location of active contacts in clinical responders and a suggested guideline for targeting. J. Neurosurg. 111, 1209–1215. doi: 10.3171/2008.10.JNS08763
Hanson, T. L., Fuller, A. M., Lebedev, M. A., Turner, D. A., and Nicolelis, M. A. (2012). Subcortical neuronal ensembles: an analysis of motor task association, tremor, oscillations, and synchrony in human patients. J. Neurosci. 32, 8620–8632. doi: 10.1523/JNEUROSCI.0750-12.2012
Hardenacke, K., Kuhn, J., Lenartz, D., Maarouf, M., Mai, J. K., Bartsch, C., et al. (2013a). Stimulate or degenerate: deep brain stimulation of the nucleus basalis Meynert in Alzheimer dementia. World Neurosurg. 80, S27.e35–S27.e43. doi: 10.1016/j.wneu.2012.12.005
Hardenacke, K., Shubina, E., Buhrle, C. P., Zapf, A., Lenartz, D., Klosterkotter, J., et al. (2013b). Deep brain stimulation as a tool for improving cognitive functioning in Alzheimer's dementia: a systematic review. Front. Psychiatry 4:159. doi: 10.3389/fpsyt.2013.00159
Hartmann, C. J., Lujan, J. L., Chaturvedi, A., Goodman, W. K., Okun, M. S., Mcintyre, C. C., et al. (2015). Tractography activation patterns in dorsolateral prefrontal cortex suggest better clinical responses in OCD DBS. Front. Neurosci. 9:519. doi: 10.3389/fnins.2015.00519
Heldman, D. A., Pulliam, C. L., Urrea Mendoza, E., Gartner, M., Giuffrida, J. P., Montgomery, E. B. Jr., et al. (2016). Computer-guided deep brain stimulation programming for parkinson's disease. Neuromodulation 19, 127–132. doi: 10.1111/ner.12372
Henderson, J. M. (2012). “Connectomic surgery”: diffusion tensor imaging (DTI) tractography as a targeting modality for surgical modulation of neural networks. Front. Integr. Neurosci. 6:15. doi: 10.3389/fnint.2012.00015
Henderson, J. M., Pell, M., O'sullivan, D. J., Mccusker, E. A., Fung, V. S., Hedges, P., et al. (2002). Postmortem analysis of bilateral subthalamic electrode implants in Parkinson's disease. Mov. Disord. 17, 133–137. doi: 10.1002/mds.1261
Herron, J. A., Thompson, M. C., Brown, T., Chizeck, H. J., Ojemann, J. G., and Ko, A. L. (2017). Chronic electrocorticography for sensing movement intention and closed-loop deep brain stimulation with wearable sensors in an essential tremor patient. J. Neurosurg. 127, 580–587. doi: 10.3171/2016.8.JNS16536
Hescham, S., Lim, L. W., Jahanshahi, A., Steinbusch, H. W., Prickaerts, J., Blokland, A., et al. (2013). Deep brain stimulation of the forniceal area enhances memory functions in experimental dementia: the role of stimulation parameters. Brain Stimul. 6, 72–77. doi: 10.1016/j.brs.2012.01.008
Hill, K. K., Campbell, M. C., Mcneely, M. E., Karimi, M., Ushe, M., Tabbal, S. D., et al. (2013). Cerebral blood flow responses to dorsal and ventral STN DBS correlate with gait and balance responses in Parkinson's disease. Exp. Neurol. 241, 105–112. doi: 10.1016/j.expneurol.2012.12.003
Holtzheimer, P. E., Kelley, M. E., Gross, R. E., Filkowski, M. M., Garlow, S. J., Barrocas, A., et al. (2012). Subcallosal cingulate deep brain stimulation for treatment-resistant unipolar and bipolar depression. Arch. Gen. Psychiatry 69, 150–158. doi: 10.1001/archgenpsychiatry.2011.1456
Horn, A., Reich, M., Vorwerk, J., Li, N., Wenzel, G., Fang, Q., et al. (2017). Connectivity Predicts deep brain stimulation outcome in Parkinson disease. Ann. Neurol. 82, 67–78. doi: 10.1002/ana.24974
Kent, A. R., and Grill, W. M. (2012). Recording evoked potentials during deep brain stimulation: development and validation of instrumentation to suppress the stimulus artefact. J. Neural Eng. 9:036004. doi: 10.1088/1741-2560/9/3/036004
Kent, A. R., Swan, B. D., Brocker, D. T., Turner, D. A., Gross, R. E., and Grill, W. M. (2015). Measurement of evoked potentials during thalamic deep brain stimulation. Brain Stimul. 8, 42–56. doi: 10.1016/j.brs.2014.09.017
Khobragade, N., Graupe, D., and Tuninetti, D. (2015). Towards fully automated closed-loop Deep Brain Stimulation in Parkinson's disease patients: a LAMSTAR-based tremor predictor. Conf. Proc. IEEE Eng. Med. Biol. Soc. 2015, 2616–2619. doi: 10.1109/EMBC.2015.7318928
Kuhn, A. A., Kupsch, A., Schneider, G. H., and Brown, P. (2006). Reduction in subthalamic 8-35 Hz oscillatory activity correlates with clinical improvement in Parkinson's disease. Eur. J. Neurosci. 23, 1956–1960. doi: 10.1111/j.1460-9568.2006.04717.x
Kuhn, A. A., Tsui, A., Aziz, T., Ray, N., Brucke, C., Kupsch, A., et al. (2009). Pathological synchronisation in the subthalamic nucleus of patients with Parkinson's disease relates to both bradykinesia and rigidity. Exp. Neurol. 215, 380–387. doi: 10.1016/j.expneurol.2008.11.008
Laxton, A. W., Tang-Wai, D. F., Mcandrews, M. P., Zumsteg, D., Wennberg, R., Keren, R., et al. (2010). A phase I trial of deep brain stimulation of memory circuits in Alzheimer's disease. Ann. Neurol. 68, 521–534. doi: 10.1002/ana.22089
Leuthardt, E. C., Schalk, G., Moran, D., and Ojemann, J. G. (2006). The emerging world of motor neuroprosthetics: a neurosurgical perspective. Neurosurgery 59, 1–14. discussion 1-14. doi: 10.1227/01.NEU.0000221506.06947.AC
Lieber, B., Taylor, B. E., Appelboom, G., Mckhann, G., and Connolly, E. S. Jr. (2015). Motion sensors to assess and monitor medical and surgical management of parkinson disease. World Neurosurg. 84, 561–566. doi: 10.1016/j.wneu.2015.03.024
Little, S., Beudel, M., Zrinzo, L., Foltynie, T., Limousin, P., Hariz, M., et al. (2016a). Bilateral adaptive deep brain stimulation is effective in Parkinson's disease. J. Neurol. Neurosurg. Psychiatr. 87, 717–721. doi: 10.1136/jnnp-2015-310972
Little, S., and Brown, P. (2012). What brain signals are suitable for feedback control of deep brain stimulation in Parkinson's disease? Ann. N. Y. Acad. Sci. 1265, 9–24. doi: 10.1111/j.1749-6632.2012.06650.x
Little, S., Tripoliti, E., Beudel, M., Pogosyan, A., Cagnan, H., Herz, D., et al. (2016b). Adaptive deep brain stimulation for Parkinson's disease demonstrates reduced speech side effects compared to conventional stimulation in the acute setting. J. Neurol. Neurosurg. Psychiatr. 87, 1388–1389. doi: 10.1136/jnnp-2016-313518
Lozano, A. M., Fosdick, L., Chakravarty, M. M., Leoutsakos, J. M., Munro, C., Oh, E., et al. (2016). A phase II study of fornix deep brain stimulation in mild Alzheimer's disease. J. Alzheimers. Dis. 54, 777–787. doi: 10.3233/JAD-160017
Lujan, J. L., Chaturvedi, A., Choi, K. S., Holtzheimer, P. E., Gross, R. E., Mayberg, H. S., et al. (2013). Tractography-activation models applied to subcallosal cingulate deep brain stimulation. Brain Stimul. 6, 737–739. doi: 10.1016/j.brs.2013.03.008
Mackinnon, C. D., Webb, R. M., Silberstein, P., Tisch, S., Asselman, P., Limousin, P., et al. (2005). Stimulation through electrodes implanted near the subthalamic nucleus activates projections to motor areas of cerebral cortex in patients with Parkinson's disease. Eur. J. Neurosci. 21, 1394–1402. doi: 10.1111/j.1460-9568.2005.03952.x
Maling, N., Hashemiyoon, R., Foote, K. D., Okun, M. S., and Sanchez, J. C. (2012). Increased thalamic gamma band activity correlates with symptom relief following deep brain stimulation in humans with Tourette's syndrome. PLoS ONE 7:e44215. doi: 10.1371/annotation/446ec4cb-63da-42d2-afc6-7e8459b2abbe
Marsden, J., Limousin-Dowsey, P., Fraix, V., Pollak, P., Odin, P., and Brown, P. (2001). Intermuscular coherence in Parkinson's disease: effects of subthalamic nucleus stimulation. Neuroreport 12, 1113–1117. doi: 10.1097/00001756-200105080-00013
Martens, H. C., Toader, E., Decre, M. M., Anderson, D. J., Vetter, R., Kipke, D. R., et al. (2011). Spatial steering of deep brain stimulation volumes using a novel lead design. Clin. Neurophysiol. 122, 558–566. doi: 10.1016/j.clinph.2010.07.026
Matias, C. M., Silva, D., Machado, A. G., and Cooper, S. E. (2016). “Rescue” of bilateral subthalamic stimulation by bilateral pallidal stimulation: case report. J. Neurosurg. 124, 417–421. doi: 10.3171/2015.1.JNS141604
Mayberg, H. S., Brannan, S. K., Tekell, J. L., Silva, J. A., Mahurin, R. K., Mcginnis, S., et al. (2000). Regional metabolic effects of fluoxetine in major depression: serial changes and relationship to clinical response. Biol. Psychiatry 48, 830–843. doi: 10.1016/S0006-3223(00)01036-2
Mayberg, H. S., Lozano, A. M., Voon, V., Mcneely, H. E., Seminowicz, D., Hamani, C., et al. (2005). Deep brain stimulation for treatment-resistant depression. Neuron 45, 651–660. doi: 10.1016/j.neuron.2005.02.014
Meidahl, A. C., Tinkhauser, G., Herz, D. M., Cagnan, H., Debarros, J., and Brown, P. (2017). Adaptive deep brain stimulation for movement disorders: the long road to clinical therapy. Mov. Disord. 32, 810–819. doi: 10.1002/mds.27022
Mielke, M. M., Okonkwo, O. C., Oishi, K., Mori, S., Tighe, S., Miller, M. I., et al. (2012). Fornix integrity and hippocampal volume predict memory decline and progression to Alzheimer's disease. Alzheimers Dement. 8, 105–113. doi: 10.1016/j.jalz.2011.05.2416
Moran, A., Bergman, H., Israel, Z., and Bar-Gad, I. (2008). Subthalamic nucleus functional organization revealed by parkinsonian neuronal oscillations and synchrony. Brain 131, 3395–3409. doi: 10.1093/brain/awn270
Morita, H., Hass, C. J., Moro, E., Sudhyadhom, A., Kumar, R., and Okun, M. S. (2014). Pedunculopontine nucleus stimulation: where are we now and what needs to be done to move the field forward? Front. Neurol. 5:243. doi: 10.3389/fneur.2014.00243
Neumann, W. J., Huebl, J., Brucke, C., Gabriels, L., Bajbouj, M., Merkl, A., et al. (2014). Different patterns of local field potentials from limbic DBS targets in patients with major depressive and obsessive compulsive disorder. Mol. Psychiatry 19, 1186–1192. doi: 10.1038/mp.2014.2
Neumann, W. J., Jha, A., Bock, A., Huebl, J., Horn, A., Schneider, G. H., et al. (2015). Cortico-pallidal oscillatory connectivity in patients with dystonia. Brain 138, 1894–1906. doi: 10.1093/brain/awv109
Neumann, W. J., Staub, F., Horn, A., Schanda, J., Mueller, J., Schneider, G. H., et al. (2016). Deep brain recordings using an implanted pulse generator in Parkinson's disease. Neuromodulation 19, 20–24. doi: 10.1111/ner.12348
Noor, M. S., Murari, K., Mccracken, C. B., and Kiss, Z. H. (2016). Spatiotemporal dynamics of cortical perfusion in response to thalamic deep brain stimulation. Neuroimage 126, 131–139. doi: 10.1016/j.neuroimage.2015.11.017
Odekerken, V. J., Boel, J. A., Schmand, B. A., De Haan, R. J., Figee, M., Van Den Munckhof, P., et al. (2016). GPi vs. STN deep brain stimulation for Parkinson disease: three-year follow-up. Neurology 86, 755–761. doi: 10.1212/WNL.0000000000002401
Okun, M. S., Foote, K. D., Wu, S. S., Ward, H. E., Bowers, D., Rodriguez, R. L., et al. (2013). A trial of scheduled deep brain stimulation for Tourette syndrome: moving away from continuous deep brain stimulation paradigms. JAMA Neurol. 70, 85–94. doi: 10.1001/jamaneurol.2013.580
Oswal, A., Beudel, M., Zrinzo, L., Limousin, P., Hariz, M., Foltynie, T., et al. (2016). Deep brain stimulation modulates synchrony within spatially and spectrally distinct resting state networks in Parkinson's disease. Brain 139, 1482–1496. doi: 10.1093/brain/aww048
Ponce, F. A., Asaad, W., Foote, K. D., Anderson, W. S., Cosgrove, R., Baltuch, G. H., et al. (2015). 130 Bilateral fornix deep brain stimulation for alzheimer disease: surgical safety in the advance trial. Neurosurgery 62(Suppl. 1), 207. doi: 10.1227/01.neu.0000467092.68817.3e
Priori, A., Foffani, G., Rossi, L., and Marceglia, S. (2013a). Adaptive deep brain stimulation (aDBS) controlled by local field potential oscillations. Exp. Neurol. 245, 77–86. doi: 10.1016/j.expneurol.2012.09.013
Priori, A., Giannicola, G., Rosa, M., Marceglia, S., Servello, D., Sassi, M., et al. (2013b). Deep brain electrophysiological recordings provide clues to the pathophysiology of Tourette syndrome. Neurosci. Biobehav. Rev. 37, 1063–1068. doi: 10.1016/j.neubiorev.2013.01.011
Quinn, E. J., Blumenfeld, Z., Velisar, A., Koop, M. M., Shreve, L. A., Trager, M. H., et al. (2015). Beta oscillations in freely moving Parkinson's subjects are attenuated during deep brain stimulation. Mov. Disord. 30, 1750–1758. doi: 10.1002/mds.26376
Riva-Posse, P., Choi, K. S., Holtzheimer, P. E., Mcintyre, C. C., Gross, R. E., Chaturvedi, A., et al. (2014). Defining critical white matter pathways mediating successful subcallosal cingulate deep brain stimulation for treatment-resistant depression. Biol. Psychiatry 76, 963–969. doi: 10.1016/j.biopsych.2014.03.029
Rosa, M., Arlotti, M., Ardolino, G., Cogiamanian, F., Marceglia, S., Di Fonzo, A., et al. (2015). Adaptive deep brain stimulation in a freely moving Parkinsonian patient. Mov. Disord. 30, 1003–1005. doi: 10.1002/mds.26241
Rouse, A. G., Stanslaski, S. R., Cong, P., Jensen, R. M., Afshar, P., Ullestad, D., et al. (2011). A chronic generalized bi-directional brain-machine interface. J. Neural Eng. 8:036018. doi: 10.1088/1741-2560/8/3/036018
Roy, S. H., Cole, B. T., Gilmore, L. D., De Luca, C. J., Thomas, C. A., Saint-Hilaire, M. M., et al. (2013). High-resolution tracking of motor disorders in Parkinson's disease during unconstrained activity. Mov. Disord. 28, 1080–1087. doi: 10.1002/mds.25391
Salanova, V., Witt, T., Worth, R., Henry, T. R., Gross, R. E., Nazzaro, J. M., et al. (2015). Long-term efficacy and safety of thalamic stimulation for drug-resistant partial epilepsy. Neurology 84, 1017–1025. doi: 10.1212/WNL.0000000000001334
Santaniello, S., Fiengo, G., Glielmo, L., and Grill, W. M. (2011). Closed-loop control of deep brain stimulation: a simulation study. IEEE Trans. Neural Syst. Rehabil. Eng. 19, 15–24. doi: 10.1109/TNSRE.2010.2081377
Schlaepfer, T. E., Bewernick, B. H., Kayser, S., Madler, B., and Coenen, V. A. (2013). Rapid effects of deep brain stimulation for treatment-resistant major depression. Biol. Psychiatry 73, 1204–1212. doi: 10.1016/j.biopsych.2013.01.034
Schlenstedt, C., Shalash, A., Muthuraman, M., Falk, D., Witt, K., and Deuschl, G. (2017). Effect of high-frequency subthalamic neurostimulation on gait and freezing of gait in Parkinson's disease: a systematic review and meta-analysis. Eur. J. Neurol. 24, 18–26. doi: 10.1111/ene.13167
Seminowicz, D. A., Mayberg, H. S., Mcintosh, A. R., Goldapple, K., Kennedy, S., Segal, Z., et al. (2004). Limbic-frontal circuitry in major depression: a path modeling metanalysis. Neuroimage 22, 409–418. doi: 10.1016/j.neuroimage.2004.01.015
Sharma, M., Deogaonkar, M., and Rezai, A. (2015). Assessment of potential targets for deep brain stimulation in patients with Alzheimer's disease. J. Clin. Med. Res. 7, 501–505. doi: 10.14740/jocmr2127w
Shukla, P., Basu, I., Graupe, D., Tuninetti, D., and Slavin, K. V. (2012). A neural network-based design of an on-off adaptive control for Deep Brain Stimulation in movement disorders. Conf. Proc. IEEE Eng. Med. Biol. Soc. 2012, 4140–4143. doi: 10.1109/EMBC.2012.6346878
Shull, P. B., Jirattigalachote, W., Hunt, M. A., Cutkosky, M. R., and Delp, S. L. (2014). Quantified self and human movement: a review on the clinical impact of wearable sensing and feedback for gait analysis and intervention. Gait Posture 40, 11–19. doi: 10.1016/j.gaitpost.2014.03.189
Silberstein, P., Kuhn, A. A., Kupsch, A., Trottenberg, T., Krauss, J. K., Wohrle, J. C., et al. (2003). Patterning of globus pallidus local field potentials differs between Parkinson's disease and dystonia. Brain 126, 2597–2608. doi: 10.1093/brain/awg267
Sriram, A., Foote, K. D., Oyama, G., Kwak, J., Zeilman, P. R., and Okun, M. S. (2014). Brittle dyskinesia following STN but not GPi deep brain stimulation. Tremor Other Hyperkinet. Mov. (N. Y). 4, 242. doi: 10.7916/D8KS6PPR
Stanslaski, S., Afshar, P., Cong, P., Giftakis, J., Stypulkowski, P., Carlson, D., et al. (2012). Design and validation of a fully implantable, chronic, closed-loop neuromodulation device with concurrent sensing and stimulation. IEEE Trans. Neural Syst. Rehabil. Eng. 20, 410–421. doi: 10.1109/TNSRE.2012.2183617
Steeves, T. D., Day, L., Dykeman, J., Jette, N., and Pringsheim, T. (2012). The prevalence of primary dystonia: a systematic review and meta-analysis. Mov. Disord. 27, 1789–1796. doi: 10.1002/mds.25244
Steigerwald, F., Muller, L., Johannes, S., Matthies, C., and Volkmann, J. (2016). Directional deep brain stimulation of the subthalamic nucleus: a pilot study using a novel neurostimulation device. Mov. Disord. 31, 1240–1243. doi: 10.1002/mds.26669
Steiner, L. A., Neumann, W. J., Staub-Bartelt, F., Herz, D. M., Tan, H., Pogosyan, A., et al. (2017). Subthalamic beta dynamics mirror Parkinsonian bradykinesia months after neurostimulator implantation. Mov. Disord. doi: 10.1002/mds.27068
Stypulkowski, P. H., Stanslaski, S. R., Denison, T. J., and Giftakis, J. E. (2013). Chronic evaluation of a clinical system for deep brain stimulation and recording of neural network activity. Stereotact. Funct. Neurosurg. 91, 220–232. doi: 10.1159/000345493
Stypulkowski, P. H., Stanslaski, S. R., Jensen, R. M., Denison, T. J., and Giftakis, J. E. (2014). Brain stimulation for epilepsy–local and remote modulation of network excitability. Brain Stimul. 7, 350–358. doi: 10.1016/j.brs.2014.02.002
Swann, N. C., De Hemptinne, C., Miocinovic, S., Qasim, S., Wang, S. S., Ziman, N., et al. (2016). Gamma oscillations in the hyperkinetic state detected with chronic human brain recordings in parkinson's disease. J. Neurosci. 36, 6445–6458. doi: 10.1523/JNEUROSCI.1128-16.2016
Sweet, J. A., Eakin, K. C., Munyon, C. N., and Miller, J. P. (2014). Improved learning and memory with theta-burst stimulation of the fornix in rat model of traumatic brain injury. Hippocampus 24, 1592–1600. doi: 10.1002/hipo.22338
Tinkhauser, G., Pogosyan, A., Little, S., Beudel, M., Herz, D. M., Tan, H., et al. (2017). The modulatory effect of adaptive deep brain stimulation on beta bursts in Parkinson's disease. Brain 140, 1053–1067. doi: 10.1093/brain/awx010
Trager, M. H., Koop, M. M., Velisar, A., Blumenfeld, Z., Nikolau, J. S., Quinn, E. J., et al. (2016). Subthalamic beta oscillations are attenuated after withdrawal of chronic high frequency neurostimulation in Parkinson's disease. Neurobiol. Dis. 96, 22–30. doi: 10.1016/j.nbd.2016.08.003
Vandewalle, V., Van Der Linden, C., Groenewegen, H. J., and Caemaert, J. (1999). Stereotactic treatment of Gilles de la Tourette syndrome by high frequency stimulation of thalamus. Lancet 353, 724. doi: 10.1016/S0140-6736(98)05964-9
Vansteensel, M. J., Pels, E. G., Bleichner, M. G., Branco, M. P., Denison, T., Freudenburg, Z. V., et al. (2016). Fully Implanted Brain-Computer Interface in a Locked-In Patient with ALS. N. Engl. J. Med. 375, 2060–2066. doi: 10.1056/NEJMoa1608085
Volkmann, J., Chabardes, S., Steinke, G. K., and Carcieri, S. (2016). 375 DIRECT DBS: a prospective, multicenter clinical trial with blinding for a directional deep brain stimulation lead. Neurosurgery 63 (Suppl. 1), 211–212. doi: 10.1227/01.neu.0000489863.00935.ea
Waldau, B., Clayton, D. A., Gasperson, L. B., and Turner, D. A. (2011). Analysis of the time course of the effect of subthalamic nucleus stimulation upon hand function in Parkinson's patients. Stereotact. Funct. Neurosurg. 89, 48–55. doi: 10.1159/000323340
Wang, D. D., De Hemptinne, C., Miocinovic, S., Qasim, S. E., Miller, A. M., Ostrem, J. L., et al. (2016). Subthalamic local field potentials in Parkinson's disease and isolated dystonia: an evaluation of potential biomarkers. Neurobiol. Dis. 89, 213–222. doi: 10.1016/j.nbd.2016.02.015
Weinberger, M., Mahant, N., Hutchison, W. D., Lozano, A. M., Moro, E., Hodaie, M., et al. (2006). Beta oscillatory activity in the subthalamic nucleus and its relation to dopaminergic response in Parkinson's disease. J. Neurophysiol. 96, 3248–3256. doi: 10.1152/jn.00697.2006
Whitmer, D., De Solages, C., Hill, B., Yu, H., Henderson, J. M., and Bronte-Stewart, H. (2012). High frequency deep brain stimulation attenuates subthalamic and cortical rhythms in Parkinson's disease. Front. Hum. Neurosci. 6:155. doi: 10.3389/fnhum.2012.00155
Widge, A. S., and Sahay, A. (2016). Closing the loop in deep brain stimulation for psychiatric disorders: lessons from motor neural prosthetics. Neuropsychopharmacology 41, 379–380. doi: 10.1038/npp.2015.241
Williams, L., Mcgovern, E., Kimmich, O., Molloy, A., Beiser, I., Butler, J. S., et al. (2017). Epidemiological, clinical and genetic aspects of adult onset isolated focal dystonia in Ireland. Eur. J. Neurol. 24, 73–81. doi: 10.1111/ene.13133
Wingeier, B., Tcheng, T., Koop, M. M., Hill, B. C., Heit, G., and Bronte-Stewart, H. M. (2006). Intra-operative STN DBS attenuates the prominent beta rhythm in the STN in Parkinson's disease. Exp. Neurol. 197, 244–251. doi: 10.1016/j.expneurol.2005.09.016
Yamamoto, T., Katayama, Y., Ushiba, J., Yoshino, H., Obuchi, T., Kobayashi, K., et al. (2013). On-demand control system for deep brain stimulation for treatment of intention tremor. Neuromodulation 16, 230–235; discussion 235. doi: 10.1111/j.1525-1403.2012.00521.x
Yanagisawa, T., Yamashita, O., Hirata, M., Kishima, H., Saitoh, Y., Goto, T., et al. (2012). Regulation of motor representation by phase-amplitude coupling in the sensorimotor cortex. J. Neurosci. 32, 15467–15475. doi: 10.1523/JNEUROSCI.2929-12.2012
Keywords: deep brain stimulation, epilepsy, Parkinson's disease, responsive brain stimulation, beta hypersynchrony, phase amplitude coupling, evoked field potentials, closed loop
Citation: Hoang KB, Cassar IR, Grill WM and Turner DA (2017) Biomarkers and Stimulation Algorithms for Adaptive Brain Stimulation. Front. Neurosci. 11:564. doi: 10.3389/fnins.2017.00564
Received: 16 August 2017; Accepted: 25 September 2017;
Published: 10 October 2017.
Edited by:Ioan Opris, Leonard M. Miller School of Medicine, United States
Reviewed by:Francesco Sammartino, The Ohio State University Columbus, United States
Martijn Beudel, University Medical Center Groningen, Netherlands
Simon J. Little, University College London, United Kingdom
Damian Marc Herz, University of Oxford, United Kingdom
Copyright © 2017 Hoang, Cassar, Grill and Turner. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Dennis A. Turner, firstname.lastname@example.org