Altered Directed Functional Connectivity of the Hippocampus in Mild Cognitive Impairment and Alzheimer’s Disease: A Resting-State fMRI Study

Introduction

Alzheimer’s disease (AD) is a common and progressive neurodegenerative disorder of the nervous system occurring in elderly individuals (Brookmeyer et al., 2007). AD is the most common form of dementia, which is characterized by memory impairment and cognitive function decline. Mild cognitive impairment (MCI) is generally considered an intermediate disease state between normal aging and AD and is characterized by significant cognitive impairment in the absence of dementia. MCI patients have a high risk of transitioning to AD. Previous studies have shown that approximately 10–15% of MCI patients per year progress to AD, whereas only 1–2% of cognitively normal aged people develop AD (Davatzikos, 2009). Dementia not only significantly affects the quality of life of elderly individuals but also entails heavy financial and psychological burdens for the family and society. Unlike AD, the irreversible pathophysiological changes in dementia can be delayed or prevented with early diagnosis and treatment. Therefore, it is crucial to develop accurate diagnostic methods and to study the pathological process underlying the transition from MCI to AD.

The hippocampus is generally considered one of the earliest affected brain regions in patients with AD (Braak and Braak, 1997). Various neuroimaging studies have demonstrated abnormal structure and function of the hippocampus in patients with AD and MCI. β-Amyloid abnormalities and tau pathology in the preclinical stages of AD initially appear in the hippocampus (Braak and Braak, 1991; Hanseeuw et al., 2016; Serra et al., 2018). Longitudinal studies have shown significant volume loss in the hippocampus during the progression of AD, and there is a direct relationship with cognitive decline (Everitt and Dunn, 2013; Joko et al., 2016). Altered functional connectivity (FC) of the hippocampus in patients with MCI and AD has attracted increasing attention from researchers. Wang et al. (2006) studied connectivity changes between the hippocampus and all other brain regions in AD patients and found disrupted FC between the hippocampus and a number of regions including the medial prefrontal cortex, ventral anterior cingulate cortex, right inferotemporal cortex, right superior and middle temporal gyrus, and posterior cingulate cortex. Kim et al. (2013) used structural and fMRI data to examine the aberrant patterns of FC between the hippocampus and the rest of the brain and discovered reduced FC between the hippocampus and precuneus in AD patients. Sohn et al. (2014) investigated FC between the hippocampus and several specific brain regions in amnestic MCI and AD patients using rs-fMRI data. Tahmasian et al. (2015) performed seed-based FC analyses of the hippocampus in subjects with MCI or AD and normal controls (NCs). The results indicated that the intrinsic connectivity between the hippocampus and precuneus was significantly reduced, and hippocampal glucose metabolism was increased in the patient groups. Sun et al. (2017) studied FC of the medial temporal brain regions in MCI, AD, and NC subjects and found a significant difference in FC between the bilateral perirhinal cortex and right hippocampus.

Functional connectivity only reflects the interactions between different brain regions, but effective connectivity is able to explore the direction and intensity of information flow in the interacting brain regions and offers a better understanding of the interaction patterns of different brain regions. Liu et al. (2012) investigated effective connectivity between resting state networks in AD patients and NCs and found that the interactions between resting-state networks in AD patients and NCs were different. Zhong et al. (2014) found differences in effective connectivity of the default mode network (DMN) between AD patients and NCs. The most common methods for studying effective connectivity include structural equation models (SEMs), dynamic causal modeling (DCM), and Granger causality analysis (GCA). The SEMs and DCM are based on theoretical assumptions and specify hypotheses in terms of different models or architectures (Bajaj et al., 2016). Unlike SEMs and DCM, GCA does not require theoretical assumptions about the existence and direction of influence between any two regions. The need for theoretical assumptions also means that SEMs and DCM may lead to erroneous conclusions due to any misspecification. Additionally, the models required for SEMs and DCM cannot represent networks with large numbers of nodes (Roebroeck et al., 2005; Zhao et al., 2016; Zhang et al., 2017), and GCA is sufficiently flexible to accommodate hemodynamic variability (Bressler and Seth, 2011).

Numerous studies have demonstrated the effectiveness of measuring the directed connectivity of fMRI time series with GCA (Liao et al., 2011; Wen et al., 2013; Liang et al., 2014; Khazaee et al., 2017). Liang et al. (2014) identified the patterns of effective connectivity among four important resting-state networks, i.e., the DMN, hippocampal–cortical memory network, frontoparietal control network, and dorsal attention network, via GCA in amnestic MCI patients. Those researchers found that the directed connections between areas in the four networks were significantly altered in aMCI patients compared with healthy controls. Khazaee et al. (2017) applied GCA to construct the whole-brain directed network with rs-fMRI data from MCI, AD, and NC subjects and subsequently performed a classification of the three groups using directed graph measures. An accuracy of 93.3% was eventually achieved. A large number of studies have shown that FC between the hippocampus and other brain regions was abnormal in MCI and AD patients, and these abnormalities might be associated with the pathology of MCI and AD. However, little research has examined the abnormal directed connectivity of the hippocampus in MCI and AD patients, and therefore, the alterations in the directed connectivity patterns of the hippocampus in MCI and AD patients are largely unknown.

In the current study, to identify the directed connectivity changes in the brain related to AD progression, we applied GCA to explore the resting-state-directed connectivity of the hippocampus in MCI and AD patients. We used the hippocampus as the seed region and detected directed FC between the hippocampus and other brain regions using voxel wise GCA.

Materials and Methods

Participants

All of the data used in this study were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database¹. The purpose of the ADNI is to study the pathogenesis and prevention of AD by analyzing a variety of types of medical imaging data. The rs-fMRI data of 29 patients with AD (average age = 72.33 years; 18 females), 65 patients with MCI (average age = 71.8 years; 29 females), and 30 NC subjects (average age = 74.18 years; 19 females) (Table 1) were analyzed in this study. All participants were right-handed and had no history of neurological or psychiatric disorders. The patients with AD had a Mini-Mental State Examination (MMSE) score of 14–26, a Clinical Dementia Rating (CDR) of 0.5 or 1.0 and met the National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer’s Disease and Related Disorders Association (NINCDS/ADRDA) criteria for probable AD. The MCI patients had MMSE scores of 23–30 and CDR scores of 0.5. The NC subjects were non-depressed, non-MCI, and non-demented and had MMSE scores of 24–30 and CDR scores of 0. To assess test–retest reliability, 19 patients with AD, 37 patients with MCI, and 19 NC subjects were scanned twice. The mean interval between two scans was 3 months.

TABLE 1

Table 1. Demographic and clinical data.

Data Acquisition and Preprocessing

All subjects underwent rs-fMRI in a 3T MR scanner (Siemens Trio 3-Tesla scanner, Siemens, Erlangen, Germany). During the scan, participants were asked to relax with their eyes closed but not to fall asleep (Jack et al., 2008). Each scan consisted of 140 contiguous EPI functional volumes with the scan parameters set as follows: slice number = 48, slice thickness = 3.3 mm, repetition time (TR) = 3,000 ms, echo time (TE) = 30 ms, field of view = 192 × 192 mm, matrix = 64 × 64 mm, and flip angle = 80°. Preprocessing of the rs-fMRI data was performed using the Data Processing Assistant for Resting-State fMRI (DPARSF) toolbox (Yan and Zang, 2010) and the SPM8 package². The preprocessing steps were applied as follows: the first 10 volumes of the time series data were discarded due to signal equilibrium and allow the participants to adapt to the scanning noise; slice timing was applied to compensate for the time difference between different slices in each volume; realignment for head movement compensation was applied using a six-parameter rigid-body spatial transformation; all images were normalized into the Montreal Neurological Institute (MNI) space; the resulting images were detrended to reduce the effects of low-frequency drift, smoothed using a Gaussian filter with FWHM = 4 mm, and bandpass filtered (0.01–0.08 Hz) to remove high frequency physiological noise; and finally, a Friston-24 parameter and parameters for the global mean signal, cerebrospinal fluid signal, and white matter signal were regressed out as nuisance covariates for the subsequent analysis (Kelly et al., 2008).

Definition of Seed Regions

In the rs-fMRI data analysis for each individual, the bilateral hippocampal ROIs were defined using free software in the rs-fMRI data analysis toolkit REST³. The ROIs were extracted from the Anatomical Automatic Labeling (AAL) template (Tzourio-Mazoyer et al., 2002). For each seed region, the BOLD time series of the voxels within the seed region were averaged to generate the reference time series for this seed region (Figure 1).

FIGURE 1

Figure 1. Regions of interest, including the left hippocampus and right hippocampus.

Directed Brain Functional Connectivity

Multivariate GCA was applied to each voxel in the whole brain to obtain the directed brain FC from the seed points to other voxels in the whole brain and the reverse impact intensities from other voxels in the whole brain to the seed points. The signed-path multivariate Granger causality coefficients of each pair of time series were calculated using REST-GCA software (Zang et al., 2012). The bivariate Granger causality of two time series X(t) and Y(t) can be formulated by a vector autoregressive model (Hamilton et al., 2009):

$$Y_t=\sum _{i=1}^p{A}_i{X}_{(t-i)}+\sum _{i=1}^p{B}_i{Y}_{(t-i)}+C{Z}_t+{\epsilon }_t(1)$$

$$X_t=\sum _{i=1}^p{A}_i^{\prime }{Y}_{(t-i)}+\sum _{i=1}^p{B}_i^{\prime }{X}_{t-i}+C^{\prime }{Z}_t+{\epsilon }_t^{\prime }(2)$$

where p is the model order, i.e., the maximum number of lagged samples, A′_i [formula (1)] and A_i [formula (2)] are the signed-path coefficients, B_i [formula (1)] and B′_i [formula (2)] are autoregression coefficients, ε_t [formula (1)] and ε′_t [formula (2)] are residuals, and Z_t represents the covariates (e.g., head motion, global trend, and time series from certain brain areas). The time series X_t significantly Granger-causes the time series Y_t if the signed-path coefficient A_i is significantly larger or smaller than zero, and vice versa, i.e., Y_t can be defined as a significant Granger-cause to X_t if the signed-path coefficient A′_i is significantly larger or smaller than zero. Multivariate Granger causality is a generalization of the above bivariate model by including more than two variables.

Statistical Analysis

Demographic and clinical data were analyzed using the Statistical Package for Social Sciences (SPSS 20.0) software. Continuous variables are presented as the means and standard deviations (SD). Categorical data are presented as numbers and percentages. Group differences in sex were assessed with a two-tailed Pearson chi-square test, and the remaining variables were tested using one-way analyses of variance (ANOVA) with group (NC, MCI, AD) as the between-subjects factor. All p-values of <0.05 were considered statistically significant.

The GCA FC maps were analyzed based on voxel wise comparisons across the whole brain, which was accomplished using the Statistical Analysis function in the REST software. The calculated intensity values were normalized (Fisher z-transformation), and two-sample t-tests were applied to identify regions showing significant differences in directed FC between any two groups with age and sex removed as covariates. The threshold for significant differences between groups was set to p < 0.05 with a minimum cluster size of 85 contiguous voxels (Zheng et al., 2017).

Spearman’s correlation was used to assess the relationship between the GCA coefficients for the abnormal directional connections and MMSE, FAQ, and CDR in the three groups using SPSS 20.0 software.

Test–Retest Reliability

Consistent with previous research (Braun et al., 2012; Plichta et al., 2012; Cao et al., 2014), we calculated a commonly used index, namely, the intraclass correlation coefficient (ICC) (Shrout and Fleiss, 2015), to investigate the test–retest reliability of the abnormal directional connections between the three groups. The ICC values were calculated according to the following equation:

$$ICC=\frac{M{S}_{\mathrm{\lambda }}-M{S}_{\epsilon }}{M{S}_{\mathrm{\lambda }}+(k-1)M{S}_{\epsilon }+\frac{k}{n}(M{S}_{\mathrm{\pi }}-M{S}_{\epsilon })}(3)$$

where MS_λ is the between-subject mean square, MS_ε is the residual mean square, MS_π is the between-scan mean square, n is the number of subjects, and k is the number of repeated observations per subject. Here, ICC values close to 1 indicate perfect agreement between the two scans, while ICC values close to 0 (or negative) indicate poor or no agreement. In this study, we used a standard scale to classify reliability (Winer, 1962; Sampat et al., 2006), with an ICC value from 0 to 0.25 indicating poor reliability; 0.25 to 0.4 indicating low reliability; 0.4 to 0.6 indicating fair reliability; 0.6 to 0.75 indicating good reliability; and 0.75 to 1.0 indicating excellent reliability.

Results

Demographic and Clinical Data

The demographic and clinical data for each group are presented in Table 1. No significant differences were observed in sex or age among the three groups (p > 0.05). However, the MMSE, CDR, and FAQ scores were significantly different (p < 0.001, Bonferroni correction) among the three groups.

Altered Hippocampal Directed Functional Connectivity: Pairwise Comparisons

We present the average GCA coefficients for the abnormal directional connections between the hippocampus and the whole brain within each group (NC, MCI, and AD). The results are shown in Supplementary Tables S1, S2. The pairwise comparisons of differences in hippocampal connectivity were obtained using the REST two-sample t-tests. In the directed FC from the left hippocampus to the whole brain, the MCI group, compared with the NC group, showed significantly decreased connectivity to the right inferior temporal gyrus, right middle temporal gyrus, right parahippocampal gyrus, and part of the prefrontal cortex. Enhanced connectivity was detected from the left hippocampus to the left inferior temporal gyrus, left anterior cingulate and paracingulate gyri, and right inferior frontal gyrus, triangular portion (Figure 2A and Table 2). Compared with the NC group, the AD group showed strengthened connectivity from the left hippocampus to the left inferior temporal gyrus and left precuneus and weakened connectivity from the left hippocampus to the right temporal pole: superior temporal gyrus, right caudate nucleus, right posterior cingulate gyrus, and right superior frontal gyrus (Figure 2B and Table 2). Compared with the MCI group, the AD group demonstrated increased connectivity from the left hippocampus to regions of the right cerebellum, left middle occipital gyrus, and right thalamus and decreased connectivity from the left hippocampus to the bilateral temporal pole, superior temporal gyrus, right rolandic operculum, left anterior cingulate and paracingulate gyri, and left superior frontal gyrus (Figure 2C and Table 2). The differences between groups in directed FC from the whole brain to the left hippocampus are shown in Figures 2D–F and Table 2. The detailed results of the pairwise comparisons regarding the directed FC between the right hippocampus and the whole brain are displayed in Figure 3 and Table 3.

FIGURE 2

Figure 2. Directed functional connectivity showing significant differences in the left hippocampus and whole brain pairwise comparisons. From the left hippocampus to whole brain, panel (A) represents the directed functional connectivity showing significant differences between the MCI and NC groups, panel (B) represents the directed functional connectivity showing significant differences between the AD and NC groups, and panel (C) represents the directed functional connectivity showing significant differences between the AD and MCI groups. From whole brain to the left hippocampus, panel (D) represents the directed functional connectivity showing significant differences between the MCI and NC groups, panel (E) represents the directed functional connectivity showing significant differences between the AD and NC groups, and panel (F) represents the directed functional connectivity showing significant differences between the AD and MCI groups. The red/yellow-colored brain regions indicate increased GCA values between groups. The blue/green-colored brain regions indicate decreased GCA values between groups.

TABLE 2

Table 2. Directed functional connectivity showing significant differences in the left hippocampus and the whole brain pairwise comparisons.

FIGURE 3

Figure 3. Directed functional connectivity showing significant differences in the right hippocampus and whole brain pairwise comparisons. From the right hippocampus to whole brain, panel (A) represents the directed functional connectivity showing significant differences between the MCI and NC groups, panel (B) represents the directed functional connectivity showing significant differences between the AD and NC groups, and panel (C) represents the directed functional connectivity showing significant differences between the AD and MCI groups. From whole brain to the right hippocampus, panel (D) represents the directed functional connectivity showing significant differences between the MCI and NC groups, panel (E) represents the directed functional connectivity showing significant differences between the AD and NC groups, and panel (F) represents the directed functional connectivity showing significant differences between the AD and MCI groups. The red/yellow-colored brain regions indicate increased GCA values between groups. The blue/green-colored brain regions indicate decreased GCA values between groups.

TABLE 3

Table 3. Directed functional connectivity showing significant differences in the right hippocampus and the whole brain pairwise comparisons.

Figure 4A shows the significantly altered directed FC between the left hippocampus and the whole brain in the MCI group compared with the NC group. The difference focuses primarily on the connectivity from the left hippocampus to other brain regions. The connectivity from the left hippocampus to the right middle temporal gyrus and the right cerebellum was decreased, whereas the left inferior temporal gyrus, left anterior cingulate and paracingulate gyri, and the middle frontal gyrus all showed enhanced directed FC to the left hippocampus to varying degrees. Figure 4B indicates the difference in the directed FC between the left hippocampus and other brain regions in the NC group and the AD group. The connectivity from the left hippocampus to the left inferior temporal gyrus was demonstrated to be enhanced in the AD group, which was similar to the findings in the MCI group. However, the differences mainly occurred in the connectivity from other brain regions to the left hippocampus. Figure 4C shows the differences in directed FC between the left hippocampus and the whole brain in the MCI and AD groups. A large number of abnormal connections were identified, but this analysis mostly showed decreased directed connectivity. Figure 5A illustrates the significantly altered directed FC between the right hippocampus and the whole brain in the MCI group compared with the NC group. There were few abnormal connections. Figure 5B indicates the difference in the directed FC between the right hippocampus and other brain regions in the NC group and the AD group. The differences are primarily found in the connectivity from the right hippocampus to other brain regions. Figure 5C shows the differences in the directed FC between the right hippocampus and the whole brain in the MCI and AD groups. A large number of abnormal connections were noted, but these were mainly concentrated in regions that received information from the right hippocampus.

FIGURE 4

Figure 4. Differences in directed functional connectivity from the left hippocampus to the whole brain and from the whole brain to the left hippocampus between each pair of groups. Panel (A) represents the comparison between the MCI and NC groups, panel (B) represents the comparison between the AD and NC groups, and panel (C) represents the comparison between the AD and MCI groups. The red line denotes that the GCA value in the former group was higher than the latter group, and the blue line denotes that the GCA value in the former group was lower than the latter group. The solid line indicates the directed functional connectivity from the hippocampus to other brain regions, and the dashed line indicates the directed functional connectivity from other brain regions to the hippocampus.

FIGURE 5

Figure 5. Differences in directed functional connectivity from the right hippocampus to the whole brain and from the whole brain to the right hippocampus between each pair of groups. Panel (A) represents the comparison between the MCI and NC groups, panel (B) represents the comparison between the AD and NC groups, and panel (C) represents the comparison between the AD and MCI groups. The red line denotes that the GCA value in the former group was higher than the latter group, and the blue line denotes that the GCA value in the former group was lower than the latter group. The solid line indicates the directed functional connectivity from the hippocampus to other brain regions, and the dashed line indicates the directed functional connectivity from other brain regions to the hippocampus.

Relationships Between the Abnormal Directional Connections and Cognitive and Clinical Measurements

Simultaneously, in order to explore the potential relationship between the abnormal directional connections and cognitive and clinical measurements, we found some significant correlations between the GCA coefficients for the abnormal directional connections and MMSE, CDR, and FAQ in the three groups. The results are shown in Supplementary Tables S3, S4. For example, the GCA coefficients from the left hippocampus to left inferior temporal gyrus (r = −0.214, p = 0.045) and to left precuneus (r = −0.300, p = 0.025) were negatively correlated with MMSE in the three groups, and the GCA coefficient from the left hippocampus to left anterior cingulate and paracingulate gyri was positively correlated with CDR (r = 0.286, p = 0.006) and FAQ (r = 0.301, p = 0.004) in NC and MCI groups. Moreover, the GCA coefficients from the right hippocampus to right middle frontal gyrus, from right superior frontal gyrus to the left hippocampus, and from left middle frontal gyrus to the right hippocampus were significantly correlated with MMSE, CDR, and FAQ in NC and AD groups (showed in Supplementary Tables S3, S4).

Test–Retest Reliability of the Abnormal Directional Connections Between the Three Groups

To further understand the reliability of the GCA differences among the three groups, we calculated the ICC values of the abnormal directional connections among the three groups and found fair average reliability of the abnormal directional connections (showed in Supplementary Figures S1, S2). For instance, our study found that the interconnection between the left hippocampus and inferior temporal gyrus showed good reliability in NC and MCI groups. Moreover, the directional FC from the left hippocampus to right middle temporal gyrus, left anterior cingulate and paracingulate gyri, left middle frontal gyrus, right superior frontal gyrus, and right inferior frontal gyrus, triangular portion showed low to good reliability in NC and MCI groups.

Discussion

In the current study, we used the hippocampus (HIP) as connective node and applied the GCA coefficient to investigate the directed relationship between the HIP and the whole brain. The results revealed alterations in the directed FCs from the HIP to the whole brain and from the whole brain to the HIP in patients with MCI and AD. Furthermore, significant differences among the three groups were mainly found in the temporal lobe, frontal lobe, and cingulate cortex. Within these regions, the main brain regions showing abnormalities included ITG, right PCUN, MTG, left STG, MFG, IFG, left ACG, and right INS. Notably, most of these differences were significantly correlated with cognitive and clinical measurements in the three groups.

Abnormal Directed Connectivity Between the HIP and the Default Mode Network

Most of the above regions belong to the DMN, which is considered responsible for episodic memory formation and attention (Cechetto and Weishaupt, 2016). The DMN is thought to be primarily responsible for internally focused thought processes, such as autobiographical memory and experience of the self. Previous studies have consistently demonstrated that the DMN is the first network to be affected in AD, and decreased DMN FC is known to occur in AD patients (Ashwal, 2017; Brown et al., 2019).

Specifically, our study found the directed FCs from the left HIP to left ITG and from the right HIP to right PCUN in MCI and AD patients were stronger than NCs. Actually, the ITG is located at the end of the ventral visual stream (Tanaka, 1996) and is considered relevant to long-term visual memory storage (Miyashita, 1993) and cognitive learning. Furthermore, the PCUN is also critical to visuospatial imaging, retrieval of episodic memory and information processing of self-related information (Cavanna and Trimble, 2006; Hebscher et al., 2017; Mazzoni et al., 2019). Hence, this finding may indicate that these abnormal FCs might be associated with cognitive decline and visuospatial disability in MCI and AD patients. Notably, according to the research by Convit et al. (2000), the ITG might be the first temporal lobe neocortical site affected in AD, and atrophy in this region could be used to distinguish AD from non-demented individuals. This may be related to the fact that the directed FC from left ITG to the left HIP only weakens in AD patients, and may mean that ITG have not fully atrophy during the MCI group compared to the AD group.

Comparing with NCs, the directed FC between the HIP and MTG was significantly decreased in patients. Interestingly, the directed FC from the left HIP to right MTG was significantly decreased in MCI patients only, and the directed FC from left MTG to right HIP was significantly decreased in AD patients only. Many studies have shown that the MTG plays an important role in language function (Mohammed et al., 2015; Khazaee et al., 2017) and that the gray matter volume of the MTG in MCI patients was significant different than that in controls. Consistent with these findings, Yan et al. (2013) found decreased effective connectivity among MTG and the HIP in patients with MCI, compared with controls, and this impaired connectivity was associated with patients’ cognitive performance in an auditory verbal learning task. Therefore, there may exist a compensation mechanism and the influence inconsistency of left and right MTG for the language function, in the process of developing from MCI to AD. In addition, comparing with NCs, the directed FCs from the left HIP to right PHG were significantly decreased in MCI patients, and the directed FC from the right HIP to left STG was significantly decreased in AD patients. The PHG plays an essential role in memory generation as a bridge between the HIP and cortex (Bar et al., 2008), and the STG has been reported to be a key region in emotional perception caused by facial stimulation and processing of auditory language and has been implicated as a critical structure in social cognition (Bigler et al., 2007). These changes might be related to the clinical manifestation of cognitive impairment in AD patients with dementia.

Abnormal Directed Connectivity Between the HIP and the Executive Control Network

The directed FCs between the HIP and selected brain regions in the executive control network (ECN), such as SFG, MFG, and IFG, were abnormal. Consistent with our finding, a body of research has demonstrated that functional brain activity within portions of the ECN was abnormal in patients with MCI and AD (Firbank et al., 2016; Zhao et al., 2018). Generally, the ECN is considered responsible for the extrinsic awareness that regulates the executive functions that control and mediate cognitive processes, including working memory, reasoning, flexibility, problem solving, and planning (Zhao et al., 2018; Brown et al., 2019).

Specifically, the directed FCs from the left HIP to right SFG and from left MFG to the right HIP were significantly decreased in MCI and AD patients. In fact, the SFG (Khazaee et al., 2015) and the MFG (Levine et al., 2015; Liu et al., 2015) are important components of the dorsolateral prefrontal cortex that play an essential role in visual working memory (Oliveri et al., 2001). Furthermore, Cai et al. (2017) found that the dorsolateral prefrontal cortex and medial prefrontal cortex were the core nodes in the ECN and that they showed different connection patterns in patients with MCI and AD. Evidently, these changes in connectivity might explain why AD patients increasingly suffer from disruptions in visuospatial skills and memory impairment. Notably, the directed FC from the left HIP to right IFGtriang was significantly increased in MCI patients only, whereas the significant increase of this directed FC was observed in the opposite direction in AD patients. This may indicate that IFGtriang has a regulatory effect on cognitive control and memory retrieval in patients with AD.

Abnormal Directed Connectivity Between the HIP and the Salience Network

As the functional module that plays a vital role in communication, social behavior, and self-awareness (Uddin, 2017), the salience network (SN) and its interactions with the HIP showed significant abnormalities. The SN is a large-scale paralimbic–limbic network anchored in the anterior insula and dorsal anterior cingulate cortex, with prominent subcortical nodes in the affect and reward processing systems (Menon, 2015). He et al. (2014) and Chand et al. (2017) found that the structure and function of the SN was disrupted in patients with MCI and AD. These results also indicated that the effective connections between the SN and other brain regions in MCI and AD patients may be different than those in NCs. Hence, the disruption in the SN found in this study might be associated with cognitive decline in patients with MCI and AD.

Notably, the directed FC from the left HIP to left ACG was significantly enhanced in MCI patients but obviously weakened in AD patients. Nevertheless, the directed FC from left ACG to the HIP was visibly increased in AD patients. These findings indicate that a compensatory mechanism is present during the development of AD pathology. In fact, according to research by Apps M A, the ACG plays an important role in monitoring the outcomes of decisions in uncertain or volatile environments and might be an advanced control structure responsible for behavior planning and the execution of executive network functions (Apps et al., 2009).

More interestingly, the directed FC from the HIP to right INS in AD patients showed a consistent weakening trend compared with that in NCs. Nevertheless, directed FC from right INS to the right HIP was significantly increased in patients with AD compared to those with MCI. These findings may be similar to the compensatory mechanism described above and may be important because the INS is usually considered to play an important role in emotional regulation and the control of body balance. Moreover, Kurth et al. (2010) suggested that the INS is related to social emotion, sensorimotor function, sense of smell and taste, and cognitive functions. Hence, the unusual interaction between the HIP and INS might be one reason why patients with AD showed changes in personality and behavior, cognitive decline, and executive dysfunction.

Abnormal Directed Connectivity Between the HIP and Other Brain Regions

The current study found the directed FC from right SMA to the left HIP was increased in MCI patients. Consistent with these results, a previous study had reported the gradual loss of the sensorimotor cortex with the progression of AD (Frisoni et al., 2009), and functional alterations in the SMA in AD patients have been demonstrated in rs-fMRI studies (Brier et al., 2012). Moreover, the directed FC from the right HIP to left PCL decreased in MCI patients, and the directed FC from right PCL to the right HIP decreased in AD patients. These changes might explain symptoms such as apraxia and executive function in late AD.

Notably, our study showed that the directed FCs between the HIP and other brain regions in patients with MCI had been disrupted to a certain degree but that there were only abnormal connections with few brain regions. Nevertheless, in AD patients, the mass of affected voxels was larger, the number of widely distributed brain regions was larger, and the higher levels of statistical significance than MCI patients. These results might mean that during the transition from MCI to AD, a large number of brain regions become impaired, the directed FCs between the HIP and a large number of brain regions become disrupted, and the direction and intensity of information flow becomes altered, which might lead to clinical manifestations such as memory deficits, cognitive decline, and executive dysfunction in AD patients.

Additionally, one of the interesting findings was that the abnormal brain regions associated with the left HIP in MCI patients were primarily from the brain regions which receive information from the left HIP, whereas the abnormal brain regions associated with the left HIP in the AD patients were primarily from the brain regions which transmit information to the left HIP. This difference might be an imaging marker for the discrimination between MCI and AD and requires further study. Moreover, the current study showed that almost all brain regions with abnormal connectivity presented with unilateral abnormalities, with some exceptions. The abnormal FC was asymmetric in the two hemispheres, which was consistent with previous studies (Kim et al., 2012; Wachinger et al., 2018).

Correlations Between Abnormal Directed Connectivity and Cognitive and Clinical Measurements

We performed correlation analyses between the GCA coefficients for the abnormal directional FCs and cognitive and clinical measurements (MMSE, CDR, and FAQ). These three cognitive and clinical measurements provide a quantitative assessment of cognitive function and are widely used (Ciesielska et al., 2016; Kaur et al., 2016; Kim et al., 2017). The higher the MMSE scores indicate the higher the cognitive ability; the lower functional performance is associated with higher FAQ scores, and the higher CDR scores indicate the presence of dementia. Overall, most of these abnormal directional FCs were significantly correlated with MMSE, CDR, and FAQ. Specifically, the directed FC from the left HIP to left ITG and MMSE were significantly negatively correlated, which indicated that the lower the MMSE, the stronger the FC. This is also consistent with our finding that this abnormal directed FC might be associated with cognitive decline in MCI and AD patients. Moreover, the directed FCs from the left HIP to left MFG and from the right HIP to left STG were significantly negatively correlated with CDR and FAQ in the three groups. This is not only consistent with the results of our discussion above, but also indicates that the patient’s visual working memory function is gradually decreasing. More consistently, the directed FC from the left HIP to left ACG was significantly positively correlated with CDR and FAQ in MCI patients, and was significantly negatively correlated with CDR and FAQ in AD patients. This indicates that the compensatory mechanism occurs in the brain during disease progression.

Limitation

A limitation of this study is that the number of subjects used to assess the test–retest reliability of the abnormal directed FC is small, which may lead to potential instability of ICC values. In this study, we performed cross-group merging on the retest subjects and performed ICC analysis. We found fair average reliability of the abnormal directional FCs. Nevertheless, some abnormal directional FCs still have low reliability. This may be due to the small number of objects and the large between-subject mean square. The results in need for further validation with a larger dataset.

Conclusion

In conclusion, this study reveals significant differences in directed FC between the hippocampus and other brain regions among NC, MCI, and AD subjects, and these differences were significantly correlated with cognitive and clinical measurements. These results might indicate patterns of alterations in the transmission and reception of information with the evolution of the disease. The analysis of abnormal directed connectivity might provide an additional target for the prevention and treatment of AD. Moreover, selected alterations could be reliable and used as discriminant features to classify NC, MCI, and AD groups. These possibilities require further study.

Alzheimer’s Disease Neuroimaging Initiative

The data used in the preparation of this article were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database (adni.loni.usc.edu). As such, the investigators within the ADNI contributed to the design and implementation of the ADNI and/or provided data but did not participate in the analysis or writing of this report. A complete listing of the ADNI investigators can be found at https://adni.loni.usc.edu/wp-content/uploads/how_to_apply/ADNI_Acknowledgement_List.pdf.

Data Availability Statement

All datasets generated for this study are included in the article/Supplementary Material.

Ethics Statement

The studies involving human participants were reviewed and approved by The Alzheimer’s Disease Neuroimaging Initiative (ADNI) database. The patients/participants provided their written informed consent to participate in this study.

Author Contributions

JXu performed the experiment and completed the manuscript. HG, HC, ZC, XW, and YG provided suggestions for this study. BW and JXi provided guidance throughout the study.

Funding

This work was supported by the National Natural Science Foundation of China (61503272, 61672374, 61873178, and 61876124), the Natural Science Foundation of Shanxi (201801D121135), the International Science and Technology Cooperation Project of Shanxi (201803D421047), and the Youth Science and Technology Research Fund (201701D221119).

Conflict of Interest

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.

Acknowledgments

We would like to thank the AJE team for the professional language editing services.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnagi.2019.00326/full#supplementary-material

Footnotes

1. ^ http://adni.loni.ucla.edu
2. ^ http://www.fil.ion.ucl.ac.uk/spm
3. ^ http://restfmri.net/forum/REST_V1.8

References

Apps, M., Balsters, J., and Ramnani, N. (2009). Anterior cingulate cortex: monitoring the outcomes of others’ decisions. Neuroimage 47, 424–435. doi: 10.1080/17470919.2011.638799

PubMed Abstract | CrossRef Full Text | Google Scholar

Ashwal, S. (2017). “Disorders of consciousness in children,” in Swaiman’s Pediatric Neurology, 6th Edn, eds K. F. Swaiman, S. Ashwal, D. M. Ferriero, N. F. Schor, R. S. Finkel, A. L. Gropman, et al. (Amsterdam: Elsevier), 767–780. doi: 10.1016/b978-0-323-37101-8.00101-6

CrossRef Full Text | Google Scholar

Bajaj, S., Adhikari, B. M., Friston, K. J., and Dhamala, M. (2016). Bridging the gap: dynamic causal modeling and granger causality analysis of resting state fMRI. Brain Connect. 6, 652–661. doi: 10.1089/brain.2016.0422

PubMed Abstract | CrossRef Full Text | Google Scholar

Bar, M., Aminoff, E., and Schacter, D. L. (2008). Scenes unseen: the parahippocampal cortex intrinsically subserves contextual associations, not scenes or places per se. J. Neurosci. 28, 8539–8544. doi: 10.1523/jneurosci.0987-08.2008

CrossRef Full Text | Google Scholar

Bigler, E. D., Mortensen, S., Neeley, E. S., Ozonoff, S., Krasny, L., Johnson, M., et al. (2007). Superior temporal gyrus, language function, and autism. Dev. Neuropsychol. 31, 217–238. doi: 10.1080/87565640701190841

PubMed Abstract | CrossRef Full Text | Google Scholar

Braak, H., and Braak, E. (1991). Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol. 82, 239–259. doi: 10.1007/bf00308809

PubMed Abstract | CrossRef Full Text | Google Scholar

Braak, H., and Braak, E. (1997). Staging of alzheimer-related cortical destruction. Int. Psychoger. 33, 403–408. doi: 10.1159/000116984

PubMed Abstract | CrossRef Full Text | Google Scholar

Braun, U., Plichta, M. M., Esslinger, C., Sauer, C., Haddad, L., Grimm, O., et al. (2012). Test–retest reliability of resting-state connectivity network characteristics using fMRI and graph theoretical measures. Neuroimage 59, 1404–1412. doi: 10.1016/j.neuroimage.2011.08.044

PubMed Abstract | CrossRef Full Text | Google Scholar

Bressler, S. L., and Seth, A. K. (2011). Wiener–granger causality: a well established methodology. Neuroimage 58, 323–329. doi: 10.1016/j.neuroimage.2010.02.059

PubMed Abstract | CrossRef Full Text | Google Scholar

Brier, M. R., Thomas, J. B., Snyder, A. Z., Benzinger, T. L., Zhang, D., Raichle, M. E., et al. (2012). Loss of intranetwork and internetwork resting state functional connections with Alzheimer’s disease progression. J. Neurosci. 32, 8890–8899. doi: 10.1523/JNEUROSCI.5698-11.2012

PubMed Abstract | CrossRef Full Text | Google Scholar

Brookmeyer, R., Johnson, E., Ziegler-Graham, K., and Arrighi, H. M. (2007). Forecasting the global burden of Alzheimer’s disease. Alzheimer’s Dement. 3, 186–191.

Google Scholar

Brown, C. A., Schmitt, F. A., Smith, C. D., and Gold, B. T. (2019). Distinct patterns of default mode and executive control network circuitry contribute to present and future executive function in older adults. NeuroImage 195, 320–332. doi: 10.1016/j.neuroimage.2019.03.073

PubMed Abstract | CrossRef Full Text | Google Scholar

Cai, S., Peng, Y., Chong, T., Zhang, Y., Von Deneen, K. M., Huang, L., et al. (2017). Differentiated effective connectivity patterns of the executive control network in progressive MCI: a potential biomarker for predicting AD. Curr. Alzheimer Res. 14, 937–950. doi: 10.2174/1567205014666170309120200

PubMed Abstract | CrossRef Full Text | Google Scholar

Cao, H., Plichta, M., Schäfer, A., Haddad, L., Grimm, O., Schneider, M., et al. (2014). Test-retest reliability of fMRI-based graph theoretical properties during working memory, emotion processing, and resting state. Neuroimage 84, 888–900. doi: 10.1016/j.neuroimage.2013.09.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Cavanna, A. E., and Trimble, M. R. (2006). The precuneus: a review of its functional anatomy and behavioural correlates. Brain 129, 564–583. doi: 10.1093/brain/awl004

PubMed Abstract | CrossRef Full Text | Google Scholar

Cechetto, D., and Weishaupt, N. (2016). The Cerebral Cortex in Neurodegenerative and Neuropsychiatric Disorders: Experimental Approaches to Clinical Issues. Cambridge, MA: Academic Press.

Google Scholar

Chand, G. B., Wu, J., Hajjar, I., and Qiu, D. (2017). Interactions of the salience network and its subsystems with the default-mode and the central-executive networks in normal aging and mild cognitive impairment. Brain Connect. 7, 401–412. doi: 10.1089/brain.2017.0509

PubMed Abstract | CrossRef Full Text | Google Scholar

Ciesielska, N., Sokołowski, R., Mazur, E., Podhorecka, M., Polak-Szabela, A., and Kędziora-Kornatowska, K. (2016). Is the montreal cognitive assessment (MoCA) test better suited than the mini-mental state examination (MMSE) in mild cognitive impairment (MCI) detection among people aged over 60? Meta Anal. Psych. Polska 50, 1039–1052. doi: 10.12740/PP/45368

PubMed Abstract | CrossRef Full Text | Google Scholar

Convit, A., De Asis, J., De Leon, M. J., Tarshish, C. Y., De Santi, S., and Rusinek, H. (2000). Atrophy of the medial occipitotemporal, inferior, and middle temporal gyri in non-demented elderly predict decline to Alzheimer’s disease☆. Neurobiol. Aging 21, 19–26. doi: 10.1016/s0197-4580(99)00107-4

CrossRef Full Text | Google Scholar

Davatzikos, C. (2009). Baseline and longitudinal patterns of brain atrophy in MCI patients and their use in prediction of short-term conversion to Alzheimer’s disease: results from ADNI. Alzheimers Dement. 44, 1415–1422. doi: 10.1016/j.neuroimage.2008.10.031

PubMed Abstract | CrossRef Full Text | Google Scholar

Everitt, B. S., and Dunn, G. (2013). Applied Multivariate Data Analysis, 2 Edn. London: Pearson.

Google Scholar

Firbank, M., Kobeleva, X., Cherry, G., Killen, A., Gallagher, P., Burn, D. J., et al. (2016). Neural correlates of attention−executive dysfunction in lewy body dementia and Alzheimers disease. Hum. Brain Mapp. 37, 1254–1270. doi: 10.1002/hbm.23100

PubMed Abstract | CrossRef Full Text | Google Scholar

Frisoni, G. B., Prestia, A., Rasser, P. E., Bonetti, M., and Thompson, P. M. (2009). In vivo mapping of incremental cortical atrophy from incipient to overt Alzheimer’s disease. J. Neurol. 256, 916–924. doi: 10.1007/s00415-009-5040-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Hamilton, J. P., Thomason, M. E., Gotlib, I. H., and Saad, Z. S. (2009). “Granger causality via vector autoregression tuned for FMRI data analysis,” in Proceedings 17th Scientific Meeting, International Society for Magnetic Resonance in Medicine, Honolulu, 1718.

Google Scholar

Hanseeuw, B. J., Schultz, A. P., Betensky, R. A., Sperling, R. A., and Johnson, K. A. (2016). Decreased hippocampal metabolism in high-amyloid mild cognitiveimpairment. Alzheimers Dement. 12, 1288–1296. doi: 10.1016/j.jalz.2016.06.2357

PubMed Abstract | CrossRef Full Text | Google Scholar

He, X., Qin, W., Liu, Y., Zhang, X., Duan, Y., Song, J., et al. (2014). Abnormal salience network in normal aging and in amnestic mild cognitive impairment and Alzheimer’s disease. Hum. Brain Mapp. 35, 3446–3464. doi: 10.1002/hbm.22414

PubMed Abstract | CrossRef Full Text | Google Scholar

Hebscher, M., Levine, B., and Gilboa, A. (2017). The precuneus and hippocampus contribute to individual differences in the unfolding of spatial representations during episodic autobiographical memory. Neuropsychologia 110, 123–133. doi: 10.1016/j.neuropsychologia.2017.03.029

PubMed Abstract | CrossRef Full Text | Google Scholar

Jack, C., Bernstein, M. A., Fox, N. C., Thompson, P., Alexander, G., Harvey, D., et al. (2008). The Alzheimer’s Disease neuroimaging initiative (ADNI): MRI methods. J. Magn. Reson. Imaging. 27, 685–691.

Google Scholar

Joko, T., Washizuka, S., Sasayama, D., Inuzuka, S., Ogihara, T., Yasaki, T., et al. (2016). Patterns of hippocampal atrophy differ among Alzheimer’s disease, amnestic mild cognitive impairment, and late-life depression. Psychogeriatr. Official J. Japn. Psychogeriatr. Soc. 16, 355–361. doi: 10.1111/psyg.12176

PubMed Abstract | CrossRef Full Text | Google Scholar

Kaur, N., Belchior, P., Gelinas, I., and Bier, N. (2016). Critical appraisal of questionnaires to assess functional impairment in individuals with mild cognitive impairment. Int. Psychogeriatr. 28, 1425–1439. doi: 10.1017/S104161021600017X

PubMed Abstract | CrossRef Full Text | Google Scholar

Kelly, A. M. C., Uddin, L. Q., Biswal, B. B., Castellanos, F. X., and Milham, M. P. (2008). Competition between functional brain networks mediates behavioral variability. Neuroimage 39, 527–537. doi: 10.1016/j.neuroimage.2007.08.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Khazaee, A., Ebrahimzadeh, A., and Babajani-Feremi, A. (2015). Identifying patients with Alzheimer’s disease using resting-state fMRI and graph theory. Clin. Neurophysiol. 126, 2132–2141. doi: 10.1016/j.clinph.2015.02.060

PubMed Abstract | CrossRef Full Text | Google Scholar

Khazaee, A., Ebrahimzadeh, A., and Babajani-Feremi, A. (2017). Classification of patients with MCI and AD from healthy controls using directed graph measures of resting-state fMRI. Behav. Brain Res. 322, 339–350. doi: 10.1016/j.bbr.2016.06.043

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, J., Kim, Y. H., and Lee, J. H. (2013). Hippocampus–precuneus functional connectivity as an early sign of Alzheimer’s disease: a preliminary study using structural and functional magnetic resonance imaging data. Brain Res. 1495, 18–29. doi: 10.1016/j.brainres.2012.12.011

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, J. H., Lee, J. W., Kim, G. H., Roh, J. H., Kim, M.-J., Seo, S. W., et al. (2012). Cortical asymmetries in normal, mild cognitive impairment, and Alzheimer’s disease. Neurobiol. Aging 33, 1959–1966. doi: 10.1016/j.neurobiolaging.2011.06.026

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, J. W., Min, S. B., and Bo, K. S. (2017). Clinical dementia rating orientation score as an excellent predictor of the progression to Alzheimer s Disease in mild cognitive impairment. Psychiatry Investig. 14, 420–426. doi: 10.4306/pi.2017.14.4.420

PubMed Abstract | CrossRef Full Text | Google Scholar

Kurth, F., Zilles, K., Fox, P. T., Laird, A. R., and Eickhoff, S. B. (2010). A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis. Brain Struc. Func. 214, 519–534. doi: 10.1007/s00429-010-0255-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Levine, M. E., Lu, A. T., Bennett, D. A., and Horvath, S. (2015). Epigenetic age of the pre-frontal cortex is associated with neuritic plaques, amyloid load, and Alzheimer’s disease related cognitive functioning. Aging 7, 1198–1121.

Google Scholar

Liang, P., Li, Z., Deshpande, G., Wang, Z., Hu, X., and Li, K. (2014). Altered causal connectivity of resting state brain networks in amnesic MCI. Plos One 9:e88476. doi: 10.1371/journal.pone.0088476

PubMed Abstract | CrossRef Full Text | Google Scholar

Liao, W., Ding, J., Marinazzo, D., Xu, Q., Wang, Z., Yuan, C., et al. (2011). Small-world directed networks in the human brain: multivariate Granger causality analysis of resting-state fMRI. Neuroimage 54, 2683–2694. doi: 10.1016/j.neuroimage.2010.11.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, Y., Yu, J.-T., Wang, H.-F., Han, P.-R., Tan, C.-C., Wang, C., et al. (2015). APOE genotype and neuroimaging markers of Alzheimer’s disease: systematic review and meta-analysis. J. Neurol. Neurosurg. Psychiatry 86, 127–134. doi: 10.1136/jnnp-2014-307719

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, Z., Zhang, Y., Bai, L., Yan, H., Dai, R., Zhong, C., et al. (2012). Investigation of the effective connectivity of resting state networks in Alzheimer’s disease: a functional MRI study combining independent components analysis and multivariate granger causality analysis. Nmr. Biomed. 25, 1311–1320. doi: 10.1002/nbm.2803

PubMed Abstract | CrossRef Full Text | Google Scholar

Mazzoni, G., Clark, A., De Bartolo, A., Guerrini, C., Nahouli, Z., Duzzi, D., et al. (2019). Brain activation in Highly superior autobiographical memory: the role of the precuneus in the autobiographical memory retrieval network. Cortex. 120, 588–602. doi: 10.1016/j.cortex.2019.02.020

PubMed Abstract | CrossRef Full Text | Google Scholar

Menon, V. (2015). “Salience Network,” in Brain Mapping, ed A.W. Toga. Waltham: Academic Press, 597–611.

Google Scholar

Miyashita, Y. (1993). Inferior temporal cortex: where visual perception meets memory. Annu. Rev. Neurosci. 16, 245–263. doi: 10.1146/annurev.ne.16.030193.001333

CrossRef Full Text | Google Scholar

Mohammed, G., Qi, Z., Warren, B., Loewenstein, D. A., Ranjan, D., and Malek, A. (2015). Inclusion of neuropsychological scores in atrophy models improves diagnostic classification of Alzheimer’s Disease and mild cognitive impairment. Comput. Intell. Neurosci. 2015:56.

Google Scholar

Oliveri, M., Turriziani, P., Carlesimo, G., Koch, G., Tomaiuolo, F., Panella, M., et al. (2001). Parieto-frontal interactions in visual-object and visual-spatial working memory: evidence from transcranial magnetic stimulation. Cereb. Cortex 11, 606–618. doi: 10.1093/cercor/11.7.606

PubMed Abstract | CrossRef Full Text | Google Scholar

Plichta, M. M., Schwarz, A. J., Grimm, O., Morgen, K., Mier, D., Haddad, L., et al. (2012). Test-retest reliability of evoked BOLD signals from a cognitive-emotive fMRI test battery. Neuroimage 60, 1746–1758. doi: 10.1016/j.neuroimage.2012.01.129

PubMed Abstract | CrossRef Full Text | Google Scholar

Roebroeck, A., Formisano, E., and Goebel, R. (2005). Mapping directed influence over the brain using Granger causality and fMRI. Neuroimage 25, 230–242. doi: 10.1016/j.neuroimage.2004.11.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Sampat, M. P., Whitman, G. J., Stephens, T. W., Broemeling, L. D., Heger, N. A., Bovik, A. C., et al. (2006). The reliability of measuring physical characteristics of spiculated masses on mammography. Br. J. Radiol. 2:S134.

PubMed Abstract | Google Scholar

Serra, L., Bozzali, M., Fadda, L., De Simone, M. S., Bruschini, M., Perri, R., et al. (2018). The role of hippocampus in the retrieval of autobiographical memories in patients with amnestic mild cognitive impairment due to Alzheimer’s disease. J. Neuropsychol. doi: 10.1111/jnp.12174 [Epub ahead of print].

CrossRef Full Text | PubMed Abstract | Google Scholar

Shrout, P. E., and Fleiss, J. L. (2015). Intraclass correlations: uses in assessing rater reliability. Psychol. Bull. 86, 420–428. doi: 10.1037//0033-2909.86.2.420

PubMed Abstract | CrossRef Full Text | Google Scholar

Sohn, W. S., Yoo, K., Na, D. L., and Yong, J. (2014). Progressive Changes in Hippocampal Resting-state Connectivity Across Cognitive impairment: a cross-sectional study from normal to Alzheimer Disease. Alzheimer Dis. Assoc Disord. 28, 239–246. doi: 10.1097/WAD.0000000000000027

PubMed Abstract | CrossRef Full Text | Google Scholar

Sun, Y., Wang, Y., Lu, J., Liu, R., and Schwarz, C. G. (2017). Disrupted functional connectivity between perirhinal and parahippocampal cortices with hippocampal subfields in patients with mild cognitive impairment and Alzheimer’s disease. Oncotarget 8, 99112–99124. doi: 10.18632/oncotarget.17944

PubMed Abstract | CrossRef Full Text | Google Scholar

Tahmasian, M., Pasquini, L., Scherr, M., Meng, C., Forster, S., Mulej Bratec, S., et al. (2015). The lower hippocampus global connectivity, the higher its local metabolism in Alzheimer disease. Neurology 84, 1956–1963. doi: 10.1212/WNL.0000000000001575

PubMed Abstract | CrossRef Full Text | Google Scholar

Tanaka, K. (1996). Inferotemporal cortex and object vision. Annu. Rev. Neurosci. 19, 109–139. doi: 10.1146/annurev.neuro.19.1.109

PubMed Abstract | CrossRef Full Text | Google Scholar

Tzourio-Mazoyer, N., Landeau, B., Papathanassiou, D., Crivello, F., Etard, O., Delcroix, N., et al. (2002). Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single-subject brain. Neuroimage 15, 273–289. doi: 10.1006/nimg.2001.0978

PubMed Abstract | CrossRef Full Text | Google Scholar

Uddin, L. Q. (2017). “Chapter 6 - future directions in salience network research,” in Salience Network of the Human Brain, ed. L. Q. Uddin, (San Diego: Academic Press), 29–32. doi: 10.1016/b978-0-12-804593-0.00006-0

CrossRef Full Text | Google Scholar

Wachinger, C., Nho, K., Saykin, A. J., Reuter, M., and Rieckmann, A., and Alzheimer’s Disease Neuroimaging Initiative. (2018). A longitudinal imaging genetics study of neuroanatomical asymmetry in Alzheimer’s disease. Biol. Psychiatry 84, 522–530. doi: 10.1016/j.biopsych.2018.04.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, L., Zang, Y., He, Y., Liang, M., Zhang, X., Tian, L., et al. (2006). Changes in hippocampal connectivity in the early stages of Alzheimer’s disease: evidence from resting state fMRI. Neuroimage 31, 496–504. doi: 10.1016/j.neuroimage.2005.12.033

PubMed Abstract | CrossRef Full Text | Google Scholar

Wen, X., Wu, X., Li, R., Fleisher, A. S., Reiman, E. M., Wen, X., et al. (2013). Alzheimer’s disease-related changes in regional spontaneous brain activity levels and inter-region interactions in the default mode network. Brain Res. 1509, 58–65. doi: 10.1016/j.brainres.2013.03.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Winer, B. J. (1962). Statistical Principles in Experimental Design. Int. Stud. Ed. 29, 7304–7309.

Google Scholar

Yan, C. G., and Zang, Y. F. (2010). DPARSF: A MATLAB Toolbox for “Pipeline”. Data Analysis of Resting-State fMRI. Front. Syst. Neurosci. 4:13. doi: 10.3389/fnsys.2010.00013

PubMed Abstract | CrossRef Full Text | Google Scholar

Yan, H., Zhang, Y., Chen, H., Wang, Y., and Liu, Y. (2013). Altered effective connectivity of the default mode network in resting-state amnestic type mild cognitive impairment. J. Int. Neuropsychol. Soc. 19, 1–10. doi: 10.1017/S1355617712001580

PubMed Abstract | CrossRef Full Text | Google Scholar

Zang, Z.-X., Yan, C.-G., Dong, Z.-Y., Huang, J., and Zang, Y.-F. (2012). Granger causality analysis implementation on MATLAB: a graphic user interface toolkit for fMRI data processing. J. Neurosci. Methods 203, 418–426. doi: 10.1016/j.jneumeth.2011.10.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, G. J., Wang, Y. J., and Li, B. (2017). Analysis of the effective connectivity of brain network based on transfer entropy. Computer Science and Technology 1111–1119. doi: 10.1142/9789813146426_0125

CrossRef Full Text | Google Scholar

Zhao, Q., Lu, H., Metmer, H., Li, W. X., and Lu, J. (2018). Evaluating functional connectivity of executive control network and frontoparietal network in Alzheimer’s disease. Brain Res. 1678, 262–272. doi: 10.1016/j.brainres.2017.10.025

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhao, Z., Wang, X., Fan, M., Yin, D., Sun, L., Jia, J., et al. (2016). Altered effective connectivity of the primary motor cortex in stroke: a resting-state fMRI Study with granger causality analysis. Plos One 11:e0166210. doi: 10.1371/journal.pone.0166210

PubMed Abstract | CrossRef Full Text | Google Scholar

Zheng, L. J., Yang, G. F., Zhang, X. Y., Wang, Y. F., Liu, Y., Zheng, G., et al. (2017). Altered amygdala and hippocampus effective connectivity in mild cognitive impairment patients with depression: a resting-state functional MR imaging study with granger causality analysis. Oncotarget 8:25021. doi: 10.18632/oncotarget.15335

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhong, Y., Huang, L., Cai, S., Zhang, Y., Deneen, K. M. V., Ren, A., et al. (2014). Altered effective connectivity patterns of the default mode network in Alzheimer’s disease: AN fMRI study. Neurosci. Lett. 578, 171–175. doi: 10.1016/j.neulet.2014.06.043

PubMed Abstract | CrossRef Full Text | Google Scholar