ORIGINAL RESEARCH article
Sec. Headache and Neurogenic Pain
Response Predictors of Repetitive Neuromuscular Magnetic Stimulation in the Preventive Treatment of Episodic Migraine
- 1Division of Pediatric Neurology and Developmental Medicine and LMU Center for Children With Medical Complexity, Dr. von Hauner Children's Hospital, LMU Hospital, Ludwig-Maximilians-Universität, Munich, Germany
- 2Department of Diagnostic and Interventional Neuroradiology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany
- 3TUM-Neuroimaging Center, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany
- 4Department of Neurosurgery, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany
- 5Department of Diagnostic and Interventional Radiology, University Hospital Ulm, Ulm, Germany
Background: Repetitive neuromuscular magnetic stimulation (rNMS) of the trapezius muscles showed beneficial effects in preventing episodic migraine. However, clinical characteristics that predict a favorable response to rNMS are unknown. The objective of this analysis is to identify such predictors.
Methods: Thirty participants with a diagnosis of episodic migraine (mean age: 24.8 ± 4.0 years, 29 females), who were prospectively enrolled in two non-sham-controlled studies evaluating the effects of rNMS were analyzed. In these studies, the interventional stimulation of the bilateral trapezius muscles was applied in six sessions and distributed over two consecutive weeks. Baseline and follow-up assessments included the continuous documentation of a headache calendar over 30 days before and after the stimulation period, the Migraine Disability Assessment Score (MIDAS) questionnaire (before stimulation and 90 days after stimulation), and measurements of pain pressure thresholds (PPTs) above the trapezius muscles by algometry (before and after each stimulation session). Participants were classified as responders based on a ≥25% reduction in the variable of interest (headache frequency, headache intensity, days with analgesic intake, MIDAS score, left-sided PPTs, right-sided PPTs). Post-hoc univariate and multivariate binary logistic regression analyses were performed.
Results: Lower headache frequency (P = 0.016) and intensity at baseline (P = 0.015) and a migraine diagnosis without a concurrent tension-type headache component (P = 0.011) were significantly related to a ≥25% reduction in headache frequency. Higher headache frequency (P = 0.052) and intensity at baseline (P = 0.014) were significantly associated with a ≥25% reduction in monthly days with analgesic intake. Lower right-sided PPTs at baseline were significantly related to a ≥25% increase in right-sided PPTs (P = 0.015) and left-sided PPTs (P =0.030). Performance of rNMS with higher stimulation intensities was significantly associated with a ≥25% reduction in headache intensity (P = 0.046).
Conclusions: Clinical headache characteristics at baseline, the level of muscular hyperalgesia, and stimulation intensity may inform about how well an individual patient responds to rNMS. These factors may allow an early identification of patients that would most likely benefit from rNMS.
Migraine is one of the most prevalent neurological disorders worldwide, with more than one billion affected people in 2016 and a significant impact on health-related quality of life, work productivity, and social relationships (1–3). Migraine is countervailed by a multimodal approach of lifestyle management, psychoeducation, psychotherapeutic intervention, and pharmacotherapy (4–6). Medication for migraine attacks is well-established and widely used; yet, responsiveness to prophylactic treatment varies and treatment adherence is often poor (e.g., due to side effects or insufficient adjustment of dosage) (7, 8). Against this background, innovative non-pharmacological treatment options are highly required (4, 8–10).
Neurostimulation represents a non-pharmacological treatment alternative that has emerged over the recent years (11–14). It aims at modifying the complex processes and interactions in and in-between the central, peripheral, and/or autonomous nervous system through externally applied electrical or magnetically induced stimuli. Several approaches exist, including: transcranial magnetic stimulation (TMS), transcranial direct current stimulation (tDCS), occipital nerve stimulation (ONS), transcutaneous supraorbital nerve stimulation (tSNS), transcutaneous vagus nerve stimulation (tVNS), and remote electrical neurostimulation (REN) of cutaneous sensory afferents of the upper arm (10, 15–22).
Furthermore, repetitive neuromuscular magnetic stimulation (rNMS) has been introduced lately, targeting to the neck and shoulder muscles to prevent attacks in episodic migraine (23–25). Specifically, rNMS has been reported to be safe, feasible, well-tolerated, and well-accepted (23–25). Moreover, promising effects of rNMS in terms of a reduction in headache frequency, headache intensity, migraine-associated disability, and muscular hypersensitivity have been reported (23–25). It is hypothesized that rNMS intervenes at the terminal branches of the motor and afferent nerves in the region within the induced electromagnetic field, thus directly and indirectly leading to an increase of proprioceptive sensation (26, 27). The trigemino-cervical complex (TCC) serves as a gateway for this bottom-up approach and its translation to modulate the central mechanisms of nociception (10, 28, 29).
However, rNMS demands a commitment in terms of patient's and therapist's resources. Stimulators are increasingly available on the markets, but, they are still by far more expensive than devices for transcutaneous electrical nerve stimulation (tENS), which limits availability. Therefore, recommending rNMS for migraine prevention anticipates thorough consideration of which patient may benefit the most in the context of an individualized multimodal treatment paradigm. However, no data on the predictors of a treatment response to rNMS nor to any other neurostimulating approach are available. The aim of this study was to assess clinical headache and muscular characteristics as well as technical aspects of the stimulation protocol that are associated with a positive treatment response to rNMS regarding headache frequency, headache intensity, burden of migraine, frequency of analgesic intake, and level of muscular hyperalgesia.
The protocols of the two non-sham-controlled studies that form the basis of the present analyses were approved by the institutional review boards of both universities of Munich. The studies were conducted in accordance with the Declaration of Helsinki. Written informed consent was obtained from all participants.
For the analysis of response predictors, the baseline, treatment, and follow-up charts of 30 participants who received rNMS to the upper trapezius muscles during two previous prospective non-sham-controlled clinical studies have been reviewed (23–25). The following inclusion criteria were applied during those studies: (1) age between 18 and 35 years, (2) episodic migraine [according to the German version of the headache questionnaire modified according to the International Classification of Headache Disorders (ICHD), 3rd beta edition (30–32)], (3) at least one active myofascial trigger point (mTrP) in one of the upper trapezius muscles (identified by a physiotherapist specialized in manual palpation of mTrPs), and (4) no metallic implants (e.g., pacemaker, cochlear implants). The following criteria were defined as exclusion criteria: (1) chronic migraine (≥15 headache days per month for >3 months) (30), (2) any neurological disorder except for primary headache, (3) intake of any medication for migraine prophylaxis, and (4) pregnancy.
During the previous studies, each participant underwent six sessions of rNMS in regular intervals during two consecutive weeks (e.g., Monday/Wednesday/Friday or Tuesday/Thursday/Saturday) (23–25). A Nexstim eXimia NBS System with a figure-of-eight stimulation coil was used for rNMS (version 4.3; Nexstim Oy, Helsinki, Finland). Before starting the first rNMS session, the stimulation intensity (% of maximum stimulator output) was determined individually for the trapezius muscles and was kept for both sides for the following sessions. Individual stimulation intensities were set by increasing the intensity in 5% steps until participants reported a discomfortable sensation (defined as a score of 5 on a 0–10 visual analog scale). Next, this intensity was decreased by 5% so that a comfortable and non-painful stimulation over 15 min was possible (23–25). Stimulation targeted to the left and right upper trapezius muscles – focusing on the mTrP with the highest intensity of referred pain—for 15 min per side during each session. Stimulation of each side consisted of 20 bursts with a total of 6.000 stimuli and a 20-Hz frequency. A single burst lasted 15 s and was composed of 300 stimuli, followed by a relaxation time of 30 s.
Baseline and Follow-up Assessments
The German version of the headache questionnaire modified according to the ICHD (3rd beta edition) (30–32), the headache calendar of the German Migraine and Headache Society (DMKG) (33), and the Migraine Disability Assessment Score (MIDAS) questionnaire (34, 35) were applied. The presence of aura symptoms and an association with tension-type headache (TTH) were documented as well.
To evaluate the headache frequency and characteristics, participants were asked to fill in the headache calendar of the DMKG on a daily basis in the 30 days before the first rNMS session. Numerous items of each headache attack like date, trigger mechanisms (stress, relaxation, disturbance of sleep-awake rhythm, or menstruation), intensity, duration, quality, localization, forerunning symptoms (scintillating scotoma, paresthesia, or aphasia), concomitant symptoms (nausea, vomiting, photophobia, phonophobia or odor-sensitivity), drug intake, dosage form, and pain relief were recorded with the help of the calendar. Subsequently, the participants filled in the headache diary during the course of the 30 days after the last rNMS intervention, defined as the follow-up period.
Moreover, participants were advised to fill in the MIDAS questionnaire to evaluate the impairment by headache events in different aspects of daily life before and after the application of rNMS. As the MIDAS questionnaire is evaluating a period of 90 days, this questionnaire had to be completed prior to the first rNMS session (evaluating the 90 pre-interventional days) and 90 days after the last session (evaluating the 90 post-interventional days). Measurements of PPTs were performed with an analog algometer by applying pressure with its rubber tip of 1 cm2 perpendicularly to the determined mTrPs. The pressure was increased with a velocity of 1 kg/s/cm2 until the local PPT was attained according to the participant. This algometry was conducted three times per side before and after rNMS during each of the six sessions, and the average of each three measurements was calculated afterwards (36, 37). In this context, the PPT was defined as the cut-off value between mere pressure and pressure-induced painful perception (37–41).
SPSS (version 25.0; IBM SPSS Statistics for Windows, Armonk, NY, USA) was used for statistical data analyses. Response to rNMS was investigated by categorizing participants into responders and non-responders according to a ≥25% response criterion for the following outcomes: (1) headache frequency, (2) headache intensity, (3) MIDAS score, (4) days with analgesic intake per month, (5) left-sided PPT, and (6) right-sided PPT. The following potential predictors were evaluated: (1) age, (2) headache type (episodic migraine, episodic migraine with concurrent TTH diagnosis), (3) pre-interventional headache frequency, (4) pre-interventional headache intensity, (5) pre-interventional MIDAS score, (6) pre-interventional days with analgesic intake per month, (7), pre-interventional left-sided PPT, (8) pre-interventional right-sided PPT, and (9) stimulation intensity. Differences between pre- and post-interventional values of predictor variables were assessed using paired t-tests.
We performed univariate binary logistic regression analyses to assess the influence of each potential predictor on the outcome variable. To assess whether the regression model is better fitted than a null model, the Omnibus test was used. Further, multivariate binary logistic regression analyses (with a backward elimination approach) were used to evaluate the combined influence of potential predictors on the response (≥25% response rate) to rNMS. The Benjamini-Hochberg procedure with a false discovery rate (FDR) of 10% was used to adjust for multiple testing. The statistical significance for all tests was set at α = 0.05.
Thirty participants who received rNMS applied to the bilateral trapezius muscles were included in the analysis. All participants had a diagnosis of episodic migraine, and 10 subjects had an additional diagnosis of concurrent TTH (33.3%). Participants were on average 24.8 ± 4.0 years old (age range: 19–35 years) and 29 of the participants were female (96.7%). Demographics as well as baseline and follow-up characteristics are summarized in Table 1.
Table 1. Descriptive statistics of n = 30 patients affected by episodic migraine participating in two pilot studies of repetitive neuromuscular magnetic stimulation applied to the trapezius muscles.
Response set to a level of ≥25% was achieved in 50% of this cohort (n = 15) in terms of decreases in headache frequency, in 13% of participants (n = 4) in terms of decreases in headache intensity, in 73% of participants (n = 22) in terms of decreases in the MIDAS score, in 50% of participants (n = 15) in terms of decreases in monthly days with analgesic intake, and in 53% of participants (n= 16) in terms of increases in left-sided PPTs as well as in 60% of participants (n = 18) in terms of increases in right-sided PPTs, respectively. The results of the univariate analyses are summarized in Table 2.
Table 2. Results of the univariate analyses of response predictors of repetitive neuromuscular magnetic stimulation applied to the trapezius muscles in patients affected by episodic migraine.
The multivariate analyses revealed the following results (Table 3): headache type as well as pre-interventional headache frequency and headache intensity were significantly associated with responsiveness in terms of a ≥25% reduction in headache frequency. Responders had on average lower pre-interventional headache frequency (responders: 7.4 ± 3.4 days/month; non-responders: 8.9 ± 5.4 days/month) and intensity (responders: 5.0 ± 1.3 points; non-responders: 5.5 ± 1.5 points on a 10-point visual analog scale). In addition, responders were more often diagnosed with migraine without a concurrent diagnosis of TTH [responders: 12 participants without a TTH diagnosis (80%); non-responders: 8 participants without a TTH diagnosis (53.3%)]. The pre-interventional headache intensity was significantly associated with responsiveness in terms of a ≥25% reduction in monthly days with analgesic intake. The association of pre-interventional headache frequency with responsiveness showed a statistical trend (P = 0.052). Responders had on average higher pre-interventional headache frequency (responders: 9.0 ± 5.6 days/month; non-responders: 7.3 ± 3.0 days/month) and intensity (responders: 5.7 ± 1.4 points; non-responders: 4.7 ± 1.1 points on a 10-point visual analog scale).
Table 3. Results of the multivariate analyses of response predictors of repetitive neuromuscular magnetic stimulation applied to the trapezius muscles in n = 30 patients affected by episodic migraine.
The pre-interventional right-sided PPT was significantly associated with responsiveness in terms of a ≥25% increase in the right-sided PPTs. Responders had on average lower pre-interventional right-sided PPTs (responders: 2.0 ± 0.9; non-responders: 2.4 ± 0.7). The pre-interventional right-sided PPT was significantly associated with responsiveness in terms of a ≥25% increase in the left-sided PPTs. Responders had on average lower pre-interventional right-sided PPTs (responders: 1.9 ± 0.7; non-responders: 2.6 ± 0.8). Stimulation intensity was significantly associated with responsiveness in terms of a ≥25% reduction in headache intensity. Responders received rNMS with higher stimulation intensities on average (responders: 29.3 ± 4.4% of maximum stimulator output; non-responders: 23.5 ± 4.3% of maximum stimulator output).
No statistically significant predictors were identified for responsiveness in terms of a ≥25% reduction in MIDAS scores (P > 0.05).
In migraine research, neurostimulation methods are emerging non-invasive, non-pharmacological approaches, for which efficacy data is available but information on clinical baseline characteristics associated with positive treatment response are still lacking (11, 12). This study points at clinical headache and muscular characteristics as well as a technical factor as potential predictors for a beneficial response to rNMS in participants with episodic migraine. Reductions in headache frequency (from 8.17 to 6.33 headache days per month) and in MIDAS scores (from 26.3 reflecting severe disability to 15.3 reflecting moderate disability) were observed after application of rNMS compared to the baseline status, whereas no significant changes were found for headache intensity or duration.
Participants achieving a reduction in headache frequency of at least 25% had on average lower headache frequency, lower headache intensity, and were more often diagnosed with migraine without a TTH component at baseline. Responsiveness in terms of ≥25% reduction in monthly analgesic intake days was associated with higher mean headache intensity at baseline and higher headache frequency by trend. Regarding muscular involvement, participants achieving a ≥25% increase in right- and left-sided PPTs had on average lower baseline right-sided PPTs. From the technical perspective, participants with a decrease of at least 25% in headache intensity received rNMS with higher mean stimulation intensities. All those findings are in agreement with the current concept of migraine pathophysiology, which includes not only central pain mechanisms but also points at muscular involvement of the neck muscles (7, 42–44). Clinically, particularly the involvement of the upper trapezius muscles has been described more pronounced in migraine than in episodic TTH (45, 46). Supported by muscular imaging by advanced techniques like muscle T2 mapping of the trapezius muscles, the clinical signs might be considered surrogates of muscular neuroinflammation (47, 48). This imaging finding could be seen in line with the framework of the TCC (28, 29).
The level of sensitization and impairment of the nociceptive feedback control systems may eventually be more easily amenable by a tailored treatment approach the lower the baseline headache frequency and intensity are. This may imply to consider a neuromodulatory approach early during the course of disease, before perpetuation of the disorder. With respect to this assumption, a follow-up rNMS study involving patients suffering from chronic migraine would be of interest, as well as long-term follow-up investigations to assess the sustainability of the beneficial effects in different subgroups of patients (e.g., episodic migraine vs. high-frequent episodic migraine vs. chronic migraine). Treating migraine via the bottom-up approach allows the modulation of the afferent input to the TCC and, in consequence, of the central pain processing mechanisms (10, 28, 29). Since TTH is associated with different pathophysiological mechanisms, patients with migraine having a concurrent TTH component might respond to rNMS to a lesser extent (49–52).
Patients who are more frequently or more intensely affected by migraine may also use more medication for pain relief. Hence, a decrease of the intake of analgesics is likely to reflect a lower headache frequency and/or intensity as a positive response to rNMS. The better treatment response in patients with a higher level of muscular hyperalgesia supports the concept of the bottom-up approach, as well. In this regard, rNMS targeting the part of the trapezius muscles that is included in the TCC is particularly effective in patients with a high level of muscular involvement. Specifically, the impact of the stimulation intensity on the outcome might reflect a dose-effect relationship. Given the novelty of the rNMS approach, no comparisons of different stimulation protocols have been conducted yet.
Of note, we chose a reduction of ≥25% as responder rate since clinical experience support that responder rates lower than 50% are also clinically meaningful in the context of non-pharmacological preventive treatments (53). This is especially true for the cohort of this study since it involves participants suffering from frequent episodic migraine (up to 26 headache days per month).
Data on the predictors of treatment response to other non-invasive methods of neurostimulation (e.g., TMS, tDCS, or tENS of cranial nerves) for the prevention of migraine is lacking so far. Only one study examined potential predictors for the response to invasive ONS in refractory chronic headache (54). It showed that shorter unilateral headache attacks and prior response to a pharmacologically induced occipital nerve block were associated with a greater likelihood for a positive response to invasive ONS (54).
When interpreting the results of this analysis the following limitations should be respected. First, the sample size is low, which does not allow for an extrapolation to the general population of migraine patients. Second, the analysis relies on data retrieved from not-sham-controlled pilot studies, which is why placebo effects in the context of response level cannot be excluded. Further research is needed to evaluate the association of clinical as well as muscular characteristics and technical aspects to treatment response for neurostimulation therapy. In addition, future studies should investigate rNMS in a higher number of patients as well as in sham-controlled settings to assess and correct for a potential placebo effect. Future studies could for instance assess further predictors like age at onset of migraine, overall duration of migraine (55), number of local spots of muscular hyperalgesia (i.e., mTrPs), fluid biomarkers (e.g., calcitonin gene-related peptide), or biomarkers based on novel muscular imaging methods (e.g., T2 mapping derived from magnetic resonance imaging of the trapezius muscles) (47, 48). Since our results derive from a cohort of young adults with episodic migraine, future studies should include other migraine cohorts as well (e.g., pediatric populations). Further, this study did not assess variables reflecting central sensitization (e.g., allodynia), and it did not systematically assess common comorbidities like depression or anxiety. Future studies should implement such comorbidities in their study design. In addition, different classifications of responsiveness should be considered, for example ≥25% vs. ≥50% response, excellent responders (56), full-length responders, or wearing-off responders (57). Moreover, the establishment of standardized protocols for treatment and for data collection during baseline and follow-up are necessary for reliable data analysis and bias exclusion (55, 58). The identification of potential predictors for the different neurostimulation approaches and for a larger cohort of patients could enable an individually tailored, efficacy-predicting tool (score chart) in a multimodal therapy setting (59).
This analysis informs about predictors of treatment response to rNMS applied to the upper trapezius muscle in a cohort of young adults affected by episodic migraine. Findings demonstrate that some clinical headache characteristics at baseline (headache frequency, headache intensity, and headache diagnosis), the level of muscular hyperalgesia expressed by PPTs at baseline, as well as technical aspects during rNMS (stimulation intensity) may deliver information on how well an individual patient may respond to rNMS. These factors may allow early identification of patients who would experience benefits of rNMS based on their initial clinical presentation. This is important as rNMS represents an innovative and promising treatment approach that is, however, restricted to single headache centers at the current stage, only. Further, to establish a treatment option like rNMS in a cost- and time-efficient manner, the individual counseling on the treatment options in the context of a multimodal regimen should be based on all evidence available.
Data Availability Statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
The studies involving human participants were reviewed and approved by Ethikkommission TUM & LMU. The patients/participants provided their written informed consent to participate in this study.
TR and FTF conducted the clinical studies on which the analysis of the paper is based on with support of BK and HK and under the supervision of NS, FH, and MNL. CB and NS conducted the statistical analysis with support of TB and LA. CB, TR, MB, NS, SK, MNL, and FH discussed and interpreted the findings and gave their expert opinion with regards to all analyses. CB, TR, and MB drafted the manuscript. GU, PS, and ML compiled tables. All authors reviewed, commented on and contributed to the final manuscript. All authors have agreed to this final version of the article being submitted.
MNL received grants from the Deutsches Zentrum für Luft- und Raumfahrt (DLR-PT). MNL and FH received a grant Innovationsfonds of the joint federal committee of health insurance companies (GBA) for a nation-wide study on an early multimodal intervention program for children with migraine. The work of MB is supported by the Bavarian Gender Equality Grant of the Free State of Bavaria, the German Migraine and Headache Society (DMKG), Germany, and the ZNS-Hannelore-Kohl Stiftung, Germany. The work of NS is supported by the Dr. Ing. Leonhard Lorenz Foundation, the German Migraine and Headache Society (DMKG), and the Joachim Herz Foundation.
Conflict of Interest
The Division of Pediatric Neurology and Developmental Medicine, Dr. von Hauner Children's Hospital, LMU Hospital, Munich Germany is provided by an emFieldPro magnetic stimulator by Zimmer MedizinSysteme GmbH (Neu-Ulm, Germany). NS and SK received honoraria from Nexstim Plc (Helsinki, Finland). SK received honoraria from Brainlab AG (Munich, Germany), Spineart (Frankfurt, Germany), Ulrich Medical (Ulm, Germany), Zeiss Meditec (Jena, Germany), and Medtronic (Dublin, Ireland).
The remaining 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.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
DMKG, German Migraine and Headache Society; ICHD, international classification of headache disorders; MIDAS, migraine disability assessment; mTrP, myofascial trigger point; ONS, occipital nerve stimulation; PPT, pressure pain threshold; QoL, quality of life; REN, remote electrical neurostimulation; rNMS, repetitive neuromuscular magnetic stimulation; TCC, trigemino-cervical complex; tDCS, transcranial direct current stimulation; tENS, transcutaneous electrical nerve stimulation; TMS, transcranial magnetic stimulation; TTH, tension-type headache; tSNS, transcutaneous supraorbital nerve stimulation; tVNS, transcutaneous vagus nerve stimulation.
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Keywords: headache, migraine, neurostimulation, non-invasive neuromodulation, repetitive peripheral magnetic stimulation, myofascial trigger point, preventive migraine therapy, migraine prevention
Citation: Börner C, Renner T, Trepte-Freisleder F, Urban G, Schandelmaier P, Lang M, Lechner MF, Koenig H, Klose B, Albers L, Krieg SM, Baum T, Heinen F, Landgraf MN, Sollmann N and Bonfert MV (2022) Response Predictors of Repetitive Neuromuscular Magnetic Stimulation in the Preventive Treatment of Episodic Migraine. Front. Neurol. 13:919623. doi: 10.3389/fneur.2022.919623
Received: 14 April 2022; Accepted: 21 June 2022;
Published: 28 July 2022.
Edited by:Massimiliano Valeriani, Bambino Gesù Children's Hospital (IRCCS), Italy
Reviewed by:Marco Russo, IRCCS Local Health Authority of Reggio Emilia, Italy
Luciana Mendonça Barbosa, University of São Paulo, Brazil
Copyright © 2022 Börner, Renner, Trepte-Freisleder, Urban, Schandelmaier, Lang, Lechner, Koenig, Klose, Albers, Krieg, Baum, Heinen, Landgraf, Sollmann and Bonfert. 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) and the copyright owner(s) 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: Nico Sollmann, firstname.lastname@example.org
†These authors have contributed equally to this work and share first authorship