Cargando…
The modulation effects of repeated transcutaneous auricular vagus nerve stimulation on the functional connectivity of key brainstem regions along the vagus nerve pathway in migraine patients
BACKGROUND: Previous studies have shown a significant response to acute transcutaneous vagus nerve stimulation (taVNS) in regions of the vagus nerve pathway, including the nucleus tractus solitarius (NTS), raphe nucleus (RN) and locus coeruleus (LC) in both healthy human participants and migraine pa...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275573/ https://www.ncbi.nlm.nih.gov/pubmed/37333617 http://dx.doi.org/10.3389/fnmol.2023.1160006 |
_version_ | 1785059901152690176 |
---|---|
author | Huang, Yiting Zhang, Yue Hodges, Sierra Li, Hui Yan, Zhaoxian Liu, Xian Hou, Xiaoyan Chen, Weicui Chai-Zhang, Thalia Kong, Jian Liu, Bo |
author_facet | Huang, Yiting Zhang, Yue Hodges, Sierra Li, Hui Yan, Zhaoxian Liu, Xian Hou, Xiaoyan Chen, Weicui Chai-Zhang, Thalia Kong, Jian Liu, Bo |
author_sort | Huang, Yiting |
collection | PubMed |
description | BACKGROUND: Previous studies have shown a significant response to acute transcutaneous vagus nerve stimulation (taVNS) in regions of the vagus nerve pathway, including the nucleus tractus solitarius (NTS), raphe nucleus (RN) and locus coeruleus (LC) in both healthy human participants and migraine patients. This study aims to investigate the modulation effect of repeated taVNS on these brainstem regions by applying seed-based resting-state functional connectivity (rsFC) analysis. METHODS: 70 patients with migraine were recruited and randomized to receive real or sham taVNS treatments for 4 weeks. fMRI data were collected from each participant before and after 4 weeks of treatment. The rsFC analyses were performed using NTS, RN and LC as the seeds. RESULTS: 59 patients (real group: n = 33; sham group: n = 29) completed two fMRI scan sessions. Compared to sham taVNS, real taVNS was associated with a significant reduction in the number of migraine attack days (p = 0.024) and headache pain intensity (p = 0.008). The rsFC analysis showed repeated taVNS modulated the functional connectivity between the brain stem regions of the vagus nerve pathway and brain regions associated with the limbic system (bilateral hippocampus), pain processing and modulation (bilateral postcentral gyrus, thalamus, and mPFC), and basal ganglia (putamen/caudate). In addition, the rsFC change between the RN and putamen was significantly associated with the reduction in the number of migraine days. CONCLUSION: Our findings suggest that taVNS can significantly modulate the vagus nerve central pathway, which may contribute to the potential treatment effects of taVNS for migraine. Clinical Trial Registration: http://www.chictr.org.cn/hvshowproject.aspx?id=11101, identifier ChiCTR-INR-17010559. |
format | Online Article Text |
id | pubmed-10275573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102755732023-06-17 The modulation effects of repeated transcutaneous auricular vagus nerve stimulation on the functional connectivity of key brainstem regions along the vagus nerve pathway in migraine patients Huang, Yiting Zhang, Yue Hodges, Sierra Li, Hui Yan, Zhaoxian Liu, Xian Hou, Xiaoyan Chen, Weicui Chai-Zhang, Thalia Kong, Jian Liu, Bo Front Mol Neurosci Molecular Neuroscience BACKGROUND: Previous studies have shown a significant response to acute transcutaneous vagus nerve stimulation (taVNS) in regions of the vagus nerve pathway, including the nucleus tractus solitarius (NTS), raphe nucleus (RN) and locus coeruleus (LC) in both healthy human participants and migraine patients. This study aims to investigate the modulation effect of repeated taVNS on these brainstem regions by applying seed-based resting-state functional connectivity (rsFC) analysis. METHODS: 70 patients with migraine were recruited and randomized to receive real or sham taVNS treatments for 4 weeks. fMRI data were collected from each participant before and after 4 weeks of treatment. The rsFC analyses were performed using NTS, RN and LC as the seeds. RESULTS: 59 patients (real group: n = 33; sham group: n = 29) completed two fMRI scan sessions. Compared to sham taVNS, real taVNS was associated with a significant reduction in the number of migraine attack days (p = 0.024) and headache pain intensity (p = 0.008). The rsFC analysis showed repeated taVNS modulated the functional connectivity between the brain stem regions of the vagus nerve pathway and brain regions associated with the limbic system (bilateral hippocampus), pain processing and modulation (bilateral postcentral gyrus, thalamus, and mPFC), and basal ganglia (putamen/caudate). In addition, the rsFC change between the RN and putamen was significantly associated with the reduction in the number of migraine days. CONCLUSION: Our findings suggest that taVNS can significantly modulate the vagus nerve central pathway, which may contribute to the potential treatment effects of taVNS for migraine. Clinical Trial Registration: http://www.chictr.org.cn/hvshowproject.aspx?id=11101, identifier ChiCTR-INR-17010559. Frontiers Media S.A. 2023-06-02 /pmc/articles/PMC10275573/ /pubmed/37333617 http://dx.doi.org/10.3389/fnmol.2023.1160006 Text en Copyright © 2023 Huang, Zhang, Hodges, Li, Yan, Liu, Hou, Chen, Chai-Zhang, Kong and Liu. https://creativecommons.org/licenses/by/4.0/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. |
spellingShingle | Molecular Neuroscience Huang, Yiting Zhang, Yue Hodges, Sierra Li, Hui Yan, Zhaoxian Liu, Xian Hou, Xiaoyan Chen, Weicui Chai-Zhang, Thalia Kong, Jian Liu, Bo The modulation effects of repeated transcutaneous auricular vagus nerve stimulation on the functional connectivity of key brainstem regions along the vagus nerve pathway in migraine patients |
title | The modulation effects of repeated transcutaneous auricular vagus nerve stimulation on the functional connectivity of key brainstem regions along the vagus nerve pathway in migraine patients |
title_full | The modulation effects of repeated transcutaneous auricular vagus nerve stimulation on the functional connectivity of key brainstem regions along the vagus nerve pathway in migraine patients |
title_fullStr | The modulation effects of repeated transcutaneous auricular vagus nerve stimulation on the functional connectivity of key brainstem regions along the vagus nerve pathway in migraine patients |
title_full_unstemmed | The modulation effects of repeated transcutaneous auricular vagus nerve stimulation on the functional connectivity of key brainstem regions along the vagus nerve pathway in migraine patients |
title_short | The modulation effects of repeated transcutaneous auricular vagus nerve stimulation on the functional connectivity of key brainstem regions along the vagus nerve pathway in migraine patients |
title_sort | modulation effects of repeated transcutaneous auricular vagus nerve stimulation on the functional connectivity of key brainstem regions along the vagus nerve pathway in migraine patients |
topic | Molecular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275573/ https://www.ncbi.nlm.nih.gov/pubmed/37333617 http://dx.doi.org/10.3389/fnmol.2023.1160006 |
work_keys_str_mv | AT huangyiting themodulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT zhangyue themodulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT hodgessierra themodulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT lihui themodulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT yanzhaoxian themodulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT liuxian themodulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT houxiaoyan themodulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT chenweicui themodulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT chaizhangthalia themodulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT kongjian themodulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT liubo themodulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT huangyiting modulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT zhangyue modulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT hodgessierra modulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT lihui modulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT yanzhaoxian modulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT liuxian modulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT houxiaoyan modulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT chenweicui modulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT chaizhangthalia modulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT kongjian modulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients AT liubo modulationeffectsofrepeatedtranscutaneousauricularvagusnervestimulationonthefunctionalconnectivityofkeybrainstemregionsalongthevagusnervepathwayinmigrainepatients |