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Baseline functional connectivity may predict placebo responses to accelerated rTMS treatment in major depression
Although in theory sham repetitive transcranial magnetic stimulation (rTMS) has no inherent therapeutic value, nonetheless, such placebo stimulations may have relevant therapeutic effects in clinically depressed patients. On the other hand, antidepressant responses to sham rTMS are quite heterogeneo...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267925/ https://www.ncbi.nlm.nih.gov/pubmed/31633261 http://dx.doi.org/10.1002/hbm.24828 |
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author | Wu, Guo‐Rong Wang, Xiaowan Baeken, Chris |
author_facet | Wu, Guo‐Rong Wang, Xiaowan Baeken, Chris |
author_sort | Wu, Guo‐Rong |
collection | PubMed |
description | Although in theory sham repetitive transcranial magnetic stimulation (rTMS) has no inherent therapeutic value, nonetheless, such placebo stimulations may have relevant therapeutic effects in clinically depressed patients. On the other hand, antidepressant responses to sham rTMS are quite heterogeneous across individuals and its neural underpinnings have not been explored yet. The current brain imaging study aims to detect baseline neural fingerprints resulting in clinically beneficial placebo rTMS treatment responses. We collected resting‐state functional magnetic resonance imaging data prior to a registered randomized clinical trial of accelerated placebo stimulation protocol in patients documented with treatment‐resistant depression (http://clinicaltrials.gov/show/NCT01832805). In addition to global brain connectivity and rostral anterior cingulate cortex (rACC) seed‐based functional connectivity (FC), elastic‐net regression and cross‐validation procedures were used to identify baseline intrinsic brain connectivity biomarkers for sham‐rTMS responses. Placebo responses to accelerated sham rTMS were correlated with baseline global brain connectivity in the rACC/ventral medial prefrontal cortex (vmPFC). Concerning the rACC seed‐based FC analysis, the placebo response was associated positively with the precuneus/posterior cingulate (PCun/PCC) cortex and negatively with the middle frontal gyrus. Our findings provide first brain imaging evidence for placebo responses to sham stimulation being predictable from rACC rsFC profiles, especially in brain areas implicated in (re)appraisal and self‐focus processes. |
format | Online Article Text |
id | pubmed-7267925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72679252020-06-12 Baseline functional connectivity may predict placebo responses to accelerated rTMS treatment in major depression Wu, Guo‐Rong Wang, Xiaowan Baeken, Chris Hum Brain Mapp Research Articles Although in theory sham repetitive transcranial magnetic stimulation (rTMS) has no inherent therapeutic value, nonetheless, such placebo stimulations may have relevant therapeutic effects in clinically depressed patients. On the other hand, antidepressant responses to sham rTMS are quite heterogeneous across individuals and its neural underpinnings have not been explored yet. The current brain imaging study aims to detect baseline neural fingerprints resulting in clinically beneficial placebo rTMS treatment responses. We collected resting‐state functional magnetic resonance imaging data prior to a registered randomized clinical trial of accelerated placebo stimulation protocol in patients documented with treatment‐resistant depression (http://clinicaltrials.gov/show/NCT01832805). In addition to global brain connectivity and rostral anterior cingulate cortex (rACC) seed‐based functional connectivity (FC), elastic‐net regression and cross‐validation procedures were used to identify baseline intrinsic brain connectivity biomarkers for sham‐rTMS responses. Placebo responses to accelerated sham rTMS were correlated with baseline global brain connectivity in the rACC/ventral medial prefrontal cortex (vmPFC). Concerning the rACC seed‐based FC analysis, the placebo response was associated positively with the precuneus/posterior cingulate (PCun/PCC) cortex and negatively with the middle frontal gyrus. Our findings provide first brain imaging evidence for placebo responses to sham stimulation being predictable from rACC rsFC profiles, especially in brain areas implicated in (re)appraisal and self‐focus processes. John Wiley & Sons, Inc. 2019-10-21 /pmc/articles/PMC7267925/ /pubmed/31633261 http://dx.doi.org/10.1002/hbm.24828 Text en © 2019 The Authors. Human Brain Mapping published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Wu, Guo‐Rong Wang, Xiaowan Baeken, Chris Baseline functional connectivity may predict placebo responses to accelerated rTMS treatment in major depression |
title | Baseline functional connectivity may predict placebo responses to accelerated rTMS treatment in major depression |
title_full | Baseline functional connectivity may predict placebo responses to accelerated rTMS treatment in major depression |
title_fullStr | Baseline functional connectivity may predict placebo responses to accelerated rTMS treatment in major depression |
title_full_unstemmed | Baseline functional connectivity may predict placebo responses to accelerated rTMS treatment in major depression |
title_short | Baseline functional connectivity may predict placebo responses to accelerated rTMS treatment in major depression |
title_sort | baseline functional connectivity may predict placebo responses to accelerated rtms treatment in major depression |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267925/ https://www.ncbi.nlm.nih.gov/pubmed/31633261 http://dx.doi.org/10.1002/hbm.24828 |
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