| Literature DB >> 33267920 |
Megumi Kinjo1, Masataka Wada1, Shinichiro Nakajima1, Sakiko Tsugawa1, Tomomi Nakahara1, Daniel M Blumberger2, Masaru Mimura1, Yoshihiro Noda1.
Abstract
Major depressive disorder (MDD) is a mental illness with high socio-economic burden, but its pathophysiology has not been fully elucidated. Recently, the cortical excitatory and inhibitory imbalance hypothesis and neuroplasticity hypothesis have been proposed for MDD. Although several studies have examined the neurophysiological profiles in MDD using transcranial magnetic stimulation (TMS), a meta-analysis of TMS neurophysiology has not been performed. The objective of this study was to compare TMS-electromyogram (TMS-EMG) findings between patients with MDD and healthy controls (HCs). To this end, we examined whether patients with MDD have lower short-interval cortical inhibition (SICI) which reflects gamma-aminobutyric acid (GABA)A receptor-mediated activity, lower cortical silent period (CSP) which represents GABAB receptor-mediated activity, higher intracortical facilitation (ICF) which reflects glutamate N-methyl-D-aspartate receptor-mediated activity, and the lower result of paired associative stimulation (PAS) paradigm which shows the level of neuroplasticity in comparison with HC. Further, we explored the effect of clinical and demographic factors that may influence TMS neurophysiological indices. We first searched and identified research articles that conducted single- or paired-pulse TMS-EMG on patients with MDD and HC. Subsequently, we extracted the data from the included studies and meta-analyzed the data with the comprehensive meta-analysis software. Patients with MDD were associated with lower SICI, lower CSP, potentially higher ICF, and lower PAS compared with HC. Our results confirmed the proposed hypotheses, suggesting the usefulness of TMS neurophysiology as potential diagnostic markers of MDD.Entities:
Keywords: TMS neurophysiology; cortical excitability; cortical inhibition; excitatory and inhibitory imbalance hypothesis; major depressive disorder; neuroplasticity hypothesis
Year: 2020 PMID: 33267920 PMCID: PMC7856413 DOI: 10.1017/S0033291720004729
Source DB: PubMed Journal: Psychol Med ISSN: 0033-2917 Impact factor: 7.723