Neuropsychopharmacology Reports (Sep 2024)

Neurophysiological profiles of patients with bipolar disorders as probed with transcranial magnetic stimulation: A systematic review

  • Keita Taniguchi,
  • Naotsugu Kaneko,
  • Masataka Wada,
  • Sotaro Moriyama,
  • Shinichiro Nakajima,
  • Masaru Mimura,
  • Yoshihiro Noda

DOI
https://doi.org/10.1002/npr2.12458
Journal volume & issue
Vol. 44, no. 3
pp. 572 – 584

Abstract

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Abstract Aim Bipolar disorder (BD) has a significant impact on global health, yet its neurophysiological basis remains poorly understood. Conventional treatments have limitations, highlighting the need for a better understanding of the neurophysiology of BD for early diagnosis and novel therapeutic strategies. Design Employing a systematic review approach of the PRISMA guidelines, this study assessed the usefulness and validity of transcranial magnetic stimulation (TMS) neurophysiology in patients with BD. Methods Databases searched included PubMed, MEDLINE, Embase, and PsycINFO, covering studies from January 1985 to January 2024. Results Out of 6597 articles screened, nine studies met the inclusion criteria, providing neurophysiological insights into the pathophysiological basis of BD using TMS–electromyography and TMS–electroencephalography methods. Findings revealed significant neurophysiological impairments in patients with BD compared to healthy controls, specifically in cortical inhibition and excitability. In particular, short‐interval cortical inhibition (SICI) was consistently diminished in BD across the studies, which suggests a fundamental impairment of cortical inhibitory function in BD. This systematic review corroborates the potential utility of TMS neurophysiology in elucidating the pathophysiological basis of BD. Specifically, the reduced cortical inhibition in the SICI paradigm observed in patients with BD suggests gamma‐aminobutyric acid (GABA)‐A receptor‐mediated dysfunction, but results from other TMS paradigms have been inconsistent. Thus, complex neurophysiological processes may be involved in the pathological basis underlying BD. This study demonstrated that BD has a neural basis involving impaired GABAergic function, and it is highly expected that further research on TMS neurophysiology will further elucidate the pathophysiological basis of BD.

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