| Literature DB >> 35444257 |
Masataka Wada1, Yoshihiro Noda1, Yusuke Iwata2, Sakiko Tsugawa1, Kazunari Yoshida1,3,4,5, Hideaki Tani1, Yoji Hirano6,7, Shinsuke Koike8, Daiki Sasabayashi9,10, Haruyuki Katayama1, Eric Plitman11, Kazutaka Ohi12, Fumihiko Ueno1,5,13, Fernando Caravaggio5,13, Teruki Koizumi1,14, Philip Gerretsen5,13,15,16, Takefumi Suzuki2, Hiroyuki Uchida1, Daniel J Müller3,5,16, Masaru Mimura1, Gary Remington5,16, Anthony A Grace17, Ariel Graff-Guerrero5,13,15,16, Shinichiro Nakajima18,19.
Abstract
Antipsychotic drugs are the mainstay in the treatment of schizophrenia. However, one-third of patients do not show adequate improvement in positive symptoms with non-clozapine antipsychotics. Additionally, approximately half of them show poor response to clozapine, electroconvulsive therapy, or other augmentation strategies. However, the development of novel treatment for these conditions is difficult due to the complex and heterogenous pathophysiology of treatment-resistant schizophrenia (TRS). Therefore, this review provides key findings, potential treatments, and a roadmap for future research in this area. First, we review the neurobiological pathophysiology of TRS, particularly the dopaminergic, glutamatergic, and GABAergic pathways. Next, the limitations of existing and promising treatments are presented. Specifically, this article focuses on the therapeutic potential of neuromodulation, including electroconvulsive therapy, repetitive transcranial magnetic stimulation, transcranial direct current stimulation, and deep brain stimulation. Finally, we propose multivariate analyses that integrate various perspectives of the pathogenesis, such as dopaminergic dysfunction and excitatory/inhibitory imbalance, thereby elucidating the heterogeneity of TRS that could not be obtained by conventional statistics. These analyses can in turn lead to a precision medicine approach with closed-loop neuromodulation targeting the detected pathophysiology of TRS.Entities:
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Year: 2022 PMID: 35444257 DOI: 10.1038/s41380-022-01572-0
Source DB: PubMed Journal: Mol Psychiatry ISSN: 1359-4184 Impact factor: 15.992