Dopaminergic dysfunction and excitatory/inhibitory imbalance in treatment-resistant schizophrenia and novel neuromodulatory treatment

神经调节 神经科学 多巴胺能 氯氮平 脑深部刺激 精神分裂症(面向对象编程) 磁刺激 心理学 谷氨酸的 电休克疗法 抗精神病药 医学 刺激 多巴胺 精神科 帕金森病 疾病 内科学 谷氨酸受体 认知 受体
作者
Masataka Wada,Yoshihiro Noda,Yusuke Iwata,Sakiko Tsugawa,Kazunari Yoshida,Hideaki Tani,Yoji Hirano,Shinsuke Koike,Daiki Sasabayashi,Haruyuki Katayama,Eric Plitman,Kazutaka Ohi,Fumihiko Ueno,Fernando Caravaggio,Teruki Koizumi,Philip Gerretsen,Takefumi Suzuki,Hiroyuki Uchida,Daniel J. Müller,Masaru Mimura
出处
期刊:Molecular Psychiatry [Springer Nature]
卷期号:27 (7): 2950-2967 被引量:115
标识
DOI:10.1038/s41380-022-01572-0
摘要

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.
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