TY - JOUR
T1 - Dopaminergic dysfunction and excitatory/inhibitory imbalance in treatment-resistant schizophrenia and novel neuromodulatory treatment
AU - Wada, Masataka
AU - Noda, Yoshihiro
AU - Iwata, Yusuke
AU - Tsugawa, Sakiko
AU - Yoshida, Kazunari
AU - Tani, Hideaki
AU - Hirano, Yoji
AU - Koike, Shinsuke
AU - Sasabayashi, Daiki
AU - Katayama, Haruyuki
AU - Plitman, Eric
AU - Ohi, Kazutaka
AU - Ueno, Fumihiko
AU - Caravaggio, Fernando
AU - Koizumi, Teruki
AU - Gerretsen, Philip
AU - Suzuki, Takefumi
AU - Uchida, Hiroyuki
AU - Müller, Daniel J.
AU - Mimura, Masaru
AU - Remington, Gary
AU - Grace, Anthony A.
AU - Graff-Guerrero, Ariel
AU - Nakajima, Shinichiro
N1 - Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2022/7
Y1 - 2022/7
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85128444952&partnerID=8YFLogxK
U2 - 10.1038/s41380-022-01572-0
DO - 10.1038/s41380-022-01572-0
M3 - 総説
C2 - 35444257
AN - SCOPUS:85128444952
SN - 1359-4184
VL - 27
SP - 2950
EP - 2967
JO - Molecular Psychiatry
JF - Molecular Psychiatry
IS - 7
ER -