TY - JOUR
T1 - Toward recovery in schizophrenia
T2 - Current concepts, findings, and future research directions
AU - Onitsuka, Toshiaki
AU - Hirano, Yoji
AU - Nakazawa, Takanobu
AU - Ichihashi, Kayo
AU - Miura, Kenichiro
AU - Inada, Ken
AU - Mitoma, Ryo
AU - Yasui-Furukori, Norio
AU - Hashimoto, Ryota
N1 - Funding Information:
Japan Agency for Medical Research and Development (AMED) under grant number JP21dm0207069 (TO). Japan Society for the Promotion of Science (JSPS) KAKENHI under grant numbers JP20KK0193, JP18K07604, JP19H00630, JP19H03579, JP21H02851; AMED under grant number JP19dm0107124; and the 2019 SIRS Research Fund Award from Schizophrenia International Research Society (YH). AMED under grant numbers JP21wm0425012 and JP20gm1310003, the Takeda Science Foundation (TN). AMED under grant number JP21dm0207069, JSPS KAKENHI (20K06920) (KM). Brain/MINDS & beyond studies (grant number JP21dm0307002) from AMED; AMED under grant numbers JP21dk0307083, JP21dk0307103, JP21uk1024002, and JP21wm0425012; JSPS Grant‐in‐Aid for Scientific Research (B) JP20H03611 and for Specially Promoted Research JP19H05467; and SENSHIN Medical Research Foundation and Intramural Research Grant (3‐1) for Neurological and Psychiatric Disorders of NCNP (RH).
Publisher Copyright:
© 2022 The Authors. Psychiatry and Clinical Neurosciences © 2022 Japanese Society of Psychiatry and Neurology.
PY - 2022/7
Y1 - 2022/7
N2 - Schizophrenia was initially defined as “dementia praecox” by E. Kraepelin, which implies progressive deterioration. However, recent studies have revealed that early effective intervention may lead to social and functional recovery in schizophrenia. In this review, we provide an overview of current concepts in schizophrenia and pathophysiological hypotheses. In addition, we present recent findings from clinical and basic research on schizophrenia. Recent neuroimaging and neurophysiological studies have consistently revealed specific biological differences in the structure and function of the brain in those with schizophrenia. From a basic research perspective, to determine the essential pathophysiology underlying schizophrenia, it is crucial that findings from all lines of inquiry—induced pluripotent stem cell (iPSC)-derived neural cells from patients, murine models expressing genetic mutations identified in patients, and patient clinical data—be integrated to contextualize the analysis results. However, the findings remain insufficient to serve as a diagnostic tool or a biomarker for predicting schizophrenia-related outcomes. Collaborations to conduct clinical research based on the patients' and their families' values are just beginning, and further development is expected.
AB - Schizophrenia was initially defined as “dementia praecox” by E. Kraepelin, which implies progressive deterioration. However, recent studies have revealed that early effective intervention may lead to social and functional recovery in schizophrenia. In this review, we provide an overview of current concepts in schizophrenia and pathophysiological hypotheses. In addition, we present recent findings from clinical and basic research on schizophrenia. Recent neuroimaging and neurophysiological studies have consistently revealed specific biological differences in the structure and function of the brain in those with schizophrenia. From a basic research perspective, to determine the essential pathophysiology underlying schizophrenia, it is crucial that findings from all lines of inquiry—induced pluripotent stem cell (iPSC)-derived neural cells from patients, murine models expressing genetic mutations identified in patients, and patient clinical data—be integrated to contextualize the analysis results. However, the findings remain insufficient to serve as a diagnostic tool or a biomarker for predicting schizophrenia-related outcomes. Collaborations to conduct clinical research based on the patients' and their families' values are just beginning, and further development is expected.
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U2 - 10.1111/pcn.13342
DO - 10.1111/pcn.13342
M3 - Review article
C2 - 35235256
AN - SCOPUS:85127451382
SN - 1323-1316
VL - 76
SP - 282
EP - 291
JO - Psychiatry and clinical neurosciences
JF - Psychiatry and clinical neurosciences
IS - 7
ER -