TY - JOUR
T1 - Subcortical volumetric alterations in four major psychiatric disorders
T2 - a mega-analysis study of 5604 subjects and a volumetric data-driven approach for classification
AU - Okada, Naohiro
AU - Fukunaga, Masaki
AU - Miura, Kenichiro
AU - Nemoto, Kiyotaka
AU - Matsumoto, Junya
AU - Hashimoto, Naoki
AU - Kiyota, Masahiro
AU - Morita, Kentaro
AU - Koshiyama, Daisuke
AU - Ohi, Kazutaka
AU - Takahashi, Tsutomu
AU - Koeda, Michihiko
AU - Yamamori, Hidenaga
AU - Fujimoto, Michiko
AU - Yasuda, Yuka
AU - Hasegawa, Naomi
AU - Narita, Hisashi
AU - Yokoyama, Satoshi
AU - Mishima, Ryo
AU - Kawashima, Takahiko
AU - Kobayashi, Yuko
AU - Sasabayashi, Daiki
AU - Harada, Kenichiro
AU - Yamamoto, Maeri
AU - Hirano, Yoji
AU - Itahashi, Takashi
AU - Nakataki, Masahito
AU - Hashimoto, Ryu Ichiro
AU - Tha, Khin K.
AU - Koike, Shinsuke
AU - Matsubara, Toshio
AU - Okada, Go
AU - van Erp, Theo G.M.
AU - Jahanshad, Neda
AU - Yoshimura, Reiji
AU - Abe, Osamu
AU - Onitsuka, Toshiaki
AU - Watanabe, Yoshiyuki
AU - Matsuo, Koji
AU - Yamasue, Hidenori
AU - Okamoto, Yasumasa
AU - Suzuki, Michio
AU - Turner, Jessica A.
AU - Thompson, Paul M.
AU - Ozaki, Norio
AU - Kasai, Kiyoto
AU - Hashimoto, Ryota
N1 - Publisher Copyright:
© The Author(s) 2023.
PY - 2023/12
Y1 - 2023/12
N2 - Differential diagnosis is sometimes difficult in practical psychiatric settings, in terms of using the current diagnostic system based on presenting symptoms and signs. The creation of a novel diagnostic system using objective biomarkers is expected to take place. Neuroimaging studies and others reported that subcortical brain structures are the hubs for various psycho-behavioral functions, while there are so far no neuroimaging data-driven clinical criteria overcoming limitations of the current diagnostic system, which would reflect cognitive/social functioning. Prior to the main analysis, we conducted a large-scale multisite study of subcortical volumetric and lateralization alterations in schizophrenia, bipolar disorder, major depressive disorder, and autism spectrum disorder using T1-weighted images of 5604 subjects (3078 controls and 2526 patients). We demonstrated larger lateral ventricles volume in schizophrenia, bipolar disorder, and major depressive disorder, smaller hippocampus volume in schizophrenia and bipolar disorder, and schizophrenia-specific smaller amygdala, thalamus, and accumbens volumes and larger caudate, putamen, and pallidum volumes. In addition, we observed a leftward alteration of lateralization for pallidum volume specifically in schizophrenia. Moreover, as our main objective, we clustered the 5,604 subjects based on subcortical volumes, and explored whether data-driven clustering results can explain cognitive/social functioning in the subcohorts. We showed a four-biotype classification, namely extremely (Brain Biotype [BB] 1) and moderately smaller limbic regions (BB2), larger basal ganglia (BB3), and normal volumes (BB4), being associated with cognitive/social functioning. Specifically, BB1 and BB2–3 were associated with severe and mild cognitive/social impairment, respectively, while BB4 was characterized by normal cognitive/social functioning. Our results may lead to the future creation of novel biological data-driven psychiatric diagnostic criteria, which may be expected to be useful for prediction or therapeutic selection.
AB - Differential diagnosis is sometimes difficult in practical psychiatric settings, in terms of using the current diagnostic system based on presenting symptoms and signs. The creation of a novel diagnostic system using objective biomarkers is expected to take place. Neuroimaging studies and others reported that subcortical brain structures are the hubs for various psycho-behavioral functions, while there are so far no neuroimaging data-driven clinical criteria overcoming limitations of the current diagnostic system, which would reflect cognitive/social functioning. Prior to the main analysis, we conducted a large-scale multisite study of subcortical volumetric and lateralization alterations in schizophrenia, bipolar disorder, major depressive disorder, and autism spectrum disorder using T1-weighted images of 5604 subjects (3078 controls and 2526 patients). We demonstrated larger lateral ventricles volume in schizophrenia, bipolar disorder, and major depressive disorder, smaller hippocampus volume in schizophrenia and bipolar disorder, and schizophrenia-specific smaller amygdala, thalamus, and accumbens volumes and larger caudate, putamen, and pallidum volumes. In addition, we observed a leftward alteration of lateralization for pallidum volume specifically in schizophrenia. Moreover, as our main objective, we clustered the 5,604 subjects based on subcortical volumes, and explored whether data-driven clustering results can explain cognitive/social functioning in the subcohorts. We showed a four-biotype classification, namely extremely (Brain Biotype [BB] 1) and moderately smaller limbic regions (BB2), larger basal ganglia (BB3), and normal volumes (BB4), being associated with cognitive/social functioning. Specifically, BB1 and BB2–3 were associated with severe and mild cognitive/social impairment, respectively, while BB4 was characterized by normal cognitive/social functioning. Our results may lead to the future creation of novel biological data-driven psychiatric diagnostic criteria, which may be expected to be useful for prediction or therapeutic selection.
UR - http://www.scopus.com/inward/record.url?scp=85166679340&partnerID=8YFLogxK
U2 - 10.1038/s41380-023-02141-9
DO - 10.1038/s41380-023-02141-9
M3 - 学術論文
C2 - 37537281
AN - SCOPUS:85166679340
SN - 1359-4184
VL - 28
SP - 5206
EP - 5216
JO - Molecular Psychiatry
JF - Molecular Psychiatry
IS - 12
ER -