TY - JOUR
T1 - Differences in functional connectivity networks related to the midbrain dopaminergic system-related area in various psychiatric disorders
AU - Nakamura, Yuko
AU - Okada, Naohiro
AU - Koshiyama, Daisuke
AU - Kamiya, Kouhei
AU - Abe, Osamu
AU - Kunimatsu, Akira
AU - Okanoya, Kazuo
AU - Kasai, Kiyoto
AU - Koike, Shinsuke
N1 - Publisher Copyright:
© The Author(s) 2020. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. All rights reserved.
PY - 2020/9/1
Y1 - 2020/9/1
N2 - Objective: Disruptions in the dopamine system have been observed in psychiatric disorders. Since dopamine is mainly produced in the ventral tegmental area (VTA), elucidating the differences in the VTA neural network across psychiatric disorders would facilitate a greater understanding of the pathophysiological mechanisms underlying these disorders. However, no study has compared VTA-seed-based functional connectivity across psychiatric disorders. Therefore, we conducted a resting-state functional magnetic resonance imaging (rs-fMRI) study to perform a seed-based fMRI analysis, using the VTA as a seed. Methods: We included participants with major depressive disorder (MDD; n = 45), schizophrenia (n = 32), and bipolar disorder (BPD; n = 30), along with healthy control participants (n = 46) who were matched for age, gender, and handedness. Results: The results showed that patients with MDD and BPD had altered VTA-related connectivity in the superior frontal gyrus, frontal pole regions, hippocampus, cerebellum, and posterior cingulate cortex. Some of these differences in connectivity were also found between affective disorders and schizophrenia; however, there were no differences between the schizophrenia and control groups. Connectivity between the VTA and the hippocampus was correlated with positive symptoms in the schizophrenia group. The connectivity was not associated with medication dose, and the results remained significant after controlling for dose. Conclusions: The results suggest that altered brain functional connectivity related to VTA networks could be associated with the distinctive pathophysiologies of psychiatric disorders, especially affective disorders.
AB - Objective: Disruptions in the dopamine system have been observed in psychiatric disorders. Since dopamine is mainly produced in the ventral tegmental area (VTA), elucidating the differences in the VTA neural network across psychiatric disorders would facilitate a greater understanding of the pathophysiological mechanisms underlying these disorders. However, no study has compared VTA-seed-based functional connectivity across psychiatric disorders. Therefore, we conducted a resting-state functional magnetic resonance imaging (rs-fMRI) study to perform a seed-based fMRI analysis, using the VTA as a seed. Methods: We included participants with major depressive disorder (MDD; n = 45), schizophrenia (n = 32), and bipolar disorder (BPD; n = 30), along with healthy control participants (n = 46) who were matched for age, gender, and handedness. Results: The results showed that patients with MDD and BPD had altered VTA-related connectivity in the superior frontal gyrus, frontal pole regions, hippocampus, cerebellum, and posterior cingulate cortex. Some of these differences in connectivity were also found between affective disorders and schizophrenia; however, there were no differences between the schizophrenia and control groups. Connectivity between the VTA and the hippocampus was correlated with positive symptoms in the schizophrenia group. The connectivity was not associated with medication dose, and the results remained significant after controlling for dose. Conclusions: The results suggest that altered brain functional connectivity related to VTA networks could be associated with the distinctive pathophysiologies of psychiatric disorders, especially affective disorders.
KW - Psychiatric disorders
KW - Resting-state functional magnetic resonance imaging
KW - The ventral tegmental area
UR - http://www.scopus.com/inward/record.url?scp=85092145223&partnerID=8YFLogxK
U2 - 10.1093/schbul/sbz121
DO - 10.1093/schbul/sbz121
M3 - 記事
C2 - 31901932
AN - SCOPUS:85092145223
SN - 0586-7614
VL - 46
SP - 1239
EP - 1248
JO - Schizophrenia Bulletin
JF - Schizophrenia Bulletin
IS - 5
ER -