期刊
SCHIZOPHRENIA BULLETIN
卷 44, 期 1, 页码 65-74出版社
OXFORD UNIV PRESS
DOI: 10.1093/schbul/sbx028
关键词
schizophrenia; bipolar disorder; major depressive disorder; gray matter volume; white matter integrity
类别
资金
- National Natural Science Foundation of China [81271499, 81571311, 81571331]
- National Key Research and Development Program [2016YFC0904300, 2016YFC1306900]
- National High Tech Development Plan (863) [2015AA020513]
- NATIONAL INSTITUTE OF MENTAL HEALTH [T32MH016804] Funding Source: NIH RePORTER
Background: Schizophrenia (SZ), bipolar disorder (BD), and major depressive disorder (MDD) are distinct diagnostic categories in current psychiatric nosology, yet there is increasing evidence for shared clinical and biological features in these disorders. No previous studies have examined brain structural features concurrently in these 3 disorders. The aim of this study was to identify the extent of shared and distinct brain alterations in SZ, BD, and MDD. Methods: We examined gray matter (GM) volume and white matter (WM) integrity in a total of 485 individuals (135 with SZ, 86 with BD, 108 with MDD, and 156 healthy controls [HC]) who underwent high-resolution structural magnetic resonance imaging (MRI) and diffusion tensor imaging (DTI) at a single site. Results: Significant 4-group (SZ, BD, MDD, and HC groups) differences (P < .05, corrected) in GM volumes were found primarily in the paralimbic and heteromodal corticies. Post hoc analyses showed that the SZ, BD, and MDD groups shared GM volume decreases in 87.9% of the total regional volume with significant 4-group differences. Significant 4-group differences in WM integrity (P < .05 corrected) were found in callosal, limbic-paralimbic-hetermodal, cortico-cortical, thalamocortical and cerebellar WM. Post hoc analyses revealed that the SZ and BD groups shared WM alterations in all regions, while WM alterations were not observed with MDD. Conclusions: Our findings of common alterations in SZ, BD, and MDD support the presence of core neurobiological disruptions in these disorders and suggest that neural structural distinctions between these disorders may be less prominent than initially postulated, particularly between SZ and BD
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