Asphyxia at birth affects brain structure in patients on the schizophrenia-bipolar disorder spectrum and healthy participants

被引:13
作者
Wortinger, Laura Anne [1 ,2 ]
Engen, Kristine [1 ,2 ]
Barth, Claudia [2 ]
Andreassen, Ole A. [2 ,3 ]
Jorgensen, Kjetil Nordbo [1 ,2 ]
Agartz, Ingrid [1 ,2 ,4 ]
机构
[1] Diakonhjemmet Hosp, Dept Psychiat Res, Oslo, Norway
[2] Univ Oslo, Inst Clin Med, NORMENT, Oslo, Norway
[3] Oslo Univ Hosp, Div Mental Hlth & Addict, NORMENT, Oslo, Norway
[4] Karolinska Inst, Ctr Psychiat Res, Dept Clin Neurosci, Stockholm, Sweden
关键词
Asphyxia; bipolar disorder; caudate; intracranial volume; schizophrenia; surface area; OBSTETRIC COMPLICATIONS; SURFACE-AREA; LONGITUDINAL CHANGES; CORTICAL MORPHOLOGY; INTRACRANIAL VOLUME; HIPPOCAMPAL VOLUME; FETAL HYPOXIA; ABNORMALITIES; RISK; CAUDATE;
D O I
10.1017/S0033291720002779
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background Uncertainty exists about what causes brain structure alterations associated with schizophrenia (SZ) and bipolar disorder (BD). Whether a history of asphyxia-related obstetric complication (ASP) - a common but harmful condition for neural tissue - contributes to variations in adult brain structure is unclear. We investigated ASP and its relationship to intracranial (ICV), global brain volumes and regional cortical and subcortical structures. Methods A total of 311 patients on the SZ - BD spectrum and 218 healthy control (HC) participants underwent structural magnetic resonance imaging. They were evaluated for ASP using prospective information obtained from the Medical Birth Registry of Norway. Results In all groups, ASP was related to smaller ICV, total brain, white and gray matter volumes and total surface area, but not to cortical thickness. Smaller cortical surface areas were found across frontal, parietal, occipital, temporal and insular regions. Smaller hippocampal, amygdala, thalamus, caudate and putamen volumes were reported for all ASP subgroups. ASP effects did not survive ICV correction, except in the caudate, which remained significantly smaller in both patient ASP subgroups, but not in the HC. Conclusions Since ASP was associated with smaller brain volumes in all groups, the genetic risk of developing a severe mental illness, alone, cannot easily explain the smaller ICV. Only the smaller caudate volumes of ASP patients specifically suggest that injury from ASP can be related to disease development. Our findings give support for the ICV as a marker of aberrant neurodevelopment and ASP in the etiology of brain development in BD and SZ.
引用
收藏
页码:1050 / 1059
页数:10
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