Sex Differences in Variability of Brain Structure Across the Lifespan

被引:27
|
作者
Forde, Natalie J. [1 ]
Jeyachandra, Jerrold [1 ]
Joseph, Michael [1 ]
Jacobs, Grace R. [1 ,2 ]
Dickie, Erin [1 ]
Satterthwaite, Theodore D. [3 ,4 ]
Shinohara, Russell T. [5 ,6 ]
Ameis, Stephanie H. [1 ,7 ]
Voineskos, Aristotle N. [1 ,7 ]
机构
[1] Ctr Addict & Mental Hlth, Campbell Family Mental Hlth Res Inst, Toronto, ON M5T 1R8, Canada
[2] Univ Toronto, Fac Med, Inst Med Sci, Toronto, ON M5S 1A8, Canada
[3] Univ Penn, Dept Psychiat, Philadelphia, PA 19104 USA
[4] Penn CHOP Lifespan Brain Inst, Philadelphia, PA 19104 USA
[5] Univ Penn, Penn Stat Imaging & Visualizat Ctr, Dept Biostat Epidemiol & Informat, Philadelphia, PA 19104 USA
[6] Univ Penn, Ctr Biomed Image Comp & Analyt, Dept Radiol, Philadelphia, PA 19103 USA
[7] Univ Toronto, Fac Med, Dept Psychiat, Toronto, ON M5T 1R8, Canada
关键词
healthy variation; sex differences; surface area; variability; vulnerability for disease; SURFACE-BASED ANALYSIS; HUMAN CEREBRAL-CORTEX; OPEN ACCESS SERIES; CORTICAL DEVELOPMENT; MRI DATA; GENDER; VOLUME; NETWORKS; DISEASE; MECP2;
D O I
10.1093/cercor/bhaa123
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Several brain disorders exhibit sex differences in onset, presentation, and prevalence. Increased understanding of the neurobiology of sex-based differences in variability across the lifespan can provide insight into both disease vulnerability and resilience. In n = 3069 participants, from 8 to 95 years of age, we found widespread greater variability in males compared with females in cortical surface area and global and subcortical volumes for discrete brain regions. In contrast, variance in cortical thickness was similar for males and females. These findings were supported by multivariate analysis accounting for structural covariance, and present and stable across the lifespan. Additionally, we examined variability among brain regions by sex. We found significant age-by-sex interactions across neuroimaging metrics, whereby in very early life males had reduced among-region variability compared with females, while in very late life this was reversed. Overall, our findings of greater regional variability, but less among-region variability in males in early life may aid our understanding of sex-based risk for neurodevelopmental disorders. In contrast, our findings in late life may provide a potential sex-based risk mechanism for dementia.
引用
收藏
页码:5420 / 5430
页数:11
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