Mankiw Catherine, Park Min Tae M, Reardon P K, Fish Ari M, Clasen Liv S, Greenstein Deanna, Giedd Jay N, Blumenthal Jonathan D, Lerch Jason P, Chakravarty M Mallar, Raznahan Armin
Developmental Neurogenomics Unit, Child Psychiatry Branch, National Institute of Mental Health, Bethesda, Maryland 20892.
Cerebral Imaging Center, Douglas Mental Health University Institute, Montreal, Quebec H4H 1R3, Canada.
J Neurosci. 2017 May 24;37(21):5221-5231. doi: 10.1523/JNEUROSCI.2158-16.2017. Epub 2017 Mar 17.
The cerebellum is a large hindbrain structure that is increasingly recognized for its contribution to diverse domains of cognitive and affective processing in human health and disease. Although several of these domains are sex biased, our fundamental understanding of cerebellar sex differences-including their spatial distribution, potential biological determinants, and independence from brain volume variation-lags far behind that for the cerebrum. Here, we harness automated neuroimaging methods for cerebellar morphometrics in 417 individuals to (1) localize normative male-female differences in raw cerebellar volume, (2) compare these to sex chromosome effects estimated across five rare sex (X/Y) chromosome aneuploidy (SCA) syndromes, and (3) clarify brain size-independent effects of sex and SCA on cerebellar anatomy using a generalizable allometric approach that considers scaling relationships between regional cerebellar volume and brain volume in health. The integration of these approaches shows that (1) sex and SCA effects on raw cerebellar volume are large and distributed, but regionally heterogeneous, (2) human cerebellar volume scales with brain volume in a highly nonlinear and regionally heterogeneous fashion that departs from documented patterns of cerebellar scaling in phylogeny, and (3) cerebellar organization is modified in a brain size-independent manner by sex (relative expansion of total cerebellum, flocculus, and Crus II-lobule VIIIB volumes in males) and SCA (contraction of total cerebellar, lobule IV, and Crus I volumes with additional X- or Y-chromosomes; X-specific contraction of Crus II-lobule VIIIB). Our methods and results clarify the shifts in human cerebellar organization that accompany interwoven variations in sex, sex chromosome complement, and brain size. Cerebellar systems are implicated in diverse domains of sex-biased behavior and pathology, but we lack a basic understanding of how sex differences in the human cerebellum are distributed and determined. We leverage a rare neuroimaging dataset to deconvolve the interwoven effects of sex, sex chromosome complement, and brain size on human cerebellar organization. We reveal topographically variegated scaling relationships between regional cerebellar volume and brain size in humans, which (1) are distinct from those observed in phylogeny, (2) invalidate a traditional neuroimaging method for brain volume correction, and (3) allow more valid and accurate resolution of which cerebellar subcomponents are sensitive to sex and sex chromosome complement. These findings advance understanding of cerebellar organization in health and sex chromosome aneuploidy.
小脑是后脑的一个大型结构,其在人类健康和疾病中对认知和情感加工的不同领域所做的贡献日益受到认可。尽管其中一些领域存在性别差异,但我们对小脑性别差异的基本理解,包括其空间分布、潜在的生物学决定因素以及与脑容量变化的独立性,远远落后于对大脑的理解。在这里,我们利用自动神经成像方法对417名个体的小脑形态进行测量,以(1)定位正常男性和女性在原始小脑体积上的差异,(2)将这些差异与在五种罕见的性(X/Y)染色体非整倍体(SCA)综合征中估计的性染色体效应进行比较,以及(3)使用一种可推广的异速生长方法来阐明性别和SCA对小脑解剖结构的脑容量独立效应,该方法考虑了健康状态下区域小脑体积与脑容量之间的缩放关系。这些方法的整合表明,(1)性别和SCA对原始小脑体积的影响很大且分布广泛,但在区域上是异质的;(2)人类小脑体积与脑容量以高度非线性且区域异质的方式缩放,这与系统发育中记录的小脑缩放模式不同;(3)小脑组织在脑容量独立的方式下因性别(男性小脑总体积、绒球和 Crus II - 小叶 VIIIB 体积相对增大)和 SCA(额外的 X 或 Y 染色体导致小脑总体积、小叶 IV 和 Crus I 体积缩小;Crus II - 小叶 VIIIB 的 X 特异性缩小)而发生改变。我们的方法和结果阐明了伴随性别、性染色体组成和脑容量交织变化的人类小脑组织的变化。小脑系统涉及多种性别差异行为和病理学领域,但我们对人类小脑中性别差异如何分布和确定缺乏基本的了解。我们利用一个罕见的神经成像数据集来解卷积性别、性染色体组成和脑容量对人类小脑组织的交织效应。我们揭示了人类区域小脑体积与脑容量之间地形上多样的缩放关系,这些关系(1)与系统发育中观察到的不同,(2)使传统的脑容量校正神经成像方法无效,(3)允许更有效和准确地分辨哪些小脑亚成分对性别和性染色体组成敏感。这些发现推进了对健康状态下和性染色体非整倍体中小脑组织的理解。