Pham Linh, Guma Elisa, Ellegood Jacob, Lerch Jason P, Raznahan Armin
Section on Developmental Neurogenomics, Human Genetics Branch, National Institute of Mental Health, Bethesda, MD, 20892, USA.
Wellcome Centre for Integrative Neuroimaging, University of Oxford, Oxford, OX3 9DU, UK.
Biol Sex Differ. 2025 Jul 1;16(1):47. doi: 10.1186/s13293-025-00728-1.
Structural covariance within the brain is thought to reflect inter-regional sharing of developmental influences. This hypothesis has proved difficult to test but can be informatively probed by the study of sex differences. Here, we use neuroimaging in humans and mice to study sex-differences in anatomical covariance- asking (1) are there sex differences in structural covariance and (2) do regions that share the same developmental influences, as exhibited by shared sex differences in volume, also show shared sex differences in volume covariance. This study design illuminates both the biology of sex-differences and theoretical models for anatomical covariance- benefitting from tests of inter-species convergence.
Brain volume correlations for males and females across 255 regions in mice (n = 423) and 378 regions in humans (n = 436) were calculated using volumetric measures obtained from structural MRI. Mean correlations for each sex were compared within species to determine whether covariance sex differences exist. Specific covariances with strong sex differences in each species were identified via permutation tests for statistical significance. Brain maps of regional average structural covariance sex-bias were generated for mice and humans. Regional average structural covariance sex-bias and volumetric sex-bias were correlated to identify whether these features align in their direction of sex-bias.
We find that volumetric structural covariance is stronger in adult females than males for both wild-type mice and healthy human subjects: 98% of comparisons with statistically significant covariance sex differences in mice are female-biased, while 76% of such comparisons are female-biased in humans (q < 0.05). Regional covariance and volumetric sex-biases have weak inverse relationships to each other in both species: volumetrically male-biased regions contain more female-biased covariations, while volumetrically female-biased regions have more male-biased covariations (mice: r = -0.185, p = 0.002; humans: r = -0.189, p = 0.001).
Our results identify a tendency for females to show stronger neuroanatomical covariance across species. These structural covariance sex differences are also partially related to regional sex differences in volume for both species, suggesting that stronger structural covariance in females could be an evolutionarily conserved feature - partially shaped by the same developmental influences that mediate volumetric sex-biases.
大脑内的结构协方差被认为反映了发育影响的区域间共享。这一假设已被证明难以检验,但可以通过对性别差异的研究进行有益的探索。在此,我们使用人类和小鼠的神经成像来研究解剖协方差中的性别差异——探究(1)结构协方差中是否存在性别差异,以及(2)在体积上表现出相同发育影响的区域,在体积协方差中是否也表现出相同的性别差异。这种研究设计既阐明了性别差异的生物学机制,也为解剖协方差的理论模型提供了信息——受益于种间趋同的检验。
使用从结构MRI获得的体积测量值,计算了小鼠(n = 423)255个区域和人类(n = 436)378个区域中雄性和雌性的脑体积相关性。在物种内比较每种性别的平均相关性,以确定协方差性别差异是否存在。通过置换检验确定每种物种中具有强烈性别差异的特定协方差的统计显著性。生成了小鼠和人类区域平均结构协方差性别偏差的脑图谱。将区域平均结构协方差性别偏差与体积性别偏差相关联,以确定这些特征在性别偏差方向上是否一致。
我们发现,对于野生型小鼠和健康人类受试者,成年雌性的体积结构协方差均强于雄性:在小鼠中,98%具有统计学显著协方差性别差异的比较偏向雌性,而在人类中,此类比较的76%偏向雌性(q < 0.05)。在两个物种中,区域协方差和体积性别偏差之间的反向关系都很弱:体积上偏向雄性的区域包含更多偏向雌性的协方差,而体积上偏向雌性的区域具有更多偏向雄性的协方差(小鼠:r = -0.185,p = 0.002;人类:r = -0.189,p = 0.001)。
我们的结果确定了雌性在跨物种中表现出更强神经解剖协方差的趋势。这些结构协方差性别差异也与两个物种的区域体积性别差异部分相关,这表明雌性更强的结构协方差可能是一种进化上保守的特征——部分由介导体积性别偏差的相同发育影响塑造。