Schmitt J Eric, Lenroot Rhoshel K, Ordaz Sarah E, Wallace Gregory L, Lerch Jason P, Evans Alan C, Prom Elizabeth C, Kendler Kenneth S, Neale Michael C, Giedd Jay N
Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA.
Neuroimage. 2009 Aug 1;47(1):56-64. doi: 10.1016/j.neuroimage.2008.06.039. Epub 2008 Jul 11.
The role of genetics in driving intracortical relationships is an important question that has rarely been studied in humans. In particular, there are no extant high-resolution imaging studies on genetic covariance. In this article, we describe a novel method that combines classical quantitative genetic methodologies for variance decomposition with recently developed semi-multivariate algorithms for high-resolution measurement of phenotypic covariance. Using these tools, we produced correlational maps of genetic and environmental (i.e. nongenetic) relationships between several regions of interest and the cortical surface in a large pediatric sample of 600 twins, siblings, and singletons. These analyses demonstrated high, fairly uniform, statistically significant genetic correlations between the entire cortex and global mean cortical thickness. In agreement with prior reports on phenotypic covariance using similar methods, we found that mean cortical thickness was most strongly correlated with association cortices. However, the present study suggests that genetics plays a large role in global brain patterning of cortical thickness in this manner. Further, using specific gyri with known high heritabilities as seed regions, we found a consistent pattern of high bilateral genetic correlations between structural homologues, with environmental correlations more restricted to the same hemisphere as the seed region, suggesting that interhemispheric covariance is largely genetically mediated. These findings are consistent with the limited existing knowledge on the genetics of cortical variability as well as our prior multivariate studies on cortical gyri.
遗传学在驱动皮质内关系中的作用是一个重要问题,但在人类中很少得到研究。特别是,目前尚无关于遗传协方差的高分辨率成像研究。在本文中,我们描述了一种新方法,该方法将用于方差分解的经典定量遗传方法与最近开发的用于高分辨率测量表型协方差的半多变量算法相结合。使用这些工具,我们在一个包含600对双胞胎、兄弟姐妹和独生子女的大型儿科样本中,绘制了几个感兴趣区域与皮质表面之间的遗传和环境(即非遗传)关系的相关图谱。这些分析表明,整个皮质与全球平均皮质厚度之间存在高度、相当均匀且具有统计学意义的遗传相关性。与之前使用类似方法进行的表型协方差报告一致,我们发现平均皮质厚度与联合皮质的相关性最强。然而,本研究表明,遗传学在以这种方式塑造皮质厚度的全球脑模式中起着很大作用。此外,使用具有已知高遗传力的特定脑回作为种子区域,我们发现结构同源物之间存在一致的高双侧遗传相关性模式,而环境相关性则更多地局限于与种子区域相同的半球,这表明半球间协方差在很大程度上是由遗传介导的。这些发现与关于皮质变异性遗传学的现有有限知识以及我们之前对皮质脑回的多变量研究一致。