Rezaie Roozbeh, Daly Eileen M, Cutter William J, Murphy Declan G M, Robertson Dene M W, DeLisi Lynn E, Mackay Clare E, Barrick Thomas R, Crow Timothy J, Roberts Neil
School of Clinical Sciences, University of Liverpool, UK.
Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 5;150B(1):74-85. doi: 10.1002/ajmg.b.30772.
The cognitive deficits present in individuals with sex chromosome aneuploidies suggest that hemispheric differentiation of function is determined by an X-Y homologous gene [Crow (1993); Lancet 342:594-598]. In particular, females with Turner's syndrome (TS) who have only one X-chromosome exhibit deficits of spatial ability whereas males with Klinefelter's syndrome (KS) who possess a supernumerary X-chromosome are delayed in acquiring words. Since spatial and verbal abilities are generally associated with right and left hemispheric function, such deficits may relate to anomalies of cerebral asymmetry. We therefore applied a novel image analysis technique to investigate the relationship between sex chromosome dosage and structural brain asymmetry. Specifically, we tested Crow's prediction that the magnitude of the brain torque (i.e., a combination of rightward frontal and leftward occipital asymmetry) would, as a function of sex chromosome dosage, be respectively decreased in TS women and increased in KS men, relative to genotypically normal controls. We found that brain torque was not significantly different in TS women and KS men, in comparison to controls. However, TS women exhibited significantly increased leftward brain asymmetry, restricted to the posterior of the brain and focused on the superior temporal and parietal-occipital association cortex, while KS men showed a trend for decreased brain asymmetry throughout the frontal lobes. The findings suggest that the number of sex chromosomes influences the development of brain asymmetry not simply to modify the torque but in a complex pattern along the antero-posterior axis.
性染色体非整倍体个体中出现的认知缺陷表明,功能的半球分化是由X-Y同源基因决定的[克劳(1993年);《柳叶刀》342:594 - 598]。特别是,患有特纳综合征(TS)的女性只有一条X染色体,表现出空间能力缺陷,而患有克兰费尔特综合征(KS)的男性有一条额外的X染色体,在学习语言方面存在延迟。由于空间和语言能力通常与左右半球功能相关,这些缺陷可能与脑不对称异常有关。因此,我们应用了一种新颖的图像分析技术来研究性染色体剂量与脑结构不对称之间的关系。具体而言,我们检验了克劳的预测,即相对于基因正常的对照组,脑扭矩(即向右的额叶和向左的枕叶不对称的组合)的大小将根据性染色体剂量分别在TS女性中降低,在KS男性中增加。我们发现,与对照组相比,TS女性和KS男性的脑扭矩没有显著差异。然而,TS女性表现出明显增加的向左脑不对称,仅限于脑后部,集中在颞上叶和顶枕联合皮层,而KS男性在整个额叶显示出脑不对称降低的趋势。这些发现表明,性染色体的数量影响脑不对称的发展,不仅简单地改变扭矩,而且沿着前后轴以复杂的模式影响。