Research Imaging Center, University of Texas Health Science Center San Antonio, San Antonio, TX 78284, USA.
Neuroimage. 2010 Nov 15;53(3):1109-16. doi: 10.1016/j.neuroimage.2010.01.078. Epub 2010 Jan 29.
We analyzed the degree of genetic control over intersubject variability in the microstructure of cerebral white matter (WM) using diffusion tensor imaging (DTI). We performed heritability, genetic correlation and quantitative trait loci (QTL) analyses for the whole-brain and 10 major cerebral WM tracts. Average measurements for fractional anisotropy (FA), radial (L( perpendicular)) and axial (L( vertical line)) diffusivities served as quantitative traits. These analyses were done in 467 healthy individuals (182 males/285 females; average age 47.9+/-13.5 years; age range: 19-85 years), recruited from randomly-ascertained pedigrees of extended families. Significant heritability was observed for FA (h(2)=0.52+/-0.11; p=10(-7)) and L( perpendicular) (h(2)=0.37+/-0.14; p=0.001), while L( vertical line) measurements were not significantly heritable (h(2)=0.09+/-0.12; p=0.20). Genetic correlation analysis indicated that the FA and L( perpendicular) shared 46% of the genetic variance. Tract-wise analysis revealed a regionally diverse pattern of genetic control, which was unrelated to ontogenic factors, such as tract-wise age-of-peak FA values and rates of age-related change in FA. QTL analysis indicated linkages for whole-brain average FA (LOD=2.36) at the marker D15S816 on chromosome 15q25, and for L( perpendicular) (LOD=2.24) near the marker D3S1754 on the chromosome 3q27. These sites have been reported to have significant co-inheritance with two psychiatric disorders (major depression and obsessive-compulsive disorder) in which patients show characteristic alterations in cerebral WM. Our findings suggest that the microstructure of cerebral white matter is under a strong genetic control and further studies in healthy as well as patients with brain-related illnesses are imperative to identify the genes that may influence cerebral white matter.
我们使用弥散张量成像(DTI)分析了脑白质(WM)微观结构中个体间变异性的遗传控制程度。我们对全脑和 10 个主要脑 WM 束进行了遗传力、遗传相关性和数量性状位点(QTL)分析。各向异性分数(FA)、径向(L( perpendicular))和轴向(L( vertical line))扩散率的平均测量值作为定量特征。这些分析是在 467 名健康个体(182 名男性/285 名女性;平均年龄 47.9+/-13.5 岁;年龄范围:19-85 岁)中进行的,这些个体是从扩展家族的随机确定的家系中招募的。FA(h(2)=0.52+/-0.11;p=10(-7))和 L( perpendicular)(h(2)=0.37+/-0.14;p=0.001)具有显著的遗传力,而 L( vertical line)的测量值没有显著的遗传力(h(2)=0.09+/-0.12;p=0.20)。遗传相关性分析表明,FA 和 L( perpendicular) 共享 46%的遗传方差。束状分析显示遗传控制的区域多样性模式,这与发育因素无关,例如束状年龄峰 FA 值和 FA 与年龄相关的变化率。QTL 分析表明,全脑平均 FA 的连锁(LOD=2.36)位于染色体 15q25 上的标记 D15S816 处,L( perpendicular) 的连锁(LOD=2.24)位于染色体 3q27 上的标记 D3S1754 附近。这些位点与两种精神疾病(重度抑郁症和强迫症)有显著的共同遗传,这些疾病患者的脑 WM 表现出特征性改变。我们的研究结果表明,脑白质的微观结构受强烈的遗传控制,在健康人群以及与大脑相关疾病的患者中进行进一步研究对于确定可能影响脑白质的基因至关重要。