Genetics of microstructure of cerebral white matter using diffusion tensor imaging

被引:127
|
作者
Kochunov, P. [1 ,2 ]
Glahn, D. C. [1 ,3 ,4 ]
Lancaster, J. L. [1 ]
Winkler, A. M. [3 ]
Smith, S. [5 ]
Thompson, P. M. [6 ]
Almasy, L. [2 ]
Duggirala, R. [2 ]
Fox, P. T. [1 ]
Blangero, J. [2 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Res Imaging Ctr, San Antonio, TX 78284 USA
[2] SW Fdn Biomed Res, San Antonio, TX 78284 USA
[3] Inst Living, Olin Neuropsychiat Res Ctr, Hartford, CT USA
[4] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA
[5] Univ Oxford, FMRIB Ctr, Oxford, England
[6] Univ Calif Los Angeles, Sch Med, Dept Neurol, Los Angeles, CA 90024 USA
基金
英国工程与自然科学研究理事会;
关键词
White matter; Diffusion tensor imaging; DTI; Heritability; Linkage; BRAIN FIBER ARCHITECTURE; TRAIT LINKAGE ANALYSIS; SPATIAL STATISTICS; CORPUS-CALLOSUM; FRACTIONAL ANISOTROPY; SUSCEPTIBILITY LOCI; MULTIVARIATE TESTS; VOXELWISE ANALYSIS; MEXICAN-AMERICANS; WILLIAMS-SYNDROME;
D O I
10.1016/j.neuroimage.2010.01.078
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 to) and axial (L-parallel to) 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 to (h(2) = 0.37 +/- 0.14; p=0.001), while L-parallel to measurements were not significantly heritable (h(2)= 0.09 +/- 0.12; p = 0.20). Genetic correlation analysis indicated that the FA and L-perpendicular to 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 to (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. (c) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1109 / 1116
页数:8
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