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COMPARISON OF FRACTIONAL AND GEODESIC ANISOTROPY IN DIFFUSION TENSOR IMAGES OF 90 MONOZYGOTIC AND DIZYGOTIC TWINS.90对同卵和异卵双胞胎扩散张量图像中分数各向异性与测地线各向异性的比较。
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Extending genetic linkage analysis to diffusion tensor images to map single gene effects on brain fiber architecture.将基因连锁分析扩展至扩散张量成像,以绘制单基因对脑纤维结构的影响图谱。
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Genetics of primary cerebral gyrification: Heritability of length, depth and area of primary sulci in an extended pedigree of Papio baboons.原发性脑回发育的遗传学:狒狒 Papio 一个扩展家系中初级脑沟长度、深度和面积的遗传力。
Neuroimage. 2010 Nov 15;53(3):1126-34. doi: 10.1016/j.neuroimage.2009.12.045. Epub 2009 Dec 24.
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Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies.皮质厚度或灰质体积?影像学遗传学研究中表型选择的重要性。
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Analysis of genetic variability and whole genome linkage of whole-brain, subcortical, and ependymal hyperintense white matter volume.全脑、皮质下和室管膜下脑白质高信号体积的遗传变异性和全基因组连锁分析。
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Genetics of brain fiber architecture and intellectual performance.脑纤维结构与智力表现的遗传学
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Evaluation of 14 nonlinear deformation algorithms applied to human brain MRI registration.应用于人类脑磁共振成像配准的14种非线性变形算法的评估。
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Temporal and spatial development of axonal maturation and myelination of white matter in the developing brain.发育中大脑白质轴突成熟和髓鞘形成的时空发育
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A tensor-based morphometry study of genetic influences on brain structure using a new fluid registration method.一项使用新型流体配准方法对基因对脑结构影响的基于张量的形态测量学研究。
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利用弥散张量成像技术研究脑白质微观结构的遗传学。

Genetics of microstructure of cerebral white matter using diffusion tensor imaging.

机构信息

Research Imaging Center, University of Texas Health Science Center San Antonio, San Antonio, TX 78284, USA.

出版信息

Neuroimage. 2010 Nov 15;53(3):1109-16. doi: 10.1016/j.neuroimage.2010.01.078. Epub 2010 Jan 29.

DOI:10.1016/j.neuroimage.2010.01.078
PMID:20117221
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2888778/
Abstract

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.

摘要

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。