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儿茶酚-O-甲基转移酶的单倍型调节与智力相关的脑白质完整性。

Haplotypes of catechol-O-methyltransferase modulate intelligence-related brain white matter integrity.

机构信息

LIAMA Center for Computational Medicine, National Laboratory of Pattern Recognition, Institute of Automation, Chinese Academy of Sciences, Beijing 100190, PR China.

出版信息

Neuroimage. 2010 Mar;50(1):243-9. doi: 10.1016/j.neuroimage.2009.12.020. Epub 2009 Dec 11.

Abstract

Twin studies have indicated a common genetic origin for intelligence and for variations in brain morphology. Our previous diffusion tensor imaging studies found an association between intelligence and white matter integrity of specific brain regions or tracts. However, specific genetic determinants of the white matter integrity of these brain regions and tracts are still unclear. In this study, we assess whether and how catechol-O-methyltransferase (COMT) gene polymorphisms affect brain white matter integrity. We genotyped twelve single nucleotide polymorphisms (SNPs) within the COMT gene and performed haplotype analyses on data from 79 healthy subjects. Our subjects had the same three major COMT haplotypes (termed the HPS, APS and LPS haplotypes) as previous studies have reported as regulating significantly different levels of enzymatic activity and dopamine. We used the mean fractional anisotropy (FA) values from four regions and five tracts of interest to assess the effect of COMT polymorphisms, including the well-studied val158met SNP and the three main haplotypes that we had identified, on intelligence-related white matter integrity. We identified an association between the mean FA values of two regions in the bilateral prefrontal lobes and the COMT haplotypes, rather than between them and val158met. The haplotype-FA value associations modulated nonlinearly and fit an inverted U-model. Our findings suggest that COMT haplotypes can nonlinearly modulate the intelligence-related white matter integrity of the prefrontal lobes by more significantly influencing prefrontal dopamine variations than does val158met.

摘要

双生子研究表明,智力和大脑形态变化具有共同的遗传基础。我们之前的弥散张量成像研究发现,智力与特定脑区或脑区束的白质完整性之间存在关联。然而,这些脑区和脑区束的白质完整性的特定遗传决定因素仍不清楚。在这项研究中,我们评估儿茶酚-O-甲基转移酶(COMT)基因多态性是否以及如何影响大脑白质完整性。我们对 COMT 基因中的 12 个单核苷酸多态性(SNP)进行了基因分型,并对 79 名健康受试者的数据进行了单倍型分析。我们的受试者与之前的研究一样,具有三种主要的 COMT 单倍型(称为 HPS、APS 和 LPS 单倍型),这些单倍型调节着显著不同水平的酶活性和多巴胺。我们使用了四个感兴趣的区域和五个感兴趣的束的平均分数各向异性(FA)值来评估 COMT 多态性对与智力相关的白质完整性的影响,包括研究得很好的 val158met SNP 和我们之前确定的三种主要单倍型。我们发现双侧前额叶两个区域的平均 FA 值与 COMT 单倍型之间存在关联,而不是与 val158met 之间存在关联。单倍型- FA 值的关联呈非线性变化,符合倒 U 型模型。我们的研究结果表明,COMT 单倍型可以通过更显著地影响前额叶多巴胺变化,而非线性地调节前额叶与智力相关的白质完整性,而 val158met 则不能。

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