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认知能力、个体内变异性以及儿茶酚-O-甲基转移酶和脑源性神经营养因子的常见遗传变异:基于人群的老年人群纵向研究。

Cognitive ability, intraindividual variability, and common genetic variants of catechol-O-methyltransferase and brain-derived neurotrophic factor: a longitudinal study in a population-based sample of older adults.

机构信息

Department of Genome Biology, John Curtin School of Medical Research, Australian National University.

Department of Human Development and Family Studies, Colorado State University.

出版信息

Psychol Aging. 2014 Jun;29(2):393-403. doi: 10.1037/a0035702.

Abstract

Genetic differences play a significant role in generating individual differences in cognitive abilities. Studies have linked common polymorphisms (valine to methionine substitution; VAL/MET) in the catechol-O-methyltransferase (COMT) and brain-derived neurotrophic factor (BDNF) to cognitive differences between individuals. However, not all studies support these associations and hence, the impact of these polymorphisms on cognition is unclear. Here, we investigated the effect of COMT VAL158MET and BDNF VAL66MET polymorphisms and their interaction on cognitive performance measured longitudinally over 8 years in a population-based sample of older adults (60-64 years at baseline; n = 400). We used multilevel models to examine differences between individuals with different genotypes in performance on psychometric tests while controlling for age, sex, and education. We observed significant main and interaction effects of COMT and BDNF genotypes on reaction time (RT) and intraindividual variability in RT (IIV-RT). Subjects with at least one copy of the COMTMET allele (which is associated with higher prefrontal dopamine) had significantly faster RT (both simple and choice RT) and less IIV-RT in both tasks than those without the COMTMET allele when they also carried one or more BDNFMET alleles (which is associated with lower activity-dependent BDNF secretion). However, RT and IIV-RT did not differ significantly between the COMT genotypes in the absence of the BDNFMET allele. These polymorphisms had no significant effect on within person change in RT or IIV-RT. Our findings indicate that the interaction between common variants of COMT and BDNF explain individual differences in RT and IIV-RT but do not explain age-related decline in these abilities.

摘要

遗传差异在产生认知能力的个体差异方面起着重要作用。研究已经将儿茶酚-O-甲基转移酶(COMT)和脑源性神经营养因子(BDNF)中的常见多态性(缬氨酸到蛋氨酸取代;VAL/MET)与个体之间的认知差异联系起来。然而,并非所有研究都支持这些关联,因此这些多态性对认知的影响尚不清楚。在这里,我们研究了 COMT VAL158MET 和 BDNF VAL66MET 多态性及其相互作用对认知表现的影响,该认知表现是通过对基于人群的老年成年人(基线时 60-64 岁;n=400)进行的 8 年纵向测量得出的。我们使用多层次模型来检查具有不同基因型的个体在心理测试中的表现差异,同时控制年龄、性别和教育程度。我们观察到 COMT 和 BDNF 基因型对反应时间(RT)和 RT 个体内变异性(IIV-RT)的显著主效应和相互作用效应。至少携带一个 COMTMET 等位基因(与前额叶多巴胺水平升高有关)的受试者在两个任务中的 RT(简单 RT 和选择 RT)更快,IIV-RT 更小,而那些没有 COMTMET 等位基因的受试者在携带一个或多个 BDNFMET 等位基因(与 BDNF 分泌活性降低有关)时也是如此。然而,在没有 BDNFMET 等位基因的情况下,COMT 基因型之间的 RT 和 IIV-RT 没有显著差异。这些多态性对 RT 或 IIV-RT 没有显著影响。我们的研究结果表明,COMT 和 BDNF 常见变体之间的相互作用可以解释 RT 和 IIV-RT 的个体差异,但不能解释这些能力的年龄相关下降。

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