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BDNF gene effects on brain circuitry replicated in 455 twins.BDNF 基因对大脑回路的影响在 455 对双胞胎中得到复制。
Neuroimage. 2011 Mar 15;55(2):448-54. doi: 10.1016/j.neuroimage.2010.12.053. Epub 2010 Dec 30.
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Effect of brain-derived neurotrophic factor Val66Met polymorphism and serum levels on the progression of mild cognitive impairment.脑源性神经营养因子 Val66Met 多态性和血清水平对轻度认知障碍进展的影响。
World J Biol Psychiatry. 2010 Sep;11(6):774-80. doi: 10.3109/15622971003797241.
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BDNF Val66Met polymorphism is associated with cognitive impairment in Italian patients with Parkinson's disease.脑源性神经营养因子 Val66Met 多态性与意大利帕金森病患者的认知障碍有关。
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Genetic and vascular modifiers of age-sensitive cognitive skills: effects of COMT, BDNF, ApoE, and hypertension.年龄敏感性认知技能的遗传和血管调节因素:儿茶酚-O-甲基转移酶、脑源性神经营养因子、载脂蛋白E及高血压的影响
Neuropsychology. 2009 Jan;23(1):105-116. doi: 10.1037/a0013487.
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BDNF val66met influences time to onset of levodopa induced dyskinesia in Parkinson's disease.脑源性神经营养因子缬氨酸66蛋氨酸影响帕金森病中左旋多巴诱发异动症的发病时间。
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BDNF is a novel marker of cognitive function in ageing women: the DR's EXTRA Study.脑源性神经营养因子是老年女性认知功能的新型标志物:DR的EXTRA研究。
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7
Association study of brain-derived neurotrophic factor and apolipoprotein E polymorphisms and cognitive function in aged males without dementia.脑源性神经营养因子和载脂蛋白E基因多态性与无痴呆老年男性认知功能的关联研究
Neurosci Lett. 2008 Mar 12;433(2):158-62. doi: 10.1016/j.neulet.2007.12.057. Epub 2008 Jan 10.
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Association between genetic variants of IL-1beta, IL-6 and TNF-alpha cytokines and cognitive performance in the elderly general population of the MEMO-study.MEMO研究中老年普通人群中白细胞介素-1β、白细胞介素-6和肿瘤坏死因子-α细胞因子基因变异与认知能力的关联。
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Brain-derived neurotrophic factor polymorphism Val66Met influences cognitive abilities in the elderly.脑源性神经营养因子多态性Val66Met影响老年人的认知能力。
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Preservation of gray matter volume in multiple sclerosis patients with the Met allele of the rs6265 (Val66Met) SNP of brain-derived neurotrophic factor.脑源性神经营养因子rs6265(Val66Met)单核苷酸多态性的Met等位基因对多发性硬化症患者灰质体积的保护作用
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脑源性神经营养因子(BDNF)基因:在MEMO研究的正常认知衰老过程中对认知功能的性别特异性作用?

Brain-derived neurotrophic factor (BDNF) gene: a gender-specific role in cognitive function during normal cognitive aging of the MEMO-Study?

作者信息

Laing Katharine R, Mitchell David, Wersching Heike, Czira Maria E, Berger Klaus, Baune Bernhard T

机构信息

Department of Psychology, School of Social Sciences and Psychology, James Cook University, Townsville, QLD 4811, Australia.

出版信息

Age (Dordr). 2012 Aug;34(4):1011-22. doi: 10.1007/s11357-011-9275-8. Epub 2011 Jun 22.

DOI:10.1007/s11357-011-9275-8
PMID:21695421
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3682062/
Abstract

Cognitive aging processes are underpinned by multiple processes including genetic factors. The brain-derived neurotrophic factor (BDNF) has been suggested to be involved in age-related cognitive decline in otherwise healthy individuals. The gender-specific role of the BDNF gene in cognitive aging remains unclear. The identification of genetic biomarkers might be a useful approach to identify individuals at risk of cognitive decline during healthy aging processes. The aim of this study was to investigate the associations between three single-nucleotide polymorphisms (SNPs) in the BDNF gene and domains of cognitive functioning in normal cognitive aging. The sample, comprising 369 participants (M = 72.7 years, SD = 4.45 years), completed an extensive neuropsychological test battery measuring memory, motor function, and perceptual speed. The relationships between the SNPs rs6265, rs7103411, and rs7124442 and cognitive domains were examined. While significant main effects of BDNF SNPs on cognitive function were found for the association between rs7103411 and memory performance, gender-specific analyses revealed for females significant main effects of rs7103411 for memory and of rs6265 for perceptual speed independent of the APOE*E4 status and education. The finding for the association between rs6265 and perceptual speed in females remained significant after Bonferroni correction for multiple comparisons. None of the analyses showed significant results for males. This study is the first to implicate that the SNPs rs6265 and rs7103411 affect cognitive function in the elderly in a gender-specific way.

摘要

认知衰老过程由包括遗传因素在内的多种过程所支撑。脑源性神经营养因子(BDNF)被认为与原本健康个体的年龄相关认知衰退有关。BDNF基因在认知衰老中的性别特异性作用仍不清楚。识别遗传生物标志物可能是识别健康衰老过程中认知衰退风险个体的一种有用方法。本研究的目的是调查BDNF基因中的三个单核苷酸多态性(SNP)与正常认知衰老中认知功能领域之间的关联。该样本包括369名参与者(平均年龄M = 72.7岁,标准差SD = 4.45岁),他们完成了一系列广泛的神经心理学测试,以测量记忆、运动功能和感知速度。研究了SNP rs6265、rs7103411和rs7124442与认知领域之间的关系。虽然发现BDNF SNP对认知功能有显著的主效应,即rs7103411与记忆表现之间的关联,但性别特异性分析显示,对于女性而言,rs7103411对记忆有显著主效应,rs6265对感知速度有显著主效应,且独立于APOE*E4状态和教育程度。在进行多重比较的Bonferroni校正后,rs6265与女性感知速度之间的关联结果仍然显著。所有分析对男性均未显示出显著结果。本研究首次表明,SNP rs6265和rs7103411以性别特异性方式影响老年人的认知功能。