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首页> 外文期刊>Neurobiology of Aging: Experimental and Clinical Research >Sex-dependent effect of the BDNF Val66Met polymorphism on executive functioning and processing speed in older adults: evidence from the health ABC study
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Sex-dependent effect of the BDNF Val66Met polymorphism on executive functioning and processing speed in older adults: evidence from the health ABC study

机译:BDNF Val66met多态性对老年人执行功能和加工速度的性依赖性效应:来自健康ABC学习的证据

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Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism may be an important source of heterogeneity seen in cognitive aging, although the specific relationship between this polymorphism and cognition remains controversial and may depend on the sex of participants. We assessed 2668 older black and white adults and fit linear mixed models to digit symbol substitution test (DSST) performance assessed in years 0 (baseline), 4, 7, and 9 to examine the interaction between sex and BDNF genotype on the intercept (i.e., estimated baseline DSST) and change in DSST over 9 years, adjusted for covariates. Sex interacted with BDNF genotype to predict DSST intercept (F[1,1599] = 7.4, p 0.01) and 9-year change (F [1,1183] = 4.1, p = 0.04) in white participants only. Initially, white male Val/Val carriers had lower DSST scores (37.6, SE = 0.8) in comparison with male Met carriers (difference, -1.7; 95% CI, -3.2 to -0.3) and female Val/Val carriers (difference, -5.6; 95% CI, -6.8 to -4.3). White female Met carriers showed a slower rate of change (annual rate of change = -0.6, SE = 0.1) in comparison with female Val/Val carriers (difference, -0.2; 95% CI, -0.4 to -0.02) and male Met carriers (difference, -0.3; 95% CI, -0.5 to -0.02). Our findings suggest that BDNF Val66Met and sex should be considered in future endeavors aimed at treating or preventing neurodegenerative disorders. (C) 2018 Elsevier Inc. All rights reserved.
机译:脑衍生的神经营养因子(BDNF)Val66met多态性可能是认知老龄化中观察到的异质性的重要来源,但这种多态性和认知之间的具体关系仍然存在争议,并且可能取决于参与者的性别。我们评估了2668年较旧的黑白成人,并将线性混合模型拟合到数年0(基线),4,7和9年评估的数字符号替代测试(DSST)性能,以检查性别和BDNF基因型对截距之间的相互作用(即,估计基线DSST)和DSST的变化超过9年,调整了协变量。性别与BDNF基因型相互作用以预测DSST截距(F [1,1599] = 7.4,P& 0.01),并且仅在白色参与者中(F [1,1183] = 4.1,p = 0.04)。最初,与男性Met载体(差异为-1.7; 95%CI,-3.2至-0.3)和母VAL载体(差异,差异, -5.6; 95%CI,-6.8至-4.3)。与雌性VAL载体相比载体(差异,-0.3; 95%CI,-0.5至-0.02)。我们的研究结果表明,应在未来的旨在治疗或预防神经变性障碍的努力中考虑BDNF Val66met和性别。 (c)2018年Elsevier Inc.保留所有权利。

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