Matyi Joshua, Tschanz JoAnn T, Rattinger Gail B, Sanders Chelsea, Vernon Elizabeth K, Corcoran Chris, Kauwe John S K, Buhusi Mona
Department of Psychology, Utah State University.
Center for Epidemiologic Studies, Utah State University.
J Gerontol A Biol Sci Med Sci. 2017 Nov 9;72(12):1607-1613. doi: 10.1093/gerona/glx092.
Neurotrophins, including nerve-growth factor and brain-derived neurotrophic factor, have been implicated in Alzheimer's disease (AD). Associations between AD and neurotrophin signaling genes have been inconsistent, with few studies examining sex differences in risk. We examined four single-nucleotide polymorphisms (SNPs) involved in neurotrophin signaling (rs6265, rs56164415, rs2289656, rs2072446) and risk for AD by sex in a population-based sample of older adults. Three thousand four hundred and ninety-nine individuals without dementia at baseline [mean (standard deviation) age = 74.64 (6.84), 58% female] underwent dementia screening and assessment over four triennial waves. Cox regression was used to examine time to AD or right censoring for each SNP. Female carriers of the minor T allele for rs2072446 and rs56164415 had a 60% (hazard ratio [HR] = 1.60, 95% confidence interval [CI] = 1.02-2.51) and 93% (HR = 1.93, 95% CI = 1.30-2.84) higher hazard for AD, respectively, than male noncarriers of the T allele. Furthermore, male carriers of the T allele of rs2072446 had a 61% lower hazard (HR = 0.39, 95% CI = 0.14-1.06) than male noncarriers at trend-level significance (p = .07). The association between certain neurotrophin gene polymorphisms and AD differs by sex and may explain inconsistent findings in the literature.
神经营养因子,包括神经生长因子和脑源性神经营养因子,与阿尔茨海默病(AD)有关。AD与神经营养因子信号基因之间的关联并不一致,很少有研究考察风险中的性别差异。我们在一个基于人群的老年人样本中,按性别研究了参与神经营养因子信号传导的四个单核苷酸多态性(SNP,即rs6265、rs56164415、rs2289656、rs2072446)与AD风险的关系。3499名基线时无痴呆的个体[平均(标准差)年龄=74.64(6.84),58%为女性]在四个三年期随访中接受了痴呆筛查和评估。采用Cox回归分析每个SNP至AD发生或右侧删失的时间。rs2072446和rs56164415次要T等位基因的女性携带者发生AD的风险分别比T等位基因的男性非携带者高60%(风险比[HR]=1.60,95%置信区间[CI]=1.02 - 2.51)和93%(HR = 1.93,95% CI = 1.30 - 2.84)。此外,rs2072446的T等位基因男性携带者的风险比男性非携带者低61%(HR = 0.39,95% CI = 0.14 - 1.06),在趋势水平上具有显著性(p = 0.07)。某些神经营养因子基因多态性与AD之间的关联存在性别差异,这可能解释了文献中不一致的研究结果。