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首页> 外文期刊>International psychogeriatrics >Polymorphisms of the estrogen receptor alpha (ESR1) gene and the risk of Alzheimer's disease in a southern Chinese community.
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Polymorphisms of the estrogen receptor alpha (ESR1) gene and the risk of Alzheimer's disease in a southern Chinese community.

机译:雌激素受体α(ESR1)基因的多态性与南部华人社区的阿尔茨海默氏病风险。

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摘要

BACKGROUND: Alzheimer's disease (AD) is a neurodegenerative disease with a higher prevalence in women. Expression of estrogen receptor 1 (ESR1) gene has been identified throughout the brain. Owing to the putative neuroprotective effects of estrogen, estrogen receptor gene is a potential candidate modulating the development of AD. Preliminary associations between two polymorphisms of ESR1 (PvuII and XbaI) gene and AD have been reported. METHODS: In this study, 16 single nucleotide polymorphisms (SNPs) of the ESR1 gene (including four commonly studied ESR1 SNPs and 12 other tagging SNPs selected from the HapMap database) were investigated to further evaluate the association between ESR1 polymorphisms and the risk of AD in the Chinese population. RESULTS: A total of 233 Chinese AD patients and 245 age-matched elderly control subjects were recruited. Genetic associations were analyzed by chi-square test and interaction effect was analysed by logistic regression analysis. Five SNPs (clustered between intron 3 and intron 7) were associated with the risk of AD (p-value ranges from 0.001 to 0.035); another two SNPs (located on exon 2 and intron 2) were shown to modulate the age-at-onset (AAO) in AD (p-value = 0.036 and 0.011). CONCLUSIONS: ESR1 gene polymorphisms may be associated with the AAO in AD. The present results provided information for possible associations between certain polymorphisms of ESR1 gene and the risk of AD.
机译:背景:阿尔茨海默氏病(AD)是一种在女性中患病率较高的神经退行性疾病。雌激素受体1(ESR1)基因的表达已在整个大脑中被确认。由于雌激素的假定的神经保护作用,雌激素受体基因是调节AD发展的潜在候选者。据报道,ESR1的两个多态性(PvuII和XbaI)与AD之间存在初步关联。方法:在这项研究中,ESR1基因的16个单核苷酸多态性(SNP)(包括从HapMap数据库中选择的四个常见的ESR1 SNP和12个其他标记SNP)被调查,以进一步评估ESR1多态性与AD风险之间的关联。在中国人口中。结果:总共招募了233名中国AD患者和245名年龄相匹配的老年对照受试者。通过卡方检验分析遗传关联,并通过逻辑回归分析分析相互作用效应。五个SNP(内含子3和内含子7之间)与AD风险相关(p值范围为0.001至0.035);另有两个SNP(位于外显子2和内含子2上)可调节AD的发病年龄(AAO)(p值= 0.036和0.011)。结论:ESR1基因多态性可能与AD中的AAO有关。本结果为ESR1基因某些多态性与AD风险之间可能的关联提供了信息。

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