Suppr超能文献

组织蛋白酶 D(224C/T)多态性增加了男性患阿尔茨海默病的风险。

The cathepsin D (224C/T) polymorphism confers an increased risk to develop Alzheimer's disease in men.

机构信息

Department of Child and Adolescent Psychiatry, LVR Klinikum Essen, University of Duisburg-Essen, Germany.

出版信息

J Gerontol A Biol Sci Med Sci. 2010 Mar;65(3):219-24. doi: 10.1093/gerona/glp209. Epub 2010 Jan 18.

Abstract

The lysosomal protease cathepsin D is likely involved in beta-amyloidogenesis in Alzheimer's disease (AD). There is evidence for a single nucleotide polymorphism (rs17571) of the cathepsin D gene to be associated with increased AD risk. However, little is known about gender-specific differences. Therefore, we performed a genetic association study focusing on gender-specific differences in 434 participants (219 AD and 215 controls). Screening of the rs17571 shows a significantly higher proportion of T-allele carriers among male Alzheimer patients (28.5%) when compared with male controls (13.8%, p = .013, p(corr) = .039). The odds ratio was 2.48 (95% confidence interval: 1.14-5.58). There was no significant difference in the T-allele distribution in women. Including APOE4 status and age did not have an additional effect on the morbidity risk. Thus, our results support the idea that rs17571 confers an increased risk for AD in men but not in women. Further investigation should substantiate the role of gender for AD risk of rs17571.

摘要

溶酶体蛋白酶组织蛋白酶 D 可能参与阿尔茨海默病(AD)中的β-淀粉样蛋白生成。有证据表明组织蛋白酶 D 基因的单核苷酸多态性(rs17571)与 AD 风险增加相关。然而,关于性别特异性差异知之甚少。因此,我们进行了一项遗传关联研究,重点关注 434 名参与者(219 名 AD 患者和 215 名对照)中的性别特异性差异。rs17571 的筛查显示,与男性对照组(13.8%,p=.013,p(corr)=.039)相比,男性 AD 患者的 T 等位基因携带者比例明显更高(28.5%)。比值比为 2.48(95%置信区间:1.14-5.58)。女性 T 等位基因分布无显著差异。包括 APOE4 状态和年龄对发病率风险没有额外影响。因此,我们的结果支持 rs17571 增加男性而非女性 AD 风险的观点。进一步的研究应该证实性别对 rs17571 的 AD 风险的作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验