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机构地区:[1]首都医科大学宣武医院神经内科,北京100053
出 处:《中华神经科杂志》2008年第12期802-807,共6页Chinese Journal of Neurology
基 金:国家973计划基金资助项目(2006ch500700);北京自然科学基金重点资助项目(7071004)
摘 要:目的通过检测载脂蛋白D基因(apolipoprotein D gene,ApoD)单核苷酸多态位点,探讨其与北方汉族人群散发性阿尔茨海默病(sporadic Alzheimer’s disease,SAD)的相关性。方法应用聚合酶链反应(PCR)及直接测序筛查ApoD基因所有外显子及其两端内含子多态位点。选取等位基因频率大于10%的位点,利用PCR-限制性片段长度多态性(PCR—RFLP)技术,采用病例封照相关性研究方法,研究256例SAD患者以及294名健康人的ApoD多态位点与SAD发病的关系。同时对位点间的连锁不平衡及构建的单体型进行相关性分析。结果ApoD第2号外显子存在T/C多态性(rs5952),第3号内含子(rs1568566)存在C/T多态性。ApoD m5952T/C和rs1568566C/T等位基因频率和基因型频率在SAD组和对照组间的分布差异有统计学意义。Logistic回归分析表明携带rs5952C或rs1568566T等位基因分别增加SAD发病风险:校正后rs5952 χ^2=9.282(P=0.002);m1568566 χ^2=5.072(P=0.024)。进一步分析证实性别和ApoD多态性存在交互作用。rs5952-rs1568566位点间存在连锁不平衡。结论北方汉族人ApoD基因存在第2号外显子m5952和第3号内含子rs15685662个多态位点;ApoD多态可增加SAD发病风险;携带rs5952T或rs1568566C单体型可能对SAD的发病有一定的保护作用。Objective To investigate whether polymorphisms of apolipoprotein D gene (APOD) have an effect on the risk for sporadic Alzheimer' s disease (SAD). Methods Combination of polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) and DNA sequencing technique to screen all exons ( 1-5 ), along with flanking exon-intron boundaries of the APOD gene. We investigated the polymorphisms of APOD in 256 SAD patients and 294 healthy controls from North China by PCR-RFLP technique. Association of every polymorphism with AD was analyzed in this case-control study. Results Two ApoD (rs5952 and rs1568566) polymorphisms were detected and there were significant differences in the genotype or allele frequencies for the 2 ApoD polymorphisms respectively between cases and controls. Logistic analysis showed that rs5952C or rs1568566T allele carrier increased the risk for SAD ( rs5952 adjusted OR = 1. 817, 95% CI 1. 237-2. 669, χ^2 = 9. 282, P = 0. 002 ; rs1568566 adjusted OR = 1. 563, 95% CI 1. 060--2. 306, χ^2 = 5. 072, P = 0. 024). The ApoD polymorphisms showed gender specific associations. The linkage disequilibrium of the 2 single nucleotide polymorphism loci was found between rs5952 and rs1568566 of ApoD. Conclusion Polymorphisms of rs5952 and rs1568566 in ApoD might play an important role in modifying risk for SAD.
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