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机构地区:[1]辽宁医学院公共卫生学院,辽宁锦州121001
出 处:《现代预防医学》2016年第4期580-583,共4页Modern Preventive Medicine
基 金:辽宁省大学生创新创业训练计划项目(201410160050)
摘 要:目的探讨尼古丁乙酰胆碱受体α3亚基(α-3 nicotinic acetylcholine receptor,CHRNA3)基因rs1051730位点多态性与慢性阻塞性肺疾病(Chronic Obstructive Pulmonary Disease,COPD)发病风险的关系。方法检索Pub Med、CNKI等中、英文数据库,收集有关rs1051730位点多态性与COPD关联性的病例对照研究,提取相关数据进行Meta分析,计算OR值及其95%置信区间(95%Confidence Intervals,95%CI),根据研究对象种族进行亚组分析。结果共有7篇文献纳入本研究,累计病例数5259名,对照组11 913名。Meta分析结果显示,在显性遗传模型(CT+TT vs CC)条件下,rs1051730与COPD发病风险相关(OR=1.22,95%CI=1.12~1.32,P〈0.001);亚组分析结果显示,该关联性仅存在于欧洲人种中(OR=1.11,95%CI=1.12~1.32,P〈0.001),而在中国汉族人群中,rs1051730与COPD无关联(OR=1.23,95%CI=0.90~1.67,P=0.191)。等位基因模型(T vs C)和隐性模型(TT vs CT+CC)条件下均得出类似结论。结论 CHRNA3基因rs1051730位点多态性与欧洲人群COPD发病相关,携带T等位基因能够显著增加COPD的发病风险。Objective This work was to explore the correlation between the polymorphism of rs1051730 in an CHRNA3 subunit (α-3 nicotinic acetyleholine receptor) with chronic obstructive pulmonary disease (COPD). Methods A comprehensive literature research was conducted to find studies reporting correlation between rs1051730 and COPD. ORs (Pooled odds ratios) with 95% CIs (95% confidence intervals) were calculated. Subgroup analyses were conducted according to the ethnicity of the study population. Results A total of 7 articles with 5259 cases and 11913 controls were included in this analysis. Under dominant model (CT+TT vs CC), significant correlation between rs1051730 and COPD were identified (OR=1.22, 95% CI=1.12-1.32, P〈0.001). However, this correlation only existed among European (OR=1.11, 95% CI=1.12-1.32, P〈0.001), not Chinese (OR=1.23, 95% CI=0.90-1.67, P=0.191). The similar results were found by both allele model (T vs C) and recessive model (TT vs CT+CC). Condusion Rs1051730 in CHRNA3 was associated with COPD among European, and the T allele could increase the COPD risk.
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