首页> 美国卫生研究院文献>Oncotarget >Associations between two common single nucleotide polymorphisms (rs2241766 and rs1501299) of ADIPOQ gene and coronary artery disease in type 2 diabetic patients: a systematic review and meta-analysis
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Associations between two common single nucleotide polymorphisms (rs2241766 and rs1501299) of ADIPOQ gene and coronary artery disease in type 2 diabetic patients: a systematic review and meta-analysis

机译:ADIPOQ基因的两种常见单核苷酸多态性(rs2241766和rs1501299)与2型糖尿病患者冠状动脉疾病之间的关联:系统评价和荟萃分析

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摘要

ADIPOQ gene polymorphisms were indicated to be associated with coronary artery disease (CAD) in diabetic patients, however, published studies reported inconsistent results. We performed this meta-analysis to reach a more accurate estimation of the relationship between two common ADIPOQ genetic polymorphisms (rs2241766 and rs1501299) and CAD risk in diabetic patients. Eligible studies were retrieved by searching PubMed, Embase, Wangfang, VIP database and China National Knowledge Infrastructure databases. Included and excluded criteria were formulated. The case group was diabetic patients with CAD, and the control group was diabetic subjects without CAD. Summary odds rations (ORs) and 95% confidence intervals (CIs) were used to evaluate ADIPOQ polymorphisms associations with CAD risk in diabetic group. Heterogeneity was evaluated by Q statistic and I2 statistic. A total of twelve published articles, involving 3996 cases and 8876 controls were included in this meta-analysis. The pooled results from rs1501299 polymorphism showed decreased risk in homozygote model (TT VS GG: OR=0.67, 95%CI=0.54-0.83). Heterogeneity was detected in our study. Sensitivity analysis and subgroup analysis were conducted in the meta-analysis. For rs2241766 polymorphism, an increased risk was detected in Caucasian subgroup in heterozygote model (CT VS TT: OR=1.19, 95%CI=1.00-1.42). In genotyping method (PCR-RFLP) subgroup, an increased risk was found in recessive model (GG VS GT+TT: OR=2.05, 95%CI=1.23-3.39). In the sensitivity analysis of rs1501299, decreased risk was detected in allelic model (T VS G: OR=0.86, 95%CI=0.76-0.98) and recessive model (TT VS TG+GG: OR=0.47, 95%CI=0.33-0.67). Publication bias is not observed in our results. Our meta-analysis suggests that the rs1501299 polymorphism may play a protective role in CAD in diabetic patients. The rs2241766 polymorphism is found to be associated with a significant increase in CAD risk in Caucasian and genotyping method (PCR-RFLP) subgroups. Further studies are needed to confirm the prediagnostic effect of the two gene polymorphisms in CAD risk in diabetic patients.
机译:据指出,ADIPOQ基因多态性与糖尿病患者的冠状动脉疾病(CAD)有关,但是,已发表的研究报道了不一致的结果。我们进行了这项荟萃分析,以更准确地估计糖尿病患者中两种常见的ADIPOQ基因多态性(rs2241766和rs1501299)与CAD风险之间的关系。通过搜索PubMed,Embase,Wangfang,VIP数据库和中国国家知识基础设施数据库来检索符合条件的研究。制定了纳入和排除标准。病例组是患有CAD的糖尿病患者,对照组是没有CAD的糖尿病患者。摘要赔率(OR)和95%置信区间(CI)用于评估ADIPOQ多态性与糖尿病组CAD风险的关联。通过Q统计量和I 2 统计量评估异质性。本荟萃分析共纳入12篇发表的文章,涉及3996例病例和8876例对照。 rs1501299多态性的汇总结果显示,纯合子模型的风险降低(TT VS GG:OR = 0.67,95%CI = 0.54-0.83)。在我们的研究中检测到异质性。在荟萃分析中进行了敏感性分析和亚组分析。对于rs2241766多态性,在杂合子模型中的白种人亚组中检测到风险增加(CT VS TT:OR = 1.19,95%CI = 1.00-1.42)。在基因分型方法(PCR-RFLP)亚组中,隐性模型的风险增加(GG VS GT + TT:OR = 2.05,95%CI = 1.23-3.39)。在rs1501299的敏感性分析中,在等位基因模型(T VS G:OR = 0.86,95%CI = 0.76-0.98)和隐性模型(TT VS TG + GG:OR = 0.47,95%CI = 0.33)中发现风险降低-0.67)。我们的结果未发现出版偏见。我们的荟萃分析表明,rs1501299基因多态性可能在糖尿病患者的CAD中起保护作用。发现rs2241766基因多态性与白种人和基因分型方法(PCR-RFLP)亚组的CAD风险显着增加有关。需要进一步的研究来确认这两种基因多态性对糖尿病患者的CAD风险的预诊断作用。

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