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促红细胞生成素基因多态性与糖尿病微血管并发症风险之间的关联。

Associations between erythropoietin polymorphisms and risk of diabetic microvascular complications.

作者信息

Li Hua, Xu Huipu, Li Yuerong, Zhao Dongdong, Ma Baoxin

机构信息

Department of Oncology, The Affiliated Hospital of Binzhou Medical University, Binzhou, Shandong 256603, China.

Department of Cardiology, The Affiliated Hospital of Binzhou Medical University, Binzhou, Shandong 256603, China.

出版信息

Oncotarget. 2017 Nov 27;8(68):112675-112684. doi: 10.18632/oncotarget.22699. eCollection 2017 Dec 22.

Abstract

We conducted a meta-analysis to evaluate the relationship between erythropoietin (EPO) polymorphisms and diabetic microvascular complications. We searched the PubMed, Embase, Cochrane library, Web of Science, Wanfang, and Chinese National Knowledge Infrastructure databases for appropriate studies. Odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to evaluate the associations. Ultimately, eight studies consisting of 2,861 cases and 2,136 controls were identified and included in our meta-analysis. Results with our genotype model indicated an association between rs1617640 polymorphisms and diabetic microvascular complications (TT vs. GG: OR = 1.544, 95% CI = 1.089-2.189, = 0.015). No clear associations between the rs1617640 and rs507392 polymorphisms and diabetic retinopathy were observed. By contrast, rs551238 polymorphisms were associated with increased diabetic retinopathy risk (allele model: OR = 0.774, 95% CI = 0.658-0.911, = 0.002; genotype model: AC vs. CC: OR = 0.598, 95% CI = 0.402-0.890, = 0.011; dominant model: OR = 0.561, 95% CI = 0.385-0.817, = 0.003; recessive model: OR = 0.791, 95% CI = 0.643-0.973, = 0.026). These results indicate that EPO polymorphisms are a risk factor for diabetic microvascular complications.

摘要

我们进行了一项荟萃分析,以评估促红细胞生成素(EPO)基因多态性与糖尿病微血管并发症之间的关系。我们在PubMed、Embase、Cochrane图书馆、Web of Science、万方和中国知网数据库中检索了相关研究。计算了具有95%置信区间(CI)的比值比(OR)来评估关联。最终,确定了八项研究,包括2861例病例和2136例对照,并纳入我们的荟萃分析。我们的基因型模型结果表明,rs1617640基因多态性与糖尿病微血管并发症之间存在关联(TT与GG:OR = 1.544,95%CI = 1.089 - 2.189,P = 0.015)。未观察到rs1617640和rs507392基因多态性与糖尿病视网膜病变之间存在明显关联。相比之下,rs551238基因多态性与糖尿病视网膜病变风险增加相关(等位基因模型:OR = 0.774,95%CI = 0.658 - 0.911,P = 0.002;基因型模型:AC与CC:OR = 0.598,95%CI = 0.495402 - 0.890,P = 0.011;显性模型:OR = 0.561,95%CI = 0.385 - 0.817,P = 0.003;隐性模型:OR = 0.791,95%CI = 0.643 - 0.973,P = 0.026)。这些结果表明,EPO基因多态性是糖尿病微血管并发症的一个危险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ca/5762540/ad4dc32ec76d/oncotarget-08-112675-g001.jpg

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