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69C>T 多态性与 2 型糖尿病风险:系统评价和更新的荟萃分析。

69C>T Polymorphism and the Risk of Type 2 Diabetes Mellitus: A Systematic Review and Updated Meta-Analysis.

机构信息

College of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, South Korea.

出版信息

Front Endocrinol (Lausanne). 2021 Apr 23;12:639524. doi: 10.3389/fendo.2021.639524. eCollection 2021.

DOI:10.3389/fendo.2021.639524
PMID:33967955
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8104122/
Abstract

BACKGROUND

The ATP-binding cassette transporter A1 is likely associated with the risk of type 2 diabetes mellitus (T2DM) β cell function modification, but the evidence on the association remains unclear. This study aimed to investigate the relationship between the 69C>T polymorphism and the risk of T2DM through a systematic review and meta-analysis.

MATERIALS AND METHODS

The PubMed, Web of Science, and Embase databases were searched for qualified studies published until August 2020. Studies that included the association between the 69C>T polymorphism and the risk of T2DM were reviewed. The odds ratios (ORs) and 95% confidence intervals (CIs) were evaluated.

RESULTS

We analyzed data from a total of 10 studies involving 17,742 patients. We found that the CC or CT genotype was associated with increased risk of T2DM than the TT genotype (OR, 1.41; 95% CI, 1.02-1.93). In the Asian population, the C allele carriers had a higher risk of T2DM than those with the TT genotype; the ORs of the CC and CT genotypes were 1.80 (95% CI, 1.21-2.68) and 1.61 (95% CI, and 1.29-2.01), respectively.

CONCLUSIONS

This meta-analysis confirmed that the 69C>T genotype showed a decrease risk of T2DM compared to the CC or CT genotypes.

摘要

背景

ATP 结合盒转运蛋白 A1 可能与 2 型糖尿病(T2DM)β细胞功能改变的风险相关,但关于该相关性的证据仍不清楚。本研究旨在通过系统评价和荟萃分析来探讨 69C>T 多态性与 T2DM 风险之间的关系。

材料和方法

检索 PubMed、Web of Science 和 Embase 数据库,纳入截至 2020 年 8 月发表的合格研究。评估 69C>T 多态性与 T2DM 风险之间的关联研究。评估比值比(ORs)和 95%置信区间(CIs)。

结果

我们分析了共 10 项研究的数据,这些研究共纳入了 17742 名患者。我们发现 CC 或 CT 基因型与 T2DM 风险增加有关,而 TT 基因型则不然(OR,1.41;95%CI,1.02-1.93)。在亚洲人群中,C 等位基因携带者发生 T2DM 的风险高于 TT 基因型携带者;CC 和 CT 基因型的 OR 值分别为 1.80(95%CI,1.21-2.68)和 1.61(95%CI,1.29-2.01)。

结论

这项荟萃分析证实,与 CC 或 CT 基因型相比,69C>T 基因型与 T2DM 风险降低有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07b2/8104122/b90d861f85da/fendo-12-639524-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07b2/8104122/b92d225a45d6/fendo-12-639524-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07b2/8104122/a0f8c8ed0477/fendo-12-639524-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07b2/8104122/b90d861f85da/fendo-12-639524-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07b2/8104122/b92d225a45d6/fendo-12-639524-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07b2/8104122/a0f8c8ed0477/fendo-12-639524-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07b2/8104122/b90d861f85da/fendo-12-639524-g003.jpg

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