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亚洲人群中变异对2型糖尿病的影响:一项系统评价和荟萃分析。

The Effect of Variation on Type 2 Diabetes Mellitus in the Asian Population: A Systematic Review and Meta-Analysis.

作者信息

Virginia Dita Maria, Dwiprahasto Iwan, Wahyuningsih Mae Sri Hartati, Nugrahaningsih Dwi Aris Agung

机构信息

Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia.

Faculty of Pharmacy, Sanata Dharma University, Yogyakarta, Indonesia.

出版信息

Malays J Med Sci. 2022 Jun;29(3):5-16. doi: 10.21315/mjms2022.29.3.2. Epub 2022 Jun 28.

Abstract

The prevalence of type 2 diabetes mellitus (T2DM) is increasing among Asians. The adenosine monophosphate-activated protein kinase (AMPK) increases T2DM risk through insulin resistance. Glucose levels are related to AMPK subunit α2 encoded by . This systematic review and meta-analysis aimed to analyse the association between variation and T2DM risk. Publication search related to and T2DM used PubMed, ProQuest, and ScienceDirect databases. Article selection based on inclusion and exclusion criteria only included Japanese and Chinese populations. This meta-analysis used five genotype models to estimate the effect of variation and T2DM risk. Additionally, a fixed-effect model was selected to measure the pooled size effect if > 0.05 or I < 50%. Qualitative analysis included four eligible studies, and meta-analysis included only two studies because both showed data concerning rs2746342 variation. Patients with G allele are 1.45 times more likely to have T2DM than patients with T allele (95% confidence interval [CI]: 1.20, 1.76; : 0.0001). Notably, patients who had GG genotype have 1.96 times higher risk of T2DM compared with those with TT genotype (95% CI: 1.34, 2.87; : 0.0005), dominant model (odds ratio [OR]: 1.75; 95% CI: 1.32, 2.31; : 0.001), and recessive model (OR: 1.43; 95% CI: 1.01, 2.01; : 0.04). variation, especially in rs2746342, has an association with T2DM risk in the G allele, additive, dominant, and recessive models. G allele might be the most contributable factor in increasing T2DM susceptibility.

摘要

2型糖尿病(T2DM)在亚洲人群中的患病率正在上升。腺苷单磷酸激活蛋白激酶(AMPK)通过胰岛素抵抗增加T2DM风险。血糖水平与 所编码的AMPK亚基α2相关。本系统评价和荟萃分析旨在分析 变异与T2DM风险之间的关联。与 和T2DM相关的文献检索使用了PubMed、ProQuest和ScienceDirect数据库。基于纳入和排除标准的文章选择仅纳入了日本和中国人群。本荟萃分析使用了五种基因型模型来估计 变异和T2DM风险的影响。此外,如果I²>0.05或I<50%,则选择固定效应模型来测量合并效应量。定性分析纳入了四项符合条件的研究,荟萃分析仅纳入了两项研究,因为这两项研究均显示了有关rs2746342变异的数据。携带G等位基因的患者患T2DM的可能性是携带T等位基因患者的1.45倍(95%置信区间[CI]:1.20,1.76;P=0.0001)。值得注意的是,与携带TT基因型的患者相比,携带GG基因型的患者患T2DM的风险高1.96倍(95%CI:1.34,2.87;P=0.0005),显性模型(优势比[OR]:1.75;95%CI:1.32,2.31;P=0.001),隐性模型(OR:1.43;95%CI:1.01,2.01;P=0.04)。 变异,尤其是rs2746342,在G等位基因、加性、显性和隐性模型中与T2DM风险相关。G等位基因可能是增加T2DM易感性的最主要因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ca/9249426/50bb603aea5f/02mjms2903_raf1.jpg

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