亚洲妇女易患妊娠期糖尿病遗传因素的荟萃分析

Sharifah Nurdiyana Syed Mohd Bahktiar, Muhammad Hisyam Jamari, Nurul Aishah Wan Noor, Rabia’tul A’dawiyah Ariff Fadzilah, Muhamad Zafri Abdul Karim, H. Abdul Halim, Noor Fatihah Abu, Teh Lay Kek, M. Z. Salleh
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引用次数: 1

摘要

一项荟萃分析旨在确定增加亚洲妊娠期糖尿病(GDM)风险的显著风险等位基因,以帮助高危妇女进行基因分型决策。使用PubMed、Science Direct和HuGE navigator检索2000年1月至2018年11月的相关研究。数据提取由5位审稿人完成。使用Review Manager 5.3,确定了11个snp与GDM风险之间的关联。计算具有95%置信区间(95% CI)的优势比(ORs)、异质性检验和发表偏倚。如果p值≤0.05,则结果被认为是显著的。根据纳入和排除标准确定了21项研究。从研究的11个遗传变异中,发现9个与GDM易感性显著相关,但异质性不同。等位基因、显性和隐性遗传模型显示MTNR1B (rs138753、rs10830963)和CDKAL1 (rs7754840)与GDM显著相关。使用等位基因和隐性模型发现IGF2BP2 (rs4402960)与GDM有显著关联。对于TCF7L2 (rs7903146),使用等位基因、显性和超显性模型发现显著关联。KCNQ1 (rs2237892)仅在显性模型中与GDM相关。GSTM1(缺失)、GSTT1(缺失)和GSTP1 (rs1695)也与GDM易感性增加密切相关。然而,MTNR1B (rs10830962)和PPARγ2与亚洲人群GDM风险缺乏相关性。在亚洲人群中,9种基因变异与GDM风险增加有关。建议对这些多态性进行筛查,以确定有风险的孕妇,以进行预防和个性化干预。
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Meta-Analysis of the Genetic Factors that Predisposed Asian Women to Gestational Diabetes Mellitus
A meta-analysis was conducted to determine the significant risk alleles which increase the risks of gestational diabetes mellitus (GDM) in Asian to help in decision-making for genotyping of women at risk. PubMed, Science Direct and HuGE navigator were used to identify relevant studies from January 2000 to November 2018. Data extraction was done by five reviewers. Using Review Manager 5.3, association between 11 SNPs and risks of GDM was determined. Odds ratios (ORs) with 95% confidence intervals (95% CI), test of heterogeneity and publication bias were calculated. The result was considered significant if p-value ≤ 0.05. Twenty-one studies were identified based on the inclusion and exclusion criteria. From 11 genetic variants studied, 9 were found to have significant association with GDM susceptibility with different heterogeneity. Allelic, dominant and recessive genetic models show MTNR1B (rs138753, rs10830963) and CDKAL1 (rs7754840) are significantly associated with GDM. IGF2BP2 (rs4402960) was found to have significant association with GDM using allelic and recessive models. For TCF7L2 (rs7903146), significant association was found using allelic, dominant and over dominant models. KCNQ1 (rs2237892) showed association with GDM in dominant model only. Strong associations with increased susceptibility for GDM were also found for GSTM1 (deletion), GSTT1 (deletion) and GSTP1 (rs1695). However, MTNR1B (rs10830962) and PPARγ2 are lack of association with GDM risk in Asian population. Nine genetic variants were associated with increased GDM risk in Asian population. Screening of these polymorphisms to identify pregnant women at risk is recommended for prevention and personalised intervention.
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审稿时长
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