Kanthimathi Sekar, Chidambaram Manickam, Bodhini Dhanasekaran, Liju Samuel, Bhavatharini Aruyerchelvan, Uma Ram, Anjana Ranjit Mohan, Mohan Viswanathan, Radha Venkatesan
Madras Diabetes Research Foundation, No. 4, Conran Smith Road, Gopalapuram, Chennai, India.
Division of Experimental Genetics, Sidra Medical and Research Center, Out-Patient Clinic, C6-73003, PO Box 26999, Al Luqta Street, Education City North Campus, Qatar Foundation, Doha, Qatar.
Mol Genet Genomics. 2017 Jun;292(3):585-591. doi: 10.1007/s00438-017-1292-6. Epub 2017 Feb 11.
Earlier studies have provided evidence that the gestational diabetes mellitus (GDM) and Type 2 diabetes mellitus (T2DM) share common genetic background. A recent genome wide association study (GWAS) showed a strong association of six novel gene variants with T2DM among south Asians but not with Europeans. The aim of this study was to investigate whether these variants that confer susceptibility to T2DM in Asian Indian population also correlate with GDM in Asian Indian population. In addition to these novel variants, three T2DM associated SNPs that were previously identified by GWAS in Caucasian populations, which also showed association with T2DM in south Indian population in our previous study were also evaluated for their susceptibility to GDM in our population. The study groups comprised unrelated pregnant women with GDM (n = 518) and pregnant women with normal glucose tolerance (NGT) (n = 1220). A total of nine SNPs in or near nine loci, namely AP3S2 (rs2028299), BAZ1B (rs12056034), CDKN2A/B (rs7020996), GRB14 (rs3923113), HHEX (rs7923837), HMG20A (rs7178572), HNF4A (rs4812829), ST6GAL1 (rs16861329) and VPS26A (rs1802295) were genotyped using the MassARRAY system. Among these nine SNPs that previously showed an association with T2DM in Asian Indians, HMG20A (rs7178572) and HNF4A (rs4812829) gene variants showed a significant association with GDM. The risk alleles of rs7178572 in HMG20A and rs4812829 in HNF4A gene conferred 1.24 and 1.28 times higher risk independently and about 1.44 and 1.97 times increased susceptibility to GDM for one and two risk genotypes, respectively. We report that the HMG20A (rs7178572) and HNF4A (rs4812829) variants that have previously shown a strong association with T2DM in Asian Indians also contributes significant risk to GDM in this population. This is the first report of the association of HMG20A (rs7178572) and HNF4A (rs4812829) variants with GDM.
早期研究已提供证据表明,妊娠期糖尿病(GDM)和2型糖尿病(T2DM)具有共同的遗传背景。最近一项全基因组关联研究(GWAS)显示,六个新的基因变异与南亚人群的T2DM密切相关,但与欧洲人群无关。本研究的目的是调查这些在亚洲印度人群中赋予T2DM易感性的变异是否也与亚洲印度人群的GDM相关。除了这些新变异外,还对先前在高加索人群中通过GWAS鉴定出的三个与T2DM相关的单核苷酸多态性(SNP)进行了评估,在我们之前的研究中,这三个SNP在南印度人群中也与T2DM相关,此次对其在我们人群中对GDM的易感性进行评估。研究组包括患有GDM的无亲缘关系孕妇(n = 518)和葡萄糖耐量正常(NGT)的孕妇(n = 1220)。使用MassARRAY系统对九个基因座内或附近的总共九个SNP进行基因分型,这九个基因座分别为AP3S2(rs2028299)、BAZ1B(rs12056034)、CDKN2A/B(rs7020996)、GRB14(rs3923113)、HHEX(rs7923837)、HMG20A(rs7178572)、HNF4A(rs4812829)、ST6GAL1(rs16861329)和VPS26A(rs1802295)。在这九个先前显示与亚洲印度人群T2DM相关的SNP中,HMG20A(rs7178572)和HNF4A(rs4812829)基因变异与GDM显著相关。HMG20A中rs7178572的风险等位基因和HNF4A中rs4812829的风险等位基因分别独立地使风险增加1.24倍和1.28倍,对于一种和两种风险基因型,对GDM的易感性分别增加约1.44倍和1.97倍。我们报告称,先前在亚洲印度人群中显示与T2DM密切相关的HMG20A(rs7178572)和HNF4A(rs4812829)变异也对该人群的GDM构成显著风险。这是关于HMG20A(rs7178572)和HNF4A(rs4812829)变异与GDM关联的首次报告。