Hsueh Kuan-Chun, Nfor Oswald Ndi, Hsu Shu-Yi, Yang Shun-Fa, Liaw Yung-Po
Department of Surgery, Tungs' Taichung Metro Harbor Hospital, Taichung, Taiwan.
Department of Post-Baccalaureate Medicine, College of Medicine, National Chung Hsing University, Taichung, Taiwan.
Front Genet. 2022 Mar 7;13:822700. doi: 10.3389/fgene.2022.822700. eCollection 2022.
Type 2 diabetes (T2D) and liver cirrhosis remain significant public health threats in Taiwan. These conditions are reported to be associated with the rs738409 polymorphism of the in European populations. We assessed the effect of T2D and rs738409 polymorphism on liver cirrhosis among Taiwan Biobank (TWB) participants. In total, 17,985 participants in TWB had their health records linked to the National Health Insurance Research Database (NHIRD). Participants included those who visited the assessment centers between 2008 and 2015, with an age range between 30 and 70 years of age. We performed logistic regression analysis to investigate the odds ratios (OR) for liver cirrhosis among participants based on the T2D status and rs738409 genotypes. Genotyping was performed using the Axiom Genome-Wide TWB Array Plate. In our analysis, 150 of the 17,619 eligible participants were identified as cirrhosis cases. Based on the univariate analysis, liver cirrhosis was positively associated with T2D (OR, 1.83; 95% CI 1.23-2.70) whereas, the variant rs738409 was not (regardless of the genetic model). The variant and T2D, however, showed significant interactions in the additive, genotype, and dominant models ( values of 0.0302, 0.0395, and 0.0455, respectively). We observed a statistically significant association between T2D and liver cirrhosis and variant rs738409 with an OR of 1.71 (95% CI, 1.03-2.84) for individuals carrying a G allele compared to those with a C allele and 2.92 (95% CI 1.07-7.99) for GG compared to CC individuals. According to our study, Taiwanese adults with T2D and the rs738409 GG genotype are more likely to develop liver cirrhosis.
2型糖尿病(T2D)和肝硬化仍是台湾地区重大的公共卫生威胁。据报道,在欧洲人群中,这些疾病与[具体基因]的rs738409多态性有关。我们评估了T2D和rs738409多态性对台湾生物银行(TWB)参与者肝硬化的影响。TWB共有17985名参与者,其健康记录与“全民健康保险研究数据库”(NHIRD)相关联。参与者包括2008年至2015年间前往评估中心的人群,年龄在30至70岁之间。我们进行了逻辑回归分析,以研究基于T2D状态和rs738409基因型的参与者患肝硬化的比值比(OR)。基因分型使用Axiom全基因组TWB阵列板进行。在我们的分析中,17619名符合条件的参与者中有150人被确定为肝硬化病例。基于单因素分析,肝硬化与T2D呈正相关(OR,1.83;95%CI 1.23 - 2.70),而rs738409变体则不然(无论遗传模型如何)。然而,该变体与T2D在加性、基因型和显性模型中显示出显著的相互作用(P值分别为0.0302、0.0395和0.0455)。我们观察到T2D与肝硬化以及rs738409变体之间存在统计学上的显著关联,与携带C等位基因的个体相比,携带G等位基因的个体患肝硬化的OR为1.71(95%CI,1.03 - 2.84),与CC个体相比,GG个体的OR为2.92(95%CI 1.07 - 7.99)。根据我们的研究,患有T2D且rs738409基因型为GG的台湾成年人更易患肝硬化。