Sun Lu-Lu, Zhang Si-Jia, Chen Mei-Jun, Elena Kazakova, Qiao Hong
Department of Endocrinology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150000, China.
Chin Med J (Engl). 2017 May 5;130(9):1055-1061. doi: 10.4103/0366-6999.204926.
Four single nucleotide polymorphisms (SNPs) in the modulator recognition factor 2/AT-rich interaction domain 5B (MRF2/ARID5B) gene located at chromosome 10q21.2 have been shown to be associated with both type 2 diabetes mellitus (T2DM) and coronary artery disease in a Japanese cohort. This study aimed to investigate the relationship between these SNPs (rs2893880, rs10740055, rs7087507, rs10761600) and new-onset T2DM and lipid metabolism in a Northern Chinese population.
This was a case-control study. The rs2893880, rs10740055, rs7087507, and rs10761600 genetic variants were genotyped by SNPscan and analyzed in relation to T2DM susceptibility in 2000 individuals (999 with newly diagnosed T2DM and 1001 controls without diabetes mellitus). Associations between the MRF2/ARID5B genetic models and T2DM were determined by multivariate logistic regression.
Regarding the rs10740055 SNP, AA was associated with a higher risk of T2DM compared with codominant-type CC (adjusted by sex, age, and body mass index [BMI], P= 0.041, odds ratio [OR] = 1.421, 95% confidence interval [CI] 1.014-1.991). Meanwhile, AA individuals were at increased risk of presenting with T2DM compared with individuals with CC or a single C (adjusted by sex, age, and BMI, P= 0.034, OR = 1.366, 95% CI 1.023-1.824). With respect to rs10761600, AT contributed to a higher risk of T2DM compared with AA (adjusted by sex, age, and BMI, P= 0.013, OR = 1.585, 95% CI 1.101-2.282), while TT also increased the risk of presenting with T2DM compared with AA or A (adjusted by sex, age, and BMI, P= 0.004, OR = 1.632, 95% CI 1.166-2.284). High-density lipoprotein cholesterol (HDL-C) levels were significantly different among the three genotypes of rs7087507 in the controls (P = 0.048) (GG>GA).
The present results identified MRF2/ARID5B as a potential susceptibility gene for new-onset T2DM in a Northern Chinese population, while the rs7087507 SNP was associated with HDL-C levels. Further larger studies are required to validate these findings.
位于10号染色体q21.2的调节因子识别因子2/富含AT交互结构域5B(MRF2/ARID5B)基因中的四个单核苷酸多态性(SNP)已被证明与日本人群中的2型糖尿病(T2DM)和冠状动脉疾病均相关。本研究旨在调查中国北方人群中这些SNP(rs2893880、rs10740055、rs7087507、rs10761600)与新发T2DM及脂质代谢之间的关系。
这是一项病例对照研究。通过SNPscan对rs2893880、rs10740055、rs7087507和rs10761600基因变异进行基因分型,并在2000名个体(999例新诊断的T2DM患者和1001名无糖尿病的对照者)中分析其与T2DM易感性的关系。通过多因素逻辑回归确定MRF2/ARID5B基因模型与T2DM之间的关联。
关于rs10740055 SNP,与共显性类型CC相比(经性别、年龄和体重指数[BMI]校正,P = 0.041,比值比[OR] = 1.421,95%置信区间[CI] 1.014 - 1.991),AA与T2DM风险较高相关。同时,与CC或单个C个体相比,AA个体患T2DM的风险增加(经性别、年龄和BMI校正,P = 0.034,OR = 1.366,95% CI 1.023 - 1.824)。关于rs10761600,与AA相比,AT导致T2DM风险较高(经性别、年龄和BMI校正,P = 0.013,OR = 1.585,95% CI 1.101 - 2.282),而与AA或A相比,TT也增加了患T2DM的风险(经性别、年龄和BMI校正,P = 0.004,OR = 1.632,95% CI 1.166 - 2.284)。在对照组中,rs7087507的三种基因型之间的高密度脂蛋白胆固醇(HDL-C)水平存在显著差异(P = 0.048)(GG>GA)。
目前的结果确定MRF2/ARID5B是中国北方人群新发T2DM的一个潜在易感基因,而rs7087507 SNP与HDL-C水平相关。需要进一步开展更大规模的研究来验证这些发现。