Contribution of ENPP1, TCF7L2, and FTO polymorphisms to type 2 diabetes in mixed ancestry ethnic population of South Africa

被引:19
作者
Yako, Yandiswa Y. [1 ]
Madubedube, Jabulisile H. [2 ]
Kengne, Andre P. [3 ,4 ]
Erasmus, Rajiv T. [5 ,6 ]
Pillay, Tahir S. [7 ]
Matsha, Tandi E. [2 ]
机构
[1] Univ Witwatersrand, Fac Hlth Sci, Dept Surg, ZA-2050 Johannesburg, South Africa
[2] Cape Peninsula Univ Technol, Fac Hlth & Wellness Sci, Dept Biomed Sci, ZA-7530 Cape Town, South Africa
[3] South African Med Res Council, Noncommunicable Dis Res Unit, Cape Town, South Africa
[4] Univ Cape Town, Dept Med, ZA-7925 Cape Town, South Africa
[5] Natl Hlth Lab Serv, Fac Med & Hlth Sci, Div Chem Pathol, Cape Town, South Africa
[6] Univ Stellenbosch, Cape Town, South Africa
[7] Univ Pretoria, Inst Cellular & Mol Med Mol Endocrinol, ZA-0002 Pretoria, South Africa
基金
英国医学研究理事会;
关键词
Type; 2; diabetes; genetics; ENPP1; TCF7L2; FTO; Africa; GENOME-WIDE ASSOCIATION; BODY-MASS INDEX; GENETIC-VARIANTS; K121Q POLYMORPHISM; INSULIN-RESISTANCE; CHINESE POPULATION; EUROPEAN POPULATIONS; PREVENTION PROGRAM; RISK; OBESITY;
D O I
10.4314/ahs.v15i4.14
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Transcription factor 7-like 2 gene (TCF7L2), fat mass and obesity-associated gene (FTO), and ectonucleotide pyrophosphatase/phosphodiesterase gene (ENPP1) are known risk loci for type 2 diabetes (T2DM) mostly in European populations. Objectives: To assess the association of these genes with T2DM risk in a South African mixed-ancestry population. Methods: Five hundred and sixty six participants were genotyped for ENPP1-rs997509 and -rs1044498, FTO-9941349 and -rs3751812, TCF7L2-rs12255372 and -rs7903146 polymorphisms using Taqman genotyping assays and validated by automated sequencing to assess the association of the polymorphisms with cardiometabolic traits. Results: In logistic regression models adjusted for age, sex, body mass index (BMI) and insulin resistance, minor allele of rs997509 was associated with a higher risk of prevalent T2DM under a recessive model [odd ratio 4.60 (95% confidence interval: 1.07 to 19.86); p = 0.040]. Under additive model, the rs7903146 [1.43 (1.00 to 2.04); p=0.053] and rs9941349 [1.43 (1.00 to 2.04); p = 0.052] minor alleles showed marginally significant associations with a high risk of T2DM. However, only the rs7903146 alleles (p=0.011) and genotypes (p=0.025) distributions were statistically significantly different between diabetic and non-diabetic individuals. Conclusion: Our findings demonstrate that ENPP1, TCF7L2, and FTO may predispose to T2DM in the mixed-ancestry population.
引用
收藏
页码:1149 / 1160
页数:12
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