Association between rs2278426 (C/T) and rs892066 (C/G) variants of ANGPTL8 (betatrophin) and susceptibility to type2 diabetes mellitus

被引:10
作者
Ghasemi, Hassan [1 ]
Karimi, Jamshid [2 ]
Khodadadi, Iraj [2 ]
Saidijam, Massoud [3 ]
Tavilani, Heidar [2 ]
机构
[1] Abadan Sch Med Sci, Abadan, Iran
[2] Hamadan Univ Med Sci, Sch Med, Dept Biochem, Hamadan, Iran
[3] Hamadan Univ Med Sci, Ctr Mol Med, Hamadan, Iran
关键词
ANGPTL8; insulin resistance; polymorphism; rs2278426; type 2 diabetes mellitus; ANGIOPOIETIN-LIKE PROTEIN; BETA-CELL PROLIFERATION; INSULIN-RESISTANCE; HDL-CHOLESTEROL; PAX GENES; IDENTIFICATION; INHIBITION; MUTATIONS; LIPASIN; MASS;
D O I
10.1002/jcla.22649
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background Angiopoietin-like protein 8 (ANGPTL8) is a hormone that mainly secreted from the liver and adipose tissue and plays an important role in the proliferation of pancreatic beta cells and lipid metabolism. Therefore, we studied the association of ANGPTL8 rs2278426 (C/T) and rs892066 (C/G) polymorphisms with the risk of type 2 diabetes mellitus (T2DM) and their association with biochemical parameters. Methods Two hundred and eighty-eight subjects (controls; n = 138 and type 2 diabetic patients; n = 150) were enrolled in this study. Direct haplotyping was performed using amplification-refractory mutation system (ARMS)-RFLP-PCR. Results The CT genotype frequency of rs2278426 (C/T) variant was significantly higher in T2DM patients compared to the controls group (P = 0.02), and there was a significant association between this genotype and increased risk of T2DM (OR: 2.41, CI: 1.26-4.59, P = 0.007). In addition, there was a significant relationship between CT genotype of this variant and high-density lipoprotein cholesterol (HDL-C), fasting blood sugar (FBS), insulin, insulin resistance and glycated hemoglobin (P < 0.05). Furthermore, bioinformatics analysis revealed that arginine (Arg) to tryptophan (Trp) substitution at rs2278426 position causes structural instability of ANGPTL8 protein. Genotype and allele distribution of rs892066 (C/G) was not statistically significant in T2DM patients compared to the control group. The distribution of haplotypes had no significant difference between controls and T2DM patients (P = 0.24). Conclusion Our results suggest that the rs2278426 (C/T) variant is associated with increased risk of T2DM and may cause dyslipidemia due to its effect on decreasing HDL-C levels.
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页数:8
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