Association of adiponectin gene polymorphisms and their haplotypes with type 2 diabetes and related metabolic traits in an Iranian population

被引:3
作者
Joshaghani, Hamid Reza [1 ]
Kokhaei, Parviz [2 ]
Barati, Mehdi [2 ]
Pakdel, Abbas [3 ,4 ]
Mohammadzadeh, Ghorban [5 ]
Bandegi, Navid [6 ]
Bandegi, Ahmad Reza [7 ]
机构
[1] Golestan Univ Med Sci, Biochem & Metab Disorders Res Ctr, Gorgan, Golestan, Iran
[2] Semnan Univ Med Sci, Canc Res Ctr, Semnan, Iran
[3] Semnan Univ Med Sci, Nervous Syst Stem Cells Res Ctr, Semnan, Iran
[4] Semnan Univ Med Sci, Fac Med, Dept Biochem, Semnan 1513138111, Iran
[5] Ahvaz Jundishapur Univ Med Sci, Fac Med, Hyperlipidemia Res Ctr, Dept Clin Biochem, Ahvaz, Iran
[6] Birjand Univ Med Sci, Fac Med, Birjand, Iran
[7] Semnan Univ Med Sci, Res Ctr Physiol, Semnan, Iran
关键词
Adiponectin; Type 2 diabetes mellitus; Gene polymorphism; Iran; SINGLE-NUCLEOTIDE POLYMORPHISMS; CORONARY-ARTERY-DISEASE; ADIPOQ GENE; MELLITUS; RISK; SUSCEPTIBILITY; VARIANTS; CHINESE;
D O I
10.1007/s13410-019-00785-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Adiponectin is an adipocyte-secreted protein that contributes to glucose homeostasis. Contradictory reports are available on single nucleotide polymorphisms (SNPs) in the adiponectin gene and the risk of type 2 diabetes (T2D). We investigate the association of adiponectin gene SNPs (+45T/G and +276G/T) with serum adiponectin, insulin resistance, lipid profile, and T2D risk in an Iranian population. Method The +45T/G and +276G/T SNPs were genotyped in 211 non-familial T2D patients and 202 non-diabetic subjects by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and TaqMan probe, respectively. Results T2D was associated with a decrease in serum adiponectin level. The G allele and the GG and TG genotypes of +45T/G SNP were more abundant than the T allele and the TT genotype in T2D patients compared with controls (p < 0.001). The risk of T2D in individuals with the GG and TG genotypes of +45T/G SNP was 4 and 2 times more than that with the TT genotype, respectively. There was no statistically significant difference in the frequencies of allele and genotype of +276G/T SNP between the control and T2D groups. The presence of +45G/+276G haplotype was associated with an increased risk of T2D (OR = 2.01, 95% CI = 1.34-3.03,p = 0.04). Conclusion Therefore, our results showed that +45T/G SNP is associated with the risk of T2D higher than +276G/T SNP in the studied population.
引用
收藏
页码:216 / 222
页数:7
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