Common Variants of Inflammatory Cytokine Genes Are Associated with Risk of Nephropathy in Type 2 Diabetes among Asian Indians

被引:68
作者
Ahluwalia, Tarunveer Singh
Khullar, Madhu
Ahuja, Monica
Kohli, Harbir Singh
Bhansali, Anil
Mohan, Viswanathan
Venkatesan, Radha
Rai, Taranjit Singh
Sud, Kamal
Singal, Pawan K.
机构
[1] Department of Nephrology, Post Graduate Institute of Medical Education and Research, Chandigarh
[2] Department of Endocrinology, Post Graduate Institute of Medical Education and Research, Chandigarh
[3] Department of Experimental Medicine and Biotechnology, Post Graduate Institute of Medical Education and Research, Chandigarh
[4] Madras Diabetes Research Foundation, Dr. Mohan's Diabetes Specialties Centre, Gopalapuram, Chennai
[5] Institute of Cardiovascular Sciences, St Boniface General Hospital Research Centre, University of Manitoba, Winnipeg, MB
关键词
MONOCYTE CHEMOATTRACTANT PROTEIN-1; PROMOTER POLYMORPHISM; RENAL-INSUFFICIENCY; CANDIDATE GENE; CCR5; DISEASE; EPIDEMIOLOGY; PROGRESSION; TGF-BETA-1; JAPANESE;
D O I
10.1371/journal.pone.0005168
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Background: Inflammatory cytokine genes have been proposed as good candidate genes for conferring susceptibility to diabetic nephropathy. In the present study, we examined the combined effect of multiple alleles of pro inflammatory cytokine genes for determining the risk of nephropathy in type 2 diabetic patients. Methodology/Principal Findings: Eight single nucleotide polymorphisms (SNPs) of pro-inflammatory cytokine genes (CCL2, TGFB1, IL8, CCR5, and MMP9) were genotyped in two independently ascertained type 2 diabetic cohorts with (DN) and without nephropathy (DM); consisting of patients from North India (n = 495) and South India (n = 188). Genotyping was carried out using PCR, allele specific oligonucleotide-PCR (ASO-PCR), PCR-RFLP and TaqMan allelic discrimination assays and the gene-gene interaction among genetic variants were determined by multi dimensional reduction (MDR) software. Serum high sensitive CRP (hs-CRP) levels were measured by ELISA. The hs-CRP levels were significantly higher in DN as compared to the DM group (p < 0.05). The CCL2, IL8, CCR5 and MMP9 polymorphisms were found to be associated with the risk of diabetic nephropathy. Frequency of CCL2 II, IL8 -251AA, CCR5 59029AA and MMP9 279Gln/Gln genotypes were significantly higher in DN than in DM group (p < 0.05) and associated with an increased risk of nephropathy in both North and South Indian cohorts. CCR5 DD and IL8 -251AA genotypes were more prevalent in North Indian DN group only. The co-occurrence of risk associated genotypes (II, -2518GG (CCL2), DD (CCR5) and 279Gln/Gln (MMP9) conferred a tenfold increased risk of nephropathy among type 2 diabetics (p < 0.0002). Conclusion: The present study highlights that common variants of inflammatory cytokine genes exert a modest effect on risk of DN and a combination of risk alleles confer a substantial increased risk of nephropathy in type 2 diabetes among Asian Indians.
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页数:10
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