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Association of chemokine gene variants with end stage renal disease in North Indian population.
- Source :
-
Transplant immunology [Transpl Immunol] 2013 Jun; Vol. 28 (4), pp. 189-92. Date of Electronic Publication: 2013 Apr 21. - Publication Year :
- 2013
-
Abstract
- Background & Aim: The progression rate of chronic kidney disease (CKD) to its end-stage renal disease (ESRD), and the development and severity of various complications, are indirectly influenced by genetic and epigenetic factors. Chemokines are small inducible pro-inflammatory cytokines, which are implicated in many biological processes like migration of leukocytes, angiogenesis, tumor growth and metastasis. We tested association of four single nucleotide polymorphisms (SNPs) viz. CCL2I/D, CCL2A2518G, CXCL12G801A and CXCR2(+1208)C/T among individuals with ESRD (end stage renal disease) and normal healthy controls from North Indian population.<br />Materials and Method: CCL2I/D, CCL2A2518G, CXCL12G801A and CXCR2(+1208)C/T were genotyped in blood samples of hospital-based case-control study comprising of 200 ESRD cases and 200 healthy controls using Restriction Fragment Length Polymorphism (RFLP) and ARMS (Amplification Refractory Mutation Specific) PCR methodology.<br />Results: A significant association was found in CXCL12G801A with ESRD risk. In case of CXCL12G801A polymorphism heterozygous (GA) genotype showed significant risk (p=0.039; OR=1.55) whereas A allele carrier (GA+AA) also exhibited risk with ESRD (p=0.045, OR=1.59). In CXCR2(+1208)C/T polymorphism, the heterozygous genotype (CT) showed significant risk for ESRD (p=0.028; OR=1.65) and combination of CT+TT demonstrated significant high risk for ESRD (p=0.036; OR=1.52). In case of CCL2I/D, the variant genotype (D/D) showed reduced risk for ESRD patients. Upon analyzing the gene-gene interaction between CXCR2 and CXCL12, the combination (CT-GA) showed 2.65 fold risk for ESRD (p=0.018).<br />Conclusion: Our results indicated that polymorphism in CXCL12G801A and CXCR2(+1208)C/T showed high risk for ESRD in North Indian population. However, CCL2I/D showed reduced risk and CCL2A2518G exhibited no association. Study with large sample size and diverse ethnicity is required to validate these observations.<br /> (Copyright © 2013 Elsevier B.V. All rights reserved.)
- Subjects :
- Adult
Case-Control Studies
Female
Genetic Association Studies
Genetic Predisposition to Disease
Genotype
Humans
India
Male
Nucleic Acid Amplification Techniques
Polymorphism, Restriction Fragment Length
Polymorphism, Single Nucleotide
Chemokine CCL2 genetics
Chemokine CCL21 genetics
Chemokine CXCL12 genetics
Kidney Failure, Chronic genetics
Receptors, Interleukin-8B genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1878-5492
- Volume :
- 28
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Transplant immunology
- Publication Type :
- Academic Journal
- Accession number :
- 23615182
- Full Text :
- https://doi.org/10.1016/j.trim.2013.04.004