CCL2 single nucleotide polymorphism of rs1024611 implicates prominence of inflammatory cascade by univariate modeling in Indian AMD.

The role of chemotactic protein CCL2/MCP-1 has been widely explored in age related macular degeneration (AMD) patients as well as animal models through our previous studies.Aim of the study was to examine the association of another variance of CCL2, rs1024611 in pathophysiology of AMD.This particula...

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Main Authors: Neel Kamal Sharma, Kaushal Sharma, Ramandeep Singh, Suresh Kumar Sharma, Akshay Anand
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5903598?pdf=render
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spelling doaj-4feef80e6db4471c837925c545c567692020-11-25T01:46:31ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01134e019342310.1371/journal.pone.0193423CCL2 single nucleotide polymorphism of rs1024611 implicates prominence of inflammatory cascade by univariate modeling in Indian AMD.Neel Kamal SharmaKaushal SharmaRamandeep SinghSuresh Kumar SharmaAkshay AnandThe role of chemotactic protein CCL2/MCP-1 has been widely explored in age related macular degeneration (AMD) patients as well as animal models through our previous studies.Aim of the study was to examine the association of another variance of CCL2, rs1024611 in pathophysiology of AMD.This particular SNP has been found to be involved in inflammatory processes in various diseases. Total 171 subjects were recruited in the study with all demographic details by administering a standard questionnaire. SNP analysis was performed with TaqMan assay. Linear univariate and ANCOVA modeling was performed to show the interaction of rs1024611 with another SNP variant of CCL-2/CCR-2 (rs4586 and rs1799865) and impact of individual genotypes on CCL-2 expression in the context of AMD pathology.Results showed that both heterozygous (AG, p = 0.01) and homozygous (GG, p = 0.0001) genotypes are associated with AMD pathology. Allele frequency analysis showed that 'G' allele is frequent in AMD patients as compared to controls (p = 0.0001). Moreover, AMD patients who smoke were found to be associated with 'AG' genotype (p = 0.0145). Although, we did not find any significant interaction between the SNP variants by linear univariate analysis but results show the effect of 'CT' genotype on 'TT' genotype in rs4586 by considering rs1024611 as covariate.Based on these results it is imperative that CCL2 mediated pathology may be associated with AMD.http://europepmc.org/articles/PMC5903598?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Neel Kamal Sharma
Kaushal Sharma
Ramandeep Singh
Suresh Kumar Sharma
Akshay Anand
spellingShingle Neel Kamal Sharma
Kaushal Sharma
Ramandeep Singh
Suresh Kumar Sharma
Akshay Anand
CCL2 single nucleotide polymorphism of rs1024611 implicates prominence of inflammatory cascade by univariate modeling in Indian AMD.
PLoS ONE
author_facet Neel Kamal Sharma
Kaushal Sharma
Ramandeep Singh
Suresh Kumar Sharma
Akshay Anand
author_sort Neel Kamal Sharma
title CCL2 single nucleotide polymorphism of rs1024611 implicates prominence of inflammatory cascade by univariate modeling in Indian AMD.
title_short CCL2 single nucleotide polymorphism of rs1024611 implicates prominence of inflammatory cascade by univariate modeling in Indian AMD.
title_full CCL2 single nucleotide polymorphism of rs1024611 implicates prominence of inflammatory cascade by univariate modeling in Indian AMD.
title_fullStr CCL2 single nucleotide polymorphism of rs1024611 implicates prominence of inflammatory cascade by univariate modeling in Indian AMD.
title_full_unstemmed CCL2 single nucleotide polymorphism of rs1024611 implicates prominence of inflammatory cascade by univariate modeling in Indian AMD.
title_sort ccl2 single nucleotide polymorphism of rs1024611 implicates prominence of inflammatory cascade by univariate modeling in indian amd.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description The role of chemotactic protein CCL2/MCP-1 has been widely explored in age related macular degeneration (AMD) patients as well as animal models through our previous studies.Aim of the study was to examine the association of another variance of CCL2, rs1024611 in pathophysiology of AMD.This particular SNP has been found to be involved in inflammatory processes in various diseases. Total 171 subjects were recruited in the study with all demographic details by administering a standard questionnaire. SNP analysis was performed with TaqMan assay. Linear univariate and ANCOVA modeling was performed to show the interaction of rs1024611 with another SNP variant of CCL-2/CCR-2 (rs4586 and rs1799865) and impact of individual genotypes on CCL-2 expression in the context of AMD pathology.Results showed that both heterozygous (AG, p = 0.01) and homozygous (GG, p = 0.0001) genotypes are associated with AMD pathology. Allele frequency analysis showed that 'G' allele is frequent in AMD patients as compared to controls (p = 0.0001). Moreover, AMD patients who smoke were found to be associated with 'AG' genotype (p = 0.0145). Although, we did not find any significant interaction between the SNP variants by linear univariate analysis but results show the effect of 'CT' genotype on 'TT' genotype in rs4586 by considering rs1024611 as covariate.Based on these results it is imperative that CCL2 mediated pathology may be associated with AMD.
url http://europepmc.org/articles/PMC5903598?pdf=render
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