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Variations in host genes encoding adhesion molecules and susceptibility to falciparum malaria in India
BACKGROUND: Host adhesion molecules play a significant role in the pathogenesis of Plasmodium falciparum malaria and changes in their structure or levels in individuals can influence the outcome of infection. The aim of this study was to investigate the association of SNPs of three adhesion molecule...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2612678/ https://www.ncbi.nlm.nih.gov/pubmed/19055786 http://dx.doi.org/10.1186/1475-2875-7-250 |
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author | Sinha, Swapnil Qidwai, Tabish Kanchan, Kanika Anand, Prerna Jha, Ganga N Pati, Sudhanshu S Mohanty, Sanjib Mishra, Saroj K Tyagi, Prajesh K Sharma, Surya K Venkatesh, Vimala Habib, Saman |
author_facet | Sinha, Swapnil Qidwai, Tabish Kanchan, Kanika Anand, Prerna Jha, Ganga N Pati, Sudhanshu S Mohanty, Sanjib Mishra, Saroj K Tyagi, Prajesh K Sharma, Surya K Venkatesh, Vimala Habib, Saman |
author_sort | Sinha, Swapnil |
collection | PubMed |
description | BACKGROUND: Host adhesion molecules play a significant role in the pathogenesis of Plasmodium falciparum malaria and changes in their structure or levels in individuals can influence the outcome of infection. The aim of this study was to investigate the association of SNPs of three adhesion molecule genes, ICAM1, PECAM1 and CD36, with severity of falciparum malaria in a malaria-endemic and a non-endemic region of India. METHODS: The frequency distribution of seven selected SNPs of ICAM1, PECAM1 and CD36 was determined in 552 individuals drawn from 24 populations across India. SNP-disease association was analysed in a case-control study format. Genotyping of the population panel was performed by Sequenom mass spectroscopy and patient/control samples were genotyped by SNaPshot method. Haplotypes and linkage disequilibrium (LD) plots were generated using PHASE and Haploview, respectively. Odds-ratio (OR) for risk assessment was estimated using EpiInfo™ version 3.4. RESULTS: Association of the ICAM1 rs5498 (exon 6) G allele and the CD36 exon 1a A allele with increased risk of severe malaria was observed (severe versus control, OR = 1.91 and 2.66, P = 0.02 and 0.0012, respectively). The CD36 rs1334512 (-53) T allele as well as the TT genotype associated with protection from severe disease (severe versus control, TT versus GG, OR = 0.37, P = 0.004). Interestingly, a SNP of the PECAM1 gene (rs668, exon 3, C/G) with low minor allele frequency in populations of the endemic region compared to the non-endemic region exhibited differential association with disease in these regions; the G allele was a risk factor for malaria in the endemic region, but exhibited significant association with protection from disease in the non-endemic region. CONCLUSION: The data highlights the significance of variations in the ICAM1, PECAM1 and CD36 genes in the manifestation of falciparum malaria in India. The PECAM1 exon 3 SNP exhibits altered association with disease in the endemic and non-endemic region. |
format | Text |
id | pubmed-2612678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26126782008-12-31 Variations in host genes encoding adhesion molecules and susceptibility to falciparum malaria in India Sinha, Swapnil Qidwai, Tabish Kanchan, Kanika Anand, Prerna Jha, Ganga N Pati, Sudhanshu S Mohanty, Sanjib Mishra, Saroj K Tyagi, Prajesh K Sharma, Surya K Venkatesh, Vimala Habib, Saman Malar J Research BACKGROUND: Host adhesion molecules play a significant role in the pathogenesis of Plasmodium falciparum malaria and changes in their structure or levels in individuals can influence the outcome of infection. The aim of this study was to investigate the association of SNPs of three adhesion molecule genes, ICAM1, PECAM1 and CD36, with severity of falciparum malaria in a malaria-endemic and a non-endemic region of India. METHODS: The frequency distribution of seven selected SNPs of ICAM1, PECAM1 and CD36 was determined in 552 individuals drawn from 24 populations across India. SNP-disease association was analysed in a case-control study format. Genotyping of the population panel was performed by Sequenom mass spectroscopy and patient/control samples were genotyped by SNaPshot method. Haplotypes and linkage disequilibrium (LD) plots were generated using PHASE and Haploview, respectively. Odds-ratio (OR) for risk assessment was estimated using EpiInfo™ version 3.4. RESULTS: Association of the ICAM1 rs5498 (exon 6) G allele and the CD36 exon 1a A allele with increased risk of severe malaria was observed (severe versus control, OR = 1.91 and 2.66, P = 0.02 and 0.0012, respectively). The CD36 rs1334512 (-53) T allele as well as the TT genotype associated with protection from severe disease (severe versus control, TT versus GG, OR = 0.37, P = 0.004). Interestingly, a SNP of the PECAM1 gene (rs668, exon 3, C/G) with low minor allele frequency in populations of the endemic region compared to the non-endemic region exhibited differential association with disease in these regions; the G allele was a risk factor for malaria in the endemic region, but exhibited significant association with protection from disease in the non-endemic region. CONCLUSION: The data highlights the significance of variations in the ICAM1, PECAM1 and CD36 genes in the manifestation of falciparum malaria in India. The PECAM1 exon 3 SNP exhibits altered association with disease in the endemic and non-endemic region. BioMed Central 2008-12-04 /pmc/articles/PMC2612678/ /pubmed/19055786 http://dx.doi.org/10.1186/1475-2875-7-250 Text en Copyright © 2008 Sinha et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Sinha, Swapnil Qidwai, Tabish Kanchan, Kanika Anand, Prerna Jha, Ganga N Pati, Sudhanshu S Mohanty, Sanjib Mishra, Saroj K Tyagi, Prajesh K Sharma, Surya K Venkatesh, Vimala Habib, Saman Variations in host genes encoding adhesion molecules and susceptibility to falciparum malaria in India |
title | Variations in host genes encoding adhesion molecules and susceptibility to falciparum malaria in India |
title_full | Variations in host genes encoding adhesion molecules and susceptibility to falciparum malaria in India |
title_fullStr | Variations in host genes encoding adhesion molecules and susceptibility to falciparum malaria in India |
title_full_unstemmed | Variations in host genes encoding adhesion molecules and susceptibility to falciparum malaria in India |
title_short | Variations in host genes encoding adhesion molecules and susceptibility to falciparum malaria in India |
title_sort | variations in host genes encoding adhesion molecules and susceptibility to falciparum malaria in india |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2612678/ https://www.ncbi.nlm.nih.gov/pubmed/19055786 http://dx.doi.org/10.1186/1475-2875-7-250 |
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