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Association of the GNAS locus with severe malaria.

Authors :
Auburn, Sarah
Diakite, Mahamadou
Fry, Andrew E.
Ghansah, Anita
Campino, Susana
Richardson, Anna
Jallow, Muminatou
Sisay-Joof, Fatou
Pinder, Margaret
Griffiths, Michael J.
Peshu, Norbert
Williams, Thomas N.
Marsh, Kevin
Molyneux, Malcolm E.
Taylor, Terrie E.
Koram, Kwadwo A.
Oduro, Abraham R.
Rogers, William O.
Rockett, Kirk A.
Haldar, Kasturi
Source :
Human Genetics; Dec2008, Vol. 124 Issue 5, p499-506, 8p, 5 Charts, 3 Graphs
Publication Year :
2008

Abstract

Functional studies have demonstrated an interaction between the stimulatory G protein alpha subunit (G-alpha-s) and the malaria parasite at a cellular level. Obstruction of signal transduction via the erythrocyte G-alpha-s subunit reduced invasion by Plasmodium falciparum parasites. We sought to determine whether this signal pathway had an impact at the disease level by testing polymorphisms in the gene encoding G-alpha-s ( GNAS) for association with severe malaria in a large multi-centre study encompassing family and case–control studies from The Gambia, Kenya and Malawi, and a case–control study from Ghana. We gained power to detect association using meta-analysis across the seven studies, with an overall sample size approximating 4,000 cases and 4,000 controls. Out of 12 SNPs investigated in the 19 kb GNAS region, four presented signals of association ( P < 0.05) with severe malaria. The strongest single-locus association demonstrated an odds ratio of 1.13 (1.05–1.21), P = 0.001. Three of the loci presenting significant associations were clustered at the 5-prime end of the GNAS gene. Accordingly, haplotypes constructed from these loci demonstrated significant associations with severe malaria [OR = 0.88 (0.81–0.96), P = 0.005 and OR = 1.12 (1.03–1.20), P = 0.005]. The evidence presented here indicates that the influence of G-alpha-s on erythrocyte invasion efficacy may, indeed, alter individual susceptibility to disease. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03406717
Volume :
124
Issue :
5
Database :
Complementary Index
Journal :
Human Genetics
Publication Type :
Academic Journal
Accession number :
35417653
Full Text :
https://doi.org/10.1007/s00439-008-0575-8