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Haplotypic analysis of tag SNPs of the interleukin-18 gene in relation to cardiovascular disease events: the MORGAM Project

Authors :
Marie-Lise, Grisoni
Carole, Proust
Mervi, Alanne
Maylis, DeSuremain
Veikko, Salomaa
Kari, Kuulasmaa
François, Cambien
Viviane, Nicaud
Birgitta, Stegmayr
Jarmo, Virtamo
Denis, Shields
Frank, Kee
Laurence, Tiret
Alun, Evans
David-Alexandre, Tregouet
K, Asplund
Source :
European Journal of Human Genetics, European Journal of Human Genetics; Vol 16, Grisoni, M L, Proust, C, Alanne, M, DeSuremain, M, Salomaa, V, Kuulasmaa, K, Cambien, F, Nicaud, V, Stegmayr, B, Virtamo, J, Shields, D, Kee, F, Tiret, L, Evans, A & Tregouet, D A 2008, ' Haplotypic analysis of tag SNPs of the interleukin-18 gene in relation to cardiovascular disease events: the MORGAM Project ' European Journal of Human Genetics, vol 16, no. 12, pp. 1512-1520 . DOI: 10.1038/ejhg.2008.127
Publication Year :
2008

Abstract

Interleukin-18 (IL-18) is a key inflammatory molecule suspected of being involved in the etiology of cardiovascular diseases (CVD). Five single nucleotide polymorphisms (SNPs) capturing the common genetic variation of the IL-18 gene (tag SNPs) were genotyped in five European prospective CVD cohorts including 1933 cases and 1938 non-cases as part of the MORGAM Project. Not a single SNP was found associated with CVD. However, a significant (P=0.002) gene-smoking interaction was observed. In smokers, the -105T allele was more frequent in cases than in non-cases (0.29 vs 0.25) and associated with an increased risk of disease (odds ratio (OR)=1.25 (1.07-1.45), P=0.005), whereas the inverse relationship tended to be observed in non-smokers (OR=0.90 (0.78-1.02), P=0.131). The gene-smoking interaction was broadly homogenous across the cohorts and was also observed through haplotype analyses. In conclusion, using the concerted effort of several European prospective CVD cohorts, we are able to show that one IL-18 tag SNP interacts with smoking to modulate the risk of developing CVD.

Details

Language :
English
ISSN :
14765438 and 10184813
Volume :
16
Issue :
12
Database :
OpenAIRE
Journal :
European Journal of Human Genetics
Accession number :
edsair.doi.dedup.....44308bafe675ccd45b50677b73ebd647
Full Text :
https://doi.org/10.1038/ejhg.2008.127