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

Grisoni, Marie-Lise (author)
Proust, Carole (author)
Alanne, Mervi (author)
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DeSuremain, Maylis (author)
Salomaa, Veikko (author)
Kuulasmaa, Kari (author)
Cambien, François (author)
Nicaud, Viviane (author)
Stegmayr, Birgitta (author)
Umeå universitet,Medicin
Virtamo, Jarmo (author)
Shields, Denis (author)
Kee, Frank (author)
Tiret, Laurence (author)
Evans, Alun (author)
Tregouet, David-Alexandre (author)
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 (creator_code:org_t)
2008-07-16
2008
English.
In: European Journal of Human Genetics. - : Springer Science and Business Media LLC. - 1018-4813 .- 1476-5438. ; 16:12, s. 1512-20
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • 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.

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