Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions.

Journal Article (Journal Article)

BACKGROUND: Common diseases such as coronary heart disease (CHD) are complex in etiology. The interaction of genetic susceptibility with lifestyle factors may play a prominent role. However, gene-lifestyle interactions for CHD have been difficult to identify. Here, we investigate interaction of smoking behavior, a potent lifestyle factor, with genotypes that have been shown to associate with CHD risk. METHODS: We analyzed data on 60 919 CHD cases and 80 243 controls from 29 studies for gene-smoking interactions for genetic variants at 45 loci previously reported to be associated with CHD risk. We also studied 5 loci associated with smoking behavior. Study-specific gene-smoking interaction effects were calculated and pooled using fixed-effects meta-analyses. Interaction analyses were declared to be significant at a P value of <1.0×10-3 (Bonferroni correction for 50 tests). RESULTS: We identified novel gene-smoking interaction for a variant upstream of the ADAMTS7 gene. Every T allele of rs7178051 was associated with lower CHD risk by 12% in never-smokers (P=1.3×10-16) in comparison with 5% in ever-smokers (P=2.5×10-4), translating to a 60% loss of CHD protection conferred by this allelic variation in people who smoked tobacco (interaction P value=8.7×10-5). The protective T allele at rs7178051 was also associated with reduced ADAMTS7 expression in human aortic endothelial cells and lymphoblastoid cell lines. Exposure of human coronary artery smooth muscle cells to cigarette smoke extract led to induction of ADAMTS7. CONCLUSIONS: Allelic variation at rs7178051 that associates with reduced ADAMTS7 expression confers stronger CHD protection in never-smokers than in ever-smokers. Increased vascular ADAMTS7 expression may contribute to the loss of CHD protection in smokers.

Full Text

Duke Authors

Cited Authors

  • Saleheen, D; Zhao, W; Young, R; Nelson, CP; Ho, W; Ferguson, JF; Rasheed, A; Ou, K; Nurnberg, ST; Bauer, RC; Goel, A; Do, R; Stewart, AFR; Hartiala, J; Zhang, W; Thorleifsson, G; Strawbridge, RJ; Sinisalo, J; Kanoni, S; Sedaghat, S; Marouli, E; Kristiansson, K; Hua Zhao, J; Scott, R; Gauguier, D; Shah, SH; Smith, AV; van Zuydam, N; Cox, AJ; Willenborg, C; Kessler, T; Zeng, L; Province, MA; Ganna, A; Lind, L; Pedersen, NL; White, CC; Joensuu, A; Edi Kleber, M; Hall, AS; März, W; Salomaa, V; O'Donnell, C; Ingelsson, E; Feitosa, MF; Erdmann, J; Bowden, DW; Palmer, CNA; Gudnason, V; Faire, UD; Zalloua, P; Wareham, N; Thompson, JR; Kuulasmaa, K; Dedoussis, G; Perola, M; Dehghan, A; Chambers, JC; Kooner, J; Allayee, H; Deloukas, P; McPherson, R; Stefansson, K; Schunkert, H; Kathiresan, S; Farrall, M; Marcel Frossard, P; Rader, DJ; Samani, NJ; Reilly, MP

Published Date

  • June 13, 2017

Published In

Volume / Issue

  • 135 / 24

Start / End Page

  • 2336 - 2353

PubMed ID

  • 28461624

Pubmed Central ID

  • PMC5612779

Electronic International Standard Serial Number (EISSN)

  • 1524-4539

Digital Object Identifier (DOI)

  • 10.1161/CIRCULATIONAHA.116.022069


  • eng

Conference Location

  • United States