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ALOX5AP variants are associated with in-stent restenosis after percutaneous coronary intervention.

Publication ,  Journal Article
Shah, SH; Hauser, ER; Crosslin, D; Wang, L; Haynes, C; Connelly, J; Nelson, S; Johnson, J; Gadson, S; Nelson, CL; Seo, D; Gregory, S ...
Published in: Atherosclerosis
November 2008

BACKGROUND: Use of drug-eluting stents (DES) has reduced in-stent restenosis after percutaneous coronary intervention (PCI); however, DES are associated with late stent thrombosis. There is no accurate way to predict in-stent restenosis, although risk factors for atherosclerosis overlap those for in-stent restenosis. Therefore, we evaluated atherosclerosis candidate genes for association with in-stent restenosis. METHODS: We identified 46 consecutive cases that had undergone PCI with bare-metal stents who subsequently developed symptomatic in-stent restenosis of the target lesion (>/=75% luminal narrowing) within 6 months. Forty-six age-, race-, vessel-diameter- and sex-matched controls without in-stent restenosis after PCI with bare-metal stent were also identified. Single-nucleotide polymorphisms (SNPs, N=82) from 39 candidate atherosclerosis genes were genotyped. Multivariable logistic regression models were used to test for association. RESULTS: Five SNPs were associated with in-stent restenosis. Three ALOX5AP SNPs were most strongly associated, two with increased risk (OR 3.74, p=0.01; OR 3.46, p=0.02), and the third with decreased risk of in-stent restenosis (OR 0.09, p=0.004). Two ALOX5AP haplotypes were associated with in-stent restenosis (HapB: OR 3.13, p=0.03); and a haplotype similar to HapA: OR 0.14, p=0.0009). CONCLUSIONS: ALOX5AP, a gene within the inflammatory leukotriene pathway linked to and associated with coronary atherosclerosis, is also associated with in-stent restenosis. Genotyping these variants may help identify those at risk for in-stent restenosis who would benefit most from use of DES.

Duke Scholars

Published In

Atherosclerosis

DOI

EISSN

1879-1484

Publication Date

November 2008

Volume

201

Issue

1

Start / End Page

148 / 154

Location

Ireland

Related Subject Headings

  • Risk Factors
  • Polymorphism, Single Nucleotide
  • Middle Aged
  • Membrane Proteins
  • Male
  • Humans
  • Haplotypes
  • Graft Occlusion, Vascular
  • Genetic Association Studies
  • Female
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Shah, S. H., Hauser, E. R., Crosslin, D., Wang, L., Haynes, C., Connelly, J., … Newby, L. K. (2008). ALOX5AP variants are associated with in-stent restenosis after percutaneous coronary intervention. Atherosclerosis, 201(1), 148–154. https://doi.org/10.1016/j.atherosclerosis.2008.01.011
Shah, Svati H., Elizabeth R. Hauser, David Crosslin, Liyong Wang, Carol Haynes, Jessica Connelly, Sarah Nelson, et al. “ALOX5AP variants are associated with in-stent restenosis after percutaneous coronary intervention.Atherosclerosis 201, no. 1 (November 2008): 148–54. https://doi.org/10.1016/j.atherosclerosis.2008.01.011.
Shah SH, Hauser ER, Crosslin D, Wang L, Haynes C, Connelly J, et al. ALOX5AP variants are associated with in-stent restenosis after percutaneous coronary intervention. Atherosclerosis. 2008 Nov;201(1):148–54.
Shah, Svati H., et al. “ALOX5AP variants are associated with in-stent restenosis after percutaneous coronary intervention.Atherosclerosis, vol. 201, no. 1, Nov. 2008, pp. 148–54. Pubmed, doi:10.1016/j.atherosclerosis.2008.01.011.
Shah SH, Hauser ER, Crosslin D, Wang L, Haynes C, Connelly J, Nelson S, Johnson J, Gadson S, Nelson CL, Seo D, Gregory S, Kraus WE, Granger CB, Goldschmidt-Clermont P, Newby LK. ALOX5AP variants are associated with in-stent restenosis after percutaneous coronary intervention. Atherosclerosis. 2008 Nov;201(1):148–154.
Journal cover image

Published In

Atherosclerosis

DOI

EISSN

1879-1484

Publication Date

November 2008

Volume

201

Issue

1

Start / End Page

148 / 154

Location

Ireland

Related Subject Headings

  • Risk Factors
  • Polymorphism, Single Nucleotide
  • Middle Aged
  • Membrane Proteins
  • Male
  • Humans
  • Haplotypes
  • Graft Occlusion, Vascular
  • Genetic Association Studies
  • Female