Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarction
- PMID: 21757122
- DOI: 10.1016/j.jacc.2010.11.075
Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarction
Abstract
Objectives: The purpose of this study was to test whether the 9p21.3 variant rs1333040 influences the occurrence of new cardiovascular events and coronary atherosclerosis progression after early-onset myocardial infarction.
Background: 9p21.3 genetic variants are associated with ischemic heart disease, but it is not known whether they influence prognosis after an acute coronary event.
Methods: Within the Italian Genetic Study of Early-onset Myocardial Infarction, we genotyped rs1333040 in 1,508 patients hospitalized for a first myocardial infarction before the age of 45 years who underwent coronary angiography without index event coronary revascularization. They were followed up for major cardiovascular events and angiographic coronary atherosclerosis progression.
Results: Over 16,599 person-years, there were 683 cardiovascular events and 492 primary endpoints: 77 cardiovascular deaths, 223 reoccurrences of myocardial infarction, and 383 coronary artery revascularizations. The rs1333040 genotype had a significant influence (p = 0.01) on the primary endpoint, with an adjusted hazard ratio of 1.19 (95% confidence interval [CI]: 1.08 to 1.37) for heterozygous carriers and 1.41 (95% CI: 1.06 to 1.87) for homozygous carriers. Analysis of the individual components of the primary endpoints provided no significant evidence that the rs1333040 genotype influenced the hazard of cardiovascular death (p = 0.24) or the reoccurrence of myocardial infarction (p = 0.57), but did provide significant evidence that it influenced on the hazard of coronary revascularization, with adjusted heterozygous and homozygous ratios of 1.38 (95% CI: 1.17 to 1.63) and 1.90 (95% CI: 1.36 to 2.65) (p = 0.00015), respectively. It also significantly influenced the angiographic endpoint of coronary atherosclerosis progression (p = 0.002).
Conclusions: In early-onset myocardial infarction, the 9p21.3 variant rs1333040 affects the progression of coronary atherosclerosis and the probability of coronary artery revascularization during long-term follow-up.
Copyright © 2011 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
Comment in
-
The 9p21.3 genetic region and coronary heart disease where do we go from here?J Am Coll Cardiol. 2011 Jul 19;58(4):435-7. doi: 10.1016/j.jacc.2011.01.053. J Am Coll Cardiol. 2011. PMID: 21757123 No abstract available.
Similar articles
-
Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease.Circ Cardiovasc Genet. 2008 Dec;1(2):85-92. doi: 10.1161/CIRCGENETICS.108.793158. Circ Cardiovasc Genet. 2008. PMID: 19956784 Free PMC article.
-
The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease.Eur Heart J. 2010 Dec;31(24):3017-23. doi: 10.1093/eurheartj/ehq272. Epub 2010 Aug 20. Eur Heart J. 2010. PMID: 20729229 Free PMC article.
-
Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease.Circ J. 2012;76(4):950-6. doi: 10.1253/circj.cj-11-1166. Epub 2012 Feb 9. Circ J. 2012. PMID: 22322877 Free PMC article.
-
The association of 9p21-3 locus with coronary atherosclerosis: a systematic review and meta-analysis.BMC Med Genet. 2014 Jun 6;15:66. doi: 10.1186/1471-2350-15-66. BMC Med Genet. 2014. PMID: 24906238 Free PMC article. Review.
-
Matrix metalloproteinases in coronary artery disease and myocardial infarction.Basic Res Cardiol. 2023 May 9;118(1):18. doi: 10.1007/s00395-023-00987-2. Basic Res Cardiol. 2023. PMID: 37160529 Free PMC article. Review.
Cited by
-
Genetic variants at chromosome 9p21 and risk of first versus subsequent coronary heart disease events: a systematic review and meta-analysis.J Am Coll Cardiol. 2014 Jun 3;63(21):2234-45. doi: 10.1016/j.jacc.2014.01.065. Epub 2014 Mar 7. J Am Coll Cardiol. 2014. PMID: 24607648 Free PMC article. Review.
-
The 9p21 locus is associated with coronary artery disease and cardiovascular events in the presence (but not in the absence) of coronary calcification.PLoS One. 2014 Apr 14;9(4):e94823. doi: 10.1371/journal.pone.0094823. eCollection 2014. PLoS One. 2014. PMID: 24732910 Free PMC article.
-
The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey).Int J Endocrinol. 2015;2015:164652. doi: 10.1155/2015/164652. Epub 2015 May 18. Int J Endocrinol. 2015. PMID: 26089876 Free PMC article.
-
Association of Low Expression of NUMB in Peripheral Blood with Acute Myocardial Infarction.Cardiol Res Pract. 2022 Apr 26;2022:7981637. doi: 10.1155/2022/7981637. eCollection 2022. Cardiol Res Pract. 2022. PMID: 35529060 Free PMC article.
-
Microbial modulation of cardiovascular disease.Nat Rev Microbiol. 2018 Mar;16(3):171-181. doi: 10.1038/nrmicro.2017.149. Epub 2018 Jan 8. Nat Rev Microbiol. 2018. PMID: 29307889 Free PMC article. Review.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical