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Title of article :
Influence of 9p21.3 Genetic Variants on Clinical and Angiographic Outcomes in Early-Onset Myocardial Infarction
Author/Authors :
Ardissino، نويسنده , , Diego and Berzuini، نويسنده , , Carlo and Merlini، نويسنده , , Piera Angelica and Mannuccio Mannucci، نويسنده , , Pier and Surti، نويسنده , , Aarti and Burtt، نويسنده , , Noel and Voight، نويسنده , , Benjamin and Tubaro، نويسنده , , Marco and Peyvandi، نويسنده , , Flora and Spreafico، نويسنده , , Marta and Celli، نويسنده , , Patrizia and Lina، نويسنده , , Daniela and Notara، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
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Abstract :
Objectives rpose 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. ound genetic variants are associated with ischemic heart disease, but it is not known whether they influence prognosis after an acute coronary event. s 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. s 6,599 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). sions ly-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.
Keywords :
Outcomes , rs1333040 , early-onset myocardial infarction , 9p21.3 genetic variants
Journal title :
JACC (Journal of the American College of Cardiology)
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