This case-control study included 127 consecutive patients aged ≤45 years with a diagnosis of STEMI who were admitted to a cardiovascular intensive care unit and 127 controls recruited between January 2006 and March 2007. Participants were genotyped for the 4G/5G polymorphism using the polymerase chain reaction and restriction fragment length polymorphism analysis, and their plasma PAI-1 concentrations were measured. Informed consent was obtained from all participants.
There was a significant difference in genotype distribution between the 2 groups (Pc;.002). The 4G allele occurred more frequently in the patient group (P=.032). In addition, there were significant independent associations between STEMI and the 4G allele (ie, 4G/4G plus 4G/5G; odds ratio [OR] =2.29; 95 % confidence interval [CI], 1.12-4.68; P=.022), smoking (OR=23.23; 95 % CI, 8.92-60.47; Pc;.001), a family history of cardiovascular disease (OR=4.66; 95 % CI, 2.06-10.52; P=.001) and hypertension (OR=5.42; 95 % CI, 1.67-17.56; P=.005). The plasma PAI-1 concentration was higher in individuals who were homozygous for the 4G allele (Pc;.001).
The study findings indicate that the 4G allele is an independent risk factor for acute myocardial infarction in young patients, as are smoking, hypertension, and a family history of inherited cardiovascular disease.