{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T14:46:13Z","timestamp":1791902773307,"version":"4.3.4"},"reference-count":21,"publisher":"S. Karger AG","issue":"3","license":[{"start":{"date-parts":[[2010,1,1]],"date-time":"2010-01-01T00:00:00Z","timestamp":1262304000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.karger.com\/Services\/SiteLicenses"},{"start":{"date-parts":[[2010,1,1]],"date-time":"2010-01-01T00:00:00Z","timestamp":1262304000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.karger.com\/Services\/SiteLicenses"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Cardiology"],"published-print":{"date-parts":[[2010]]},"abstract":"<jats:p>&lt;i&gt;Objectives:&lt;\/i&gt; The \u2013765G&gt;C variation (rs20417 SNP) in the promoter of cyclooxygenase-2 (COX-2) gene has been demonstrated to lower COX-2 enzyme activity in the vasculature, thus affecting atherosclerotic plaque growth and stability. Therefore, this genetic variant may be a candidate influencing the residual risk. &lt;i&gt;Methods:&lt;\/i&gt; In 285 coronary patients the incidence of major adverse cardiovascular events (MACEs), defined as a composite of cardiovascular deaths, non-fatal myocardial infarction and stroke, unstable angina and revascularization procedures, was monitored for a median of 7.8 years. The genotypes were obtained in 231 patients (81%) by PCR amplification and FAU I digestion. &lt;i&gt;Results:&lt;\/i&gt; 89 MACEs (38.5%) were recorded during the follow-up in genotyped patients. Their incidence was not different in patients with GC or CC when compared with those with GG genotype (46.2 vs. 35.5% respectively; p = 0.14). Kaplan-Meyer analysis did not demonstrate any influence of &lt;i&gt;COX-2&lt;\/i&gt; genotypes on the event-free survival time (log-rank p = 0.55). After controlling for confounders, the \u2013765G&gt;C carrier status was not associated with significant variation in the risk of MACE or its individual components. &lt;i&gt;Conclusions:&lt;\/i&gt; These results suggest that the functional G\u2013765C variant in the &lt;i&gt;COX-2&lt;\/i&gt; gene is not a significant predictor of the recurrence of ischemic events in coronary patients.<\/jats:p>","DOI":"10.1159\/000298880","type":"journal-article","created":{"date-parts":[[2010,3,19]],"date-time":"2010-03-19T11:27:05Z","timestamp":1268998025000},"page":"236-242","source":"Crossref","is-referenced-by-count":6,"title":["Functional rs20417 SNP (\u2013765G&gt;C) of Cyclooxygenase-2 Gene Does Not Predict the Risk of Recurrence of Ischemic Events in Coronary Patients: Results of a 7-Year Prospective 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