کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2930319 | 1576263 | 2011 | 4 صفحه PDF | دانلود رایگان |

Background: Premature cardiovascular disease (CVD) is treated in the same way as CVD of advanced age. However, in patients with premature CVD and a family history of CVD, different —possibly genetic— mechanisms may underlie this disease, which current medical treatment is not targeted to. This suggests that subjects with a genetic predisposition to CVD are more likely to have recurrent cardiovascular events.Methods: We retrospectively investigated 291 patients with premature CVD and assessed the amount of recurrent events according to family history in a follow-up period of 31 years. Premature CVD was defined as an event < 51 years for men or < 56 for women. We used a Cox proportional hazards model to estimate the relationship between a positive family history and recurrence of cardiovascular events.Results: Patients with recurrent events had more often a positive family history (60.0% vs. 47.1%; p < 0.05), were more often smokers (85.2% vs. 70.7%; p < 0.05), had more often hypertension (36.3% vs. 23.6%; p < 0.05) and had a longer follow-up period (10.0 years vs. 5.4 years; p < 0.001) than patients without recurrent events. After adjusting for these differences and modelling time to events, a positive family history was independently associated with recurrent events (Hazard ratio 1.31 (95% confidence intervals (CI) 1.01-1.72; p < 0.05)).Conclusions: Patients with a genetic predisposition for CVD are at risk for recurrent events, after adjusting for risk factors and other confounders. This might imply that in subjects with a genetic predisposition for CVD different pathophysiological mechanisms are active, leading to recurrent events.
Journal: International Journal of Cardiology - Volume 153, Issue 1, 17 November 2011, Pages 64–67