Patients with premature cardiovascular disease and a positive family history for cardiovascular disease are prone to recurrent events

被引:15
|
作者
Mulders, Ties A. [2 ,3 ,4 ]
Meyer, Zainna [2 ]
van der Donk, Christel [2 ]
Kroon, Abraham A. [2 ,4 ]
Ferreira, Isabel [2 ,5 ]
Stehouwer, Coen D. A. [2 ,4 ]
Pinto-Sietsma, Sara-Joan [1 ,3 ]
机构
[1] Acad Med Ctr, Dept Clin Epidemiol Biostat & Bioinformat, NL-1100 DD Amsterdam, Netherlands
[2] Univ Med Ctr Maastricht, Dept Internal Med, Div Gen Internal Med, Subdiv Vasc Med, Maastricht, Netherlands
[3] Acad Med Ctr, Dept Internal Med, Div Vasc Med, NL-1100 DD Amsterdam, Netherlands
[4] Univ Med Ctr Maastricht, Cardiovasc Res Inst Maastricht CARIM, Maastricht, Netherlands
[5] Univ Med Ctr Maastricht, Dept Clin Epidemiol & Med Technol Assessment KEMT, Maastricht, Netherlands
关键词
Premature cardiovascular disease; Positive family history; CORONARY-HEART-DISEASE; FACTOR-V-LEIDEN; MYOCARDIAL-INFARCTION; RISK; SUSCEPTIBILITY; SMOKING; PROTEIN;
D O I
10.1016/j.ijcard.2010.08.040
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:64 / 67
页数:4
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