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The epidemiological concept of residual risk

机译:残留风险的流行病学概念

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Residual cardiovascular risk can be defined as the residual risk of incident vascular events or progression of established vascular damage persisting in patients treated with current evidence-based recommended care including the risk that established from risk factors, such as dyslipidemia, high blood pressure, and the risk related to emerging or newer risk factors. The concept clearly derives from intervention trials, mainly the statin trials, and there is a lot of debate about the residual risk conferred by other lipid components, in particular low levels of HDL cholesterol and high levels of triglycerides. A meta-analysis of 53 fibrates (16,802 subjects) and 30 niacin trials (4,749 subjects) revealed an average HDL-C increase of 10% with fibrates and 16% with niacin, a triglyceride decrease of 36% with fibrates and 20% with niacin, and a LDL-C decrease of 8% with fibrates and 14% with niacin. These lipid changes resulted in similar overall reductions in major coronary events evidenced by a 25% decrease with fibrates and 27% with niacin. However, recent analyses of the primary and secondary prevention trials like JUPITER, Treating to New Targets (TNT) and PROVE-IT TIMI 22 force to reconsider the issue. In these three trials, HDL-C was useful in the initial risk assessment but when LDL-C was aggressively lowered the residual risk predictive value of HDL-C was markedly attenuated. Also epidemiological studies evaluate the residual risk in treated hypertensives and dyslipidemic subjects within a general population. The PRIME study in Northern Ireland and France and the Progetto CUORE study in Italy, both with a 10-year follow-up were able to test the hypothesis of the residual cardiovascular risk in treated hypertensives, because the proportion of treated dyslipidemic subjects was too low at baseline. In both studies treatment with antihypertensive agents was associated with a sizeable residual cardiovascular risk with the hazard ratio of 1.5–1.7, suggesting that more efficient risk reduction strategies in hypertension should be developed as a priority. In conclusion residual cardiovascular risk should be better studied in cardiovascular epidemiology, refining the methods to evaluate it, to consider measures of exposure to the modifiable risk factors and indicators of treatment (both at pharmacological and lifestyle level) over the time. Repeated measures and cohortal follow-up are needed and also new statistical methods are necessary to evaluate the residual risk to understand how to reduce it.
机译:残余心血管风险可定义为接受当前循证推荐治疗的患者中发生的血管事件或已确立的血管损害进展持续的残余风险,包括由血脂异常,高血压和高血脂等危险因素确定的风险。与新兴或较新的风险因素相关的风险。该概念显然源自干预试验,主要是他汀类药物试验,关于其他脂质成分(尤其是低水平的HDL胆固醇和高水平的甘油三酸酯)赋予的残留风险,存在很多争议。对53个贝特类药物(16,802名受试者)和30个烟酸试验(4,749名受试者)进行的荟萃分析显示,贝特类药物的HDL-C平均升高10%,烟酸中HDL-C的平均升高,贝特类药物的甘油三酸酯降低36%,烟酸中甘油三酸酯的降低20% ,贝特类药物降低LDL-C 8%,烟酸降低LDL-C 14%。这些脂质的变化导致主要冠状动脉事件的总体减少量相似,贝特类药物减少25%,烟酸减少27%。但是,最近对初级和二级预防试验(如JUPITER,治疗新靶点(TNT)和PROVE-IT TIMI 22)的分析迫使我们重新考虑这个问题。在这三项试验中,HDL-C在初始风险评估中很有用,但是当LDL-C大幅降低时,HDL-C的残留风险预测值显着减弱。流行病学研究还评估了普通人群中已治疗的高血压和血脂异常受试者的残留风险。在北爱尔兰和法国进行的PRIME研究以及在意大利进行的Progetto CUORE研究(均进行了10年的随访)能够验证治疗后的高血压患者残留心血管风险的假说,因为血脂异常患者的比例过低在基线。在两项研究中,使用降压药治疗均会导致相当大的残余心血管风险,危险比为1.5-1.7,这表明应优先开发更有效的降低高血压风险策略。总之,应该在心血管流行病学中更好地研究剩余的心血管风险,完善评估方法,考虑一段时间内暴露于可改变的危险因素和治疗指标(包括药理学和生活方式水平)的措施。需要重复测量和队列随访,还需要新的统计方法来评估残留风险以了解如何降低残留风险。

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