Gianfagna Francesco, Veronesi Giovanni, Guasti Luigina, Chambless Lloyd E, Brambilla Paolo, Corrao Giovanni, Mancia Giuseppe, Cesana Giancarlo, Ferrario Marco M
Research Centre in Epidemiology and Preventive Medicine - EPIMED, Department of Clinical and Experimental Medicine, University of Insubria, Via O Rossi 9, 21100 Varese, Italy.
Research Centre in Epidemiology and Preventive Medicine - EPIMED, Department of Clinical and Experimental Medicine, University of Insubria, Via O Rossi 9, 21100 Varese, Italy; Research Centre on Dyslipidemia, Department of Clinical and Experimental Medicine, University of Insubria, Viale Borri 57, 21100 Varese, Italy.
Atherosclerosis. 2014 Sep;236(1):175-81. doi: 10.1016/j.atherosclerosis.2014.06.029. Epub 2014 Jul 14.
We assessed predictive abilities and clinical utility of CVD risk algorithms including ApoB and ApoAI among non-diabetic subjects with metabolic syndrome (MetS).
Three independent population-based cohorts (3677 35-74 years old) were enrolled in Northern Italy, adopting standardized MONICA procedures. Through Cox models, we assessed the associations between lipid measures and first coronary events, as well as the changes in discrimination and reclassification (NRI) when standard lipids or apolipoproteins were added to the CVD risk algorithm including non-lipids risk factors. Finally, the best models including lipids or apolipoproteins were compared.
During the 14.5 years median follow-up time, 164 coronary events were validated. All measures showed statistically significant associations with the endpoint, while in the MetS subgroup HDL-C and ApoAI (men, HR = 1.59; 95%CI: 0.96-2.65) were not associated. Models including HDL-C plus TC and ApoB plus ApoAI for lipids and apolipoproteins, respectively, showed the best predictive values. When ApoB plus ApoAI replaced TC plus HDL-C, NRI values improved in subjects with MetS (13.8; CI95%: -5.1,53.1), significantly in those previously classified at intermediate risk (44.5; CI95% 13.8,129.6). In this subgroup, 5.5% of subjects was moved in the high (40.0% of expected events) and 17.0% in the low risk class (none had an event at 10 years).
ApoB and ApoAI could improve coronary risk prediction when used as second level biomarkers in non-diabetic subjects with MetS classified at intermediate risk. The absence of cases moved downward suggests the gain in avoiding treatments in non-cases and favor the use of apolipoproteins for risk assessment.
我们评估了心血管疾病(CVD)风险算法(包括载脂蛋白B和载脂蛋白AI)在患有代谢综合征(MetS)的非糖尿病受试者中的预测能力和临床效用。
在意大利北部招募了三个独立的基于人群的队列(3677名35 - 74岁),采用标准化的莫尼卡(MONICA)程序。通过Cox模型,我们评估了血脂指标与首次冠状动脉事件之间的关联,以及当将标准血脂或载脂蛋白添加到包括非血脂风险因素的CVD风险算法中时,判别能力和重新分类(净重新分类指数,NRI)的变化。最后,比较了包含血脂或载脂蛋白的最佳模型。
在14.5年的中位随访期内,验证了164例冠状动脉事件。所有指标均显示与终点有统计学显著关联,而在MetS亚组中,高密度脂蛋白胆固醇(HDL - C)和载脂蛋白AI(男性,风险比[HR] = 1.59;95%置信区间[CI]:0.96 - 2.65)无关联。分别包含HDL - C加总胆固醇(TC)以及载脂蛋白B加载脂蛋白AI的血脂和载脂蛋白模型显示出最佳预测值。当载脂蛋白B加载脂蛋白AI取代TC加HDL - C时,MetS受试者的NRI值有所改善(13.8;95%CI: - 5.1,53.1),在先前分类为中等风险的受试者中显著改善(44.5;95%CI 13.8,129.6)。在该亚组中,5.5%的受试者被重新分类为高风险(占预期事件的40.0%),17.0%被重新分类为低风险(10年内均无事件发生)。
在分类为中等风险的患有MetS的非糖尿病受试者中,当将载脂蛋白B和载脂蛋白AI用作二级生物标志物时,可改善冠状动脉风险预测。没有病例被向下重新分类,这表明在非患病个体中避免治疗的益处增加,支持使用载脂蛋白进行风险评估。