主持海报会议II:预防和卫生政策

J. Skoumas, K. Aznaouridis, VMetaxa, F. Platsouka, L. Papadimitriou, C. Pitsavos, C. Stefanadis, M. Lorgeril, P. Salen, F. Laporte, A. Castelnuovo, V. Krogh, M. Donati, A. Tverdal, F. Visseren, A. Algra
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摘要

M135代谢综合征是家族性合并高脂血症患者预后的预测因子CMasoura, J Skoumas, K Aznaouridis, VMetaxa, F Platsouka, L Papadimitriou, C Pitsavos, C Stefanadis主题:脂质与动脉粥样硬化目的:家族性合并高脂血症(FCH)是一种与早发心血管疾病相关的多基因脂质疾病。目前尚不清楚代谢综合征(MetS)是否调节FCH患者的心血管风险。方法:我们对644例FCH患者(421例男性)进行了9.2 3.6年的前瞻性研究。在开始治疗前,在入组时评估人口统计学特征和生化参数。MetS的诊断基于改进的ATP III标准(葡萄糖> 100mg /dl)。在随访期间记录硬心血管终点,如急性心肌梗死(AMI)和心血管死亡。结果:323例MetS患者年龄较大(50.8 - 10.2岁vs. 46.7 - 11.0岁,öÀ<0.001),甘油三酯和葡萄糖水平较高,但与没有MetS的患者相比,他们的HDL-C水平较低(均öÀ<0.001)。总胆固醇没有差异。合并终点(AMI/死亡)发生在29例MetS患者和9例无MetS患者中(9.0% vs. 2.8%, P=0.001)。Kaplan-Meier分析显示,两组无事件生存率差异有统计学意义(P=0.005,图)。多因素分析(Cox回归)显示,入组时met预测AMI/死亡与年龄、性别或既往心血管疾病无关(校正优势比2.25,95% CI 1.06-4.75, P=0.034)。结论:MetS是FCH患者主要心血管事件的独立预测因子。
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Moderated Poster Session II: Prevention and health policy
M135 Metabolic syndrome is a predictor of outcome in patients with familial combined hyperlipidemia CMasoura, J Skoumas, K Aznaouridis, VMetaxa, F Platsouka, L Papadimitriou, C Pitsavos, C Stefanadis Athens, Greece Topic: Lipids and atherosclerosis Purpose: Familial combined hyperlipidemia (FCH) is a polygenic lipid disorder associated with premature cardiovascular disease. It is unknown whether metabolic syndrome (MetS) modulates cardiovascular risk in FCH patients. Methods: We studied prospectively 644 FCH patients (421 men) for 9.2 3.6 years. Demographic characteristics and biochemical parameters were evaluated at enrolment, before the initiation of treatment. The diagnosis of MetS was based on the modified ATP III criteria (glucose >100 mg/dl). Hard cardiovascular end-points, like acute myocardial infarction (AMI) and cardiovascular death, were recorded during the follow-up. Results: The 323 patients with MetS were older (50.8 10.2 vs. 46.7 11.0 years, öÀ<0.001) and had higher triglyceride and glucose levels, but they had lower HDL-C levels compared with patients without MetS (all öÀ<0.001). There was no difference in total cholesterol. The combined endpoint (AMI/death) occurred in 29 patients with MetS and in 9 patients without MetS (9.0% vs. 2.8%, P=0.001). Kaplan-Meier analysis showed a significant difference in the event-free survival between the 2 groups (P=0.005, figure). Multivariate analysis (Cox regression) showed that MetS at enrolment predicts AMI/death independent of age, sex or previous cardiovascular disease (adjusted odds ratio 2.25, 95% CI 1.06-4.75, P=0.034). Conclusions: MetS represents an independent predictor of major cardiovascular events in FCH patients.
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