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代谢综合征是否真的能预测心血管疾病和全因死亡率,并且与组成代谢综合征的各项变量无关?——Dubbo 研究。

Is prediction of cardiovascular disease and all-cause mortality genuinely driven by the metabolic syndrome, and independently from its component variables? The Dubbo study.

机构信息

University of NSW, Lipid Research Department, St Vincent's Hospital, Sydney, NSW 2010, Australia.

出版信息

Heart Lung Circ. 2011 Apr;20(4):214-9. doi: 10.1016/j.hlc.2010.12.005. Epub 2011 Feb 24.

Abstract

BACKGROUND

The Metabolic Syndrome (MetS) predicts an increased risk of cardiovascular disease and all-cause mortality. Is this prediction genuinely driven by the syndrome and independently from its component variables?

METHODS

A longitudinal cohort study in Dubbo, Australia of 2805 men and women ≥60 years followed for 16 years from 1988. Cox proportional hazards models were calculated for coronary heart disease (CHD), ischaemic stroke and all-cause mortality with MetS as an independent variable. Separate models included the MetS variable, with or without the presence of one of its five component variables.

RESULTS

MetS was present in 33% of subjects. Obesity was present in 43% of those with MetS, high blood pressure in 99%, elevated triglycerides in 83%, low HDL-C in 75% and glycaemia in 48%. With respect to CHD and all-cause mortality, prediction by MetS was similar in the presence or absence of individual component factors (e.g. hazard ratio (95% CI) for CHD by MetS when low HDL-C present 1.60(1.39-1.84) and 1.67(1.37-2.04) when low HDL-C absent). With stroke, prediction by MetS was lost in the absence of elevated triglycerides or glycaemia factors (e.g. hazard ratio for stroke by MetS when glycaemia present 1.59(1.24-2.05) and 1.08(0.82-1.42) when glycaemia absent).

CONCLUSIONS

The findings suggest that prediction of CHD and all-cause mortality is genuinely driven by the MetS and independently of its component variables. Prediction of ischaemic stroke is more complex, with some components providing prediction independently from the MetS.

摘要

背景

代谢综合征(MetS)可预测心血管疾病和全因死亡率的风险增加。这种预测是否真的是由该综合征驱动的,而与综合征的组成变量无关?

方法

这是一项在澳大利亚达博进行的纵向队列研究,共纳入了 2805 名年龄≥60 岁的男性和女性,他们于 1988 年开始随访,随访时间为 16 年。使用 Cox 比例风险模型计算了代谢综合征作为独立变量时的冠心病(CHD)、缺血性卒中和全因死亡率。单独的模型包括代谢综合征变量,以及是否存在其五个组成变量中的一个。

结果

33%的受试者存在代谢综合征。在患有代谢综合征的人群中,肥胖的发生率为 43%,高血压为 99%,甘油三酯升高为 83%,高密度脂蛋白胆固醇降低为 75%,血糖升高为 48%。就 CHD 和全因死亡率而言,在存在或不存在个别组成因素的情况下,代谢综合征的预测结果相似(例如,当低 HDL-C 存在时,代谢综合征与 CHD 的风险比(95%CI)为 1.60(1.39-1.84),当低 HDL-C 不存在时为 1.67(1.37-2.04))。对于中风,在不存在甘油三酯或血糖升高因素的情况下,代谢综合征的预测结果消失(例如,当血糖存在时,代谢综合征与中风的风险比为 1.59(1.24-2.05),当血糖不存在时为 1.08(0.82-1.42))。

结论

研究结果表明,CHD 和全因死亡率的预测确实是由代谢综合征驱动的,而与综合征的组成变量无关。缺血性中风的预测更为复杂,一些组成部分独立于代谢综合征提供预测。

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