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首页> 外文期刊>European journal of internal medicine >Prospective study of metabolic syndrome as a mortality marker in chronic coronary heart disease patients
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Prospective study of metabolic syndrome as a mortality marker in chronic coronary heart disease patients

机译:代谢综合征作为慢性冠心病患者死亡率标志物的前瞻性研究

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Abstract Background We aimed to clarify the impact of metabolic syndrome (MetS) as assessed by different definitions on the cardiovascular mortality in patients with coronary heart disease (CHD). Methods A total of 1692 patients, 6–24months after myocardial infarction and/or coronary revascularization at baseline, were followed in a prospective cohort study. MetS was identified using four different definitions: standard National Cholesterol Education Program definition (NCEP-ATPIII) based on the presence of ≥3 of the following factors: increased waist circumference, raised blood pressure, hypetriglyceridemia, low high-density lipoprotein cholesterol, and increased fasting glycemia; modified NCEP-ATPIII definition (similar, but omitting antihypertensive treatment as an alternative criterion); presence of “atherogenic dyslipidemia”; or “hypertriglyceridemic waist”. The primary outcome was a fatal cardiovascular event at 5years. Results During 5-year follow-up, 117 patients (6.9%) died from a cardiovascular cause. Patients with MetS by modified NCEP-ATPIII ( n =1066, 63.0% of the whole sample) had significantly higher 5-year cardiovascular mortality [adjusted hazard risk ratio (HRR) 2.01 [95%CI:1.26–3.22]; p =0.003] than subjects without MetS. However, when testing single MetS component factors, the majority of attributable mortality risk was driven by increased fasting glycemia (≥5.6mmol/L) [HRR 2.69 (95%CI:1.29–5.62), p =0.009] and the significance of MetS disappeared. None of the other MetS definitions, i.e., standard NCEP-ATPIII ( n =1210; 71.5%), “hypertriglyceridemic waist” ( n =455; 26.9%) or “atherogenic dyslipidemia” ( n =223; 13.2%) were associated with any significant mortality risk. Conclusions The co-incidence of MetS has a limited mortality impact in CHD patients, while an increase in fasting glycemia seems to be more a specific marker of mortality risk. Highlights ? Metabolic syndrome seems to have only a minor clinical relevance in coronary patients. ? Mild increase of fasting glycaemia effectively identified additive mortality risk. ? Other metabolic syndrome components did not improved the prediction model.
机译:摘要背景我们旨在阐明代谢综合征(METS)的影响,如不同定义对冠心病(CHD)患者心血管死亡率的不同定义。方法在预期的队列研究中,共有1692名患者,6-24个患者,在基线的心肌梗死和/或冠状动脉血管内血管内血管内化。使用四种不同的定义鉴定了Mets:标准国家胆固醇教育计划定义(NCEP-ATPIII)基于以下因素的存在:增加腰围,升高的血压,低密度血症,低密度脂蛋白胆固醇,增加禁食糖血症;改性NCEP-ATPIII定义(类似但省略抗高血压治疗作为替代标准);存在“致动脉粥样硬化血症血症”;或“高甘油植染腰”。主要结果是5年的致命心血管事件。结果在5年的随访期间,117名患者(6.9%)从心血管原因中死亡。通过改性的NCEP-ATPIII(N = 1066,63.0%的整个样品的Mets患者具有明显更高的5年血管死亡率[调整后危害风险比(HRR)2.01 [95%CI:1.26-3.22]; P = 0.003]比没有满足的主体。然而,当测试单一的Mets组分因子时,大多数可归因的死亡率风险由增加的血糖(≥5.6mmol/ l)(HRR 2.69(95%CI:1.29-5.62),P = 0.009]和Mets的重要性驱动消失了。其他METS定义都没有,即标准NCEP-ATPIII(n = 1210; 71.5%),“高甘油植体腰部”(n = 455; 26.9%)或“致动脉粥样脂质血症”(n = 223; 13.2%)与之有关任何显着的死亡风险。结论Mets的共发病率在CHD患者中具有有限的死亡率影响,而禁食糖血症的增加似乎具有更多的死亡风险标记。强调 ?代谢综合征似乎只具有冠状动脉患者的轻微临床相关性。还禁食血脂症的轻度增加有效地确定了添加剂死亡率风险。还其他代谢综合征组件没有改善预测模型。

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