Use of Framinghamrisk score and new biomarkers to predict cardiovascular mortality in older people: population based observational cohort study

被引:246
作者
de Ruijter, Wouter
Westendorp, Rudi G. J. [2 ]
Assendelft, Willem J. J. [1 ]
den Elzen, Wendy P. J. [1 ]
de Craen, Anton J. M. [2 ]
le Cessie, Saskia [3 ]
Gussekloo, Jacobijn [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Publ Hlth & Primary Care, NL-2300 RA Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Gerontol & Geriat, NL-2300 RA Leiden, Netherlands
[3] Leiden Univ, Dept Med Stat, NL-2300 RA Leiden, Netherlands
来源
BMJ-BRITISH MEDICAL JOURNAL | 2009年 / 338卷
关键词
C-REACTIVE PROTEIN; CORONARY-HEART-DISEASE; MYOCARDIAL-INFARCTION; BLOOD-PRESSURE; RISK-FACTORS; INFLAMMATORY MARKERS; PLASMA HOMOCYSTEINE; NATRIURETIC PEPTIDE; MULTIPLE BIOMARKERS; PRIMARY PREVENTION;
D O I
10.1136/bmj.a3083
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives To investigate the performance of classic risk factors, and of some new biomarkers, in predicting cardiovascular mortality in very old people from the general population with no history of cardiovascular disease. Design The Leiden 85-plus Study (1997-2004) is an observational prospective cohort study with 5 years of follow-up. Setting General population of the city of Leiden, the Netherlands. Participants Population based sample of participants aged 85 years (215 women and 87 men) with no history of cardiovascular disease; no other exclusion criteria. Main measurements Cause specific mortality was registered during follow-up. All classic risk factors included in the Framingham risk score (sex, systolic blood pressure, total and high density lipoprotein cholesterol, diabetes mellitus, smoking and electrocardiogram based left ventricular hypertrophy), as well as plasma concentrations of the new biomarkers homocysteine, folic acid, C reactive protein, and interleukin 6, were assessed at baseline. Results During follow-up, 108 of the 302 participants died; 32% (35/108) of deaths were from cardiovascular causes. Classic risk factors did not predict cardiovascular mortality when used in the Framingham risk score (area under receiver operating characteristic curve 0.53, 95% confidence interval 0.42 to 0.63) or in a newly calibrated model (0.53, 0.43 to 0.64). Of the new biomarkers studied, homocysteine had most predictive power (0.65, 0.55 to 0.75). Entering any additional risk factor or combination of factors into the homocysteine prediction model did not increase its discriminative power. Conclusions In very old people from the general population with no history of cardiovascular disease, concentrations of homocysteine alone can accurately identify those at high risk of cardiovascular mortality, whereas classic risk factors included in the Framingham risk score do not. These preliminary findings warrant validation in a separate cohort.
引用
收藏
页码:219 / 222
页数:8
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