Cystatin C and risk of vascular and nonvascular mortality: a prospective cohort study of older men

被引:24
|
作者
Emberson, J. R. [1 ]
Haynes, R.
Dasgupta, T.
Mafham, M.
Landray, M. J.
Baigent, C.
Clarke, R.
机构
[1] Univ Oxford, Clin Trial Serv Unit, Oxford OX3 7LF, England
基金
英国医学研究理事会;
关键词
aging; epidemiology; kidney; risk factors; GLOMERULAR-FILTRATION-RATE; CHRONIC KIDNEY-DISEASE; CARDIOVASCULAR EVENTS; SERUM CREATININE; CIVIL-SERVANTS; HEART-DISEASE; FOLLOW-UP; RE-SURVEY; STRATIFICATION; CHOLESTEROL;
D O I
10.1111/j.1365-2796.2010.02214.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Emberson JR, Haynes R, Dasgupta T, Mafham M, Landray MJ, Baigent C, Clarke R (University of Oxford, Oxford, UK). Cystatin C and risk of vascular and nonvascular mortality: a prospective cohort study of older men. J Intern Med 2010; 268: 145-154. Objective. To assess the relevance of cystatin C, as a marker of mild-to-moderate renal impairment, for vascular and nonvascular mortality in older people. Design. Prospective cohort study. Setting. Re-survey in 1997 to 1998 of survivors in the 1970 Whitehall study of London civil servants. Subjects. Five thousand three hundred and seventy-one men (mean age at resurvey: 77 years) who took part in the resurvey and had plasma cystatin C concentration measured. Main outcome measures. Cause-specific mortality over subsequent 11 years (1997 to 2008). Methods. Cox regression was used to estimate the associations of cystatin C with vascular and nonvascular mortality, before and after adjustment for prior disease and other risk factors (including lifetime blood pressure). Results. During an 11.0-year follow-up period, there were 1171 deaths from vascular causes [26 per 1000 per year (py)] and 1615 deaths from nonvascular causes (36 per 1000 py). Compared with men with cystatin C in the bottom fifth of the distribution, men in the top 10th had about two-fold higher mortality rates from vascular and nonvascular mortality (fully adjusted P both < 0.001) even after adjustment for prior disease and all measured confounders, including lifetime blood pressure. The fully adjusted relative risks per 50% higher cystatin C concentrations were 1.66 [95% CI 1.48 to 1.85] for vascular mortality, 1.92 [95% CI 1.66 to 2.22] for ischaemic heart disease mortality and 1.46 [95% CI 1.31 to 1.61] for nonvascular mortality. Conclusions. In older men, plasma concentration of cystatin C, probably as a marker of mild renal disease, is a strong independent predictor of both vascular and nonvascular mortality.
引用
收藏
页码:145 / 154
页数:10
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