Literature DB >> 17601544

Red cell distribution width as a novel prognostic marker in heart failure: data from the CHARM Program and the Duke Databank.

G Michael Felker1, Larry A Allen, Stuart J Pocock, Linda K Shaw, John J V McMurray, Marc A Pfeffer, Karl Swedberg, Duolao Wang, Salim Yusuf, Eric L Michelson, Christopher B Granger.   

Abstract

OBJECTIVES: The goal of this study was to identify potentially novel laboratory markers of risk in chronic heart failure patients.
BACKGROUND: Although a variety of prognostic markers have been described in heart failure, a systematic assessment of routine laboratory values has not been reported.
METHODS: All 2,679 symptomatic chronic heart failure patients from the North American CHARM (Candesartan in Heart Failure: Assessment of Reduction in Mortality and Morbidity) program had a wide range of laboratory measures performed at a core facility, enabling us to assess the relationship between routine blood tests and outcomes using a Cox proportional hazards model. We then replicated our findings in a cohort of 2,140 heart failure patients from the Duke Databank.
RESULTS: Among 36 laboratory values considered in the CHARM program, higher red cell distribution width (RDW) showed the greatest association with morbidity and mortality (adjusted hazard ratio 1.17 per 1-SD increase, p < 0.001). Higher RDW was among the most powerful overall predictors, with only age and cardiomegaly showing a better independent association with outcome. This finding was replicated in the Duke Databank, in which higher RDW was strongly associated with all-cause mortality (adjusted hazard ratio 1.29 per 1 SD, p < 0.001), second only to age as a predictor of outcome.
CONCLUSIONS: In 2 large contemporary heart failure populations, RDW was found to be a very strong independent predictor of morbidity and mortality. Understanding how and why this marker is associated with outcome may provide novel insights into heart failure pathophysiology.

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Year:  2007        PMID: 17601544     DOI: 10.1016/j.jacc.2007.02.067

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


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