CLINICAL RESEARCH: HEART FAILURE
Red Cell Distribution Width as a Novel Prognostic Marker in Heart FailureData From the CHARM Program and the Duke Databank
G. Michael Felker, MD, MHS, FACC*,*,
Larry A. Allen, MD*,
Stuart J. Pocock, PhD1, ,
Linda K. Shaw, MS*,
John J.V. McMurray, MD, FACC1, ,
Marc A. Pfeffer, MD, PhD, FACC1, ,
Karl Swedberg, MD, PhD, FACC1,||,
Duolao Wang, PhD ,
Salim Yusuf, DPhil, FACC1,¶,
Eric L. Michelson, MD, FACC2,#,
Christopher B. Granger, MD, FACC1,* for the CHARM Investigators
* Duke Clinical Research Institute, Durham, North Carolina
London School of Hygiene and Tropical Medicine, London, United Kingdom
University of Glasgow, Glasgow, United Kingdom
Brigham and Womens Hospital, Boston, Massachusetts
|| Department of Medicine, Sahlgrenska University Hospital/Östra, Göteburg, Sweden
¶ McMaster University, Hamilton, Ontario, Canada
# AstraZeneca LP, Wilmington, Delaware.
Manuscript received January 9, 2007;
revised manuscript received February 23, 2007,
accepted February 25, 2007.
* Reprint requests and correspondence: Dr. G. Michael Felker, Duke Clinical Research Institute, 2400 Pratt Street, Room 0311 Terrace Level, DUMC Box 3850, Durham, North Carolina 27715. (Email: michael.felker{at}duke.edu).
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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Abbreviations and Acronyms
| | ACE = angiotensin-converting enzyme | | HR = hazard ratio | | NYHA = New York Heart Association | | RDW = red cell distribution width |
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