Red cell distribution width, C-reactive protein, the complete blood count, and mortality in patients with coronary disease and a normal comparison population

Red cell distribution width (RDW) is associated with morbidity and mortality in coronary artery disease (CAD), but the connection of RDW with chronic inflammation is equivocal. In 1,489 patients with CAD and 8.4–15.2years of follow-up all-cause mortality and RDW were studied using Cox regression. RD...

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Veröffentlicht in:Clinica chimica acta 2011-11, Vol.412 (23-24), p.2094-2099
Hauptverfasser: Lappé, Jason M., Horne, Benjamin D., Shah, Svati H., May, Heidi T., Muhlestein, Joseph B., Lappé, Donald L., Kfoury, Abdallah G., Carlquist, John F., Budge, Deborah, Alharethi, Rami, Bair, Tami L., Kraus, William E., Anderson, Jeffrey L.
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container_end_page 2099
container_issue 23-24
container_start_page 2094
container_title Clinica chimica acta
container_volume 412
creator Lappé, Jason M.
Horne, Benjamin D.
Shah, Svati H.
May, Heidi T.
Muhlestein, Joseph B.
Lappé, Donald L.
Kfoury, Abdallah G.
Carlquist, John F.
Budge, Deborah
Alharethi, Rami
Bair, Tami L.
Kraus, William E.
Anderson, Jeffrey L.
description Red cell distribution width (RDW) is associated with morbidity and mortality in coronary artery disease (CAD), but the connection of RDW with chronic inflammation is equivocal. In 1,489 patients with CAD and 8.4–15.2years of follow-up all-cause mortality and RDW were studied using Cox regression. RDW and its associations with inflammation, liver function, renal function, and body mass were assessed. A population of 449 normal (No-CAD) patients also was evaluated. RDW predicted all-cause mortality in a step-wise manner (HR=1.37 per quintile; 95% CI=1.29, 1.46; p-trend
doi_str_mv 10.1016/j.cca.2011.07.018
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In 1,489 patients with CAD and 8.4–15.2years of follow-up all-cause mortality and RDW were studied using Cox regression. RDW and its associations with inflammation, liver function, renal function, and body mass were assessed. A population of 449 normal (No-CAD) patients also was evaluated. RDW predicted all-cause mortality in a step-wise manner (HR=1.37 per quintile; 95% CI=1.29, 1.46; p-trend&lt;0.001). A significant but meaningless correlation between RDW and high-sensitivity C-reactive protein (hsCRP) was identified (r=0.181; p&lt;0.001). With full adjustment, RDW remained significant (p-trend&lt;0.001) and the strongest predictor of mortality among all factors included in the model. RDW also strongly predicted all-cause mortality in the normal control population (HR=1.33 per quintile, CI=1.15, 1.55; p-trend&lt;0.001), but hsCRP did not predict mortality among normal controls. RDW was associated with mortality in patients with CAD and may provide clinically useful prognostication. 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In 1,489 patients with CAD and 8.4–15.2years of follow-up all-cause mortality and RDW were studied using Cox regression. RDW and its associations with inflammation, liver function, renal function, and body mass were assessed. A population of 449 normal (No-CAD) patients also was evaluated. RDW predicted all-cause mortality in a step-wise manner (HR=1.37 per quintile; 95% CI=1.29, 1.46; p-trend&lt;0.001). A significant but meaningless correlation between RDW and high-sensitivity C-reactive protein (hsCRP) was identified (r=0.181; p&lt;0.001). With full adjustment, RDW remained significant (p-trend&lt;0.001) and the strongest predictor of mortality among all factors included in the model. RDW also strongly predicted all-cause mortality in the normal control population (HR=1.33 per quintile, CI=1.15, 1.55; p-trend&lt;0.001), but hsCRP did not predict mortality among normal controls. RDW was associated with mortality in patients with CAD and may provide clinically useful prognostication. Although RDW was correlated with hsCRP, they were independent predictors of mortality. RDW has been incorporated into risk prediction tool using data from basic chemistries available at: http://intermountainhealthcare.org/IMRS. ► Red cell distribution width (RDW) is associated with mortality in CAD patients. ► The etiology of RDW elevation is unknown. ► Elevation of RDW is not due to chronic inflammation as measured by hsCRP. ► RDW is also associated with mortality in controls and is not a coronary disease-specific or heart failure-specific marker. ► Despite an unknown pathophysiology, elevated RDW is a strong predictor of mortality.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>21821014</pmid><doi>10.1016/j.cca.2011.07.018</doi><tpages>6</tpages></addata></record>
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subjects Aged
Blood Cell Count
Blood cells
C-Reactive Protein - metabolism
Case-Control Studies
CBC
Coronary disease
Coronary Disease - blood
Coronary Disease - mortality
Erythrocytes - metabolism
Female
Humans
Male
Middle Aged
Mortality
Proportional Hazards Models
RDW
title Red cell distribution width, C-reactive protein, the complete blood count, and mortality in patients with coronary disease and a normal comparison population
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