Journal Home
Search for

Volume 147, Issue 5, Pages 931-938 (May 2004)


View previous. 42 of 42

Independent prognostic value of elevated high-sensitivity C-reactive protein in chronic heart failure

Wei-Hsian Yin, MDade, Jaw-Wen Chen, MDce, Hsu-Lung Jen, MDa, Meng-Cheng Chiang, MDa, Wen-Pin Huang, MDa, An-Ning Feng, MDa, Mason Shing Young, MD, FACCb, Shing-Jong Lin, MD, PhDcdeCorresponding Author Informationemail address

Received 16 May 2003; accepted 17 November 2003.

Abstract 

Background

The serum concentration of C-reactive protein (CRP) is mildly elevated in patients with chronic congestive heart failure (CHF), but this level falls well within the range found in healthy subjects. Standard clinical assays for CRP lack sensitivity within the low reference range and thus cannot be used effectively for routine clinical risk prediction. Because assays for high-sensitivity CRP (hsCRP) are now available, we can measure hsCRP to determine its predictive value for the prognosis of patients with CHF.

Methods

Serum levels of hsCRP in 108 patients with CHF and left ventricular ejection fraction (LVEF) <50% were examined. Major adverse cardiac events (death, heart transplantation, or hospitalization with worsening heart failure) during a median follow-up period of 403 days were determined.

Results

The concentrations of hsCRP in this study population were significantly increased with the severity of CHF. In a multivariate analysis, LVEF and serum levels of hsCRP were independent significant predictors for adverse outcomes in these patients (hazard ratio, 3.714, P = .024, and hazard ratio, 2.584, P = .047, respectively). However, hsCRP was minimally correlated with LVEF (r = −0.167, P = .084). Further analysis indicated that hsCRP might identify a different high-risk group and could improve risk stratification beyond that of LVEF.

Conclusions

These findings suggest that an elevated level of hsCRP is an independent predictor of prognosis in CHF and can provide additional prognostic information for the risk stratification and treatment in patients with chronic CHF.

a Division of Cardiology, Taipei, Taiwan

b Department of Internal Medicine, Cheng-Hsin General Hospital, Taipei, Taiwan

c Division of Cardiology, Taipei Veterans General Hospital, Taipei, Taiwan

d Institute of Clinical Medicine, Taipei, Taiwan

e Cardiovascular Research Center, National Yang-Ming University School of Medicine, Taipei, Taiwan

Corresponding Author InformationReprint requests: Shing-Jong Lin, MD, PhD, Division of Cardiology, Taipei Veterans General Hospital, 201, Sec 2, Shih-Pai Rd, Taipei 112, Taiwan.

PII: S0002-8703(03)00859-7

doi:10.1016/j.ahj.2003.11.021


View previous. 42 of 42