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Clinical Chemistry 54: 335-342, 2008. First published December 21, 2007; 10.1373/clinchem.2007.100271
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Right arrow Proteomics and Protein Markers
(Clinical Chemistry. 2008;54:335-342.)
© 2008 American Association for Clinical Chemistry, Inc.


Proteomics and Protein Markers

Prospective Study of High-Sensitivity C-Reactive Protein as a Determinant of Mortality: Results from the MONICA/KORA Augsburg Cohort Study, 1984–1998

Wolfgang Koenig1,a, Natalie Khuseyinova1, Jens Baumert2 and Christa Meisinger2,3

1 Department of Internal Medicine II–Cardiology, University of Ulm Medical Center, Ulm, Germany; 2 Helmholtz Center Munich, German Research Center for Environment and Health (GmbH), Institute of Epidemiology, Neuherberg, Germany; 3 MONICA/KORA Myocardial Infarction Registry, Central Hospital Augsburg, Germany.

aAddress correspondence to this author at: Department of Internal Medicine II– Cardiology, University of Ulm Medical Center, Robert-Koch Str. 8, D-89081 Ulm, Germany. Fax +49-731-500-45021; e-mail wolfgang.koenig{at}uniklinik-ulm.de.

Background: C-reactive protein (CRP), an exquisitely sensitive systemic marker of inflammation, has emerged as an independent predictor of cardiovascular diseases (CVD). Because other chronic diseases are also associated with an inflammatory response, we sought to assess the association of high-sensitivity CRP (hsCRP) with total and cause-specific mortality in a large cohort of middle-aged men.

Methods: We measured hsCRP at baseline in 3620 middle-aged men, randomly drawn from 3 samples of the general population in the Augsburg area (Southern 0Germany) in 1984–85, 1989–90, and 1994–95. Outcome was defined as all deaths, fatal CVD, fatal coronary heart disease (CHD) including sudden cardiac deaths, and cancer deaths.

Results: During an average follow-up of 7.1 years, 408 deaths occurred (CVD 196, CHD 129, cancer 127). In multivariable Cox regression analysis, subjects with hsCRP >3 mg/L at baseline showed an almost 2-fold increased risk to die vs those with hsCRP <1 mg/L [hazard ratio (HR) 1.88, 95% CI 1.41–2.52]. HRs were 2.15 (95% CI 1.39–3.34) for fatal CVD, 1.74 (1.04–2.92) for fatal CHD, and 1.65 (1.01–2.68) for cancer mortality. In contrast, neither total nor HDL cholesterol significantly predicted all-cause or cancer mortality, and cholesterol had only modest effects on CVD mortality.

Conclusions: Our results suggest that increased circulating hsCRP concentrations are associated with an increased risk of death from several widespread chronic diseases. Persistently increased hsCRP is a sensitive and valuable nonspecific indicator of an ongoing disease process that deserves serious and careful medical attention.




The following articles in journals at HighWire Press have cited this article:


Home page
Clin. Chem.Home page
P. M Ridker
High-Sensitivity C-Reactive Protein as a Predictor of All-Cause Mortality: Implications for Research and Patient Care
Clin. Chem., February 1, 2008; 54(2): 234 - 237.
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