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CRP in cardiovascular disease
Mahir Karakas1, Wolfgang Koenig
1Department of Internal Medicine II - Cardiology, University of Ulm Medical Center, Ulm, Germany.
Insights
High-sensitivity C-reactive protein (hsCRP) identifies individuals at elevated cardiovascular risk, even with normal cholesterol. Statin therapy, as shown in the JUPITER trial, significantly reduces cardiovascular events in these patients.
Area of Science:
- Cardiology
- Biomarkers
- Preventive Medicine
Background:
- Traditional cardiovascular risk factors inadequately identify all at-risk individuals.
- High-sensitivity C-reactive protein (hsCRP) is a widely studied blood biomarker for cardiovascular risk.
- While associations exist, the causal link between CRP and coronary heart disease (CHD) is debated, with Mendelian randomization studies suggesting it may not be causal.
Purpose of the Study:
- To evaluate if individuals with normal low-density lipoprotein cholesterol but elevated hsCRP levels represent a high-risk population.
- To determine if statin treatment benefits this specific high-risk group.
Main Methods:
- The JUPITER trial randomized 17,802 apparently healthy individuals to receive either 20 mg of rosuvastatin daily or a placebo.
- Participants had normal low-density lipoprotein cholesterol levels but elevated hsCRP.
Main Results:
- Rosuvastatin significantly reduced the incidence of major cardiovascular events by 44% compared to placebo.
- The primary endpoint rates were 0.77 per 100 person-years for rosuvastatin and 1.36 per 100 person-years for placebo.
- hsCRP may serve as an integrative marker, identifying high-risk subjects by reflecting overall inflammatory burden.
Conclusions:
- Elevated hsCRP in individuals with normal LDL cholesterol identifies a population that benefits from statin therapy.
- The JUPITER trial findings support the clinical utility of hsCRP in cardiovascular risk assessment and prevention.
- hsCRP's role in identifying high-risk individuals warrants further consideration in clinical practice.
Abstract:
In primary prevention, traditional risk factors are a useful first step in determining who is at cardiovascular risk, however, it has been noted that a considerable number of those at risk cannot be identified on the basis of traditional risk factors alone. Among blood biomarkers, C-reactive protein (CRP), measured by high-sensitivity assays (hsCRP), has received widespread interest and a large database has been accumulated on its potential role as a predictor of cardiovascular risk, although observed associations between circulating CRP and coronary heart disease (CHD) are unlikely to be causal, as recently indicated by various Mendelian randomization studies. In a meta-analysis of 22 prospective studies, the multivariable adjusted, combined odds ratio for CRP to predict CHD, comparing extreme tertiles, was 1.58 (95% confidence interval, 1.48-1.68). Several recent studies showed a significant contribution of CRP to coronary risk prediction independent of the Framingham Risk Score, with better discrimination, calibration and improved, albeit modest reclassification of subjects at risk. To test the hypothesis whether or not subjects with normal low-density lipoprotein cholesterol but elevated CRP represent a population at increased risk that might benefit from statin treatment, the JUPITER trial randomized 17,802 apparently healthy persons to either 20 mg rosuvastatin daily or placebo. Rosuvastatin significantly reduced the incidence of major cardiovascular events. The rates of the primary endpoint (composite of nonfatal myocardial infarction, nonfatal stroke, hospitalization for unstable angina, revascularization, and confirmed death from cardiovascular causes) were 0.77 and 1.36 per 100 person-years of follow-up in the rosuvastatin and placebo groups, respectively. Relative risk reduction was 44%. CRP may have more accurately selected high-risk subjects due to its association with very many risk factors, thus representing an integrative marker of the total inflammatory burden of an individual. JUPITER has revitalized the discussion on CRP in clinical practice and will make it more difficult in the future to neglect the evidence built around CRP and cardiovascular risk.
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