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High-sensitivity C-reactive protein and cardiovascular disease: a resolute belief or an elusive link?

Omair Yousuf1, Bibhu D Mohanty, Seth S Martin

  • 1Johns Hopkins Ciccarone Center for Prevention of Heart Disease, Baltimore, Maryland 21287, USA. oyousuf1@jhmi.edu

Insights

High-sensitivity C-reactive protein (hsCRP) is linked to cardiovascular disease risk but lacks definitive proof of causation. Its clinical utility in risk prediction and statin therapy guidance remains debated, with no clear consensus on optimal use.

Area of Science:

  • Cardiovascular Medicine
  • Inflammation Biology
  • Biomarker Research

Background:

  • Inflammation is integral to atherosclerosis and cardiovascular (CV) event risk.
  • High-sensitivity C-reactive protein (hsCRP) is a prominent inflammatory biomarker studied for CV risk assessment.
  • While associated with CV disease (CVD) risk, hsCRP's causative role in atherothrombosis is not definitively established by randomized trials.

Purpose of the Study:

  • To review the current understanding and clinical application of hsCRP in cardiovascular medicine.
  • To evaluate hsCRP's biological role, epidemiological associations, biomarker quality, and utility in guiding statin therapy.
  • To clarify the debate surrounding hsCRP's incremental predictive value beyond conventional risk factors.

Main Methods:

  • Literature review of hsCRP's biology, epidemiology, and clinical utility.
  • Analysis of hsCRP's role in atherosclerosis and association with cardiovascular disease (CVD).
  • Examination of hsCRP as a risk biomarker and its application in statin therapy decisions.

Main Results:

  • hsCRP is implicated in vascular remodeling and plaque development, correlating with increased CVD risk.
  • Evidence for hsCRP as a causative factor in atherothrombosis is limited.
  • The incremental predictive value of hsCRP in risk stratification beyond traditional factors is debated.

Conclusions:

  • Despite guidelines, consensus on optimal hsCRP use in clinical practice, particularly for primary prevention and statin therapy, is lacking.
  • Further understanding of hsCRP's role is needed to guide treatment decisions effectively.
  • The clinical utility of hsCRP for risk prediction and therapy guidance requires careful consideration.

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