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New risk markers may change the HeartScore risk classification significantly in one-fifth of the population

M H Olsen1, T W Hansen, M K Christensen

  • 1Research Center for Prevention and Health, Glostrup, Denmark. mho@dadlnet.dk

Insights

Urine albumin/creatinine ratio (UACR) and high-sensitivity C-reactive protein (hsCRP) improve cardiovascular risk prediction, especially in lower-risk individuals. These biomarkers help refine risk classification beyond traditional methods like HeartScore.

Area of Science:

  • Cardiology
  • Biomarkers
  • Risk Prediction

Background:

  • Cardiovascular disease remains a leading cause of mortality globally.
  • Accurate risk stratification is crucial for effective primary prevention strategies.
  • Current risk scores may not fully capture individual risk, particularly in lower-risk populations.

Purpose of the Study:

  • To evaluate the added value of urine albumin/creatinine ratio (UACR), high-sensitivity C-reactive protein (hsCRP), and N-terminal pro-brain natriuretic peptide (Nt-proBNP) to existing cardiovascular risk prediction models.
  • To assess the impact of these biomarkers on risk reclassification in different population subgroups.

Main Methods:

  • A Danish population cohort of 2460 individuals was stratified into three groups: those with existing cardiovascular disease/diabetes, high-risk (HeartScore >5%), and low-moderate risk (HeartScore <5%).
  • The study followed participants for 9.5 years, monitoring a composite endpoint of cardiovascular death, non-fatal myocardial infarction, or stroke (CEP).
  • Statistical analyses, including hazard ratios and interaction tests, were used to determine the predictive value of UACR, hsCRP, and Nt-proBNP.

Main Results:

  • UACR and hsCRP significantly predicted CEP across all risk groups, whereas Nt-proBNP showed predictive value primarily in higher-risk individuals.
  • In the low-moderate risk group, UACR or hsCRP identified a subgroup (16%) experiencing one-third of CEPs.
  • In patients with known cardiovascular disease or diabetes, combining UACR and Nt-proBNP identified a low-risk subgroup (52%) experiencing only 15% of CEPs.
  • The addition of UACR and hsCRP (for low-moderate risk) or UACR and Nt-proBNP (for high-risk) significantly reclassified risk in 19% of the population.

Conclusions:

  • UACR and hsCRP are valuable additions to cardiovascular risk prediction, particularly for refining risk assessment in low-to-moderate risk populations.
  • Nt-proBNP may offer additional prognostic information in patients with established cardiovascular disease or diabetes.
  • These biomarkers enhance the accuracy of risk stratification, potentially leading to more personalized preventive strategies.

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