Prediction of Cardiovascular Disease Risk by Cardiac Biomarkers in 2 United Kingdom Cohort Studies: Does Utility

Paul Welsh1, Carole Hart1, Olia Papacosta1

  • 1From the Institute of Cardiovascular and Medical Sciences, BHF Glasgow Cardiovascular Research Centre (P.W., D.P., N.S.), Institute of Health and Wellbeing (C.H., G.W.), and Robertson Centre for Biostatistics (A.M., H.M.), University of Glasgow, Glasgow, United Kingdom; Department of Primary Care and Population Health, University College London, London, United Kingdom (O.P., S.R., P.W., G.W.); and Helmsley Medical Centre, Helmsley, York, United Kingdom (M.U.).

Insights

Cardiac biomarkers like NT-proBNP and troponin T can improve cardiovascular disease risk prediction, especially when using specific risk thresholds for treatment decisions.

Area of Science:

  • Cardiology
  • Biomarker Research
  • Preventive Medicine

Background:

  • Cardiovascular disease (CVD) remains a leading cause of mortality.
  • Accurate risk prediction is crucial for timely intervention.
  • Established risk scores have limitations in identifying all at-risk individuals.

Purpose of the Study:

  • To evaluate the predictive ability of NT-proBNP, high-sensitivity troponin T, and midregional pro adrenomedullin for CVD events.
  • To determine if these biomarkers improve existing CVD risk prediction models.
  • To assess the impact of biomarker addition on clinical decision-making for preventive treatments.

Main Methods:

  • Utilized data from the British Regional Heart Study (BRHS) and MIDSPAN Family Study (MFS).
  • Employed Cox regression models adjusted for classical risk factors.
  • Assessed improvements in C-index and risk reclassification using NT-proBNP and other biomarkers.

Main Results:

  • NT-proBNP and high-sensitivity troponin T generally associated with increased CVD risk.
  • NT-proBNP significantly improved risk prediction in the BRHS cohort.
  • Improvements in risk classification were threshold-dependent, particularly for NT-proBNP and troponin T.

Conclusions:

  • Cardiac biomarkers, notably NT-proBNP, can enhance CVD risk assessment.
  • The clinical utility of adding biomarkers depends on the chosen risk threshold for initiating preventive therapies.
  • Further research may refine biomarker integration into clinical practice for personalized CVD prevention.

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