Predicting cardiovascular disease risk across the atherosclerotic disease continuum

Katrina K Poppe1,2, Sue Wells1, Rod Jackson1

  • 1Section of Epidemiology and Biostatistics, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand.

Insights

A new cardiovascular disease (CVD) risk equation (PREDICT-2°) was developed for secondary prevention, complementing primary prevention scores. This highlights a CVD risk continuum, showing limitations of a one-size-fits-all approach for those with existing atherosclerotic CVD.

Area of Science:

  • Cardiology
  • Public Health
  • Epidemiology

Background:

  • Cardiovascular disease (CVD) guidelines typically separate primary and secondary prevention strategies.
  • Existing risk equations primarily focus on primary prevention, leaving a gap in assessing risk for individuals with established atherosclerotic cardiovascular disease (ASCVD).
  • A nuanced understanding of CVD risk distribution is crucial for effective population health management.

Purpose of the Study:

  • To develop a novel risk equation (PREDICT-2°) for estimating the 5-year risk of CVD event recurrence in patients with known ASCVD.
  • To complement existing primary prevention risk equations (PREDICT-1°).
  • To describe the distribution of CVD risk across the general population, particularly highlighting differences between those with and without ASCVD.

Main Methods:

  • Utilized data from a large primary care cohort (PREDICT) including adults aged 30-79 years who underwent routine CVD risk assessment between 2007-2016.
  • Developed a new Cox regression model for PREDICT-2° to calculate 5-year CVD event recurrence risk in patients with ASCVD.
  • Calculated 5-year CVD risk for individuals without ASCVD using established PREDICT-1° equations.

Main Results:

  • The study identified 475,161 patients, with 12% having a history of ASCVD.
  • For individuals without ASCVD, median 5-year CVD risks were 2.2% for women and 3.5% for men.
  • For individuals with ASCVD, the new PREDICT-2° equation showed significantly higher median 5-year risks: 21% for women and 23% for men.

Conclusions:

  • Developed PREDICT-2° risk scores for individuals with ASCVD, enhancing current risk assessment tools.
  • Demonstrated that median CVD risk is approximately eight-fold higher in individuals with ASCVD compared to those without.
  • Highlighted a CVD risk continuum and the inadequacy of a 'one-size-fits-all' approach for managing ASCVD patients, emphasizing the need for tailored risk assessment.
Abstract

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