Incorporating kidney disease measures into cardiovascular risk prediction: Development and validation in 9 million

Kunihiro Matsushita1, Simerjot K Jassal2, Yingying Sang1

  • 1Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.

Eclinicalmedicine
|November 5, 2020
PubMed

Insights

CKD Patch improves cardiovascular disease risk prediction by incorporating kidney function measures. This method enhances existing risk calculators, providing more accurate assessments for patients with chronic kidney disease.

Area of Science:

  • Cardiology
  • Nephrology
  • Epidemiology

Background:

  • Chronic kidney disease (CKD) measures like eGFR and albuminuria are crucial for cardiovascular disease (CVD) risk prediction.
  • Current clinical guidelines lack standardized methods for integrating CKD measures into CVD risk prediction.
  • CKD Patch offers a validated approach to calibrate and enhance CVD risk predictions using CKD measures.

Purpose of the Study:

  • To develop and validate the CKD Patch method for improving CVD risk prediction.
  • To incorporate estimated glomerular filtration rate (eGFR) and albuminuria into established risk calculators.
  • To enhance the prediction of atherosclerotic CVD (ASCVD) and CVD mortality.

Main Methods:

  • Developed "CKD Patches" using data from 4,143,535 adults across 35 datasets.
  • Incorporated eGFR and albuminuria to enhance the Pooled Cohort Equation (PCE) for ASCVD and Systematic COronary Risk Evaluation (SCORE) for CVD mortality.
  • Validated the CKD Patch approach in 4,932,824 adults from 37 independent datasets.

Main Results:

  • CKD Patch significantly improved CVD mortality and ASCVD risk prediction in validation datasets (e.g., Δc-statistic 0.027 for CVD mortality, 0.010 for ASCVD).
  • Risk prediction for CVD mortality was substantially increased in individuals with very high-risk CKD (2.64-fold), high-risk CKD (1.86-fold), and moderate-risk CKD (1.37-fold) compared to SCORE.
  • Corresponding risk enhancements for ASCVD with PCE were 1.55-fold, 1.24-fold, and 1.21-fold, respectively, indicating underestimation by traditional methods in CKD patients.

Conclusions:

  • CKD Patch provides a quantitative method to enhance ASCVD and CVD mortality risk prediction.
  • This approach can be applied to risk equations recommended in major US and European guidelines.
  • Utilizing CKD measures with CKD Patch leads to more accurate CVD risk assessments for patients with chronic kidney disease.
Abstract

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