Cardiovascular risk prediction in people with chronic kidney disease

Kunihiro Matsushita1, Shoshana H Ballew, Josef Coresh

  • 1aDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health bWelch Center for Prevention, Epidemiology, and Clinical Research, Baltimore, Maryland, USA.

Insights

Measures of chronic kidney disease (CKD), such as albuminuria and estimated glomerular filtration rate (eGFR), significantly improve cardiovascular disease (CVD) risk prediction. Albuminuria shows a more pronounced effect than eGFR, suggesting updated guidelines are needed.

Area of Science:

  • Nephrology
  • Cardiology
  • Epidemiology

Background:

  • Clinical guidelines lack consistency on using chronic kidney disease (CKD) measures for cardiovascular disease (CVD) risk prediction.
  • Existing studies often use varied definitions and statistical methods, hindering direct comparisons.

Purpose of the Study:

  • To review recent literature on the utility of CKD measures in predicting CVD risk.
  • To inform potential updates to clinical guidelines regarding CVD risk assessment in CKD patients.

Main Methods:

  • Review of recent literature on CKD and CVD risk prediction.
  • Analysis of a large individual-level meta-analysis from the CKD Prognosis Consortium (over 630,000 participants).
  • Inclusion of studies examining creatinine-based eGFR, albuminuria, cystatin C, β2-microglobulin, coronary artery calcium, and cardiac troponins.

Main Results:

  • Estimated glomerular filtration rate (eGFR) and albuminuria improve CVD risk prediction beyond traditional factors, especially for CVD mortality and heart failure.
  • Albuminuria provides a more significant improvement in CVD risk prediction compared to eGFR.
  • Additional biomarkers like cystatin C, β2-microglobulin, coronary artery calcium, and cardiac troponins may further enhance CVD prediction in CKD.

Conclusions:

  • CKD measures, particularly albuminuria, are valuable additions to CVD risk prediction models.
  • Further research and guideline updates are necessary to integrate these biomarkers effectively.
  • The utility of specific biomarkers depends on the CVD outcome, population, and data availability.
Abstract

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