A retrospective study on development and internal validation of cardiovascular disease risk prediction model for

Huixia Liu1, Jing Xiong1

  • 1Department of Nephrology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Peerj
|June 10, 2026
PubMed

Insights

Cardiovascular disease (CVD) risk in chronic kidney disease (CKD) patients is better predicted by a new model including inflammatory and imaging markers. This model improves upon traditional risk factors for CKD stages 3-5.

Area of Science:

  • Nephrology
  • Cardiology
  • Biomarkers

Background:

  • Cardiovascular disease (CVD) is the primary cause of death in chronic kidney disease (CKD) patients.
  • Traditional CVD risk factors are less effective in predicting outcomes in advanced CKD.
  • Novel biomarkers are needed to improve CVD risk prediction in CKD.

Purpose of the Study:

  • To develop and validate a 5-year CVD risk prediction model for CKD stages 3-5.
  • To integrate clinical, laboratory, and imaging parameters into the prediction model.
  • To enhance the accuracy of CVD risk assessment in CKD patients.

Main Methods:

  • Recruited 301 CKD stages 3-5 patients with follow-up until July 2022.
  • Utilized LASSO and multivariable logistic regression to identify predictors.
  • Internally validated the model using tenfold cross-validation and assessed performance with c-statistic and Hosmer-Lemeshow test.

Main Results:

  • 169 (56.1%) patients experienced a CVD event within 5 years.
  • C-reactive protein (CRP) and interventricular septum thickness (IVS) improved predictive performance when added to traditional factors.
  • The full model achieved an AUC of 0.845 (95% CI [0.802-0.888]) with excellent calibration.

Conclusions:

  • A validated clinical risk prediction model for 5-year CVD events in CKD stages 3-5 was established.
  • The model incorporates readily available clinical, inflammatory, and imaging variables.
  • This tool aims to improve CVD risk prediction and management in CKD patients.
Abstract

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