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  6. Validation Of The Klinrisk Chronic Kidney Disease Progression Model In The Fidelity Population

Validation of the Klinrisk chronic kidney disease progression model in the FIDELITY population

Navdeep Tangri1,2, Thomas Ferguson1,2, Silvia J Leon2,3

  • 1Department of Internal Medicine, Max Rady College of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.

Clinical Kidney Journal
|April 23, 2024

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View abstract on PubMed

Summary
This summary is machine-generated.

Klinrisk, a laboratory-based model, accurately predicts chronic kidney disease (CKD) progression in patients with type 2 diabetes. This tool aids in early identification of high-risk individuals, potentially delaying disease advancement.

Area of Science:

  • Nephrology
  • Clinical Epidemiology
Keywords:
Klinriskchronic kidney diseaseexternal validationkidney failure

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  • Biostatistics
  • Background:

    • Chronic kidney disease (CKD) affects over 800 million globally and is often underdiagnosed.
    • Early detection and intervention are crucial for slowing CKD progression.
    • Klinrisk is a validated model using laboratory data to predict CKD progression risk.

    Purpose of the Study:

    • To externally validate the Klinrisk model's predictive accuracy for CKD progression.
    • To assess Klinrisk's performance in a diverse patient population with CKD and type 2 diabetes within the FIDELITY trials.
    • To investigate potential interactions between finerenone treatment and risk prediction.

    Main Methods:

    • The FIDELITY trial cohort, including patients with CKD and type 2 diabetes, was used for validation up to 4 years.
    • Primary outcomes included a 40% or 57% decrease in estimated glomerular filtration rate (eGFR) or kidney failure.
    • Model performance was evaluated using area under the receiver operating characteristic curve (AUC) and calibration plots.

    Main Results:

    • Klinrisk demonstrated strong predictive accuracy for the primary outcome at 2 years (AUC=0.81) and 4 years (AUC=0.86).
    • The model showed appropriate calibration, with Brier scores of 0.067 (2 years) and 0.115 (4 years).
    • No significant interaction was found between finerenone treatment and CKD progression risk (P=0.31).

    Conclusions:

    • The Klinrisk model is accurate and useful for identifying patients at high risk of CKD progression.
    • Laboratory-based risk prediction facilitates early detection and management strategies for CKD.
    • The findings support the use of Klinrisk in clinical practice for proactive CKD patient care.
    laboratory-based prediction model