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Predicting Lifetime Risk of Kidney Failure Using Age and a Single eGFR Measurement.

Ryo Enoki1, Mariko Miyazaki1, Enyu Imai2

  • 1Department of Nephrology, Graduate School of Medicine, Tohoku University, Sendai 980-8574, Japan.

Journal of Clinical Medicine
|April 14, 2026
PubMed
Summary
This summary is machine-generated.

A new age + estimated glomerular filtration rate (eGFR) model simplifies chronic kidney disease (CKD) risk stratification at initial visits. This tool aids in guiding surveillance and early interventions for better patient outcomes.

Keywords:
age–eGFR indexchronic kidney disease progressioneGFR trajectory modelingsingle-point risk assessment

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Area of Science:

  • Nephrology
  • Geriatrics
  • Predictive Modeling

Background:

  • Chronic kidney disease (CKD) prognosis typically relies on longitudinal data, complicating initial risk assessment.
  • Current clinical decisions based on estimated glomerular filtration rate (eGFR) often neglect patient age.
  • A simplified predictive model is needed to address these limitations.

Purpose of the Study:

  • To develop a simplified predictive model for progressive CKD incorporating patient age and eGFR.
  • To quantify the impact of clinical interventions like smoking cessation and pharmacotherapies on CKD progression.
  • To evaluate the clinical utility of the age + eGFR model compared to conventional methods.

Main Methods:

  • Utilized a historical dataset from the pre-renin-angiotensin system inhibitor (RASi) and pre-sodium-glucose cotransporter 2 inhibitor (SGLT2i) era (1988-2003).
  • Developed heatmaps to predict the probability of reaching eGFR < 30 mL/min/1.73 m² by age 80.
  • Assessed predictive performance using calibration, discrimination metrics, and decision curve analysis.

Main Results:

  • Age and eGFR showed a correlation with CKD progression risk; e.g., at age 40, an eGFR of ~57 mL/min/1.73 m² indicated a 50% risk of reaching stage 4 CKD by age 80.
  • The age + eGFR model demonstrated acceptable calibration and discrimination.
  • Smoking cessation reduced risk by 9.4-11.2%; combined RASi and SGLT2i treatment reduced progression probability by 31.2-40.0%.

Conclusions:

  • The age + eGFR rule offers a simple, interpretable method for age-adjusted risk stratification using a single eGFR measurement.
  • This heuristic may enhance clinical utility in guiding surveillance intensity and early intervention strategies.
  • External validation is necessary before widespread clinical application.