Variability in eGFR and the Risk of Adverse Kidney Outcomes and All-Cause Mortality

Key Points Increased eGFR variability over 3 years independently predicts a higher risk of kidney outcomes and all-cause mortality. This association remained consistent across subgroups and sensitivity analyses. Routine eGFR variability assessment may enable identification of high-risk patients and provide an opportunity for the initiation of interventions. Background eGFR variability may predict adverse outcomes, such as cardiovascular events and mortality, yet its influence on kidney impairment progression in routine clinical practice is not well described. Methods This retrospective cohort study used longitudinal eGFR data from MedicineInsight, a comprehensive primary care database. We included adults (18 years or older) with at least three eGFR measurements over 3 years between January 1, 2011, and December 31, 2018. eGFR variability between visits was assessed using the coefficient of variation and categorized into groups by quintiles. A kidney composite end point, comprising a sustained 40% decline in eGFR from baseline, a sustained eGFR of <15 ml/min per 1.73 m 2 , and all-cause mortality, was tracked over a 3-year follow-up. Cox proportional hazards models quantified the association between eGFR variability and outcomes. Results Among 754,306 patients, with a mean age of 59.1 years and 58.0% female, higher eGFR variability was associated with an increased risk of the kidney composite end point (hazard ratio, 2.17;95% confidence interval, 2.03 to 2.32) for the highest versus lowest fifth after adjusting for mean eGFR and eGFR slope, as well as other cardiovascular disease risk factors and medication use. Similar trends were observed for components of the primary outcome and across all subgroups including age, sex, hypertension, diabetes, and baseline eGFR. Conclusions Increased eGFR variability independently predicts adverse kidney outcomes, underscoring its potential as a clinical biomarker for identifying high-risk patients. Including eGFR variability in routine kidney assessments may improve risk stratification, enabling timely interventions and potentially enhancing patient outcomes in primary care.

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Publication Details

Journal
Kidney360
Published
2025-10-27
DOI
https://doi.org/10.34067/kid.0000000988
Primary Topic
Cardiac Imaging and Diagnostics
Type
article
Field-Weighted Citation Impact
0.00

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article

Variability in eGFR and the Risk of Adverse Kidney Outcomes and All-Cause Mortality

Takaya Sasaki, Brendon Lange Neuen, Hannah Wallace, Jeffrey T. Ha et al.
Kidney360
Cardiac Imaging and Diagnostics
article

Variability in eGFR and the Risk of Adverse Kidney Outcomes and All-Cause Mortality

Takaya Sasaki, Brendon Lange Neuen, Hannah Wallace, Jeffrey T. Ha, Mark Woodward, Paul E. Ronksley, Takashi Yokoo, John Chalmers, Daniel Bekele Ketema, Luke Buizen, Sunil V. Badve, Martin Gallagher, Sradha S. Kotwal, Min Jun, Meg Jardine, Katie Harris
article en

Abstract

Key Points Increased eGFR variability over 3 years independently predicts a higher risk of kidney outcomes and all-cause mortality. This association remained consistent across subgroups and sensitivity analyses. Routine eGFR variability assessment may enable identification of high-risk patients and provide an opportunity for the initiation of interventions. Background eGFR variability may predict adverse outcomes, such as cardiovascular events and mortality, yet its influence on kidney impairment progression in routine clinical practice is not well described. Methods This retrospective cohort study used longitudinal eGFR data from MedicineInsight, a comprehensive primary care database. We included adults (18 years or older) with at least three eGFR measurements over 3 years between January 1, 2011, and December 31, 2018. eGFR variability between visits was assessed using the coefficient of variation and categorized into groups by quintiles. A kidney composite end point, comprising a sustained 40% decline in eGFR from baseline, a sustained eGFR of <15 ml/min per 1.73 m 2 , and all-cause mortality, was tracked over a 3-year follow-up. Cox proportional hazards models quantified the association between eGFR variability and outcomes. Results Among 754,306 patients, with a mean age of 59.1 years and 58.0% female, higher eGFR variability was associated with an increased risk of the kidney composite end point (hazard ratio, 2.17;95% confidence interval, 2.03 to 2.32) for the highest versus lowest fifth after adjusting for mean eGFR and eGFR slope, as well as other cardiovascular disease risk factors and medication use. Similar trends were observed for components of the primary outcome and across all subgroups including age, sex, hypertension, diabetes, and baseline eGFR. Conclusions Increased eGFR variability independently predicts adverse kidney outcomes, underscoring its potential as a clinical biomarker for identifying high-risk patients. Including eGFR variability in routine kidney assessments may improve risk stratification, enabling timely interventions and potentially enhancing patient outcomes in primary care.

Kidney360Vol. 7(2)
Jikei University School of Medicine (JP), The University of Sydney (AU), University of Calgary (CA), The George Institute for Global Health (GB), Concord Repatriation General Hospital (AU), Liverpool Hospital (AU), UNSW Sydney (AU), Prince of Wales Hospital (AU), The George Institute for Global Health (AU), St George Hospital (AU), Alberta Kidney Disease Network (CA), National Health and Medical Research Council (AU), Imperial College London (GB)
Eli Lilly and Company, National Institutes of Health
Openalex Percentile: Top 54%
Cardiac Imaging and Diagnostics
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