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The Impact of Primary Renal Diagnosis on Prognosis and the Varying Predictive Power of Albuminuria in the NURTuRE-CKD Study

McDonnell, Thomas; Kalra, Philip A.; Vuilleumier, Nicolas; Cockwell, Paul; Wheeler, David C.; Fraser, Simon DS; Banks, Rosamonde E.; Taal, Maarten W.

Authors

Thomas McDonnell

Philip A. Kalra

Nicolas Vuilleumier

Paul Cockwell

David C. Wheeler

Simon DS Fraser

Rosamonde E. Banks



Abstract

Introduction: The definition of CKD is broad, which neglects the heterogeneity of risk across primary renal diseases.

Methods: The National Unified Renal Translational Research Enterprise (NURTuRE)-CKD is an ongoing UK, prospective multicenter cohort study of 2,996 adults with an eGFR of 15-59 mL/min/1.73 m2 or eGFR ≥60 mL/min/1.73 m2 with a urine albumin-to-creatinine ratio (uACR) >30 mg/mmol. Outcomes and predictive performance of eGFR and uACR were subcategorized by ERA-EDTA primary renal diagnosis (PRD) codes.

Results: 2,638 participants were included, with baseline median eGFR of 33.5 mL/min/1.73 m2 and uACR 29.8 mg/mmol. Over a median 49.2 months follow-up, 630 (23.9%) experienced kidney failure (KF), and 352 (13.3%) died before KF, the median eGFR slope was -1.97 mL/min/1.73 m2/year. There were significant differences in risk across the PRD, persisting after adjustment for age, sex, baseline eGFR, and modifiable risk factors (blood pressure, HbA1c, and renin-angiotensin-aldosterone system inhibitors). Diabetic kidney disease (DKD), glomerulonephritis, and familial/hereditary nephropathy were associated with the greatest risk, while tubulointerstitial disease and vasculitis carried a low risk of KF. eGFR had good predictive accuracy across all PRD. However, the addition of uACR showed variable benefit, depending on the PRD. The largest benefit was seen in vasculitis, renal vascular, and DKD groups, but uACR added no predictive value to the familial/hereditary group.

Conclusion: Significant differences in the risk of kidney-related outcomes occurred across the various primary renal diagnoses persisting after adjustment for age, sex, baseline eGFR, and modifiable risk factors. Albuminuria's discriminatory ability as a biomarker of progression varies by diagnosis. CKD care should, therefore, take a personalized approach that always considers the primary renal diagnosis.

Citation

McDonnell, T., Kalra, P. A., Vuilleumier, N., Cockwell, P., Wheeler, D. C., Fraser, S. D., Banks, R. E., & Taal, M. W. (2024). The Impact of Primary Renal Diagnosis on Prognosis and the Varying Predictive Power of Albuminuria in the NURTuRE-CKD Study. American Journal of Nephrology, 1-12. https://doi.org/10.1159/000541770

Journal Article Type Article
Acceptance Date Sep 29, 2024
Online Publication Date Oct 4, 2024
Publication Date Oct 4, 2024
Deposit Date Oct 3, 2024
Publicly Available Date Oct 5, 2025
Journal American Journal of Nephrology
Print ISSN 0250-8095
Electronic ISSN 1421-9670
Publisher Karger Publishers
Peer Reviewed Peer Reviewed
Pages 1-12
DOI https://doi.org/10.1159/000541770
Keywords Albuminuria; Chronic kidney disease; Precision medicine; Primary renal diagnosis; Risk stratification.
Public URL https://nottingham-repository.worktribe.com/output/40285561
Publisher URL https://karger.com/ajn/article/doi/10.1159/000541770/914344/The-Impact-of-Primary-Renal-Diagnosis-on-Prognosis