Discordance in Creatinine- and Cystatin C–Based eGFR and Clinical Outcomes

Michelle M. Estrella(Kidney Research UK), Shoshana H. Ballew(Kidney Research UK), Yingying Sang(Kidney Research UK), Morgan E. Grams(Kidney Research UK), Josef Coresh(Kidney Research UK), Aditya Surapaneni(Kidney Research UK), Natalia Alencar de Pinho(Inserm), Johan Ärnlöv(Dalarna University), Hermann Brenner(German Cancer Research Center), Juan Jesús Carrero(Kidney Research UK), Teresa K. Chen(Kidney Research UK), Debbie L. Cohen(University of Pennsylvania), Mary Cushman(University of Vermont), Ron T. Gansevoort(University Medical Center Groningen), Shih‐Jen Hwang(National Institutes of Health), Lesley A. Inker(Tufts Medical Center), Joachim H. Ix(UC San Diego Health System), Keiko Kabasawa(Kidney Research UK), Tsuneo Konta(Yamagata University), Jennifer S. Lees(Kidney Research UK), Kevan R. Polkinghorne(Kidney Research UK), Michael G. Shlipak(Kidney Research UK), Robin W.M. Vernooij(Utrecht University), David C. Wheeler(University College London), Ashok K. Yadav(Post Graduate Institute of Medical Education and Research), Andrew S. Levey(Tufts Medical Center), Kai‐Uwe Eckardt(Friedrich-Alexander-Universität Erlangen-Nürnberg), Teresa K. Chen(Kidney Research UK), Yingying Sang(Kidney Research UK), Morgan E. Grams(Kidney Research UK), Josef Coresh(Kidney Research UK), Steven J. Chadban(Kidney Research UK), Kevan Polkinghorne(Kidney Research UK), Nisha Bansal(Kidney Research UK), Joachim H. Ix(UC San Diego Health System), Michael G. Shlipak(Kidney Research UK), Marie-Hélène Metzger(Kidney Research UK), Bénédicte Stengel(Kidney Research UK), Martin Landray(Kidney Research UK), John Townend(Kidney Research UK), Jonathan Emberson(Kidney Research UK), Chi‐yuan Hsu(Kidney Research UK), Wei Yang(Kidney Research UK), Amanda Anderson(Kidney Research UK), Hermann Brenner(German Cancer Research Center), Dietrich Rothenbacher(Kidney Research UK), Ben Schöttker(Kidney Research UK), Hannah Stocker(Kidney Research UK), Daniel Levy(Kidney Research UK), Martin Larson(Kidney Research UK), Anna Köttgen(Kidney Research UK), Peggy Sekula(Kidney Research UK), Ulla T. Schultheiß(Kidney Research UK), Markus P. Schneider(Kidney Research UK), Vivek Kumar(Kidney Research UK), Manisha Sahay(Kidney Research UK), Narayan Prasad(Kidney Research UK), Robin W.M. Vernooij(Utrecht University), Andrew S. Levey(Tufts Medical Center), Lesley A. Inker(Tufts Medical Center), Mark J. Sarnak(Kidney Research UK), Orlando M. Gutiérrez(Kidney Research UK), Mary Cushman(University of Vermont), Stephan J. L. Bakker(Kidney Research UK), Lyanne M. Kieneker(Kidney Research UK), Marco van Londen(Kidney Research UK), Katharine L. Cheung(Kidney Research UK), Titilayo O. Ilori(Kidney Research UK), Edouard L. Fu(Kidney Research UK), Anne‐Laure Faucon(Kidney Research UK), Aurora Caldinelli(Kidney Research UK), Antoine Créon(Kidney Research UK), Tsuneo Konta(Yamagata University), Kazunobu Ichikawa(Kidney Research UK), Satoru Nagase(Kidney Research UK), Masafumi Watanabe(Kidney Research UK), Jennifer S. Lees(Kidney Research UK), Patrick B. Mark(Kidney Research UK), Anders Larsson(Kidney Research UK), Vilmantas Giedraitis(Kidney Research UK), Keiko Kabasawa(Kidney Research UK), Yumi Ito(Kidney Research UK), Junta Tanaka(Kidney Research UK), Ichiei Narita(Kidney Research UK), Michelle M. Estrella(Kidney Research UK), Shoshana H. Ballew(Kidney Research UK), Juan Jesús Carrero(Kidney Research UK), Ron T. Gansevoort(University Medical Center Groningen), Kunihiro Matsushita(Kidney Research UK), Dorothea Nitsch(Kidney Research UK), Angela Yee‐Moon Wang(Kidney Research UK), Carina Flaherty(Kidney Research UK), Aditya Surapaneni(Kidney Research UK)
JAMA
November 7, 2025
Cited by 6Open Access
Full Text

Abstract

Importance: Estimated glomerular filtration rates (eGFRs) can differ according to whether creatinine or cystatin C is used for the eGFR calculation, but the prevalence and importance of these differences remain unclear. Objectives: To evaluate the prevalence of a discordance between cystatin C-based eGFR (eGFRcys) and creatinine-based eGFR (eGFRcr), identify characteristics associated with greater discordance, and evaluate associations of discordance with adverse outcomes. Data Sources: Participants in the Chronic Kidney Disease Prognosis Consortium (CKD-PC). Study Selection: Participants with concurrent cystatin C and creatinine measurements and clinical outcome measurement. Data Extraction and Synthesis: Between April 2024 and August 2025, data were synthesized using individual-level meta-analysis. Main Outcomes and Measures: The primary independent measurement was a large negative eGFR difference (eGFRdiff), defined as an eGFRcys that was at least 30% lower than eGFRcr. Secondary (dependent) outcomes included all-cause and cardiovascular mortality, atherosclerotic cardiovascular disease, heart failure, and kidney failure with replacement therapy. Results: A total of 821 327 individuals from 23 outpatient cohorts (mean [SD] age, 59 [12] years; 48% female; 13.5% with diabetes; 40% with hypertension) and 39 639 individuals from 2 inpatient cohorts (mean [SD] age, 67 [16] years; 31% female; 30% with diabetes; 72% with hypertension) were included. Among outpatient participants, 11% had a large negative eGFRdiff (range, 3%-50%). Among inpatients, 35% had a large negative eGFRdiff. Among outpatient participants, at a mean (SD) follow-up of 11 (4) years, a large negative eGFRdiff, compared with an eGFRdiff between -30% and 30%, was associated with higher rates of all-cause mortality (28.4 vs 16.8 per 1000 person-years [PY]; hazard ratio [HR], 1.69 [95% CI, 1.57-1.82]), cardiovascular mortality (6.1 vs 3.8 per 1000 PY; HR, 1.61 [95% CI, 1.48-1.76]), atherosclerotic cardiovascular disease (13.3 vs 9.8 per 1000 PY; HR, 1.35 [95% CI, 1.27-1.44]), heart failure (13.2 vs 8.6 per 1000 PY; HR, 1.54 [95% CI, 1.40-1.68]), and kidney failure with replacement therapy (2.7 vs 2.1 per 1000 PY; HR, 1.29 [95% CI, 1.13-1.47]). Conclusions and Relevance: In the CKD-PC, 11% of outpatient participants and 35% of hospitalized patients had an eGFRcys that was at least 30% lower than their eGFRcr. In the outpatient setting, presence of eGFRcys at least 30% lower than eGFRcr was associated with significantly higher rates of all-cause mortality, cardiovascular events, and kidney failure.


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