» Articles » PMID: 39950153

Clinically Meaningful EGFR Slope As a Surrogate Endpoint Differs Across CKD Stages and Slope Evaluation Periods: the CKD-JAC Study

Abstract

Background: The slope of estimated glomerular filtration rate (eGFR) is a promising surrogate endpoint in patients with chronic kidney disease (CKD). However, current evidence is mainly derived from Western populations with CKD stages 1-3. In addition, stage-by-stage analysis has never been formally performed.

Methods: We analyzed data from the Chronic Kidney Disease Japan Cohort Study, which included a large proportion of patients with CKD stages 4 and 5. We estimated eGFR slopes over three evaluation periods (0.5, 1, and 2 years) using mixed effects models and examined their associations with kidney failure with replacement therapy across CKD stages.

Results: Of 2713 patients with an available 1-year eGFR slope, 985 subsequently initiated kidney replacement therapy. Overall, a slower eGFR decline was strongly associated with a lower risk of subsequent kidney failure with replacement therapy. The association was pronounced with higher baseline CKD stages and attenuated with shorter evaluation periods. The estimated deceleration in eGFR decline over 1 year associated with a 20% lower risk of subsequent kidney failure with replacement therapy was 1.91 (1.60-2.37), 1.12 (1.00-1.28), and 1.06 (0.81-1.60) ml/min/1.73 m per year in patients with CKD stages 3, 4, and 5, respectively.

Conclusion: Our results support the potential of eGFR slope as a surrogate across different stages of CKD in Asians and suggest that a shorter evaluation period than 2 years may be feasible for patients with late-stage CKD. Our findings provide valuable insights for the future design of clinical trials in CKD patients, especially those with more advanced CKD.

References
1.
Inker L, Heerspink H, Tighiouart H, Levey A, Coresh J, Gansevoort R . GFR Slope as a Surrogate End Point for Kidney Disease Progression in Clinical Trials: A Meta-Analysis of Treatment Effects of Randomized Controlled Trials. J Am Soc Nephrol. 2019; 30(9):1735-1745. PMC: 6727261. DOI: 10.1681/ASN.2019010007. View

2.
Levey A, Gansevoort R, Coresh J, Inker L, Heerspink H, Grams M . Change in Albuminuria and GFR as End Points for Clinical Trials in Early Stages of CKD: A Scientific Workshop Sponsored by the National Kidney Foundation in Collaboration With the US Food and Drug Administration and European Medicines Agency. Am J Kidney Dis. 2019; 75(1):84-104. DOI: 10.1053/j.ajkd.2019.06.009. View

3.
Looker H, Mauer M, Saulnier P, Harder J, Nair V, Boustany-Kari C . Changes in Albuminuria But Not GFR are Associated with Early Changes in Kidney Structure in Type 2 Diabetes. J Am Soc Nephrol. 2019; 30(6):1049-1059. PMC: 6551789. DOI: 10.1681/ASN.2018111166. View

4.
Chin M, Bakris G, Block G, Chertow G, Goldsberry A, Inker L . Bardoxolone Methyl Improves Kidney Function in Patients with Chronic Kidney Disease Stage 4 and Type 2 Diabetes: Post-Hoc Analyses from Bardoxolone Methyl Evaluation in Patients with Chronic Kidney Disease and Type 2 Diabetes Study. Am J Nephrol. 2018; 47(1):40-47. PMC: 5841134. DOI: 10.1159/000486398. View

5.
Coresh J, Heerspink H, Sang Y, Matsushita K, Arnlov J, Astor B . Change in albuminuria and subsequent risk of end-stage kidney disease: an individual participant-level consortium meta-analysis of observational studies. Lancet Diabetes Endocrinol. 2019; 7(2):115-127. PMC: 6379893. DOI: 10.1016/S2213-8587(18)30313-9. View