Literature DB >> 31495881

Choice of endpoint in kidney outcome trials: considerations from the EMPA-REG OUTCOME® trial.

Vlado Perkovic1, Audrey Koitka-Weber2,3,4, Mark E Cooper3, Guntram Schernthaner5, Egon Pfarr2, Hans J Woerle2, Maximilian von Eynatten2, Christoph Wanner4.   

Abstract

BACKGROUND: Doubling of serum creatinine [equivalent to 57% reduction in estimated glomerular filtration rate (eGFR)] is an established surrogate for end-stage kidney disease (ESKD); however, this endpoint necessitates lengthy follow-up and large sample sizes in clinical trials. We explored whether alternative eGFR decline thresholds provide more feasible surrogate kidney endpoints.
METHODS: The study involved post hoc analysis of the EMPA-REG OUTCOME® trial. Adults with type 2 diabetes, high cardiovascular risk and eGFR ≥30 mL/min/1.73 m2 were assigned empagliflozin 10 mg or 25 mg (n = 4687) or placebo (n = 2333), on top of standard of care. We assessed composite endpoints incorporating different eGFR decline thresholds (≥30, ≥40, ≥50 or ≥57%) combined with initiation of renal replacement therapy (RRT) or renal death. This trial is registered with ClinicalTrials.gov (NCT01131676).
RESULTS: Empagliflozin versus placebo significantly lowered the risk of decline in eGFR for each threshold listed above, combined with initiation of RRT or renal death, ranging from a hazard ratio (HR) of 0.81 [95% confidence interval (CI) 0.72-0.91] for endpoints based on 30% eGFR decline to an HR of 0.37 (0.23-0.61) for endpoints based on 57% eGFR decline. Lower thresholds (e.g. 30%) were associated with higher event rates but weaker treatment effects. The time to the 95% CI of the HR falling to <1.0 decreased with increasing eGFR threshold.
CONCLUSIONS: The composite of 40% decline in eGFR, ESKD or renal death appears to provide reliable results similar to the traditional 57% decline in eGFR.
© The Author(s) 2019. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.

Entities:  

Keywords:  CKD; ESKD; GFR; clinical trial; type 2 diabetes

Year:  2020        PMID: 31495881     DOI: 10.1093/ndt/gfz179

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  6 in total

1.  Dipeptidyl peptidase-4 inhibitors, glucagon-like peptide 1 receptor agonists and sodium-glucose co-transporter-2 inhibitors for people with cardiovascular disease: a network meta-analysis.

Authors:  Takayoshi Kanie; Atsushi Mizuno; Yoshimitsu Takaoka; Takahiro Suzuki; Daisuke Yoneoka; Yuri Nishikawa; Wilson Wai San Tam; Jakub Morze; Andrzej Rynkiewicz; Yiqiao Xin; Olivia Wu; Rui Providencia; Joey Sw Kwong
Journal:  Cochrane Database Syst Rev       Date:  2021-10-25

2.  Design, recruitment, and baseline characteristics of the EMPA-KIDNEY trial.

Authors: 
Journal:  Nephrol Dial Transplant       Date:  2022-06-23       Impact factor: 7.186

Review 3.  Review of potential biomarkers of inflammation and kidney injury in diabetic kidney disease.

Authors:  Vuthi Khanijou; Neda Zafari; Melinda T Coughlan; Richard J MacIsaac; Elif I Ekinci
Journal:  Diabetes Metab Res Rev       Date:  2022-07-11       Impact factor: 8.128

Review 4.  GLP-1 Receptor Agonists and Diabetic Kidney Disease: A Call of Attention to Nephrologists.

Authors:  José Luis Górriz; María José Soler; Juan F Navarro-González; Clara García-Carro; María Jesús Puchades; Luis D'Marco; Alberto Martínez Castelao; Beatriz Fernández-Fernández; Alberto Ortiz; Carmen Górriz-Zambrano; Jorge Navarro-Pérez; Juan José Gorgojo-Martinez
Journal:  J Clin Med       Date:  2020-03-30       Impact factor: 4.241

Review 5.  The Effect of Glucagon-Like Peptide-1 Receptor Agonists on Renal Outcomes in Type 2 Diabetes.

Authors:  Win L Yin; Steve C Bain; Thinzar Min
Journal:  Diabetes Ther       Date:  2020-03-17       Impact factor: 2.945

6.  Urinary Galectin-3 as a Novel Biomarker for the Prediction of Renal Fibrosis and Kidney Disease Progression.

Authors:  Shuo-Ming Ou; Ming-Tsun Tsai; Huan-Yuan Chen; Fu-An Li; Kuo-Hua Lee; Wei-Cheng Tseng; Fu-Pang Chang; Yao-Ping Lin; Ruey-Bing Yang; Der-Cherng Tarng
Journal:  Biomedicines       Date:  2022-03-02
  6 in total

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