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Abstract: SA-OR013

Association of eGFR Decline with Clinical Outcomes in Real-World US Patients with CKD

Session Information

Category: CKD (Non-Dialysis)

  • 2301 CKD (Non-Dialysis): Epidemiology, Risk Factors, and Prevention

Authors

  • Erickson, Kevin F., Baylor College of Medicine, Department of Medicine-Nephrology, Houston, Texas, United States
  • Modley, Ben, leads.healthcare, Staufen, Germany
  • Winkelmayer, Wolfgang C., Baylor College of Medicine, Department of Medicine-Nephrology, Houston, Texas, United States
  • Fotheringham, James, Sheffield University, School of Medicine and Population Health, Sheffield, United Kingdom
  • Zhang, Ling, Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, Connecticut, United States
  • Du, Chengan, Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, Connecticut, United States
  • Steubl, Dominik, Boehringer Ingelheim International GmbH & Co. KG, Ingelheim am Rhein, Germany
  • Wittrup-Jensen, Villum, Boehringer Ingelheim International GmbH & Co. KG, Ingelheim am Rhein, Germany
  • Akehurst, Ronald L., Lumanity, London, United Kingdom
  • Boersma, Cornelis, University of Groningen, Faculty of Medical Sciences, Groningen, Netherlands
  • Postma, Maarten J., Health-Ecore B.V., Zeist, Netherlands
Background

Estimated glomerular filtration rate (eGFR) decline is a surrogate endpoint in clinical trials for chronic kidney disease (CKD) widely accepted by regulatory authorities as a valid predictor of kidney failure. However, uptake of eGFR decline in real-world practice as a formal indicator of adverse outcomes is limited. This study explored the clinical significance of a sustained ≥40% eGFR decline as a predictor of kidney failure and cardiovascular (CV) outcomes in real-world US patients.

Methods

We used US Optum Market Clarity database linked claims and electronic health records (10/2015–9/2023) to identify patients with CKD, defined as ≥2 eGFR measures <90 mL/min/1.73 m2 within 1 year and ≥90 days apart. A baseline (BL) period of ≤3 years, based on a median follow-up of 2–2.4 years in CKD trials, was defined by the time from first eGFR value at start of baseline until ≥40% decline in eGFR (start of follow-up).1,2 To eliminate immortal time bias, controls without ≥40% eGFR decline were matched to cases at BL. Time-to-event analyses were conducted to estimate the incidence and rate ratios of kidney failure, CV death, and hospitalizations for myocardial infarction, heart failure, or stroke during follow-up in cases vs controls, adjusted for BL covariates.

Results

116,828 cases with ≥40% eGFR decline were matched to 414,084 controls. Mean follow-up was 3.4 years. Incidence rates of all study outcomes were >2-fold increased among cases vs controls (p<0.0001, Table 1).

Conclusion

These findings show a strong association between ≥40% eGFR decline over a 3-year period and longer-term adverse clinical outcomes in patients with CKD, thus supporting its potential as an effective risk predictor for kidney and CV complications and outcomes.

1Heerspink HJL, et al. N Engl J Med. 2020;383(15):1436-1446.
2The E-KCG, et al. N Engl J Med. 2023;388(2):117-127.

Funding

  • Commercial Support – Boehringer Ingelheim

Digital Object Identifier (DOI)