Population-wide eGFR percentiles in younger adults and clinical outcomes

Author:

Hussain Junayd123,Imsirovic Haris1,Talarico Robert1,Akbari Ayub4,Ravani Pietro56,Tanuseputro Peter127,Hundemer Gregory L247ORCID,Ramsay Tim17ORCID,Tangri Navdeep8,Knoll Greg A47,Bugeja Ann147ORCID,Sood Manish M247

Affiliation:

1. School of Epidemiology and Public Health, University of Ottawa , Ottawa, Ontario , Canada

2. Institute of Clinical Evaluative Sciences (ICES) , Ottawa, Ontario , Canada

3. Michael G. DeGroote School of Medicine, McMaster University , Hamilton, Ontario , Canada

4. Division of Nephrology, Department of Medicine, The Ottawa Hospital , Ottawa, Ontario , Canada

5. Department of Medicine, University of Calgary , Calgary, Alberta , Canada

6. Department of Community Health Sciences, University of Calgary , Calgary, Alberta , Canada

7. Ottawa Hospital Research Institute, The Ottawa Hospital , Ottawa, Ontario , Canada

8. Division of Nephrology, Max Rady College of Medicine, University of Manitoba , Winnipeg, Manitoba , Canada

Abstract

ABSTRACT Background and hypothesis Identifying meaningful estimated glomerular filtration rate (eGFR) reductions in younger adults (<65 years) could guide prevention efforts. To aid in interpretation and identification of young adults at risk, we examined the association of population-level eGFR percentiles relative to the median by age and clinical outcomes. Methods We conducted a retrospective cohort study of 8.7 million adults from Ontario, Canada aged from 18 to 65 years from 2008 to 2021 with an eGFR measure (both single outpatient value and repeat measures). We calculated median eGFR values by age and examined the association of reduced eGFR percentiles (≤10th, 5th, 2.5th, and 1st) with outcomes using time to event models. Outcomes were a composite of all-cause mortality, major adverse cardiac outcomes (MACE) with/without heart failure (MACE+), and kidney failure as well as each component individually. Results From the age of 18 to 65, the median eGFR declined with age (range 128 to 90) and across percentiles [eGFR ranges 102 to 68 for ≤10th, 96 to 63 for ≤5th, 90 to 58 for ≤2.5th and 83 to 54 for 1st]. The adjusted rate for any adverse outcome was elevated at ≤10th percentile (HR 1.14 95%CI 1.10–1.18) and was consistent for all-cause mortality, MACE, MACE+, and predominant for kidney failure (HR 5.57 95%CI 3.79–8.19) compared to the median eGFR for age. Young adults with an eGFR in the lower percentiles were less likely to be referred to a specialist, have a repeat eGFR, or albumin to creatinine ratio measure. Conclusions eGFR values at the 10th percentile or lower based on a population-level distribution are associated with adverse clinical outcomes and in younger adults (18 to 39) this corresponds to a higher level of eGFR that may be underrecognized. Application of population-based eGFR percentiles may aid interpretation and improve identification of younger adults at risk.

Funder

Ottawa Hospital

Academic Medical Organization Innovation Fund

Publisher

Oxford University Press (OUP)

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