GFR estimation based on standardized creatinine and cystatin C: a European multicenter analysis in older adults

Author:

Björk Jonas12,Bäck Sten Erik3,Ebert Natalie4,Evans Marie5,Grubb Anders3,Hansson Magnus6,Jones Ian7,Lamb Edmund J.8,Martus Peter9,Schaeffner Elke4,Sjöström Per7,Nyman Ulf10

Affiliation:

1. Division of Occupational and Environmental Medicine , Lund University , Lund , Sweden

2. Clinical Studies Sweden, Forum South , Skåne University Hospital , Lund , Sweden

3. Department of Clinical Chemistry , Skåne University Hospital , Lund , Sweden

4. Division of Nephrology and Intensive Care Medicine, Charite´ Campus Virchow , Berlin , Germany

5. Department of Clinical Sciences Intervention and Technology , Karolinska Institute and Karolinska University Hospital Huddinge , Stockholm , Sweden

6. Department of Clinical Chemistry , Karolinska Institute and Karolinska University Hospital Huddinge , Stockholm , Sweden

7. Faculty of Medicine and Health , Örebro University , Örebro , Sweden

8. Clinical Biochemistry , East Kent Hospitals University NHS Foundation Trust , Canterbury, Kent , UK

9. Institute of Medical Biostatistics , Eberhard Karls University Tübingen , Tübingen , Germany

10. Department of Translational Medicine, Division of Medical Radiology , Lund University , Malmö , Sweden , Phone: +46-733-842244

Abstract

Abstract Background: Although recommended by the Kidney Disease Improving Global Outcomes, the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPICR) creatinine equation was not targeted to estimate glomerular filtration rate (eGFR) among older adults. The Berlin Initiative Study (BIS1CR) equation was specifically developed in older adults, and the Lund-Malmö revised (LMRCR) and the Full Age Spectrum (FASCR) equations have shown promising results in older adults. Our aim was to validate these four creatinine equations, including addition of cystatin C in a large multicenter cohort of Europeans ≥70 years. Methods: A total of 3226 individuals (2638 with cystatin C) underwent GFR measurement (mGFR; median, 44 mL/min/1.73 m2) using plasma iohexol clearance. Bias, precision (interquartile range [IQR]), accuracy (percent of estimates ±30% of mGFR, P30), eGFR accuracy diagrams and probability diagrams to classify mGFR<45 mL/min/1.73 m2 were compared. Results: The overall results of BIS1CR/CKD-EPICR/FASCR/LMRCR were as follows: median bias, 1.7/3.6/0.6/−0.7 mL/min/1.73 m2; IQR, 11.6/12.3/11.1/10.5 mL/min/1.73 m2; and P30, 77.5%/76.4%/80.9%/83.5% (significantly higher for LMR, p<0.001). Substandard P30 (<75%) was noted for all equations at mGFR<30 mL/min/1.73 m2, and at body mass index values <20 and ≥35 kg/m2. LMRCR had the most stable performance across mGFR subgroups. Only LMRCR and FASCR had a relatively constant small bias across eGFR levels. Probability diagrams exhibited wide eGFR intervals for all equations where mGFR<45 could not be confidently ruled in or out. Adding cystatin C improved P30 accuracy to 85.7/86.8/85.7/88.7 for BIS2CR+CYS/CKD-EPICR+CYS/FASCR+CYS/MEANLMR+CAPA. Conclusions: LMRCR and FASCR seem to be attractive alternatives to CKD-EPICR in estimating GFR by creatinine-based equations in older Europeans. Addition of cystatin C leads to important improvement in estimation performance.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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