Performance of Cystatin C– and Creatinine-Based Estimated Glomerular Filtration Rate Equations Depends on Patient Characteristics

Author:

Meeusen Jeffrey W1,Rule Andrew D23,Voskoboev Nikolay1,Baumann Nikola A1,Lieske John C12

Affiliation:

1. Department of Laboratory Medicine and Pathology

2. Department of Internal Medicine, Division of Nephrology and Hypertension, and

3. Department of Health Sciences Research Division of Epidemiology, Mayo Clinic, Rochester, MN

Abstract

Abstract BACKGROUND The Kidney Disease Improving Global Outcomes (KDIGO) guideline recommends use of a cystatin C–based estimated glomerular filtration rate (eGFR) to confirm creatinine-based eGFR between 45 and 59 mL · min−1 · (1.73 m2)−1. Prior studies have demonstrated that comorbidities such as solid-organ transplant strongly influence the relationship between measured GFR, creatinine, and cystatin C. Our objective was to evaluate the performance of cystatin C–based eGFR equations compared with creatinine-based eGFR and measured GFR across different clinical presentations. METHODS We compared the performance of the CKD-EPI 2009 creatinine-based estimated GFR equation (eGFRCr) and the newer CKD-EPI 2012 cystatin C–based equations (eGFRCys and eGFRCr-Cys) with measured GFR (iothalamate renal clearance) across defined patient populations. Patients (n = 1652) were categorized as transplant recipients (n = 568 kidney; n = 319 other organ), known chronic kidney disease (CKD) patients (n = 618), or potential kidney donors (n = 147). RESULTS eGFRCr-Cys showed the most consistent performance across different clinical populations. Among potential kidney donors without CKD [stage 2 or higher; eGFR >60 mL · min−1 · (1.73 m2)−1], eGFRCys and eGFRCr-Cys demonstrated significantly less bias than eGFRCr; however, all 3 equations substantially underestimated GFR when eGFR was <60 mL · min−1 · (1.73 m2)−1. Among transplant recipients with CKD stage 3B or greater [eGFR <45 mL · min−1 · (1.73 m2)−1], eGFRCys was significantly more biased than eGFRCr. No clear differences in eGFR bias between equations were observed among known CKD patients regardless of eGFR range or in any patient group with a GFR between 45 and 59 mL · min−1 · (1.73 m2)−1. CONCLUSIONS The performance of eGFR equations depends on patient characteristics that are readily apparent on presentation. Among the 3 CKD-EPI equations, eGFRCr-Cys performed most consistently across the studied patient populations.

Funder

Mayo Foundation

Mayo Clinic

NIDDK

National Center for Advancing Translational Sciences

NIH

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

Reference28 articles.

1. Estimating glomerular filtration rate from serum creatinine and cystatin C;Inker;N Engl J Med,2012

2. KDIGO 2012 Clinical Practice Guideline for the evaluation and management of chronic kidney disease;Kidney Disease: Improving Global Outcomes (KDIGO) CKD Work Group;Kidney Int Suppl,2013

3. Glomerular filtration rate estimated by cystatin C among different clinical presentations;Rule;Kidney Int,2006

4. Performance of creatinine-based GFR estimating equations in solid-organ transplant recipients;Shaffi;Am J Kidney Dis,2014

5. Relative performance of the MDRD and CKD-EPI equations for estimating glomerular filtration rate among patients with varied clinical presentations;Murata;Clin J Am Soc Nephrol,2011

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