Analytical Validation of GFR NMR : A Blood-Based Multiple Biomarker Assay for Accurate Estimation of Glomerular Filtration Rate.
Markus FuhrmannAmauri Schwaeble SantamariaRenee ScottJeffrey W MeeusenMarianna FernandesJohn VenzVictoria RotheFrank StämmlerJochen EhrichEric SchifferPublished in: Diagnostics (Basel, Switzerland) (2022)
Accurate and precise monitoring of kidney function is critical for a timely and reliable diagnosis of chronic kidney disease (CKD). The determination of kidney function usually involves the estimation of the glomerular filtration rate (eGFR). We recently reported the clinical performance of a new eGFR equation (GFR NMR ) based on the nuclear magnetic resonance (NMR) measurement of serum myo-inositol, valine, and creatinine, in addition to the immunoturbidometric quantification of serum cystatin C, age and sex. We now describe the analytical performance evaluation of GFR NMR according to the Clinical and Laboratory Standards Institute guidelines. Within-laboratory coefficients of variation (CV%) of the GFR NMR equation did not exceed 4.3%, with a maximum CV% for repeatability of 3.7%. Between-site reproducibility (three sites) demonstrated a maximum CV% of 5.9%. GFR NMR stability was demonstrated for sera stored for up to 8 days at 2-10°C and for NMR samples stored for up to 10 days in the NMR device at 6 ± 2°C. Substance interference was limited to 4/40 (10.0%) of the investigated substances, resulting in an underestimated GFR NMR (for glucose and metformin) or a loss of results (for naproxen and ribavirin) for concentrations twice as high as usual clinical doses. The analytical performances of GFR NMR, combined with its previously reported clinical performance, support the potential integration of this NMR method into clinical practice.