4.4 Article

Frequency of Renal Monitoring - Creatinine and Cystatin C (FORM-2C): an observational cohort study of patients with reduced eGFR in primary care

Journal

BRITISH JOURNAL OF GENERAL PRACTICE
Volume 71, Issue 710, Pages E677-+

Publisher

ROYAL COLL GENERAL PRACTITIONERS
DOI: 10.3399/BJGP.2020.0940

Keywords

chronic kidney diseases; creatinine cystatin C; estimated glomerular filtration rate; primary care

Funding

  1. National Institute for Health Research (NIHR) Programme Grants for Applied Research [RP-PG-1210-12003]
  2. University of Oxford
  3. National Institutes of Health Research (NIHR) [RP-PG-1210-12003] Funding Source: National Institutes of Health Research (NIHR)

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This study compared the effectiveness of estimating eGFR using serum creatinine and serum cystatin C for predicting renal function decline in patients with eGFR of 30-89 ml/min/1.73 m(2). The results showed that in patients with eGFR <60 ml/min/1.73 m(2), serum cystatin C-derived eGFR was more predictive than serum creatinine-derived eGFR for future decline in kidney function.
Background Monitoring is the mainstay of chronic kidney disease management in primary care; however, them is little evidence about the best way to do this. Aim To compare the effectiveness of estimated glomerular filtration rate (eGFR) derived from serum creatinine and serum cystatin C to predict renal function decline among those with a recent eGFR of 30-89 ml/min/1.73 m(2). Design and setting Observational cohort study in UK primary care. Method Serum creatinine and serum cystatin C were both measured at seven study visits over 2 years in 750 patients aged >= 18 years with an eGFR of 30-89 ml/min/1.73 m(2) within the previous year The primary outcome was change in eGFR derived from serum creatinine or serum cystatin C between 6 and 24 months. Results Average change in eGFR was 0.51 ml/min/1.73 m(2)/year when estimated by serum creatinine and -2.35 ml/min/1.73 m(2)/year when estimated by serum cystatin C. The c-statistic for predicting renal decline using serum creatinine derived eGFR was 0.495 [95% confidence interval [Cl] = 0.471 to 0.519]. The equivalent c-statistic using serum cystatin C-derived eGFR was 0.497 [95% Cl. 0.468 to 0.525). Similar results were obtained when restricting analyses to those aged >= 75 or <75 years. or with eGFR >= 60 ml/min/1.73 m(2). In those with eGFR <60 ml/min/1.73 m(2). serum cystatin C-derived eGFR was more predictive than serum creatinine-derived eGFR for future decline in kidney function. Conclusion In the primary analysis neither eGFR estimated from serum creatinine nor from serum cystatin C predicted future change in kidney function. partly due to small changes during 2 years. In some secondary analyses there was a suggestion that serum cystatin C was a more useful biomarker to estimate eGFR, especially in those with a baseline eGFR <60 ml/min/1.73 m(2).

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