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Cystatin C: an improved estimator of glomerular filtration rate?

Omar F Laterza1, Christopher P Price, Mitchell G Scott

  • 1Washington University School of Medicine, Department of Pathology and Immunology, Division of Laboratory Medicine, Box 8118, 660 S. Euclid Ave., St. Louis, MO 63110, USA.

Clinical Chemistry
|April 30, 2002
PubMed

Insights

Serum creatinine (SCr) is a common marker for kidney function, but cystatin C (CysC) may offer advantages. This review suggests CysC performs at least as well as SCr and may be superior in specific patient groups for assessing glomerular filtration rate (GFR).

Area of Science:

  • Nephrology
  • Clinical Chemistry
  • Biomarker Analysis

Background:

  • Glomerular filtration rate (GFR) is crucial for assessing kidney function.
  • Current endogenous markers like serum creatinine (SCr) have limitations in certain clinical scenarios.
  • Cystatin C (CysC) is an alternative endogenous marker for GFR estimation.

Purpose of the Study:

  • To critically review the utility of cystatin C (CysC) for GFR assessment.
  • To evaluate CysC's performance, particularly in patient populations where it may outperform SCr.
  • To examine the evolution of CysC immunoassays, reference intervals, and diagnostic accuracy.

Main Methods:

  • Narrative review of primarily recent publications (last 5 years).
  • Medline search (June 2000-September 2001) for studies on CysC and GFR.
  • Inclusion criteria: >75 individuals (excluding renal transplant studies) and accepted GFR gold standards.

Main Results:

  • CysC levels in blood are independent of age and sex.
  • Of 24 studies on clinical utility, 15 found CysC superior to SCr, and 9 found it equivalent.
  • Summary ROC analysis of 20 studies indicates CysC is likely superior to SCr for detecting impaired GFR.

Conclusions:

  • Cystatin C (CysC) demonstrates at least equivalent performance to serum creatinine (SCr) in the general population.
  • CysC is likely superior to SCr for GFR assessment in specific patient subpopulations.
  • Further investigation into CysC's role in diverse clinical settings is warranted.
Abstract

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