A Risk Score to Guide Cystatin C Testing to Detect Occult-Reduced Estimated Glomerular Filtration Rate

Carmen A Peralta1, Paul Muntner, Rebecca Scherzer

  • 1San Francisco Veterans Affairs Medical, San Francisco, Calif., USA.

Insights

A new risk score can identify individuals with reduced kidney function (eGFRcys<60) missed by standard creatinine tests. This tool helps screen patients effectively for better health outcomes.

Area of Science:

  • Nephrology
  • Clinical Chemistry
  • Epidemiology

Background:

  • Occult-reduced estimated glomerular filtration rate (eGFR<60 ml/min/1.73 m2) detected by serum cystatin C but missed by creatinine poses a high risk for complications.
  • There is a need for tools to guide cystatin C testing among individuals with preserved kidney function based on creatinine (eGFRcreat>60 ml/min/1.73 m2).

Purpose of the Study:

  • To develop and validate a risk score for identifying individuals with reduced eGFR by cystatin C (eGFRcys<60 ml/min/1.73 m2).
  • To assess the utility of this risk score in guiding cystatin C testing in clinical practice.

Main Methods:

  • Development of a risk score using logistic regression with Bayesian model averaging in the REGARDS study.
  • External validation of the risk score in the NHANES III study.
  • Assessment of performance using calibration and discrimination measures.

Main Results:

  • Among 24,877 adults with eGFRcreat>60, 13.5% had reduced eGFRcys.
  • Older age, Black race, smoking, higher BMI, lower eGFRcreat, diabetes, hypertension, and cardiovascular disease history were associated with reduced eGFRcys (p<0.001).
  • The risk score achieved a c-statistic of 0.87 (REGARDS) and 0.84 (NHANES), identifying 72% of occult-reduced eGFR cases by screening only 22% of participants.

Conclusions:

  • A risk score utilizing readily accessible clinical characteristics can effectively identify individuals with reduced eGFRcys missed by creatinine-based assessments.
  • This tool can aid in targeted cystatin C testing, improving the detection of kidney function decline.
Abstract

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