Abstract

Glomerular filtration rate (GFR) is routinely estimated using endogenous biomarkers due to the complexity of direct measurement methods. Cystatin C is a protease inhibitor produced in all nucleated cells. It is freely filtered and then catabolized by renal tubular cells. Therefore, plasma concentration of cystatin C depends primarily on GFR. Serum cystatin C is less affected by muscle mass, diet, race, gender and age than creatinine. In the general population, equations to estimate GFR based on cystatin C do not have a better performance than those based on creatinine. However, formulas that combine creatinine and cystatin C are more accurate and precise. Estimation of GFR based on cystatin C could be useful in populations in which creatinine value may be biased, such as people with extremely low or high muscle mass, cirrhosis and chronic cardiorenal syndrome. Due to its higher cost in comparison to creatinine, we recommend measuring cystatin C on these clinical situations and when a more accurate estimation of GFR is required.

Highlights

  • Recibido el 23 de diciembre de 2019, aceptado el 6 de abril de Correspondencia a: Dr Juan Pablo Huidobro Diagonal Paraguay 362, 4to piso

  • Cystatin C is a protease inhibitor produced in all nucleated cells

  • Serum cystatin C is less affected by muscle mass, diet, race, gender and age than creatinine

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Summary

ARTÍCULO DE REVISIÓN

Uso de la cistatina C como biomarcador para estimar la tasa de filtración glomerular Juan Pablo Huidobro E.1, Ana María Guzmán[2], Rodrigo Tagle[1]

Use of cystatin C to estimate glomerular filtration rate
Características de la cistatina C
Fórmulas que incluyen cistatina C
Secreción tubular

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