Copious Podocyturia without Proteinuria and with Normal Renal Function in a Young Adult with Fabry Disease

法布里病青年患者出现大量足细胞尿,无蛋白尿,肾功能正常

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作者:H Trimarchi, R Canzonieri, A Muryan, A Schiel, A Araoz, M Forrester, A Karl, F Lombi, J Andrews, V Pomeranz, T Rengel, E Zotta

Abstract

The time for starting a patient with Fabry disease on enzyme replacement therapy is still a matter of debate, particularly when no overt classical clinical signs or symptoms are present. With respect to Fabry nephropathy, a dual problem coexists: the reluctance of many nephrologists to start enzyme replacement infusion until signs of renal disease appear as the appearance of proteinuria or an elevation in serum creatinine and the lack of validated biomarkers of early renal damage. In this regard, proteinuria is nowadays considered as an early and appropriate marker of kidney disease and of cardiovascular morbidity and mortality. However, in this report we demonstrate that podocyturia antedates the classical appearance of proteinuria and could be considered as an even earlier biomarker of kidney damage. Podocyturia may be a novel indication for the initiation of therapy in Fabry disease.

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