Urine podocin:nephrin mRNA ratio (PNR) as a podocyte stress biomarker
Author(s) -
Akihiro Fukuda,
Larysa Wickman,
Madhusudan Venkatareddy,
S. Q. Wang,
Mosharaf Chowdhury,
Jocelyn Wiggins,
Karen Shedden,
Roger C. Wiggins
Publication year - 2012
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/gfs313
Subject(s) - podocin , nephrin , podocyte , medicine , focal segmental glomerulosclerosis , proteinuria , glomerulosclerosis , urine , albuminuria , renal function , creatinine , endocrinology , kidney , urology
Proteinuria and/or albuminuria are widely used for noninvasive assessment of kidney diseases. However, proteinuria is a nonspecific marker of diverse forms of kidney injury, physiologic processes and filtration of small proteins of monoclonal and other pathologic processes. The opportunity to develop new glomerular disease biomarkers follows the realization that the degree of podocyte depletion determines the degree of glomerulosclerosis, and if persistent, determines the progression to end-stage kidney disease (ESKD). Podocyte cell lineage-specific mRNAs can be recovered in urine pellets of model systems and in humans. In model systems, progressive glomerular disease is associated with decreased nephrin mRNA steady-state levels compared with podocin mRNA. Thus, the urine podocin:nephrin mRNA ratio (PNR) could serve as a useful progression biomarker. The use of podocyte-specific transcript ratios also circumvents many problems inherent to urine assays.
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