Consequences of Nephrotic Proteinuria and Nephrotic Syndrome after Kidney Transplant
María José Ortega, Miguel Martínez-Belotto, Cristina García-Majado, Lara Belmar, Covadonga López del Moral, Jose María Gómez-Ortega, Rosalía Valero, Juan Carlos Ruiz, Emilio Rodrigo

TL;DR
Nephrotic proteinuria and syndrome after kidney transplants are common and strongly linked to poor outcomes, with early development of syndrome indicating worse survival.
Contribution
The study provides new insights into the clinical and histopathological features of nephrotic-range proteinuria and its association with graft survival after kidney transplantation.
Findings
Nephrotic-range proteinuria occurred in 18.6% of kidney transplants.
Graft survival dropped from 75.8% at 12 months to 38% at 5 years after NP onset.
Early development of nephrotic syndrome was linked to higher graft loss risk.
Abstract
Proteinuria is the main predictor of kidney graft loss. However, there is little information regarding the consequences of nephrotic proteinuria (NP) and nephrotic syndrome (NS) after a kidney transplant. We aimed to describe the clinical and histopathological characteristics of kidney recipients with nephrotic-range proteinuria and compare the graft surveillance between those who developed NS and those who did not. A total of 204 patients (18.6% of kidney transplants in the study period) developed NP, and 68.1% of them had NS. Of the 110 patients who underwent a graft biopsy, 47.3% exhibited ABMR, 21.8% the recurrence of glomerulonephritis, 9.1% IFTA, and 7.3% de novo glomerulonephritis. After a median follow-up of 97.5 months, 64.1% experienced graft loss. The graft survival after the onset of NP declined from 75.8% at 12 months to 38% at 5 years, without significant differences…
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Taxonomy
TopicsRenal Diseases and Glomerulopathies · Pregnancy and Medication Impact · Renal Transplantation Outcomes and Treatments
