| Literature DB >> 30411406 |
Natàlia Puig-Gay1, Conxita Jacobs-Cacha1,2, Joana Sellarès2, Lluís Guirado3, Francisco González Roncero4, Carlos Jiménez5, Sofía Zárraga6, Javier Paul7, Ricardo Lauzurica8, Ángel Alonso9, Ana Fernández10, Isabel Beneyto11, Auxiliadora Mazuecos12, Domingo Hernández13, Alberto Rodriguez-Benot14, Antonio Franco15, Luisa Jimeno16, Marta Crespo17, Anna Meseguer1, Francesc Moreso2, Daniel Seron2, Joan Lopez-Hellin1, Carmen Cantarell2.
Abstract
Recurrence of idiopathic focal segmental glomerulosclerosis (FSGS) is a serious complication after kidney transplantation. FSGS relapse is suspected by a sudden increase in proteinuria but there is not an accurate noninvasive diagnostic tool to confirm this entity or to detect patients at risk. We aimed to validate the diagnostic performance of ApoA-Ib to detect FSGS relapses by measuring urinary ApoA-Ib in a retrospective cohort of 61 kidney transplanted patients (37 FSGS and 24 non-FSGS). In addition, to assess the ApoA-Ib predictive ability, ApoA-Ib was measured periodically in a prospective cohort of 13 idiopathic FSGS patients who were followed during 1 year after transplantation. ApoA-Ib had a sensitivity of 93.3% and a specificity of 90.9% to diagnose FSGS relapses, with a high negative predictive value (95.2%), confirming our previous results. In the prospective cohort, ApoA-Ib predated the recurrence in four of five episodes observed. In the nonrelapsing group (n = 9), ApoA-Ib was negative in 37 of 38 samples. ApoA-Ib has the potential to be a good diagnostic biomarker of FSGS relapses, providing a confident criterion to exclude false positives even in the presence of high proteinuria. It has also the potential to detect patients at risk of relapse, even before transplantation.Entities:
Keywords: apolipoprotein A-I; focal segmental glomerulosclerosis; kidney transplantation; recurrence
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Year: 2018 PMID: 30411406 DOI: 10.1111/tri.13372
Source DB: PubMed Journal: Transpl Int ISSN: 0934-0874 Impact factor: 3.782