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Urinary biomarkers of chronic allograft nephropathy.
Cassidy, Hilary; Slyne, Jennifer; O'Kelly, Patrick; Traynor, Carol; Conlon, Peter J; Johnston, Olwyn; Slattery, Craig; Ryan, Michael P; McMorrow, Tara.
Afiliação
  • Cassidy H; School of Biomolecular and Biomedical Science, Conway Institute, University College Dublin, Belfield, Dublin, Ireland.
  • Slyne J; School of Biomolecular and Biomedical Science, Conway Institute, University College Dublin, Belfield, Dublin, Ireland.
  • O'Kelly P; Department of Nephrology & Transplantation, Beaumont Hospital, Beaumont, Dublin, Ireland.
  • Traynor C; Nephrology Department, Mater Misercordiae University Hospital, Dublin, Ireland.
  • Conlon PJ; Department of Nephrology & Transplantation, Beaumont Hospital, Beaumont, Dublin, Ireland.
  • Johnston O; Gordon & Leslie Diamond Centre, Division of Nephrology, University of British Columbia, Vancouver, Canada.
  • Slattery C; School of Biomolecular and Biomedical Science, Conway Institute, University College Dublin, Belfield, Dublin, Ireland.
  • Ryan MP; School of Biomolecular and Biomedical Science, Conway Institute, University College Dublin, Belfield, Dublin, Ireland.
  • McMorrow T; School of Biomolecular and Biomedical Science, Conway Institute, University College Dublin, Belfield, Dublin, Ireland.
Proteomics Clin Appl ; 9(5-6): 574-85, 2015 Jun.
Article em En | MEDLINE | ID: mdl-25951805
ABSTRACT

PURPOSE:

Chronic allograft nephropathy (CAN) is widely accepted as the leading cause of renal allograft loss after the first year post transplantation. This study aimed to identify urinary biomarkers that could predict CAN in transplant patients. EXPERIMENTAL

DESIGN:

The study included 34 renal transplant patients with histologically proven CAN and 36 renal transplant patients with normal renal function. OrbiTrap MS was utilized to analysis a urinary fraction in order to identify other members of a previously identified biomarker tree . This novel biomarker pattern offers the potential to distinguish between transplant recipients with CAN and those with normal renal function.

RESULTS:

The primary node of the biomarker pattern was reconfirmed as ß2 microglobulin. Three other members of this biomarker pattern were identified neutrophil gelatinase-associated lipocalin, clusterin, and kidney injury biomarker 1. Significantly higher urinary concentrations of these proteins were found in patients with CAN compared to those with normal kidney function. CONCLUSIONS AND CLINICAL RELEVANCE While further validation in a larger more-diverse patient population is required to determine if this biomarker pattern provides a potential means of diagnosing CAN by noninvasive methods in a clinical setting, this study clearly demonstrates the biomarkers' ability to stratify patients based on transplant function.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fragmentos de Peptídeos / Proteinúria / Rejeição de Enxerto / Nefropatias Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Proteomics Clin Appl Assunto da revista: BIOQUIMICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Irlanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fragmentos de Peptídeos / Proteinúria / Rejeição de Enxerto / Nefropatias Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Proteomics Clin Appl Assunto da revista: BIOQUIMICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Irlanda