Literature DB >> 23331756

Early plasma soluble receptor for advanced glycation end-product levels are associated with bronchiolitis obliterans syndrome.

R J Shah1, S L Bellamy, J C Lee, E Cantu, J M Diamond, N Mangalmurti, S M Kawut, L B Ware, J D Christie.   

Abstract

Early epithelial injury after lung transplantation may contribute to development of bronchiolitis obliterans syndrome (BOS). We evaluated the relationship between early postoperative soluble receptor for advanced glycation end-product (sRAGE) levels, a marker of type I alveolar cell injury and BOS. We performed a cohort study of 106 lung transplant recipients between 2002 and 2006 at the University of Pennsylvania with follow-up through 2010. Plasma sRAGE was measured 6 and 24 h after transplantation. Cox proportional hazards models were used to evaluate the association between sRAGE and time to BOS, defined according to ISHLT guidelines. Sixty (57%) subjects developed BOS. The average time to BOS was 3.4 years. sRAGE levels measured at 6 h (HR per SD of sRAGE: 1.69, 95% CI: 1.11, 2.57, p = 0.02) and 24 h (HR per SD of sRAGE: 1.74, 95% CI: 1.14, 2.65, p = 0.01) were associated with an increased hazard of BOS. Multivariable Cox regression indicated this relationship was independent of potential confounders. Elevated plasma sRAGE levels measured in the immediate postoperative period are associated with the development of BOS. Early epithelial injury after transplantation may contribute to the development of fibrosis in BOS. © Copyright 2013 The American Society of Transplantation and the American Society of Transplant Surgeons.

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Year:  2013        PMID: 23331756      PMCID: PMC3582806          DOI: 10.1111/ajt.12062

Source DB:  PubMed          Journal:  Am J Transplant        ISSN: 1600-6135            Impact factor:   8.086


  30 in total

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Review 3.  Chronic allograft rejection: epidemiology, diagnosis, pathogenesis, and treatment.

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4.  Plasma levels of receptor for advanced glycation end products, blood transfusion, and risk of primary graft dysfunction.

Authors:  Jason D Christie; Chirag V Shah; Steven M Kawut; Nilam Mangalmurti; David J Lederer; Joshua R Sonett; Vivek N Ahya; Scott M Palmer; Keith Wille; Vibha Lama; Pali D Shah; Ashish Shah; Ann Weinacker; Clifford S Deutschman; Benjamin A Kohl; Ejigayehu Demissie; Scarlett Bellamy; Lorraine B Ware
Journal:  Am J Respir Crit Care Med       Date:  2009-08-06       Impact factor: 21.405

5.  Plasma receptor for advanced glycation end products and clinical outcomes in acute lung injury.

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6.  The role of the receptor for advanced glycation end-products in lung fibrosis.

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8.  Loss of RAGE in pulmonary fibrosis: molecular relations to functional changes in pulmonary cell types.

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9.  Ischemia- reperfusion injury and its influence on the epigenetic modification of the donor kidney genome.

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Authors:  Hsi-Min Hsiao; Davide Scozzi; Jason M Gauthier; Daniel Kreisel
Journal:  Curr Opin Organ Transplant       Date:  2017-02       Impact factor: 2.640

Review 3.  Protein biomarkers associated with primary graft dysfunction following lung transplantation.

Authors:  B C S Hamilton; J Kukreja; L B Ware; M A Matthay
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4.  An obligatory role for club cells in preventing obliterative bronchiolitis in lung transplants.

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Review 5.  Biomarkers of lung injury in cardiothoracic surgery.

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Journal:  Dis Markers       Date:  2015-03-17       Impact factor: 3.434

6.  Local and systemic RAGE axis changes in pulmonary hypertension: CTEPH and iPAH.

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8.  Blood Gene Expression Predicts Bronchiolitis Obliterans Syndrome.

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Review 9.  The role of innate immunity in the long-term outcome of lung transplantation.

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