Literature DB >> 29377268

Elevated donor plasminogen activator inhibitor-1 levels and the risk of primary graft dysfunction.

Barbara C S Hamilton1, Gabriela R Dincheva1, Hanjing Zhuo1, Jeffrey A Golden1, Marek Brzezinski1, Jonathan P Singer1, Michael A Matthay1, Jasleen Kukreja1.   

Abstract

Primary graft dysfunction (PGD) following lung transplantation is associated with elevated recipient plasma levels of plasminogen activator inhibitor-1 (PAI-1) and the receptor for advanced glycation end products (RAGE). However, the significance of these biomarkers in the donor plasma is uncertain. We hypothesized that elevated donor plasma levels of PAI-1 and RAGE would be associated with recipient PGD. We carried out a prospective unmatched case-control study of double-lung transplant recipients between May 2014 and September 2015. We compared donor plasma levels of PAI-1 and RAGE using rank-sum tests and t tests, in 12 recipients who developed PGD grade 2 or 3 within 72 hours postoperatively with 13 recipients who did not. Recipients who developed PGD had higher donor plasma levels of PAI-1 than recipients who did not (median 2.7 ng/mL vs 1.4; P = .03). Recipients with PGD also had numerically higher donor plasma levels of RAGE than recipients without PGD, although this difference did not achieve statistical significance (median 1061 pg/mL vs 679; P = .12). Systemic inflammatory responses in the donor, as reflected by elevated plasma levels of PAI-1, may contribute to the risk of developing PGD. Rapid biomarker assessment of easily available plasma samples may assist in donor lung selection and risk stratification.
© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  biomarker; donor; lung transplantation; plasminogen activator inhibitor 1; primary graft dysfunction

Mesh:

Substances:

Year:  2018        PMID: 29377268      PMCID: PMC5924447          DOI: 10.1111/ctr.13210

Source DB:  PubMed          Journal:  Clin Transplant        ISSN: 0902-0063            Impact factor:   2.863


  25 in total

1.  Objective Estimates Improve Risk Stratification for Primary Graft Dysfunction after Lung Transplantation.

Authors:  R J Shah; J M Diamond; E Cantu; J Flesch; J C Lee; D J Lederer; V N Lama; J Orens; A Weinacker; D S Wilkes; D Roe; S Bhorade; K M Wille; L B Ware; S M Palmer; M Crespo; E Demissie; J Sonnet; A Shah; S M Kawut; S L Bellamy; A R Localio; J D Christie
Journal:  Am J Transplant       Date:  2015-04-15       Impact factor: 8.086

2.  Report of the ISHLT Working Group on Primary Lung Graft Dysfunction part II: definition. A consensus statement of the International Society for Heart and Lung Transplantation.

Authors:  Jason D Christie; Martin Carby; Remzi Bag; Paul Corris; Marshall Hertz; David Weill
Journal:  J Heart Lung Transplant       Date:  2005-06-04       Impact factor: 10.247

3.  Interleukin-8 release during early reperfusion predicts graft function in human lung transplantation.

Authors:  Marc De Perrot; Yasuo Sekine; Stefan Fischer; Thomas K Waddell; Karen McRae; Mingyao Liu; Dennis A Wigle; Shaf Keshavjee
Journal:  Am J Respir Crit Care Med       Date:  2002-01-15       Impact factor: 21.405

4.  Nutritional assessment of the lung transplant patient: body mass index as a predictor of 90-day mortality following transplantation.

Authors:  J Madill; C Gutierrez; J Grossman; J Allard; C Chan; M Hutcheon; S H Keshavjee
Journal:  J Heart Lung Transplant       Date:  2001-03       Impact factor: 10.247

5.  A panel of lung injury biomarkers enhances the definition of primary graft dysfunction (PGD) after lung transplantation.

Authors:  Rupal J Shah; Scarlett L Bellamy; A Russell Localio; Nancy Wickersham; Joshua M Diamond; Ann Weinacker; Vibha N Lama; Sangeeta Bhorade; John A Belperio; Maria Crespo; Ejigayehu Demissie; Steven M Kawut; Keith M Wille; David J Lederer; James C Lee; Scott M Palmer; Jonathan Orens; John Reynolds; Ashish Shah; David S Wilkes; Lorraine B Ware; Jason D Christie
Journal:  J Heart Lung Transplant       Date:  2012-06-12       Impact factor: 10.247

6.  Receptor for advanced glycation end products in donor lungs is associated with primary graft dysfunction after lung transplantation.

Authors:  A Pelaez; S D Force; A A Gal; D C Neujahr; A M Ramirez; P M Naik; D A Quintero; A V Pileggi; K A Easley; R Echeverry; E C Lawrence; D M Guidot; P O Mitchell
Journal:  Am J Transplant       Date:  2010-02-01       Impact factor: 8.086

7.  Concomitant endothelin-1 overexpression in lung transplant donors and recipients predicts primary graft dysfunction.

Authors:  M Salama; O Andrukhova; M A Hoda; S Taghavi; P Jaksch; G Heinze; W Klepetko; S Aharinejad
Journal:  Am J Transplant       Date:  2010-01-05       Impact factor: 8.086

8.  Pre-implantation multiple cytokine mRNA expression analysis of donor lung grafts predicts survival after lung transplantation in humans.

Authors:  H Kaneda; T K Waddell; M de Perrot; X-H Bai; C Gutierrez; T Arenovich; C Chaparro; M Liu; S Keshavjee
Journal:  Am J Transplant       Date:  2006-03       Impact factor: 8.086

9.  Elevated levels of the receptor for advanced glycation end products, a marker of alveolar epithelial type I cell injury, predict impaired alveolar fluid clearance in isolated perfused human lungs.

Authors:  Raphael Briot; James A Frank; Tokujiro Uchida; Jae W Lee; Carolyn S Calfee; Michael A Matthay
Journal:  Chest       Date:  2008-11-18       Impact factor: 9.410

10.  Using the inherent chemistry of the endothelin-1 peptide to develop a rapid assay for pre-transplant donor lung assessment.

Authors:  Andrew T Sage; Xiaohui Bai; Marcelo Cypel; Mingyao Liu; Shaf Keshavjee; Shana O Kelley
Journal:  Analyst       Date:  2015-12-21       Impact factor: 4.616

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