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

Journal Article (Clinical Trial;Journal Article;Multicenter Study)

RATIONALE: The receptor for advanced glycation end products (RAGE) is an important marker of lung epithelial injury and may be associated with impaired alveolar fluid clearance. We hypothesized that patients with primary graft dysfunction (PGD) after lung transplantation would have higher RAGE levels in plasma than patients without PGD. OBJECTIVES: To test the association of soluble RAGE (sRAGE) levels with PGD in a prospective, multicenter cohort study. METHODS: We measured plasma levels of sRAGE at 6 and 24 hours after allograft reperfusion in 317 lung transplant recipients at seven centers. The primary outcome was grade 3 PGD (Pa(O(2))/Fi(O(2)) < 200 with alveolar infiltrates) within the first 72 hours after transplantation. MEASUREMENTS AND MAIN RESULTS: Patients who developed PGD had higher levels of sRAGE than patients without PGD at both 6 hours (median 9.3 ng/ml vs. 7.5 ng/ml, respectively; P = 0.028) and at 24 hours post-transplantation (median 4.3 ng/ml vs. 1.9 ng/ml, respectively; P < 0.001). Multivariable logistic regression analyses indicated that the relationship between levels of sRAGE and PGD was attenuated by elevated right heart pressures and by the use of cardiopulmonary bypass. Median sRAGE levels were higher in subjects with cardiopulmonary bypass at both 6 hours (P = 0.003) and 24 hours (P < 0.001). sRAGE levels at 6 hours were significantly associated with intraoperative red cell transfusion (Spearman's rho = 0.39, P = 0.002 in those with PGD), and in multivariable linear regression analyses this association was independent of confounding variables (P = 0.02). CONCLUSIONS: Elevated plasma levels of sRAGE are associated with PGD after lung transplantation. Furthermore, plasma sRAGE levels are associated with blood product transfusion and use of cardiopulmonary bypass.

Full Text

Duke Authors

Cited Authors

  • Christie, JD; Shah, CV; Kawut, SM; Mangalmurti, N; Lederer, DJ; Sonett, JR; Ahya, VN; Palmer, SM; Wille, K; Lama, V; Shah, PD; Shah, A; Weinacker, A; Deutschman, CS; Kohl, BA; Demissie, E; Bellamy, S; Ware, LB; Lung Transplant Outcomes Group,

Published Date

  • November 15, 2009

Published In

Volume / Issue

  • 180 / 10

Start / End Page

  • 1010 - 1015

PubMed ID

  • 19661249

Pubmed Central ID

  • PMC2778153

Electronic International Standard Serial Number (EISSN)

  • 1535-4970

Digital Object Identifier (DOI)

  • 10.1164/rccm.200901-0118OC


  • eng

Conference Location

  • United States