Plasma Levels of Receptor for Advanced Glycation End Products, Blood Transfusion, and Risk of Primary Graft Dysfunction

被引:114
|
作者
Christie, Jason D. [1 ,2 ]
Shah, Chirag V. [2 ]
Kawut, Steven M. [2 ,3 ]
Mangalmurti, Nilam
Lederer, David J. [5 ]
Sonett, Joshua R. [6 ]
Ahya, Vivek N.
Palmer, Scott M. [7 ]
Wille, Keith [8 ]
Lama, Vibha [9 ]
Shah, Pali D. [10 ]
Shah, Ashish [10 ]
Weinacker, Ann [11 ]
Deutschman, Clifford S. [4 ]
Kohl, Benjamin A. [4 ]
Demissie, Ejigayehu [2 ]
Bellamy, Scarlett [2 ]
Ware, Lorraine B. [12 ]
机构
[1] Univ Penn, Sch Med, Div Pulm Allergy & Crit Care Med, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Biostat & Epidemiol, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Penn Cardiovasc Inst, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Med, Dept Anesthesia & Crit Care, Philadelphia, PA 19104 USA
[5] Columbia Univ Coll Phys & Surg, Div Pulm Allergy & Crit Care Med, New York, NY 10032 USA
[6] Columbia Univ Coll Phys & Surg, Dept Surg, New York, NY 10032 USA
[7] Duke Univ, Div Pulm Allergy & Crit Care Med, Raleigh, NC USA
[8] Univ Alabama, Div Pulm & Crit Care Med, Birmingham, AL USA
[9] Univ Michigan, Div Pulm Allergy & Crit Care Med, Ann Arbor, MI 48109 USA
[10] Johns Hopkins Univ Hosp, Dept Med, Div Pulm Allergy & Crit Care Med, Baltimore, MD 21205 USA
[11] Stanford Univ, Div Pulm & Crit Care Med, Palo Alto, CA 94304 USA
[12] Vanderbilt Univ, Div Allergy Pulm & Crit Care Med, Nashville, TN USA
关键词
primary graft dysfunction; reperfusion injury; lung transplantation; receptor for advanced glycation end products; acute lung injury; ISHLT WORKING GROUP; ACUTE LUNG INJURY; RESPIRATORY-DISTRESS-SYNDROME; ENDOTHELIAL-CELL DYSFUNCTION; REPERFUSION INJURY; DIABETIC VASCULOPATHY; SOLUBLE RECEPTOR; TRANSPLANTATION; RAGE; ISCHEMIA;
D O I
10.1164/rccm.200901-0118OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
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 PG D 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(O2)/Fi(O2) < 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 P = 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.
引用
收藏
页码:1010 / 1015
页数:6
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