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

被引:3
作者
Hamilton, Barbara C. S. [1 ]
Dincheva, Gabriela R. [1 ]
Zhuo, Hanjing [1 ]
Golden, Jeffrey A. [1 ]
Brzezinski, Marek [1 ]
Singer, Jonathan P. [1 ]
Matthay, Michael A. [1 ]
Kukreja, Jasleen [1 ]
机构
[1] Univ Calif San Francisco, Dept Surg, San Francisco, CA 94143 USA
关键词
biomarker; donor; lung transplantation; plasminogen activator inhibitor 1; primary graft dysfunction; GLYCATION END-PRODUCTS; ACUTE LUNG INJURY; I CELL INJURY; TRANSPLANTATION; RECEPTOR; EXPRESSION; INTERLEUKIN-8; DEFINITION; BIOMARKERS; PERFUSION;
D O I
10.1111/ctr.13210
中图分类号
R61 [外科手术学];
学科分类号
摘要
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.
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页数:7
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