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Abrogation of graft ischemia‐reperfusion injury in ischemia‐free liver transplantation

Background Ischemia‐reperfusion injury (IRI) is considered an inherent component of organ transplantation that compromises transplant outcomes and organ availability. The ischemia‐free liver transplantation (IFLT) procedure has been developed to avoid interruption of blood supply to liver grafts. It...

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Published in:Clinical and translational medicine 2022-04, Vol.12 (4), p.e546-n/a
Main Authors: Guo, Zhiyong, Xu, Jinghong, Huang, Shanzhou, Yin, Meixian, Zhao, Qiang, Ju, Weiqiang, Wang, Dongping, Gao, Ningxin, Huang, Changjun, Yang, Lu, Chen, Maogen, Zhang, Zhiheng, Zhu, Zebin, Wang, Linhe, Zhu, Caihui, Zhang, Yixi, Tang, Yunhua, Chen, Haitian, Liu, Kunpeng, Lu, Yuting, Ma, Yi, Hu, Anbin, Chen, Yinghua, Zhu, Xiaofeng, He, Xiaoshun
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Language:English
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Summary:Background Ischemia‐reperfusion injury (IRI) is considered an inherent component of organ transplantation that compromises transplant outcomes and organ availability. The ischemia‐free liver transplantation (IFLT) procedure has been developed to avoid interruption of blood supply to liver grafts. It is unknown how IFLT might change the characteristics of graft IRI. Methods Serum and liver biopsy samples were collected from IFLT and conventional liver transplantation (CLT) recipients. Pathological, metabolomics, transcriptomics, and proteomics analyses were performed to identify the characteristic changes in graft IRI in IFLT. Results Peak aspartate aminotransferase (539.59 ± 661.76 U/L versus 2622.28 ± 3291.57 U/L) and alanine aminotransferase (297.64 ± 549.50 U/L versus 1184.16 ± 1502.76 U/L) levels within the first 7 days and total bilirubin levels by day 7 (3.27 ± 2.82 mg/dl versus 8.33 ± 8.76 mg/dl) were lower in the IFLT versus CLT group (all p values 
ISSN:2001-1326
2001-1326
DOI:10.1002/ctm2.546