: Livers from donations after circulatory death (DCDs) are very sensitive to ischemia/reperfusion injury and thus need careful reconditioning, such as normothermic regional perfusion (NRP). So far, its impact on DCDs has not been thoroughly investigated. This pilot cohort study aimed to explore the NRP impact on liver function by evaluating dynamic changes of circulating markers and hepatic gene expression in 9 uncontrolled DCDs (uDCDs) and 10 controlled DCDs. At NRP start, controlled DCDs had lower plasma levels of inflammatory and liver damage markers, including α-glutathione s-transferase, sorbitol-dehydrogenase, malate dehydrogenase 1, liver-type arginase-1, and keratin-18, but higher levels of osteopontin, sFas, flavin mononucleotide, and succinate than uDCDs. During 4-hour NRP, some damage and inflammatory markers increased in both groups, while IL-6, HGF, and osteopontin increased only in uDCDs. At the NRP end, the tissue expression of early transcriptional regulators, apoptosis, and autophagy mediators was higher in uDCDs than in controlled DCDs. In conclusion, despite initial differences in liver damage biomarkers, the uDCD group was characterized by a major gene expression of regenerative and repair factors after the NRP procedure. Correlative analysis among circulating/tissue biomarkers and the tissue congestion/necrosis degree revealed new potential candidate biomarkers.

An extensive evaluation of hepatic markers of damage and regeneration in controlled and uncontrolled donation after circulatory death / Basta, Giuseppina; Melandro, Fabio; Babboni, Serena; Del Turco, Serena; Ndreu, Rudina; Torri, Francesco; Martinelli, Caterina; Silvestrini, Beatrice; Peris, Adriano; Lazzeri, Chiara; Guarracino, Fabio; Morganti, Riccardo; Maremmani, Paolo; Bertini, Pietro; De Simone, Paolo; Ghinolfi, Davide. - In: LIVER TRANSPLANTATION. - ISSN 1527-6465. - Publish Ahead of Print:(2023). [10.1097/LVT.0000000000000122]

An extensive evaluation of hepatic markers of damage and regeneration in controlled and uncontrolled donation after circulatory death

Melandro, Fabio;
2023

Abstract

: Livers from donations after circulatory death (DCDs) are very sensitive to ischemia/reperfusion injury and thus need careful reconditioning, such as normothermic regional perfusion (NRP). So far, its impact on DCDs has not been thoroughly investigated. This pilot cohort study aimed to explore the NRP impact on liver function by evaluating dynamic changes of circulating markers and hepatic gene expression in 9 uncontrolled DCDs (uDCDs) and 10 controlled DCDs. At NRP start, controlled DCDs had lower plasma levels of inflammatory and liver damage markers, including α-glutathione s-transferase, sorbitol-dehydrogenase, malate dehydrogenase 1, liver-type arginase-1, and keratin-18, but higher levels of osteopontin, sFas, flavin mononucleotide, and succinate than uDCDs. During 4-hour NRP, some damage and inflammatory markers increased in both groups, while IL-6, HGF, and osteopontin increased only in uDCDs. At the NRP end, the tissue expression of early transcriptional regulators, apoptosis, and autophagy mediators was higher in uDCDs than in controlled DCDs. In conclusion, despite initial differences in liver damage biomarkers, the uDCD group was characterized by a major gene expression of regenerative and repair factors after the NRP procedure. Correlative analysis among circulating/tissue biomarkers and the tissue congestion/necrosis degree revealed new potential candidate biomarkers.
2023
liver transplantation machine perfusion, nrp
01 Pubblicazione su rivista::01a Articolo in rivista
An extensive evaluation of hepatic markers of damage and regeneration in controlled and uncontrolled donation after circulatory death / Basta, Giuseppina; Melandro, Fabio; Babboni, Serena; Del Turco, Serena; Ndreu, Rudina; Torri, Francesco; Martinelli, Caterina; Silvestrini, Beatrice; Peris, Adriano; Lazzeri, Chiara; Guarracino, Fabio; Morganti, Riccardo; Maremmani, Paolo; Bertini, Pietro; De Simone, Paolo; Ghinolfi, Davide. - In: LIVER TRANSPLANTATION. - ISSN 1527-6465. - Publish Ahead of Print:(2023). [10.1097/LVT.0000000000000122]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1676755
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