Albumin in decompensated cirrhosis: new concepts and perspectives
The pathophysiological background of decompensated cirrhosis is characterised by a systemic proinflammatory and pro-oxidant milieu that plays a major role in the development of multiorgan dysfunction. Such abnormality is mainly due to the systemic spread of bacteria and/or bacterial products from th...
| Autores: | , , , , , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2020 |
| País: | España |
| Institución: | Universidad de Barcelona |
| Repositorio: | Dipòsit Digital de la UB |
| OAI Identifier: | oai:diposit.ub.edu:2445/173020 |
| Acceso en línea: | https://hdl.handle.net/2445/173020 |
| Access Level: | acceso abierto |
| Palabra clave: | Cirrosi hepàtica Albúmines Hepatic cirrhosis Albumins |
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Albumin in decompensated cirrhosis: new concepts and perspectivesBernardi, MauroAngeli, PaoloClària i Enrich, JoanMoreau, RichardGinès i Gibert, PereJalan, RajivCaraceni, PaoloFernández, JavierGerbes, Alexander L.O'Brien, Alastair J.Trebicka, JonelThevenot, ThierryArroyo, VicenteCirrosi hepàticaAlbúminesHepatic cirrhosisAlbuminsThe pathophysiological background of decompensated cirrhosis is characterised by a systemic proinflammatory and pro-oxidant milieu that plays a major role in the development of multiorgan dysfunction. Such abnormality is mainly due to the systemic spread of bacteria and/or bacterial products from the gut and danger-associated molecular patterns from the diseased liver triggering the release of proinflammatory mediators by activating immune cells. The exacerbation of these processes underlies the development of acute-on-chronic liver failure. A further mechanism promoting multiorgan dysfunction and failure likely consists with a mitochondrial oxidative phosphorylation dysfunction responsible for systemic cellular energy crisis. The systemic proinflammatory and pro-oxidant state of patients with decompensated cirrhosis is also responsible for structural and functional changes in the albumin molecule, which spoil its pleiotropic non-oncotic properties such as antioxidant, scavenging, immune-modulating and endothelium protective functions. The knowledge of these abnormalities provides novel targets for mechanistic treatments. In this respect, the oncotic and non-oncotic properties of albumin make it a potential multitarget agent. This would expand the well-established indications to the use of albumin in decompensated cirrhosis, which mainly aim at improving effective volaemia or preventing its deterioration. Evidence has been recently provided that long-term albumin administration to patients with cirrhosis and ascites improves survival, prevents complications, eases the management of ascites and reduces hospitalisations. However, variant results indicate that further investigations are needed, aiming at confirming the beneficial effects of albumin, clarifying its optimal dosage and administration schedule and identify patients who would benefit most from long-term albumin administration.BMJ Publishing Group2020info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://hdl.handle.net/2445/173020Articles publicats en revistes (Biomedicina)reponame:Dipòsit Digital de la UBinstname:Universidad de BarcelonaInglésReproducció del document publicat a: https://doi.org/10.1136/gutjnl-2019-318843Gut, 2020, vol. 69, num. 6, p. 1127-1138https://doi.org/10.1136/gutjnl-2019-318843cc by-nc (c) Bernardi et al., 2020http://creativecommons.org/licenses/by-nc/3.0/es/info:eu-repo/semantics/openAccessoai:diposit.ub.edu:2445/1730202026-05-27T06:46:51Z |
| dc.title.none.fl_str_mv |
Albumin in decompensated cirrhosis: new concepts and perspectives |
| title |
Albumin in decompensated cirrhosis: new concepts and perspectives |
| spellingShingle |
Albumin in decompensated cirrhosis: new concepts and perspectives Bernardi, Mauro Cirrosi hepàtica Albúmines Hepatic cirrhosis Albumins |
| title_short |
Albumin in decompensated cirrhosis: new concepts and perspectives |
| title_full |
Albumin in decompensated cirrhosis: new concepts and perspectives |
| title_fullStr |
Albumin in decompensated cirrhosis: new concepts and perspectives |
| title_full_unstemmed |
Albumin in decompensated cirrhosis: new concepts and perspectives |
| title_sort |
Albumin in decompensated cirrhosis: new concepts and perspectives |
| dc.creator.none.fl_str_mv |
Bernardi, Mauro Angeli, Paolo Clària i Enrich, Joan Moreau, Richard Ginès i Gibert, Pere Jalan, Rajiv Caraceni, Paolo Fernández, Javier Gerbes, Alexander L. O'Brien, Alastair J. Trebicka, Jonel Thevenot, Thierry Arroyo, Vicente |
| author |
Bernardi, Mauro |
| author_facet |
Bernardi, Mauro Angeli, Paolo Clària i Enrich, Joan Moreau, Richard Ginès i Gibert, Pere Jalan, Rajiv Caraceni, Paolo Fernández, Javier Gerbes, Alexander L. O'Brien, Alastair J. Trebicka, Jonel Thevenot, Thierry Arroyo, Vicente |
| author_role |
author |
| author2 |
Angeli, Paolo Clària i Enrich, Joan Moreau, Richard Ginès i Gibert, Pere Jalan, Rajiv Caraceni, Paolo Fernández, Javier Gerbes, Alexander L. O'Brien, Alastair J. Trebicka, Jonel Thevenot, Thierry Arroyo, Vicente |
| author2_role |
author author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
Cirrosi hepàtica Albúmines Hepatic cirrhosis Albumins |
| topic |
Cirrosi hepàtica Albúmines Hepatic cirrhosis Albumins |
| description |
The pathophysiological background of decompensated cirrhosis is characterised by a systemic proinflammatory and pro-oxidant milieu that plays a major role in the development of multiorgan dysfunction. Such abnormality is mainly due to the systemic spread of bacteria and/or bacterial products from the gut and danger-associated molecular patterns from the diseased liver triggering the release of proinflammatory mediators by activating immune cells. The exacerbation of these processes underlies the development of acute-on-chronic liver failure. A further mechanism promoting multiorgan dysfunction and failure likely consists with a mitochondrial oxidative phosphorylation dysfunction responsible for systemic cellular energy crisis. The systemic proinflammatory and pro-oxidant state of patients with decompensated cirrhosis is also responsible for structural and functional changes in the albumin molecule, which spoil its pleiotropic non-oncotic properties such as antioxidant, scavenging, immune-modulating and endothelium protective functions. The knowledge of these abnormalities provides novel targets for mechanistic treatments. In this respect, the oncotic and non-oncotic properties of albumin make it a potential multitarget agent. This would expand the well-established indications to the use of albumin in decompensated cirrhosis, which mainly aim at improving effective volaemia or preventing its deterioration. Evidence has been recently provided that long-term albumin administration to patients with cirrhosis and ascites improves survival, prevents complications, eases the management of ascites and reduces hospitalisations. However, variant results indicate that further investigations are needed, aiming at confirming the beneficial effects of albumin, clarifying its optimal dosage and administration schedule and identify patients who would benefit most from long-term albumin administration. |
| publishDate |
2020 |
| dc.date.none.fl_str_mv |
2020 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/2445/173020 |
| url |
https://hdl.handle.net/2445/173020 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Reproducció del document publicat a: https://doi.org/10.1136/gutjnl-2019-318843 Gut, 2020, vol. 69, num. 6, p. 1127-1138 https://doi.org/10.1136/gutjnl-2019-318843 |
| dc.rights.none.fl_str_mv |
cc by-nc (c) Bernardi et al., 2020 http://creativecommons.org/licenses/by-nc/3.0/es/ info:eu-repo/semantics/openAccess |
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cc by-nc (c) Bernardi et al., 2020 http://creativecommons.org/licenses/by-nc/3.0/es/ |
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openAccess |
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application/pdf |
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BMJ Publishing Group |
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BMJ Publishing Group |
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Articles publicats en revistes (Biomedicina) reponame:Dipòsit Digital de la UB instname:Universidad de Barcelona |
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Universidad de Barcelona |
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Dipòsit Digital de la UB |
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Dipòsit Digital de la UB |
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