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Application of anti-inflammatory treatment in two different ovine Acute Respiratory Distress Syndrome injury models: a preclinical randomized intervention study

Whilst the presence of 2 subphenotypes among the heterogenous Acute Respiratory Distress Syndrome (ARDS) population is becoming clinically accepted, subphenotype-specific treatment efficacy has yet to be prospectively tested. We investigated anti-inflammatory treatment in different ARDS models in sh...

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Autores principales: Wildi, Karin, Livingstone, Samantha, Ainola, Carmen, Colombo, Sebastiano Maria, Heinsar, Silver, Sato, Noriko, Sato, Kei, Bouquet, Mahé, Wilson, Emily, Abbate, Gabriella, Passmore, Margaret, Hyslop, Kieran, Liu, Keibun, Wang, Xiaomeng, Palmieri, Chiara, See Hoe, Louise E., Jung, Jae-Seung, Ki, Katrina, Mueller, Christian, Laffey, John, Pelosi, Paolo, Li Bassi, Gianluigi, Suen, Jacky, Fraser, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589361/
https://www.ncbi.nlm.nih.gov/pubmed/37863994
http://dx.doi.org/10.1038/s41598-023-45081-8
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author Wildi, Karin
Livingstone, Samantha
Ainola, Carmen
Colombo, Sebastiano Maria
Heinsar, Silver
Sato, Noriko
Sato, Kei
Bouquet, Mahé
Wilson, Emily
Abbate, Gabriella
Passmore, Margaret
Hyslop, Kieran
Liu, Keibun
Wang, Xiaomeng
Palmieri, Chiara
See Hoe, Louise E.
Jung, Jae-Seung
Ki, Katrina
Mueller, Christian
Laffey, John
Pelosi, Paolo
Li Bassi, Gianluigi
Suen, Jacky
Fraser, John
author_facet Wildi, Karin
Livingstone, Samantha
Ainola, Carmen
Colombo, Sebastiano Maria
Heinsar, Silver
Sato, Noriko
Sato, Kei
Bouquet, Mahé
Wilson, Emily
Abbate, Gabriella
Passmore, Margaret
Hyslop, Kieran
Liu, Keibun
Wang, Xiaomeng
Palmieri, Chiara
See Hoe, Louise E.
Jung, Jae-Seung
Ki, Katrina
Mueller, Christian
Laffey, John
Pelosi, Paolo
Li Bassi, Gianluigi
Suen, Jacky
Fraser, John
author_sort Wildi, Karin
collection PubMed
description Whilst the presence of 2 subphenotypes among the heterogenous Acute Respiratory Distress Syndrome (ARDS) population is becoming clinically accepted, subphenotype-specific treatment efficacy has yet to be prospectively tested. We investigated anti-inflammatory treatment in different ARDS models in sheep, previously shown similarities to human ARDS subphenotypes, in a preclinical, randomized, blinded study. Thirty anesthetized sheep were studied up to 48 h and randomized into: (a) OA: oleic acid (n = 15) and (b) OA-LPS: oleic acid and subsequent lipopolysaccharide (n = 15) to achieve a PaO(2)/FiO(2) ratio of < 150 mmHg. Then, animals were randomly allocated to receive treatment with methylprednisolone or erythromycin or none. Assessed outcomes were oxygenation, pulmonary mechanics, hemodynamics and survival. All animals reached ARDS. Treatment with methylprednisolone, but not erythromycin, provided the highest therapeutic benefit in Ph2 animals, leading to a significant increase in PaO(2)/FiO(2) ratio by reducing pulmonary edema, dead space ventilation and shunt fraction. Animals treated with methylprednisolone displayed a higher survival up to 48 h than all others. In animals treated with erythromycin, there was no treatment benefit regarding assessed physiological parameters and survival in both phenotypes. Treatment with methylprednisolone improves oxygenation and survival, more so in ovine phenotype 2 which resembles the human hyperinflammatory subphenotype.
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spelling pubmed-105893612023-10-22 Application of anti-inflammatory treatment in two different ovine Acute Respiratory Distress Syndrome injury models: a preclinical randomized intervention study Wildi, Karin Livingstone, Samantha Ainola, Carmen Colombo, Sebastiano Maria Heinsar, Silver Sato, Noriko Sato, Kei Bouquet, Mahé Wilson, Emily Abbate, Gabriella Passmore, Margaret Hyslop, Kieran Liu, Keibun Wang, Xiaomeng Palmieri, Chiara See Hoe, Louise E. Jung, Jae-Seung Ki, Katrina Mueller, Christian Laffey, John Pelosi, Paolo Li Bassi, Gianluigi Suen, Jacky Fraser, John Sci Rep Article Whilst the presence of 2 subphenotypes among the heterogenous Acute Respiratory Distress Syndrome (ARDS) population is becoming clinically accepted, subphenotype-specific treatment efficacy has yet to be prospectively tested. We investigated anti-inflammatory treatment in different ARDS models in sheep, previously shown similarities to human ARDS subphenotypes, in a preclinical, randomized, blinded study. Thirty anesthetized sheep were studied up to 48 h and randomized into: (a) OA: oleic acid (n = 15) and (b) OA-LPS: oleic acid and subsequent lipopolysaccharide (n = 15) to achieve a PaO(2)/FiO(2) ratio of < 150 mmHg. Then, animals were randomly allocated to receive treatment with methylprednisolone or erythromycin or none. Assessed outcomes were oxygenation, pulmonary mechanics, hemodynamics and survival. All animals reached ARDS. Treatment with methylprednisolone, but not erythromycin, provided the highest therapeutic benefit in Ph2 animals, leading to a significant increase in PaO(2)/FiO(2) ratio by reducing pulmonary edema, dead space ventilation and shunt fraction. Animals treated with methylprednisolone displayed a higher survival up to 48 h than all others. In animals treated with erythromycin, there was no treatment benefit regarding assessed physiological parameters and survival in both phenotypes. Treatment with methylprednisolone improves oxygenation and survival, more so in ovine phenotype 2 which resembles the human hyperinflammatory subphenotype. Nature Publishing Group UK 2023-10-20 /pmc/articles/PMC10589361/ /pubmed/37863994 http://dx.doi.org/10.1038/s41598-023-45081-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wildi, Karin
Livingstone, Samantha
Ainola, Carmen
Colombo, Sebastiano Maria
Heinsar, Silver
Sato, Noriko
Sato, Kei
Bouquet, Mahé
Wilson, Emily
Abbate, Gabriella
Passmore, Margaret
Hyslop, Kieran
Liu, Keibun
Wang, Xiaomeng
Palmieri, Chiara
See Hoe, Louise E.
Jung, Jae-Seung
Ki, Katrina
Mueller, Christian
Laffey, John
Pelosi, Paolo
Li Bassi, Gianluigi
Suen, Jacky
Fraser, John
Application of anti-inflammatory treatment in two different ovine Acute Respiratory Distress Syndrome injury models: a preclinical randomized intervention study
title Application of anti-inflammatory treatment in two different ovine Acute Respiratory Distress Syndrome injury models: a preclinical randomized intervention study
title_full Application of anti-inflammatory treatment in two different ovine Acute Respiratory Distress Syndrome injury models: a preclinical randomized intervention study
title_fullStr Application of anti-inflammatory treatment in two different ovine Acute Respiratory Distress Syndrome injury models: a preclinical randomized intervention study
title_full_unstemmed Application of anti-inflammatory treatment in two different ovine Acute Respiratory Distress Syndrome injury models: a preclinical randomized intervention study
title_short Application of anti-inflammatory treatment in two different ovine Acute Respiratory Distress Syndrome injury models: a preclinical randomized intervention study
title_sort application of anti-inflammatory treatment in two different ovine acute respiratory distress syndrome injury models: a preclinical randomized intervention study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589361/
https://www.ncbi.nlm.nih.gov/pubmed/37863994
http://dx.doi.org/10.1038/s41598-023-45081-8
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