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Oxidative stress, redox status and surfactant metabolism in mechanically ventilated patients receiving different approaches to oxygen therapy (MecROX): an observational study protocol for mechanistic evaluation

Oxidative stress, redox status and surfactant metabolism in mechanically ventilated patients receiving different approaches to oxygen therapy (MecROX): an observational study protocol for mechanistic evaluation
Oxidative stress, redox status and surfactant metabolism in mechanically ventilated patients receiving different approaches to oxygen therapy (MecROX): an observational study protocol for mechanistic evaluation

BACKGROUND: MecROX is a mechanistic sub-study of the UK-ROX trial which was designed to evaluate the clinical and cost-effectiveness of a conservative approach to oxygen therapy for invasively ventilated adults in intensive care. This is based on the scientific rationale that excess oxygen is harmful. Epithelial cell damage with alveolar surfactant deficiency is characteristic of hyperoxic acute lung injury. Additionally, hyperoxaemia (excess blood oxygen levels) may exacerbate whole-body oxidative stress leading to cell death, autophagy, mitochondrial dysfunction, bioenergetic failure and multi-organ failure resulting in poor clinical outcomes. However, there is a lack of in-vivo human models evaluating the mechanisms that underpin oxygen-induced organ damage in mechanically ventilated patients.

AIM: The aim of the MecROX mechanistic sub-study is to assess lung surfactant composition and global systemic redox status to provide a mechanistic and complementary scientific rationale to the UK-ROX trial findings. The objectives are to quantify in-vivo surfactant composition, synthesis, and metabolism with markers of oxidative stress and systemic redox disequilibrium (as evidenced by alterations in the 'reactive species interactome') to differentiate between groups of conservative and usual oxygen targets.

METHODS AND DESIGN: After randomisation into the UK-ROX trial, 100 adult participants (50 in the conservative and 50 in usual care group) will be recruited at two trial sites. Blood and endotracheal samples will be taken at 0, 48 and 72 hours following an infusion of 3 mg/kg methyl-D 9-choline chloride. This is a non-radioactive, stable isotope of choline (vitamin), which has been extensively used to study surfactant phospholipid kinetics in humans. This study will mechanistically evaluate the in-vivo surfactant synthesis and breakdown (by hydrolysis and oxidation), oxidative stress and redox disequilibrium from sequential plasma and bronchial samples using an array of analytical platforms. We will compare conservative and usual oxygenation groups according to the amount of oxygen administered. Trial registration: ISRCTNISRCTN61929838, 27/03/2023 https://doi.org/10.1186/ISRCTN61929838.

Hyperoxia, Mechanical ventilation, Oxidative stress, Oxygen, Redox, Surfactant
2633-4402
23
Dushianthan, Ahilanandan
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Martin, Daniel
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Mouncey, Paul
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Shahid, Tasnin
8bed7f4b-5c2e-44b1-8d2a-04d64aac58d7
Lampro, Lamprini
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Johnson, Amelia Francis
2daf5d55-4f4d-415d-93d4-7ef5c53c76fd
Goss, Victoria
ef02be5d-9318-4f7d-b076-3153555980d0
Cazley, Angelica
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Herbert, William
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Jones, William
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Lamond, Mark
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Neyroud, Florence
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Salmon, Karen
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Lentaigne, Julian
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Minnion, Magdalena
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Panchal, Madhuri
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Koster, Grielof
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Moyses, Helen
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Postle, Anthony D
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Feelisch, Martin
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Grocott, Michael P W
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Dushianthan, Ahilanandan
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Martin, Daniel
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Mouncey, Paul
98f436c1-b1ec-4d6f-8d4d-2f5e4c59a4c2
Shahid, Tasnin
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Lampro, Lamprini
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Johnson, Amelia Francis
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Goss, Victoria
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Cazley, Angelica
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Herbert, William
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Jones, William
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Lamond, Mark
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Neyroud, Florence
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Salmon, Karen
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Lentaigne, Julian
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Minnion, Magdalena
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Panchal, Madhuri
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Koster, Grielof
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Moyses, Helen
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Postle, Anthony D
0fa17988-b4a0-4cdc-819a-9ae15c5dad66
Feelisch, Martin
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Grocott, Michael P W
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Dushianthan, Ahilanandan, Martin, Daniel, Mouncey, Paul, Shahid, Tasnin, Lampro, Lamprini, Johnson, Amelia Francis, Goss, Victoria, Cazley, Angelica, Herbert, William, Jones, William, Lamond, Mark, Neyroud, Florence, Salmon, Karen, Lentaigne, Julian, Minnion, Magdalena, Panchal, Madhuri, Koster, Grielof, Moyses, Helen, Postle, Anthony D, Feelisch, Martin and Grocott, Michael P W (2024) Oxidative stress, redox status and surfactant metabolism in mechanically ventilated patients receiving different approaches to oxygen therapy (MecROX): an observational study protocol for mechanistic evaluation. NIHR open research, 4, 23, [23]. (doi:10.3310/nihropenres.13567.2).

Record type: Article

Abstract

BACKGROUND: MecROX is a mechanistic sub-study of the UK-ROX trial which was designed to evaluate the clinical and cost-effectiveness of a conservative approach to oxygen therapy for invasively ventilated adults in intensive care. This is based on the scientific rationale that excess oxygen is harmful. Epithelial cell damage with alveolar surfactant deficiency is characteristic of hyperoxic acute lung injury. Additionally, hyperoxaemia (excess blood oxygen levels) may exacerbate whole-body oxidative stress leading to cell death, autophagy, mitochondrial dysfunction, bioenergetic failure and multi-organ failure resulting in poor clinical outcomes. However, there is a lack of in-vivo human models evaluating the mechanisms that underpin oxygen-induced organ damage in mechanically ventilated patients.

AIM: The aim of the MecROX mechanistic sub-study is to assess lung surfactant composition and global systemic redox status to provide a mechanistic and complementary scientific rationale to the UK-ROX trial findings. The objectives are to quantify in-vivo surfactant composition, synthesis, and metabolism with markers of oxidative stress and systemic redox disequilibrium (as evidenced by alterations in the 'reactive species interactome') to differentiate between groups of conservative and usual oxygen targets.

METHODS AND DESIGN: After randomisation into the UK-ROX trial, 100 adult participants (50 in the conservative and 50 in usual care group) will be recruited at two trial sites. Blood and endotracheal samples will be taken at 0, 48 and 72 hours following an infusion of 3 mg/kg methyl-D 9-choline chloride. This is a non-radioactive, stable isotope of choline (vitamin), which has been extensively used to study surfactant phospholipid kinetics in humans. This study will mechanistically evaluate the in-vivo surfactant synthesis and breakdown (by hydrolysis and oxidation), oxidative stress and redox disequilibrium from sequential plasma and bronchial samples using an array of analytical platforms. We will compare conservative and usual oxygenation groups according to the amount of oxygen administered. Trial registration: ISRCTNISRCTN61929838, 27/03/2023 https://doi.org/10.1186/ISRCTN61929838.

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More information

Published date: 2024
Additional Information: Copyright: © 2024 Dushianthan A et al.
Keywords: Hyperoxia, Mechanical ventilation, Oxidative stress, Oxygen, Redox, Surfactant

Identifiers

Local EPrints ID: 493723
URI: http://eprints.soton.ac.uk/id/eprint/493723
ISSN: 2633-4402
PURE UUID: 50319b01-8f51-42fa-a690-e71b6b65d35f
ORCID for Ahilanandan Dushianthan: ORCID iD orcid.org/0000-0002-0165-3359
ORCID for Anthony D Postle: ORCID iD orcid.org/0000-0001-7361-0756
ORCID for Martin Feelisch: ORCID iD orcid.org/0000-0003-2320-1158
ORCID for Michael P W Grocott: ORCID iD orcid.org/0000-0002-9484-7581

Catalogue record

Date deposited: 11 Sep 2024 17:19
Last modified: 14 Sep 2024 01:57

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Contributors

Author: Ahilanandan Dushianthan ORCID iD
Author: Daniel Martin
Author: Paul Mouncey
Author: Tasnin Shahid
Author: Lamprini Lampro
Author: Amelia Francis Johnson
Author: Victoria Goss
Author: Angelica Cazley
Author: William Herbert
Author: William Jones
Author: Mark Lamond
Author: Florence Neyroud
Author: Karen Salmon
Author: Julian Lentaigne
Author: Magdalena Minnion
Author: Madhuri Panchal
Author: Grielof Koster
Author: Helen Moyses
Author: Martin Feelisch ORCID iD

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