Exhaled Volatile Organic Compounds Precedes Pulmonary Injury in a Swine Pulmonary Oxygen Toxicity Model

PurposeInspiring high partial pressure of oxygen (FiO2 > 0.6) for a prolonged duration can lead to lung damage termed pulmonary oxygen toxicity (PO2T). While current practice is to limit oxygen exposure, there are clinical and military scenarios where higher FiO2 levels and partial pressures...

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Main Authors: William A. Cronin, Angela S. Forbes, Kari L. Wagner, Peter Kaplan, Renee Cataneo, Michael Phillips, Richard Mahon, Aaron Hall
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-12-01
Series:Frontiers in Physiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fphys.2019.01297/full
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spelling doaj-fbe1c79725d74144ac62848ec1037b642020-11-25T01:19:34ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2019-12-011010.3389/fphys.2019.01297476816Exhaled Volatile Organic Compounds Precedes Pulmonary Injury in a Swine Pulmonary Oxygen Toxicity ModelWilliam A. Cronin0William A. Cronin1Angela S. Forbes2Kari L. Wagner3Peter Kaplan4Renee Cataneo5Michael Phillips6Richard Mahon7Richard Mahon8Aaron Hall9Walter Reed National Military Medical Center, Bethesda, MD, United StatesUndersea Medicine Department, Naval Medical Research Center, Silver Spring, MD, United StatesWalter Reed National Military Medical Center, Bethesda, MD, United StatesWalter Reed National Military Medical Center, Bethesda, MD, United StatesBreath Research Laboratory, Menssana Research, Inc., Newark, NJ, United StatesBreath Research Laboratory, Menssana Research, Inc., Newark, NJ, United StatesBreath Research Laboratory, Menssana Research, Inc., Newark, NJ, United StatesUndersea Medicine Department, Naval Medical Research Center, Silver Spring, MD, United StatesHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD, United StatesUndersea Medicine Department, Naval Medical Research Center, Silver Spring, MD, United StatesPurposeInspiring high partial pressure of oxygen (FiO2 > 0.6) for a prolonged duration can lead to lung damage termed pulmonary oxygen toxicity (PO2T). While current practice is to limit oxygen exposure, there are clinical and military scenarios where higher FiO2 levels and partial pressures of oxygen are required. The purpose of this study is to develop a non-invasive breath-based biomarker to detect PO2T prior to the onset of clinical symptoms.MethodsMale Yorkshire swine (20–30 kg) were placed into custom airtight runs and randomized to air (0.209 FiO2, n = 12) or oxygen (>0.95 FiO2, n = 10) for 72 h. Breath samples, arterial blood gases, and vital signs were assessed every 12 h. After 72 h of exposure, animals were euthanized and the lungs processed for histology and wet-dry ratios.ResultsSwine exposed to hyperoxia developed pulmonary injury consistent with PO2T. Histology of oxygen-exposed swine showed pulmonary lymphatic congestion, epithelial sloughing, and neutrophil transmigration. Pulmonary injury was also evidenced by increased interstitial edema and a decreased PaO2/FiO2 ratio in the oxygen group when compared to the air control group. Breath volatile organic compound (VOC) sample analysis identified six VOCs that were combined into an algorithm which generated a breath score predicting PO2T with a ROC/AUC curve of 0.72 defined as a of PaO2/FiO2 ratio less than 350 mmHg.ConclusionExposing swine to 72 h of hyperoxia induced a pulmonary injury consistent with human clinical endpoints of PO2T. VOC analysis identified six VOCs in exhaled breath that preceded PO2T. Results show promise that a simple, non-invasive breath test could potentially predict the risk of pulmonary injury in humans exposed to high partial pressures of oxygen.https://www.frontiersin.org/article/10.3389/fphys.2019.01297/fullpulmonary oxygen toxicityvolatile organic compoundshyperoxiaswineprediction
collection DOAJ
language English
format Article
sources DOAJ
author William A. Cronin
William A. Cronin
Angela S. Forbes
Kari L. Wagner
Peter Kaplan
Renee Cataneo
Michael Phillips
Richard Mahon
Richard Mahon
Aaron Hall
spellingShingle William A. Cronin
William A. Cronin
Angela S. Forbes
Kari L. Wagner
Peter Kaplan
Renee Cataneo
Michael Phillips
Richard Mahon
Richard Mahon
Aaron Hall
Exhaled Volatile Organic Compounds Precedes Pulmonary Injury in a Swine Pulmonary Oxygen Toxicity Model
Frontiers in Physiology
pulmonary oxygen toxicity
volatile organic compounds
hyperoxia
swine
prediction
author_facet William A. Cronin
William A. Cronin
Angela S. Forbes
Kari L. Wagner
Peter Kaplan
Renee Cataneo
Michael Phillips
Richard Mahon
Richard Mahon
Aaron Hall
author_sort William A. Cronin
title Exhaled Volatile Organic Compounds Precedes Pulmonary Injury in a Swine Pulmonary Oxygen Toxicity Model
title_short Exhaled Volatile Organic Compounds Precedes Pulmonary Injury in a Swine Pulmonary Oxygen Toxicity Model
title_full Exhaled Volatile Organic Compounds Precedes Pulmonary Injury in a Swine Pulmonary Oxygen Toxicity Model
title_fullStr Exhaled Volatile Organic Compounds Precedes Pulmonary Injury in a Swine Pulmonary Oxygen Toxicity Model
title_full_unstemmed Exhaled Volatile Organic Compounds Precedes Pulmonary Injury in a Swine Pulmonary Oxygen Toxicity Model
title_sort exhaled volatile organic compounds precedes pulmonary injury in a swine pulmonary oxygen toxicity model
publisher Frontiers Media S.A.
series Frontiers in Physiology
issn 1664-042X
publishDate 2019-12-01
description PurposeInspiring high partial pressure of oxygen (FiO2 > 0.6) for a prolonged duration can lead to lung damage termed pulmonary oxygen toxicity (PO2T). While current practice is to limit oxygen exposure, there are clinical and military scenarios where higher FiO2 levels and partial pressures of oxygen are required. The purpose of this study is to develop a non-invasive breath-based biomarker to detect PO2T prior to the onset of clinical symptoms.MethodsMale Yorkshire swine (20–30 kg) were placed into custom airtight runs and randomized to air (0.209 FiO2, n = 12) or oxygen (>0.95 FiO2, n = 10) for 72 h. Breath samples, arterial blood gases, and vital signs were assessed every 12 h. After 72 h of exposure, animals were euthanized and the lungs processed for histology and wet-dry ratios.ResultsSwine exposed to hyperoxia developed pulmonary injury consistent with PO2T. Histology of oxygen-exposed swine showed pulmonary lymphatic congestion, epithelial sloughing, and neutrophil transmigration. Pulmonary injury was also evidenced by increased interstitial edema and a decreased PaO2/FiO2 ratio in the oxygen group when compared to the air control group. Breath volatile organic compound (VOC) sample analysis identified six VOCs that were combined into an algorithm which generated a breath score predicting PO2T with a ROC/AUC curve of 0.72 defined as a of PaO2/FiO2 ratio less than 350 mmHg.ConclusionExposing swine to 72 h of hyperoxia induced a pulmonary injury consistent with human clinical endpoints of PO2T. VOC analysis identified six VOCs in exhaled breath that preceded PO2T. Results show promise that a simple, non-invasive breath test could potentially predict the risk of pulmonary injury in humans exposed to high partial pressures of oxygen.
topic pulmonary oxygen toxicity
volatile organic compounds
hyperoxia
swine
prediction
url https://www.frontiersin.org/article/10.3389/fphys.2019.01297/full
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