An RCT of acute health effects in COPD-patients after passive vape exposure from e-cigarettes

Background: E-cigarette use has been shown to have short-term acute effects among active users but less is known of the acute passive effects, particularly among individuals with existing respiratory diseases. Objective: To investigate local and systemic effects of short-term passive vape exposure a...

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Veröffentlicht in:European clinical respiratory journal 2021-01, Vol.8 (1), p.1861580
Hauptverfasser: Rosenkilde Laursen, Karin, Bønløkke, Jakob Hjort, Bendstrup, Elisabeth, Bilde, Merete, Glasius, Marianne, Heitmann Gutzke, Vibeke, Puthukkadan Moosakutty, Shamjad, Olin, Anna-Carin, Ravn, Peter, Østergaard, Kirsten, Sigsgaard, Torben
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container_title European clinical respiratory journal
container_volume 8
creator Rosenkilde Laursen, Karin
Bønløkke, Jakob Hjort
Bendstrup, Elisabeth
Bilde, Merete
Glasius, Marianne
Heitmann Gutzke, Vibeke
Puthukkadan Moosakutty, Shamjad
Olin, Anna-Carin
Ravn, Peter
Østergaard, Kirsten
Sigsgaard, Torben
description Background: E-cigarette use has been shown to have short-term acute effects among active users but less is known of the acute passive effects, particularly among individuals with existing respiratory diseases. Objective: To investigate local and systemic effects of short-term passive vape exposure among patients with mild or moderate chronic obstructive pulmonary disease (COPD). Methods: In a double-blinded crossover study 16 non-smoking COPD-patients (mean age 68) were randomly exposed for 4 h to passive vape (median PM 2.5 : 18 µg/m 3 (range: 8-333)) and clean air (PM 2.5  
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Objective: To investigate local and systemic effects of short-term passive vape exposure among patients with mild or moderate chronic obstructive pulmonary disease (COPD). Methods: In a double-blinded crossover study 16 non-smoking COPD-patients (mean age 68) were randomly exposed for 4 h to passive vape (median PM 2.5 : 18 µg/m 3 (range: 8-333)) and clean air (PM 2.5  &lt; 6 µg/m 3 ) separated by 14 days. Particles were measured using an ultrafine particle counter (P-TRAK) and a scanning mobility particle sizer (SMPS). Health effects including Surfactant Protein-A (SP-A) and albumin in exhaled air, spirometry, FeNO, and plasma proteins were evaluated before, right after, and 24 hours after exposure. Participants reported symptoms throughout exposure sessions. Data were analyzed using mixed models. Results: SP-A in exhaled air was negatively affected by exposure to vape and several plasma proteins increased significantly. Throat irritation was more pronounced during passive vape exposure, while FVC and FEV 1 decreased, however, not significantly. Conclusions: SP-A in exhaled air and some plasma proteins were affected by passive vape in patients with COPD indicating inflammation, showing that passive vape exposure is potentially harmful.</description><identifier>ISSN: 2001-8525</identifier><identifier>EISSN: 2001-8525</identifier><identifier>DOI: 10.1080/20018525.2020.1861580</identifier><identifier>PMID: 33456728</identifier><language>eng</language><publisher>United States: Taylor &amp; Francis</publisher><subject>Chronic obstructive pulmonary disease ; COPD ; Electronic cigarettes ; Electronic nicotine delivery systems ; exposure ; human ; human exposure ; Lungmedicin och allergi ; particulate matter ; Proteins ; RCT ; Respiratory Medicine and Allergy ; Respiratory System ; secondhand vape ; spirometry ; Vaping</subject><ispartof>European clinical respiratory journal, 2021-01, Vol.8 (1), p.1861580</ispartof><rights>2020 The Author(s). Published by Informa UK Limited, trading as Taylor &amp; Francis Group. 2020</rights><rights>2020 The Author(s). Published by Informa UK Limited, trading as Taylor &amp; Francis Group.</rights><rights>2020 The Author(s). Published by Informa UK Limited, trading as Taylor &amp; Francis Group. This work is licensed under the Creative Commons Attribution – Non-Commercial License http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 The Author(s). Published by Informa UK Limited, trading as Taylor &amp; Francis Group. 2020 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c600t-68073bbe88af0bd44a3cbeb350aa110432c41a65b0a80ebebe7a50f14490fc33</citedby><cites>FETCH-LOGICAL-c600t-68073bbe88af0bd44a3cbeb350aa110432c41a65b0a80ebebe7a50f14490fc33</cites><orcidid>0000-0002-4404-6989 ; 0000-0002-2043-7571 ; 0000-0002-1955-6661 ; 0000-0002-4238-6963 ; 0000-0002-8247-6576 ; 0000-0003-1621-8058 ; 0000-0002-2112-514X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7781946/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7781946/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,27502,27924,27925,53791,53793,59143,59144</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33456728$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://gup.ub.gu.se/publication/301560$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Rosenkilde Laursen, Karin</creatorcontrib><creatorcontrib>Bønløkke, Jakob Hjort</creatorcontrib><creatorcontrib>Bendstrup, Elisabeth</creatorcontrib><creatorcontrib>Bilde, Merete</creatorcontrib><creatorcontrib>Glasius, Marianne</creatorcontrib><creatorcontrib>Heitmann Gutzke, Vibeke</creatorcontrib><creatorcontrib>Puthukkadan Moosakutty, Shamjad</creatorcontrib><creatorcontrib>Olin, Anna-Carin</creatorcontrib><creatorcontrib>Ravn, Peter</creatorcontrib><creatorcontrib>Østergaard, Kirsten</creatorcontrib><creatorcontrib>Sigsgaard, Torben</creatorcontrib><title>An RCT of acute health effects in COPD-patients after passive vape exposure from e-cigarettes</title><title>European clinical respiratory journal</title><addtitle>Eur Clin Respir J</addtitle><description>Background: E-cigarette use has been shown to have short-term acute effects among active users but less is known of the acute passive effects, particularly among individuals with existing respiratory diseases. Objective: To investigate local and systemic effects of short-term passive vape exposure among patients with mild or moderate chronic obstructive pulmonary disease (COPD). Methods: In a double-blinded crossover study 16 non-smoking COPD-patients (mean age 68) were randomly exposed for 4 h to passive vape (median PM 2.5 : 18 µg/m 3 (range: 8-333)) and clean air (PM 2.5  &lt; 6 µg/m 3 ) separated by 14 days. Particles were measured using an ultrafine particle counter (P-TRAK) and a scanning mobility particle sizer (SMPS). Health effects including Surfactant Protein-A (SP-A) and albumin in exhaled air, spirometry, FeNO, and plasma proteins were evaluated before, right after, and 24 hours after exposure. Participants reported symptoms throughout exposure sessions. Data were analyzed using mixed models. Results: SP-A in exhaled air was negatively affected by exposure to vape and several plasma proteins increased significantly. Throat irritation was more pronounced during passive vape exposure, while FVC and FEV 1 decreased, however, not significantly. 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Objective: To investigate local and systemic effects of short-term passive vape exposure among patients with mild or moderate chronic obstructive pulmonary disease (COPD). Methods: In a double-blinded crossover study 16 non-smoking COPD-patients (mean age 68) were randomly exposed for 4 h to passive vape (median PM 2.5 : 18 µg/m 3 (range: 8-333)) and clean air (PM 2.5  &lt; 6 µg/m 3 ) separated by 14 days. Particles were measured using an ultrafine particle counter (P-TRAK) and a scanning mobility particle sizer (SMPS). Health effects including Surfactant Protein-A (SP-A) and albumin in exhaled air, spirometry, FeNO, and plasma proteins were evaluated before, right after, and 24 hours after exposure. Participants reported symptoms throughout exposure sessions. Data were analyzed using mixed models. Results: SP-A in exhaled air was negatively affected by exposure to vape and several plasma proteins increased significantly. 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subjects Chronic obstructive pulmonary disease
COPD
Electronic cigarettes
Electronic nicotine delivery systems
exposure
human
human exposure
Lungmedicin och allergi
particulate matter
Proteins
RCT
Respiratory Medicine and Allergy
Respiratory System
secondhand vape
spirometry
Vaping
title An RCT of acute health effects in COPD-patients after passive vape exposure from e-cigarettes
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