Short halt in vaping modifies cardiorespiratory parameters and urine metabolome: a randomized trial.

Department of Cardiology, Erasme University Hospital, Université Libre de Bruxelles, Brussels, Belgium.Institute for Translational Research in Cardiovascular and Respiratory Sciences, Université Libre de Bruxelles, Brussels, Belgium.Department of Human Biology and Toxicology, University of Mons, Mons, Belgium.Department of Cardiology, Erasme University Hospital, Université Libre de Bruxelles, Brussels, Belgium.Institute for Translational Research in Cardiovascular and Respiratory Sciences, Université Libre de Bruxelles, Brussels, Belgium.Department of Human Biology and Toxicology, University of Mons, Mons, Belgium.Laboratory of Toxicology and Applied Pharmacology, Institute of Experimental and Clinical Research, Université Catholique de Louvain, Brussels, Belgium.Department of Cardiology, Erasme University Hospital, Université Libre de Bruxelles, Brussels, Belgium.Institute for Translational Research in Cardiovascular and Respiratory Sciences, Université Libre de Bruxelles, Brussels, Belgium.Department of Clinical Chemistry, Université Libre de Bruxelles, Brussels, Belgium.Chest Department, Erasme University Hospital, Université Libre de Bruxelles, Brussels, Belgium.Department of Cardiology, Centre Hospitalier Universitaire Saint-Pierre, Université Libre de Bruxelles, Brussels, Belgium.Cardio-Pulmonary Exercise Laboratory, Université Libre de Bruxelles, Brussels, Belgium.Cardio-Pulmonary Exercise Laboratory, Université Libre de Bruxelles, Brussels, Belgium.Department of Cardiology, Erasme University Hospital, Université Libre de Bruxelles, Brussels, Belgium.Institute for Translational Research in Cardiovascular and Respiratory Sciences, Université Libre de Bruxelles, Brussels, Belgium.

American journal of physiology. Lung cellular and molecular physiology. 2020;(2):L331-L344
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Abstract

Propylene glycol and glycerol are e-cigarette constituents that facilitate liquid vaporization and nicotine transport. As these small hydrophilic molecules quickly cross the lung epithelium, we hypothesized that short-term cessation of vaping in regular users would completely clear aerosol deposit from the lungs and reverse vaping-induced cardiorespiratory toxicity. We aimed to assess the acute effects of vaping and their reversibility on biological/clinical cardiorespiratory parameters [serum/urine pneumoproteins, hemodynamic parameters, lung-function test and diffusing capacities, transcutaneous gas tensions (primary outcome), and skin microcirculatory blood flow]. Regular e-cigarette users were enrolled in this randomized, investigator-blinded, three-period crossover study. The periods consisted of nicotine-vaping (nicotine-session), nicotine-free vaping (nicotine-free-session), and complete cessation of vaping (stop-session), all maintained for 5 days before the session began. Multiparametric metabolomic analyses were used to verify subjects' protocol compliance. Biological/clinical cardiorespiratory parameters were assessed at the beginning of each session (baseline) and after acute vaping exposure. Compared with the nicotine- and nicotine-free-sessions, a specific metabolomic signature characterized the stop-session. Baseline serum club cell protein-16 was higher during the stop-session than the other sessions (P < 0.01), and heart rate was higher in the nicotine-session (P < 0.001). Compared with acute sham-vaping in the stop-session, acute nicotine-vaping (nicotine-session) and acute nicotine-free vaping (nicotine-free-session) slightly decreased skin oxygen tension (P < 0.05). In regular e-cigarette-users, short-term vaping cessation seemed to shift baseline urine metabolome and increased serum club cell protein-16 concentration, suggesting a decrease in lung inflammation. Additionally, acute vaping with and without nicotine decreased slightly transcutaneous oxygen tension, likely as a result of lung gas exchanges disturbances.

Methodological quality

Publication Type : Randomized Controlled Trial

Metadata

MeSH terms : Heart