The Study of ELEctronic Cigarette Toxicity in a Human Model in Vivo Model of Inflammation and Vascular Dysfunction — SELECT  

Acute Lung Injury Clinical Trial

Official title: The Study of ELEctronic Cigarette Toxicity in a Human Model in Vivo Model of Inflammation and Vascular Dysfunction (SELECT)

Status Recruiting

Clinical Trial Summary

To carry out a prospective cohort study of healthy volunteers, assessing differences between baseline pulmonary inflammation, response to LPS inhalation and endothelial function, as measured by flow mediated dilation between, electronic cigarette uses, cigarette smokers and non smokers.

Clinical Trial Description

Background. Since their introduction, electronic cigarette (EC) use has increased substantially. Perhaps most concerning is the increased use amongst adolescents. Many e-cigarette users believe that electronic cigarettes are safer than conventional cigarettes [1]. However, the toxicities of electronic cigarettes, including those in the lung, are relatively poorly studied. Notably, early studies suggest that electronic cigarettes are not harmless. The fine and ultra-fine particles could deposit in the lungs and lead to harm. Animal studies of electronic cigarettes have been associated with a number of pulmonary toxicities, including increased inflammation and oxidative stress in the lung [2] as well as impaired pulmonary immunity [3, 4]. EC vapour reduces indoor air quality by increasing the concentrations of particulate matter, particle number concentrations, polycyclic aromatic hydrocarbons (PAH) which are known carcinogens [5]. Early studies on cardiovascular function also suggests harm from the constituents of EC vapour such as the direct effects of nicotine, carbonyls as well as fine and ultrafine particles [6].

There is limited understanding of the adverse effects of EC vapour of the pulmonary or cardiovascular physiology and additional studies, particularly in humans, are needed to better characterize the acute toxicities of electronic cigarettes

Hypothesis Our hypothesis is, when compared to cigarette or e-cigarette naïve healthy volunteers;

1. E-cigarette users will have a higher baseline pulmonary inflammation

2. E-cigarette users will have an exaggerated immune response after LPS inhalation

3. E-cigarettes users will have endothelial dysfunction as measured by FMD of the brachial artery

Trial design Prospective cohort study of healthy subjects exposed to inhaled LPS.

Population Healthy subjects, including electronic cigarette users, cigarette smokers and controls will be recruited by advertising.

Intervention Bronchoscopy and blood sampling to assess baseline pulmonary and systemic inflammation and injury and in response to inhaled LPS 50 mcg. Flow mediated dilation (FMD) of brachial artery to study endothelial dysfunction.

After informed consent, their baseline FMD of brachial artery will be measured as well as lung function. FMD of brachial artery will be measured within 5 mins of use of e-cigarette to reflect the acute effects of e-cigarette on systemic endothelial dysfunction. Bronchoscopy with BAL, blood and urine sampling will be performed. This will enable us to measure the baseline inflammation and markers of cellular injury without inhaled LPS. At 24 hours the subject will return and lung function will be measured and blood sampling will be performed.

Six weeks later, the above procedure will be repeated but with LPS stimulation. The subject will once again attend the hospital and lung function will be measured, blood and urine sampling will be performed. Subjects will inhale LPS (from Escherichia coli O26:B6, 50 μg; Sigma-Aldrich, St. Louis, MO) using a dosimeter. Bronchoscopy with BAL will be undertaken 6 hours following LPS inhalation. Prior to bronchoscopy, lung function will be measured in order to ensure that they may safely undergo LPS inhalation. At 24 hours subjects will return and lung function will be measured and blood sampling will be performed. The time points for BAL and plasma sampling are chosen to obtain insight into both cytokine/chemokine release and neutrophil recruitment after pulmonary delivery of LPS.

Statistical considerations The primary exposure variable will be e-cigarette exposure; the primary outcome variable will be plasma and BAL biomarkers of injury and inflammation. Given that early studies of electronic cigarettes suggest that they may be associated with inflammation, we have used BAL absolute neutrophil count, a key marker of inflammation, to inform our sample size. Based on data from controls in our prior study, a cohort of 10 e-cigarette users and 10 controls should be able to detect a minimal difference of 7.09 x 105 cells in the BAL after LPS inhalation between groups with 80% power using Wilcoxon Rank Sum testing. Of note, this is similar to the difference we observed between smokers and non-smokers after LPS in our prior study [7]. Additionally, we will compare biomarkers of inflammation and injury in electronic cigarette users to those from conventional cigarette smokers using Wilcoxon Rank Sum testing. All data will be analysed using STATA 13.1 (StataCorp LP, College Station, TX).

Study Monitoring Site monitoring will be directed by the sponsor according to the study risk assessment. Site visits will be performed on a regular basis as required by the sponsor to ensure that all regulatory requirements are met and to monitor the quality of the data collected. The CRF will be used for source data verification. ;

Related Conditions & MeSH terms

• Acute Lung Injury
• Inflammation
• Lung Injury
• Respiratory Distress Syndrome, Adult

• NCT number: NCT02739438
• Study type: Observational
• Source: Queen's University, Belfast
• Contact: Murali Shyamsundar, PhD
• Phone: 02890 976381
• Email: murali.shyamsundar@qub.ac.uk
• Status: Recruiting
• Start date: February 1, 2017
• Completion date: December 2019