An interventional study of I quit ordinary smoking (IQOS) and Conventional cigarette in Smoking Cessation, sponsored by University of Athens. Status unknown at 1 site in Greece. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-04-24.
Sponsored by University of Athens · Not applicable, Interventional, and Prevention
I quit ordinary smoking (IQOS) is proposed as a bridge to smoking cessation. In this study the investigators will examine its effects on aortic elasticity, glycocalyx integrity, and exhaled carbon monoxide (CO) concentration, both acutely and after 1 month of use.
Two smokers groups matched for age and sex will be assessed:
In the acute phase all 60 smokers will undergo a "sham" smoking for 7 minutes. Afterwards all 60 smokers will be randomized to smoke either a normal cigarette or IQOS and the after 60 minute washout period these subjects will be crossed over to the altenate mode of smoking (IQOS or normal cigarette respectively).
After the completion of the acute phase all 60 smokers will start the use of IQOS for one month.
In the acute phase, measurements will be performed at baseline, after sham smoking and after smoking of the normal cigarette or IQOS. The chronic phase measurements will be performed 1 month after use IQOS. Thirty current smokers of similar age and sex will serve as controls and will have measurements at baseline and 1 month after baseline assessment.
In both phases the investigators will assess: a) the aortic pulse wave velocity (PWV) and augmentation index (AIx) by Arteriograph and Complior; b) the perfusion boundary region of the sublingual arterial microvessels using Sideview, Darkfield imaging (Microscan, Glycocheck); c) the exhaled carbon monoxide (CO) level (parts per million -ppm) as a smoking status marker; d) the vital signs; e) an electrocardiogram; and f) plasma levels of C- reactive protein (CRP), transforming growth factor-b (TGF-b), lipoprotein associated phospholipase A2 (LP- LPA2), tumor necrosis factor- α (TNF-α), interleukins 6 and 10 (IL-6 and -10), procollagen propeptide type III (PIIINP), matrix metalloproteinase 2 and 9 (MMP-2 and -9), and macrophage-colony stimulating factor (MCSF), malondialdehyde (MDA) and protein carbonyls (PCs).
Exclusion Criteria:
I quit ordinary smoking (IQOS) assistes cessation program
Device: I quit ordinary smoking (IQOS)
Conventional cigarette smoking continuation
Other: Conventional cigarette
I quit ordinary smoking (IQOS) assisted cessation program
Conventional cigarette smoking continuation
Acute I quit ordinary smoking (IQOS) effects on pulse wave velocity
Acute I quit ordinary smoking (IQOS) effects on pulse wave velocity (PWV, m/s) using tonometry
Time frame: 7 minutes
Acute I quit ordinary smoking (IQOS) effects on Exhaled Carbon monoxide (CO)
CO concentration was measured the exhaled carbon as parts per million-ppm by the device Smokerlyzer, Covita, Bedfont, CA, USA). Participants were instructed not to smoke the night before and the morning before the CO measurements and to hold their breath for 10 sec before exhaling to the mouthpiece.
Time frame: 7 minutes
Acute I quit ordinary smoking (IQOS) effects on endothelial glycocalyx thickness
Acute I quit ordinary smoking (IQOS) effects on endothelial glycocalyx thickness as assessed by perfused boundary region (PBR, micrometers) of the sublinqual arterial microvessels
Time frame: 7 minutes
Chronic I quit ordinary smoking (IQOS) effects on pulse wave velocity
Chronic I quit ordinary smoking (IQOS) effects on pulse wave velocity (PWV, m/s) using tonometry
Time frame: 1 month
Chronic I quit ordinary smoking (IQOS) effects on endothelial glycocalyx thickness
Chronic I quit ordinary smoking (IQOS) effects on endothelial glycocalyx thickness as assessed by perfused boundary region (PBR, micrometers) of the sublinqual arterial microvessels
Time frame: 1 month
Chronic I quit ordinary smoking (IQOS) effects in left ventricular function
Left Ventricular function is assessed by Global Longitudinal Strain by speckle tracking echocardiography
Time frame: 1 month
Chronic I quit ordinary smoking (IQOS) effects on endothelial function
Endothelial function was assessed by measuring coronary flow reserve of Left anterior descending artery. Coronary flow reserve was estimated by Doppler echocardiography as the ratio of coranary flow velocity after bolus intravenous adenosine infusion to coronary flow velocity at rest.
Time frame: 1 month
Chronic I quit ordinary smoking (IQOS) effects on endothelial function
Endothelial function was assessed by measuring Flow Mediated Vasodilation (FMD) using sonography. During a FMD test, vasodilation occurs following an acute increase in blood flow, typically induced via circulatory arrest in the arm (supra-systolic cuff occlusion) for a period of time. FMD is the percent of increase in brachial artery diameter after occlusion.
Time frame: 1 month
Chronic I quit ordinary smoking (IQOS) effects on Exhaled Carbon monoxide (CO)
CO concentration was measured the exhaled carbon as parts per million-ppm by the device Smokerlyzer, Covita, Bedfont, CA, USA). Participants were instructed not to smoke the night before and the morning before the CO measurements and to hold their breath for 10 sec before exhaling to the mouthpiece.
Time frame: 1 month
Acute I quit ordinary smoking (IQOS) effects on platelet activation.
Platelet activation was estimated by measuring blood levels of Thromboxane B2 (Thromboxane B2 EIA Kit Cayman Ann Arbor MI USA) A commercially available ELISA kit was used with an assay range 1.6-1000 pg/ml.
Time frame: 7 minutes
Chronic I quit ordinary smoking (IQOS) effects on myocardial work.
Myocardial work (MW) was estimated by combining echo-derived left ventricular (LV) strain with brachial blood pressure to construct LV strain-pressure curves non-invasively. Brachial cuff systolic pressure measurements provide the peak systolic LV pressure value, which is combined with the input of valvular timing events that define isovolumetric and ejection phases, allowing the construction of an LV-pressure curve. This is combined with LV strain data into a pressure-strain loop (PSL), the area within which represents MW. Global MW index (GWI) is defined as the work within the LV PSL from mitral valve closure to mitral valve opening, while constructive MW (GCW) is the component of MW that contributes to LV ejection. On the contrary, wasted MW (GWW) is the work wasted as myocyte lengthening during systole, which does not contribute to LV ejection. MW efficiency (GWE) is defined as the ratio of GCW to the sum of GCW and GWW \[GWE= GCW/ (GCW+GWW)\].
Time frame: 1 month
Chronic I quit ordinary smoking (IQOS) effects on arterial stiffness.
Arterial stiffness was estimated by calculating Total arterial compliance (TAC). TAC was evaluated utilising the stroke volume (SV) to pulse pressure (PP) ratio (SV/PP), based on the two-element Windkessel model; SV measurements were derived from two-dimensional echocardiography.
Time frame: 1 month
Chronic I quit ordinary smoking (IQOS) effects on platelet activation.
Platelet activation was estimated by measuring blood levels of Thromboxane B2 (Thromboxane B2 EIA Kit Cayman Ann Arbor MI USA) A commercially available ELISA kit was used with an assay range 1.6-1000 pg/ml.
Time frame: 1 month
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University of Athens