Objective: To evaluate the impact of heated versus combustion tobacco products on progression of atherosclerosis in patients with CAD unable(unwilling) to quit smoking. Rationale: Despite the efforts to curb smoking and full awareness of its deleterious health impact, smoking remains a significant contributor to morbidity and mortality. Some health impact of smoking may be improved by other forms of cigarettes than traditional combustion, especially for subjects unwilling or unable to stop smoking. As recently as 2020, one of heated tobacco products (HTP)(IQOS) was FDA Authorized as a 'Reduced Exposure' product. The available evidence to date allows to conclude that the IQOS system heats tobacco but does not burn it, which significantly reduces the production of harmful and potentially harmful chemicals. Scientific studies have shown that switching completely from conventional cigarettes to the IQOS system significantly reduced body's exposure to harmful or potentially harmful chemicals. There is also evidence indicating lower levels of inflammatory markers and improved vascular function associated with use of heated tobacco products. However, it is unknown whether the reduction in the exposure translates into potential reduction of harm within cardiovascular system, as compared to the traditional (combustion) cigarettes. The evidence is of crucial importance for patients with cardiovascular diseases, medical community, and national health authorities planning evidence based policies regarding HTP/cigarettes.
Objective: To evaluate the impact of heated versus combustion tobacco products on progression of atherosclerosis in patients with CAD unable(unwilling) to quit smoking. Background Despite the efforts to curb smoking and full awareness of its deleterious health impact, smoking remains a significant contributor to morbidity and mortality. Some health impact of smoking may be improved by other forms of cigarettes than traditional combustion, especially for subjects unwilling or unable to stop smoking. As recently as 2020, one of heated tobacco products (HTP)(IQOS) was FDA Authorized as a 'Reduced Exposure' product. The available evidence to date allows to conclude that the IQOS system heats tobacco but does not burn it, which significantly reduces the production of harmful and potentially harmful chemicals. Scientific studies have shown that switching completely from conventional cigarettes to the IQOS system significantly reduced body's exposure to harmful or potentially harmful chemicals. There is also evidence indicating lower levels of inflammatory markers and improved vascular function associated with use of heated tobacco products. However, it is unknown whether the reduction in the exposure translates into potential reduction of harm within cardiovascular system, as compared to the traditional (combustion) cigarettes. The evidence is of crucial importance for patients with cardiovascular diseases, medical community, and national health authorities planning evidence based policies regarding HTP/cigarettes. Methods: Prospective, single-centre, open-label, randomised study including 180 stable patients with coronary artery disease (CAD) as diagnosed on CCTA, without indications for invasive treatment, unable(unwilling) to quit smoking, randomised 1:1 to either heated (group H) or combustion (group C) tobacco products and followed for 18 months. The follow-up is accomplished with CCTA scan. The study clinical visits are planned at 1, 3, 6, 12, and 18 months. The primary outcome is change in non calcified plaque volume at 18 months between H and C groups (intention to treat design).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Enrollment
180
Patients unable (unwilling) to stop smoking will be randomized to either combustion (C) or heated (H) tobacco groups.
National Institute of Cardiology
Warsaw, Poland
RECRUITINGChange in non calcified plaque volume between H and C groups ("intention to treat")
CCTA based evaluation
Time frame: 0-18 months
Change in total plaque volume
CCTA based evaluation
Time frame: 0-18 months
Change in plaque volume components (low attenuation, fibrous-fatty, fibrous, non-calcified plaque, calcified plaque)
CCTA based evaluation
Time frame: 0-18 months
Change in non calcified plaque volume between H and C groups ("as treated")
CCTA based evaluation
Time frame: 0-18 months
Change in lipid metabolism
Total cholesterol (TC) Triglycerides (TG) Lipoproteins: low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C) Apolipoproteins: apolipoprotein A1 (ApoA1), apolipoprotein B (ApoB) Lipoprotein(a) Lp(a)
Time frame: 0-18 months
Change in oxidative stress
8-Epi prostaglandin F2 alpha (8 epi PGF2α) Myeloperoxidase (MPO)
Time frame: 0-18 months
Change in inflammation
High-sensitivity C-reactive protein (hs CRP) White blood cell (WBC) counts Homocysteine Interleukins (IL-6) Fibrinogen
Time frame: 0-18 months
Change in platelet activation
11-dehydro-thromboxane B2 (11 DTX B2) Plasminogen activator inhibitor-1 (PAI-1) Tissue plasminogen activator (t-PA) Platelet count Mean platelet volume (MPV)
Time frame: 0-18 months
Change in endothelial dysfunction
P-selectin Metalloproteinase 9 (MMP-9)
Time frame: 0-18 months
Change in haemodynamic stress
N-terminal pro b-type natriuretic peptide (NT-proBNP)
Time frame: 0-18 months
Change in myocardial injury
high-sensitivity troponin T (hs-TnT)
Time frame: 0-18 months
Change in glycemia control
Fasting Blood Glucose, HbA1c
Time frame: 0-18 months
Change in physical activity
self reported, mobile device monitoring
Time frame: 0-18 months
Change in exposure to nicotine
4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol , Nicotine equivalents in spot urine , 2-cyanoethylmercapturic acid
Time frame: 0-18 months
SAFETY (ADVERSE OUTCOMES)
Independent DSMB will evaluate the outcomes
Time frame: 0-18 months
Change in self reported product use
Time frame: 0-18 months
Change in quality of life
EQ5D-5L
Time frame: 0-18 months
Cost/effectiveness analysis
Time frame: 0-18 months
Subgroup analysis (AGE/SEX/CO-MORBIDITIES)
Time frame: 1-18 months
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