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2.
Hellenic J Cardiol ; 67: 28-35, 2022.
Article in English | MEDLINE | ID: mdl-35605944

ABSTRACT

BACKGROUND: Fagerstrom score is a validated marker of nicotine addiction in smokers. METHODS: In a prospective study, we investigated a) the predictive value of Fagerstrom score for the smoking status in patients early after acute myocardial infarction (AMI) and b) the effectiveness of medically assisted smoking cessation programs in the prevention of relapsing to smoking post discharge. In 103 smokers (58 ± 12 years, 79.6% males), we assessed Fagerstrom score during hospitalization for AMI. Patients filled a dedicated questionnaire including data on family, marital and educational status, habits related to smoking and were followed-up at 3 and 6 months after discharge. RESULTS: Twenty-eight patients (27.2%) did not quit smoking throughout the 6-months follow-up period (Fagerstrom score:8.1 ± 1.6), 39 patients (37.8%) ceased smoking at 3 months but relapsed to smoking at 6 months (score:6.8 ± 2.1), and only 34 patients (33%) had ceased smoking for 6 consecutive months (score:5.2 ± 2 p < 0.05 for all comparisons between subgroups). By multivariate analysis, Fagerstrom score remained a significant predictor of smoking cessation at 6 months (OR: 0.72, 95%CI: 0.60--0.86, p < 0.001). Out of 73 patients who abstained from smoking for the first 3 months post-AMI, those who participated in a smoking cessation program displayed lower rate of relapsing to smoking compared with those who opted to cease smoking without any support (33.3% vs 61.8% p = 0.012). CONCLUSION: Fagerstrom score is a useful predictor of smoking cessation 6 months post-AMI. Patients participating in a smoking cessation program display lower relapse rates post-discharge suggesting the need of well-organized smoking cessation clinics for secondary prevention of heart disease.


Subject(s)
Aftercare , Myocardial Infarction , Female , Hospitalization , Humans , Male , Myocardial Infarction/epidemiology , Myocardial Infarction/therapy , Patient Discharge , Prospective Studies , Recurrence , Smoking/adverse effects , Smoking/epidemiology
3.
Sci Rep ; 11(1): 11808, 2021 06 03.
Article in English | MEDLINE | ID: mdl-34083663

ABSTRACT

We compared the effects of Heat-not-Burn cigarette (HNBC) to those of tobacco cigarette (Tcig), on myocardial, coronary and arterial function as well as on oxidative stress and platelet activation in 75 smokers. In the acute study, 50 smokers were randomised into smoking a single Tcig or a HNBC and after 60 min were crossed-over to the alternate smoking. For chronic phase, 50 smokers were switched to HNBC and were compared with an external group of 25 Tcig smokers before and after 1 month. Exhaled carbon monoxide (CO), pulse wave velocity (PWV), malondialdehyde (MDA) and thromboxane B2 (TxB2) were assessed in the acute and chronic study. Global longitudinal strain (GLS), myocardial work index (GWI), wasted myocardial work (GWW), coronary flow reserve (CFR), total arterial compliance (TAC) and flow-mediated dilation (FMD) were assessed in the chronic study. Acute HNBC smoking caused a smaller increase of PWV than Tcig (change 1.1 vs 0.54 m/s, p < 0.05) without change in CO and biomarkers in contrast to Tcig. Compared to Tcig, switching to HNBC for 1-month improved CO, FMD, CFR, TAC, GLS, GWW, MDA, TxB2 (differences 10.42 ppm, 4.3%, 0.98, 1.8 mL/mmHg, 2.35%, 19.72 mmHg%, 0.38 nmol/L and 45 pg/mL respectively, p < 0.05). HNBCs exert a less detrimental effect on vascular and cardiac function than tobacco cigarettes.Trial registration Registered on https://clinicaltrials.gov/ (NCT03452124, 02/03/2018).


Subject(s)
Blood Circulation , Cardiovascular Physiological Phenomena , Cigarette Smoking/adverse effects , Coronary Circulation , Adult , Aged , Biomarkers , Female , Heart Disease Risk Factors , Heart Function Tests , Humans , Male , Middle Aged , Oxidative Stress , Platelet Activation
5.
Food Chem Toxicol ; 141: 111389, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32343994

ABSTRACT

We examined the effects of electronic cigarette on platelet and vascular function after 4 months of use compared to tobacco smoking. Forty smokers without cardiovascular disease were randomized to smoke either conventional cigarettes or an electronic cigarette (nicotine concentration of 12 mg/ml). At baseline and after four months, we measured a) platelet function by Platelet Function Analyzer PFA-100 and Light Transmission Aggregometry, b) pulse wave velocity, c) plasma malondialdehyde levels as oxidative stress index and d) the exhaled CO level. After 4 months, continuation of conventional cigarette smoking further impaired platelet function compared to vaping as assessed by PFA (mean increase 27.1 vs 11.6 s, p for interaction = 0.048) and by LTA (decline 24.1 vs 9.4%, p for interaction = 0.045). Conversely, compared to smoking, vaping resulted in greater reduction of exhaled CO (6.9 ppm vs 2.6, p for interaction < 0.001), improvement of PWV (decrease of 0.8 m/s vs increase of 0.8 m/s, p for interaction = 0.020) and reduction of MDA (reduction 0.13 vs increase 0.19 nmol/L, p for interaction = 0.035). Switching to electronic cigarette for 4 months has a neutral effect on platelet function while it reduces arterial stiffness and oxidative stress compared to tobacco smoking.


Subject(s)
Blood Platelets/drug effects , Electronic Nicotine Delivery Systems , Endothelium, Vascular/drug effects , Nicotine/pharmacology , Endothelium, Vascular/physiology , Humans
6.
Atherosclerosis ; 262: 123-130, 2017 07.
Article in English | MEDLINE | ID: mdl-28549278

ABSTRACT

BACKGROUND AND AIMS: The effects of medically-aided smoking cessation on vascular function and oxidative stress are not fully clarified. METHODS: One hundred eighty-eight current smokers were randomized to varenicline or nicotine replacement treatment (NRT) for a 3-month period. We assessed: (a) augmentation index (Aix) and pulse wave velocity (PWV); (b) perfusion boundary region (PBR) of sublingual microvasculature (range:5-25 µm), an index of the endothelial glycocalyx thickness, using Sideview, Darkfield imaging; (c) the exhaled CO; and (d) the malondialdehyde (MDA) and protein carbonyls (PC) plasma levels, as markers of oxidative stress, at baseline and after 3 and 12 months. RESULTS: After 3 months of treatment, CO, MDA, PC and Aix were decreased in all subjects (median CO: 25 vs. 6 ppm, MDA: 0.81 vs. 0.63 nmol/L, PC: 0.102, vs. 0.093 nmol/mg protein, Aix: 13% vs. 9%, p < 0.05) while PWV remained unchanged. Endothelial glycocalyx integrity showed a greater improvement in the varenicline than the NRT treatment (PBR range 5-9 µm: 1.07 ± 0.02 vs. 1.17 ± 0.02 µm, p = 0.03) in parallel with the greater CO reduction (5 vs. 7 ppm, p = 0.02). At 1-year follow-up, MDA, PC, Aix and PBR at 5-25 µm range were further improved in subjects who abstained from smoking (n = 84 out of 188), while the above markers and PWV deteriorated in relapsed smokers (p < 0.05). CONCLUSIONS: A smoking cessation program using varenicline or NRT for 3 months resulted in a decrease of CO, oxidative stress, arterial stiffness and restored endothelial glycocalyx. These effects were more evident after varenicline treatment, likely because of a greater CO reduction, and were maintained after 1 year only in subjects who abstained from smoking.


Subject(s)
Endothelial Cells/drug effects , Glycocalyx/drug effects , Nicotinic Agonists/therapeutic use , Oxidative Stress/drug effects , Smoking Cessation/methods , Smoking/drug therapy , Tobacco Use Cessation Devices , Tobacco Use Disorder/drug therapy , Varenicline/therapeutic use , Vascular Stiffness/drug effects , Adult , Aged , Breath Tests , Carbon Monoxide/metabolism , Endothelial Cells/metabolism , Endothelial Cells/pathology , Female , Glycocalyx/metabolism , Glycocalyx/pathology , Greece , Humans , Male , Malondialdehyde/metabolism , Middle Aged , Nicotinic Agonists/adverse effects , Protein Carbonylation/drug effects , Pulse Wave Analysis , Smoking/metabolism , Smoking/pathology , Smoking/physiopathology , Time Factors , Tobacco Use Cessation Devices/adverse effects , Tobacco Use Disorder/metabolism , Tobacco Use Disorder/pathology , Tobacco Use Disorder/physiopathology , Treatment Outcome , Varenicline/adverse effects
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