Tobacco Consumption and Toxicant Exposure of Cigarette Smokers Using Electronic Cigarettes

被引:56
|
作者
Pulvers, Kim [1 ]
Emami, Ashley S. [1 ]
Nollen, Nicole L. [2 ]
Romero, Devan R. [3 ]
Strong, David R. [4 ]
Benowitz, Neal L. [5 ,6 ]
Ahluwalia, Jasjit S. [7 ]
机构
[1] Calif State Univ San Marcos, Dept Psychol, 333 S Twin Oaks Valley Rd, San Marcos, CA 92096 USA
[2] Univ Kansas, Sch Med, Dept Prevent Med & Publ Hlth, Kansas City, KS USA
[3] Calif State Univ San Marcos, Dept Kinesiol, San Marcos, CA USA
[4] Univ Calif San Diego, Dept Family Med & Publ Hlth, San Diego, CA 92103 USA
[5] Univ Calif San Francisco, Sch Med, Dept Med, Div Clin Pharmacol, San Francisco, CA USA
[6] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
[7] Rutgers State Univ, Sch Publ Hlth, Piscataway, NJ USA
关键词
METABOLITE 4-(METHYLNITROSAMINO)-1-(3-PYRIDYL)-1-BUTANOL; SMOKING REDUCTION; NICOTINE; DEPENDENCE; CARCINOGEN; BIOMARKERS; COTININE; BENEFITS; BELIEFS;
D O I
10.1093/ntr/ntw333
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
There is considerable debate about the benefits and risks of electronic cigarettes (ECs). To better understand the risk-benefit ratio of ECs, more information is needed about net nicotine consumption and toxicant exposure of cigarette smokers switching to ECs. Forty cigarette smokers (a parts per thousand 1 year of smoking) interested in switching to ECs but not necessarily quitting smoking were enrolled in a 4-week observational study and provided an e-Go C non-variable battery and refillable atomizers and choice of eight flavors in 12 or 24 mg nicotine dosage. Measurement of urinary cotinine (metabolite of nicotine), 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL; a pulmonary carcinogen), and eight volatile organic compounds (VOCs) that are toxic tobacco smoke constituents was conducted at baseline and week 4. All participants with follow-up data (92.5%) reported using the study EC. Of the 40 smokers, 16 reported no cigarettes at week 2 (40%) and six continued to report no cigarettes at week 4 (15%). Change in nicotine intake over the 4 weeks was non-significant (p = .90). Carbon monoxide (p < .001), NNAL (p < .01) and metabolites of benzene (p < .01) and acrylonitrile (p = .001) were significantly decreased in the study sample. Smokers switching exclusively to ECs for at least half of the study period demonstrated significant reductions in metabolites of ethylene oxide (p = .03) and acrylamide (p < .01). Smokers using ECs over 4 weeks maintained cotinine levels and experienced significant reductions in carbon monoxide, NNAL, and two out of eight measured VOC metabolites. Those who switched exclusively to ECs for at least half of the study period significantly reduced two additional VOCs. This study extends current literature by measuring change in smoking dependence and disease-associated biomarkers, NNAL and a panel of eight common VOCs that are toxic tobacco smoke constituents in smokers who switch to ECs. The findings support the idea of harm reduction, however some levels of toxicant exposure are still of clinical concern, particularly for dual users. Extrapolation of these results must be careful to separate the different toxic exposure results for exclusive switchers versus dual cigarette + EC users, and not to equate harm reduction with the idea that using ECs is harmless.
引用
收藏
页码:206 / 214
页数:9
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