Pub Date : 2025-11-21eCollection Date: 2025-01-01DOI: 10.18332/tid/211500
Jimin Lee, Youngmee Kim, Won-Kyung Cho
Introduction: Given the shared risk profiles and interdependence of smoking and drinking behaviors, this study aimed to examine factors associated with smoking and alcohol consumption among older adult Korean men.
Methods: This was a secondary cross-sectional analysis of data pooled from the Korea National Health and Nutrition Examination Survey (KNHANES) conducted between 2007 and 2019, encompassing 7259 men aged ≥65 years. The participants were divided into the non-smoking/non-drinking, smoking/non-drinking, non-smoking/drinking, and smoking/drinking groups, and the sociodemographic and various health-related data collected via questionnaires and blood tests were used for multinomial logistic regression.
Results: When examining factors associated with each group using the non-smoking/non-drinking group as the reference group, several associated factors were identified. For example, not participating in regular exercise (AOR=1.31; 95% CI: 1.06-1.61; p=0.011), perceived health status as poor/very poor (AOR=1.56; 95% CI: 1.21-2.00; p<0.001), and skipping breakfast (AOR=1.90; 95% CI: 1.22-2.98; p=0.005) were some of the factors positively associated with the smoking/non-drinking group. Conversely BMI ≥25 (AOR=1.44; 95% CI: 1.12-1.83; p=0.004), elevated triglyceride levels (AOR=1.03; 95% CI: 1.03-1.05; p<0.001), and more daily fat intake (AOR=1.20; 95% CI: 1.03-1.40; p=0.019) were positively associated with the non-smoking/drinking group. Higher triglyceride levels (AOR=1.03; 95% CI: 1.01-1.05; p<0.001), depressive mood (AOR=2.10; 95% CI: 1.20-3.67; p=0.009), and more daily fat intake (AOR=1. 27; 95% CI: 1.07-1.51; p=0.007) were positively associated with the smoking/drinking group.
Conclusions: Metabolic changes, such as higher triglyceride levels, were more common in the drinking groups, whereas negative emotions were more prevalent among smokers. These findings may highlight the need for targeted interventions to promote healthier lifestyles among older adults; however, further research is necessary to revalidate our study findings.
{"title":"Secondary cross-sectional analysis of smoking and drinking factors among older Korean men: A 13-year national survey.","authors":"Jimin Lee, Youngmee Kim, Won-Kyung Cho","doi":"10.18332/tid/211500","DOIUrl":"10.18332/tid/211500","url":null,"abstract":"<p><strong>Introduction: </strong>Given the shared risk profiles and interdependence of smoking and drinking behaviors, this study aimed to examine factors associated with smoking and alcohol consumption among older adult Korean men.</p><p><strong>Methods: </strong>This was a secondary cross-sectional analysis of data pooled from the Korea National Health and Nutrition Examination Survey (KNHANES) conducted between 2007 and 2019, encompassing 7259 men aged ≥65 years. The participants were divided into the non-smoking/non-drinking, smoking/non-drinking, non-smoking/drinking, and smoking/drinking groups, and the sociodemographic and various health-related data collected via questionnaires and blood tests were used for multinomial logistic regression.</p><p><strong>Results: </strong>When examining factors associated with each group using the non-smoking/non-drinking group as the reference group, several associated factors were identified. For example, not participating in regular exercise (AOR=1.31; 95% CI: 1.06-1.61; p=0.011), perceived health status as poor/very poor (AOR=1.56; 95% CI: 1.21-2.00; p<0.001), and skipping breakfast (AOR=1.90; 95% CI: 1.22-2.98; p=0.005) were some of the factors positively associated with the smoking/non-drinking group. Conversely BMI ≥25 (AOR=1.44; 95% CI: 1.12-1.83; p=0.004), elevated triglyceride levels (AOR=1.03; 95% CI: 1.03-1.05; p<0.001), and more daily fat intake (AOR=1.20; 95% CI: 1.03-1.40; p=0.019) were positively associated with the non-smoking/drinking group. Higher triglyceride levels (AOR=1.03; 95% CI: 1.01-1.05; p<0.001), depressive mood (AOR=2.10; 95% CI: 1.20-3.67; p=0.009), and more daily fat intake (AOR=1. 27; 95% CI: 1.07-1.51; p=0.007) were positively associated with the smoking/drinking group.</p><p><strong>Conclusions: </strong>Metabolic changes, such as higher triglyceride levels, were more common in the drinking groups, whereas negative emotions were more prevalent among smokers. These findings may highlight the need for targeted interventions to promote healthier lifestyles among older adults; however, further research is necessary to revalidate our study findings.</p>","PeriodicalId":23202,"journal":{"name":"Tobacco Induced Diseases","volume":"23 ","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12639415/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145588701","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-21eCollection Date: 2025-01-01DOI: 10.18332/tid/209609
Xingyi Zhang, Ting Chen, Guoyue Zhang, Xianzhi Du, Rui Xu
Introduction: Preserved ratio impaired spirometry (PRISm) is a new and variable phenotype of spirometry impairment that was first defined by the Global Initiative for Chronic Obstructive Lung Disease (GOLD) in 2023. The identification of high-risk factors for the progression from PRISm to COPD remains insufficient at present.
Methods: Mendelian randomization (MR) analysis was conducted using genome-wide association study (GWAS) summary statistics. Genetic instruments for smoking behavior were derived from the GWAS & Sequencing Consortium of Alcohol and Nicotine use (GSCAN) (n=607291), while PRISm case-control data were sourced from the UK Biobank (n=296282). The inverse-variance weighted (IVW) method served as the primary analytical approach, supplemented by heterogeneity assessment, pleiotropy evaluation, and sensitivity analyses. For the meta-analysis, PubMed, Embase, Cochrane Library, and Web of Science were systematically searched from inception to 31 December 2024, to identify relevant studies that followed up on the changes in spirometry among individuals with PRISm or studies that reported the possible factors related to the changes in spirometry among individuals with PRISm. The risk of bias and the quality of the included studies were assessed using the Newcastle-Ottawa Scale (NOS).
Results: The MR analysis identified 85 SNPs as genetic instruments, revealing a modest causal link between cigarette smoking and PRISm prevalence (IVW: OR=1.01-1.02, p=0.048). The meta-analysis of 14 studies (n=7336 PRISm cases) shows 20.8% (95% CI: 15.6-25.9) progress to COPD at follow-up, with no significant difference by follow-up duration (<5 vs ≥5 years). Persistent PRISm occurs in 41.5% (95% CI: 35.8-47.2), more frequently in long-term follow-up subgroups. Baseline 'chest distress/dyspnea' (OR=3.81; 95% CI: 1.47-9.84) and 'current smoking' (OR=2.18; 95% CI: 1.14-4.15) significantly predict progression, while respiratory symptoms, FEV1/FVC ratio, TLC%, and FVC% show no association.
Conclusions: Our findings suggest a modest causal link between cigarette smoking and PRISm prevalence. The progression of PRISm to COPD within 5 years is approximately 20.8%. Among individuals with PRISm at the first visit, 'chest distress or dyspnea' and 'current smoking' are potential clinical risk factors for the progression of PRISm to COPD.
保存比例肺功能受损(PRISm)是肺功能受损的一种新的可变表型,于2023年由全球慢性阻塞性肺疾病倡议(GOLD)首次定义。目前,从PRISm到COPD进展的高危因素的识别仍然不足。方法:采用全基因组关联研究(GWAS)汇总统计进行孟德尔随机化(MR)分析。吸烟行为的遗传工具来自酒精和尼古丁使用GWAS和测序联盟(GSCAN) (n=607291),而PRISm病例对照数据来自英国生物银行(n=296282)。以反方差加权法(IVW)为主要分析方法,辅以异质性评价、多效性评价和敏感性分析。meta分析系统检索了PubMed、Embase、Cochrane Library和Web of Science从启动到2024年12月31日,以确定随访PRISm患者肺活量变化的相关研究或报告PRISm患者肺活量变化可能相关因素的研究。采用纽卡斯尔-渥太华量表(NOS)对纳入研究的偏倚风险和质量进行评估。结果:MR分析确定了85个snp作为遗传工具,揭示了吸烟与PRISm患病率之间的适度因果关系(IVW: OR=1.01-1.02, p=0.048)。14项研究(n=7336例PRISm病例)的荟萃分析显示,随访期间20.8% (95% CI: 15.6-25.9)进展为COPD,随访时间差异无统计学意义(1/FVC比、TLC%和FVC%无相关性)。结论:我们的研究结果表明吸烟与PRISm患病率之间存在适度的因果关系。PRISm在5年内发展为COPD的比例约为20.8%。在首次就诊时患有PRISm的患者中,“胸闷或呼吸困难”和“当前吸烟”是PRISm进展为COPD的潜在临床危险因素。
{"title":"Causal association between cigarette smoking and the prevalence of preserved ratio impaired spirometry (PRISm), and the progression risk factors of PRISm: A study based on Mendelian randomization and meta-analysis.","authors":"Xingyi Zhang, Ting Chen, Guoyue Zhang, Xianzhi Du, Rui Xu","doi":"10.18332/tid/209609","DOIUrl":"10.18332/tid/209609","url":null,"abstract":"<p><strong>Introduction: </strong>Preserved ratio impaired spirometry (PRISm) is a new and variable phenotype of spirometry impairment that was first defined by the Global Initiative for Chronic Obstructive Lung Disease (GOLD) in 2023. The identification of high-risk factors for the progression from PRISm to COPD remains insufficient at present.</p><p><strong>Methods: </strong>Mendelian randomization (MR) analysis was conducted using genome-wide association study (GWAS) summary statistics. Genetic instruments for smoking behavior were derived from the GWAS & Sequencing Consortium of Alcohol and Nicotine use (GSCAN) (n=607291), while PRISm case-control data were sourced from the UK Biobank (n=296282). The inverse-variance weighted (IVW) method served as the primary analytical approach, supplemented by heterogeneity assessment, pleiotropy evaluation, and sensitivity analyses. For the meta-analysis, PubMed, Embase, Cochrane Library, and Web of Science were systematically searched from inception to 31 December 2024, to identify relevant studies that followed up on the changes in spirometry among individuals with PRISm or studies that reported the possible factors related to the changes in spirometry among individuals with PRISm. The risk of bias and the quality of the included studies were assessed using the Newcastle-Ottawa Scale (NOS).</p><p><strong>Results: </strong>The MR analysis identified 85 SNPs as genetic instruments, revealing a modest causal link between cigarette smoking and PRISm prevalence (IVW: OR=1.01-1.02, p=0.048). The meta-analysis of 14 studies (n=7336 PRISm cases) shows 20.8% (95% CI: 15.6-25.9) progress to COPD at follow-up, with no significant difference by follow-up duration (<5 vs ≥5 years). Persistent PRISm occurs in 41.5% (95% CI: 35.8-47.2), more frequently in long-term follow-up subgroups. Baseline 'chest distress/dyspnea' (OR=3.81; 95% CI: 1.47-9.84) and 'current smoking' (OR=2.18; 95% CI: 1.14-4.15) significantly predict progression, while respiratory symptoms, FEV<sub>1</sub>/FVC ratio, TLC%, and FVC% show no association.</p><p><strong>Conclusions: </strong>Our findings suggest a modest causal link between cigarette smoking and PRISm prevalence. The progression of PRISm to COPD within 5 years is approximately 20.8%. Among individuals with PRISm at the first visit, 'chest distress or dyspnea' and 'current smoking' are potential clinical risk factors for the progression of PRISm to COPD.</p>","PeriodicalId":23202,"journal":{"name":"Tobacco Induced Diseases","volume":"23 ","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12639413/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145588624","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction: Smoking is well-established as the primary risk factor for laryngeal cancer, yet high-quality clinical randomized controlled trials are lacking. To address this gap, we utilized Mendelian randomization (MR), a novel research approach that offers an alternative to traditional randomized controlled trials. Our study aimed to reaffirm the connection between smoking and laryngeal cancer, while also contributing new insights for global public health prevention.
Methods: We performed a two-sample MR analysis using publicly released genome-wide association studies (GWAS) statistics. Smoking as exposure and laryngeal cancer as outcome. The inverse-variance weighted (IVW) method was used to analyze the genetic causal association between smoking and laryngeal cancer. We applied four complementary methods, including weighted median, weighted mode, MR-Egger regression, and MR pleiotropy residual sum and outlier (MR-PRESSO) to detect and correct for the effect of horizontal pleiotropy.
Results: Based on IVW, we found a causal association between smoking (cigarettes per day) and laryngeal cancer (OR=9.55; 95% CI: 1.26-72.27; p=0.03). There was a potential genetic causal association between smoking and laryngeal cancer. No heterogeneity (Q=34.06, p=0.89) or horizontal pleiotropy (Egger intercept, p=0.69) was found in any of the analyses. Sensitivity analyses confirmed robustness (MR-PRESSO global test, p=0.96). None of the leave-one-out tests in the analyses found any SNP that could affect the results of MR.
Conclusions: Genetic liability to smoking is associated with a higher risk of laryngeal cancer. Our findings support a genetic link between smoking and laryngeal cancer, underscoring the importance of smoking prevention in public health strategies.
{"title":"Causal association of smoking and laryngeal cancer: A Mendelian randomization study.","authors":"Fengbo Yang, Xing Chen, Ruoying Wei, Ping Lv, Mohammed Abdelfatah Alhoot","doi":"10.18332/tid/209744","DOIUrl":"10.18332/tid/209744","url":null,"abstract":"<p><strong>Introduction: </strong>Smoking is well-established as the primary risk factor for laryngeal cancer, yet high-quality clinical randomized controlled trials are lacking. To address this gap, we utilized Mendelian randomization (MR), a novel research approach that offers an alternative to traditional randomized controlled trials. Our study aimed to reaffirm the connection between smoking and laryngeal cancer, while also contributing new insights for global public health prevention.</p><p><strong>Methods: </strong>We performed a two-sample MR analysis using publicly released genome-wide association studies (GWAS) statistics. Smoking as exposure and laryngeal cancer as outcome. The inverse-variance weighted (IVW) method was used to analyze the genetic causal association between smoking and laryngeal cancer. We applied four complementary methods, including weighted median, weighted mode, MR-Egger regression, and MR pleiotropy residual sum and outlier (MR-PRESSO) to detect and correct for the effect of horizontal pleiotropy.</p><p><strong>Results: </strong>Based on IVW, we found a causal association between smoking (cigarettes per day) and laryngeal cancer (OR=9.55; 95% CI: 1.26-72.27; p=0.03). There was a potential genetic causal association between smoking and laryngeal cancer. No heterogeneity (Q=34.06, p=0.89) or horizontal pleiotropy (Egger intercept, p=0.69) was found in any of the analyses. Sensitivity analyses confirmed robustness (MR-PRESSO global test, p=0.96). None of the leave-one-out tests in the analyses found any SNP that could affect the results of MR.</p><p><strong>Conclusions: </strong>Genetic liability to smoking is associated with a higher risk of laryngeal cancer. Our findings support a genetic link between smoking and laryngeal cancer, underscoring the importance of smoking prevention in public health strategies.</p>","PeriodicalId":23202,"journal":{"name":"Tobacco Induced Diseases","volume":"23 ","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12639414/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145588660","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-20eCollection Date: 2025-01-01DOI: 10.18332/tid/211432
Anthony A Laverty, Jennie C Parnham, Martin McKee, Filippos T Filippidis, Nicholas S Hopkinson
Introduction: There are growing concerns that advertising and promotion on social media are driving youth use of tobacco and e-cigarettes. The UK provides an instructive example as it has high levels of e-cigarette use, high levels of social media use and a restrictive tobacco control environment. Existing evidence in the UK, however, has not focused on children, and has not been updated to reflect changes in patterns of social media use and in the use of these products. The aim of this study is to assess the associations of social media use with smoking and vaping.
Methods: Using data from the United Kingdom Household Longitudinal Study on adolescents aged 10-17 years between 2015-2023, we employed generalized estimating equation (GEE) models to estimate the relationships between time spent on social media and likelihood of smoking tobacco and using e-cigarettes. Models were controlled for possible confounders including sociodemographics and whether children lived in a home with e-cigarette use or tobacco smoking. We included data from 9359 participants with 25704 observations.
Results: Current cigarette smoking was reported by 4.9% of the sample and current e-cigarette use by 3.1%. Our adjusted models found strong relationships between time spent on social media and both smoking and vaping (p for trend <0.001). For example, use of social media for ≥7 hours/day was linked to greater odds of tobacco (adjusted odds ratio, AOR=5.13; 95% CI: 3.32-7.95) and e-cigarette use (AOR=4.26; CI: 2.25-8.08).
Conclusions: This study finds associations between time spent on social media and both smoking and vaping among children. Enforcing regulations on content and restricting the duration of social media use may be warranted to protect children's health.
{"title":"Social media use and child cigarette smoking and e-cigarette use: A cohort study 2015-2023.","authors":"Anthony A Laverty, Jennie C Parnham, Martin McKee, Filippos T Filippidis, Nicholas S Hopkinson","doi":"10.18332/tid/211432","DOIUrl":"10.18332/tid/211432","url":null,"abstract":"<p><strong>Introduction: </strong>There are growing concerns that advertising and promotion on social media are driving youth use of tobacco and e-cigarettes. The UK provides an instructive example as it has high levels of e-cigarette use, high levels of social media use and a restrictive tobacco control environment. Existing evidence in the UK, however, has not focused on children, and has not been updated to reflect changes in patterns of social media use and in the use of these products. The aim of this study is to assess the associations of social media use with smoking and vaping.</p><p><strong>Methods: </strong>Using data from the United Kingdom Household Longitudinal Study on adolescents aged 10-17 years between 2015-2023, we employed generalized estimating equation (GEE) models to estimate the relationships between time spent on social media and likelihood of smoking tobacco and using e-cigarettes. Models were controlled for possible confounders including sociodemographics and whether children lived in a home with e-cigarette use or tobacco smoking. We included data from 9359 participants with 25704 observations.</p><p><strong>Results: </strong>Current cigarette smoking was reported by 4.9% of the sample and current e-cigarette use by 3.1%. Our adjusted models found strong relationships between time spent on social media and both smoking and vaping (p for trend <0.001). For example, use of social media for ≥7 hours/day was linked to greater odds of tobacco (adjusted odds ratio, AOR=5.13; 95% CI: 3.32-7.95) and e-cigarette use (AOR=4.26; CI: 2.25-8.08).</p><p><strong>Conclusions: </strong>This study finds associations between time spent on social media and both smoking and vaping among children. Enforcing regulations on content and restricting the duration of social media use may be warranted to protect children's health.</p>","PeriodicalId":23202,"journal":{"name":"Tobacco Induced Diseases","volume":"23 ","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12641251/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145606222","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-19eCollection Date: 2025-01-01DOI: 10.18332/tid/209954
Anasua Kundu, Anna Feore, Nada Abu-Zarour, Sherald Sanchez, Megan Sutton, Kyran Sachdeva, Siddharth Seth, Robert Schwartz, Michael Chaiton
Introduction: In this review, we aimed to explore whether nicotine e-cigarette or vaping product use impact respiratory health.
Methods: We searched CINAHL, Embase, MEDLINE, PsycINFO, PubMed and Cochrane library databases initially in January 2023 and updated the search in January 2024. We included peer-reviewed human, animal, cell/in vitro original studies published between July 2021 and December 2023 but excluded qualitative studies. Three types of e-cigarette exposure were examined: acute, short-to-medium term, and long-term.
Results: We included 119 studies in the main analysis, and 5 in meta-analysis. Over half of the studies had low risk of bias. Non-smoker current vapers had higher incident risk of respiratory symptoms (relative risk, RR=1.90; 95% CI: 1.28-2.83) but statistically non-significant risk of chronic obstructive pulmonary disease (COPD) (RR=2.53; 95% CI: 0.96-6.67) compared to never users. They also had lower incident risk of respiratory symptoms compared to non-vaper current smokers (RR=0.75; 95% CI: 0.64-0.89) and dual users (dual use vs vaping, RR=1.26; 95% CI: 1.03-1.55). Dual users had higher risk of incidence of respiratory symptoms and prevalence of COPD compared to never users (RR=2.53; 95% CI: 1.44-4.45 and RR=3.86; 95% CI: 1.49-10.02, respectively), and the risk was statistically similar to non-vaper current smokers (RR=0.97; 95% CI: 0.84-1.14 and RR=1.15; 95% CI: 1.00-1.33, respectively). All meta-analysis findings were of 'very low' to 'low' certainty evidence. Of the studies not included in meta-analysis, we found 'moderate' certainty evidence of higher risk of respiratory symptoms, COPD, asthma, lung inflammation and damage in non-smoker current vapers compared to non-users, inconsistent findings on the risk of COVID-19 and other respiratory infections, and no significant association with e-cigarette associated lung injury.
Conclusions: E-cigarettes are associated with harms to the respiratory system. Further longitudinal research with special attention to measuring effects in different e-cigarette user populations are warranted.
{"title":"Evidence update on the respiratory health effects of vaping e-cigarettes: A systematic review and meta-analysis.","authors":"Anasua Kundu, Anna Feore, Nada Abu-Zarour, Sherald Sanchez, Megan Sutton, Kyran Sachdeva, Siddharth Seth, Robert Schwartz, Michael Chaiton","doi":"10.18332/tid/209954","DOIUrl":"10.18332/tid/209954","url":null,"abstract":"<p><strong>Introduction: </strong>In this review, we aimed to explore whether nicotine e-cigarette or vaping product use impact respiratory health.</p><p><strong>Methods: </strong>We searched CINAHL, Embase, MEDLINE, PsycINFO, PubMed and Cochrane library databases initially in January 2023 and updated the search in January 2024. We included peer-reviewed human, animal, cell/<i>in vitro</i> original studies published between July 2021 and December 2023 but excluded qualitative studies. Three types of e-cigarette exposure were examined: acute, short-to-medium term, and long-term.</p><p><strong>Results: </strong>We included 119 studies in the main analysis, and 5 in meta-analysis. Over half of the studies had low risk of bias. Non-smoker current vapers had higher incident risk of respiratory symptoms (relative risk, RR=1.90; 95% CI: 1.28-2.83) but statistically non-significant risk of chronic obstructive pulmonary disease (COPD) (RR=2.53; 95% CI: 0.96-6.67) compared to never users. They also had lower incident risk of respiratory symptoms compared to non-vaper current smokers (RR=0.75; 95% CI: 0.64-0.89) and dual users (dual use vs vaping, RR=1.26; 95% CI: 1.03-1.55). Dual users had higher risk of incidence of respiratory symptoms and prevalence of COPD compared to never users (RR=2.53; 95% CI: 1.44-4.45 and RR=3.86; 95% CI: 1.49-10.02, respectively), and the risk was statistically similar to non-vaper current smokers (RR=0.97; 95% CI: 0.84-1.14 and RR=1.15; 95% CI: 1.00-1.33, respectively). All meta-analysis findings were of 'very low' to 'low' certainty evidence. Of the studies not included in meta-analysis, we found 'moderate' certainty evidence of higher risk of respiratory symptoms, COPD, asthma, lung inflammation and damage in non-smoker current vapers compared to non-users, inconsistent findings on the risk of COVID-19 and other respiratory infections, and no significant association with e-cigarette associated lung injury.</p><p><strong>Conclusions: </strong>E-cigarettes are associated with harms to the respiratory system. Further longitudinal research with special attention to measuring effects in different e-cigarette user populations are warranted.</p>","PeriodicalId":23202,"journal":{"name":"Tobacco Induced Diseases","volume":"23 ","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12628669/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145565652","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction: Bipolar disorder is a periodic episode of extreme fluctuations in emotion that has been shown to be associated with smoking and irritability, but the relationship between the three has not been studied, especially in terms of genetic causality. This study aimed to obtain potential causal estimates of the association between irritability and bipolar disorder while quantifying the mediating effects of the modifiable risk factor, smoking.
Methods: This study used a two-step Mendelian randomization (MR) method and employed the inverse variance weighted method for the two-sample MR, utilizing SNPs as genetic instruments. Sensitivity analyses were conducted to detect heterogeneity and horizontal pleiotropy.
Results: Irritability (OR=3.13; 95% CI: 1.23-7.93; p=0.016) and smoking (OR=2.00; 95% CI: 1.47-2.37; p<0.001) were significantly associated with bipolar disorder from a genetic perspective. Irritability was associated with a higher risk of smoking (OR=1.21; 95% CI: 1.07-1.37; p=0.002). Sensitivity analyses confirmed the robustness of these results. Mediation analysis indicated that smoking partially mediated the potential pathway from irritability and bipolar disorder, with the proportion of the effect of irritability on bipolar disorder mediated by smoking being 11.76% (95% CI: 2-21; p=0.012).
Conclusions: Smoking plays a mediating role in the potential causal pathway linking irritability and bipolar disorder, suggesting that smoking cessation interventions may possibly help mitigate the risk of bipolar disorder among individuals with heightened irritability.
{"title":"The causal mediating effect of smoking on the relationship between irritability and bipolar disorder: A two-step Mendelian randomization study.","authors":"Qianying Hu, Chaoyan Yue, Yifeng Xu, Jianhua Chen, Xin Luo, Enzhao Cong","doi":"10.18332/tid/209615","DOIUrl":"10.18332/tid/209615","url":null,"abstract":"<p><strong>Introduction: </strong>Bipolar disorder is a periodic episode of extreme fluctuations in emotion that has been shown to be associated with smoking and irritability, but the relationship between the three has not been studied, especially in terms of genetic causality. This study aimed to obtain potential causal estimates of the association between irritability and bipolar disorder while quantifying the mediating effects of the modifiable risk factor, smoking.</p><p><strong>Methods: </strong>This study used a two-step Mendelian randomization (MR) method and employed the inverse variance weighted method for the two-sample MR, utilizing SNPs as genetic instruments. Sensitivity analyses were conducted to detect heterogeneity and horizontal pleiotropy.</p><p><strong>Results: </strong>Irritability (OR=3.13; 95% CI: 1.23-7.93; p=0.016) and smoking (OR=2.00; 95% CI: 1.47-2.37; p<0.001) were significantly associated with bipolar disorder from a genetic perspective. Irritability was associated with a higher risk of smoking (OR=1.21; 95% CI: 1.07-1.37; p=0.002). Sensitivity analyses confirmed the robustness of these results. Mediation analysis indicated that smoking partially mediated the potential pathway from irritability and bipolar disorder, with the proportion of the effect of irritability on bipolar disorder mediated by smoking being 11.76% (95% CI: 2-21; p=0.012).</p><p><strong>Conclusions: </strong>Smoking plays a mediating role in the potential causal pathway linking irritability and bipolar disorder, suggesting that smoking cessation interventions may possibly help mitigate the risk of bipolar disorder among individuals with heightened irritability.</p>","PeriodicalId":23202,"journal":{"name":"Tobacco Induced Diseases","volume":"23 ","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12598469/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145496967","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-07eCollection Date: 2025-01-01DOI: 10.18332/tid/210669
Catherine O Egbe, Mukhethwa Londani, Siphesihle Gwambe, Leonce Sessou, Omotayo F Fagbule, Stella A Bialous
Introduction: The tobacco 'endgame' concept proposes moving beyond traditional tobacco control measures towards a tobacco-free future. The aim of this study is to investigate the perceptions of tobacco control stakeholders in Africa on their agreement with what endgame approaches are suited for the region to achieve a tobacco-free society.
Methods: Data were collected using a web-based cross-sectional survey hosted on Redcap. A total of 146 stakeholders from 28 African countries took the survey. Participants rated agreement with 11 proposed endgame approaches drawn from the literature and the qualitative phase of this study. Descriptive analysis was used to summarize stakeholders' level of agreement while bivariate (chi-squared and Fisher's exact tests) and adjusted modified Poisson regression analyses examined association between agreement/disagreement to endgame approaches and demographic factors. Data were analyzed using STATA v17.
Results: All participants agreed to an integrated endgame approach while over 90% agreed with six measures (having non-addictive cigarettes, making cigarette unappealing, tobacco-free generation, regulated market model, quota/sinking lid and specific approaches for Africa). Agreements ranged from 70-85% for price caps, performance-based regulation, and non-combustible nicotine products, while only 35% supported government takeover of tobacco companies. Adjusted Poisson regression analyses showed that female stakeholders were less likely to support restricting tobacco sales by year of birth (relative risk ratio, RRR=0.89) and price caps (RRR=0.78), while PhD holders were more likely to support restricting tobacco sales by year of birth (RRR=1.29) and price caps (RRR=1.27). Stakeholders from Southern Africa were less likely to support a state takeover of tobacco companies (RRR=0.40) and performance-based regulation (RRR=0.76). Having more than 20 years of tobacco control experience lowered the support of price caps endgame measures (RRR=0.45).
Conclusions: Policymakers are encouraged to use insights from this study to consider multifaceted approaches aimed at addressing the problem of commercial tobacco in the African region and pave the way for a tobacco-free Africa.
{"title":"Support for tobacco endgame approaches: Results from a web-based survey of stakeholders from 28 African countries.","authors":"Catherine O Egbe, Mukhethwa Londani, Siphesihle Gwambe, Leonce Sessou, Omotayo F Fagbule, Stella A Bialous","doi":"10.18332/tid/210669","DOIUrl":"10.18332/tid/210669","url":null,"abstract":"<p><strong>Introduction: </strong>The tobacco 'endgame' concept proposes moving beyond traditional tobacco control measures towards a tobacco-free future. The aim of this study is to investigate the perceptions of tobacco control stakeholders in Africa on their agreement with what endgame approaches are suited for the region to achieve a tobacco-free society.</p><p><strong>Methods: </strong>Data were collected using a web-based cross-sectional survey hosted on Redcap. A total of 146 stakeholders from 28 African countries took the survey. Participants rated agreement with 11 proposed endgame approaches drawn from the literature and the qualitative phase of this study. Descriptive analysis was used to summarize stakeholders' level of agreement while bivariate (chi-squared and Fisher's exact tests) and adjusted modified Poisson regression analyses examined association between agreement/disagreement to endgame approaches and demographic factors. Data were analyzed using STATA v17.</p><p><strong>Results: </strong>All participants agreed to an integrated endgame approach while over 90% agreed with six measures (having non-addictive cigarettes, making cigarette unappealing, tobacco-free generation, regulated market model, quota/sinking lid and specific approaches for Africa). Agreements ranged from 70-85% for price caps, performance-based regulation, and non-combustible nicotine products, while only 35% supported government takeover of tobacco companies. Adjusted Poisson regression analyses showed that female stakeholders were less likely to support restricting tobacco sales by year of birth (relative risk ratio, RRR=0.89) and price caps (RRR=0.78), while PhD holders were more likely to support restricting tobacco sales by year of birth (RRR=1.29) and price caps (RRR=1.27). Stakeholders from Southern Africa were less likely to support a state takeover of tobacco companies (RRR=0.40) and performance-based regulation (RRR=0.76). Having more than 20 years of tobacco control experience lowered the support of price caps endgame measures (RRR=0.45).</p><p><strong>Conclusions: </strong>Policymakers are encouraged to use insights from this study to consider multifaceted approaches aimed at addressing the problem of commercial tobacco in the African region and pave the way for a tobacco-free Africa.</p>","PeriodicalId":23202,"journal":{"name":"Tobacco Induced Diseases","volume":"23 ","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12598468/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145496954","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-06eCollection Date: 2025-01-01DOI: 10.18332/tid/211071
Yabin Xing, Wei Wen, Gang Wang, Kecheng Du
Introduction: In China, cigarettes function as both consumer goods and 'social currency'. Despite increased awareness of smoking risks, cigarette gifting persists. This study examines whether graphic warning images and price increases can reduce the social value of cigarettes in gifting contexts.
Methods: A survey experiment was conducted (n=744), randomly assigning participants to a control group (n=189), a price treatment group (n=285), and an image warning group (n=270). Eligible participants were adults with stable incomes. Participants in the price treatment group viewed the same cigarette brands as in the control condition but with retail prices doubled relative to the market price, whereas those in the image treatment group viewed cigarette packs with added graphic warning images while prices remained unchanged. The primary outcomes were willingness to gift or receive cigarettes in strong and weak relationships (1=very unwilling to 5=very willing) and brand tier preference (1=low, 2=mid, 3=high), and logistic regressions were applied to assess treatment effects. All comparisons were made against the control group, and logistic regression results are presented as coefficients (β) with 95% confidence intervals (CI).
Results: Graphic warning images significantly reduced willingness to gift cigarettes (β= -0.88; 95% CI: -1.33 - -0.42, p<0.001) and expectations to receive cigarettes (β= -0.62; 95% CI: -1.08 - -0.16, p<0.01) in weak relationships but had no significant effect in strong relationships. Price increases did not affect gifting willingness but reduced brand preference in weak relationships (β= -0.67; 95% CI: -1.11 - -0.23, p<0.01).
Conclusions: Graphic warnings effectively weaken the symbolic value of cigarettes in non-intimate relationships, while price increases alone are insufficient. Tobacco control strategies should prioritize altering symbolic meanings rather than relying solely on economic measures.
{"title":"Reframing cigarettes as social currency: A randomized survey experiment on the role of warning images and pricing.","authors":"Yabin Xing, Wei Wen, Gang Wang, Kecheng Du","doi":"10.18332/tid/211071","DOIUrl":"10.18332/tid/211071","url":null,"abstract":"<p><strong>Introduction: </strong>In China, cigarettes function as both consumer goods and 'social currency'. Despite increased awareness of smoking risks, cigarette gifting persists. This study examines whether graphic warning images and price increases can reduce the social value of cigarettes in gifting contexts.</p><p><strong>Methods: </strong>A survey experiment was conducted (n=744), randomly assigning participants to a control group (n=189), a price treatment group (n=285), and an image warning group (n=270). Eligible participants were adults with stable incomes. Participants in the price treatment group viewed the same cigarette brands as in the control condition but with retail prices doubled relative to the market price, whereas those in the image treatment group viewed cigarette packs with added graphic warning images while prices remained unchanged. The primary outcomes were willingness to gift or receive cigarettes in strong and weak relationships (1=very unwilling to 5=very willing) and brand tier preference (1=low, 2=mid, 3=high), and logistic regressions were applied to assess treatment effects. All comparisons were made against the control group, and logistic regression results are presented as coefficients (β) with 95% confidence intervals (CI).</p><p><strong>Results: </strong>Graphic warning images significantly reduced willingness to gift cigarettes (β= -0.88; 95% CI: -1.33 - -0.42, p<0.001) and expectations to receive cigarettes (β= -0.62; 95% CI: -1.08 - -0.16, p<0.01) in weak relationships but had no significant effect in strong relationships. Price increases did not affect gifting willingness but reduced brand preference in weak relationships (β= -0.67; 95% CI: -1.11 - -0.23, p<0.01).</p><p><strong>Conclusions: </strong>Graphic warnings effectively weaken the symbolic value of cigarettes in non-intimate relationships, while price increases alone are insufficient. Tobacco control strategies should prioritize altering symbolic meanings rather than relying solely on economic measures.</p>","PeriodicalId":23202,"journal":{"name":"Tobacco Induced Diseases","volume":"23 ","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12598467/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145496926","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction: Smoking is the leading, preventable factor which significantly increases the likelihood of household relative poverty in China. This study aimed to explore the association between smoking and relative poverty across different households and provide evidence for targeted tobacco control measures and poverty reduction policies.
Methods: This study adopted a longitudinal design using two waves of unbalanced panel data from the China Family Panel Studies (CFPS) conducted in 2018 and 2020. Data were collected through structured questionnaires and self-reported responses. Smoking status of household members was considered the exposure factor, while household relative poverty status, measured by the Foster-Greer-Thorbecke indices, served as the outcome variable. A panel logit random effects model was employed to estimate the determinants of relative poverty across households with varying smoking status.
Results: At the 50% median income poverty line, China's relative poverty headcount ratio was 22.15% in 2018 and 22.54% in 2020, with the poverty gap index declining from 11.08% to 10.82% and the squared poverty gap index increasing slightly from 7.13% to 7.17%. Former-smoking households showed the highest poverty incidence (26.3% in 2018; 26.24% in 2020), followed by current-smoking (24.94%; 23.28%) and non-smoking households (22.75%; 22.37%). The panel logit model revealed significantly higher likelihood for current-smoking (adjusted odds ratio, AOR=1.63; 95% CI: 1.44-1.86, p<0.01) and former-smoking households (AOR=1.95; 95% CI: 1.60-2.36, p<0.01) compared to non-smoking households. Additional factors associated with increased odds of poverty included having ≥65 years members, members with chronic disease, and members reporting a two-week illness (all p<0.01).
Conclusions: We conclude that China faces a substantial challenge of relative poverty, with tobacco use significantly increasing the likelihood of household poverty. Potential policy directions may include evaluating the effects of adjusting tobacco excise taxes and reforming tax collection mechanisms, exploring rural smokers' preferences for smoking cessation information to inform the development of targeted interventions and so on.
{"title":"An observational study on the association between smoking and relative poverty in China: Evidence from two waves of China Family Panel Studies.","authors":"Qiaoying Wei, Hao Wang, Quan Wan, Shenglin Liang, Wenpeng Pang, Qian Zeng, Peipei Chai","doi":"10.18332/tid/210322","DOIUrl":"10.18332/tid/210322","url":null,"abstract":"<p><strong>Introduction: </strong>Smoking is the leading, preventable factor which significantly increases the likelihood of household relative poverty in China. This study aimed to explore the association between smoking and relative poverty across different households and provide evidence for targeted tobacco control measures and poverty reduction policies.</p><p><strong>Methods: </strong>This study adopted a longitudinal design using two waves of unbalanced panel data from the China Family Panel Studies (CFPS) conducted in 2018 and 2020. Data were collected through structured questionnaires and self-reported responses. Smoking status of household members was considered the exposure factor, while household relative poverty status, measured by the Foster-Greer-Thorbecke indices, served as the outcome variable. A panel logit random effects model was employed to estimate the determinants of relative poverty across households with varying smoking status.</p><p><strong>Results: </strong>At the 50% median income poverty line, China's relative poverty headcount ratio was 22.15% in 2018 and 22.54% in 2020, with the poverty gap index declining from 11.08% to 10.82% and the squared poverty gap index increasing slightly from 7.13% to 7.17%. Former-smoking households showed the highest poverty incidence (26.3% in 2018; 26.24% in 2020), followed by current-smoking (24.94%; 23.28%) and non-smoking households (22.75%; 22.37%). The panel logit model revealed significantly higher likelihood for current-smoking (adjusted odds ratio, AOR=1.63; 95% CI: 1.44-1.86, p<0.01) and former-smoking households (AOR=1.95; 95% CI: 1.60-2.36, p<0.01) compared to non-smoking households. Additional factors associated with increased odds of poverty included having ≥65 years members, members with chronic disease, and members reporting a two-week illness (all p<0.01).</p><p><strong>Conclusions: </strong>We conclude that China faces a substantial challenge of relative poverty, with tobacco use significantly increasing the likelihood of household poverty. Potential policy directions may include evaluating the effects of adjusting tobacco excise taxes and reforming tax collection mechanisms, exploring rural smokers' preferences for smoking cessation information to inform the development of targeted interventions and so on.</p>","PeriodicalId":23202,"journal":{"name":"Tobacco Induced Diseases","volume":"23 ","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12584675/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145453101","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}