Department of Biostatistics and Data Science, The University of Texas Health Science Center at Houston, School of Public Health, Austin.
Michael and Susan Dell Center for Healthy Living, The University of Texas Health Science Center at Houston, School of Public Health, Austin.
JAMA Netw Open. 2024 May 1;7(5):e2410740. doi: 10.1001/jamanetworkopen.2024.10740.
The association of use of electronic nicotine delivery systems (ENDS) with the age of asthma onset is unknown.
To explore the association of past 30-day ENDS use with the age of asthma onset in adults and youths who did not have asthma or chronic obstructive pulmonary disease and never used cigarettes.
DESIGN, SETTING, AND PARTICIPANTS: This cohort study was a secondary analysis of waves 1 to 6 of the US nationally representative Population of Tobacco and Health Study (2013-2021). Eligible participants included adults (≥18 years) and youths (12-17 years) who did not have asthma or chronic obstructive pulmonary disease at the first wave of participation. Data analysis was conducted from September 2022 to April 2024.
Past 30-day ENDS use at the first wave of participation in the study preceding the onset of asthma.
Lower and upper age limits were estimated using the age reported at the first wave of participation and the number of weeks between follow-up waves until asthma was first reported or censored. The association of past 30-day ENDS use with the age of asthma onset was estimated using weighted interval-censoring Cox regression. The cumulative hazard function for the age of asthma onset was estimated using interval-censoring survival analysis.
A total of 24 789 participants were included, with 7766 adults (4461 female [weighted percentage, 59.11%] and 3305 male [weighted percentage, 40.89%]), representing 80.0 million adults, and 17 023 youths (8514 female [weighted percentage, 50.60%] and 8496 male [weighted percentage 49.32%]), representing 33.9 million youths. By age 27 years, 6.2 per 1000 adults reported asthma incidence (hazard ratio [HR], 0.62%; 95% CI, 0.46%-0.75%). While controlling for covariates, there was a 252% increased risk of the onset of asthma at earlier ages for adults who used ENDS in the past 30 days vs adults who did not (adjusted HR, 3.52; 95% CI, 1.24-10.02). For youths, there was no association of ENDS use in the past 30 days with age of asthma onset (adjusted HR, 1.79; 95% CI, 0.67-4.77), which could be due to a lack of statistical power.
In this cohort study, past 30-day ENDS use among adults was associated with earlier ages of asthma onset. These findings suggest that prevention and cessation programs directed to adults who use ENDS are needed to educate the public, protect public health, prevent adverse health outcomes, and motivate users to stop. Furthermore, modifying symptom-screening asthma guidelines, resulting in earlier asthma detection and treatment, may reduce morbidity and mortality due to asthma.
使用电子尼古丁传送系统(ENDS)与哮喘发病年龄之间的关联尚不清楚。
探讨过去 30 天内使用ENDS 与未患哮喘或慢性阻塞性肺疾病且从未使用过香烟的成年人和青少年哮喘发病年龄之间的关系。
设计、地点和参与者:这是一项对美国全国代表性烟草与健康研究(2013-2021 年)的第 1 至 6 波次的二次分析的队列研究。合格的参与者包括首次参加研究时没有哮喘或慢性阻塞性肺疾病的成年人(≥18 岁)和青少年(12-17 岁)。数据分析于 2022 年 9 月至 2024 年 4 月进行。
在哮喘发病前的研究第一波次中过去 30 天内使用ENDS。
使用首次参加研究时报告的年龄和随访波次之间的周数来估计下限和上限年龄,直到首次报告哮喘或被删失为止。使用加权间隔 censoring Cox 回归估计过去 30 天内使用 ENDS 与哮喘发病年龄之间的关系。使用间隔 censoring 生存分析估计哮喘发病年龄的累积风险函数。
共纳入 24789 名参与者,其中 7766 名成年人(4461 名女性[加权百分比,59.11%]和 3305 名男性[加权百分比,40.89%]),代表 8000 万成年人,以及 17023 名青少年(8514 名女性[加权百分比,50.60%]和 8496 名男性[加权百分比,49.32%]),代表 3390 万青少年。到 27 岁时,有 6.2%的成年人报告哮喘发病率(风险比[HR],0.62%;95%CI,0.46%-0.75%)。在控制了混杂因素后,与未使用 ENDS 的成年人相比,过去 30 天内使用 ENDS 的成年人哮喘发病年龄提前 2.52 倍(调整后的 HR,3.52;95%CI,1.24-10.02)。对于青少年,过去 30 天内使用 ENDS 与哮喘发病年龄之间没有关联(调整后的 HR,1.79;95%CI,0.67-4.77),这可能是由于缺乏统计学效力。
在这项队列研究中,成年人过去 30 天内使用 ENDS 与哮喘发病年龄提前有关。这些发现表明,需要针对使用 ENDS 的成年人制定预防和戒烟计划,以教育公众,保护公共健康,预防不良健康后果,并促使使用者戒烟。此外,修改以症状为导向的哮喘筛查指南,导致更早发现和治疗哮喘,可能会降低哮喘引起的发病率和死亡率。