Abstract
Background Use of electronic cigarettes (e-cigarettes) is prevalent among adolescents and young adults, but there has been limited knowledge about health consequences in human populations. We conduct a systematic review and meta-analysis of results on respiratory disorders from studies of general-population samples and consider the mapping of these results to findings about biological processes linked to e-cigarettes in controlled laboratory studies.
Method We conducted a literature search and meta-analysis of epidemiological studies on the association of e-cigarette use with asthma and with COPD. We discuss findings from laboratory studies about effects of e-cigarettes on four biological processes: cytotoxicity, oxidative stress/inflammation, susceptibility to infection and genetic expression.
Results Epidemiological studies, both cross-sectional and longitudinal, show a significant association of e-cigarette use with asthma and COPD, controlling for cigarette smoking and other covariates. For asthma (n=15 studies), the pooled adjusted odds ratio (aOR) was 1.39 (95% CI 1.28–1.51); for COPD (n=9 studies) the aOR was 1.49 (95% CI 1.36–1.65). Laboratory studies consistently show an effect of e-cigarettes on biological processes related to respiratory harm and susceptibility to illness, with e-cigarette conditions differing significantly from clean-air controls, although sometimes less than for cigarettes.
Conclusions The evidence from epidemiological studies meets established criteria for consistency, strength of effect, temporality, and in some cases a dose–response gradient. Biological plausibility is indicated by evidence from multiple laboratory studies. We conclude that e-cigarette use has consequences for asthma and COPD, which is of concern for respirology and public health.
Abstract
Epidemiological studies show a relationship of e-cigarette use with asthma and COPD, and laboratory studies show their adverse effects on four biological processes. It can be concluded that e-cigarette use is of significant concern for public health. https://bit.ly/3drH4pj
Introduction
Use of electronic cigarettes (e-cigarettes) and other types of electronic nicotine delivery systems is currently prevalent among adolescents and young adults [1, 2]. Recent surveys show that nicotine-based e-cigarette use is common [3] and indicate that 27.5% of US high school students are current e-cigarette users [4]. This prevalence has raised concern among a broad range of public health researchers and laboratory scientists [5–8].
While there has been considerable research on the correlates of e-cigarette use [9, 10], there has been less knowledge about health consequences in human populations. A report compiled early in 2017 concluded there was no definitive evidence on whether e-cigarettes cause respiratory disease in humans [11]. However, since then there has been considerable evidence on health variables from epidemiological investigations of large general-population samples, from laboratory studies of biological processes linked to e-cigarettes, and from case reports based on patients who have provided examples of respiratory disease associated with e-cigarette use [12–17].
The aim of this article is to provide a comprehensive review and meta-analysis of evidence from epidemiological studies about the association of e-cigarette use with asthma and COPD in human populations and to discuss this evidence in relation to findings from controlled laboratory studies of biological processes affected by e-cigarette use. Epidemiological studies indicate findings that occur in the natural environment of the participants and allow control for potential confounders. Laboratory studies have particular evidentiary value because they use experimental methods that allow for strict causal conclusions. Our review considers data from adolescents as well as adults, because of the prognostic significance of early respiratory symptomatology for lung disease at later ages [18–20]. We do not consider research on e-cigarettes and cardiovascular disease [21, 22] and we do not cover research on epigenetic and intergenerational effects [23–26].
For the epidemiological evidence, we provide a comprehensive review of all available studies and provide a meta-analysis of aggregate effect sizes across studies of asthma and COPD. For laboratory research, we discuss selected studies that are most relevant for interpreting the epidemiological findings on respiratory outcomes, as detailed reviews of laboratory research are available in focused areas [27, 28]. The present article is the first to conceptually link the epidemiological findings to evidence from laboratory research and to discuss the implications of these bodies of research when considered together.
Evidence from epidemiological studies
Epidemiological studies on the association of e-cigarettes (or synonyms thereof) with asthma and COPD (or synonyms thereof) in general populations were identified through searches on PsycINFO and PubMed, contacts with other investigators, and searching abstracts from recent research meetings. The search was conducted in March 2020.
The Preferred Reporting Items for Systematic Reviews and Meta-Analyses charts (figure 1) show how exclusion and inclusion criteria were applied for identified entries on asthma and COPD. Entries were coded and evaluated for appropriateness. To be included in the review, a study had to have a large representative sample, reasonable measures of e-cigarette use and cigarette smoking, a reasonable measure of respiratory disorder, and a comparison group of nonusers of e-cigarettes and combustible cigarettes (or repeated measures of the participants). Two of the authors (TW and SS) independently examined all entries and agreed on how studies met the criteria. Of 875 entries identified for asthma, 15 studies met all inclusion criteria; of 855 entries identified for COPD, nine studies met all criteria.
Flow chart for selection of studies a) asthma; b) COPD.
Four general issues are important for interpretation of this literature. First, because combustible cigarette smoking is correlated with e-cigarette use [29–31] and is a risk factor for respiratory disease, it is crucial to control for this correlation in multivariable analyses. As noted in the tables, most of the studies did control for cigarette smoking, indicating that observed effects for e-cigarettes are not attributable to confounding with smoking. Second, when e-cigarette use and cigarette smoking are entered together in a multivariable analysis, if they both show significant contributions to respiratory disease (i.e. additive effects) then the implication is that persons who both use e-cigarettes and smoke cigarettes will be worse off than exclusive e-cigarette users or exclusive smokers. Notes about additive effects are provided in the tables. Third, it is possible that the association between smoking and respiratory disease is different for persons who use e-cigarettes (i.e. interaction effect). This may be tested by a stratified analysis or by entering a cross-product term for e-cigarettes and smoking in a multivariable analysis in addition to their main effects. Interaction tests are noted in the tables. An interaction with OR >1 would indicate that the association of e-cigarette use with respiratory outcomes is greater among those who smoke (i.e. synergistic effect); OR <1 would indicate that e-cigarette use has a greater effect among nonsmokers (i.e. inverse interaction). Fourth, with cross-sectional data, the finding of a positive association for e-cigarettes and respiratory disease could be interpreted as meaning that persons who develop disease quit smoking cigarettes and take up e-cigarettes (i.e. reverse causation). This possibility may be addressed in cross-sectional data through internal analyses that logically would work either for or against an interpretation of reverse causation. Alternatively, longitudinal data showing that e-cigarette use precedes disease development in time would work against a reverse-causation interpretation. This issue is addressed in the review of the studies.
Epidemiological studies of asthma
Characteristics of studies of asthma are presented in table 1. Studies of adolescents typically used school-based data collection and criterion variables indicating diagnosis of asthma by a health professional. The participants in these studies were mostly high-school students (aged 15–18 years). Studies of adults used direct interview and telephone survey methods. Multivariable analyses typically adjusted for demographics, cigarette smoking, and other relevant covariates.
Epidemiological studies of e-cigarette use and asthma/bronchitis
Asthma among East Asian adolescents
All four studies [32–35] found the likelihood of respiratory symptoms to be significantly higher among e-cigarette users, with additive effects for e-cigarettes and smoking. Cho and Paik [32] also reported that e-cigarette users had more days absent from school because of asthma, an external validation. Kim et al. [33] and Lee et al. [34] found significant associations of e-cigarettes with asthma in pooled samples of middle- and high-school students. Cho and Paik [32] performed a cross-product test and found an inverse interaction: the association of e-cigarette use with asthma was significant among never-smokers, but was nonsignificant among smokers. Confirming these results, Wang et al. [35] reported a stronger association of e-cigarette use with respiratory symptoms among never-smokers. In these studies, the finding of a significant association with respiratory disease among never-smokers works against an interpretation of reverse causation.
Statewide surveys of asthma in Florida
Choi and Bernat [36] reported a stronger association of e-cigarettes with asthma for current (30-day) use (adjusted (a)OR=2.20) than for lifetime use (aOR=1.72). Another study [37] reported a significant association of e-cigarette use with asthma in the whole sample in a Florida survey conducted in a different year. Two analyses focusing on adolescents with asthma found own e-cigarette use [36] or second-hand exposure to e-cigarette aerosol [38] associated with higher likelihood of having had an asthma attack during the past year.
Regional and national surveys on asthma
A Canadian study [39] noted a significant association of ever e-cigarette use with lifetime asthma and a study in Hawaii [40] found a significant association of e-cigarette use with current asthma, controlling for cigarette smoking and other covariates (e.g. obesity). Similarly, a study with a US national sample [41] indicated a significant association of e-cigarette use with asthma controlling for cigarette smoking, marijuana use and other covariates. In two studies [40, 41], e-cigarette use and cigarette smoking made additive contributions to likelihood of asthma; cross-product tests for interaction between e-cigarette and cigarette smoking were mostly nonsignificant.
Bronchitis among high-school students
In a California study [42], chronic bronchitis was coded if in the previous 12 months a participant had daily cough, congestion or phlegm for 3 months in a row other than when having a cold. An analysis for the total sample showed significant associations of both e-cigarette use and smoking with chronic bronchitis and also showed a dose–response effect: the likelihood of bronchitis was higher with more frequent e-cigarette use. A significant association of e-cigarette use with bronchitis among never-smokers was noted, but a comparable analysis for smokers was not reported.
E-cigarette use and asthma among adults
In a national web-based survey conducted from 2013 through 2017 [43], current e-cigarette use was positively associated with a diagnosis of asthma and with a breathing-difficulty score. In Hawaii data from the Behavioral Risk Factor Surveillance Survey (BRFSS), e-cigarette use was significantly associated with asthma only among nonsmokers [44], similar to findings from three adolescent studies [32, 35, 42]. Osei et al. [45] pooled data from 2 years of national BRFSS data and noted a significant association of current e-cigarette use with current asthma among persons who had never smoked. They also noted a dose–response effect: a greater likelihood of asthma with more frequent e-cigarette use. Bhatta and Glantz [46] used longitudinal data from a national household interview study, the Population Assessment of Tobacco and Health (PATH), to predict incident (i.e. new) asthma at waves 2 and 3 among persons who were free of asthma at wave 1. There was a significant relationship of baseline e-cigarette use to incident asthma in this prospective analysis.
Epidemiological studies of COPD
In studies of respiratory disorder among adults (table 2), the criterion variable typically involved having been diagnosed with COPD (and sometimes other respiratory conditions) by a doctor, nurse or other health professional. Seven studies were cross-sectional and two were longitudinal. Multivariable analyses adjusted for covariates similar to those used for asthma, including demographics, cigarette smoking and obesity.
Epidemiological studies of e-cigarette use and respiratory disorders
US national sample (PATH)
In an analysis of PATH data [47], participants were classified as nonusers, exclusive e-cigarette users, exclusive smokers or dual users. Respiratory disease was coded if a respondent said they been told by a doctor they had any of COPD, chronic bronchitis, emphysema or asthma. Results showed that current exclusive e-cigarette users had a higher likelihood of respiratory disease compared with nonusers, and dual users had an even higher likelihood. Another analysis of PATH data using a propensity-matching design to control for a range of confounders [48] showed that current e-cigarette users had a higher likelihood of COPD compared with matched controls and a stratified analysis showed an inverse interaction: a much stronger association of e-cigarette use with COPD among nonsmokers compared with the rest of the sample. Li et al. [49] analysed seven specific symptoms of respiratory illness (e.g. wheezing, dry cough) in wave 2 PATH data. They found that exclusive e-cigarette use was positively related to most of the symptoms and this was not accounted for by smoking history. Dual users had greater risk for respiratory symptomatology compared with solo e-cigarette users (i.e. additive effects).
COPD in US samples
Data from a US national sample [43] indicated current exclusive e-cigarette use was significantly associated with diagnosed COPD, with the greatest likelihood of COPD found among dual users. A study with BRFSS data from Hawaii [44] found a significant inverse interaction: the association of exclusive e-cigarette use with COPD was stronger among nonsmokers compared with smokers. Analysis of national BRFSS data based on both ever- and current e-cigarette use [50] also showed an association of e-cigarette use with COPD that was stronger among nonsmokers than among smokers. This study reported a dose–response effect and emphasised that dual users were notably worse off for COPD.
Respiratory symptoms in regional samples from Sweden
Data from Sweden [51] included measures tapping occurrence of five specific respiratory symptoms (e.g. long-standing cough, sputum production). Among never-smokers, the association of e-cigarette use with likelihood of respiratory symptoms was marginally significant, but this may have been influenced by small cell size, as the overall rate of e-cigarette use in this sample was relatively low (2% of the population). Stratified analyses suggested e-cigarette use adding to risk among both former smokers and current smokers, but direct tests for additive effects were not conducted.
Longitudinal studies of respiratory disease
Prospective analyses of wave 1 through wave 3 PATH data [46] tested the relationship of e-cigarette use at baseline to new disease at follow-up (chronic bronchitis, emphysema or COPD) among persons who were free of disease at wave 1. Significant predictive effects were found for both prior and current e-cigarette use. Tests for additive effects indicated dual users were significantly worse off than exclusive e-cigarette users or exclusive smokers (aOR=3.30). In the COPDGene study [52], participants were aged 45–80 years and had ≥10 pack-years of smoking history. Respiratory disease status was indexed at baseline through lung function tests and self-report of chronic bronchitis and COPD; follow-up measures were obtained at 6-month intervals. Longitudinal analyses controlling for baseline clinical variables indicated e-cigarette use was related to a higher prevalence of chronic bronchitis and an increased number of COPD exacerbations. Participants who used e-cigarettes were more likely to have progression of lung disease on lung function tests, although this was nonsignificant with adjustment for covariates.
Meta-analysis
The meta-analysis was based on adjusted odds ratios for e-cigarette use that controlled for cigarette smoking and other disease-related risk factors (compare with [10]). The meta-analysis for asthma was based on 11 studies of adolescents and four studies of adults (table 1) having a total of 971 278 participants. A random effects meta-analysis indicated the pooled aOR for asthma was 1.39 (95% CI 1.28–1.51) for e-cigarette users compared to non-e-cigarette users (figure 2a). We observed moderate heterogeneity in the results (Q14=28.20, p=0.01; I2=50%), because the international studies exhibited greater heterogeneity than US-based studies. A separate meta-analysis of the four adult studies indicated a significant aOR of 1.40 (95% CI 1.23–1.58, data not shown) hence it was appropriate to include these with the adolescent studies.
Forest plots for meta-analysis of studies a) asthma; b) COPD.
The meta-analysis for COPD or composite respiratory symptoms was based on nine studies of adults (table 2) having a total of 1 023 494 participants. A random-effects meta-analysis indicated the pooled aOR for respiratory disease was 1.49 (95% CI 1.36–1.65) for e-cigarette users compared to non-e-cigarette users (figure 2b). We observed no significant evidence of heterogeneity in these studies (Q8=6.41, p=0.60; I2=0%). (A sensitivity analysis supporting these findings is presented in the supplementary material.)
Summary of epidemiological studies
A significant association of e-cigarette use with respiratory disorder was found across 23 of the 24 studies reviewed, and e-cigarette use typically added independently to risk derived from cigarette smoking. The studies had large representative samples drawn from multiple states and countries, and the analyses included a number of covariates so as to rule out several possible types of confounding. Methodological characteristics of the research were generally strong, and independent methodological studies have supported both the validity of self-reports of substance use (e.g. [53, 54]) and the reliability and validity of health measures in large-scale surveys for adolescents [55, 56] and for adults [57–59]. Moreover, several studies provided external validation for self-report findings (e.g. through school absences); this makes interpretation of the findings as deriving from an “ill worker's effect” (i.e. persons with disease simply reporting a stereotypic cause) not very plausible. A limitation that could be noted is that most studies were cross-sectional. However, a reverse-causality interpretation is not very plausible, because several cross-sectional studies showed a significant association of e-cigarette use with respiratory disease among never-smokers; and longitudinal studies showing e-cigarette use to predict onset of respiratory disease from a disease-free baseline [46, 52] also make reverse causation unlikely.
Evidence from laboratory studies
Laboratory studies provide experimental evidence about effects of e-cigarettes on four types of biological processes that are linked to respiratory outcomes. While other processes are possibly implicated, such as fine particulate matter [60, 61], these are the areas where the most direct evidence is available. We discuss representative laboratory studies on these topics because extensive narrative reviews are available elsewhere [27, 28, 62]. We note that although nicotine itself has adverse effects on pulmonary variables [63, 64], in a number of studies the effects observed for e-cigarettes are independent of nicotine content, hence are attributable to other components of e-cigarette liquid or aerosol. In our discussion we do not address the question of whether e-cigarettes have lower levels of carcinogenic toxicants associated with combustible cigarettes. While this tends to be the case for known carcinogens (e.g. [65]), there are conditions where effects of e-cigarettes on other biological processes are comparable to those of cigarettes and there is evidence that new types of toxicants may emerge from the mixing and heating of e-cigarette humectants and flavourings [66]. Thus, we believe a key question is whether effects of e-cigarettes on biological processes differ significantly from clean-air controls, indicating actual harm to lung/airway tissues. In addition, we consider how levels of biological effects differ for e-cigarettes and cigarettes.
Cytotoxic effects
In [67], cells exposed for 1–48 h to e-cigarette aerosol extracts showed concentration-dependent cytotoxic effects and reduced cell proliferation for five of the 11 products tested (supplementary table S5). Leigh et al. [68] found that cell metabolic activity and viability were both decreased in the e-cigarette condition compared to an air control. Another study [69] found that all e-cigarette brands tested had cytotoxic effects. In one study [67], effects for e-cigarettes were sometimes less than for cigarettes, but in another [69], the effect for DNA damage was comparable to that for cigarettes. Rowell et al. [70] found that e-cigarettes produced decreases in cell viability, proliferation and metabolism compared with the control condition, and a study with JUUL brand e-cigarettes showed that pod fluids were cytotoxic in two assays for all flavours [71]. In these studies, cinnamon, menthol, vanilla and berry or fruit flavourings were found to have particularly cytotoxic effects.
In one recent study, most of the 20 popular e-liquids screened showed evidence of significant toxicity [72]. Escobar et al. [73] tested the effects of three aerosolised humectants (propylene glycol, glycerol and propylene glycol + glycerol) with no flavourings added. Evidence of cytotoxicity was found for aerosolised humectants and evidence was found for increases in two pro-inflammatory cytokines, interleukin (IL)-6 and IL-8, and indices of cellular stress. Thus, evidence was found for biological effects of basic constituents of e-cigarettes, aside from contributions from flavourings.
Oxidative stress and inflammation
Oxidative stress is an important process in the aetiology of lung disease [74], and a number of studies have shown e-cigarettes to be related to indices of oxidative stress (supplementary table S6). In studies including both human cells and animal models [75], oxidative stress was increased and cell viability decreased in the e-cigarette condition compared to a clean-air control. Other studies have also found an impact of e-cigarettes on oxidative stress and effects for disrupting lung functioning, with some effects independent of flavourings [76, 77]. Studies by Lerner et al. [78] showed that exposure to e-cigarettes reduced cell viability, increased reactive oxygen species and produced an increase in the inflammatory cytokines IL-6 and IL-8 (compare with [79]). Larcombe et al. [80] found that mice exposed to e-cigarette aerosol had impaired lung function and changes in airway reactivity. Effects for e-cigarettes were less than for cigarettes [75, 76], but in other studies [78, 80] some effects were comparable to or greater than those for cigarettes. An in vivo study based on human nonsmokers [81] found increases over time in blood markers for oxidative stress and inflammation and evidence that oxidants were released into the blood (compare with [82]). A cell study with human alveolar macrophages [83] found a dose-dependent reduction in cell viability (i.e. e-cigarettes increased cytotoxicity) together with increase in the production of reactive oxygen species and pro-inflammatory cytokines (e.g. IL-6, tumour necrosis factor-α) and decrease in phagocytosis (i.e. bacteria-killing) ability. Notably, some studies found that heating of e-liquids increased the magnitude of adverse effects.
Linkages to immune function and susceptibility to infection
In a mixed-methods study [84], cells cultured with various concentrations of e-liquid and inoculated with human rhinovirus had higher levels of viral load and decreased host defence molecule expression, and infected mice exposed to e-cigarettes showed higher viral load (supplementary table S7). Studies with macrophages and an animal model [85] indicated that e-cigarette exposure reduced antimicrobial activity, and a controlled-infection study with mice indicated greater methicillin-resistant Staphylococcus aureus bacterial burden and higher mortality in the e-cigarette condition. In a series of cell studies and in vivo studies [86], lungs of mice exposed to e-cigarette aerosol and infected with Streptococcus pneumoniae showed increased bacterial burden, and mice infected with influenza virus showed a higher rate of mortality in the e-cigarette condition compared to a clean-air control. Similarly, Gilpin et al. [87] and Gómez et al. [88] exposed macrophages and several types of bacteria (e.g. influenza, pneumonia) to e-cigarette aerosol extract and found increased bacterial virulence and inflammatory potential as well as decreased bacteria-killing ability. A mouse study [89] found similar effects for macrophages and found increased morbidity and mortality among influenza-infected animals, independent of nicotine. Human studies [90] have found that e-cigarette users showed markers for increased oxidative stress and inflammatory response and aberrant neutrophil activation and mucus ratios, all of which could be involved in respiratory disease (compare with [91]). In another study, proteins associated with membrane formation and mucus formation were uniquely affected in e-cigarette users so as to increase susceptibility to respiratory infections [92]. Clapp et al. [93] found a suppressed host defense mechanism: exposure to one e-liquid reduced the motility and the beat frequency of lung cilia, hence impairing an essential respiratory defence mechanism, similar to effects found by Garcia-Arcos et al. [91]. Although these studies demonstrated effects of flavourings, some also found significant adverse effects for humectants alone. In several studies [87–92] some effects of e-cigarettes on immune function were less than for cigarettes, but some were equal to cigarettes.
In the most recent studies, four common flavouring chemicals affected human neutrophils, an important part of the innate immune response, in a dose-dependent manner [94] and three of the four flavourings impaired defence against S. aureus. Similarly, Corriden et al. [95] exposed neutrophil cells and mice to e-cigarette aerosol and found that exposure reduced several measures of neutrophil function and increased the number of bacteria found at an infection site. In a related study [96], proteases linked to respiratory disease were elevated in both e-cigarette users and smokers. Related effects were found in two other studies [97, 98].
Genetic effects
Yu et al. [99] found that exposure to e-cigarette aerosol produced increased cell death and DNA damage compared to untreated cells (supplementary table S8). A human study [100] found that of 543 genes available for comparison, 358 genes were differentially expressed when comparing e-cigarette users with nonusers, the differences generally being consistent with immune suppression. Some effects were six times greater for e-cigarettes than for cigarettes. A comparison of cigarette smokers and e-cigarette users [101] showed that genes downregulated for both groups (i.e. common effects) tended to be ones involved in cilia assembly and movement; PCR validation indicated that both e-cigarettes and cigarettes interfered with ciliated cells in the airway epithelium. Ganapathy et al. [102] found a dose-dependent effect of e-cigarettes on DNA damage. Two related studies [103, 104] confirmed effects for impaired cell functioning and increased interference with DNA repair mechanisms. Two of the studies [99, 102] found that the effect of e-cigarettes on DNA damage and other processes was comparable to effects observed for cigarettes.
In the most recent work, an in vivo human study [105] found larger numbers of differentially expressed transcripts in exclusive smokers and e-cigarette users compared to controls (1726 versus 1152). Only 299 of the differences were common to smokers and e-cigarette users, indicating their effects were through largely different mechanisms. Song et al. [106] analysed cells from bronchoscopies and found a large number of differentially expressed transcripts (n=2452) for e-cigarette users and smokers compared to nonsmokers. Inflammation processes were implicated, in that e-cigarette users had higher inflammatory infiltrates than nonsmokers, but levels tended to be lower than for smokers.
Summary of laboratory studies
Laboratory studies have shown e-cigarettes to have effects on four biological processes that are relevant for respiratory disease. Evidence is found for exposure to e-cigarette liquid or aerosol producing cytotoxic effects and oxidative stress. Results for inflammation are less consistent, but effects on cytokines and other indices of inflammation have been found in several studies. Both cell studies and animal models indicate that bacterial virulence and indices of susceptibility to infection are increased by e-cigarette exposure and that bacteria- and virus-infected animals show higher morbidity and mortality when they are exposed to e-cigarette aerosol. Finally, studies of genetic variables have found e-cigarettes to cause DNA damage and e-cigarette use to suppress genes involved in immune function, with pathways that can be distinct from those found for cigarettes. While comments have been made about specific aspects for some of the studies [107–110], the finding of biological effects for e-cigarettes across four outcome domains in both cell cultures, animal models and human studies shows a replicable body of findings linking e-cigarettes to several biological processes involved in the pathogenesis of respiratory disease in humans.
General discussion
The aim of this article is to provide an integrative review of the relation between e-cigarette use and respiratory health outcomes by considering findings from epidemiological studies together with evidence from laboratory studies. Our epidemiological review has demonstrated a consistent association of e-cigarette use with respiratory disorder in multiple independent studies with representative samples of adolescents and adults. Laboratory studies show e-cigarette effects on four biological processes relevant for respiratory disorder and include both in vitro and in vivo studies. Risk-promoting effects have been found across four biological domains using fairly different paradigms. Thus, there is considerable evidence for a relation between e-cigarette use and respiratory disorder. In the following sections we discuss methodological issues relevant for drawing conclusions.
Alternative explanations
Studies have dealt with several alternative explanations for findings about e-cigarettes. Epidemiological studies have controlled for a number of covariates (e.g. age, sex, race/ethnicity, obesity, own smoking, second-hand smoke exposure) and these were somewhat different ones across studies, hence an argument of potential omitted-variable bias is harder to sustain. Also, significant findings from longitudinal studies and findings of associations of e-cigarette use with respiratory disease among persons who had never smoked cigarettes work against interpretations of reverse causation. While it has sometimes been suggested that persons with respiratory disease might use e-cigarettes for therapeutic purposes, it is difficult to see why they would do this given that e-cigarette aerosol has lung irritant effects (e.g. [69, 80, 84, 90, 92, 111]).
Difference from controls and from cigarettes
Laboratory studies consistently find that e-cigarette conditions significantly elevate adverse biological effects compared with clean-air or comparable control conditions, and a number of studies show e-cigarette effects comparable to those for cigarette smoke (supplementary tables S5–S8). Thus, there is consistent evidence from controlled experiments that e-cigarettes, while not having the high levels of known carcinogens associated with cigarettes [65], still can have adverse consequences from a respiratory standpoint. These concerns are supported in the present review by data showing a consistent association of e-cigarette use with respiratory disorder in large general-population samples of adolescents and adults (tables 1 and 2).
Relation to Hill's criteria
Bradford Hill's criteria were developed to provide guidance for inferring causality from epidemiological research [112] and have had an enduring impact on multiple areas of research [113–115]. Our summary of how the evidence meets these criteria is as follows.
Consistency
Our epidemiological review shows a significant association between e-cigarette use and respiratory disorder in 23 out of 24 studies, making this a highly consistent finding. In laboratory research, e-cigarettes have been found to affect disease-relevant biological processes in 35 independent studies using different methods and paradigms. Although nonsignificant conditions and null studies can be found, the consistency of confirmatory evidence is substantial.
Temporality
Finding the predictor to occur before the onset of a disease condition is a crucial criterion [112]. Prospective analyses have shown that e-cigarette use predicts onset of asthma or COPD among initially disease-free cases or worsening of respiratory symptoms over time among those with illness, controlling for baseline level [46, 52]. Together with findings from laboratory experiments where the exposure precedes the outcome, this evidence gives support for meeting the temporality criterion.
Dose–response gradient
A graded relation between level of exposure and probability of illness is another important criterion. In the present review we have noted many instances of dose–response relationships in laboratory studies. Epidemiological studies typically do not have continuous exposure data, but several have noted more recent use or greater number of days used in past month to be related to higher likelihood of respiratory disease [32, 42, 47, 51, 52]. Thus, this criterion is met to some extent, although not uniformly across the types of studies discussed.
Biological plausibility
We have shown in detail how e-cigarettes affect biological processes known to be important in the pathogenesis of human respiratory disease. This is based on experimental studies testing specific biological processes and controlled-infection studies using pathogens such as influenza and pneumonia, which are significant disease problems among humans. Thus, the finding of an association of e-cigarette use with respiratory disorder in epidemiological studies is biologically plausible because respiratory disease can develop through these mechanisms, although animal models may not directly mimic human disease.
Strength of relationship
Our meta-analysis of epidemiological studies showed the unique association between e-cigarette use and respiratory disease is an adjusted odds ratio of 1.39 for asthma and 1.45 for COPD. Whether this would be characterised as a large or small effect size is somewhat arbitrary [116], but an important consideration is that even a moderate effect size spread across a large publication can have substantial public health impact. We think the strength of relationship is such as to warrant concern about public health consequences.
Coherence with existing knowledge
Hill [112] argued that a cause–effect interpretation of data should not seriously conflict with generally known facts about the natural history and biology of the disease. Based on the evidence presented here and existing knowledge about the aetiology of respiratory disease (e.g. [28, 74]), the postulate of a relationship between e-cigarette use and respiratory disease does not seriously conflict with existing knowledge.
It should be noted that a recent development is an outbreak of severe lung disease termed e-cigarette- or vaping-associated lung injury (EVALI) [117–121]. Importantly, the e-cigarettes that these persons had been using typically contained tetrahydrocannabinol (THC) [122], and this has been accepted as one defining characteristic in the outbreak. In addition, vitamin E acetate (VEA) was detected in bronchoalveolar lavage fluid in most cases where this was available [123], and a VEA mechanism has been supported in an animal model [124]. Thus, VEA is strongly suspected of being a causal factor for EVALI, although a small minority of affected patients deny having vaped THC [125], and other constituents have been suggested for consideration [126]. Whether EVALI results from processes similar to or different from those discussed here, such as oxidative stress [126, 127], or from alternative mechanisms such as lipid deposition [128, 129], is unknown at present. The most recent brands of e-cigarettes have cytotoxic effects and disrupt lung functioning [71, 130, 131], suggesting that the issues we have noted may be contributory for EVALI. Several mechanisms should be considered, and continuing epidemiological surveillance and laboratory research are needed to determine the social and biological effects of current electronic delivery systems.
Conclusion and further research
In summary, we find that Hill's criteria have been adequately satisfied and the evidence supports the conclusion of a real relationship between e-cigarettes and respiratory disorders. There are still many questions that need to be clarified, for example whether e-cigarette use is more related to onset of disease or to exacerbation of existing symptomatology, or whether there are different types of effects at different ages. However, we think the state of the evidence is sufficient to warrant concern about the population impact of e-cigarettes [132].
The research discussed here has generally used good experimental parameters, but further research is needed to solidify knowledge about the health consequences of e-cigarettes. Toward this end, we integrate the findings in a heuristic model of e-cigarette use and respiratory disorder (figure 3). This model is testable based on methods used in prior research on behavioural consequences of e-cigarette use [10, 130]. It is not clear whether the processes we have discussed work independently or in tandem, and the model aims to clarify tests of this question.
Heuristic model for exploring relationship of e-cigarettes to respiratory outcomes.
We can suggest that e-cigarette use may affect susceptibility to infection indirectly through altering expression of genes involved in immune-system function and ciliary mobility, whereas effects of e-cigarettes on cytotoxicity and oxidative stress may occur through biochemical effects on lung or airway membranes. All three processes are hypothesised to increase the likelihood of asthma and/or COPD, possibly at different ages. Our model recognises that other risk factors for respiratory disease (e.g. cigarette smoking and obesity) have their own effects on outcomes and need to be included as covariates in research on e-cigarettes. Direct effects from e-cigarette use to asthma or COPD, not mediated through the specified biological processes, are possible in principle and are testable in appropriately designed studies. Whether direct or indirect effects are found, more would be learned by using such models to study how e-cigarette use is related to respiratory outcomes.
Epidemiological studies have consistently noted that dual users have significantly more respiratory symptomatology compared with exclusive e-cigarette users or exclusive smokers. While e-cigarette use tends to be correlated with smoking, they are not interchangeable and they produce additive effects. Laboratory studies of genetic expression also show that effects of e-cigarettes occur in part through different biological pathways than cigarettes. E-cigarette use does not merely parallel effects of smoking, but contributes independently to risk. Thus there is every reason to further pursue these questions in research conducted among smokers as well as nonsmokers.
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Footnotes
Author contributions: All authors contributed to the conception and design of the manuscript and the acquisition, analysis, and interpretation of data. All authors contributed to drafting the manuscript or critical revision for important intellectual content. All authors approve the final submitted version.
This article has supplementary material available from erj.ersjournals.com
Conflict of interest: S.S. Soneji has nothing to disclose.
Conflict of interest: K. Choi has nothing to disclose.
Conflict of interest: I. Jaspers has nothing to disclose.
Conflict of interest: E.K. Tam has nothing to disclose.
Conflict of interest: T.A. Wills reports grants from National Cancer Institute (P30 CA071789), during the conduct of the study.
Support statement: This work was supported by the National Cancer Institute (grant: P30 CA071789). Funding information for this article has been deposited with the Crossref Funder Registry.
- Received September 23, 2019.
- Accepted October 10, 2020.
- The content of this work is not subject to copyright. Design and branding are copyright ©ERS 2021
This version is distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.
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