Next Article in Journal
Single Channel Image Enhancement (SCIE) of White Blood Cells Based on Virtual Hexagonal Filter (VHF) Designed over Square Trellis
Next Article in Special Issue
Asthma: From Phenotypes to Personalized Medicine
Previous Article in Journal
Grip Strength Trajectories and Cognition in English and Chilean Older Adults: A Cross-Cohort Study
Previous Article in Special Issue
Allergic Asthma in the Era of Personalized Medicine
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Asthma and Tobacco Smoking

by
Vanesa Bellou
1,2,*,
Athena Gogali
1 and
Konstantinos Kostikas
1
1
Department of Respiratory Medicine, School of Medicine, University of Ioannina, 45110 Ioannina, Greece
2
Department of Hygiene and Epidemiology, School of Medicine, University of Ioannina, 45110 Ioannina, Greece
*
Author to whom correspondence should be addressed.
J. Pers. Med. 2022, 12(8), 1231; https://doi.org/10.3390/jpm12081231
Submission received: 28 April 2022 / Revised: 21 June 2022 / Accepted: 20 July 2022 / Published: 27 July 2022
(This article belongs to the Special Issue Asthma: From Phenotypes to Personalized Medicine)

Abstract

:
Asthma is a prevalent chronic pulmonary condition with significant morbidity and mortality. Tobacco smoking is implicated in asthma pathophysiology, diagnosis, prognosis and treatment. Smokers display increased prevalence and incidence of asthma, but a causal association cannot be claimed using existing evidence. Second-hand smoking and passive exposure to tobacco in utero and early life have also been linked with asthma development. Currently, approximately one-fourth of asthma patients are smokers. Regular smokers with asthma might display accelerated lung function decline and non-reversible airflow limitation, making their distinction from chronic obstructive pulmonary disease patients challenging. Asthma patients who smoke typically have uncontrolled disease, as shown by increased symptoms, more exacerbations and impaired quality of life. On the other hand, smoking cessation improves lung function and asthma severity. Thus, asthma patients and their caregivers should be actively questioned about their smoking status at each medical encounter, and smoking cessation ought to be strongly encouraged both for patients with asthma and their close contacts. Smokers with asthma should be provided with comprehensive smoking cessation interventions on top of other anti-asthma medications.

1. Introduction

Asthma is a common chronic airways disease characterized by variable expiratory airflow obstruction [1]. The latest Global Burden of Disease estimated the global prevalence of asthma at 262 million cases (95% UI, 224–309), based on available evidence from 2019 [2]. The trademarks of asthma are airway inflammation and airway hyperresponsiveness, manifesting with varying degrees of dyspnea, wheezing, cough and/or chest tightness. Several environmental factors, including tobacco, might trigger exacerbations of the disease, i.e., episodes in which symptoms worsen to an extent that warrants modification of a patient’s treatment [1,3].
Smoking is a hazardous health habit associated with significant morbidity and mortality population wide [4,5]. According to the latest Global Burden of Disease, tobacco is the second leading risk factor of death and the third leading risk factor of Disability-Adjusted Life Years (DALYs) worldwide, accounting for 8.71 million (95% UI, 8.12–9.31) deaths and 230 million (95% UI, 213–246) DALYs in 2019, respectively [5]. These effects are a consequence of the association of tobacco, with increased risk of a multitude of chronic diseases, as well as infections and acute health conditions [4,6].
Smoking has multiple ramifications for respiratory health [7]. The present review focused on the various links between smoking and asthma, as supported by existing literature.

2. Methods

We performed a review of the literature across two databases (PubMed and Google Scholar), using relevant keywords: asthma and tobacco, smoking or smoke. We searched for systematic reviews, meta-analyses, observational studies and clinical trials that examined the effect of various exposures to tobacco on asthma. We included all the following types of studies: studies that examined smoking as a risk factor or a prognostic factor of asthma, studies that estimated the epidemiology of smoking in patients with asthma, studies that examined diagnostic and/or therapeutic deviations in asthmatic smokers and studies that assessed the efficacy and/or efficiency of smoking cessation options among asthma patients. We excluded studies that did not involve humans and were not published in the English language. We did not enforce any limitation on the date of publication.

3. Smoking as a Risk Factor of Asthma

Current evidence suggests that asthma is not the result of a single environmental or genetic cause, but develops due to interplay between multiple genetic and environmental factors. Moreover, asthma is quite a heterogeneous disease, which is commonly categorized in phenotypes, i.e., subgroups of patients that have distinct clinical manifestations. These phenotypes are considered the output of different pathophysiological processes, suggesting that asthma is a complex disease with many mechanisms contributing to disease etiology and natural course [8,9]. A variety of risk factors and environmental exposures have been linked to asthma development, either increasing or decreasing the risk of the disease. These include demographic factors, such as age and sex; developmental factors, such as preterm birth; mode of delivery and history of infections; socioeconomic status-related factors, such as agricultural subsistence, income and daycare enrollment; dietary factors and medications; and, last but not least, inhaled exposures, such as tobacco, air pollution and air allergens [9]. The latest evidence from Global Burden of Disease placed smoking second among the leading risk factors for DALYs attributed to asthma [2].
There are a multitude of observational studies that have depicted increased prevalence of asthma in cigarette smokers [7,10,11,12,13,14,15]. Cohort studies have also shown increased incidence of asthma among cigarette smokers [7,15,16,17]. To elaborate on the association between tobacco exposure and asthma, secondhand exposure to smoking should also be considered. A few observational studies have shown increased frequency of passive smoking among patients with asthma, indicating that secondhand smoking is also a risk factor of asthma [7,18,19]. Moreover, there is emerging evidence depicting an association between the use of electronic cigarettes and asthma, chronic obstructive pulmonary disease (COPD) and their coexistence, often mentioned as asthma–COPD overlap (ACO) [20,21]. This association persisted even after controlling for tobacco smoking and other disease-relevant factors [22]. To complicate matters even more, there are data supporting that asthma is a risk factor of COPD and that the association persists even after adjusting for smoking [23].
While tobacco smoking is considered an established risk factor of asthma, a causal association cannot be claimed. The evidence supporting the association of smoking with asthma is comprised of observational studies, with many of them being cross-sectional and case-control studies [18]. These studies are prone to various biases such as confounding, reverse causality and selection bias; therefore, the study design should be examined carefully and the results interpreted with caution [24,25]. Published Mendelian Randomization studies examining a potential causal relationship between smoking and asthma had conflicting results and did not shed further light [26,27].
One of the Bradford Hill criteria required to determine if an observed association is causal is a temporal sequence, i.e., the exposure should precede the outcome [28]. It should be noted that the majority of asthma cases are diagnosed in childhood; thus, active smoking and continuous passive exposure to smoking are not likely causal factors of childhood asthma [7,8,18,29]. However, it might be the case that smoking, whether active or passive, is among the exposures causing asthma of a later onset in adult life [7,18,29,30]. The fact that asthma onset typically occurs in childhood has shifted the search for risk factors occurring in prenatal, perinatal and early life [31]. Thus, one factor that has received attention is exposure to tobacco during the years preceding childhood, which are critical for lung development [9,32].
Passive exposure to tobacco in utero and/or early life has been linked with various adverse effects on the respiratory system across the life span of exposed individuals. To elaborate, exposure to maternal smoking has been associated with increased risk of respiratory infections in childhood, wheezing, as well as diminished lung function in childhood and adolescence [32,33]. Epidemiological studies have shown that the effect on lung function persists in adult life and people exposed to maternal smoking also have higher incidences of airflow obstruction, chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis [34,35,36,37]. Regarding asthma, both maternal and paternal smoking have been associated with the development of asthma in offspring [7,38]. Recently published transgenerational studies have also depicted increased risk of asthma in children whose grandparents smoked [39,40]. Alas, more research is needed to verify this “vertical transmission” of smoking-induced asthma risk and elucidate the mechanisms behind it [41].
Taking into consideration that asthma remains a disease without a cure, public health efforts have focused on primary prevention measures to tackle its morbid impact. Therefore, population-wide measures that aim to lessen the incidence of smoking have been proposed as preventive measures to lessen the incidence of asthma in descendants of potential smokers [9,31].

4. Diagnostic Challenges for Asthmatic Smokers

Prevalence rate estimates the smoking range from 20% to 35% of asthma patients in published population-wide studies, regardless of the country of origin of the sample used. The prevalence of active smoking in patients with asthma is, therefore, approximately the same as the prevalence in the general population [18,42,43,44,45,46]. In spite of the high prevalence of smoking among patients with asthma, this group of patients is typically excluded from randomized clinical trials assessing the effectiveness of various inhaled medications in asthma patients [18,47]. Active smokers and/or patients with a smoking history of over 10 pack years were also excluded in the majority of recent randomized clinical trials conducted to examine the efficacy of biologics in severe asthma patients [48].
The main symptoms that trigger a diagnostic examination for asthma are shortness of breath, cough, chest tightness and wheezing. Typically, patients have more than one of these symptoms, and symptoms have a certain pattern: they vary over time and in intensity, tend to worsen at night and early morning and may be triggered by certain exposures, such as tobacco and allergens [1,8]. An important clinical diagnostic challenge is to distinguish between the two most prevalent airflow limitation disorders, asthma and COPD. COPD is a common chronic respiratory condition characterized by persistent symptoms and airflow limitation due to airway and/ or alveolar abnormalities. It has different pathophysiology than asthma and is typically diagnosed in midlife or old age [49,50]. The main symptoms of COPD are similar to the ones of asthma, but lack the characteristic variable pattern displayed in asthma [8,50]. Specifically, dyspnea presents on exertion in the early stages of COPD, while in asthma it is present during exposure to triggers, at night and/or during exacerbations, and asthma patients are more likely to report wheezing and less likely to have chronic bronchitis symptoms [51,52,53]. Other attributes that might be helpful for differentiating asthma from COPD include sex, information from the patient’s family and personal history (family history of asthma, allergen sensitization, history of hay fever, eczema or allergic rhinitis, presence of comorbid diseases such as cardiovascular disease) and biomarkers (eosinophils, IgE, FeNO) [52,53]. A helpful diagnostic algorithm, adapted from the Greek Guidelines for COPD, is presented in Figure 1 [54]. Last but not least, in the early stages of COPD, clinical examination is normal, as it is in asthma [8,50].
The diagnosis of asthma is made via lung function testing in patients with a clinically relevant presentation. Spirometry in asthma displays expiratory airflow limitation and excessive variability of lung function [1,8]. Existing literature has depicted that smoking initiation for the majority of people happens at a young age, and the transition to regular smoking happens between adolescence and young adulthood [55]. Nicotine dependence develops very quickly in young people with symptoms of asthma, making quitting a difficult process [56]. Asthma patients that have regularly smoked since childhood or early adulthood are more prone to impaired lung function and airway remodeling, ultimately causing fixed (non-reversible) airway obstruction [57,58,59,60,61]. This makes differentiation of asthma patients with a smoking history from COPD patients a strenuous task, given that smoking is the main risk factor of COPD and COPD patients have poorly reversible airflow limitation [50]. On top of this, certain COPD patients manifest airway hyperresponsiveness, which is the trademark feature of asthma [62]. However, the combination of greater lung function values, slower rates of lung function decline and marked airway hyperresponsiveness should steer the clinician towards an asthma diagnosis [52,53].
There are some patients that have characteristics of both asthma and COPD. This entity is better known as asthma COPD overlap (ACO), but its presence and characteristics have raised controversies among various professional societies and clinical experts. There are multiple different definitions of the disease, some of which require a known history of asthma, while others require a smoking history among other diagnostic criteria [63]. Patients with ACO display a different prognosis and need different treatment than patients with asthma and COPD, and thus should be sought after and handled accordingly. The most important therapeutic intervention in current or ex-smokers with COPD who present an asthmatic component is they should not miss the benefits of ICS in the appropriate dosing, especially in the presence of eosinophilic/T2 inflammation [64]. Existing guidelines on ACO have been revised extensively and repeatedly over the past few years to incorporate accumulating new evidence, and hopefully a consensus will be reached in the coming years [63,65].

5. Prognostic and Treatment Implications in Asthmatic Smokers

Smoking is implicated in the prognosis of asthmatic patients in a number of ways, with consequences such as increased morbidity and mortality [18,66]. These phenomena could be attributed to the modifications made by tobacco in airway morphology and the inflammatory processes of asthma [18,42]. Active smokers with asthma present increased neutrophils in induced sputum and reduced pH and squamous cell metaplasia [67]. Past smokers with asthma present airway autoimmunity and increased eosinophilic inflammation and activation, with reduced sensitivity to corticosteroids [68]. Cigarette smoking also suppresses FeNo, which is a helpful marker of asthma activity. Additionally, patients with asthma who smoke may present an accelerated rate of decline in lung function and may develop persistent airflow obstruction due to airway remodeling [57,58,59,60]. Asthmatic smokers might have aggravated small airway obstruction and an altered microbiome, with greater bacterial diversity [69,70,71]. The specific effects of smoking on distinct asthma phenotypes have not received much attention, so more research is needed to clarify the effect of smoking on different phenotypes of asthma [18,42].
Active smokers with asthma have an increased burden of symptoms, both intensity wise and frequency wise, as measured using suggested questionnaires in published studies [72,73]. Smokers with asthma exhibit higher absenteeism from work and school; have increased use of rescue medication, which is a proxy for more symptoms and inadequate disease control; and worse indices of health status compared to non-smokers [74,75]. Asthma patients who smoke have an elevated rate and severity of exacerbations [66]. Specifically, more than half of current smokers had at least one exacerbation per year requiring systemic corticosteroids, compared to 40% of former smokers [76]. Previous literature has also shown that long-term smoking directly increases the need for healthcare use in asthma patients, in the form of visits to the emergency department, visits to the general practitioner or unscheduled appointments with the pulmonologist [74,77,78]. Furthermore, smoking is linked with increased hospitalizations in asthmatic patients and asthma-related deaths [66]. Furthermore, there is scant evidence that electronic cigarette use and second-hand exposure to their aerosols may also amplify symptoms and increase exacerbations in asthma patients [79,80,81].
Furthermore, asthmatic smokers display greater prevalence of various comorbid conditions, according to published studies. These conditions include perennial rhinitis, seasonal rhinitis, lung cancer, coronary heart disease, arrhythmias, hypertension, diabetes mellitus, osteoporosis and prostate hyperplasia [82,83]. The presence of any of these comorbidities in a patient with asthma influences his overall health status, as well as the course of asthma, by means of directly damaging asthma control and potential drug interactions [83]. Taking into account all of the aforementioned information, it does not come as a surprise that ever smokers with asthma have a worse quality of life than never smokers with asthma [18].
Active smokers with asthma are less likely to adhere to proper treatment and less prone to follow asthma education programs [75]. At the same time, smoking interferes with treatment modalities received by patients with asthma because the efficacy of certain medications is altered by the smoking status of a patient. A multitude of clinical studies have shown that smokers have relative resistance to inhaled corticosteroids, which is the mainstay controller treatment option in asthma patients, according to the latest guidelines [19,84,85]. Moreover, smokers have reduced sensitivity to leukotriene receptor antagonists [85,86]. A therapeutic option to reduce exacerbations in difficult-to-treat uncontrolled asthma patients with T2 low phenotype is long-term azithromycin; however, it is effective only in non-smokers [87,88].
Combining the negative effects of smoking on asthma symptoms and exacerbations, which are the two aspects assessed to rate the control and the severity of the disease, it becomes clear that asthmatic smokers usually have more severe and uncontrolled disease and thus display a need to intensify treatment. A small number of real-life trials have shown that the main treatment options used in asthma patients remain effective in smokers, as shown in Table 1 [89,90]. ICS is the mainstay controller medication in asthmatic smokers, but patients might require higher doses due to the relative resistance they display. Fine and extra-fine particle ICS might also have an advantage over other molecules in asthmatic smokers to better target small airways [90,91,92,93]. Smokers with asthma might also benefit from earlier introduction of long-acting beta agonists or long-acting anti-cholinergics [18,42,47]. More pragmatic clinical trials, with less strict exclusion criteria, should be conducted to elucidate the comparative efficacy of various medications and treatment strategies in asthma patients [18,42,94].
Second-hand smoking ought not to be forgotten, as it impacts asthma prognosis in similar manners to active smoking. Asthma patients exposed to passive smoking present graver symptoms and more severe disease, worse health outcomes, impaired health status and quality of life and, last but not least, more exacerbations. These findings were consistent in all asthma patients regardless of age (in either children or adults) [110,111]. The harmful effects of tobacco on asthma disease control might be aggravated in patients that are concurrently exposed to indoor or outdoor air pollution. These effects include asthma control, severity of disease and lung function. Potential mechanisms of this effect include the exacerbation of inflammation and allergen-induced inflammation due to Th2 responses [112,113].

6. Smoking Cessation in Asthma Patients

The realization that asthma constitutes a syndrome rather than a single disease has created a paradigm shift in its treatment in recent years [9]. This is mainly applied to patients on the severe spectrum of the disease, i.e., patients with poor symptom control and/or frequent exacerbations while receiving maximal optimized controller therapy [48,114]. For these patients, instead of enforcing a “one size fits all” strategy, therapy is personalized depending on disease phenotype and certain patient characteristics [48]. Considering previous discussions on the various adverse effects of tobacco on the prognosis of asthma, smoking cessation is strongly encouraged by the latest guidelines on asthma management. Furthermore, tobacco smoking is nowadays considered among comorbid diseases as a treatable trait that should be targeted to improve asthma control [114,115]. Both the Global Initiative of Asthma and joint European Respiratory Society/American Thoracic Society guidelines cite smoking as a potential contributory factor of severe asthma, i.e., asthma that requires treatment with high doses of ICS, plus a second controller to achieve disease control or that remains uncontrolled [116,117].
It is established that the benefits of smoking cessation begin right after quitting and carry on throughout a person’s life. It should be stressed that smoking cessation impacts asthma patients’ overall health and physical status, as well as their asthma prognosis [4]. Published literature has illustrated various beneficial effects of smoking cessation on the prognosis of patients with asthma. In the short term, smoking cessation leads to a reduction in symptoms and less frequent use of rescue medication. In the long term, smoking cessation in asthmatics leads to improved lung function and a better quality of life. Moreover, asthma patients who quit require a smaller dose of inhaled corticosteroids to control their disease. Similar benefits of smaller magnitude have been observed for active smokers with asthma who reduced the number of cigarettes they consumed [118,119,120]. Mechanistically, smoking cessation is hypothesized to alter the inflammatory phenotype of asthmatics, which is manifested by a reduction in the number of sputum neutrophils and an increase in FeNO [118,119]. Quitting is also linked with improved airway hyperresponsiveness, as displayed by methacholine and histamine provocation testing [119,120].
Several smokers attempt to quit on their own, but quitting smoking without any aid has very low abstinence rates [121]. There is consensus that the most efficient smoking cessation intervention is a comprehensive treatment, combining behavioral counseling, pharmacotherapy and follow-up support [4,122]. Currently, there are seven effective pharmacological treatments for smoking cessation approved by the US Food and Drug Administration. These include varenicline, bupropion and five forms of nicotine replacement therapy [4,122]. The efficacy of abstinence for these options, when compared to placebo, are estimated at RR 2.24 (95% CI, 2.06–2.43) for varenicline, 1.64 (95% CI, 1.52–1.77) for bupropion, 1.49 (95% CI, 1.40–1.60) for gum, 1.64 (95% CI, 1.53–1.75) for patches, 1.52 (95% CI, 1.32–1.74) for lozenges, 1.90 (95% CI, 1.36–2.67) for inhalers and 2.02 (95% CI, 1.49–2.73) for nasal spray. The most common side effects for each of the above medications are: nausea for varenicline, insomnia for bupropion, jaw pain for gum, skin reactions for patches, hiccups for lozenges, cough for inhalers and nasal irritation for nasal spray [4,122].
The number of clinical trials examining the efficacy of various smoking cessation strategies and medication, exclusively in asthma patients, is very limited [120,123,124,125]. More clinical trials should be designed to assess and compare the effectiveness of existing smoking cessation interventions in asthma patients. Existing guidelines for asthma do not make any specific recommendations for smoking cessation interventions (i.e., specific therapeutic options and elaborate regimens or doses), while they emphasize that quitting should be encouraged and cessation support should be offered for all patients [18,75]. Published literature does not support the use of electronic cigarettes as a method to encourage smoking cessation, neither in the general population nor in asthma patients specifically [81,122].
The latest guidelines recommend that all patients should be questioned about their smoking status at every encounter, as if it were a vital sign, and suggest the use of 5As to screen for smoking in clinical settings [4,122]. Hospitalizations for an exacerbation in asthma patients could serve as an opportunity to screen for active or passive smoking. Active smokers could be provided with smoking cessation interventions, or at least be offered simple advice, and then be referred to treatment resources, such as telephone lines, websites or specialty treatment programs. This opportunity is so far underutilized in clinical practice [4,126]. Passive exposure to tobacco should not be dismissed. Adult smokers should be advised against secondhand exposure to tobacco. It is also imperative to advise parents and caregivers of asthmatic children to quit smoking, as well as to assist expectant mothers to quit [122,127,128].

7. Conclusions

Asthma and smoking intertwine in various ways (Table 2). Both active and passive smoking are commonly considered risk factors of asthma, but evidence of a causal association is conflicting. Despite the well-known hazardous effects of tobacco on respiratory health, smoking is a quite common habit among asthma patients. Smoking affects airway morphology and alters inflammation of asthmatic individuals, worsening disease prognosis and making the differential diagnosis of asthma and COPD rather laborious. Quitting smoking improves both the lung function and symptoms of asthma patients, rendering receipt of comprehensive smoking cessation interventions imperative for proper treatment.

Author Contributions

All authors have contributed equally to writing and editing this work. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest relevant to this study.

References

  1. King-Biggs, M.B. Asthma. Ann. Intern. Med. 2019, 171, ITC49. Available online: https://annals.org/aim/fullarticle/2752315/asthma (accessed on 27 April 2022). [CrossRef] [PubMed]
  2. Safiri, S.; Carson-Chahhoud, K.; Karamzad, N.; Sullman, M.J.M.; Nejadghaderi, S.A.; Taghizadieh, A.; Bell, A.W.; Kolahi, A.-A.; Ansarin, K.; Mansournia, M.A.; et al. Prevalence, Deaths, and Disability-Adjusted Life-Years Due to Asthma and Its Attributable Risk Factors in 204 Countries and Territories, 1990–2019. Chest 2022, 161, 318–329. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0012369221042069 (accessed on 27 April 2022). [CrossRef] [PubMed]
  3. McCracken, J.L.; Veeranki, S.P.; Ameredes, B.T.; Calhoun, W.J. Diagnosis and Management of Asthma in Adults. JAMA 2017, 318, 279. Available online: http://jama.jamanetwork.com/article.aspx?doi=10.1001/jama.2017.8372 (accessed on 27 April 2022). [CrossRef] [PubMed]
  4. Patel, M.S.; Patel, S.B.; Steinberg, M.B. Smoking Cessation. Ann. Intern. Med. 2021, 174, ITC177–ITC192. Available online: https://www.acpjournals.org/doi/10.7326/AITC202112210 (accessed on 27 April 2022). [CrossRef]
  5. Murray, C.J.L.; Aravkin, A.Y.; Zheng, P.; Abbafati, C.; Abbas, K.M.; Abbasi-Kangevari, M.; Abd-Allah, F.; Abdelalim, A.; Abdollahi, M.; Abdollahpour, I.; et al. Global burden of 87 risk factors in 204 countries and territories, 1990–2019: A systematic analysis for the Global Burden of Disease Study 2019. Lancet 2020, 396, 1223–1249. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0140673620307522 (accessed on 27 April 2022). [CrossRef]
  6. Sealock, T.; Sharma, S. Smoking Cessation; StatPearls Publishing: Treasure Island, FL, USA, 2022. Available online: http://www.ncbi.nlm.nih.gov/pubmed/29494049 (accessed on 27 April 2022).
  7. Jayes, L.; Haslam, P.L.; Gratziou, C.G.; Powell, P.; Britton, J.; Vardavas, C.; Jimenez-Ruiz, C.; Leonardi-Bee, J.; Tobacco Control Committee of the European Respiratory Society. SmokeHaz: Systematic Reviews and Meta-analyses of the Effects of Smoking on Respiratory Health. Chest 2016, 150, 164–179. Available online: http://www.ncbi.nlm.nih.gov/pubmed/27102185 (accessed on 27 April 2022). [CrossRef] [Green Version]
  8. Papi, A.; Brightling, C.; Pedersen, S.E.; Reddel, H.K. Asthma. Lancet 2018, 391, 783–800. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0140673617333111 (accessed on 27 April 2022). [CrossRef]
  9. Beasley, R.; Semprini, A.; Mitchell, E.A. Risk factors for asthma: Is prevention possible? Lancet 2015, 386, 1075–1085. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0140673615001567 (accessed on 27 April 2022). [CrossRef]
  10. Annesi-Maesano, I.; Oryszczyn, M.P.; Raherison, C.; Kopferschmitt, C.; Pauli, G.; Taytard, A.; de Lara, M.T.; Vervloet, D.; Charpin, D. Increased prevalence of asthma and allied diseases among active adolescent tobacco smokers after controlling for passive smoking exposure. A cause for concern? Clin. Exp. Allergy 2004, 34, 1017–1023. Available online: http://www.ncbi.nlm.nih.gov/pubmed/15248844 (accessed on 27 April 2022). [CrossRef]
  11. Langhammer, A.; Johnsen, R.; Holmen, J.; Gulsvik, A.; Bjermer, L. Cigarette smoking gives more respiratory symptoms among women than among men. The Nord-Trondelag Health Study (HUNT). J. Epidemiol. Community Health 2000, 54, 917–922. Available online: http://www.ncbi.nlm.nih.gov/pubmed/11076988 (accessed on 27 April 2022). [CrossRef] [Green Version]
  12. Chen, Y.; Dales, R.; Krewski, D.; Breithaupt, K. Increased effects of smoking and obesity on asthma among female Canadians: The National Population Health Survey, 1994-1995. Am. J. Epidemiol. 1999, 150, 255–262. Available online: http://www.ncbi.nlm.nih.gov/pubmed/10430229 (accessed on 27 April 2022). [CrossRef]
  13. Kiviloog, J.; Irnell, L.; Eklund, G. The prevalence of bronchial asthma and chronic bronchitis in smokers and non-smokers in a representative local Swedish population. Scand. J. Respir. Dis. 1974, 55, 262–276. Available online: http://www.ncbi.nlm.nih.gov/pubmed/4458061 (accessed on 27 April 2022).
  14. Flodin, U.; Jönsson, P.; Ziegler, J.; Axelson, O. An epidemiologic study of bronchial asthma and smoking. Epidemiology 1995, 6, 503–505. Available online: http://www.ncbi.nlm.nih.gov/pubmed/8562626 (accessed on 27 April 2022). [CrossRef]
  15. Torén, K.; Hermansson, B.A. Incidence rate of adult-onset asthma in relation to age, sex, atopy and smoking: A Swedish population-based study of 15813 adults. Int. J. Tuberc. Lung Dis. 1999, 3, 192–197. Available online: http://www.ncbi.nlm.nih.gov/pubmed/10094318 (accessed on 27 April 2022).
  16. Polosa, R.; Knoke, J.D.; Russo, C.; Piccillo, G.; Caponnetto, P.; Sarvà, M.; Proietti, L.; Al-Delaimy, W.K. Cigarette smoking is associated with a greater risk of incident asthma in allergic rhinitis. J. Allergy Clin. Immunol. 2008, 121, 1428–1434. Available online: http://www.ncbi.nlm.nih.gov/pubmed/18436295 (accessed on 27 April 2022). [CrossRef]
  17. Gilliland, F.D.; Islam, T.; Berhane, K.; Gauderman, W.J.; McConnell, R.; Avol, E.; Peters, J.M. Regular smoking and asthma incidence in adolescents. Am. J. Respir. Crit. Care Med. 2006, 174, 1094–1100. Available online: http://www.ncbi.nlm.nih.gov/pubmed/16973983 (accessed on 27 April 2022). [CrossRef]
  18. Polosa, R.; Thomson, N.C. Smoking and asthma: Dangerous liaisons. Eur. Respir. J. 2013, 41, 716–726. Available online: http://erj.ersjournals.com/lookup/doi/10.1183/09031936.00073312 (accessed on 27 April 2022). [CrossRef] [Green Version]
  19. Chalmers, G.W.; Macleod, K.J.; Little, S.A.; Thomson, L.J.; McSharry, C.P.; Thomson, N.C. Influence of cigarette smoking on inhaled corticosteroid treatment in mild asthma. Thorax 2002, 57, 226–230. Available online: http://www.ncbi.nlm.nih.gov/pubmed/11867826 (accessed on 27 April 2022). [CrossRef] [Green Version]
  20. Bircan, E.; Bezirhan, U.; Porter, A.; Fagan, P.; Orloff, M.S. Erratum: Electronic cigarette use and its association with asthma, chronic obstructive pulmonary disease (COPD) and asthma-COPD overlap syndrome among never cigarette smokers. Tob. Induc. Dis. 2021, 19, 74. Available online: http://www.ncbi.nlm.nih.gov/pubmed/34727146 (accessed on 27 April 2022). [CrossRef]
  21. Li, X.; Zhang, Y.; Zhang, R.; Chen, F.; Shao, L.; Zhang, L. Association Between E-Cigarettes and Asthma in Adolescents: A Systematic Review and Meta-Analysis. Am. J. Prev. Med. 2022, 62, 953–960. Available online: http://www.ncbi.nlm.nih.gov/pubmed/35337694 (accessed on 27 April 2022). [CrossRef]
  22. Wills, T.A.; Choi, K.; Pagano, I. E-Cigarette Use Associated with Asthma Independent of Cigarette Smoking and Marijuana in a 2017 National Sample of Adolescents. J. Adolesc. Health 2020, 67, 524–530. Available online: https://linkinghub.elsevier.com/retrieve/pii/S1054139X20300884 (accessed on 27 April 2022). [CrossRef]
  23. Silva, G.E.; Sherrill, D.L.; Guerra, S.; Barbee, R.A. Asthma as a Risk Factor for COPD in a Longitudinal Study. Chest 2004, 126, 59–65. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0012369215328956 (accessed on 27 April 2022). [CrossRef]
  24. Grimes, D.A.; Schulz, K.F. Bias and causal associations in observational research. Lancet 2002, 359, 248–252. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0140673602074512 (accessed on 27 April 2022). [CrossRef]
  25. Glass, T.A.; Goodman, S.N.; Hernán, M.A.; Samet, J.M. Causal inference in public health. Annu. Rev. Public Health 2013, 34, 61–75. Available online: http://www.ncbi.nlm.nih.gov/pubmed/23297653 (accessed on 27 April 2022). [CrossRef] [Green Version]
  26. Skaaby, T.; Taylor, A.E.; Jacobsen, R.K.; Paternoster, L.; Thuesen, B.H.; Ahluwalia, T.S.; Larsen, S.C.; Zhou, A.; Wong, A.; Gabrielsen, M.E.; et al. Investigating the causal effect of smoking on hay fever and asthma: A Mendelian randomization meta-analysis in the CARTA consortium. Sci. Rep. 2017, 7, 2224. Available online: http://www.nature.com/articles/s41598-017-01977-w (accessed on 27 April 2022). [CrossRef] [Green Version]
  27. Shen, M.; Liu, X.; Li, G.; Li, Z.; Zhou, H. Lifetime Smoking and Asthma: A Mendelian Randomization Study. Front. Genet. 2020, 11, 769. Available online: https://www.frontiersin.org/article/10.3389/fgene.2020.00769/full (accessed on 27 April 2022). [CrossRef]
  28. Fedak, K.M.; Bernal, A.; Capshaw, Z.A.; Gross, S. Applying the Bradford Hill criteria in the 21st century: How data integration has changed causal inference in molecular epidemiology. Emerg. Themes Epidemiol. 2015, 12, 14. Available online: http://www.ncbi.nlm.nih.gov/pubmed/26425136 (accessed on 27 April 2022). [CrossRef] [Green Version]
  29. McLeish, A.C.; Zvolensky, M.J. Asthma and Cigarette Smoking: A Review of the Empirical Literature. J. Asthma 2010, 47, 345–361. Available online: http://www.tandfonline.com/doi/full/10.3109/02770900903556413 (accessed on 27 April 2022). [CrossRef] [PubMed]
  30. Eisner, M.D. Passive Smoking and Adult Asthma. Immunol. Allergy Clin. N. Am. 2008, 28, 521–537. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0889856108000337 (accessed on 27 April 2022). [CrossRef] [PubMed]
  31. von Mutius, E.; Smits, H.H. Primary prevention of asthma: From risk and protective factors to targeted strategies for prevention. Lancet 2020, 396, 854–866. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0140673620318614 (accessed on 27 April 2022). [CrossRef]
  32. Gibbs, K.; Collaco, J.M.; McGrath-Morrow, S.A. Impact of Tobacco Smoke and Nicotine Exposure on Lung Development. Chest 2016, 149, 552–561. Available online: http://www.ncbi.nlm.nih.gov/pubmed/26502117 (accessed on 27 April 2022). [CrossRef] [Green Version]
  33. Dan, N.; Sheiner, E.; Wainstock, T.; Marks, K.; Kessous, R. Maternal Smoking during Pregnancy and the Risk for Childhood Infectious Diseases in the Offspring: A Population-Based Cohort Study. Am. J. Perinatol. 2021, 38, 166–170. Available online: http://www.ncbi.nlm.nih.gov/pubmed/31491797 (accessed on 27 April 2022). [CrossRef]
  34. Magnus, M.C.; Henderson, J.; Tilling, K.; Howe, L.D.; Fraser, A. Independent and combined associations of maternal and own smoking with adult lung function and COPD. Int. J. Epidemiol. 2018, 47, 1855–1864. Available online: http://www.ncbi.nlm.nih.gov/pubmed/30339246 (accessed on 27 April 2022). [CrossRef]
  35. Bellou, V.; Belbasis, L.; Evangelou, E. Tobacco Smoking and Risk for Pulmonary Fibrosis: A Prospective Cohort Study From the UK Biobank. Chest 2021, 160, 983–993. Available online: http://www.ncbi.nlm.nih.gov/pubmed/33905677 (accessed on 27 April 2022). [CrossRef]
  36. Dratva, J.; Zemp, E.; Dharmage, S.C.; Accordini, S.; Burdet, L.; Gislason, T.; Heinrich, J.; Janson, C.; Jarvis, D.; de Marco, R.; et al. Early Life Origins of Lung Ageing: Early Life Exposures and Lung Function Decline in Adulthood in Two European Cohorts Aged 28-73 Years. PLoS ONE 2016, 11, e0145127. [Google Scholar] [CrossRef] [Green Version]
  37. Upton, M.N.; Smith, G.D.; McConnachie, A.; Hart, C.L.; Watt, G.C.M. Maternal and personal cigarette smoking synergize to increase airflow limitation in adults. Am. J. Respir. Crit. Care Med. 2004, 169, 479–487. Available online: http://www.ncbi.nlm.nih.gov/pubmed/14630616 (accessed on 27 April 2022). [CrossRef]
  38. Lim, R.H.; Kobzik, L.; Dahl, M. Risk for Asthma in Offspring of Asthmatic Mothers versus Fathers: A Meta-Analysis. Stanojevic, S.; editor. PLoS ONE 2010, 5, e10134. [Google Scholar] [CrossRef]
  39. Lodge, C.J.; Bråbäck, L.; Lowe, A.J.; Dharmage, S.C.; Olsson, D.; Forsberg, B. Grandmaternal smoking increases asthma risk in grandchildren: A nationwide Swedish cohort. Clin. Exp. Allergy 2018, 48, 167–174. Available online: http://www.ncbi.nlm.nih.gov/pubmed/28925522 (accessed on 27 April 2022). [CrossRef]
  40. Accordini, S.; Calciano, L.; Johannessen, A.; Portas, L.; Benediktsdóttir, B.; Bertelsen, R.J.; Bråbäck, L.; Carsin, A.-E.; Dharmage, S.C.; Dratva, J.; et al. A three-generation study on the association of tobacco smoking with asthma. Int. J. Epidemiol. 2018, 47, 1106–1117. Available online: https://academic.oup.com/ije/article/47/4/1106/4925526 (accessed on 27 April 2022). [CrossRef]
  41. Arah, O.A. Commentary: Tobacco smoking and asthma: Multigenerational effects, epigenetics and multilevel causal mediation analysis. Int. J. Epidemiol. 2018, 47, 1117–1119. Available online: https://academic.oup.com/ije/article/47/4/1117/5088759 (accessed on 27 April 2022). [CrossRef]
  42. Bakakos, P.; Kostikas, K.; Loukides, S. Smoking asthma phenotype: Diagnostic and management challenges. Curr. Opin. Pulm. Med. 2016, 22, 53–58. Available online: http://www.ncbi.nlm.nih.gov/pubmed/26606078 (accessed on 27 April 2022). [CrossRef]
  43. Cerveri, I.; Cazzoletti, L.; Corsico, A.G.; Marcon, A.; Niniano, R.; Grosso, A.; Ronzoni, V.; Accordini, S.; Janson, C.; Pin, I.; et al. The impact of cigarette smoking on asthma: A population-based international cohort study. Int. Arch. Allergy Immunol. 2012, 158, 175–183. Available online: http://www.ncbi.nlm.nih.gov/pubmed/22286571 (accessed on 27 April 2022). [CrossRef] [Green Version]
  44. Kim, S.Y.; Sim, S.; Choi, H.G. Active and passive smoking impacts on asthma with quantitative and temporal relations: A Korean Community Health Survey. Sci. Rep. 2018, 8, 8614. Available online: http://www.nature.com/articles/s41598-018-26895-3 (accessed on 27 April 2022). [CrossRef]
  45. Kapetanstrataki, M.; Evangelopoulou, V.; Behrakis, P.; Tzortzi, A. Lifestyle choices of smokers: Data from the Greek National Health Survey. Pneumon 2022, 35, 1–9. Available online: http://www.pneumon.org/Lifestyle-choices-of-smokers-Data-from-the-Greek-National-Health-Survey,147114,0,2.html (accessed on 27 April 2022). [CrossRef]
  46. Ford, E.S.; Mannino, D.M.; Redd, S.C.; Moriarty, D.G.; Mokdad, A.H. Determinants of Quality of Life among People with Asthma: Findings from the Behavioral Risk Factor Surveillance System. J. Asthma 2004, 41, 327–336. Available online: http://www.tandfonline.com/doi/full/10.1081/JAS-120026090 (accessed on 27 April 2022). [CrossRef]
  47. Chatkin, J.M.; Dullius, C.R. The management of asthmatic smokers. Asthma Res. Pract. 2016, 2, 10. Available online: http://asthmarp.biomedcentral.com/articles/10.1186/s40733-016-0025-7 (accessed on 27 April 2022). [CrossRef] [Green Version]
  48. Brusselle, G.G.; Koppelman, G.H. Biologic Therapies for Severe Asthma. N. Engl. J. Med. 2022, 386, 157–171. Available online: http://www.nejm.org/doi/10.1056/NEJMra2032506 (accessed on 27 April 2022). [CrossRef] [PubMed]
  49. Global Strategy for the Diagnosis, Management and Prevention of COPD. Glob. Initiat. Chronic Obstr. Lung Dis. 2022.
  50. Rabe, K.F.; Watz, H. Chronic obstructive pulmonary disease. Lancet 2017, 389, 1931–1940. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0140673617312229 (accessed on 27 April 2022). [CrossRef]
  51. Antoniu, S.A. Descriptors of dyspnea in obstructive lung diseases. Multidiscip. Respir. Med. 2010, 5, 216. Available online: https://mrmjournal.biomedcentral.com/articles/10.1186/2049-6958-5-3-216 (accessed on 27 April 2022). [CrossRef] [PubMed] [Green Version]
  52. Marcon, A.; Locatelli, F.; Dharmage, S.C.; Svanes, C.; Heinrich, J.; Leynaert, B.; Burney, P.; Corsico, A.; Caliskan, G.; Calciano, L.; et al. The coexistence of asthma and COPD: Risk factors, clinical history and lung function trajectories. Eur. Respir. J. 2021, 58, 2004656. Available online: http://erj.ersjournals.com/lookup/doi/10.1183/13993003.04656-2020 (accessed on 27 April 2022). [CrossRef]
  53. de Marco, R.; Marcon, A.; Rossi, A.; Antó, J.M.; Cerveri, I.; Gislason, T.; Heinrich, J.; Janson, C.; Jarvis, D.; Kuenzli, N.; et al. Asthma, COPD and overlap syndrome: A longitudinal study in young European adults. Eur. Respir. J. 2015, 46, 671–679. Available online: http://erj.ersjournals.com/lookup/doi/10.1183/09031936.00008615 (accessed on 27 April 2022). [CrossRef]
  54. Hellenic Thoracic Society. National Guidelines for Chronic Obstructive Pulmonary Disease. 2021. Available online: https://hts.org.gr/302 (accessed on 19 June 2022).
  55. Reitsma, M.B.; Flor, L.S.; Mullany, E.C.; Gupta, V.; Hay, S.I.; Gakidou, E. Spatial, temporal, and demographic patterns in prevalence of smoking tobacco use and initiation among young people in 204 countries and territories, 1990–2019. Lancet Public Heal. 2021, 6, e472–e481. Available online: https://linkinghub.elsevier.com/retrieve/pii/S246826672100102X (accessed on 27 April 2022). [CrossRef]
  56. Van De Ven, M.O.M.; van Zundert, R.M.P.; Engels, R.C.M.E. Effects of asthma on nicotine dependence development and smoking cessation attempts in adolescence. J. Asthma 2013, 50, 250–259. Available online: http://www.ncbi.nlm.nih.gov/pubmed/23347267 (accessed on 27 April 2022). [CrossRef]
  57. Jang, A.-S.; Park, J.-S.; Lee, J.-H.; Park, S.-W.; Kim, D.-J.; Uh, S.-T.; Kim, Y.-H.; Park, C.-S. The impact of smoking on clinical and therapeutic effects in asthmatics. J. Korean Med. Sci. 2009, 24, 209–214. Available online: http://www.ncbi.nlm.nih.gov/pubmed/19399260 (accessed on 27 April 2022). [CrossRef]
  58. Lange, P.; Parner, J.; Vestbo, J.; Schnohr, P.; Jensen, G. A 15-year follow-up study of ventilatory function in adults with asthma. N. Engl. J. Med. 1998, 339, 1194–1200. Available online: http://www.ncbi.nlm.nih.gov/pubmed/9780339 (accessed on 27 April 2022). [CrossRef]
  59. James, A.L.; Palmer, L.J.; Kicic, E.; Maxwell, P.S.; Lagan, S.E.; Ryan, G.F.; Musk, A.W. Decline in lung function in the Busselton Health Study: The effects of asthma and cigarette smoking. Am. J. Respir. Crit. Care Med. 2005, 171, 109–114. Available online: http://www.ncbi.nlm.nih.gov/pubmed/15486340 (accessed on 27 April 2022). [CrossRef]
  60. Graff, S.; Bricmont, N.; Moermans, C.; Henket, M.; Paulus, V.; Guissard, F.; Louis, R.; Schleich, F. Clinical and biological factors associated with irreversible airway obstruction in adult asthma. Respir. Med. 2020, 175, 106202. Available online: http://www.ncbi.nlm.nih.gov/pubmed/33202369 (accessed on 27 April 2022). [CrossRef]
  61. Bakakos, A.; Vogli, S.; Dimakou, K.; Hillas, G. Asthma with Fixed Airflow Obstruction: From Fixed to Personalized Approach. J. Pers. Med. 2022, 12, 333. Available online: https://www.mdpi.com/2075-4426/12/3/333 (accessed on 27 April 2022). [CrossRef]
  62. Scichilone, N.; Battaglia, S.; La Sala, A.; Bellia, V. Clinical implications of airway hyperresponsiveness in COPD. Int. J. Chron. Obstruct. Pulmon. Dis. 2006, 1, 49–60. Available online: http://www.ncbi.nlm.nih.gov/pubmed/18046902 (accessed on 27 April 2022).
  63. Nuñez, A.; Sarasate, M.; Loeb, E.; Esquinas, C.; Miravitlles, M.; Barrecheguren, M. Practical Guide to the Identification and Diagnosis of Asthma-COPD Overlap (ACO). COPD J. Chronic Obstr. Pulm. Dis. 2019, 16, 1–7. Available online: https://www.tandfonline.com/doi/full/10.1080/15412555.2019.1575802 (accessed on 27 April 2022). [CrossRef] [PubMed]
  64. Kostikas, K.; Clemens, A.; Patalano, F. The asthma-COPD overlap syndrome: Do we really need another syndrome in the already complex matrix of airway disease? Int. J. Chron. Obstruct. Pulmon. Dis. 2016, 11, 1297–1306. Available online: https://www.dovepress.com/the-asthmandashcopd-overlap-syndrome-do-we-really-need-another-syndrom-peer-reviewed-article-COPD (accessed on 27 April 2022). [CrossRef] [PubMed] [Green Version]
  65. Miravitlles, M. Asthma-COPD Overlap (ACO) PRO-CON Debate. ACO: Call Me by My Name. COPD J. Chronic Obstr. Pulm. Dis. 2020, 17, 471–473. Available online: https://www.tandfonline.com/doi/full/10.1080/15412555.2020.1817883 (accessed on 27 April 2022). [CrossRef] [PubMed]
  66. Tupper, O.D.; Ulrik, C.S. Long-term predictors of severe exacerbations and mortality in a cohort of well-characterised adults with asthma. Respir. Res. 2021, 22, 269. Available online: http://www.ncbi.nlm.nih.gov/pubmed/34670588 (accessed on 27 April 2022). [CrossRef] [PubMed]
  67. St-Laurent, J.; Bergeron, C.; Pagé, N.; Couture, C.; Laviolette, M.; Boulet, L.-P. Influence of smoking on airway inflammation and remodelling in asthma. Clin. Exp. Allergy 2008, 38, 1582–1589. Available online: https://onlinelibrary.wiley.com/doi/10.1111/j.1365-2222.2008.03032.x (accessed on 27 April 2022). [CrossRef] [PubMed]
  68. Klein, D.K.; Silberbrandt, A.; Frøssing, L.; Hvidtfeldt, M.; von Bülow, A.; Nair, P.; Mukherjee, M.; Porsbjerg, C. Impact of former smoking exposure on airway eosinophilic activation and autoimmunity in patients with severe asthma. Eur. Respir. J. 2022, 60, 2102446. Available online: http://www.ncbi.nlm.nih.gov/pubmed/35236724 (accessed on 27 April 2022). [CrossRef] [PubMed]
  69. Chu, S.; Ma, L.; Wei, J.; Wang, J.; Xu, Q.; Chen, M.; Jiang, M.; Luo, M.; Wu, J.; Mai, L.; et al. Smoking Status Modifies the Relationship between Th2 Biomarkers and Small Airway Obstruction in Asthma. Can. Respir. J. 2021, 2021, 1918518. Available online: http://www.ncbi.nlm.nih.gov/pubmed/34876944 (accessed on 27 April 2022). [CrossRef]
  70. Kjellberg, S.; Houltz, B.K.; Zetterström, O.; Robinson, P.D.; Gustafsson, P.M. Clinical characteristics of adult asthma associated with small airway dysfunction. Respir. Med. 2016, 117, 92–102. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0954611116301147 (accessed on 27 April 2022). [CrossRef]
  71. Munck, C.; Helby, J.; Westergaard, C.G.; Porsbjerg, C.; Backer, V.; Hansen, L.H. Smoking Cessation and the Microbiome in Induced Sputum Samples from Cigarette Smoking Asthma Patients. PLoS ONE 2016, 11, e0158622. [Google Scholar] [CrossRef] [Green Version]
  72. Althuis, M.D.; Sexton, M.; Prybylski, D. Cigarette smoking and asthma symptom severity among adult asthmatics. J. Asthma 1999, 36, 257–264. Available online: http://www.ncbi.nlm.nih.gov/pubmed/10350222 (accessed on 27 April 2022). [CrossRef]
  73. Siroux, V.; Pin, I.; Oryszczyn, M.P.; Le Moual, N.; Kauffmann, F. Relationships of active smoking to asthma and asthma severity in the EGEA study. Epidemiological study on the Genetics and Environment of Asthma. Eur. Respir. J. 2000, 15, 470–477. Available online: http://www.ncbi.nlm.nih.gov/pubmed/10759439 (accessed on 27 April 2022). [CrossRef] [Green Version]
  74. Gallefoss, F.; Bakke, P.S. Does smoking affect the outcome of patient education and self-management in asthmatics? Patient Educ. Couns. 2003, 49, 91–97. Available online: http://www.ncbi.nlm.nih.gov/pubmed/12527158 (accessed on 27 April 2022). [CrossRef]
  75. Jiménez-Ruiz, C.A.; Andreas, S.; Lewis, K.E.; Tonnesen, P.; van Schayck, C.P.; Hajek, P.; Tonstad, S.; Dautzenberg, B.; Fletcher, M.; Masefield, S.; et al. Statement on smoking cessation in COPD and other pulmonary diseases and in smokers with comorbidities who find it difficult to quit. Eur. Respir. J. 2015, 46, 61–79. Available online: http://www.ncbi.nlm.nih.gov/pubmed/25882805 (accessed on 27 April 2022). [CrossRef]
  76. Tiotiu, A.; Ioan, I.; Wirth, N.; Romero-Fernandez, R.; González-Barcala, F.-J. The Impact of Tobacco Smoking on Adult Asthma Outcomes. Int. J. Environ. Res. Public Health 2021, 18, 992. Available online: https://www.mdpi.com/1660-4601/18/3/992 (accessed on 27 April 2022). [CrossRef]
  77. Kauppi, P.; Kupiainen, H.; Lindqvist, A.; Haahtela, T.; Laitinen, T. Long-term smoking increases the need for acute care among asthma patients: A case control study. BMC Pulm. Med. 2014, 14, 119. Available online: https://bmcpulmmed.biomedcentral.com/articles/10.1186/1471-2466-14-119 (accessed on 27 April 2022). [CrossRef] [Green Version]
  78. Khokhawalla, S.A.; Rosenthal, S.R.; Pearlman, D.N.; Triche, E.W. Cigarette smoking and emergency care utilization among asthmatic adults in the 2011 Asthma Call-back Survey. J. Asthma 2015, 52, 732–739. Available online: http://www.ncbi.nlm.nih.gov/pubmed/25563058 (accessed on 27 April 2022). [CrossRef]
  79. Entwistle, M.R.; Valle, K.; Schweizer, D.; Cisneros, R. Electronic cigarette (e-cigarette) use and frequency of asthma symptoms in adult asthmatics in California. J. Asthma 2021, 58, 1460–1466. Available online: http://www.ncbi.nlm.nih.gov/pubmed/32746661 (accessed on 27 April 2022). [CrossRef]
  80. Alnajem, A.; Redha, A.; Alroumi, D.; Alshammasi, A.; Ali, M.; Alhussaini, M.; Almutairi, W.; Esmaeil, A.; Ziyab, A.H. Use of electronic cigarettes and secondhand exposure to their aerosols are associated with asthma symptoms among adolescents: A cross-sectional study. Respir. Res. 2020, 21, 300. Available online: http://www.ncbi.nlm.nih.gov/pubmed/33198741 (accessed on 27 April 2022). [CrossRef]
  81. Kotoulas, S.-C.; Katsaounou, P.; Riha, R.; Grigoriou, I.; Papakosta, D.; Spyratos, D.; Porpodis, K.; Domvri, K.; Pataka, A. Electronic Cigarettes and Asthma: What Do We Know So Far? J. Pers. Med. 2021, 11, 723. Available online: http://www.ncbi.nlm.nih.gov/pubmed/34442368 (accessed on 27 April 2022).
  82. Nadeau, M.; Boulay, M.-È.; Milot, J.; Lepage, J.; Bilodeau, L.; Maltais, F.; Boulet, L.-P. Comparative prevalence of co-morbidities in smoking and non-smoking asthma patients with incomplete reversibility of airway obstruction, non-smoking asthma patients with complete reversibility of airway obstruction and COPD patients. Respir. Med. 2017, 125, 82–88. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0954611117300562 (accessed on 27 April 2022). [CrossRef] [Green Version]
  83. Tomisa, G.; Horváth, A.; Sánta, B.; Keglevich, A.; Tamási, L. Epidemiology of comorbidities and their association with asthma control. Allergy Asthma Clin. Immunol. 2021, 17, 95. Available online: http://www.ncbi.nlm.nih.gov/pubmed/34551813 (accessed on 27 April 2022). [CrossRef]
  84. Thomson, N.C. Addressing corticosteroid insensitivity in adults with asthma. Expert Rev. Respir. Med. 2016, 10, 137–156. Available online: http://www.tandfonline.com/doi/full/10.1586/17476348.2016.1133304 (accessed on 27 April 2022). [CrossRef] [PubMed] [Green Version]
  85. Thomson, N.C. Challenges in the management of asthma associated with smoking-induced airway diseases. Expert Opin. Pharmacother. 2018, 19, 1565–1579. Available online: https://www.tandfonline.com/doi/full/10.1080/14656566.2018.1515912 (accessed on 27 April 2022). [CrossRef] [PubMed]
  86. Lazarus, S.C.; Chinchilli, V.M.; Rollings, N.J.; Boushey, H.A.; Cherniack, R.; Craig, T.J.; Deykin, A.; DiMango, E.; Fish, J.E.; Ford, J.G.; et al. National Heart Lung and Blood Institute’s Asthma Clinical Research Network. Smoking affects response to inhaled corticosteroids or leukotriene receptor antagonists in asthma. Am. J. Respir. Crit. Care Med. 2007, 175, 783–790. Available online: http://www.ncbi.nlm.nih.gov/pubmed/17204725 (accessed on 27 April 2022). [CrossRef] [PubMed] [Green Version]
  87. Cameron, E.J.; Chaudhuri, R.; Mair, F.; McSharry, C.; Greenlaw, N.; Weir, C.J.; Jolly, L.; Donnelly, I.; Gallacher, K.; Morrison, D.; et al. Randomised controlled trial of azithromycin in smokers with asthma. Eur. Respir. J. 2013, 42, 1412–1415. Available online: http://erj.ersjournals.com/lookup/doi/10.1183/09031936.00093913 (accessed on 27 April 2022). [CrossRef] [PubMed]
  88. Gibson, P.G.; Yang, I.A.; Upham, J.W.; Reynolds, P.N.; Hodge, S.; James, A.L.; Jenkins, C.; Peters, M.J.; Marks, G.B.; Baraket, M.; et al. Effect of azithromycin on asthma exacerbations and quality of life in adults with persistent uncontrolled asthma (AMAZES): A randomised, double-blind, placebo-controlled trial. Lancet 2017, 390, 659–668. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0140673617312813 (accessed on 27 April 2022). [CrossRef] [Green Version]
  89. Bakakos, P.; Papakosta, D.; Loukides, S. Budesonide/formoterol via the Elpenhaler® device in asthmatic patients: A real-world effectiveness study (The BOREAS Study). Pneumon 2021, 34, 22. Available online: http://www.pneumon.org/Budesonide-formoterol-via-the-Elpenhaler-device-in-asthmatic-patients-A-real-world,144485,0,2.html (accessed on 27 April 2022). [CrossRef]
  90. Kostikas, K. Real-life effectiveness of ICS/LABA inhalers in asthma: The evidence generated and future needs for optimal patient management. Pneumon 2021, 34, 1–3. Available online: http://www.pneumon.org/Real-life-effectiveness-of-ICS-LABA-inhalers-in-nasthma-The-evidence-generated-and,144496,0,2.html (accessed on 27 April 2022). [CrossRef]
  91. Cox, C.A.; Boudewijn, I.M.; Vroegop, S.J.; Schokker, S.; Lexmond, A.J.; Frijlink, H.W.; Hagedoorn, P.; Vonk, J.M.; Farenhorst, M.P.; Ten Hacken, N.H.T.; et al. Extrafine compared to non-extrafine particle inhaled corticosteroids in smokers and ex-smokers with asthma. Respir. Med. 2017, 130, 35–42. Available online: http://www.ncbi.nlm.nih.gov/pubmed/29206631 (accessed on 27 April 2022). [CrossRef] [Green Version]
  92. Contoli, M.; Bellini, F.; Morandi, L.; Forini, G.; Bianchi, S.; Gnesini, G.; Marku, B.; Rabe, K.F.; Papi, A. Assessing small airway impairment in mild-to-moderate smoking asthmatic patients. Eur. Respir. J. 2016, 47, 1264–1267. Available online: http://www.ncbi.nlm.nih.gov/pubmed/26869674 (accessed on 27 April 2022). [CrossRef] [Green Version]
  93. Steiropoulos, P.; Bakakos, P.; Hatziagorou, E.; Katsaounou, P.; Loukides, S.; Papaioannou, A.; Porpodis, K.; Samaras, K.; Tzouvelekis, A.; Kalafatakis, K.; et al. The present and future of inhalation therapy for the management of obstructive airway diseases: Emphasis on pressurized metered-dose inhalers. Pneumon 2021, 34, 1–13. Available online: http://www.pneumon.org/The-present-and-future-of-inhalation-therapy-for-nthe-management-of-obstructive-airway,144614,0,2.html (accessed on 27 April 2022). [CrossRef]
  94. Pilette, C.; Brightling, C.; Lacombe, D.; Brusselle, G. Urgent need for pragmatic trial platforms in severe asthma. Lancet Respir. Med. 2018, 6, 581–583. Available online: https://linkinghub.elsevier.com/retrieve/pii/S2213260018302911 (accessed on 27 April 2022). [CrossRef]
  95. O’Byrne, P.M.; Lamm, C.J.; Busse, W.W.; Tan, W.C.; Pedersen, S. The Effects of Inhaled Budesonide on Lung Function in Smokers and Nonsmokers with Mild Persistent Asthma. Chest 2009, 136, 1514–1520. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0012369209607315 (accessed on 27 April 2022). [CrossRef]
  96. Bhatt, S.P.; Anderson, J.A.; Brook, R.D.; Calverley, P.M.; Celli, B.R.; Cowans, N.J.; Crim, C.; Martinez, F.J.; Newby, D.E.; Vestbo, J.; et al. Cigarette smoking and response to inhaled corticosteroids in COPD. Eur. Respir. J. 2018, 51, 1701393. Available online: http://erj.ersjournals.com/lookup/doi/10.1183/13993003.01393-2017 (accessed on 27 April 2022). [CrossRef] [Green Version]
  97. Tomlinson, J.E.M.; McMahon, A.D.; Chaudhuri, R.; Thompson, J.M.; Wood, S.F.; Thomson, N.C. Efficacy of low and high dose inhaled corticosteroid in smokers versus non-smokers with mild asthma. Thorax 2005, 60, 282–287. Available online: https://thorax.bmj.com/lookup/doi/10.1136/thx.2004.033688 (accessed on 27 April 2022). [CrossRef] [Green Version]
  98. Brusselle, G.; Peché, R.; Van den Brande, P.; Verhulst, A.; Hollanders, W.; Bruhwyler, J. Real-life effectiveness of extrafine beclometasone dipropionate/formoterol in adults with persistent asthma according to smoking status. Respir. Med. 2012, 106, 811–819. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0954611112000443 (accessed on 27 April 2022). [CrossRef] [Green Version]
  99. Clearie, K.L.; McKinlay, L.; Williamson, P.A.; Lipworth, B.J. Fluticasone/Salmeterol Combination Confers Benefits in People with Asthma Who Smoke. Chest 2012, 141, 330–338. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0012369212600695 (accessed on 27 April 2022). [CrossRef]
  100. Kerstjens, H.A.M.; Moroni-Zentgraf, P.; Tashkin, D.P.; Dahl, R.; Paggiaro, P.; Vandewalker, M.; Schmidt, H.; Engel, M.; Bateman, E.D. Tiotropium improves lung function, exacerbation rate, and asthma control, independent of baseline characteristics including age, degree of airway obstruction, and allergic status. Respir. Med. 2016, 117, 198–206. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0954611116301391 (accessed on 27 April 2022). [CrossRef] [Green Version]
  101. Magnussen, H.; Bugnas, B.; van Noord, J.; Schmidt, P.; Gerken, F.; Kesten, S. Improvements with tiotropium in COPD patients with concomitant asthma. Respir. Med. 2008, 102, 50–56. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0954611107003587 (accessed on 27 April 2022). [CrossRef] [Green Version]
  102. Jabbal, S.; Kuo, C.R.; Lipworth, B. Randomized controlled trial of triple versus dual inhaler therapy on small airways in smoking asthmatics. Clin. Exp. Allergy 2020, 50, 1140–1147. Available online: https://onlinelibrary.wiley.com/doi/10.1111/cea.13702 (accessed on 27 April 2022). [CrossRef]
  103. Chaudhuri, R.; Livingston, E.; McMahon, A.D.; Thomson, L.; Borland, W.; Thomson, N.C. Cigarette smoking impairs the therapeutic response to oral corticosteroids in chronic asthma. Am. J. Respir. Crit. Care Med. 2003, 168, 1308–1311. Available online: http://www.ncbi.nlm.nih.gov/pubmed/12893649 (accessed on 27 April 2022). [CrossRef]
  104. Price, D.; Popov, T.A.; Bjermer, L.; Lu, S.; Petrovic, R.; Vandormael, K.; Mehta, A.; Strus, J.D.; Polos, P.G.; Philip, G. Effect of montelukast for treatment of asthma in cigarette smokers. J. Allergy Clin. Immunol. 2013, 131, 763–771.e6. Available online: https://linkinghub.elsevier.com/retrieve/pii/S0091674912026747 (accessed on 27 April 2022). [CrossRef]
  105. Spears, M.; Donnelly, I.; Jolly, L.; Brannigan, M.; Ito, K.; McSharry, C.; Lafferty, J.; Chaudhuri, R.; Braganza, G.; Adcock, I.M.; et al. Effect of low-dose theophylline plus beclometasone on lung function in smokers with asthma: A pilot study. Eur. Respir. J. 2009, 33, 1010–1017. Available online: http://erj.ersjournals.com/cgi/doi/10.1183/09031936.00158208 (accessed on 27 April 2022). [CrossRef] [Green Version]
  106. Schreiber, J.; Sauerbeck, I.S.; Mailänder, C. The Long-Term Effectiveness and Safety of Omalizumab on Patient- and Physician-Reported Asthma Control: A Three-Year, Real-Life Observational Study. Adv. Ther. 2020, 37, 353–363. Available online: http://link.springer.com/10.1007/s12325-019-01135-w (accessed on 27 April 2022). [CrossRef] [PubMed] [Green Version]
  107. Morobeid, H.; Pizarro, C.; Biener, L.; Ulrich-Merzenich, G.; Kütting, D.; Nickenig, G.; Skowasch, D. Impact of prior smoking exposure and COPD comorbidity on treatment response to monoclonal antibodies in patients with severe asthma. ERJ Open Res. 2021, 7, 00190–02021. Available online: http://openres.ersjournals.com/lookup/doi/10.1183/23120541.00190-2021 (accessed on 27 April 2022). [CrossRef] [PubMed]
  108. Hansen, S.; Ulrik, C.; Hilberg, O.; Von Bülow, A.; Christiansen, A.; Johnsen, C.R.; Schmid, J.; Bjerrum, A.S.; Assing, K.; Wimmer-Aune, A.; et al. The effectiveness of anti-IL5 biologics is comparable in previous-smokers and never-smokers with severe asthma. Eur. Respir. Soc. 2021, 58, PA3742. Available online: http://erj.ersjournals.com/lookup/doi/10.1183/13993003.congress-2021.PA3742 (accessed on 27 April 2022).
  109. Crimi, C.; Campisi, R.; Cacopardo, G.; Intravaia, R.; Nolasco, S.; Porto, M.; Pelaia, C.; Crimi, N. Real-life effectiveness of mepolizumab in patients with severe refractory eosinophilic asthma and multiple comorbidities. World Allergy Organ. J. 2020, 13, 100462. Available online: http://www.ncbi.nlm.nih.gov/pubmed/32994855 (accessed on 27 April 2022). [CrossRef] [PubMed]
  110. Eisner, M.D. Directly measured second hand smoke exposure and asthma health outcomes. Thorax 2005, 60, 814–821. Available online: https://thorax.bmj.com/lookup/doi/10.1136/thx.2004.037283 (accessed on 27 April 2022). [CrossRef] [Green Version]
  111. Jang, A.-S.; Choi, I.-S.; Lee, S.; Nam, H.-S.; Kweon, S.-S.; Son, M.-H.; Lee, J.-H.; Park, S.W.; Kim, D.-J.; Uh, S.T.; et al. The effect of passive smoking on asthma symptoms, atopy, and airway hyperresponsiveness in schoolchildren. J. Korean Med. Sci. 2004, 19, 214–217. Available online: http://www.ncbi.nlm.nih.gov/pubmed/15082893 (accessed on 27 April 2022). [CrossRef]
  112. Fernandes, A.G.O.; De Souza-Machado, C.; Pinheiro, G.P.; De Oliva, S.T.; Mota, R.C.L.; De Lima, V.B.; Cruz, C.S.; Chatkin, J.M.; Cruz, A. Dual exposure to smoking and household air pollution is associated with an increased risk of severe asthma in adults in Brazil. Clin. Transl. Allergy 2018, 8, 48. Available online: https://ctajournal.biomedcentral.com/articles/10.1186/s13601-018-0235-6 (accessed on 27 April 2022). [CrossRef] [Green Version]
  113. Tatum, A.J.; Shapiro, G.G. The effects of outdoor air pollution and tobacco smoke on asthma. Immunol. Allergy Clin. N. Am. 2005, 25, 15–30. Available online: http://www.ncbi.nlm.nih.gov/pubmed/15579362 (accessed on 27 April 2022). [CrossRef]
  114. Wenzel, S.E. Severe Adult Asthmas: Integrating Clinical Features, Biology, and Therapeutics to Improve Outcomes. Am. J. Respir. Crit. Care Med. 2021, 203, 809–821. Available online: https://www.atsjournals.org/doi/10.1164/rccm.202009-3631C.I (accessed on 27 April 2022). [CrossRef]
  115. McDonald, V.M.; Clark, V.L.; Cordova-Rivera, L.; Wark, P.A.B.; Baines, K.; Gibson, P.G. Targeting treatable traits in severe asthma: A randomised controlled trial. Eur. Respir. J. 2020, 55, 1901509. Available online: http://erj.ersjournals.com/lookup/doi/10.1183/13993003.01509-2019 (accessed on 27 April 2022). [CrossRef]
  116. Holguin, F.; Cardet, J.C.; Chung, K.F.; Diver, S.; Ferreira, D.; Fitzpatrick, A.; Gaga, M.; Kellermeyer, L.; Khurana, S.; Knight, S.L.; et al. Management of severe asthma: A European Respiratory Society/American Thoracic Society guideline. Eur. Respir. J. 2020, 55, 1900588. Available online: http://erj.ersjournals.com/lookup/doi/10.1183/13993003.00588-2019 (accessed on 27 April 2022). [CrossRef] [Green Version]
  117. Chung, K.F.; Wenzel, S.E.; Brozek, J.L.; Bush, A.; Castro, M.; Sterk, P.J.; Adcock, I.M.; Bateman, E.D.; Bel, E.H.; Bleecker, E.R.; et al. International ERS/ATS guidelines on definition, evaluation and treatment of severe asthma. Eur. Respir. J. 2014, 43, 343–373. Available online: http://erj.ersjournals.com/lookup/doi/10.1183/09031936.00202013 (accessed on 27 April 2022). [CrossRef] [Green Version]
  118. Chaudhuri, R.; Livingston, E.; McMahon, A.D.; Lafferty, J.; Fraser, I.; Spears, M.; McSharry, C.P.; Thomson, N.C. Effects of Smoking Cessation on Lung Function and Airway Inflammation in Smokers with Asthma. Am. J. Respir. Crit. Care Med. 2006, 174, 127–133. Available online: http://www.atsjournals.org/doi/abs/10.1164/rccm.200510-1589O.C (accessed on 27 April 2022). [CrossRef]
  119. Westergaard, C.G.; Porsbjerg, C.; Backer, V. The effect of smoking cessation on airway inflammation in young asthma patients. Clin. Exp. Allergy 2014, 44, 353–361. Available online: https://onlinelibrary.wiley.com/doi/10.1111/cea.12243 (accessed on 27 April 2022). [CrossRef]
  120. Tønnesen, P.; Pisinger, C.; Hvidberg, S.; Wennike, P.; Bremann, L.; Westin, Å.; Thomsen, C.; Nilsson, F. Effects of smoking cessation and reduction in asthmatics. Nicotine Tob. Res. 2005, 7, 139–148. Available online: https://academic.oup.com/ntr/article-lookup/doi/10.1080/14622200412331328411 (accessed on 27 April 2022). [CrossRef]
  121. Hughes, J.R.; Keely, J.; Naud, S. Shape of the relapse curve and long-term abstinence among untreated smokers. Addiction 2004, 99, 29–38. Available online: http://www.ncbi.nlm.nih.gov/pubmed/14678060 (accessed on 27 April 2022). [CrossRef]
  122. US Preventive Services Task Force; Krist, A.H.; Davidson, K.W.; Mangione, C.M.; Barry, M.J.; Cabana, M.; Caughey, A.B.; Donahue, K.; Doubeni, C.A.; Epling, J.W.; et al. Interventions for Tobacco Smoking Cessation in Adults, Including Pregnant Persons: US Preventive Services Task Force Recommendation Statement. JAMA 2021, 325, 265–279. Available online: http://www.ncbi.nlm.nih.gov/pubmed/33464343 (accessed on 27 April 2022).
  123. Gratziou, C.; Florou, A.; Ischaki, E.; Eleftheriou, K.; Sachlas, A.; Bersimis, S.; Zakynthinos, S. Smoking cessation effectiveness in smokers with COPD and asthma under real life conditions. Respir. Med. 2014, 108, 577–583. Available online: http://www.ncbi.nlm.nih.gov/pubmed/24560410 (accessed on 27 April 2022). [CrossRef] [Green Version]
  124. Westergaard, C.G.; Porsbjerg, C.; Backer, V. The effect of Varenicline on smoking cessation in a group of young asthma patients. Respir. Med. 2015, 109, 1416–1422. Available online: http://www.ncbi.nlm.nih.gov/pubmed/26427627 (accessed on 27 April 2022). [CrossRef] [PubMed] [Green Version]
  125. Politis, A.; Ioannidis, V.; Gourgoulianis, K.I.; Daniil, Z.; Hatzoglou, C. Effects of varenicline therapy in combination with advanced behavioral support on smoking cessation and quality of life in inpatients with acute exacerbation of COPD, bronchial asthma, or community-acquired pneumonia: A prospective, open-label, preference. Chron. Respir. Dis. 2018, 15, 146–156. Available online: http://www.ncbi.nlm.nih.gov/pubmed/29117796 (accessed on 27 April 2022). [CrossRef] [PubMed]
  126. Bittner, J.C.; Hasegawa, K.; Probst, B.D.; Mould-Millman, N.-K.; Silverman, R.A.; Camargo, C.A. Smoking status and smoking cessation intervention among U.S. adults hospitalized for asthma exacerbation. Allergy Asthma Proc. 2016, 37, 318–323. Available online: http://www.ncbi.nlm.nih.gov/pubmed/27401318 (accessed on 27 April 2022). [CrossRef] [PubMed] [Green Version]
  127. Borrelli, B. Motivating parents of kids with asthma to quit smoking: The PAQS project. Health Educ. Res. 2002, 17, 659–669. Available online: https://academic.oup.com/her/article-lookup/doi/10.1093/her/17.5.659 (accessed on 27 April 2022). [CrossRef] [Green Version]
  128. Borrelli, B.; McQuaid, E.L.; Novak, S.P.; Hammond, S.K.; Becker, B. Motivating Latino caregivers of children with asthma to quit smoking: A randomized trial. J. Consult. Clin. Psychol. 2010, 78, 34–43. Available online: http://www.ncbi.nlm.nih.gov/pubmed/20099948 (accessed on 27 April 2022). [CrossRef]
Figure 1. Diagnostic algorithm for asthmatic smokers.
Figure 1. Diagnostic algorithm for asthmatic smokers.
Jpm 12 01231 g001
Table 1. Controller treatment options for asthma patients with a smoking history, according to pertinent literature.
Table 1. Controller treatment options for asthma patients with a smoking history, according to pertinent literature.
MedicationFindings from Clinical Studies
ICS ICS remain effective in asthma patients with a smoking history, but
some patients might have a blunted response to these treatments [19,95,96,97].
Higher ICS doses might be required to achieve asthma control in smokers [97].
Extrafine formulations might confer greater advantages, according to clinical data [98]
LABA Adding LABA to ICS increased airway hyperresponsiveness and airway caliber and improved
asthma symptoms in asthmatic smokers when compared to higher ICS doses [96,99].
LAMA Tiotropium is an established treatment option for asthma; however, active smokers were excluded in tiotropium trials.The benefits of tiotropium in asthma control and lung function were marginally higher in ex-smokers with asthma [100] and tiotropium has shown effectiveness in patients with concomitant asthma and COPD [101].
Additionally, triple therapy (ICS + LABA + LAMA) improved small airway outcomes in asthmatic smokers [102].
OCS Cigarette smoking diminishes the therapeutic response to OCS [103].
Macrolides Azithromycin did not improve lung function and symptoms in a clinical trial of active smokers with asthma [87].
LTRA Certain asthmatic smokers show marked improvement in asthma control after adding montelukast to ICS [86,104].
Theophylline Combination of low-dose theophylline with ICS improved lung function and symptoms in asthmatic smokers [105].
Biologics Anti-IgE is effective in active and ex-smokers [106,107].
Anti-IL5 and anti-IL5R are effective irrespective of smoking status [107,108,109].
Anti-IL4 has not been evaluated in active smokers or past smokers with over 10 pack years [48].
Abbreviations: COPD: Chronic Obstructive Pulmonary Disease; ICS: Inhaled Cortico-Steroids; LABA: Long-Acting Beta-Agonists; LAMA: Long-Acting Muscarinic Antago-nists; LTRA: LeukoTriene Receptor Antagonists; OCS: Oral CorticoSteroids.
Table 2. Summary of myths and realities of association of asthma and smoking.
Table 2. Summary of myths and realities of association of asthma and smoking.
MythReality
Smoking causes asthmaThere is no established causal association between tobacco exposure and asthma, and existing evidence is conflicting
Smoking hinders asthma diagnosisSmoking may cause fixed airway obstruction, but other disease characteristics enable accurate diagnosis
Smoking impairs asthma prognosisSmoking is associated with worse clinical outcomes and
disease control in asthma patients
Smoking interferes in asthma treatmentThe main anti-asthmatic medications remain effective in asthmatic smokers.
However, there is some evidence for reduced efficacy of inhaled corticosteroids.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Bellou, V.; Gogali, A.; Kostikas, K. Asthma and Tobacco Smoking. J. Pers. Med. 2022, 12, 1231. https://doi.org/10.3390/jpm12081231

AMA Style

Bellou V, Gogali A, Kostikas K. Asthma and Tobacco Smoking. Journal of Personalized Medicine. 2022; 12(8):1231. https://doi.org/10.3390/jpm12081231

Chicago/Turabian Style

Bellou, Vanesa, Athena Gogali, and Konstantinos Kostikas. 2022. "Asthma and Tobacco Smoking" Journal of Personalized Medicine 12, no. 8: 1231. https://doi.org/10.3390/jpm12081231

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop