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The Impact of Tobacco Use on COVID-19 Outcomes: A Systematic Review

Published online by Cambridge University Press:  01 January 2024

Jessica Baker Open the ORCID record for Jessica Baker [Opens in a new window] ,
Nandita Krishnan Open the ORCID record for Nandita Krishnan [Opens in a new window] ,
Lorien C. Abroms Open the ORCID record for Lorien C. Abroms [Opens in a new window] ,
Carla J. Berg Open the ORCID record for Carla J. Berg [Opens in a new window]  and
Renee Bittoun
Jessica Baker
Affiliation:
Department of Global Health, Milken Institute School of Public Health, The George Washington University, Washington, DC, USA
Nandita Krishnan
Affiliation:
Department of Prevention and Community Health, Milken Institute School of Public Health, The George Washington University, Washington, DC, USA
Lorien C. Abroms
Affiliation:
Department of Prevention and Community Health, Milken Institute School of Public Health, The George Washington University, Washington, DC, USA George Washington University Cancer Center, George Washington University, Washington, DC, USA
Carla J. Berg*
Affiliation:
Department of Prevention and Community Health, Milken Institute School of Public Health, The George Washington University, Washington, DC, USA George Washington University Cancer Center, George Washington University, Washington, DC, USA
*
Correspondence should be addressed to Carla J. Berg; carlaberg@gwu.edu
Rights & Permissions [Opens in a new window]

Abstract

Introduction. Tobacco use increases risks for numerous diseases, including respiratory illnesses. We examined the literature to determine whether a history of tobacco use increases risks for adverse outcomes among COVID-19 patients. Methods. We conducted a systematic search of PubMed, LitCovid, Scopus, and Europe PMC (for preprints) using COVID-19 and tobacco-related terms. We included studies of human subjects with lab-confirmed COVID-19 infections that examined tobacco use history as an exposure and used multivariable analyses. The data was collected between March 31st, 2020, and February 20th, 2021. Outcomes included mortality, hospitalization, ICU admission, mechanical ventilation, and illness severity. Results. Among the 39 studies (33 peer-reviewed, 6 preprints) included, the most common outcome assessed was mortality (n = 32). The majority of these studies (17/32) found that tobacco use increased risk, one found decreased risk, and 14 found no association. Tobacco use was associated with increased risk of hospitalization in 7 of 10 studies, ICU admission in 6 of 9 studies, mechanical ventilation in 2 of 6 studies, and illness severity in 3 of 9 studies. One study found that tobacco use history increased risk of pulmonary embolism in COVID-19 patients. Tobacco use was found to compound risks associated with diabetes (n = 1), cancer (n = 2), and chronic liver disease (n = 1). Conclusion. There is strong evidence that tobacco use increases risks of mortality and disease severity/progression among COVID-19 patients. Public health efforts during the pandemic should encourage tobacco users to quit use and seek care early and promote vaccination and other preventive behaviors among those with a history of tobacco use.

Type
Review Article
Information
Journal of Smoking Cessation , Volume 2022 , 2022 , e15
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © 2022 Jessica Baker et al.

1. Introduction

The emergence of COVID-19 in the last two years represents a grave threat to global health. Researchers have worked rapidly to better understand the risk factors associated with COVID-19, in order to prevent infections and reduce the severity of illness in those infected. Initially considered a respiratory infection, COVID-19 is now understood to be a systemic infection, which can cause a wide variety of complications throughout the body. SARS-CoV-2 commonly targets Angiotensin-Converting Enzyme 2 (ACE2) receptors in a host’s lungs and downregulates ACE2 expression [Reference Zamorano Cuervo and Grandvaux1]. ACE2 receptors are part of the Renin-Angiotensin System (RAS), which plays a complex role in regulating cardiovascular, renal, and metabolic functions. Thus, individuals living with comorbidities associated with RAS dysregulation (e.g., kidney disease, diabetes mellitus, and cardiovascular and pulmonary diseases) are at increased risk of severe COVID-19 [Reference Oakes, Fuchs, Gardner, Lazartigues and Yue2, Reference Triposkiadis, Starling, Xanthopoulos, Buter and Boudoulas3].

Tobacco use is a well-documented risk factor for hypertension, lung disease, cardiovascular disease, cancer, and diabetes and is a leading cause of chronic disease and death worldwide [Reference Husten, Remington, Brownson and Wegner4]. Additionally, cigarette smoking is a known risk factor for contracting infectious respiratory diseases such as influenza, tuberculosis, and MERS, as well as exacerbating the outcomes of those infections [Reference Arcavi and Benowitz5, Reference Park, Jung and Kim6]. Research has found that smoking increases ACE2 receptors in the lungs, indicating that smokers may be more vulnerable to infection [Reference Brake, Barnsley, Lu, McAlinden, Eapen and Sohal7, Reference Smith, Sausville and Girish8]. While the exact mechanisms of the interaction between tobacco and the RAS are complex, evidence shows that nicotine itself dysregulates the RAS [Reference Oakes, Fuchs, Gardner, Lazartigues and Yue2]. Since preexisting dysregulation of the RAS and its associated comorbidities worsen the severity and outcomes of COVID-19, understanding the impact of tobacco use on COVID-19 outcomes could significantly impact both prevention and treatment of COVID-19.

Given the explosion of research on SARS-CoV-2, systematic reviews of the literature are needed to inform evidence-based policies and practices to reduce the population impact of COVID-19. Since tobacco is a known risk factor for other infectious diseases, several reviews have focused on its impact on COVID-19 (see Table 1). The earliest review of COVID-19 and smoking that the authors are aware of was completed in March 2020 and provided initial findings from January to February 2020 [Reference Vardavas and Nikitara9]. Reviewing five relatively small studies, all from China, the study concluded that tobacco smoking likely had a negative impact on COVID-19 disease progression and outcomes. Several reviews followed in early 2020, all of which relied heavily on relatively small studies from China [Reference Berlin, Thomas, Le Faou and Cornuz10–Reference Farsalinos, Barbouni and Niaura12]. In June 2020, Gulsen et al. conducted a systematic review and meta-analysis which included 16 studies, 14 of which were from China and 2 of which were from the United States. This study more firmly concluded that a history of smoking is associated with severe COVID-19 [Reference Gülsen, Yigitbas, Uslu, Drömann and Kilinc13].

Table 1: Early and later reviews on tobacco use and COVID-19.

As more research was published in the summer and fall of 2020, reviews were able to include studies from a wider range of countries. One meta-analysis of 10 studies published in October 2020 included studies from Italy, Thailand, and the United Kingdom and specifically analyzed the association between smoking and mortality in COVID-19 patients [Reference Salah, Sharma and Mehta14]. However, this study drew only from one database (PubMed) and did not examine outcomes beyond mortality. Another review and meta-analysis included 47 peer-reviewed articles published between January and late May 2020 and analyzed the impact of smoking behavior on COVID-19 progression and mortality [Reference Patanavanich and Glantz15]. This may be the largest review to date specifically focused on tobacco use and COVID-19 outcomes, and it concluded that smoking is an independent risk factor for COVID-19 severity and death. However, some of the included studies had very small numbers of smokers (studies were excluded when the number of smokers was “zero or omitted”) and the study did not have a requirement regarding how COVID-19 was diagnosed. A literature review exploring the relationship between tobacco-related comorbidities and COVID-19 outcomes was published in November 2020 [Reference Gupta, Nethan and Mehrotra16]. This review included 23 studies published between January and September 2020. Although this was not a systematic review, it did find an association between tobacco use, cardiopulmonary diseases, and negative COVID-19 outcomes.

Finally, the most recent review at the time of this writing included 40 studies published up to December 12, 2020 [Reference Umnuaypornlert, Kanchanasurakit, Lucero-Prisno and Saokaew17]. This systematic review and meta-analysis found that current and former smoking increased the risk of COVID-19 severity and death. Of the studies included, 19 were from in China, 12 were from the US, and the rest were from other countries. Although this review assessed the quality of included studies, it did not have requirements regarding how COVID-19 was diagnosed or the number of smokers a study had to include in its sample.

The current study was aimed at identifying the impact of tobacco use on COVID-19 outcomes. Specifically, this review was aimed at adding to the existing literature in three main ways: (1) studies included had a sample of 30 or more current and former smokers, (2) only laboratory-confirmed cases of COVID-19 were included, and (3) to the extent possible, this review explored specific outcomes beyond general disease severity and mortality. Additionally, since early studies have already been heavily reviewed, we only included studies that completed data collection after March 31, 2020. Findings from this study can improve our understanding of the role of tobacco use as a risk factor for SARS-CoV-2 and facilitate our ability to draw actionable conclusions based on the available data.

2. Methods and Materials

This systematic literature review identified articles through keyword searches using the following databases: PubMed, Scopus, LitCovid, and Europe PMC (for preprints). The full list of search terms can be found in the Appendix and includes three themes: (i) terms related to tobacco such as “tobacco,” “smoking,” and “vaping”; (ii) terms related to COVID-19, including “SARS-CoV-2” and “novel coronavirus”; and (iii) terms related to outcomes, such as “mortality” and “hospitalization.”

Inclusion criteria for studies were as follows: (i) written in English; (ii) collected data between March 31, 2020, and February 20, 2021; (iii) sample size of 30 or more current or former tobacco users; (iv) lab-confirmed COVID-19 diagnosis; (v) assessed history of tobacco use as an exposure; and (vi) used multivariable analysis. Studies that were published in other languages; completed data collection before March 31, 2020; focused on animal subjects; relied on self-reported or symptom-diagnosed COVID-19; had fewer than 30 current or former tobacco users; conducted only univariate or descriptive analyses; or were unrelated to tobacco use were excluded. Case studies, ecological studies, in vitro and in silico studies, and Mendelian randomization studies were also excluded. Other reviews were included in the first stage of the search to screen for references and were then excluded.

One researcher (JB) conducted an initial screening of titles and abstracts to eliminate articles that did not meet the inclusion criteria. Two researchers (JB and NK) reviewed the remaining titles and abstracts more closely to further eliminate articles that did not meet inclusion criteria. JB and NK then conducted a full-text review of included articles. One researcher (JB) conducted the data extraction for final analysis.

Researchers used a wide variety of metrics. Lab-confirmed COVID-19 was primarily based on a positive result on an RT-PCR test. However, a few studies confirmed COVID-19 using other lab tests such as antibody or serum tests or CT radiology scans. Diagnoses based on symptoms were excluded. The type of tobacco use discussed in almost all the studies (n = 38) was combustible smoking. One study focused on smokeless tobacco. Tobacco use was most commonly reported as ever vs. never use (n = 15) or never/former/current use (n = 13). Two studies analyzed differences in pack-years smoked, where pack-years referred to the number of packs smoked per day times the number of years smoked.

Finally, “outcome” was defined as what happened after a person was infected with COVID-19. Outcomes for this analysis included the following: mortality (n = 32), hospitalization (n = 10), ICU admission (n = 9), mechanical ventilation (n = 6), and severity of illness (n = 9). Studies defined “severity” in different ways. For example, Adrish et al. [Reference Adrish, Chilimuri and Mantri18] defined severity on the basis of pneumonia and hypoxia status, while Mendy et al. [Reference Mendy, Apewokin, Wells and Morrow19] defined severity as admission to ICU or death during hospitalization. Studies focused on the incidence or transmission of COVID-19 were excluded.

3. Results

The initial search, done on February 20, 2021, identified 5,980 articles. Of these articles, 472 were published before December 2019 and removed from the Scopus search, leaving 5,508 citations. The searches were uploaded to Covidence for screening. Covidence identified 838 duplicates, which were reviewed for confirmation and then removed, leaving 4,670 articles to screen. The breakdown of the results can be seen in the PRISMA chart in Figure 1.

Figure 1: PRISMA chart.

In the first round of title and abstract screening, 4,223 articles were excluded. Many of these (n = 1,743) were thematically irrelevant. For example, they discussed adapting medical procedures in the context of COVID-19 or were otherwise unrelated to tobacco use (n = 1,056), focused on behavior or socioeconomic impacts (n = 694), focused on diseases other than COVID-19 (n = 420), or focused on incidence risk (n = 219) or were in silico, in vitro, or animal studies (n = 148). Two of the authors (JB and NK) reviewed the titles and abstracts of the remaining 447 articles. The second round of review eliminated another 309 articles, including ecological studies, case studies, reviews, and commentaries. The remaining 138 articles were included in the full-text review. Of these, a further 99 were excluded for the following reasons: only included data collected before March 31, 2020 (n = 20), sample sizes included fewer than 30 current or former tobacco users (n = 18), did not include smoking in a multivariable analysis (n = 17), included cases of COVID-19 not confirmed by lab results (n = 11), did not analyze the relationship between tobacco use and COVID-19 outcomes (n = 6), and did not include smoking as an independent variable in the analysis (n = 4). Additionally, 21 studies were excluded as they were duplicates, used the wrong study designs, or contained the wrong outcomes (e.g., incidence of COVID-19 rather than severity), and a further 2 studies were excluded because the articles were retracted.

In total, 39 studies were included in this review. At the time of the initial review, 29 of these studies were peer-reviewed manuscripts and 10 were preprints. Four preprints were subsequently published and are included in the peer-reviewed count. The characteristics of the studies can be seen in Table 2, with peer-reviewed and preprint studies listed separately. Studies had sample sizes that ranged from 101 to 406,793, with history of tobacco use sample sizes ranging from 35 to 24,484. Fourteen countries were represented by the studies, with 45% of studies done in the United States. Twenty-six studies used retrospective observational cohort designs, 8 used prospective/longitudinal study designs, 3 used case-control designs, and 2 used cross-sectional designs.

Table 2: Study characteristics and results.

OR: odds ratio; aOR: adjusted odds ratio; HR: hazard ratio; RR: relative risk; NS: not significant; pkyr: pack years. ∗Not assessed.

3.1. Mortality

Mortality was the most common outcome used across studies to assess the impact of tobacco use on COVID-19. Out of the 39 studies, 32 assessed the association between tobacco use and mortality. Of the 28 peer-reviewed articles that assessed mortality, 12 found no significant association, 15 found an increased risk of death, and one found a decreased risk of death. Of the 4 preprints that assessed mortality, 2 did not find a significant association and 2 found that tobacco use increased the risk of death. Seven articles did not report on mortality. The one article that found a significantly decreased risk of death came from Mexico, using Ministry of Health data [Reference Parra-Bracamonte, Lopez-Villalobos and Parra-Bracamonte20]. However, in a univariate analysis, the authors found a significant risk in men but not in women, which they suggested could be due to a dose-response relationship, as men are much heavier smokers than women.

A few studies focused on specific populations. Two studies among cancer patients with COVID-19 both found that tobacco use significantly increased the risk of mortality, and this was most common for patients with respiratory tract cancers [Reference Ferrari, Ferreira and Menezes21, Reference Garassino, Whisenant and Huang22]. A study on chronic liver disease patients with COVID-19 also found a significantly increased risk in this population [Reference Kim, Adeniji and Latt23].

Regarding mortality data, not all studies divided their data in the same way. Some studies analyzed former and current tobacco users separately. There was a trend in studies finding more significant risk in former smokers compared to current smokers. One factor that could explain this trend is that the pool of former smokers tended to be much larger than current smokers—often 3-5 times larger. Likewise, in some studies, the number of patients who died was very small. Even with an initial pool of 100 smokers, some studies only observed 2 or 3 deaths within that group, making statistical analysis difficult. Some of the studies that did not find a significant association in multivariable analysis found increased mortality risk in univariate analysis [Reference Adrish, Chilimuri and Mantri18, Reference Ho, Narasimhan, Sheehan, Wu and Fung24].

One study identified a dose-response effect based on pack-years, with those with a history of 30 pack-years or more having a significantly higher risk of death than those with a lower pack-year history [Reference Lowe, Zein, Hatipoglu and Attaway25]). As suggested by the Parra-Bracamonte et al. study, there might be a dose-response relationship between tobacco use history and COVID-19 mortality risk.

3.2. Disease Severity and Progression

In addition to mortality, 23 studies (19 peer-reviewed and 4 preprints) assessed a variety of other indicators for disease severity and progression (see Table 2). Eight (7 peer-reviewed and 1 preprint) studies found no significant association between tobacco use and the COVID-19 outcomes they measured. However, 15 (12 peer-reviewed and 3 preprints) studies found a significantly higher risk of disease severity or progression for people with a history of tobacco use. None of these 23 studies reported a significantly decreased risk.

Studies defined severity and progression in a wide variety of ways. The most common measures were hospitalization (n = 10), ICU admission (n = 9), the need for mechanical ventilation (n = 6), and severity (n = 9). Across the studies, tobacco smokers were found to be at significantly higher risk of hospitalization (n = 7) and ICU admission (n = 6) than nonsmokers. Two studies found smokers at increased risk of mechanical ventilation, and three found smokers to be at increased risk of severe or critical illness.

A few other outcomes were also assessed. One study found that smokers were more likely to have chest X-ray abnormalities 12 weeks after hospitalization, which correlated with longer hospital stays and longer recovery times [Reference Wallis, Heiden and Horno26]. Another study also indicated that smokers may be at risk of longer hospital stays or longer disease duration, but results were not conclusive [Reference Abbas, Nassir and Al Khames Aga27]. One study found that smokers were at higher risk of pulmonary embolism, an outcome that is associated with higher mortality [Reference Badr, Alwafi and Elrefaey28]. And finally, one study found that smokers were at increased risk of losing their sense of smell [Reference Hasan, Tamanna, Jamal and Uddin29].

Multiple studies noted the high correlation between a history of smoking and increased comorbidities, as well as the association between multiple comorbidities and increased risk of negative COVID-19 outcomes [Reference Lowe, Zein, Hatipoglu and Attaway25, Reference Bello-Chavolla, González-Díaz and Antonio-Villa30–Reference Wang, Zhong and Hurd34]. One study that compared smokers, diabetics, and diabetics who smoke found significantly worse outcomes, including increased risk of death, for the diabetics who smoke compared to the other groups [Reference Abbas, Nassir and Al Khames Aga27]. This finding highlights the crucial interaction between noncommunicable and infectious diseases.

4. Discussion

The explosion of research on COVID-19 may best be seen in NIH’s LitCovid database, which now has over 124,000 articles on the subject and sees over 2,000 new articles each week. This unparalleled rate of research offers a wealth of information, but much of the information is incomplete as we continue to learn about COVID-19 and its impacts. This review sought to organize and update existing knowledge and add to what has been done using more rigorous inclusion criteria.

The findings of this review indicate that smokers, including those who have quit, are at greater risk of developing severe COVID-19 illness compared with never smokers. As tobacco use and COVID-19 both dysregulate the RAS, ever-smokers who contracted COVID-19 were more likely to experience hospitalization, ICU admission, and death. Furthermore, the interaction of COVID-19 and smoking history was found to significantly increase the risk posed to individuals living with chronic diseases such as chronic liver disease, diabetes, and cancer [Reference Ferrari, Ferreira and Menezes21, Reference Kim, Adeniji and Latt23, Reference Abbas, Nassir and Al Khames Aga27], a finding that has not been documented in prior reviews.

In conducting this review, a number of future research directions were identified. First, several other outcomes were seen in studies that did not meet our inclusion criteria and thus were not included in this review. However, these outcomes, including stroke, blood clots, heart attacks, sepsis, mental illness, and neurological outcomes, deserve further study. Second, evidence suggests other specific patient populations with a history of smoking, such as people living with asthma and COPD, may also be at increased risk. Third, research on COVID-19 among younger populations and the impact of vaping on COVID-19 is still very limited. No studies on vaping met our inclusion criteria. Considering the growing evidence of long-lasting symptoms, neurological side effects, and other disabilities related to COVID-19, more information on how COVID-19 impacts young adults is urgently needed. Additionally, while a few articles found that noncombustible nicotine use such as hookah and vaping was correlated with increased incidence of COVID-19 [Reference Gaiha, Cheng and Halpern-Felsher35, Reference Li, Croft, Ossip and Xie36], little research has examined the association between these forms of tobacco use and COVID-19 outcomes. Finally, evidence suggests a dose-response relationship between tobacco use and health outcomes. Therefore, dosage should be considered more widely in analyses of the impact of tobacco use on COVID-19 outcomes.

4.1. Strengths and Limitations

This systematic review focused on the impact of tobacco use on COVID-19 outcomes, including hospitalization, ICU admission, mechanical ventilation, and mortality. It achieved this goal by using appropriate search terms to gather available research, applying a rigorous methodical approach, and consolidating the findings into useful results to inform public health policy. However, there are limitations. With over 2,000 articles on COVID-19 published each week, any review, including this one, is inherently behind the latest research. In an effort to mitigate this limitation, preprints were included in the analysis. However, preprints have their own limitations, as they are not yet peer-reviewed. Recognizing this limitation, we presented results of preprints separately in Table 2. While this review was able to include studies from a variety of countries, it was still limited to English-language articles, excluding work done in Chinese, Italian, Spanish, and other languages. Additionally, the wide range of measurements used across studies made comparison difficult. For example, while some studies separated current vs. former smokers, others combined all participants with a history of tobacco use into one pool. While this may solve the problem of small samples, it may also dilute the results. Perhaps most importantly, the majority of studies relied on medical records, which may be missing data or contain incomplete histories. Lowe et al. [Reference Lowe, Zein, Hatipoglu and Attaway25] point out that patients with complete records are more likely to be wealthy and regularly access healthcare, potentially leading to an underestimate of the impact of tobacco use on COVID-19 outcomes.

5. Conclusions

Tobacco use increases the risk of severe illness, hospitalization, and mortality due to COVID-19. Public health efforts to minimize these outcomes should include raising awareness of these risks, promoting the uptake of and increasing access to tobacco cessation, encouraging tobacco users to seek care early in their illness, and prioritizing vaccination for those with a history of tobacco use. Some states within the United States have prioritized tobacco users in vaccination efforts. Given the findings of this review, we recommend expanding this policy.

Appendix

A. Search Terms

A.1. PubMed and LitCovid which Recognize Mesh Terms

(“COVID-19”[Mesh] OR “Coronavirus Infections”[Mesh] OR “SARS-CoV-2”[Mesh] OR “SARS-CoV-2” OR “SARS COV 2” OR “COVID-19” OR “COVID” OR “novel coronavirus”) AND (“Smoking Devices”[Mesh] OR “Smokers”[Mesh] OR “Tobacco Use”[Mesh] OR “Tobacco Products”[Mesh] OR “Tobacco Smoke Pollution”[Mesh] OR “Vaping”[Mesh] OR “Smoking” OR “tobacco” OR “vaping” OR “cigarette” OR “Juul” OR “smoke” OR “smoked” OR “vape” OR “tobacco use”) AND (“Mortality”[Mesh] OR “Hospitalization”[Mesh] OR “Outcomes” OR “Outcome” OR “mortality” OR “death” OR “hospitalization” OR “hospitalized” OR “morbidity” OR “complication” OR “complications”)

A.2. Scopus and Europe PMC (Limited to Preprints), which Do Not Recognize Mesh Terms

(“coronavirus infections” OR sars-cov-2 OR covid-19 OR covid OR “novel coronavirus”) AND (smoking OR tobacco OR vaping OR cigarette OR juul OR smoke OR smoked OR vape OR “tobacco use”) AND (mortality OR hospitalization OR outcomes OR outcome OR death OR hospitalized OR morbidity OR complication OR complications)

Conflicts of Interest

Lorien C. Abroms receives royalties from the sale of Text2Quit and is a shareholder in Welltock, Inc. All other authors declare no conflicts of interests.

Acknowledgments

Dr. Berg is supported by the US National Institutes of Health (NIH) funding, specifically the National Cancer Institute (R01CA179422-01; PI: Berg; R01CA215155-01A1; PI: Berg; R01CA239178-01A1; MPIs: Berg, Levine), the Fogarty International Center/NIH (1R01TW010664-01; MPIs: Berg, Kegler), the National Institute of Environmental Health Sciences/Fogarty (D43ES030927-01; MPIs: Berg, Caudle, Sturua), and the National Institute on Drug Abuse (R56DA051232-01A1; MPIs: Berg, Cavazos-Rehg).

References

Zamorano Cuervo, N. and Grandvaux, N., “ACE2: evidence of role as entry receptor for SARS-CoV-2 and implications in comorbidities,” eLife, vol. 9, 2020.10.7554/eLife.61390CrossRefGoogle ScholarPubMed
Oakes, J. M., Fuchs, R. M., Gardner, J. D., Lazartigues, E., and Yue, X., “Nicotine and the renin-angiotensin system,” American Journal of Physiology. Regulatory, Integrative and Comparative Physiology, vol. 315, no. 5, pp. R895–R906, 2018.10.1152/ajpregu.00099.2018CrossRefGoogle ScholarPubMed
Triposkiadis, F., Starling, R. C., Xanthopoulos, A., Buter, J., and Boudoulas, H., “The counter regulatory axis of the lung renin-angiotensin system in severe COVID-19: physiopathology and clinical implications,” Heart, Lung and Circulation, vol. 30, no. 6, pp. 786–794, 2020.10.1016/j.hlc.2020.11.008CrossRefGoogle ScholarPubMed
Husten, C. G., “Tobacco Use,” in Chronic Disease Epidemiology, Prevention, and Control, Remington, P. L., Brownson, R. C., Wegner, M. V., Eds., pp. 117–157, American Public Health Association, 2010.Google Scholar
Arcavi, L. and Benowitz, N. L., “Cigarette smoke and infection,” JAMA Internal Medicine, vol. 164, no. 20, pp. 2206–2216, 2004.Google ScholarPubMed
Park, J. E., Jung, S., and Kim, A., “MERS transmission and risk factors: a systematic review,” BMC Public Health, vol. 18, no. 1, p. 574, 2018.10.1186/s12889-018-5484-8CrossRefGoogle ScholarPubMed
Brake, S. J., Barnsley, K., Lu, W., McAlinden, K. D., Eapen, M. S., and Sohal, S. S., “Smoking upregulates angiotensin-converting enzyme-2 receptor: a potential adhesion site for novel coronavirus SARS-CoV-2 (Covid-19),” Journal of Clinical Medicine, vol. 9, no. 3, p. 841, 2020.10.3390/jcm9030841CrossRefGoogle ScholarPubMed
Smith, J. C., Sausville, E. L., Girish, V. et al., “Cigarette smoke exposure and inflammatory signaling increase the expression of the SARS-CoV-2 receptor ACE2 in the respiratory tract,” Developmental Cell, vol. 53, pp. 514–529, 2020.10.1016/j.devcel.2020.05.012CrossRefGoogle ScholarPubMed
Vardavas, C. I. and Nikitara, K., “COVID-19 and smoking: a systematic review of the evidence,” Tobacco Induced Diseases, vol. 18, 2020.10.18332/tid/119324CrossRefGoogle ScholarPubMed
Berlin, I., Thomas, D., Le Faou, A. L., and Cornuz, J., “COVID-19 and smoking,” Nicotine and Tobacco Research, vol. 22, no. 9, pp. 1650–1652, 2020.10.1093/ntr/ntaa059CrossRefGoogle ScholarPubMed
Cattaruzza, M. S., Zagà, V., Gallus, S., D'Argenio, P., and Gorini, G., “Tobacco smoking and COVID-19 pandemic: old and new issues. A summary of the evidence from the scientific literature,” Acta bio-medica: Atenei Parmensis, vol. 91, no. 2, pp. 106–112, 2020.Google ScholarPubMed
Farsalinos, K., Barbouni, A., and Niaura, R., “Systematic review of the prevalence of current smoking among hospitalized COVID-19 patients in China: could nicotine be a therapeutic option?,” Internal and Emergency Medicine, vol. 15, pp. 845–852, 2020.10.1007/s11739-020-02355-7CrossRefGoogle Scholar
Gülsen, A., Yigitbas, B. A., Uslu, B., Drömann, D., and Kilinc, O., “The effect of smoking on COVID-19 symptom severity: systematic review and meta-analysis,” Pulmonary Medicine, vol. 2020, Article ID 7590207, 11 pages, 2020.10.1155/2020/7590207CrossRefGoogle ScholarPubMed
Salah, H. M., Sharma, T., and Mehta, J., “Smoking doubles the mortality risk in COVID-19: a meta-analysis of recent reports and potential mechanisms,” Cureus, vol. 12, no. 10, article e10837, 2020.Google ScholarPubMed
Patanavanich, R. and Glantz, S. A., “Smoking is associated with worse outcomes of COVID-19 particularly among younger adults: a systematic review and meta-analysis,” medRxiv, 2020.10.1101/2020.09.22.20199802CrossRefGoogle Scholar
Gupta, A. K., Nethan, S. T., and Mehrotra, R., “Tobacco use as a well-recognized cause of severe COVID-19 manifestations,” Respiratory Medicine, vol. 176, article 106233, 2021.10.1016/j.rmed.2020.106233CrossRefGoogle ScholarPubMed
Umnuaypornlert, A., Kanchanasurakit, S., Lucero-Prisno, D. E. I., and Saokaew, S., “Smoking and risk of negative outcomes among COVID-19 patients: a systematic review and meta-analysis,” Tobacco Induced Diseases, vol. 9, 2021.Google Scholar
Adrish, M., Chilimuri, S., Mantri, N. et al., “Association of smoking status with outcomes in hospitalised patients with COVID-19,” BMJ Open Respiratory Research, vol. 7, no. 1, article e000716, 2020.10.1136/bmjresp-2020-000716CrossRefGoogle ScholarPubMed
Mendy, A., Apewokin, S., Wells, A. A., and Morrow, A. L., “Factors associated with hospitalization and disease severity in a racially and ethnically diverse population of COVID-19 patients,” MedRxiv, 2020.10.1101/2020.06.25.20137323CrossRefGoogle Scholar
Parra-Bracamonte, G. M., Lopez-Villalobos, N., and Parra-Bracamonte, F. E., “Clinical characteristics and risk factors for mortality of patients with COVID-19 in a large data set from Mexico,” Annals of Epidemiology, vol. 52, pp. 93–98.e2, 2020.10.1016/j.annepidem.2020.08.005CrossRefGoogle Scholar
Ferrari, B. L., Ferreira, C. G., Menezes, M. et al., “Determinants of COVID-19 mortality in patients with cancer from a community oncology practice in Brazil,” JCO Oncology, vol. 7, pp. 46–55, 2021.10.1200/GO.20.00444CrossRefGoogle ScholarPubMed
Garassino, M. C., Whisenant, J. G., Huang, L. C. et al., “COVID-19 in patients with thoracic malignancies (TERAVOLT): first results of an international, registry-based, cohort study,” The Lancet Oncology, vol. 21, no. 7, 2020.10.1016/S1470-2045(20)30314-4CrossRefGoogle ScholarPubMed
Kim, D., Adeniji, N., Latt, N. et al., “Predictors of outcomes of COVID-19 in patients with chronic liver disease: US multi-center study,” Clinical Gastroenterology and Hepatology, vol. 19, no. 7, pp. 1469–1479, 2020.10.1016/j.cgh.2020.09.027CrossRefGoogle ScholarPubMed
Ho, K. S., Narasimhan, B., Sheehan, J., Wu, L., and Fung, J. Y., “Controversy over smoking in COVID-19—a real world experience in New York City,” Journal of Medical Virology, vol. 93, no. 7, pp. 4537–4543, 2020.10.1002/jmv.26738CrossRefGoogle Scholar
Lowe, K. E., Zein, J., Hatipoglu, U., and Attaway, A., “Association of smoking and cumulative pack-year exposure with COVID-19 outcomes in the Cleveland Clinic COVID-19 registry,” JAMA Internal Medicine, vol. 181, no. 5, pp. 709–711, 2021.10.1001/jamainternmed.2020.8360CrossRefGoogle Scholar
Wallis, T. J. M., Heiden, E., Horno, J. et al., “Risk factors for persistent abnormality on chest radiographs at 12-weeks post hospitalisation with PCR confirmed COVID-19,” Respiratory Research, vol. 22, p. 157, 2021.10.1186/s12931-021-01750-8CrossRefGoogle ScholarPubMed
Abbas, H. M., Nassir, K. F., Al Khames Aga, Q. A. et al., “Presenting the characteristics, smoking versus diabetes, and outcome among patients hospitalized with COVID-19,” Journal of Medical Virology, vol. 93, no. 3, pp. 1556–1567, 2021.10.1002/jmv.26487CrossRefGoogle ScholarPubMed
Badr, O. I., Alwafi, H., Elrefaey, W. A. et al., “Incidence and outcomes of pulmonary embolism among hospitalized COVID-19 patients,” International Journal of Environmental Research and Public Health, vol. 18, no. 14, p. 7645, 2021.10.3390/ijerph18147645CrossRefGoogle ScholarPubMed
Hasan, M., Tamanna, N. A., Jamal, M. N., and Uddin, J., “The prevalence of olfactory dysfunction and its associated factors in patients with COVID-19 infection,” MedRxiv, 2021.10.1101/2021.01.27.21250153CrossRefGoogle Scholar
Bello-Chavolla, O. Y., González-Díaz, A., Antonio-Villa, N. E. et al., “Unequal impact of structural health determinants and comorbidity on COVID-19 severity and lethality in older Mexican adults: considerations beyond chronological aging,” The Journals of Gerontology: Series A, vol. 76, no. 3, pp. e52–e59, 2020.Google Scholar
Pérez-Sastré, M. A., Valdés, J., and Ortiz-Hernández, L., “Clinical characteristics and severity of COVID-19 among Mexican adults,” Gaceta medica de Mexico, vol. 156, no. 5, pp. 379–387, 2020.Google ScholarPubMed
Romero, G. F., Dominguez-Castillo, E., Zheng, M. et al., Impact of tobacco smoking status on morbidity and mortality in patients hospitalized with COVID-19 pneumonia: observational study, Research Square, 2020.10.21203/rs.3.rs-107391/v1CrossRefGoogle Scholar
Ullah, A. D., Sivapalan, L., Chelala, C., and Kocher, H., “COVID-19 in patients with hepatobiliary and pancreatic diseases in East London: a single-centre cross-sectional study in East London,” BMJ Open, vol. 11, article e045077, 2021.Google Scholar
Wang, A., Zhong, X., and Hurd, Y., “Comorbidity and sociodemographic determinants in COVID-19 mortality in a US urban healthcare system,” MedRxiv, 2020.10.1101/2020.06.11.20128926CrossRefGoogle Scholar
Gaiha, S. M., Cheng, J., and Halpern-Felsher, B., “Association between youth smoking, electronic cigarette use, and COVID-19,” Journal of Adolescent Health, vol. 67, no. 4, pp. 519–523, 2020.10.1016/j.jadohealth.2020.07.002CrossRefGoogle ScholarPubMed
Li, D., Croft, D. P., Ossip, D. J., and Xie, Z., Are vabpers more susceptible to COVID-19 infection?, Pre-Print, 2020.Google ScholarPubMed
Abohamr, S. I., Abazid, R. M., Aldossari, M. A. et al., “Clinical characteristics and in-hospital mortality of COVID-19 adult patients in Saudi Arabia,” Saudi Medical Journal, vol. 41, no. 11, 2020.10.15537/smj.2020.11.25495CrossRefGoogle ScholarPubMed
Alharthy, A., Aletreby, W., Faqihi, F. et al., “Clinical characteristics and predictors of 28-day mortality in 352 critically ill patients with COVID-19: a retrospective study,” Journal of Epidemiology and Global Health, vol. 11, no. 1, p. 98, 2020.10.2991/jegh.k.200928.001CrossRefGoogle ScholarPubMed
Almazeedi, S., Al-Youha, S., Jamal, M. H. et al., “Characteristics, risk factors and outcomes among the first consecutive 1096 patients diagnosed with COVID-19 in Kuwait,” EClinical Medicine, vol. 24, article 100448, 2020.Google ScholarPubMed
Bellan, M., Patti, G., Hayden, E. et al., “Fatality rate and predictors of mortality in an Italian cohort of hospitalized COVID-19 patients,” Science Report, vol. 10, no. 1, 2020.10.1038/s41598-020-77698-4CrossRefGoogle Scholar
Chand, S., Kapoor, S., Orsi, D. et al., “COVID-19-associated critical illness-report of the first 300 patients admitted to intensive care units at a New York City medical center,” Journal of Intensive Care Medicine, vol. 35, no. 10, 2020.10.1177/0885066620946692CrossRefGoogle Scholar
Chen, L., Yu, J., He, W. et al., “Risk factors for death in 1859 subjects with COVID-19,” Leukemia (Nature), vol. 34, no. 8, pp. 2173–2183, 2020.10.1038/s41375-020-0911-0CrossRefGoogle ScholarPubMed
Chetboun, M., Raverdy, V., Labreuche, J. et al., “BMI and pneumonia outcomes in critically ill covid-19 patients: an international multicenter study,” Obesity (Silver Spring, Md.), vol. 29, no. 9, pp. 1477–1486, 2021.10.1002/oby.23223CrossRefGoogle ScholarPubMed
Di Castelnuovo, A., Bonaccio, M., Costanzo, S. et al., “Common cardiovascular risk factors and in-hospital mortality in 3, 894 patients with COVID-19: survival analysis and machine learning-based findings from the multicentre Italian CORIST study,” Nutrition, Metabolism, and Cardiovascular Diseases, vol. 30, no. 11, pp. 1899–1913, 2020.10.1016/j.numecd.2020.07.031CrossRefGoogle ScholarPubMed
Engin, A. B., Engin, E. D., and Engin, A., “Two important controversial risk factors in SARS-CoV-2 infection: obesity and smoking,” Environmental Toxicology and Pharmacology, vol. 78, article 103411, 2020.10.1016/j.etap.2020.103411CrossRefGoogle ScholarPubMed
Hamer, M., Kivimaki, M., Gale, C. R., and Batty, G. D., “Lifestyle risk factors, inflammatory mechanisms, and COVID-19 hospitalization: a community-based cohort study of 387,109 adults in UK,” Brain, Behavior, and Immunity, vol. 87, pp. 184–187, 2020.10.1016/j.bbi.2020.05.059CrossRefGoogle ScholarPubMed
Ioannou, G. N., Locke, E., Green, P. et al., “Risk factors for hospitalization, mechanical ventilation, or death among 10 131 US veterans with SARS-CoV-2 infection,” JAMA Network Open, vol. 3, no. 9, article e2022310, 2020.10.1001/jamanetworkopen.2020.22310CrossRefGoogle ScholarPubMed
Islam, M. Z., Riaz, B. K., Islam, A. N. M. S. et al., “Risk factors associated with morbidity and mortality outcomes of COVID-19 patients on the 28th day of the disease course: a retrospective cohort study in Bangladesh,” Epidemiology and Infection, vol. 148, 2020.10.1017/S0950268820002630CrossRefGoogle ScholarPubMed
Israel, A., Feldhamer, E., Lahad, A., Levin-Zamir, D., and Lavie, G., “Smoking and the risk of COVID-19 in a large observational population study,” MedRxiv, 2020.10.1101/2020.06.01.20118877CrossRefGoogle Scholar
Khawaja, A., Warwick, A., Hysi, P. et al., “Associations with COVID-19 hospitalisation amongst 406, 793 adults: the UK Biobank prospective cohort study,” MedRxiv, 2020.10.1101/2020.05.06.20092957CrossRefGoogle Scholar
Killerby, M. E., Link-Gelles, R., Haight, S. C. et al., “Characteristics associated with hospitalization among patients with COVID-19-Metropolitan Atlanta, Georgia, March-April 2020,” Morbidity and Mortality Weekly Report, vol. 69, no. 25, p. 790, 2020.10.15585/mmwr.mm6925e1CrossRefGoogle Scholar
Lohia, P., Sreeram, K., Nguyen, P. et al., “Preexisting respiratory diseases and clinical outcomes in COVID-19: a multihospital cohort study on predominantly African American population,” Respiratory Research, vol. 22, no. 1, 2021.10.1186/s12931-021-01647-6CrossRefGoogle ScholarPubMed
Palaiodimos, L., Kokkinidis, D. G., Li, W. et al., “Severe obesity, increasing age and male sex are independently associated with worse in-hospital outcomes, and higher in-hospital mortality, in a cohort of patients with COVID-19 in the Bronx, New York,” Metabolism, vol. 108, article 154262, 2020.10.1016/j.metabol.2020.154262CrossRefGoogle Scholar
Ragab, E., Mahrous, A. H., and El Sheikh, G. M., “COVID-19 infection: epidemiological, clinical, and radiological expression among adult population,” Egyptian Journal of Radiology and Nuclear Medicine, vol. 51, no. 1, 2020.10.1186/s43055-020-00341-9CrossRefGoogle Scholar
Raines, A. M., Tock, J. L., McGrew, S. J. et al., “Correlates of death among SARS-CoV-2 positive veterans: the contribution of lifetime tobacco use,” Addictive Behaviors, vol. 113, article 106692, 2021.10.1016/j.addbeh.2020.106692CrossRefGoogle ScholarPubMed
Sapienza, L. G., Nasra, K., Calsavara, V. F., Little, T. B., Narayana, V., and Abu-Isa, E., “Risk of in-hospital death associated with Covid-19 lung consolidations on chest computed tomography - a novel translational approach using a radiation oncology contour software,” European Journal of Radiology Open, vol. 8, article 100322, 2021.10.1016/j.ejro.2021.100322CrossRefGoogle ScholarPubMed
Saurabh, S., Verma, M. K., Gautam, V. et al., “Tobacco, alcohol use and other risk factors for developing symptomatic COVID-19 vs asymptomatic SARS-CoV-2 infection: a case–control study from western Rajasthan, India,” Transactions of The Royal Society of Tropical Medicine and Hygiene, vol. 15, no. 7, pp. 820–831, 2021.10.1093/trstmh/traa172CrossRefGoogle Scholar
Soares, R. C. M., Mattos, L. R., and Raposo, L. M., “Risk factors for hospitalization and mortality due to COVID-19 in Espírito Santo state, Brazil,” Am J Trop Med Hyg, vol. 103, no. 3, p. 1184, 2020.10.4269/ajtmh.20-0483CrossRefGoogle Scholar
Vilches-Moraga, A., Price, A., Braude, P. et al., “Increased care at discharge from COVID-19: the association between pre-admission frailty and increased care needs after hospital discharge; a multicentre European observational cohort study,” BMC Medicine, vol. 18, no. 1, pp. 1–9, 2020.10.1186/s12916-020-01856-8CrossRefGoogle ScholarPubMed
Figure 0

Table 1: Early and later reviews on tobacco use and COVID-19.

Figure 1

Figure 1: PRISMA chart.

Figure 2

Table 2: Study characteristics and results.