The Effect of Smoking on COVID-19 Symptom Severity: Systematic Review and Meta-Analysis

Abstract

Background

Coronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SAR2-COV-2) and was first identified in Wuhan, China, in December of 2019, but quickly spread to the rest of the world, causing a pandemic. While some studies have found no link between smoking status and severe COVID-19, others demonstrated a significant one. The present study aimed to determine the relationship between smoking and clinical COVID-19 severity via a systematic meta-analysis approach.

Methods

We searched the Google Scholar, PubMed, Scopus, Web of Science, and Embase databases to identify clinical studies suitable for inclusion in this meta-analysis. Studies reporting smoking status and comparing nonsevere and severe patients were included. Nonsevere cases were described as mild, common type, nonintensive care unit (ICU) treatment, survivors, and severe cases as critical, need for ICU, refractory, and nonsurvivors.

Results

A total of 16 articles detailing 11322 COVID-19 patients were included. Our meta-analysis revealed a relationship between a history of smoking and severe COVID-19 cases (OR = 2.17; 95% CI: 1.37–3.46; P < .001). Additionally, we found an association between the current smoking status and severe COVID-19 (OR = 1.51; 95% CI: 1.12–2.05; P < .008). In 10.7% (978/9067) of nonsmokers, COVID-19 was severe, while in active smokers, severe COVID-19 occurred in 21.2% (65/305) of cases.

Conclusion

Active smoking and a history of smoking are clearly associated with severe COVID-19. The SARS-COV-2 epidemic should serve as an impetus for patients and those at risk to maintain good health practices and discontinue smoking. The trial is registered with the International Prospective Register of Systematic Reviews (PROSPERO) CRD42020180173.

1. Introduction

Coronavirus disease 2019 (COVID-19), which is caused by severe acute respiratory syndrome coronavirus 2 (SAR2-COV-2), was first identified in Wuhan, China, in December of 2019. It has subsequently spread across the world, causing a global pandemic. This highly contagious disease has thus far infected 23.4 million people worldwide and killed approximately 808000 patients, yielding a case fatality rate (CFR) that varies between 0.7 and 12.7% (average: 3.4%) [1, 2].

COVID-19 primarily targets lung epithelial cells, causing viral pneumonia and acute respiratory distress syndrome (ARDS), especially in elderly patients. Therefore, mortality is higher in the elderly and in patients with at least one accompanying comorbid disease [3]. In the last report issued by the Centers for Disease Control and Prevention Institute, the incidence of respiratory disease was 9.2% in patients diagnosed with a severe COVID-19 clinical course [4]. Chronic obstructive pulmonary disease (COPD) and asthma are also common comorbidities in severe cases and are reported in 10.8% and 17.0%, respectively, of hospitalized patients aged ≥18 years with COVİD-19 [5].

However, it has been reported that COVID-19 progresses more severely in COPD patients [6]. Given that smoking plays an important role in the etiopathogenesis of COPD, it may have a similar effect on symptoms. In a recent meta-analysis of smoking and COVID-19 severity, smoking was found to not increase the severity of COVID-19 (odds ratio [OR], 1.69; 95% Cl: 0.41-6.92). However, only five studies were included in this meta-analysis, and heterogeneity among the studies was low (I² = 38%) [7].

In another meta-analysis involving more studies, COVID-19 severity was found to increase with smoking (OR, 1.97; 95% Cl: 0.95-4.10) [6]. To increase the statistical power of this analysis, case reports and series were also included, not just case-control studies. As previously, the heterogeneity of the studies included here was also low (I² = 44%) [6]. The different results of both meta-analyses create confusion about the issue of smoking status.

Given diverging findings in the existing literature, we systematically reviewed English-language studies to investigate whether smoking was associated with a more severe clinical course of COVID-19.

2. Material and Methods

All guidelines listed in the Preferred Reporting Items for Systematic Reviews and Meta Analyses (PRISMA) statement were followed in conducting this meta-analysis [8]. Our methodological systematic review and meta-analysis of pooled case-control studies were recorded in the International Prospective Register of Systematic Reviews (https://www.crd.york.ac.uk/prospero; registration number: CRD42020180173).

2.1. Study Search Strategy

We searched the Google Scholar, PubMed, Scopus, Web of Science, and Embase databases to identify clinical studies suitable for inclusion here. Only English-language articles published between December 2019 and April 15, 2020, were included. Case series/reports, commentaries, reviews, and editorial letters were excluded. Unpublished articles were not searched, but “ahead of print” and “first only” articles with a DOI link in the given database were included. The following search terms were used: “COVID-19,” OR “SARS-COV-2,” OR “novel coronavirus (nCOV),” AND “smoking,” OR “tobacco,” AND “clinical features,” OR “characteristic,” AND “severity,” OR “severe”.

2.2. Inclusion and Exclusion Criteria

Inclusion criteria were as follows: (i) studies that examined COVID-19 patients older than 18 years and diagnosed COVID-19 according to WHO criteria; (ii) observational, cross-sectional, prospective, or retrospective studies; (iii) studies which compared smokers with mild and severe COVID-19; (iv) studies comparing smokers with survivors and nonsurvivors of COVID-19; and (v) studies comparing smokers who developed COVID-19 that required intensive-care unit (ICU) and non-ICU treatment.

Exclusion criteria were as follows: (i) studies from the same medical center that did not contribute to meta-analysis, (ii) non-English-language studies, (iii) case reports/series, (iv) reviews, (v) editorial letters, (vi) studies lacking a full-text (unavailable or not yet published), (vii) studies without a DOI, and (viii) studies with small sample sizes (<50 patients) because of low statistical power.

2.3. Data Extraction

A researcher (AG) scanned study titles and abstracts obtained via an initial database search and included relevant ones in a secondary pool. Next, two independent researchers (AG and BU) evaluated the full text of these articles to determine whether they met study inclusion criteria. Any disputes were resolved by discussion and negotiation with a third investigator (BAY). Agreed-upon studies were included in the final meta-analysis.

The following data were obtained from all studies: title, first author, publication year, location, sample size, age (median), history of smoking (former or current), and distribution of nonsevere or severe COVID-19 status. Given these groups, we were able to compare nonsevere (mild, common type, non-ICU, survivors) and severe (critical, severe, ICU, nonsurvivors) COVID-19 cases.

2.4. Risk of Bias (Quality) Assessment

Two researchers (BAY and BU) evaluated the collected articles using the Newcastle-Ottawa scale (NOS) for study quality and risk of bias [9]. This scale evaluates three aspects of each study: (i) selection (0 to 4 points), (ii) comparability (0 to 2 points), and (iii) detection of the outcome of interest (0 to 3 points). According to the obtained total score, study quality was rated as follows: 0-3 points (poor), 4-6 points (intermediate), and 7-9 points (high). Studies with a high risk of bias were excluded during the meta-analysis phase.

2.5. Statistical Analyses

OpenMeta Analyst version 10.10 (https://www.cebm.brown.edu/open_meta) was used to calculate odds ratios with 95% confidence intervals, which are depicted using forest plots. Quantitative numbers were measured in terms of total numbers and percentages (n, %). The odds ratio of smokers among nonsevere COVID-19 and severe COVID-19 cases, as well as survivors and nonsurvivors, was calculated. Heterogeneity was evaluated with Cochran's Q, χ², and the Higgins I² test. The Higgins I² test uses a fixed effect model when I² <50%, and a random effects model when I² >50%. When heterogeneity was detected, a sensitivity adjustment was made to determine its source. This procedure was performed by leaving one study out of the analysis at a time, with a fixed effect model used after excluding heterogeneity. Publication bias was evaluated with Statsdirect version 3.2.10 (StatsDirect Ltd, Cambridge, UK) and visualized using Begg's funnel plots and Egger's test. P values (two-sided) were considered statistically significant if P < .05.

3. Results

Our initial search of international databases using the keywords described above yielded 265 articles. After duplicate articles were excluded, 197 articles remained. After article titles and abstracts were evaluated for appropriateness, a final 34 articles were found to meet study inclusion criteria. In addition, 18 of the studies for which full texts were obtained were excluded because they met exclusion criteria. A total of 16 articles met all our criteria. The relevant PRISMA study flow chart is shown in Figure 1. A quality analysis of the pooled articles included in this meta-analysis was done by applying NOS. As a result, overall quality was found to be moderate (NOS score min: 5, max: 8). Results of a quality analysis of the pooled articles are available in Table 1.

Figure 1.

PRISMA flow diagram of study selection procedures.

Table 1.

Newcastle-Ottawa scale for quality assessment and risk of bias.

Study	Year	Case selection (max. 4)	Comparability (max. 2)	Exposure/outcome (max. 3)	Total score
CDC report [4]	2020	∗∗∗∗	∗	∗∗	7
Chen Q [10]	2020	∗∗∗	∗	∗∗	6
Feng Y [11]	2020	∗∗	∗	∗∗∗	6
Goyal P [12]	2020	∗∗	—	∗∗∗	5
Guan WJ [13]	2020	∗∗	∗∗	∗∗	6
Liu W [14]	2020	∗∗	∗	∗	7
Mo P [15]	2020	∗∗	∗	∗∗∗	6
Qi D [16]	2020	∗∗∗	∗	∗∗∗	7
Shi Y [17]	2020	∗∗	∗	∗∗	5
Wang R [18]	2020	∗∗∗	∗	∗∗	6
Wan S [19]	2020	∗∗∗	∗	∗∗∗	7
Yang X [20]	2020	∗∗∗	∗∗	∗∗∗	8
Yu X [21]	2020	∗∗∗	∗∗	∗∗	7
Zhang JJ [22]	2020	∗∗∗	∗∗	∗∗	7
Zhang R [23]	2020	∗∗∗	∗	∗∗	6
Zhou F [24]	2020	∗∗∗	∗	∗∗∗	7

3.1. Features of the Included Studies

In the initial meta-analysis pool, 11322 patients with COVID-19 from 16 studies [4, 10–24] were included. However, given CDC reporting guidelines [4], 525 patients whose hospitalization statuses were reported as “unknown” were excluded from the final analysis, yielding a final 10797 patients. Of these, 9414 (87.2%) were nonsevere COVID-19 patients, while 1383 (12.8%) were severe or critical COVID-19 patients who required intensive care. Among the severe or critical patients, smoking prevalence ranged from 3.6 to 19.9% (average: 8.4%). While nine studies provided current smoker information, three provided both current smoker and former smoker information, and seven provided only historical smoking information. All of the included studies were retrospective (six multicenter and 10 single-center). A summary of the studies included in this meta-analysis is available in Table 2.

Table 2.

Features of the studies included in the meta-analysis.

First author	Location of patients	Study design	Comparison	n	Age, year	Prevalence of smoking	Former smokers	Current smokers
CDC report [4]	—	R, MC	Non-ICU vs. ICU	7162	—	261 (3.6)	165 (2.3)	96 (1.3)
Chen Q [10]	Taizhou, China	R, O, SC	Nonsevere vs. severe	145	47.5	15 (10.3)	—	—
Feng Y [11]	Wuhan, Anhui, Shanghai	R, O, MC	Moderate vs. severe, critical	454	53.0	44 (9.7)	—	—
Goyal P [12]	Newyork, USA	R, MC	Non-IMV vs. IMV	393	62.2	20 (5.1)	—	20 (5.1)
Guan WJ [13]	552 hospitals in China	R, MC	Nonsevere vs. severe	1085	47.0	158 (12.6)	21 (1.9)	137 (12.6)
Liu W [14]	Wuhan, China	R, SC	Stabilization vs. progression	78	38.0	5 (6.4)	—	—
Mo P [15]	Wuhan, China	R, SC	General vs. refractory	155	54.0	6 (3.9)	—	6 (3.9)
Qi D [16]	Chongqing, China	R, MC	Nonsevere vs. severe	267	48.0	53 (19.9)	—	—
Shi Y [ 17]	Zhejiang, China	R	Mild vs. severe	487	46.0	40 (8.2)	—	—
Wang R [18]	Fuyang, China	R, SC	Noncritical vs. ritical	125	49.4	16 (12.8)	—	16 (12.8)
Wan S [19]	Chongqing, China	R, SC	Mild vs. severe	135	47.0	9 (6.7)	—	9 (6.7)
Yang X [20]	Wuhan, China	R, O, SC	Survivors vs. nonsurvivors	52	51.9	2 (10.0)	—	—
Yu X [21]	Shanghai, China	R, SC	Nonsevere vs. severe	333	50.0	26 (7.8)	—	—
Zhang JJ [22]	Wuhan, China	R, SC	Nonsevere vs. severe	140	57.0	9 (6.4)	7 (5.0)	2 (1.4)
Zhang R [23]	Wuhan, China	R, SC	Common type vs. severe	120	45.4	6 (5.0)	—	6 (5.0)
Zhou F [24]	Wuhan, China	R, O, MC	Nonsurvivor vs. survivor	191	56.0	11 (6.0)	—	11 (6.0)

Data are presented as “n” or “n (%).” Age-related data are given as “median year.” n: population; R: retrospective; CS: cross-sectional; O: observational; IMV: invasive mechanic ventilation; ICU: intensive care unit; SC: single-center; MC: multicenter.

3.2. History of Smoking and COVID-19 Severity

The prevalence of smoking among patients with mild to moderate COVID-19 was 493/9414 (5.2%), while among severe and critical cases, it was 173/1383 (12.5%). A meta-analysis revealed a significant relationship between smoking history and severe COVID-19 (random effect model, OR = 2.17; 95% CI:1.37–3.46; P < .001) (Table 3) (Figure 2(a)). A funnel plot was used to evaluate publication bias and revealed substantial heterogeneity between the pooled studies (I² = 71.4%; P < .001) (Figure 2(b)). A sensitivity analysis conducted after removing two studies (Qi et al. [16] and Zhang et al. [23]), which were primary causes of heterogeneity, revealed that smoking was significantly related to COVID-19 severity (fixed effect model, OR = 1.85; 95% CI:1.50–2.29; P < .001) (Figure 2(c)). Furthermore, this updated analysis had low heterogeneity (I² = 40.6%; P = .06), while a funnel plot and Egger's test revealed no publication bias (tau² = −0.87, P = .16) (Figure 2(d)).

Table 3.

The relationship between history of smoking and the severity of COVID-19.

Studies	Severe COVID-19 with history of smoking			Nonsevere COVID-19 with history of smoking
Authors	Event	Total	%	Event	Total	%
CDC report [4]	38	457	8.3	208	6180	3.3
Chen et al. [10]	3	43	7.0	12	102	11.0
Feng et al. [11]	17	121	14.0	27	333	8.1
Goyal et al. [12]	6	130	4.6	14	263	5.3
Guan et al. [13]	38	172	22.0	120	913	13.0
Liu et al. [14]	3	11	27.3	2	67	2.0
Mo et al. [15]	4	85	4.7	2	70	2.9
Qi et al. [16]	31	50	62.0	22	217	10.1
Shi et al. [17]	6	49	12.2	34	438	7.8
Wang et al. [18]	7	25	28.0	9	100	9.0
Wan et al. [19]	1	40	2.5	8	95	8.4
Yang et al. [20]	0	32	0	2	20	10.0
Yu et al. [21]	2	26	8.0	24	307	8.9
Zhang et al. [22]	6	58	10.3	3	82	3.6
Zhang et al. [23]	6	30	20.0	0	90	0
Zhou et al. [24]	5	54	9.0	6	137	4.0
Total	173	1383	12.5	493	9414	5.2

Figure 2.

(a) Prevalence of smoking in severe COVID-19 patients. (b) Funnel plot for meta-analysis of the prevalence of smoking in severe COVID-19 patients. (c) Prevalence of smoking among severe COVID-19 patients after the exclusion of studies by Qi et al. [16] and Zhang et al. [23]. (d) Funnel plot for the meta-analysis of smoking among severe COVID-19 patients after the exclusion of studies by Qi D et al. [16] and Zhang R et al. [23].

3.3. Smoking Status and COVID-19 Severity

Only 10 of the pooled studies provide information about current smoking, specifically (n = 305). Current smoking prevalence in patients with mild to moderate COVID-19 was 229/7850 (2.9%), while in severe or critical cases, it was 66/1134 (5.8%). However, in 10.7% (978/9067) of nonsmokers, COVID-19 disease was severe, while in active smokers, it was severe in 21.2% (65/305) of cases (Table 4). This clearly demonstrates a significant relationship between current smoking and severe COVID-19 patients (fixed effect model, OR = 1.51; 95% CI: 1.12–2.05; z = 2.65; P = .008), with an approximate 1.5-fold increased risk of ICU admission, symptom, severity, and mortality in smokers (Figure 3(a)). In this analysis, we used a fixed effect model due to the low level of heterogeneity (I² = 48.9%; P = .40). A funnel pilot and Egger's test revealed no publication bias (tau² = 0.22, P = .77) (Figure 3(b)).

Table 4.

The relationship between smoking status and the severe COVID-19.

Studies	Current smokers with severe COVID-19			Nonsmokers with severe COVID-19
Authors	Event	Total	%	Event	Total	%
CDC report [4]	5	96	8.3	419	6901	60.7
Goyal et al. [12]	6	20	30.0	124	373	33.2
Guan et al. [13]	29	137	21.1	134	927	14.4
Mo et al. [15]	4	6	66.6	81	149	54.3
Wang et al. [18]	7	16	43.7	18	109	16.5
Wan et al. [19]	1	9	11.1	39	126	30.9
Yang et al. [20]	0	2	0	32	50	64.0
Zhang et al. [22]	2	2	100	58	138	42.0
Zhang et al. [23]	6	6	100	24	114	21.0
Zhou et al. [24]	5	11	45.4	49	180	27.2
Total	65	305	21.3	978	9067	10.7

Figure 3.

(a) Comparison of smoking status in severe COVID-19 patients. (b) Funnel plot for the meta-analysis of smoking among severe COVID-19 patients. (c) Comparison of smoking status among severe COVID-19 patients after the exclusion of a study by Zhang et al. [23]. (d) Funnel plot for the meta-analysis of smoking among severe COVID-19 patients after the exclusion of a study by Zhang et al. [23].

A sensitivity analysis conducted after removing one study (Zhang et al. [23]) revealed a similar relationship with severe COVID-19 (fixed effect model; OR = 1.36; 95% CI: 1.00–1.87; P = 0.05) and low heterogeneity (I² = 34.0%; P = .14) (Figure 3(c)). A funnel plot and Egger's test further revealed no publication bias (tau² = −0.31, P = .67) (Figure 3(d)).

4. Discussion

The present meta-analysis contained 16 studies and revealed that those with a history of smoking and active smokers had significantly increased risk for severe COVID-19. Previous studies have reported a similar result [14, 18, 23]. In addition, one prior meta-analysis reported that disease severity increased given a history of smoking (OR: 1.98) [6]. Our analysis adds to this growing consensus in the literature, invoking more studies and examining both a history of smoking and current smoking status in risk for increased COVID-19 severity.

Five prior studies have reported results which disagree with those presented here—namely, no significant difference between patients with and without a smoking history in terms of COVID-19 severity [10, 15, 21, 22, 24]. In addition, a meta-analysis performed by Lippi et al. [7] failed to find a relationship between active smoking and severe COVID-19 on Chinese patients, and another meta-analysis indicates that active smoking is not a predisposing factor for hospitalization [25]. First of all, both meta-analysis [7, 25] was not systematic and included no assessment of publication bias or study quality. As such, it should be considered only preliminary. Hence, the present systematic meta-analysis offers a more detailed view as it covers 16 studies. The heterogeneity was low to moderate, and after sensitivity adjustments, the prevalence of a history of smoking was found to be 5.2% in nonsevere COVID-19 cases and 12.5% in severe cases. Furthermore, the prevalence of active smoking was 2.9% in nonsevere COVID-19 cases and 5.8% in severe cases. Therefore, severe COVID-19 was observed almost 1.5 to 2 times more frequently in history of smoking and current smoking groups. There are studies [4, 11, 14, 16, 18, 23] and meta-analysis [6, 26–34] results supporting this finding.

In addition, a recent meta-analysis revealed that active smokers are at higher risk of mortality and serious complications [27]. Interestingly, this meta-analysis indicated that serious complications were observed in 48% of former smokers and 24% of current smokers during COVID-19 course [27]. This appears to be because former smokers have longer exposure times or accompanying diseases such as COPD due to smoking. This issue was explained recently in a rapid nonsystematic meta-analysis conducted by Guo FR, which showed that COPD increased the development of severe COVID-19 by 4.38 times [28]. These findings are supported by another rapid nonsystematic meta-analysis, suggesting that smoking increases the severity and mortality of COVID-19 in hospitalized patients [29]. In addition, a history of smoking has been reported to increase the progression of COVID-19 disease [30]. There is growing evidence to support WHO's statements that smokers are at a higher risk of developing severe COVID-19 and consequent death [31]. It seems very clear that the pandemic period is an opportunity to quit smoking due to the possibility of encountering worse clinical outcomes and complications in patients with smoking history [32].

The relationship between smoking and illness severity due to other respiratory viruses has been investigated previously. In one recent study, COPD patients who smoked had decreased leukemia inhibitory factor levels during respiratory syncytial viral infection, particularly during exacerbations, which may have contributed to lung tissue injury [35]. In addition, smoking may reduce the protective effect of influenza vaccines in elderly patients and increase the risk of hospitalization [36]. As a result, adverse effects on the lungs in smokers may aggravate the symptom severity of viral infections.

Furthermore, novel SARS-CoV-2 uses an angiotensin-converting enzyme (ACE)-2 in the lungs to enter cells and cause infection. In patients using ACE inhibitors or angiotensin II receptor blockers (ARBs) for hypertension, upregulated ACE2 expression impacts on disease course remains unclear. However, the Council on Hypertension of the European Society of Cardiology does not recommend discontinuation of ACEI and ARB medications for all patients [37]. The ACE-2 upregulation may increase infectiousness and therefore infection risk, as the SARS-COV-2 virus uses this receptor for host entry. Paradoxically, it is stated that it may be useful in protecting people from acute lung injury [38].

In one recent study, ACE-2 gene expression was upregulated in the airway epithelium of COPD patients and active smokers, thereby suggesting a mechanism by which risk for severe COVID-19 increases in smokers [39]. This upregulation may occur through the α7 subtype of nicotine acetylcholine receptors (α7-nAChR) in people who smoke and consequently consume nicotine [40]. Therefore, α7-nAChR antagonists (e.g., α-conotoxin, methyllycaconitine), which may be used to assist with smoking cessation, should be investigated for their potential impact on ACE-2 expression and thus SARS-COV-2 entry into the host [41, 42]. Furthermore, α7-nAChR and ACE-2 may be potential therapeutic targets, a topic which requires further investigation.

Common comorbidities including cardiovascular disease, chronic kidney disease, diabetes, and hypertension are associated with increased risk for severe COVID-19 [43]. Similarly, COPD is also associated with a poor clinical progression and poor outcomes despite treatment, and it was reported that the risk of severe COVID-19 was observed 4 times higher in patients with preexisting COPD than in patients without COPD [6]. This may be explained by systemic and chronic inflammation, diminished respiratory function and capacity, and COPD-related respiratory failure in some patients. The prevalence of COPD was previously reported to be 2.8% in nonsmokers, 7.6% in former smokers, and 15.2% in active smokers [44]. Given this, smoking and COPD comorbidity should be considered together as a single risk factor for severe COVID-19.

Another important point for consideration is that acute respiratory distress syndrome and cytokine storms, which are seen in some severe COVID-19 patients, are key causes of mortality in COVID-19. In these patients, proinflammatory cytokines such as interleukin (IL)-1, IL-2, IL-6, IL-8, IL-17, interferon-γ, and TNF-α are elevated, which affect patients clinical symptoms and severity [45]. Nicotine is a cholinergic agonist that acts via the a7-nAChR pathway and also inhibits proinflammatory cytokines such as IL-1, IL-6, and TNF, but has no effect on IL-10, an anti-inflammatory cytokine [46]. Therefore, nicotine may be beneficial for the treatment of severe COVID-19 when delivered via chewing gum, inhaler/aerosol, or patch [47, 48]. This potential therapeutic application should be clarified with future clinical research, however.

Several factors limit the interpretation of the present study. First, the vast majority of studies included here were retrospective epidemiological studies conducted in China. Second, some included studies did not distinguish between former or current smoking status. Third, studies classified COVID-19 cases broadly as follows: (i) mild to moderate: mild, nonsevere, common type, did not require ICU care, and COVID-19 survivors and (ii) severe: severe, critical, required ICU care, and nonsurvivors. Given these limitations, caution should be exercised while interpreting our results. Future studies may respond to these issues by defining disease severity more clearly and by obtaining more detailed information about smoking habit.

In addition to classical tobacco smoking behavior, water pipe and electronic cigarette use should not be overlooked, as these modes of consumption may increase contamination risk due to repetitive hand interactions with the mouth, carrying cigarette packets in the pockets, and blowing of smoke. Similarly, exposure to passive smoke can alter ACE-2 gene expression and cause immune system changes. Naturally, these patients also have the potential to have severe COVID-19 symptoms, and smoke exposure is a potential risk factor for those around the patient, including their friends and family.

Future studies should continue to collect nicotine consumption information, including the number of cigarettes smoked per day, passive exposure, and degree of COPD, and should evaluate the dynamics of interactions between cigarette smoking and COVID-19. In addition, the effects of various smoking habits (e.g., mild versus heavy consumption, water pipe use, and electronic cigarettes use) on the transmission of SARS-COV-2, the clinical severity of COVID-19, and the clinical progression of COVID-19 should be investigated. Finally, the relationship between COPD severity and COVID-19, and the potential therapeutic effect of nicotine on severe COVID patients should also be examined and clarified. In addition, clinicians can pay more attention to the history of smoking of COVID-19 patients, and more further research may aim to determine mechanisms that drive or decrease this risk.

5. Conclusion

The present meta-analysis revealed that active smoking and a history of smoking are significantly associated with increased COVID-19 symptom severity. The SARS-COV-2 epidemic should serve as an impetus for patients and those at risk to maintain good health practices and discontinue smoking.

Data Availability

The data [data.oma and data.xls] used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors have stated explicitly that there are no conflicts of interest in connection with this article.

Authors' Contributions

AG performed the concept of the manuscript, data collection, design of tables and figures, analysis and interpretation of data, and writing and drafting of the manuscript; BU performed the data collection and quality analysis; BAY performed the acquisition of data, quality analysis, and writing and revising the manuscript; DD and OK performed the major role in reviewing and revising the manuscript.