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. 2022 Mar 6;9:316–322. doi: 10.1016/j.toxrep.2022.02.012

Influence of tobacco smoking on the development of halitosis

Alba Romero Kauss 1, Meagan Antunes 1, Filippo Zanetti 1, Matthew Hankins 1, Julia Hoeng 1, Annie Heremans 1, Angela van der Plas 1,⁎
PMCID: PMC8908054  PMID: 35284240

Abstract

Background

Halitosis is the general term used to describe any disagreeable odor in exhaled air, regardless of whether the odorous substances originate from oral or non-oral sources. Previous research has strongly associated tobacco smoking in the development of halitosis, as it increases the synthesis of toxic volatile sulfur compounds in diseased periodontal pockets. In this review, we summarize the etiopathology and epidemiology of halitosis as well as the current evidence on the impact of smoking by means of a meta-analysis.

Methods

PubMed and Embase were searched to identify publications that reported halitosis in smokers and nonsmokers. Meta-analyses were performed if a sufficient number (n ≥ 3) of articles were available that evaluated the same outcome.

Results

The meta-analyses showed that there was an increased risk of halitosis in current smokers versus nonsmokers (odds ratios). These results were consistent both in fixed and random effects models. Even though the interstudy heterogeneity was high (I2 = 91%), sensitivity analysis by limiting the number of studies yielded similar results, with no-to-moderate heterogeneity (I2 = 0–65%). The analysis comparing ever smokers with never smokers showed no significant difference in the risk of halitosis in ever smokers. The same effect was observed when upon stratifying the analyses on the basis of ascertainment of halitosis (self-reported or measured by a Halimeter).

Conclusions

Halitosis is a common condition which can affect the quality of life of those affected. The results from this literature review and meta-analysis show that current smokers are more likely to suffer from halitosis, even if they are less likely to report it.

Keywords: Halitosis, Tobacco, Smoking, Oral health

Highlights

  • •

    Halitosis is the term used to describe any disagreeable odor in exhaled air.

  • •

    Current smokers are more likely to suffer from halitosis than nonsmokers.

  • •

    Ever smokers had a non-significantly increased halitosis risk than never smokers.

  • •

    After a sensitivity analysis the results were confirmed.

1. Introduction

Halitosis is the general term used to describe any disagreeable odor in expired air, regardless of whether the odorous substances originate from oral or non-oral sources. People who have halitosis often feel embarrassed about it and are adversely affected in terms of the social aspects of their life [1]. These social effects of halitosis usually urge compel patients to seek professional care [2]. Halitosis is considered the third most common reason for dentist visits in the United States, after caries and periodontal disease [3]. However, there should be a differentiation between genuine halitosis and pseudo-halitosis or halitophobia. In genuine halitosis, local factors as well as general factors may play a role in the etiology of the problem.

The prevalence of halitosis varies according to the study population, because the perception of halitosis differs among culturally diverse populations [4]. In Japan, population-based studies have reported the prevalence of halitosis to be 6–23% [5], [6]. A recent study conducted in Saudi Arabia found that approximately 22% of adults have self-perceived halitosis and that it was significantly associated with waterpipe tobacco smoking [7].

Additionally, approximately 25% of individuals with halitosis experience such a severe problem that it affects their social functioning. For example, individuals may feel nervous and embarrassed in the presence of other people and may avoid social contact and intimate relationships [8].

Reviews in research reports now agree that, in the vast majority of cases (80–90%), halitosis originates within the oral cavity [9], where anaerobic bacteria degrade sulfur-containing amino acids into the foul-smelling volatile sulfur compounds (VSC) hydrogen sulfide and methylmercaptan. These sulfur-containing compounds are produced by microorganisms and are often associated with bad odors. Some investigators believe that, besides VSCs, other volatiles produced by oral putrefaction processes—such as organic acids, ammonia, and amines—may also cause oral malodor [10], [11]. The two major sources for VSCs are periodontal disease and tongue coating, which is a grayish-white deposit on the tongue [12]. On the other hand, an estimated 10–20% of halitosis cases have non-oral causes [13], [14].

Previous research has shown that tobacco smoking is the second greatest offender in the development of halitosis, behind periodontal disease and the associated food stagnation. Smoking causes a decrease in the commensal population of normal flora in the oral cavity, leading to an increase in pathogenic microbes [15] as well as enhancement of microbial colonization by biofilm formation on oral epithelial cells. More importantly, a number of studies have reported that smoking increases the probability of extensive disease development [16], [17] and causes significant disruption in the oral microbiota, creating an imbalance in the oral environment. Moreover, smoking contributes to halitosis by causing hyposalivation [18], [19].

The aim of this study is to summarize of evidence on the effects of smoking on the development of halitosis by means of a meta-analysis.

2. Methods

This was a meta-analysis of interventional and observational studies performed using literature identified through PubMed and Embase. The query used in both search engines was: (halitosis OR bad breath) AND (tobacco OR smoke OR smoking OR smoker OR nicotine OR e-cigarette OR e-cig OR ENDS OR e-vapor OR heated tobacco OR IQOS OR THS OR tobacco heating). The searches were performed in the week of March 1, 2021.

Retrieval of articles was limited to those written in English and considering human populations. To verify that all available relevant publications were retrieved, the reference lists of the publications obtained through the original search were checked for additional citations.

2.1. Study selection

The following criteria were used for including publications in our review: a) case control, cohort, or interventional studies such as randomized controlled trials; b) adult human populations; c) number of patients with halitosis (self-reported or diagnosed by a Halimeter), stratified by smoking status and including sample size; and d) published between 1970 and March 1, 2021.

The exclusion criteria were as follows: a) review articles, case reports, or editorials; b) reports with incomplete data; and c) data reused in a more recent study.

2.2. Data extraction

The following information was extracted from each study: first author’s name, year of publication, study design, population characteristics, and number of participants per group.

2.3. Statistical analysis

Meta-analyses were performed when a sufficient number of articles (n ≥ 3) that evaluating the same outcome were available. The risk comparison between two groups was measured using ORs with 95% confidence intervals (CIs) and visualized using the forest plot. The Mantel–Haenszel method with inverse variance weighting was used in both fixed and random effects models to pool results. The degree of heterogeneity between the study results was tested by the inconsistency statistic (I2). Funnel plots were used to evaluate publication bias [20]. Statistical significance was assessed at α = 0.05.

The analyses were implemented using R 4.0.5. Specifically, we used the R library “meta” [21].

3. Results

The searches yielded 152 articles in PubMed and 358 in Embase. The results of both searches can be found in the PRISMA chart in Fig. 1.

Fig. 1.

Fig. 1

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PRISMA chart detailing the literature search results.

A total of 24 publications that assessed the effect of smoking status on halitosis were identified. Of these, 14 studies met the inclusion criteria for the analysis. Table 1 presents the characteristics of these studies. The remaining 10 studies were not included, as 8 of these contained incomplete information [5], [22], [23], [24], [25], [26], [27], [28], 1 included smokers and former smokers together [29] and 1 had no control group [30].

Table 1.

Characteristics of studies evaluating halitosis in smokers and nonsmokers included in the meta-analyses.

Reference Country Study design Study participants Smoking definition Diagnosis of halitosis Subgroup (halitosis, YES/NO)
Smokers Nonsmokers OR
Patient group (n) (n) (95% CI)
Al Ansari et al. [31] Kuwait Cross-sectional 1551 Kuwaiti adult subjects Smoking history Self-reported All 107/182 249/976 2.30 (1.75–3.04)
Alqatahni et al. [32] Saudi Arabia Cross-sectional 100 male participants with peri-implantitis Current smoking Self-reported All 20/15 11/21 2.55 (0.95–6.85)
AlSadhan [7] Saudi Arabia Cross-sectional Male and female students Smoking history Self-reported All 66/173 468/1636 1.33 (0.99–1.80)
Al-Zahrani et al. [33] Saudi Arabia Cross-sectional 38 consecutive type 2 diabetic patients were recruited from among patients who presented for treatment at a University hospital Smoking history Self-reported All 3/7 13/15 0.49 (0.11–2.31)
Ayo-Yusuf et al. [34] South Africa Cross-sectional 896 patients examined between January and October 2004 were retrospectively analyzed. Current smoking Halimeter: No halitosis considered in subjects with halitosis measurement of 0–1 All 119/133 206/431 1.87 (1.39–2.52)
Babazadeh et al. [35] Iran Cross-sectional 519 adolescents in Qazvin, Iran Current smoking Self-reported All 57/48 197/219 1.32 (0.86–2.03)
Eldarrat et al. [36] United Arab Emirates Cross-sectional Men and women aged between 19 and 24 years Smoking history Self-reported All 7/27 36/163 1.17 (0.47–2.91)
Jiun et al. [37] Malaysia Cross-sectional 100 smokers and 100 nonsmokers aged 18–50 years were recruited Current smoking Halimeter All 75/25 8/92 34.50 (14.71–80.92)
Lee et al. [4] South Korea Cross-sectional 54 subjects (male:female = 33:21) with a mean age of 46.0 ± 11.4 years were analyzed Smoking history Halimeter: Halitosis was measured as > 100 ppb All 8/3 23/20 2.32 (0.54–9.94)
Rech et al. [38] Brazil Cross-sectional 48 subjects (current tobacco users and never smokers, 24 each) Current smoking Self-reported All 8/16 1/23 11.50 (1.31–101.18)
Romano et al. [39] Italy Cross-sectional 736 adults (25- to 75-years-old) in a city in northern Italy Current smoking Self-reported All 76/97 307/256 0.65 (0.46–0.92)
Saadaldina et al. [40] Saudi Arabia Cross-sectional 460 adults participated in the study Smoking Self-reported All 16/19 121/304 2.12 (1.05–4.25)
Sanli et al. [41] Turkey Cross-sectional 1840 patients (823 men and 1017 women) over 25 years of age, who were admitted to a ear, nose, and throat outpatient clinic were included in the study Current smoking Self-reported All 194/515 237/1058 1.68 (1.35–2.09)
Struch et al. [42] Germany Cross-sectional Halitosis was assessed among 417 edentulous (toothless) subjects aged 40–81 years and among 2588 dentate subjects aged 20–59 years Current smoking Self-reported Dentate 207/787 173/684 1.04 (0.83–1.30)
Edentulous 10/76 12/129 1.41 (0.58–3.43)
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The meta-analysis assessing the risk of halitosis in current smokers versus nonsmokers included nine comparisons from eight studies. Both fixed and random effects models showed an increased risk for halitosis among current smokers (ORs = 1.46 [95% CI, 1.30–1.64] and OR=2.00 [95% CI, 1.25–3.21], respectively). The interstudy heterogeneity was high (I2 = 91%). Fig. 2, Fig. 3 present the forest and funnel plots related to this comparison, respectively. Overall, the funnel plots show the odds ratio and standard errors of each study are plotted on the x-axis and y-axis, respectively. The dark and light blue shaded regions represent significant effects at p = 0.05 and p = 0.01 levels of significance, respectively.

Fig. 2.

Fig. 2

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Forest plot meta-analysis of risk of halitosis in current smokers versus nonsmokers.

Fig. 3.

Fig. 3

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Funnel plot meta-analysis of risk of halitosis in current smokers versus nonsmokers.

Visual analysis of the funnel plot showed no evidence of publication bias. Because of the high heterogeneity, we performed sensitivity analysis by excluding those studies that were driving the most heterogeneity. The sensitivity analysis shown in Fig. 4 includes six studies [32], [34], [35], [41], [42], as the studies by Rech et al. [38], Jiun et al. [37], and Romano et al. [39] accounted for 20% of all interstudy heterogeneity. The results of this analysis also showed an increased risk of halitosis among current smokers in both fixed and random effects models (ORs = 1.43 [95% CI, 1.26–1.63] and OR = 1.49 [95% CI, 1.15–1.92], respectively; I2 = 65%).

Fig. 4.

Fig. 4

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Forest plot meta-analysis of risk of halitosis in current smokers versus nonsmokers (sensitivity analysis).

The meta-analysis of ever smokers versus never smokers included six studies. The fixed effects model showed an increased risk for halitosis in ever smokers versus nonsmokers (OR = 1.74 [95% CI, 1.45–2.10]), while the random effects analysis did not show a statistically significant difference in halitosis risk between the two groups (OR = 1.66 [95% CI, 1.16–2.37]). The interstudy heterogeneity was moderate (I2 = 53%). Fig. 5, Fig. 6 show the forest and the funnel plots of these analyses, respectively. Visual analysis of the funnel plot did not reveal any evidence of publication bias.

Fig. 5.

Fig. 5

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Forest plot meta-analysis of risk of halitosis in ever smokers versus never smokers.

Fig. 6.

Fig. 6

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Funnel plot meta-analysis of risk of halitosis in ever smokers versus nonsmokers.

For meta-analysis of smokers (current and ever smokers) versus nonsmokers including only those studies that used self-reporting of halitosis, 12 of the 14 studies met the inclusion criteria. The fixed effects model showed an increased risk of halitosis in smokers (OR = 1.37 [95% CI, 1.23–1.52]), while the random effects analysis did not show a statistically significant difference in halitosis risk between the two groups (OR = 1.40 [95% CI, 1.06–1.85]). The interstudy heterogeneity was high (I2 = 78%). Fig. 7, Fig. 8 show the forest and funnel plots related to this analysis, respectively. Visual analysis of the funnel plot did not reveal any evidence of publication bias.

Fig. 7.

Fig. 7

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Forest plot meta-analysis of risk of halitosis in smokers versus nonsmokers (self-reported outcome).

Fig. 8.

Fig. 8

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Funnel plot meta-analysis of risk of halitosis in smokers versus nonsmokers (self-reported outcome).

For the meta-analysis of smokers (current and ever smokers) versus nonsmokers including only those studies that used a Halimeter for diagnosis, only three studies met the inclusion criterion. The fixed effects model showed an increased risk for halitosis in smokers (OR = 2.88 [95% CI, 2.22–3.72]), while the random effects analysis did not show a statistically significant difference in halitosis risk between the two groups (OR = 5.36 [95% CI, 0.68–42.09]). The interstudy heterogeneity was high (I2 = 95%). Fig. 9, Fig. 10 show the forest and funnel plots of this analysis. Visual analysis of the funnel plot did not reveal any evidence of publication bias.

Fig. 9.

Fig. 9

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Forest plot meta-analysis of risk of halitosis in smokers versus nonsmokers (Halimeter-measured outcome).

Fig. 10.

Fig. 10

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Funnel plot meta-analysis of risk of halitosis in smokers versus nonsmokers (Halimeter-measured outcome).

4. Discussion

Halitosis is commonly defined as an unpleasant or offensive smell that is emitted from the oral cavity [43], and has a long history, dating back to 1500 BCE, as Hippocrates, the ancient Greeks, and the Romans mentioned it in their writings [12]. Halitosis poses a diagnostic problem, probably because there are many methods to measure it and because of its multifactorial etiology [44]. The aim of this manuscript was to summarize the effects of smoking on the development of halitosis by means of a meta-analysis. The meta-analysis assessing risk for halitosis in current smokers relative to nonsmokers found an increased risk for the current smoker group. These results were consistent both in fixed and random effects models. Even though the interstudy heterogeneity was high (I2 = 91%), sensitivity analysis by limiting the number of studies yielded similar results, with no-to-moderate heterogeneity (I2 = 0–65%). The analysis comparing ever smokers with never smokers showed a non-significantly increased risk of halitosis in ever smokers, which disappeared when using the random effects model. The same effect was seen when stratifying the analyses by ascertainment of halitosis (self-reported or measured by a Halimeter).

A possible reason for the high interstudy heterogeneity could be that the studies originated from very diverse populations. However, the most probable cause is the ascertainment of halitosis. This is because smokers have a greater probability of being less objective in reporting gingival conditions and halitosis [39], and, therefore, the prevalence of halitosis in these studies might be higher than that reported among the smoking groups.

Cigarette smoking is a public health problem [15] and cigarette smoke contains numerous toxicants to which smokers are regularly exposed on a periodic basis. These toxicants can potentially alter the microbial ecology of the mouth through numerous mechanisms such as antibiotic effects and oxygen deprivation [45].

A characteristic stale odor, difficult to abolish is the hallmark of the tobacco smoker [46]. Previous research has shown that tobacco smoking is the second greatest offender in the development of halitosis, behind periodontal disease and associated food stagnation. Halitosis is often unsuspected by the sufferer because of an adaptation to the smell which occurs within a short period of time (summarized by [46]). The study by Romano et al. [39] also showed that smokers had a greater probability of being less objective in reporting gingival conditions and halitosis.

Some components of tobacco combustion are actually absorbed into the blood stream via the oral mucosa or the mucosa of the lung alveoli. These substances can be exhaled because of the blood-air interchange which occurs in the lungs. The offensiveness of exhaled breath relates to the odor intensity of the tobacco used, so that cigar and pipe tobacco smokers suffer more from halitosis than those who smoke cigarettes.

Other pathways by which smoking can produce halitosis is by decreasing the commensal population of normal flora in the oral cavity, leading to an increase of pathogenic microbes, [15] as well as enhancing microbial colonization by biofilm formation on oral epithelial cells. This may impair host immune responses against pathogens and also disrupt effective nasal mucociliary clearance [47], [48]. More importantly, a number of studies have reported that smoking increases the probability of extensive disease development [16], [17] and causes a significant disruption in the oral microbiota, creating an imbalance in the oral environment. The study by Ilankizhai and Leelavathi [45] for instance, examined the changes caused by tobacco smoking on the microbial profile and oral health conditions of cigarette smokers compared to non-smokers. They found that smokers had more diverse microbial colonization than non-smokers. Staphylococcus and Bacillus species were the most prevalent bacterial isolates among smokers, followed by Enterococcus and Micrococcus species, while among non-smokers, Streptococcus was the most prevalent isolate followed by Enterococcus and Bacillus species.

Moreover, smoking contributes to halitosis by causing hyposalivation and periodontal diseases [18], [19]. The study by Rad et al. [49] evaluated the effect of smoking on salivary flow rate as well as oral and dental health in 100 smokers and 100 non-tobacco users. The authors reported that mean (± SD) salivary flow rates were 0.38 (± 0.13) ml/min in smokers and 0.56 (± 0.16) ml/min in non-smokers. The difference was statistically significant (P = 0.00001). Also, 39% of smokers and 12% of non-smokers reported experiencing at least one xerostomia symptom, with statistically significant difference between groups (p = 0.0001).

Finally, it has been shown that while the oral hygiene habits in nonsmokers and light smokers are comparable, heavy smokers have been found to have worse oral hygiene habits than nonsmokers [50].

Our analyses have some limitations. First of all, all studies included were of cross-sectional design. Also, the majority of these (n = 11) relied on the self-reporting of halitosis and only 3 had objective measurement of halitosis by using a halimeter. Of the 3 studies that used a halimeter, all of them seem to have used different definitions. The study by Ayo-Yusuf [34] measured halitosis as yes/no, the study by Lee et al. [4] used a definition of > 100 ppb while the study by Jiun et al. [37] did not specify a definition.

Our meta-analyses found that smoking is associated with the development of halitosis, most likely because of hyposalivation and periodontal diseases [18], [19] as well as by decreasing the commensal population of normal flora in the oral cavity, which leads to an increase in pathogenic microbes [15] and also enhancement of microbial colonization by biofilm formation on oral epithelial cells.

5. Conclusions

Halitosis is a common condition that can affect the quality of life of the affected individual. The results from this meta-analyses show that current smokers are more likely to suffer from halitosis than nonsmokers.

Funding

This work was supported by Philip Morris International.

CRediT authorship contribution statement

Alba Romero Kauss: Formal analysis, Writing – original draft. Meagan Antunes: Data curation. Filippo Zanetti: Conceptualization, Project administration. Matthew Hankins: Supervision, Writing – review & editing. Julia Hoeng: Conceptualization. Annie Heremans: Supervision. Angela van der Plas: Methodology, Investigation, Writing – review & editing.

Declaration of Competing Interest

This work was supported by Philip Morris International.

Handling Editor: DR. Aristidis Tsatsakis

References

  • 1.Bollen C.M., Beikler T. Halitosis: the multidisciplinary approach. Int. J. Oral Sci. 2012;4(2):55–63. doi: 10.1038/ijos.2012.39. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.van den Broek A.M., Feenstra L., de Baat C. A review of the current literature on aetiology and measurement methods of halitosis. J. Dent. 2007;35(8):627–635. doi: 10.1016/j.jdent.2007.04.009. [DOI] [PubMed] [Google Scholar]
  • 3.A.D.A Council on Scientific Affairs. J. Am. Dent. Assoc. 2003;134(35):209–214. [Google Scholar]
  • 4.Lee H.J., Kim H.M., Kim N., Oh J.C., Jo H.J., Lee J.T., et al. Association between halitosis diagnosed by a questionnaire and halimeter and symptoms of gastroesophageal reflux disease. J. Neurogastroenterol. Motil. 2014;20(4):483–490. doi: 10.5056/jnm14052. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Miyazaki H., Sakao S., Katoh Y., Takehara T. Correlation between volatile sulphur compounds and certain oral health measurements in the general population. J. Periodontol. 1995;66(8):679–684. doi: 10.1902/jop.1995.66.8.679. [DOI] [PubMed] [Google Scholar]
  • 6.Seemann R., Bizhang M., Djamchidi C., Kage A., Nachnani S. The proportion of pseudo-halitosis patients in a multidisciplinary breath malodour consultation. Int. Dent. J. 2006;56(2):77–81. doi: 10.1111/j.1875-595x.2006.tb00077.x. [DOI] [PubMed] [Google Scholar]
  • 7.AlSadhan S.A. Self-perceived halitosis and related factors among adults residing in Riyadh, Saudi Arabia. A cross sectional study. Saudi Dent. J. 2016;28(3):118–123. doi: 10.1016/j.sdentj.2016.06.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.McKeown L. Social relations and breath odour. Int. J. Dent. Hyg. 2003;1(4):213–217. doi: 10.1034/j.1601-5037.2003.00056.x. [DOI] [PubMed] [Google Scholar]
  • 9.Delanghe G., Ghyselen J., Feenstra L., van Steenberghe D. Experiences of a Belgian multidisciplinary breath odour clinic. Acta Otorhinolaryngol. Belg. 1997;51(1):43–48. [PubMed] [Google Scholar]
  • 10.Goldberg S., Kozlovsky A., Gordon D., Gelernter I., Sintov A., Rosenberg M. Cadaverine as a putative component of oral malodor. J. Dent. Res. 1994;73(6):1168–1172. doi: 10.1177/00220345940730060701. [DOI] [PubMed] [Google Scholar]
  • 11.Greenstein R.B., Goldberg S., Marku-Cohen S., Sterer N., Rosenberg M. Reduction of oral malodor by oxidizing lozenges. J. Periodontol. 1997;68(12):1176–1181. doi: 10.1902/jop.1997.68.12.1176. [DOI] [PubMed] [Google Scholar]
  • 12.Seerangaiyan K., Juch F., Winkel E.G. Tongue coating: its characteristics and role in intra-oral halitosis and general health-a review. J. Breath Res. 2018;12(3) doi: 10.1088/1752-7163/aaa3a1. [DOI] [PubMed] [Google Scholar]
  • 13.Tonzetich J. Production and origin of oral malodor: a review of mechanisms and methods of analysis. J. Periodontol. 1977;48(1):13–20. doi: 10.1902/jop.1977.48.1.13. [DOI] [PubMed] [Google Scholar]
  • 14.Durham T.M., Malloy T., Hodges E.D. Halitosis: knowing when ‘bad breath’ signals systemic disease. Geriatrics. 1993;48(8):55–59. [PubMed] [Google Scholar]
  • 15.Ogba O.M.E.J., Olorode O.A., Mbah M. Effect of tobacco smoking on oral microbial flora and the relationship with oral health in Calabar, Nigeria. Int. J. Biomed. Lab. Sci. 2017;6:1–5. [Google Scholar]
  • 16.Hujoel P.P., del Aguila M.A., DeRouen T.A., Bergstrom J. A hidden periodontitis epidemic during the 20th century? Commun. Dent. Oral Epidemiol. 2003;31(1):1–6. doi: 10.1034/j.1600-0528.2003.00061.x. [DOI] [PubMed] [Google Scholar]
  • 17.Apatzidou D.A., Riggio M.P., Kinane D.F. Impact of smoking on the clinical, microbiological and immunological parameters of adult patients with periodontitis. J. Clin. Periodontol. 2005;32(9):973–983. doi: 10.1111/j.1600-051X.2005.00788.x. [DOI] [PubMed] [Google Scholar]
  • 18.Al-Atrooshi B.A.A.-R.A. Oral halitosis and oral hygiene practices among dental students. J. Bagh. Coll. Dent. 2007;19:72–76. [Google Scholar]
  • 19.Scully C., Greenman J. Halitology (breath odour: aetiopathogenesis and management) Oral Dis. 2012;18(4):333–345. doi: 10.1111/j.1601-0825.2011.01890.x. [DOI] [PubMed] [Google Scholar]
  • 20.Macaskill P., Walter S.D., Irwig L. A comparison of methods to detect publication bias in meta-analysis. Stat. Med. 2001;20(4):641–654. doi: 10.1002/sim.698. [DOI] [PubMed] [Google Scholar]
  • 21.Schwarzer G.C., Rucker J.R., Fixed G. Effect and random effects meta-analysis. Meta-Analysis with R. 2015;XII:252. [Google Scholar]
  • 22.Kayombo C.M., Mumghamba E.G. Self-reported halitosis in relation to oral hygiene practices, oral health status, general health problems, and multifactorial characteristics among workers in Ilala and Temeke Municipals, Tanzania. Int. J. Dent. 2017;2017 doi: 10.1155/2017/8682010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Bornstein M.M., Kislig K., Hoti B.B., Seemann R., Lussi A. Prevalence of halitosis in the population of the city of Bern, Switzerland: a study comparing self-reported and clinical data. Eur. J. Oral Sci. 2009;117(3):261–267. doi: 10.1111/j.1600-0722.2009.00630.x. [DOI] [PubMed] [Google Scholar]
  • 24.Bornstein M.M., Stocker B.L., Seemann R., Burgin W.B., Lussi A. Prevalence of halitosis in young male adults: a study in swiss army recruits comparing self-reported and clinical data. J. Periodontol. 2009;80(1):24–31. doi: 10.1902/jop.2009.080310. [DOI] [PubMed] [Google Scholar]
  • 25.Kim S.Y., Sim S., Kim S.G., Park B., Choi H.G. Prevalence and associated factors of subjective halitosis in Korean adolescents. PLoS One. 2015;10(10) doi: 10.1371/journal.pone.0140214. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Tubaishat R.S., Malkawi Z.A., Albashaireh Z.S. The influence of different factors on the oral health status of smoking and nonsmoking adults. J. Contemp. Dent. Pract. 2013;14(4):731–737. doi: 10.5005/jp-journals-10024-1392. [DOI] [PubMed] [Google Scholar]
  • 27.Silva M.F., Nascimento G.G., Leite F.R.M., Horta B.L., Demarco F.F. Periodontitis and self-reported halitosis among young adults from the 1982 Pelotas Birth Cohort. Oral Dis. 2020;26(4):843–846. doi: 10.1111/odi.13286. [DOI] [PubMed] [Google Scholar]
  • 28.Setia S., Pannu P., Gambhir R.S., Galhotra V., Ahluwalia P., Sofat A. Correlation of oral hygiene practices, smoking and oral health conditions with self perceived halitosis amongst undergraduate dental students. J. Nat. Sci. Biol. Med. 2014;5(1):67–72. doi: 10.4103/0976-9668.127291. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Yahya N.A., Saub R., Nor M.M., Yusoff N. Dental patient knowledge about the effects of smoking and attitudes about the role of dentists in smoking cessation. Southeast Asian J. Trop. Med. Public Health. 2017;48(2):473–484. [PubMed] [Google Scholar]
  • 30.Barik A., Rai R.K., Chowdhury A. Tobacco use and self-reported morbidity among rural Indian adults. Prim. Health Care Res. Dev. 2016;17(5):514–523. doi: 10.1017/S146342361600013X. [DOI] [PubMed] [Google Scholar]
  • 31.Al-Ansari J.M., Boodai H., Al-Sumait N., Al-Khabbaz A.K., Al-Shammari K.F., Salako N. Factors associated with self-reported halitosis in Kuwaiti patients. J. Dent. 2006;34(7):444–449. doi: 10.1016/j.jdent.2005.10.002. [DOI] [PubMed] [Google Scholar]
  • 32.Alqahtani F., Alqhtani N., Divakar D.D., Shetty S.B., Shetty B., Alkhtani F. Self-rated peri-implant oral symptoms and clinicoradiographic characteristics in Narghile-smokers, cigarette-smokers, and nonsmokers with peri-implantitis. Clin. Implant Dent. Relat. Res. 2019;21(6):1235–1240. doi: 10.1111/cid.12864. [DOI] [PubMed] [Google Scholar]
  • 33.Al-Zahrani M.S., Zawawi K.H., Austah O.N., Al-Ghamdi H.S. Self reported halitosis in relation to glycated hemoglobin level in diabetic patients. Open Dent. J. 2011;5:154–157. doi: 10.2174/1874210601105010154. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Ayo-Yusuf O.A., Postma T.C., van Wyk C. Clinical correlates of oral malodour in a population of patients attending a preventive clinic in Pretoria, South Africa. SADJ. 2011;66(7):8–31. 326. [PubMed] [Google Scholar]
  • 35.Babazadeh S.Y.R., Pakdaman A., Kambakhsh S.M. Normative and Subjective Oral Health Evaluation among Smoking and Non-Smoking Adolescents of Qazvin, Iran, in 2015. Iran. Red. Crescent Med. J. 2017 [Google Scholar]
  • 36.Eldarrat A.H. Influence of oral health and lifestyle on oral malodour. Int. Dent. J. 2011;61(1):47–51. doi: 10.1111/j.1875-595X.2011.00010.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Jiun I.L., Siddik S.N., Malik S.N., Tin-Oo M.M., Alam M.K., Khan M.M. Association between oral hygiene status and halitosis among smokers and nonsmokers. Oral Health Prev. Dent. 2015;13(5):395–405. doi: 10.3290/j.ohpd.a33920. [DOI] [PubMed] [Google Scholar]
  • 38.Rech R.S., Santos K.W., Maahs M.A., Vidor D.C. Masticatory changes as a result of oral disorders in smokers. Int. Arch. Otorhinolaryngol. 2014;18(4):369–375. doi: 10.1055/s-0034-1385843. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Romano F., Perotto S., Bianco L., Parducci F., Mariani G.M., Aimetti M. Self-perception of periodontal health and associated factors: a cross-sectional population-based study. Int. J. Environ. Res. Public Health. 2020;17:8. doi: 10.3390/ijerph17082758. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Saadaldina S.A., Eldwakhly E., Alnazzawi A.A., Alharbi R.A., Alghamdi B.K., Abu Hammad O.A., et al. Awareness and practice of oral health measures in medina, Saudi Arabia: an observational study. Int. J. Environ. Res. Public Health. 2020;17:23. doi: 10.3390/ijerph17239112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Sanli A., Bekmez E., Yildiz G., Erdogan B.A., Yilmaz H.B., Altin G. Relationship between smoking and otorhinolaryngological symptoms. Kulak Burun Bogaz Ihtis Derg. 2016;26(1):28–33. doi: 10.5606/kbbihtisas.2016.87059. [DOI] [PubMed] [Google Scholar]
  • 42.Struch F., Schwahn C., Wallaschofski H., Grabe H.J., Volzke H., Lerch M.M., et al. Self-reported halitosis and gastro-esophageal reflux disease in the general population. J. Gen. Intern. Med. 2008;23(3):260–266. doi: 10.1007/s11606-007-0486-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Apatzidou A.D., Bakirtzoglou E., Vouros I., Karagiannis V., Papa A., Konstantinidis A. Association between oral malodour and periodontal disease-related parameters in the general population. Acta Odontol. Scand. 2013;71(1):189–195. doi: 10.3109/00016357.2011.654259. [DOI] [PubMed] [Google Scholar]
  • 44.Sombie R., Tiendrebeogo A.J.F., Guiguimde W.P.L., Guingane A., Tiendrebeogo S., Ouoba K., et al. Halitosis: multidisciplinary diagnostic and therapeutic approaches. Pan Afr. Med. J. 2018;30:201. doi: 10.11604/pamj.2018.30.201.10951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Ilankizhai R.J.L.L. Comparison of oral microbiota among smokers and non-smokers - a pilot study. Drug Invent. Today. 2018:10. [Google Scholar]
  • 46.Bastiaan R.J., Reade P.C. The effects of tobacco smoking on oral and dental tissues. Aust. Dent. J. 1976;21(4):308–315. doi: 10.1111/j.1834-7819.1976.tb01038.x. [DOI] [PubMed] [Google Scholar]
  • 47.Tamashiro E., Xiong G., Anselmo-Lima W.T., Kreindler J.L., Palmer J.N., Cohen N.A. Cigarette smoke exposure impairs respiratory epithelial ciliogenesis. Am. J. Rhinol. Allergy. 2009;23(2):117–122. doi: 10.2500/ajra.2009.23.3280. [DOI] [PubMed] [Google Scholar]
  • 48.Arcavi L., Benowitz N.L. Cigarette smoking and infection. Arch. Intern. Med. 2004;164(20):2206–2216. doi: 10.1001/archinte.164.20.2206. [DOI] [PubMed] [Google Scholar]
  • 49.Rad M., Kakoie S., Niliye Brojeni F., Pourdamghan N. Effect of long-term smoking on whole-mouth salivary flow rate and oral health. J. Dent. Res. Dent. Clin. Dent. Prospects. 2010;4(4):110–114. doi: 10.5681/joddd.2010.028. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Santos A., Pascual A., Llopis J., Giner L., Kim D.M., Levi P., Jr., et al. Self-reported oral hygiene habits in smokers and nonsmokers diagnosed with periodontal disease. Oral Health Prev. Dent. 2015;13(3):245–251. doi: 10.3290/j.ohpd.a34248. [DOI] [PubMed] [Google Scholar]

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