Abstract
Background
Oral manifestations and lesions could adversely impact the quality of people’s lives. COVID-19 infection may interact with smoking and the impact on oral manifestations is yet to be discovered.
Objectives
The aim of this study was to assess the self-reported presence of oral lesions by COVID-19-infected young adults and the differences in the association between oral lesions and COVID-19 infection in smokers and non-smokers.
Methods
This cross-sectional multi-country study recruited 18-to-23-year-old adults. A validated questionnaire was used to collect data on COVID-19-infection status, smoking and the presence of oral lesions (dry mouth, change in taste, and others) using an online platform. Multi-level logistic regression was used to assess the associations between the oral lesions and COVID-19 infection; the modifying effect of smoking on the associations.
Results
Data was available from 5,342 respondents from 43 countries. Of these, 8.1% reported COVID-19-infection, 42.7% had oral manifestations and 12.3% were smokers. A significantly greater percentage of participants with COVID-19-infection reported dry mouth and change in taste than non-infected participants. Dry mouth (11.1% vs 7.5%, p = 0.009) and change in taste (11.5% vs 2.7%, p < 0.001) were greater in COVID-19 infected than non-infected persons. The association between COVID-19-infection and dry mouth was stronger among smokers than non-smokers (AOR = 1.26 and 1.03, p = 0.09) while the association with change in taste was stronger among non-smokers (AOR = 1.22 and 1.13, p = 0.86).
Conclusion
Dry mouth and changed taste may be used as an indicator for COVID-19 infection in low COVID-19-testing environments. Smoking may modify the association between some oral lesions and COVID-19-infection.
Keywords: COVID-19, Oral lesions, Smoking, Dry mouth
Introduction
The COVID-19 pandemic has adversely affected people’s lives and caused multiple clinical manifestations (Chen et al., 2020; Zhu et al., 2020; Vinayachandran & Balasubramanian, 2021) including oral manifestations and lesions (Huang et al., 2021). Oral lesions associated with COVID-19 infection include blisters, ulcers, plaques, macule and erosion (Al-Khanati et al., 2020; Amorim dos Santos et al., 2021). A cross sectional study of COVID-19 infected patients indicated that they had aphthous-like ulcers, erythema and lichen planus (Fidan, Koyuncu & Akin, 2021). In addition, Katz & Yue (2021) reported an increased tendency for COVID-19 infection among patients with recurrent aphthous stomatitis. These manifestations could affect the quality of life of people and cause physical disability, functional limitation, and psychological disabilities (Villanueva-Vilchis et al., 2016).
Furthermore, the public health response to COVID-19 pandemic affected the mental health of many individuals because of the induced psychological distress resulting from the loss of job, uncertainties about income, prolonged isolation and poor access to social support (Kumar Kalidoss & Singh Bakshi, 2020). Shutdown of schools and poor access to support systems and movement restrictions created further stresses for many young adults. Stress is a risk factor for tobacco use (Ansell et al., 2012).
Tobacco use causes oral manifestations due to the harmful chemicals and nicotine released when tobacco is burned in the oral cavity (Ozturk, Fidanci & Unal, 2017). Tobacco smokers have oral manifestations like change in taste, hairy tongue, sore and dry throat and leukoplakia. In addition, gingival inflammation and ulcers or burns were more frequently reported in smokers than non-smokers (Patil, Bathi & Chaudhari, 2013; Amadori et al., 2017; Kumar Kalidoss & Singh Bakshi, 2020). Also, the severity of COVID-19 was reported to more severe in smokers (Gülsen et al., 2020) indicating a possible a relationship between smoking, COVID-19 infection and oral manifestations.
There is growing evidence about the association between COVID-19 and the occurrence of oral manifestations (Soares et al., 2020; Abubakr, Salem & Kamel, 2021; Fidan, Koyuncu & Akin, 2021). There are also indications that there is an increase in the proportion of people who started to smoke or increased the frequency of smoking during the pandemic (Gaiha, Cheng & Halpern-Felsher, 2020; García-Álvarez et al., 2020). There is, however, limited information on the relationship between COVID-19, smoking and oral manifestations, especially among young patients. The compromised immune system resulting from COVID-19 and the side effect of its treatment may be associated with oral lesions such as opportunistic infections of the salivary glands, dry mouth, oral ulcerations and gingivitis (Dziedzic & Wojtyczka, 2021).
Therefore, the aim of this study was to determine the association between the self-reported presence of oral manifestations in young adults from several countries and COVID-19 infection, and how this association may be modified by smoking. The null hypothesis of the study is that there is no significant difference in the self-reported presence of oral manifestations between participants infected and not infected with COVID-19, and that this difference is not modified by smoking status.
Materials and Methods
This was a cross-sectional study that collected data from 43 countries between August 2020 to January 2021 (Table S1). Ethical approval was obtained from the Research Ethics Committee of the Faculty of Dentistry, King Abdulaziz University in Saudi Arabia (#13-08-20). The study was carried out according to the Helsinki Declaration (WMA, 2001). Participants indicated consent by returning a filled questionnaire on the electronic link. Once they accessed the link, they could agree to participate, where the link takes them to the questionnaire, or not agree, where the link will exit them from the survey. Study participants were informed about the purpose of the study and the freedom to withdraw at any time and were assured of confidentiality. There was no reimbursement for study participation.
The sample size for the study was estimated to address the study aims. For the first aim, we assumed a prevalence of oral manifestations ranging from 5% to 90% in different countries, with 5% margin of error and 95% confidence level. The required sample size ranged from 73 to 383. This was increased to 167 and 460 to accommodate a non-response rate of 20% (Select Statistical Services, 2020). For the second aim where a regression analysis was to be conducted, 500 participants were needed (Nemes et al., 2009). Thus, at least 500 participants were targeted. Recruitment continued after reaching this number to ensure maximum geographic representation.
Participants were included in the study if they were young adults aged 18–23-year-old and consented to participate. Participants had to be able to read the language of the survey and have access to an electronic device connected to the internet to be able to respond to the survey.
The questionnaire was constructed in Arabic and translated by native dentists into French, Malay, Turkish and English. The content validity index (CVI) was calculated (Yusoff, 2019) for each version of the questionnaire. In addition, each version was pilot-tested by 10 participants to ensure clarity and suitability of terms. The questionnaire was uploaded to SurveyMonkey® and a tailored link was made for each data collector. All questions were mandatory; the questionnaire did not allow to leave any blank responses.
The core team (King Abdulaziz University, KAU, Saudi Arabia, and Alexandria University, Egypt) invited collaborators to recruit data from their countries/regions. Each collaborator received the study protocol, the ethical approval in addition to the customized link and details about required number of participants. We used a snowball sampling technique where country collaborators asked individuals in their network to further circulate the questionnaire link among those they knew.
Data were collected using an electronic questionnaire that comprised two sections: the first section asked about the participants’ gender, medical problems the participant had, their COVID-19 status (confirmed COVID-19 infection based on antigen or PCR test), and if they smoked. The second section asked if participants had any of the eight listed oral lesion or conditions including dental caries, stained teeth, gingival inflammation, dry mouth, change in taste, leukoplakia, burns or ulcers, or hairy tongue.
Statistical analysis
The associations between oral manifestations and COVID-19 and smoking status were assessed using the chi square test. Multilevel binary logistic regression was used to assess the relationship between each oral lesion and COVID-19 infection status, adjusted for gender, history of medical problems and smoking. Country of residence was entered into the model as random effect variable. Multilevel binary logistic regression was also used to assess whether smoking modified the association between oral manifestations and COVID-19 infection status after adjusting for gender and a history of medical problems with country entered as random effect variable. IBM SPSS for Windows version 22.0 (IBM Corp., Armonk, NY, USA) was used for statistical analysis. Adjusted odds ratios (AOR), confidence intervals (CI) and p values were calculated. Significance was set at the 5% level.
Results
The CVI for the English and Arabic versions of the questionnaire was 0.87 based on feedback from nine dentists, 0.97 for the Turkish version (seven dentists), 0.80 for the Malay version (five dentists) and 0.88 for the French version (five dentists).
Complete responses were available from 5,342 young adults from 43 countries (Table S1). Table 1 shows that 58.5% of participants were females, 13.4% had medical problems, 8.1% reported COVID-19 infection and 12.3% were smokers.
Table 1. Gender, medical problems, COVID-19 infection and smoking status of 18–23 year old persons in 43 countries (n = 5,342).
Factors | N (%) | |
---|---|---|
Gender | Male | 2,219 (41.5) |
Female | 3,123 (58.5) | |
Has medical problems | Yes | 716 (13.4) |
No | 4,626 (86.6) | |
Infected with COVID-19 | Yes | 434 (8.1) |
No | 4,908 (91.9) | |
Current smokers | Yes | 657 (12.3) |
No | 4,685 (87.7) |
Table 2 shows that 42.7% of participants reported oral manifestations. A significantly higher proportion of participants with COVID-19 infection than those without COVID-19 infection had of dry mouth, change in taste, leukoplakia, and hairy tongue (p < 0.05). A significantly higher proportion of participants who were smokers than those who are not smokers had stained teeth, gingival inflammation, dry mouth, change in taste, leukoplakia, burns or ulcers and hairy tongue (p < 0.05).
Table 2. Association between the presence of oral lesions and COVID-19 infection and smoking status (n = 5,342).
Reported oral lesions | COVID-19 infection | Smoking | Total n (%) |
||||
---|---|---|---|---|---|---|---|
Yes n (%) | No n (%) | p value | Yes n (%) | No n (%) | p value | ||
Nothing | 209 (48.2) | 2,854 (58.1) | <0.001 | 232 (35.3) | 2,831 (60.4) | <0.001 | 3,063 (57.3) |
Stained teeth | 77 (17.7) | 750 (15.3) | 0.17 | 243 (37.0) | 584 (12.5) | <0.001 | 827 (15.5) |
Dental caries | 103 (23.7) | 1,046 (21.3) | 0.24 | 156 (23.7) | 993 (21.2) | 0.14 | 1,149 (21.5) |
Gingival inflammation | 57 (13.1) | 525 (10.7) | 0.12 | 107 (16.3) | 475 (10.1) | <0.001 | 582 (10.9) |
Dry mouth | 48 (11.1) | 370 (7.5) | 0.009 | 122 (18.6) | 296 (6.3) | <0.001 | 418 (7.8) |
Change in taste | 50 (11.5) | 131 (2.7) | <0.001 | 55 (8.4) | 126 (2.7) | <0.001 | 181 (3.4) |
Leukoplakia | 20 (4.6) | 93 (1.9) | <0.001 | 25 (3.8) | 88 (1.9) | 0.001 | 113 (2.1) |
Burns or ulcers | 10 (2.3) | 59 (1.2) | 0.07 | 21 (3.2) | 48 (1.0) | <0.001 | 69 (1.3) |
Hairy tongue | 10 (2.3) | 35 (0.7) | 0.001 | 13 (2.0) | 32 (0.7) | 0.001 | 45 (0.8) |
Table 3 shows the association between oral manifestations and COVID-19 infection. There were higher odds of reporting the presence of dry mouth (AOR = 1.03, 95% CI [0.82–1.29]), change in taste (AOR = 1.16, 95% CI [0.93–1.46]), leukoplakia (AOR = 1.05, 95% CI [0.83–1.33]), and hairy tongue (AOR = 1.03, 95% CI [0.81–1.30]) among those with COVID-19 infection, although none of these associations was statistically significant.
Table 3. Association between oral lesions and COVID-19 infection and differences due to effect modification by smoking status using multi-level binary logistic regression.
Reported presence of oral lesions | All AOR (95% CI) |
Smokers AOR (95% CI) |
Non-smokers AOR (95% CI) |
p of difference due to effect modification |
---|---|---|---|---|
Stained teeth | 0.95 [0.71–1.26] | 1.24 [0.74–2.07] | 1.00 [0.79–1.26] | 0.02* |
Dental caries | 0.99 [0.79–1.23] | 1.13 [0.66–1.92] | 1.03 [0.82–1.29] | 0.59 |
Gingival inflammation | 1.00 [0.79–1.25] | 1.21 [0.71–2.07] | 1.02 [0.81–1.28] | 0.29 |
Dry mouth | 1.03 [0.82–1.29] | 1.26 [0.74–2.15] | 1.03 [0.82–1.31] | 0.09 |
Change in taste | 1.16 [0.93–1.46] | 1.13 [0.65–1.98] | 1.22 [0.96–1.54] | 0.86 |
Leukoplakia | 1.05 [0.83–1.33] | 1.06 [0.60–1.89] | 1.06 [0.83–1.35] | 0.90 |
Burns and ulcers | 1.01 [0.80–1.28] | 1.00 [0.56–1.79] | 1.03 [0.81–1.31] | 0.95 |
Hairy tongue | 1.03 [0.81–1.30] | 1.06 [0.60–1.90] | 1.03 [0.81–1.31] | 0.85 |
Notes:
An asterisk (*) indicates statistically significant at p < 0.05. Overall model was adjusted for gender, having medical problems and smoking status with country entered as random effect variable.
AOR, adjusted odds ratio; CI, confidence interval.
Table 3 also shows the effect modification in the association between oral manifestations and COVID-19 infection by smoking status presented by differences in the adjusted odds ratios between smokers and non-smokers. Smoking significantly modified the association between self-reported presence of stained teeth and COVID-19 infection with statistically significant difference between smokers and non-smokers in the strength of the association (p = 0.02).
For the other oral manifestations, the odds for the association between the presence of manifestations and COVID-19 infection were higher among smokers than non-smokers although the effect modification was not significant (p > 0.05) except for the association between COVID-19 infection and change in taste where the association was non-significantly (p = 0.86) stronger among non-smokers than smokers.
Discussion
The study showed that persons with COVID-19 infection had higher frequency of reporting dry mouth, change in taste, leukoplakia, and hairy tongue. However, after controlling for gender, having medical problems and smoking status, none of these associations was statistically significant, and the strongest association among them was for the change in taste. This suggests that underlying medical conditions and smoking may predispose persons infected with COVID-19 to these oral conditions accounting at least partly for the strength of the association between COVID-19 infection and the presence of oral manifestations or condition. Smoking significantly modified the association between COVID-19 infection and stained teeth where a directly proportional association was observed only among smokers and there was no association among non-smokers. The association between COVID-19 infection and dry mouth was stronger in smokers than in non-smokers whereas the association with change in taste was stronger among non-smokers than smokers. The null hypothesis can thus be rejected.
Our findings have implications for identifying oral manifestations associated with COVID-19 and the detection of COVID-19 infection among young adults especially in settings where the uptake of COVID-19 testing is low. In these settings, dentist’s screening for oral manifestations should have a high index of suspicion for COVID-19 when adolescents and young persons who smoke or have health problems, have oral the reported manifestations.
Similar to prior studies, we observed salivary gland-related oral manifestations such as dry mouth, and taste alteration in COVID-19 infected patients (Parma et al., 2020; Passarelli et al., 2020; Sakalli et al., 2020). The salivary gland-related oral manifestations may have resulted from the invasion of human cells by SAR-CoV-2 by binding to the angiotensin-converting enzyme two receptors in the salivary glands and on the tongue surface thereby causing inflammatory response (Xu et al., 2020).
The higher odds for a change in taste in association with COVID-19 infection than the other oral manifestations corroborate the results of a systematic review that showed a significant association between taste disorders and COVID-19 infection (Amorim dos Santos et al., 2021). This taste alteration was attributed to local inflammation of the taste buds, peripheral neurotropism and direct toxicity to taste buds, and to side effects of COVID treatment (Finsterer & Stollberger, 2020; Mahmoud et al., 2021).
The study showed that smoking modified the association between COVID-19 infection and teeth staining where the odds ratios were significantly higher in smokers than in non-smokers although these associations were not statistically significant. Nicotine significantly increases the number of Streptococcus mutans in the mouth of smokers hence promoting the formation of dental plaque that gets stained by cigarette contents (Liu et al., 2018). Smokers also had higher odds of having dry mouth than non-smokers though this finding was not significant as reported in prior studies (Villa et al., 2011; Andersson & Johannsen, 2016). Unlike prior studies, we provide evidence about this association in young people and not just adults. The results of the regression analysis, however, indicate that dry mouth association with COVID-19 may be modified by smoking.
We also observed that the association between alteration in taste and COVID-19 infection was greater in non-smokers than smokers. COVID-19 infection may cause chemosensory impairment that affects taste sensation (Parma et al., 2020), and smoking may have been associated with a lower likelihood of an alteration in taste happening for smokers as smoking already blunts the perception of flavors and elevates the taste threshold (Da Ré et al., 2018) especially the taste of salt and sugar (Da Ré et al., 2018; Duffy et al., 2019). Change in taste is becoming recognized as a COVID-19 associated manifestation. Smokers need to be warned that they may not experience this manifestation as non-smokers and should avoid a possible false sense of security against catching COVID-19 infection because of this.
The present study has some limitations. First, its cross-sectional design cannot prove causation but only suggest association. Second, self-reporting may under or overestimate the presence of some oral manifestations, although this may be the only method to assess the presence of some conditions such as change in taste. Also, a recent study compared clinical evaluation with self-reported oral conditions and showed a positive association between both reports (Nascimento et al., 2021). Future studies using clinical examination are needed to assess the prevalence of some of the oral manifestations of COVID-19 such as hairy tongue and dental caries although this examination is best conducted in a clinic with precautions to prevention cross-infection. Third, reporting smoking may be underestimated, especially by females (Hwang et al., 2018). However, the under reporting is expected to be present in both COVID-infected and non-infected AYAs which would reduce the impact of this under-reporting on the observed association. Fourth, the snowball sampling strategy used with the electronic survey at the time of COVID-19 cannot guarantee statistical representativeness although all efforts were made to ensure maximum geographic coverage to increase generalizability. This method was also used previously in previous surveys conducted during the pandemic (Leighton et al., 2021).
Conclusions
Smoking may confound the association between COVID-19 infection and the presence of some oral manifestations and modify the association with others. Policy makers, clinicians and health educators may need to take these associations into consideration when designing interventions.
Supplemental Information
Funding Statement
The authors received no funding for this work. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Additional Information and Declarations
Competing Interests
The authors declare that they have no competing interests.
Author Contributions
Maha El Tantawi conceived and designed the experiments, performed the experiments, analyzed the data, prepared figures and/or tables, authored or reviewed drafts of the article, and approved the final draft.
Heba Jafar Sabbagh conceived and designed the experiments, performed the experiments, prepared figures and/or tables, authored or reviewed drafts of the article, and approved the final draft.
Nada Abubakor Alkhateeb performed the experiments, authored or reviewed drafts of the article, participated in methodology writing and in acquiring ethical approval and data collection in their country, and approved the final draft.
Maryam Quritum conceived and designed the experiments, performed the experiments, prepared figures and/or tables, authored or reviewed drafts of the article, participated in the methodology writing and data collection, and approved the final draft.
Joud Abourdan performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Nafeesa Qureshi performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Shabnum Qureshi performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Ahmed Hamoud performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Nada Mahmoud performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Ruba Odeh performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Nuraldeen Maher Al-Khanati performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Rawiah Jaber performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Abdulrahman Loaie Balkhoyor performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Mohammed Shabi performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Morenike O. Folayan performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in her country and in editing the manuscript, and approved the final draft.
Noha Gomaa performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Raqiya Al_Nahdi performed the experiments, authored or reviewed drafts of the article, participated in writing the manuscript, and approved the final draft.
Nawal Mahmoud performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Hanane El Wazziki performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Manal Alnaas performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Bahia Samodien performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Rawa Mahmoud performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Nour Abu Assab performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Sherin Saad performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Sondos Al-Hachim performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Ali Alshaikh performed the experiments, authored or reviewed drafts of the article, participated in acquiring ethical approval and data collection in their country, and approved the final draft.
Wafaa Abdelaziz conceived and designed the experiments, performed the experiments, authored or reviewed drafts of the article, and approved the final draft.
Human Ethics
The following information was supplied relating to ethical approvals (i.e., approving body and any reference numbers):
The Research Ethics Committee of the Faculty of Dentistry, King Abdulaziz University in Saudi Arabia approved the study (13-08-20).
Data Availability
The following information was supplied regarding data availability:
The raw data with codes and labels are available in the Supplemental File.
References
- Abubakr, Salem & Kamel (2021).Abubakr N, Salem ZA, Kamel AHM. Oral manifestations in mild-to-moderate cases of COVID-19 viral infection in the adult population. Dental and Medical Problems. 2021;58(1):7–15. doi: 10.17219/dmp/130814. [DOI] [PubMed] [Google Scholar]
- Al-Khanati et al. (2020).Al-Khanati NM, Riad A, Sahloul ME, Klugar M. Aphthous-like stomatitis of COVID-19 patients: case report and review of evidence. Brazilian Journal of Oral Sciences. 2020;19:e201354. doi: 10.20396/bjos.v19i0.8661354. [DOI] [Google Scholar]
- Amadori et al. (2017).Amadori F, Bardellini E, Conti G, Majorana A. Oral mucosal lesions in teenagers: a cross-sectional study. Italian Journal of Pediatrics. 2017;43(1):50. doi: 10.1186/s13052-017-0367-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Amorim dos Santos et al. (2021).Amorim dos Santos J, Normando AGC, Carvalho da Silva RL, Acevedo AC, De Luca Canto G, Sugaya N, Santos-Silva AR, Guerra ENS. Oral manifestations in patients with COVID-19: a living systematic review. Journal of Dental Research. 2021;100(2):141–154. doi: 10.1177/0022034520957289. [DOI] [PubMed] [Google Scholar]
- Andersson & Johannsen (2016).Andersson P, Johannsen A. Dental patients’ perceptions and motivation in smoking cessation activities. Acta Odontologica Scandinavica. 2016;74(4):285–290. doi: 10.3109/00016357.2015.1114669. [DOI] [PubMed] [Google Scholar]
- Ansell et al. (2012).Ansell EB, Gu P, Tuit K, Sinha R. Effects of cumulative stress and impulsivity on smoking status. Human Psychopharmacology: Clinical and Experimental. 2012;27(2):200–208. doi: 10.1002/hup.1269. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen et al. (2020).Chen N, Zhou M, Dong X, Qu J, Gong F, Han Y, Qiu Y, Wang J, Liu Y, Wei Y, Xia J, Yu T, Zhang X, Zhang L. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet. 2020;395(10223):507–513. doi: 10.1016/S0140-6736(20)30211-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Da Ré et al. (2018).Da Ré AF, Gurgel LG, Buffon G, Moura WER, Marques Vidor DCG, Maahs MAP. Tobacco influence on taste and smell: systematic review of the literature. International Archives of Otorhinolaryngology. 2018;22(1):81–87. doi: 10.1055/s-0036-1597921. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Duffy et al. (2019).Duffy VB, Glennon SG, Larsen BA, Rawal S, Oncken C, Litt MD. Heightened olfactory dysfunction and oral irritation among chronic smokers and heightened propylthiouracil (PROP) bitterness among menthol smokers. Physiology & Behavior. 2019;201(Dec):111–122. doi: 10.1016/j.physbeh.2018.12.017. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dziedzic & Wojtyczka (2021).Dziedzic A, Wojtyczka R. The impact of coronavirus infectious disease 19 (COVID-19) on oral health. Oral Diseases. 2021;27(Suppl 3):703–706. doi: 10.1111/odi.13359. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fidan, Koyuncu & Akin (2021).Fidan V, Koyuncu H, Akin O. Oral lesions in COVID 19 positive patients. American Journal of Otolaryngology. 2021;42(3):102905. doi: 10.1016/j.amjoto.2021.102905. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Finsterer & Stollberger (2020).Finsterer J, Stollberger C. Causes of hypogeusia/hyposmia in SARS-CoV2 infected patients. Journal of Medical Virology. 2020;92(10):1793–1794. doi: 10.1002/jmv.25903. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gaiha, Cheng & Halpern-Felsher (2020).Gaiha SM, Cheng J, Halpern-Felsher B. Association between youth smoking, electronic cigarette use, and COVID-19. Journal of Adolescent Health. 2020;67(4):519–523. doi: 10.1016/j.jadohealth.2020.07.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
- García-Álvarez et al. (2020).García-Álvarez L, Fuente-Tomás L, Sáiz PA, García-Portilla MP, Bobes J. Will changes in alcohol and tobacco use be seen during the COVID-19 lockdown? Adicciones. 2020;32(2):85–89. doi: 10.20882/adicciones.1546. [DOI] [PubMed] [Google Scholar]
- Gülsen et al. (2020).Gülsen A, Yigitbas BA, Uslu B, Drömann D, Kilinc O. The effect of smoking on COVID-19 symptom severity: systematic review and meta-analysis. Pulmonary Medicine. 2020;2020(7590207):1–11. doi: 10.1155/2020/7590207. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Huang et al. (2021).Huang N, Pérez P, Kato T, Mikami Y, Okuda K, Gilmore RC, Conde CD, Gasmi B, Stein S, Beach M, Pelayo E, Maldonado JO, Lafont BA, Jang SI, Nasir N, Padilla RJ, Murrah VA, Maile R, Lovell W, Wallet SM, Bowman NM, Meinig SL, Wolfgang MC, Choudhury SN, Novotny M, Aevermann BD, Scheuermann RH, Cannon G, Anderson CW, Lee RE, Marchesan JT, Bush M, Freire M, Kimple AJ, Herr DL, Rabin J, Grazioli A, Das S, French BN, Pranzatelli T, Chiorini JA, Kleiner DE, Pittaluga S, Hewitt SM, Burbelo PD, Chertow D, Frank K, Lee J, Boucher RC, Teichmann SA, Warner BM, Byrd KM. SARS-CoV-2 infection of the oral cavity and saliva. Nature Medicine. 2021;27(5):892–903. doi: 10.1038/s41591-021-01296-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hwang et al. (2018).Hwang JH, Kim JY, Lee DH, Jung HG, Park SW. Underestimation of self-reported smoking prevalence in Korean adolescents: evidence from gold standard by combined method. International Journal of Environmental Research and Public Health. 2018;15(4):689. doi: 10.3390/ijerph15040689. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Katz & Yue (2021).Katz J, Yue S. Increased odds ratio for COVID-19 in patients with recurrent aphthous stomatitis. Journal of Oral Pathology & Medicine. 2021;50(1):114–117. doi: 10.1111/jop.13114. [DOI] [PubMed] [Google Scholar]
- Kumar Kalidoss & Singh Bakshi (2020).Kumar Kalidoss V, Singh Bakshi S. COVID-19 and smoking: an association requiring urgent attention. Journal of Smoking Cessation. 2020;15(4):223. doi: 10.1017/jsc.2020.26. [DOI] [Google Scholar]
- Leighton et al. (2021).Leighton K, Kardong-Edgren S, Schneidereith T, Foisy-Doll C. Using social media and snowball sampling as an alternative recruitment strategy for research. Clinical Simulation in Nursing. 2021;55(1):37–42. doi: 10.1016/j.ecns.2021.03.006. [DOI] [Google Scholar]
- Liu et al. (2018).Liu S, Wu T, Zhou X, Zhang B, Huo S, Yang Y, Zhang K, Cheng L, Xu X, Li M. Nicotine is a risk factor for dental caries: an in vivo study. Journal of Dental Sciences. 2018;13(1):30–36. doi: 10.1016/j.jds.2017.09.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mahmoud et al. (2021).Mahmoud MM, Abuohashish HM, Khairy DA, Bugshan AS, Khan AM, Moothedath MM. Pathogenesis of dysgeusia in COVID-19 patients: a scoping review. European Review for Medical and Pharmacological Sciences. 2021;25(2):1114–1134. doi: 10.26355/eurrev_202101_24683. [DOI] [PubMed] [Google Scholar]
- Nascimento et al. (2021).Nascimento GG, Goettems ML, Schertel Cassiano L, Horta BL, Demarco FF. Clinical and self-reported oral conditions and quality of life in the 1982 Pelotas birth cohort. Journal of Clinical Periodontology. 2021;48(9):1200–1207. doi: 10.1111/jcpe.13512. [DOI] [PubMed] [Google Scholar]
- Nemes et al. (2009).Nemes S, Jonasson JM, Genell A, Steineck G. Bias in odds ratios by logistic regression modelling and sample size. BMC Medical Research Methodology. 2009;9(1):56. doi: 10.1186/1471-2288-9-56. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ozturk, Fidanci & Unal (2017).Ozturk O, Fidanci I, Unal M. Effects of smoking on oral cavity. Journal of Experimental and Clinical Medicine. 2017;34(1):3–7. doi: 10.5835/jecm.omu.34.01.002. [DOI] [Google Scholar]
- Parma et al. (2020).Parma V, Ohla K, Veldhuizen MG, Niv MY, Kelly CE, Bakke AJ, Cooper KW, Bouysset C, Pirastu N, Dibattista M, Kaur R, Liuzza MT, Pepino MY, Schöpf V, Pereda-Loth V, Olsson SB, Gerkin RC, Rohlfs Domínguez P, Albayay J, Farruggia MC, Bhutani S, Fjaeldstad AW, Kumar R, Menini A, Bensafi M, Sandell M, Konstantinidis I, Di Pizio A, Genovese F, Öztürk L, Thomas-Danguin T, Frasnelli J, Boesveldt S, Saatci Ö, Saraiva LR, Lin C, Golebiowski J, Hwang LD, Ozdener MH, Guàrdia MD, Laudamiel C, Ritchie M, Havlícek J, Pierron D, Roura E, Navarro M, Nolden AA, Lim J, Whitcroft KL, Colquitt LR, Ferdenzi C, Brindha EV, Altundag A, Macchi A, Nunez-Parra A, Patel ZM, Fiorucci S, Philpott CM, Smith BC, Lundström JN, Mucignat C, Parker JK, van den Brink M, Schmuker M, Fischmeister FPS, Heinbockel T, Shields VDC, Faraji F, Santamaría E, Fredborg WEA, Morini G, Olofsson JK, Jalessi M, Karni N, D’Errico A, Alizadeh R, Pellegrino R, Meyer P, Huart C, Chen B, Soler GM, Alwashahi MK, Welge-Lüssen A, Freiherr J, de Groot JHB, Klein H, Okamoto M, Singh PB, Hsieh JW, Reed DR, Hummel T, Munger SD, Hayes JE. More Than Smell-COVID-19 Is Associated With Severe Impairment of Smell, Taste, and Chemesthesis. Chemical Senses. 2020;45(7):609–622. doi: 10.1093/chemse/bjaa041. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Passarelli et al. (2020).Passarelli PC, Lopez MA, Mastandrea Bonaviri GN, Garcia-Godoy F, D’Addona A. Taste and smell as chemosensory dysfunctions in COVID-19 infection. American Journal of Dentistry. 2020;33(3):135–137. [PubMed] [Google Scholar]
- Patil, Bathi & Chaudhari (2013).Patil PB, Bathi R, Chaudhari S. Prevalence of oral mucosal lesions in dental patients with tobacco smoking, chewing, and mixed habits: a cross-sectional study in South India. Journal of Family and Community Medicine. 2013;20(2):130–135. doi: 10.4103/2230-8229.114777. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sakalli et al. (2020).Sakalli E, Temirbekov D, Bayri E, Alis EE, Erdurak SC, Bayraktaroglu M. Ear nose throat-related symptoms with a focus on loss of smell and/or taste in COVID-19 patients. American Journal of Otolaryngology. 2020;41(6):102622. doi: 10.1016/j.amjoto.2020.102622. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Select Statistical Services (2020).Select Statistical Services Population proportion sample size. 2020. https://select-statistics.co.uk/calculators/sample-size-calculator-population-proportion https://select-statistics.co.uk/calculators/sample-size-calculator-population-proportion
- Soares et al. (2020).Soares CD, Carvalho RA, Carvalho KA, Carvalho MG, Almeida OP. Letter to editor: oral lesions in a patient with COVID-19. Medicina Oral Patología Oral y Cirugia Bucal. 2020;25(4):e563–e564. doi: 10.4317/medoral.24044. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Villa et al. (2011).Villa A, Polimeni A, Strohmenger L, Cicciù D, Gherlone E, Abati S. Dental patients’ self-reports of xerostomia and associated risk factors. Journal of the American Dental Association. 2011;142(7):811–816. doi: 10.14219/jada.archive.2011.0269. [DOI] [PubMed] [Google Scholar]
- Villanueva-Vilchis et al. (2016).Villanueva-Vilchis MD, López-Ríos P, García IM, Gaitán-Cepeda LA. Impact of oral mucosa lesions on the quality of life related to oral health. An etiopathogenic study. Medicina Oral Patología Oral y Cirugia Bucal. 2016;21(2):e178–e184. doi: 10.4317/medoral.20866. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vinayachandran & Balasubramanian (2021).Vinayachandran D, Balasubramanian S. Is gustatory impairment the first report of an oral manifestation in COVID-19? Oral Diseases. 2021;27(Suppl 3):748–749. doi: 10.1111/odi.13371. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WMA (2001).WMA World medical association declaration of helsinki. Ethical principles for medical research involving human subjects. Bulletin of the World Health Organization. 2001;79(4):373–374. [PMC free article] [PubMed] [Google Scholar]
- Xu et al. (2020).Xu H, Zhong L, Deng J, Peng J, Dan H, Zeng X, Li T, Chen Q. High expression of ACE2 receptor of 2019-nCoV on the epithelial cells of oral mucosa. International Journal of Oral Science. 2020;12(1):8. doi: 10.1038/s41368-020-0074-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yusoff (2019).Yusoff M. ABC of content validation and content validity index calculation. Education in Medicine Journal. 2019;11(2):49–54. doi: 10.21315/eimj2019.11.2.6. [DOI] [Google Scholar]
- Zhu et al. (2020).Zhu N, Zhang D, Wang W, Li X, Yang B, Song J, Zhao X, Huang B, Shi W, Lu R, Niu P, Zhan F, Ma X, Wang D, Xu W, Wu G, Gao GF, Tan W. A novel coronavirus from patients with pneumonia in China, 2019. New England Journal of Medicine. 2020;382(8):727–733. doi: 10.1056/NEJMoa2001017. [DOI] [PMC free article] [PubMed] [Google Scholar]
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Data Availability Statement
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The raw data with codes and labels are available in the Supplemental File.