Volume 24, Issue 5 (December & January 2021)                   J Arak Uni Med Sci 2021, 24(5): 716-729 | Back to browse issues page


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Moradi A, Ramin P. Evaluation of the Relationship Between Periapical Lesions and Tobacco Use by Panoramic Radiography in Bandar Abbas City in 1399. J Arak Uni Med Sci 2021; 24 (5) :716-729
URL: http://jams.arakmu.ac.ir/article-1-6894-en.html
1- Department of Radiology, Faculty of Dentistry, Hormozgan University of Medical Sciences, Bandar Abbas, Iran. , dr.anis moradi@gmail.com
2- Department of Radiology, Faculty of Dentistry, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
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Introduction
The epidemiological findings reveal that smoking harms various health conditions such as cardiovascular and lung disorders and periodontitis in many adult humans. However, about 35% of men and 22% of women in developed countries smoke tobacco [11]. Some studies suggest that smoking increases caries risk. Smoking has been identified as a significant risk factor for periodontal disease and accounts for more than half the cases in the population [4]. The side effects of tobacco smoking on the periodontal bone have been demonstrated in several cross-sectional and longitudinal studies [27, 31]. On this basis, it was assumed that smoking might be a risk factor for apical periodontitis, but no suggestion of a possible link between smoking and apical periodontitis or endodontics in general [22]. Thus, this study evaluates the relationship between periodontitis and tobacco use by panoramic radiography in Bandar Abbas City, Iran.
Materials and Method 
The Ethics Committee approved the protocol of the Dental Faculty of Bandar Abbas City, Iran, and each subject signed a consent form after being advised of the nature of the study. A total of 198 panoramic radiographs were classified into periapical healthy (n=99) and periapical apical (n=99) groups. The photographs were collected from the radiology department of the dentistry college of the Bandar Abbas University in 2019. Radiographs were assessed by the radiologists for the subjects who met the criteria of this study as periapical healthy or control who has no radiographically detectable periapical lesion in any teeth and periodontitis or case as a patient who has at least 1 radiographically detectable periapical lesion in a tooth. The inclusion criteria were the quality and length of root filling treatment (RFT), the number (NoRFT), and inadequate root filling treatment (RFTin), and the exclusion criteria were total teeth numbers (TTN), age, gender, the cigarette and hookah use, and dental debris. In total, 24 men and 75 women average of 35.8 years old, were and 25 men and 74 women average of 35.9 years old, were the control. Data were analyzed by SPSS software v. 23, and Chi-Square, t-test, and logistic regression tests were used. 
Results
The TTNin the periodontitis was less than the control group (P<0.05). Cigarette, hookah smokers, and RFTin in periodontitis were higher than in the control group (P<0.01). Dental plaque, age, number of smokers, RFT, and NoRFT, did not differ between groups. Tobacco, hookah use, and RFTin were higher (P<0.05) in females in periodontitis. There were no gender differences in other variables. The most significant group and gender differences (P<0.01) were found in cigarettes, hookah, tobacco, and dental plaque (Table 1). 


Logistic regression analysis was used to determine the effect of tobacco (cigarettes and hookah), smoking, hookah, tooth plaque (yes, no), TTN, RFT, NoRFT, RFTin, age, and gender on periapical status (lesion, no lesion). The Odds Ratio (OR) was for NoRFT (39.7), RFTin (36.8), hookah (8.1), tobacco (6.57), cigarettes (3.59), tooth plaque (63.6), TTN (0.98), RFT (1.4), NoRFT (7.7) and RFTin (36.8), All variables show the effect on periapical tissue (P<0.01) but not age and gender. By removing age and gender, the TTN index will also be ineffective. The highest OR among smoking variables belonged to hookah, and dental indices were NoRFT (Table 2). 


Table 3 shows cigarettes and hookah affected TTN, age, and sex (P<0.01).


Removing age, sex, and TTN means increasing the number of smokers; the TTN will also decrease. Cigarettes or hookah do not affect tooth plaque, RFT, and NoRFT.
Discussion
The people who used tobacco and hookah in the periodontitis were more significant (P<0.01) than the control group, which means smoking could be associated with periodontitis. These are consistent with Lopez-Lopez’s [11] and Correia-Sousaa’s [15] findings but not with Rodriguez’s [18] and Balto’s [19] reports. The TTNin in the control group was higher than the periodontitis (P<0.01). The periodontitis had 2 fewer teeth than the control group, which is consistent with the Bukmir [16] results. Dental plaque did not show a difference between the groups, but the logistic regression evidence revealed a high Odd Ratio (6.63) shows its effectiveness. No study was found to confirm these results. 
This study showed that TTN, RFT, and other dental indicators are significantly effective in apical periodontitis. The reported papers did not confirm the tooth plaque, but smokers had 2 fewer teeth than non-smokers and had more RFT [16]. These results were also found by Segura-Egea [28, 30] and Krall [31]. 
The logistic regression analysis showed that age had no significant effect on periodontitis. This means the probability of having a periapical lesion will not increase with age. This finding is inconsistent with reports by Moszczynski [32] and Bukmir [16], who cited the effect of age on periapical lesions, and Hirsch [33], who reported the relationship between age and dental disorders in smokers. The reason for the age difference of this study from others is probably the low age variation of the study population (35 years old); therefore, it needs further investigations with the older participating population. 
Smoking hookah, tobacco, and cigarettes negatively affected periapical tissues. The low TTN, high dental plaque, and RFT were probably the effects of tobacco smoking on the periapical tissues. Age and gender were not related to the periapical lesions.

Ethical Considerations
Compliance with ethical guidelines

Due to the lack of therapeutic intervention and the preservation of patients’ characteristics, ethical considerations are not included in this study (Code: IR.HUMS.REC.1399.384)

Funding
This article is taken from the second author's PhD dissertation in the radiology department of the School of Dentistry of Hormozgan University of Medical Sciences, Bandar Abbas.

Authors' contributions
The 1st author: Idea, conceptualization, reading photographs, the 2nd: research method, collecting samples, analyzing, writing, and final reviewing.

Conflicts of interest
The authors of the article do not declare any conflict of interest.
 

References
  1. Pinto KP, Ferreira CM, Maia LC, Sassone LC, Fidalgo TKS, Silva EJLN. Does tobacco smoking predispose to apical periodontitis and endodontic treatment need? A systematic review and meta-analysis. Int Endod J. 2020; 53(8):1068-83. [DOI:10.1111/iej.13316] [PMID]
  2. Lee LW, Lee YL, Hsiao SH, Lin HP. Bacteria in the apical root canals of teeth with apical periodontitis. J Formosan Med Asso. 2017; 116(6):448-56. [DOI:10.1016/j.jfma.2016.08.010] [PMID]
  3. Salles AG, Antunes LAA, Kuchler EC, Antunes LS. Association between apical periodontitis and interleukin gene polymorphisms: A systematic review and meta-analysis. J Endod. 2018; 44(3):355-62. [DOI:10.1016/j.joen.2017.11.001] [PMID]
  4. Hughes K, Choo M, Kuperan P, Ong CN, Aw TC. Cardiovascular risk factors in relation to cigarette smoking: A population-based survey among Asians in Singapore. Atherosclerosis. 1998; 137(2):253-8. [DOI:10.1016/S0021-9150(97)00268-2]
  5. Slama K. Current challenges in tobacco control. Int J Tuber Lung Dis. 2004; 8(10):1160-72. [PMID]
  6. Gupta R, Gupta S, Sharma S, Sinha DN, Mehrotra R. Risk of coronary heart disease among smokeless tobacco users: Results of systematic review and meta-analysis of global data. Nicotine Tobacco Res. 2019; 21(1):25-31. [DOI:10.1093/ntr/nty002] [PMID] [PMCID]
  7. Leite FRM, Nascimento GG, Scheutz F, Lopez R. Effect of smoking on periodontitis: A systematic review and meta-regression. Am J Prev Med. 2018; 54(6):831-41. [DOI:10.1016/j.amepre.2018.02.014] [PMID]
  8. WHO. WHO report on the global tobacco epidemic. Geneva: World Health Organization; 2011. https://apps.who.int/iris/handle/10665/44616
  9. Segura-Egea JJ, Martín-González J, Castellanos-Cosano L. Endodontic medicine: Connections between apical periodontitis and systemic diseases. Int Endod J. 2015; 48(10):933-51. [DOI:10.1111/iej.12507] [PMID]
  10. Krall EA Garcia C, Nunn ME, Caplan DJ, Garcia RI. Cigarette smoking increases the risk of root canal treatment. J Dent Res. 2006; 85(4):313-7. [DOI:10.1177/154405910608500406] [PMID] [PMCID]
  11. López-López J, Jané-Salas E, Martín-González J, Castellanos-Cosano L, Llamas-Carreras JM, Velasco-Ortega E, et al. Tobacco smoking and radiographic periapical status: A retrospective case-control study. J Endod. 2012; 38(5):584-8. [DOI:10.1016/j.joen.2012.02.011] [PMID]
  12. Gomes MS, Blattner TC, Sant’Ana Filho M, Grecca FS, Hugo FN, Fouad AF, et al. Can apical periodontitis modify systemic levels of inflammatory markers? A systematic review and meta-analysis. J Endod. 2013; 39(10):1205-17. [DOI:10.1016/j.joen.2013.06.014] [PMID]
  13. Ayoub CG, Aminoshariae A, Bakkar M, Ghosh S, Bonfield T, Demko C, et al. Comparison of IL-1beta, TNF-alpha, Hbd-2, and hBD-3 expression in the dental pulp of smokers versus nonsmokers. J Endod. 2017; 43(12):2009-13. [DOI:10.1016/j.joen.2017.08.017] [PMID]
  14. Fure S. Ten-year cross-sectional and incidence study of coronal and root caries and some related factors in elderly Swedish individuals. Gerodontology. 2004; 21(3):130-40. [DOI:10.1111/j.1741-2358.2004.00025.x] [PMID]
  15. Correia-Sousaa J, Madureira AR, Carvalho MF, Teles AM, Pina-Vaz I. Apical periodontitis and related risk factors: Cross-sectional study. Rev Port Estomatol Med Dent Cir Maxilofac. 2015; 56(4):226-32. [DOI:10.1016/j.rpemd.2015.08.004]
  16. Bukmir PR, Jurčević Grgić M, Brumini G, Spalj S, Pezelj-Ribaric S, Brekalo Pršo, I. Influence of tobacco smoking on dental periapical condition in a sample of Croatian adults. Wien Klin Wochenschr. 2016; 128(7-8):260-5. [DOI:10.1007/s00508-015-0910-8] [PMID]
  17. Sopinksa K, Bołtacz-Rzepkowska E. The influence of tobacco smoking on dental periapical condition in a sample of an adult population of the Łódź region, Poland. Int J Occup Med Environ Health. 2020; 33(1):45-57. [DOI:10.13075/ijomeh.1896.01460] [PMID]
  18. Rodriguez FR, Taner B, Weiger R, Walter C. Is smoking a predictor of apical periodontitis? Clin Oral Investig. 2013; 17(8):1947-55. [DOI:10.1007/s00784-012-0893-z] [PMID]
  19. Balto HA, Alabdulaaly L, Bahammam Sh, Al-Ekrish AA. Comparative analysis of prevalence of apical periodontitis in smokers and non-smokers using cone-beam computed tomography. Saudi Dent J. 2019; 31(1):52-7. [DOI:10.1016/j.sdentj.2018.09.006] [PMID] [PMCID]
  20. Ojima M, Hanioka T, Shimada K, Haresaku S, Yamamoto M, Tanaka K. The role of tobacco uses on dental care and oral disease severity within community dental clinics in Japan. Tob Induc Dis. 2013; 11(1):13. [DOI:10.1186/1617-9625-11-13] [PMID] [PMCID]
  21. Smith CS, Greenland P, Grundy MS. Beyond secondary prevention: Identifying the high-risk patient for primary prevention: Executive summary. Circulation. 2000; 101(1):111-6. [DOI:10.1161/01.cir.101.1.111] [PMID]
  22. Duncan HF, Pitt Ford TR. The potential association between smoking and endodontic disease. Int Endod J. 2006; 39(11):843-54. [DOI:10.1111/j.1365-2591.2006.01141.x] [PMID]
  23. Kirkevang L-L, Wenzel A. Risk indicators for apical periodontitis. Community Dent Oral Epidemiol. 2003; 31(1):59-67. [DOI:10.1034/j.1600-0528.2003.00032.x] [PMID]
  24. Orstavik D, Kerekes K, Eriksen HM. The periapical index: A scoring system for radiographic assessment of apical periodontitis. Endod Dent Traumatol. 1986; 2(1):20-34. [DOI:10.1111/j.1600-9657.1986.tb00119.x] [PMID]
  25. Johnson GK, Guthmiller JM. The impact of cigarette smoking on periodontal disease and treatment. Periodontol. 2007; 44(1):178-94. [PMID]
  26. Pinto JR, Bosco AF, Okamoto T, Guerra JB, Piza IG. Effects of nicotine on the healing of extraction sockets in rats. A histological study. Braz Dent J. 2002; 13(1):3-9. [PMID]
  27. Bergstrom J. Periodontitis and smoking: An evidence-based appraisal. J Evid Based Dent Pract. 2006; 6(1):33-41. [DOI:10.1016/j.jebdp.2005.12.018] [PMID]
Johnson GK, Hill M, Cigarette smoking and the periodontal patient. J Periodontol. 2004; 75(2):196-209. [PMID]
  1. Labriola A, Needleman I, Moles DR. Systematic review of the effect of smoking on nonsurgical periodontal therapy. Periodontol 2000. 2005; 37:124-37. [PMID]
  2. Cesar Neto JB, Rosa EF, Pannuti CM, Romito GA. Smoking and periodontal tissues: A review. Braz Oral Res. 2012; 26(S 1):25-31. [DOI:10.1590/S1806-83242012000700005] [PMID]
  3. César-Neto JB, Benatti BB, Sallum EA, Casati MZ, Nociti Jr FH. The influence of cigarette smoke inhalation and its cessation on the tooth-supporting alveolar bone: A histometric study in rats. J Periodontal Res. 2006; 41(2):118-23. [DOI:10.1111/j.1600-0765.2005.00844.x] [PMID]
  4. Bahammam LA. Tobacco smoking and dental periapical condition in a sample of Saudi Arabian sub-population. J King Abdulaziz Univ Med Sci. 2012; 19(1):35-41. [DOI:10.4197/Med.19-1.3]
  5. Segura-Egea JJ, Jiménez-Pinzón A, Ríos-Santos JV, Velasco-Ortega E, Cisneros-Cabello R, Poyato-Ferrera MM. High prevalence of apical periodontitis amongst smokers in a sample of Spanish adults. Int Indod J. 2008; 41(4):310-6. [DOI:10.1111/j.1365-2591.2007.01365.x] [PMID]
  6. Axelsson P, Paulander J, Lindhe J. Relationship between smoking and dental status in 35, 50, 65, and 75-year-old individuals. J Clin Periodontol. 1998; 25(4):297-305. [DOI:10.1111/j.1600-051X.1998.tb02444.x] [PMID]
  7. Segura-Egea JJ, Castellanos-Cosano L, Velasco-Ortega E, Ríos-Santos JV, Llamas-Carreras JM, Machuca G, et al. Relationship between smoking and endodontic variables in hypertensive patients. J Endod. 2011; 37(6):764-7. [DOI:10.1016/j.joen.2011.03.004] [PMID]
  8. Krall JE, Garvey A, Garcia R. Alveolar bone loss and tooth loss in male cigar and pipe smokers. J Am Dent Assoc. 2008; 130(1):57-64. [DOI:10.14219/jada.archive.1999.0029] [PMID]
  9. Moszczynski P, Żabiński Z, Rutowski J, Słowiński S, TabarowskiZ. Immunological findings in cigarette smokers. Toxicol Lett. 2001; 118(3):121-7. [DOI:10.1016/S0378-4274(00)00270-8]
  10. Hirsch JM, Livian G, Edward S, Noren JG. Tobacco habits among teenagers in the city of Göteborg, Sweden, and possible association with dental caries. Swed Dent J. 1991; 15(3):117-23. [PMID]
  11. Asikainen S, Alaluusua S. Bacteriology of dental infections. Eur Heart J. 1993; 14(S K):43-50. [PMID]
  12. Graunaite I, Lodiene G, Maciulskiene V. Pathogenesis of apical periodontitis: A literature review. J Oral Maxillofac Res. 2012; 2(4):e1. [DOI:10.5037/jomr.2011.2401] [PMID] [PMCID]
  13. Cotti E, Mercuro G, Apical periodontitis and cardiovascular diseases: Previous findings and ongoing research. Int Endod J. 2015; 48(10):926-32. [DOI:10.1111/iej.12506] [PMID]
  14. Tsai P, Torabinejad M, Rice D, Azevedo. Accuracy of cone-beam computed tomography and periapical radiography in detecting small periapical lesions. J Endod. 2012; 38(7):965-70. [DOI:10.1016/j.joen.2012.03.001] [PMID]
  15. Ahlqwist M, Halling A, Hollender L. Rotational panoramic radiography in epidemiological studies of dental health. Comparison between panoramic radiographs and intraoral full mouth surveys. Swed Dent J. 2020; 10(1-2):73-84.
  16. Muhammed AH, Manson-Hing LR. A comparison of panoramic and intraoral radiographic surveys in evaluating a dental clinic population. Oral Surg. 1982; 54(1):108-17. [DOI:10.1016/0030-4220(82)90425-X]
  17. Liang YH, Jiang L, Gao XJ, Shemesh H, Wesselink PR, Wu MK. Detection and measurement of artificial periapical lesions by cone-beam computed tomography. Int Endod J. 2014; 47(4):332-8. [DOI:10.1111/iej.12148] [PMID]
  18. Dutra KL, Haas L, Porporatti AL, Flores-Mir C, Santos JN, Mezzomo LA, et al. Diagnostic accuracy of cone-beam computed tomography and conventional radiography on apical periodontitis: A systematic review and meta-analysis. J Endod. 2016; 42(3):356-64. [DOI:10.1016/j.joen.2015.12.015] [PMID]
  19. Peterson K, Hakansson R, Hakansson J, Olsson B, Wennberg A. Follow-up study of endodontic status in an adult Swed pop. Endod Dent Traumatol. 1991; 7(5):221-5. [DOI:10.1111/j.1600-9657.1991.tb00440.x] [PMID]

 
Type of Study: Original Atricle | Subject: Oral and Maxillofacial Medicine
Received: 2021/05/10 | Accepted: 2021/07/20

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