RSS-Feed abonnieren
![](/products/assets/desktop/img/oa-logo.png)
DOI: 10.4103/ejd.ejd_99_17
Correlation of environmental tobacco smoke to gingival pigmentation and salivary alpha amylase in young adults
Publikationsverlauf
Publikationsdatum:
25. September 2019 (online)
![](https://www.thieme-connect.de/media/10.1055-s-00042133/201703/lookinside/thumbnails/10-4103-ejd-ejd_99_17_00364-1.jpg)
ABSTRACT
Objective: Passive smoking leads to melanin pigmentation on gingiva. However, documentation of gingival pigmentation and salivary amylase activity in passive smokers relative to the duration of exposure to environmental tobacco smoke (ETS), is incomplete and requires further investigation. Thus, this study aimed to assess effects of ETS exposure on gingival pigmentation in young adults. In addition, to correlate a number of years of exposure to an extent, the intensity of gingival pigmentation and salivary amylase activity. Materials and Methods: A total of 200 nonsmokers aged 18–35 years with a positive history of ETS exposure were recruited for the study. Duration and source of ETS were assessed using a questionnaire. Gingival pigmentation was assessed using gingival pigmentation index for the extent and Dummett oral pigmentation index for intensity. The skin color of all patients was also assessed. Pearson Chi-square test and one-way ANOVA was used to statistically analyze the data. Results: Number of years of exposure to passive smoking was highly significant to the extent and intensity of gingival pigmentation (P < 0.001). ETS from home environment was highly significant to the intensity of pigmentation. Environmental sources of ETS contributed to pigmentation as the majority of patients reported exposure from vehicles and workplace. The salivary amylase levels were inversely proportional to the duration of exposure to ETS. Conclusion: Within limitations of this cross-sectional observational study, it was concluded that there was a strong correlation between ETS exposure and gingival pigmentation. Duration of exposure was significant to an extent, the intensity of pigmentation and salivary amylase activity.
-
REFERENCES
- 1 Jarvis M, Tunstall-Pedoe H, Feyerabend C, Vesey C, Salloojee Y. Biochemical markers of smoke absorption and self reported exposure to passive smoking. J Epidemiol Community Health 1984; 38: 335-9
- 2 Multani S. Interrelationship of smoking, lip and gingival melanin pigmentation, and periodontal status. Addict Health 2013; 5: 57-65
- 3 Hanioka T, Tanaka K, Ojima M, Yuuki K. Association of melanin pigmentation in the gingiva of children with parents who smoke. Pediatrics 2005; 116: 186-90
- 4 Eisen D. Disorders of pigmentation in the oral cavity. Clin Dermatol 2000; 18: 579-87
- 5 Unsal E, Paksoy C, Soykan E, Elhan AH, Sahin M. Oral melanin pigmentation related to smoking in a Turkish population. Community Dent Oral Epidemiol 2001; 29: 272-7
- 6 Hedin CA, Larsson A. The ultrastructure of the gingival epithelium in smokers' melanosis. J Periodontal Res 1984; 19: 177-90
- 7 Araki S, Murata K, Ushio K, Sakai R. Dose-response relationship between tobacco consumption and melanin pigmentation in the attached gingiva. Arch Environ Health 1983; 38: 375-8
- 8 Tadakamadla J, Kumar S, Nagori A, Tibdewal H, Duraiswamy P, Kulkarni S. Effect of smoking on oral pigmentation and its relationship with periodontal status. Dent Res J (Isfahan) 2012; 9 (Suppl. 01) 112-4
- 9 Haresaku S, Hanioka T, Tsutsui A, Watanabe T. Association of lip pigmentation with smoking and gingival melanin pigmentation. Oral Dis 2007; 13: 71-6
- 10 Hajifattahi F, Azarshab M, Haghgoo R, Lesan S. Evaluation of the relationship between passive smoking and oral pigmentation in children. J Dent (Tehran) 2010; 7: 119-23
- 11 Sridharan S, Ganiger K, Satyanarayana A, Rahul A, Shetty S. Effect of environmental tobacco smoke from smoker parents on gingival pigmentation in children and young adults: A cross-sectional study. J Periodontol 2011; 82: 956-62
- 12 Madhani SM, Thomas B. Evaluation of gingival pigmentation in children exposed to and not exposed to environmental tobacco smoke. SRM J Res Dent Sci 2014; 5: 21-5
- 13 Moravej-Salehi E, Moravej-Salehi E, Hajifattahi F. Relationship of gingival pigmentation with passive smoking in women. Tanaffos 2015; 14: 107-14
- 14 Granger DA, Blair C, Willoughby M, Kivlighan KT, Hibel LC, Fortunato CK. et al. Individual differences in salivary cortisol and alpha-amylase in mothers and their infants: Relation to tobacco smoke exposure. Dev Psychobiol 2007; 49: 692-701
- 15 Avsar A, Darka O, Bodrumlu EH, Bek Y. Evaluation of the relationship between passive smoking and salivary electrolytes, protein, secretory IgA, sialic acid and amylase in young children. Arc Oral Biol 2009; 54: 457-63
- 16 Rinderknecht H, Wilding P, Haverback BJ. A new method for the determination of alpha-amylase. Experientia 1967; 23: 805
- 17 Hedin CA. Smokers' melanosis. Occurrence and localization in the attached gingiva. Arch Dermatol 1977; 113: 1533-8
- 18 Dummett CO, Gupta OP. The DOPI assessment in gingival pigmentation. J Dent Res 1966; 45: 122
- 19 Ponnaiyan D, Jegadeesan V, Perumal G, Anusha A. Correlating skin color with gingival pigmentation patterns in South Indians – A cross sectional study. Oral Health Dent Manag 2014; 13: 132-6
- 20 Sreeja C, Ramakrishnan K, Vijayalakshmi D, Devi M, Aesha I, Vijayabanu B. Oral pigmentation: A review. J Pharm Bioallied Sci 2015; 7 (Suppl. 02) 403-8
- 21 Aurrekoetxea JJ, Murcia M, Rebagliato M, Guxens M, Fernández-Somoano A, López MJ. et al. Second-hand smoke exposure in 4-year-old children in Spain: Sources, associated factors and urinary cotinine. Environ Res 2016; 145: 116-25
- 22 Cicciù M, Herford AS, Cervino G, Troiano G, Lauritano F, Laino L. Tissue fluorescence imaging (VELscope) for quick non-invasive diagnosis in oral pathology. J Craniofac Surg 2017; 28: 112-5