Correlation between periodontal pocket depth and red complex bacteria among tobacco user

https://doi.org/10.53730/ijhs.v6nS2.6561

Authors

  • Aarti Charokar Ph.D. Scholar, Department of Microbiology, RKDF Dental College & Research Centre, Bhopal (MP)
  • Abhishek Gupta Ph.D. Guide, SRK University, Bhopal (MP)
  • Vikram Singh Professor, Department of Oral Medicine & Radiology, RKDF Dental College & Research Centre, Bhopal (MP)
  • Sakshi Sharma Associate Professor, Department of Oral Medicine & Radiology, RKDF Dental College & Research Centre, Bhopal (MP)
  • Ankur Singh Rajput Assistant Professor, Department of Periodontology, RKDF Dental College & Research Centre, Bhopal (MP)
  • Pallavi Goswami PG Student, Department of Periodontology, Babu Banarasi Das College of Dental Sciences, Lucknow (UP)

Keywords:

periodontitis, BANA test, tobacco user, probing depth

Abstract

Aims- The present study is to evaluate the presence of red complex microorganism and relation with the prevalence of anaerobic bacteria and corelation with pocket depth in Periodontitis among tobacco user. Materials and Methods- The BANA (N-benzoyl-DL-arginine-naphthylamide) test was used to analyze subgingival microbiota. 400 subject age between 20-55 enrolled in this study, subject divided into three groups Tobacco Chewers, Tobacco Smokers, Both chewers and smokers and Non tobacco user. Result – The present study compared the subject with BANA test and pocket depth, the study shows tobacco smokers had deep pocket in comparison to other subject, which concluded that tobacco smokers show greater destruction of periodontium. Conclusion- Tobacco is harmful substance either it is used in any form (Chewing and Smoking), but study clearly indicate tobacco smoking are responsible for more destruction of Periodontium. The tobacco cessation programme should be implemented to prevent periodontitis and smoking prevention should be done by health education.

Downloads

Download data is not yet available.

References

Socransky SS, Haffajee AD., Cugini , M.A., Smith, C.& Kent, R.L. Jr.(1998). Microbial complexes in subgingival plaque. Journal of Clinical Microbiology, Vol.25 (No.2):134-144

Bollen C.M.L., Vandekerckhove B.N.A., Papaioannon W., Vaneldere J.,Quirynen M.(1996). Full–versus partial mouth disinfection in treatment of periodontal infections. A pilot study, long term microbiological observation. J. Clin. Periodontal Vol. 23:960-970.

Samaranayake L.(2006). Essential Microbiology for Dentistry, Churchill Livingstone Company, London: 275.

MooreW.E.C., Moore L.V.H (1994) The bacteria of periodontal disease. Periodontology 2000 Vol. 5: 66-77.

Bergstrom ,J.(1989) Cigarette smoking as risk factor in chronic periodontal disease. Community Dentistry and Oral Epidemiology, 17, 245-247.

Bergstrom, J., Eliasson, S. and Dock, J. (2000) Exposure to tobacco smoking and periodontal health. Journal of Clinical periodontology,27,61-68.

Grossi SG, Zambon JJ, Hov AW, Koch G, Dunford RG, Machtei EE et al. Assessment of risk for periodontal disease. Ris indicators for attachment loss. J Perio 1994; 65:260-267.

Haffajee AD, Socransky SS Relationship of cigarette smoking to attachment level profiles. J Clin perio 2001 28. 283-295

Loesche WJ: The identification of bacteria associated with periodontal disease and dental caries by enzymatic methods. Oral Microbial Immunol 1 : 1-6 1986.

Loesche WJ, Syed SA, Schmidt E, Morrison EC: Bacterial profiles of subgingival plaques in periodontitis. J Periodontal 56: 447-456, 1985.

Loesche WJ, Lopatin DE, Giordano J, Alcoforado G, Hujoel P. Comparision of the benzoyl-DL-arginine-naphthylamide (BANA) test, DNA probes, and immunological reagents for ability to detect anaerobic periodontal infections due to Porphyromonas gingivalis, Treponema denticola and Bacteroides forsythus. J.ClinMicrobiol. 1992 Feb; 30 (2): 427-33

Bretz WA, Eklund SA, Radicchi R, Schork MA, Schork N, Scottenfeld D, et al. The use of a rapid enzymatic assay in the field for the detection of infections associated with adult periodontitis. J public Health Dent. 1993 Dec; 53(4): 235-40

Takaishi Y, Morri H. Miki T. The benzoyl – DL arginine-naphthylamide (BANA) test and polymerase chain reaction measurement of pathogenic bacteria can assess the severity of periodontal disease. Int J Tissue React. 2003;25(1) :19-24.

C. Kazor, G. W. Taylor, and W. J. Loesche, “The prevalence of BANA-hydrolyzing periodontopathic bacteria in smokers,” Journal of Clinical Periodontology, vol. 26, no. 12, pp. 814–821, 1999.

Loesche WJ, Bretz WA, Kerschensteiner D, Stoll J, Socransky SS, Hujoel P, et al. Development of a diagnostic test for anaerobic periodontal infections based on plaque hydrolysis of benzoyl‑DL‑arginine‑naphthylamide. J Clin Microbiol1990;28:1551‑9.

Kamma JJ, NakouM, Baehni PC. Clinical and microbiological characteristics of smokers with early onset periodontitis. J Perio Res 1999; 34: 25 – 33.

Preber H, Bergstrom J, Linder LE: Occurrence of periopathogens in smoker and non-smoker patients. J Clin Periodontol 1992, 19(9 Pt1):667-671.

Hamdoon SM, Abdul Rahman Gh Y. Prevalence of Anaerobic Bacteria in Periodontitis in Relation to Pocket Depth Al- Rafidain Dent J. 2014; 14(2):320-328

Michiya Kubota1,2, Mariko Tanno-Nakanishi2, Satoru Yamada2, Effect of smoking on subgingival microflora of patients with periodontitis in Japan, BMC Oral Health 2011, 11:1.

Anil S, Hari S, Vijaykumar T. “Periodontal conditions of a selected population in Trivandrum district, Kerala, India”. Community dental oral epidemiology,1990; 18:325.

Published

25-04-2022

How to Cite

Charokar, A., Gupta, A., Singh, V., Sharma, S., Rajput, A. S., & Goswami, P. (2022). Correlation between periodontal pocket depth and red complex bacteria among tobacco user. International Journal of Health Sciences, 6(S2), 6023–6028. https://doi.org/10.53730/ijhs.v6nS2.6561

Issue

Section

Peer Review Articles

Most read articles by the same author(s)