Etiology of Black Tooth Stain in Children

Overview

The aim of the present study was to investigate the relationship between the presence of black tooth stain (BS) and dental caries incidence, dental plaque scores and to examine the colonization of Streptococcus mutans, Lactobacillus spp., Actinomyces spp. and Capnocytophaga spp. in dental plaque samples with or without BS. The socioeconomic status of the family, the oral hygiene and dietary habits of the children, medical and dental history of the children were also compared between two groups.

Full Title of Study: “Evaluation of the Etiological Factors of Black Tooth Stain in Children”

Study Type

• Study Type: Observational
• Study Design
  • Time Perspective: Cross-Sectional
• Study Primary Completion Date: June 10, 2018

Detailed Description

A total of 1000 children aged 3-12 years who applied to the Department of Pedodontics, Faculty of Dentistry, Ege University for routine dental examination were enrolled the study. From these group, children with BS (n=44) were selected as the study group. With the same number of the study group, with the same age and same sex, children without BS (n=44) were categorized as the control group. The parents were interviewed based on a structured questionnaire including questions on the socioeconomic status of the family, the oral hygiene and dietary habits of the children, medical and dental history of the children. The presence and grading of BS, dental caries incidence and dental plaque index scores were recorded by the same pediatric dentist (G.İ.). Dental examinations of the children were conducted under natural light with the aid of a dental mirror and explorer. Dental caries scores were recorded according to WHO (World Health Organization) criteria using DMFT/DMFS (decay, missing, filled, tooth/surface in permanent teeth) and dmft/dmfs indices (decay, missing, filled, tooth/surface in primary teeth). All children were classified according to the DMFT/dmft scores; Group-1: caries active (dmft+DMFT≥1), Group-2: caries-free (dmft+DMFT=0). Dental plaque scores were recorded according to Silness & Löe index. The BS scores were classified according to Gasparetto et al. The plaque samples were dispersed in a vortex mixer to obtain a homogeneous suspension and cultivated on selective VCAT medium (Oxoid) for Capnocytophaga spp., mitis salivarius agar (Difco) with 15% sucrose (Difco) and 0.2 units/mL of bacitracin (Sigma, Sigma-Aldrich Co., St Louis, MO, USA) for S. mutans , MRS Agar was used for the isolation of lactobacilli spp. (ref) and Actinomyces Selective Agar was used for the isolation of Actinomyces spp. All data were analyzed by SPPS 25.0 (SPSS Statistics for Windows, Armonk, NY: IBM Corp.). In the analysis of data, t test and Mann Whitney-U test were used for the comparison of the two groups. Categorical data were analyzed by Fisher's Exact Test and chi square test. For the significance level of the tests, p<0.05 and p<0.01 were accepted.

Interventions

• Diagnostic Test: Microbiological evaluation of dental plaques with children with or without black tooth stain
  • Evaluation of the etiological factors of black tooth stain according to the questionnaire

Arms, Groups and Cohorts

• Group 1
  • Children with black tooth stain
• Group 2
  • Children without black tooth stain

Clinical Trial Outcome Measures

Primary Measures

• Salivary bacterial level
  • Time Frame: 6 months
  • Sample collection from dental plaque

Secondary Measures

• Dental caries experience
  • Time Frame: 6 months
  • The dental caries incidence of all patients were recorded according to the dfs, DMFS indices

Participating in This Clinical Trial

Inclusion Criteria

• Cooperative children with or without black tooth stain. – Children aged between 3-12 years old. Exclusion Criteria:

• Uncooperative children. – Children who had taken antibiotic therapy within 3 months prior to the dental plaque sampling and children with any systemic disease were not included to the study. – Children having oral disease (periodontitis, oral mucosal disease etc.) – Children having autoimmune disease. – Parents refuse to sign the consent.

Gender Eligibility: All

Minimum Age: 3 Years

Maximum Age: 12 Years

Investigator Details

• Lead Sponsor
  • Ege University
• Provider of Information About this Clinical Study
  • Principal Investigator: Dilsah Cogulu, Prof. Dr. – Ege University
• Overall Official(s)
  • Dilşah Çoğulu, Prof. Dr., Study Director, Ege University, Izmir, Turkey