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Dental Plaque Microbiota in Caries-free and Caries-active Children

Completed
Conditions
Caries
Plaque
Interventions
Other: Plaque from each subject will be collected but there will be no intervention
Registration Number
NCT03906981
Lead Sponsor
Kuwait University
Brief Summary

Dental caries is a polymicrobial infection originally thought to be caused by Streptococcus mutans and Lactobacilli. However, unprecedented developments in modern molecular techniques have demonstrated that several microbial species are associated with the disease in addition to streptococci and lactobacilli. Dental caries initiation and progression is a dynamic process in which demineralization of the tooth structure, as a result of acid production from acidogenic bacteria (due to carbohydrate metabolism) is being counteracted by the remineralization of the tooth surface by strong alkali production by certain bacteria in the dental biofilm. The aim of the present study is to identify the different microbiota in the oral biofilm using new laboratory techniques as well as the levels of salivary proteins in caries-free compared with caries active Arab children.

Detailed Description

The objective of this study will be to investigate the dental plaque's microbial diversity using Human Oral Microbe Identification using Next Generation Sequencing (HOMINGS) technology in the mixed dentition as well as the levels of salivary proteins in caries-free compared with caries active Arab children. The study protocol was approved by the Health Science Center Ethical Committee at Kuwait University.

One hundred 6-9 year-old children with caries active and caries-free status will be recruited from randomly selected public schools in Kuwait. After DNA purification from supragingival plaque samples, HOMINGS will be performed. To get an insight into the host factors involved in this complex interplay between the host and the bacteria, stimulated saliva from the study subjects will be analyzed by proteomics. For children in both groups supragingival plaque samples will be collected from the buccal and lingual surfaces of all teeth. After preparing the samples, the aliquots of purified DNA samples will be shipped to The Forsyth Institute for Human Oral Microbe Identification using Next Generation Sequencing (HOMINGS) protocol.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
120
Inclusion Criteria
  • Arab 6-9 year old children
  • Healthy
  • Caries free, dmft/DMFT=0
  • Caries Active: dmft/DMFT>5
Exclusion Criteria
  • Children with a systemic disease or any drug use that could affect the microflora of the oral cavity or the salivary gland functions
  • History of salivary gland diseases
  • Those who received antibiotic therapy during the last 3 months
  • Children with severe localized or generalized periodontitis.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Caries freePlaque from each subject will be collected but there will be no intervention6-9 year old caries free children
Caries activePlaque from each subject will be collected but there will be no intervention6-9 year-old caries active (\>5 dmft/DMFT) children
Primary Outcome Measures
NameTimeMethod
Dental plaque microbiota profile2 months

Identification of dental plaque microbiota profile using HOMINGS

Secondary Outcome Measures
NameTimeMethod
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