Project 1 seeks to evaluate the effect of an antimicrobial agent applied to the mother's with the aim of reducing her levels of mutans streptococci M(MS) which, in turn, will decrease the likelihood of vertical transmission of MS to her infant. Our experience from a five year randomized trial (MITS) suggests the optimum time period for the applications of an agent so as to have an impact on the vertical transmission of MS. Previous studies provide sufficient information on the optimal concentration of chlorhexidine, an effective method of its delivery, and its efficacy in reducing oral MS levels. Total elimination or reduction of maternal oral MS over a time period should result in either; 1) a complete prevention of MS transmission or, 2) a lower degree of MS transmission or, 3) a delayed transmission of MS from mother to child. This in turn could result in a lower caries incidence in the child. In order to test the above hypotheses, a randomized active versus no treatment controlled clinical trial is proposed. Assuming the proportion of children with detectable levels of MS at 2 years of age is 16% in the treatment group, a total of 51 children are needed per group. To account for potential losses, a total of 64 infants will be included in each group. The trial will test the following two hypotheses: 1) The application of the treatment agent to the mothers dentition at 3 months intervals from six months (generally prior to the time of the child's first tooth emergence) until the second birthday of the child will result in having a larger proportion of children with undetectable levels of oral MS in saliva samples in the treatment group compared to the untreated control group, and 2) The application of the treatment agent to the mothers dentition at 3 months intervals from the time of the child's first tooth emergence until the third birthday of the child will result in a decrease incidence of dental caries in children in the treatment group compared to the untreated control group. The treatment agent we will use is a combination of chlorhexidine and Sumatara benzoin. A layer of this varnish applied to all surfaces of teeth after a dental prophylaxis will be covered by another layer of polyurethane sealant in order to achieve sustained release and to prevent the bitter taste of chlorhexidine. Treatment mothers will be given new tooth brushes after each treatment to prevent a possible source of re- colonization, namely the old tooth brushes. Precautions will be taken to prevent lactating or pregnant mothers from being exposed to these agents. Basic demographic, oral bacteriological, medical, dental, and prenatal and post natal nutritional data will be collected and immunological profiles of mother-child pairs will be evaluated. These data would be analyzed to study the natural history of MS colonization as well as to evaluate the effectiveness of the therapeutic intervention. The proposed study is conducted among a group of subjects who belong to a population sub group who is at high risk for caries or who suffer the consequences of caries most. Despite one hundred years of research, dental caries still impact heavily on the nation and its economy, and if the proposed approach of preventing tooth decay succeeds, it would have major implications.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Specialized Center (P50)
Project #
5P50DE011147-05
Application #
6104899
Study Section
Project Start
1998-09-30
Project End
2002-09-29
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
5
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
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