The goal of this R03 application is to identify markers for apical periodontitis (AP) in humans. AP represents a local immune response to the progression of microorganisms from an infected root canal space to the periapical area that results in bone resorption and affects ~27% of the general population. Recent studies have shown that genetic predisposition can contribute to an individual's susceptibility to developing AP, and that a complex signaling network operates in the determination of the nature and extent of AP progression, as well as the associated bone destructive process. Using traditional candidate gene discovery approaches, we have shown that common variants in matrix metalloproteinases, interleukins and heat shock protein genes were associated with AP. However, the genetic factors influencing apical periodontitis susceptibility have not yet been thoroughly investigated. To establish the role of genetic predisposition in the etiology of AP, in this proposal, we will perform a genome-wide association study to identify common genetic variants associated with AP risk on ~1,000 cases and controls with and without AP. We will validate the 10 top associated variants in an independent validation population, and will identify genetic risk signatures that may facilitate identification of individual predisposition to AP. Results from this study will help us understand genetic factors contributing to AP in humans, dramatically increasing knowledge of the condition and providing insights into the future development of therapeutic targets.

Public Health Relevance

Public Health Relevance Statement: Project Narrative. Apical periodontitis represents a local immune response to the progression of microorganisms from an infected root canal space to the periapical area that results in bone resorption. It affects ~27% of the general populations and if left untreated, may represent a chronic infection leading to potential systemic consequences. Importantly, a number of studies have reported on associations between AP and adverse cardiovascular outcomes, highlighting the need to identify genetic variants associated with AP. In this proposal, we will perform a genome-wide association study of apical periodontitis to delineate the genetic contributions to the condition. The proposed study is relevant to public health as it will identify targets for the development of future therapeutic agents and improve treatment outcomes and decrease treatment costs. The proposed research is relevant to Goal One of the NIDCR mission [Objective I-1: Integrate molecular, clinical, and population health approaches to improve diagnostics and optimize outcomes].

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Small Research Grants (R03)
Project #
5R03DE027494-02
Application #
9785491
Study Section
NIDR Special Grants Review Committee (DSR)
Program Officer
Wang, Lu
Project Start
2018-09-15
Project End
2020-08-31
Budget Start
2019-09-01
Budget End
2020-08-31
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Texas Health Science Center Houston
Department
Other Basic Sciences
Type
Schools of Dentistry/Oral Hygn
DUNS #
800771594
City
Houston
State
TX
Country
United States
Zip Code
77030