Association of Early Childhood Caries with Bitter Taste Receptors: A Meta-Analysis of Genome-Wide Association Studies and Transcriptome-Wide Association Study.


Journal

Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097

Informations de publication

Date de publication:
24 12 2022
Historique:
received: 19 11 2022
revised: 14 12 2022
accepted: 17 12 2022
entrez: 21 1 2023
pubmed: 22 1 2023
medline: 25 1 2023
Statut: epublish

Résumé

Although genetics affects early childhood caries (ECC) risk, few studies have focused on finding its specific genetic determinants. Here, we performed genome-wide association studies (GWAS) in five cohorts of children (aged up to 5 years, total N = 2974, cohorts: Center for Oral Health Research in Appalachia cohorts one and two [COHRA1, COHRA2], Iowa Fluoride Study, Iowa Head Start, Avon Longitudinal Study of Parents and Children [ALSPAC]) aiming to identify genes with potential roles in ECC biology. We meta-analyzed the GWASs testing ~3.9 million genetic variants and found suggestive evidence for association at genetic regions previously associated with caries in primary and permanent dentition, including the β-defensin anti-microbial proteins. We then integrated the meta-analysis results with gene expression data in a transcriptome-wide association study (TWAS). This approach identified four genes whose genetically predicted expression was associated with ECC (p-values < 3.09 × 10−6; CDH17, TAS2R43, SMIM10L1, TAS2R14). Some of the strongest associations were with genes encoding members of the bitter taste receptor family (TAS2R); other members of this family have previously been associated with caries. Of note, we identified the receptor encoded by TAS2R14, which stimulates innate immunity and anti-microbial defense in response to molecules released by the cariogenic bacteria, Streptococcus mutans and Staphylococcus aureus. These findings provide insight into ECC genetic architecture, underscore the importance of host-microbial interaction in caries risk, and identify novel risk genes.

Identifiants

pubmed: 36672800
pii: genes14010059
doi: 10.3390/genes14010059
pmc: PMC9858612
pii:
doi:

Types de publication

Meta-Analysis Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Wellcome Trust
ID : 217065/Z/19/Z
Pays : United Kingdom
Organisme : NIH HHS
ID : R01-DE014899
Pays : United States
Organisme : NIH HHS
ID : 1-U01-DE018903
Pays : United States
Organisme : NIH HHS
ID : X01-HG009878
Pays : United States
Organisme : NIH HHS
ID : P30-DE10126
Pays : United States
Organisme : NIH HHS
ID : R01-DE09551
Pays : United States
Organisme : NIDCR NIH HHS
ID : U01 DE018903
Pays : United States

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Auteurs

Ekaterina Orlova (E)

Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA 15260, USA.

Tom Dudding (T)

Bristol Dental School, University of Bristol, Bristol BS1 2LY, UK.
Medical Research Council Integrative Epidemiology Unit, Department of Population Health Sciences, University of Bristol, Bristol BS8 1QU, UK.

Jonathan M Chernus (JM)

Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA 15260, USA.

Rasha N Alotaibi (RN)

Dental Health Department, College of Applied Medical Sciences, King Saud University, Riyadh 12372, Saudi Arabia.

Simon Haworth (S)

Bristol Dental School, University of Bristol, Bristol BS1 2LY, UK.
Medical Research Council Integrative Epidemiology Unit, Department of Population Health Sciences, University of Bristol, Bristol BS8 1QU, UK.

Richard J Crout (RJ)

Department of Periodontics, School of Dentistry, West Virginia University, Morgantown, WV 26505, USA.

Myoung Keun Lee (MK)

Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, University of Pittsburgh, Pittsburgh, PA 15261, USA.

Nandita Mukhopadhyay (N)

Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, University of Pittsburgh, Pittsburgh, PA 15261, USA.

Eleanor Feingold (E)

Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA 15260, USA.
Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, University of Pittsburgh, Pittsburgh, PA 15261, USA.

Steven M Levy (SM)

Department of Preventive & Community Dentistry, University of Iowa College of Dentistry, Iowa City, IA 52242, USA.

Daniel W McNeil (DW)

Department of Psychology & Department of Dental Public Health and Professional Practice, West Virginia University, Morgantown, WV 26505, USA.

Betsy Foxman (B)

Center for Molecular and Clinical Epidemiology of Infectious Diseases, Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.

Robert J Weyant (RJ)

Dental Public Health, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.

Nicholas J Timpson (NJ)

Medical Research Council Integrative Epidemiology Unit, Department of Population Health Sciences, University of Bristol, Bristol BS8 1QU, UK.
Avon Longitudinal Study of Parents and Children, University of Bristol, Bristol BS8 1QU, UK.

Mary L Marazita (ML)

Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA 15260, USA.
Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, University of Pittsburgh, Pittsburgh, PA 15261, USA.

John R Shaffer (JR)

Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA 15260, USA.
Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, University of Pittsburgh, Pittsburgh, PA 15261, USA.

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