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Pilot GWAS of caries in African-Americans shows genetic heterogeneity.
Orlova, E; Carlson, J C; Lee, M K; Feingold, E; McNeil, D W; Crout, R J; Weyant, R J; Marazita, M L; Shaffer, J R.
Affiliation
  • Orlova E; Department of Human Genetics, Pittsburgh, USA.
  • Carlson JC; Department of Biostatistics, Graduate School of Public Health, Pittsburgh, USA.
  • Lee MK; Center for Craniofacial and Dental Genetics, Dept. of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
  • Feingold E; Department of Human Genetics, Pittsburgh, USA.
  • McNeil DW; Department of Biostatistics, Graduate School of Public Health, Pittsburgh, USA.
  • Crout RJ; Center for Craniofacial and Dental Genetics, Dept. of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
  • Weyant RJ; Departments of Psychology, & Dental Practice and Rural Health, West Virginia University, Morgantown, USA.
  • Marazita ML; Department of Periodontics, School of Dentistry, West Virginia University, Morgantown, WV, USA.
  • Shaffer JR; Department of Dental Public Health and Information Management, Pittsburgh, USA.
BMC Oral Health ; 19(1): 215, 2019 09 18.
Article de En | MEDLINE | ID: mdl-31533690
ABSTRACT

BACKGROUND:

Dental caries is the most common chronic disease in the US and disproportionately affects racial/ethnic minorities. Caries is heritable, and though genetic heterogeneity exists between ancestries for a substantial portion of loci associated with complex disease, a genome-wide association study (GWAS) of caries specifically in African Americans has not been performed previously.

METHODS:

We performed exploratory GWAS of dental caries in 109 African American adults (age > 18) and 96 children (age 3-12) from the Center for Oral Health Research in Appalachia (COHRA1 cohort). Caries phenotypes (DMFS, DMFT, dft, and dfs indices) assessed by dental exams were tested for association with 5 million genotyped or imputed single nucleotide polymorphisms (SNPs), separately in the two age groups. The GWAS was performed using linear regression with adjustment for age, sex, and two principal components of ancestry. A maximum of 1 million adaptive permutations were run to determine empirical significance.

RESULTS:

No loci met the threshold for genome-wide significance, though some of the strongest signals were near genes previously implicated in caries such as antimicrobial peptide DEFB1 (rs2515501; p = 4.54 × 10- 6) and TUFT1 (rs11805632; p = 5.15 × 10- 6). Effect estimates of lead SNPs at suggestive loci were compared between African Americans and Caucasians (adults N = 918; children N = 983). Significant (p < 5 × 10- 8) genetic heterogeneity for caries risk was found between racial groups for 50% of the suggestive loci in children, and 12-18% of the suggestive loci in adults.

CONCLUSIONS:

The genetic heterogeneity results suggest that there may be differences in the contributions of genetic variants to caries across racial groups, and highlight the critical need for the inclusion of minorities in subsequent and larger genetic studies of caries in order to meet the goals of precision medicine and to reduce oral health disparities.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Hétérogénéité génétique / Caries dentaires / Étude d&apos;association pangénomique Limites: Adult / Animals / Child / Female / Humans / Male / Middle aged / Newborn Langue: En Journal: BMC Oral Health Sujet du journal: ODONTOLOGIA Année: 2019 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Hétérogénéité génétique / Caries dentaires / Étude d&apos;association pangénomique Limites: Adult / Animals / Child / Female / Humans / Male / Middle aged / Newborn Langue: En Journal: BMC Oral Health Sujet du journal: ODONTOLOGIA Année: 2019 Type de document: Article Pays d'affiliation: États-Unis d'Amérique