Abstract | BACKGROUND: There is evidence for a genetic contribution to chronic periodontitis. In this study, we conducted a genome wide association study among 866 participants of the University of Pittsburgh Dental Registry and DNA Repository, whose periodontal diagnosis ranged from healthy (N = 767) to severe chronic periodontitis (N = 99). METHODS: Genotypingi of over half-million single nucleotide polymorphisms was determined. Analyses were done twice, first in the complete dataset of all ethnicities, and second including only samples defined as self-reported Whites. From the top 100 results, twenty single nucleotide polymorphisms had consistent results in both analyses (borderline p-values ranging from 1E-05 to 1E-6) and were selected to be tested in two independent datasets derived from 1,460 individuals from Porto Alegre, and 359 from Rio de Janeiro, Brazil. Meta-analyses of the Single nucleotide polymorphisms showing a trend for association in the independent dataset were performed. RESULTS: The rs1477403 marker located on 16q22.3 showed suggestive association in the discovery phase and in the Porto Alegre dataset (p = 0.05). The meta-analysis suggested the less common allele decreases the risk of chronic periodontitis. CONCLUSIONS: Our data offer a clear hypothesis to be independently tested regarding the contribution of the 16q22.3 locus to chronic periodontitis.
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Authors | Ping Feng, Xiaojing Wang, Priscila L Casado, Erika C Küchler, Kathleen Deeley, Jacqueline Noel, Hyongsup Kimm, Ji-Hye Kim, Alex N Haas, Valquiria Quinelato, Leticia L Bonato, Jose M Granjeiro, Cristiano Susin, Alexandre R Vieira |
Journal | BMC oral health
(BMC Oral Health)
Vol. 14
Pg. 84
(Jul 09 2014)
ISSN: 1472-6831 [Electronic] England |
PMID | 25008200
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Alleles
- Chromosome Mapping
- Chromosomes, Human, Pair 16
(genetics)
- Chromosomes, Human, Pair 21
(genetics)
- Chronic Periodontitis
(ethnology, genetics)
- Diabetes Complications
- Ethnicity
(genetics)
- Female
- Gene Frequency
(genetics)
- Genetic Markers
(genetics)
- Genetic Predisposition to Disease
(genetics)
- Genetic Variation
(genetics)
- Genome-Wide Association Study
- Genotype
- Humans
- Male
- Middle Aged
- Polymorphism, Single Nucleotide
(genetics)
- Risk Factors
- Smoking
- White People
(genetics)
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