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Genome wide association scan for chronic periodontitis implicates novel locus

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 sever...

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Autores principales: Feng, Ping, Wang, Xiaojing, Casado, Priscila L, Küchler, Erika C, Deeley, Kathleen, Noel, Jacqueline, Kimm, Hyongsup, Kim, Ji-Hye, Haas, Alex N, Quinelato, Valquiria, Bonato, Leticia L, Granjeiro, Jose M, Susin, Cristiano, Vieira, Alexandre R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4096424/
https://www.ncbi.nlm.nih.gov/pubmed/25008200
http://dx.doi.org/10.1186/1472-6831-14-84
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author Feng, Ping
Wang, Xiaojing
Casado, Priscila L
Küchler, Erika C
Deeley, Kathleen
Noel, Jacqueline
Kimm, Hyongsup
Kim, Ji-Hye
Haas, Alex N
Quinelato, Valquiria
Bonato, Leticia L
Granjeiro, Jose M
Susin, Cristiano
Vieira, Alexandre R
author_facet Feng, Ping
Wang, Xiaojing
Casado, Priscila L
Küchler, Erika C
Deeley, Kathleen
Noel, Jacqueline
Kimm, Hyongsup
Kim, Ji-Hye
Haas, Alex N
Quinelato, Valquiria
Bonato, Leticia L
Granjeiro, Jose M
Susin, Cristiano
Vieira, Alexandre R
author_sort Feng, Ping
collection PubMed
description 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: Genotyping(i) 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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spelling pubmed-40964242014-07-15 Genome wide association scan for chronic periodontitis implicates novel locus Feng, Ping Wang, Xiaojing Casado, Priscila L Küchler, Erika C Deeley, Kathleen Noel, Jacqueline Kimm, Hyongsup Kim, Ji-Hye Haas, Alex N Quinelato, Valquiria Bonato, Leticia L Granjeiro, Jose M Susin, Cristiano Vieira, Alexandre R BMC Oral Health Research Article 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: Genotyping(i) 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. BioMed Central 2014-07-09 /pmc/articles/PMC4096424/ /pubmed/25008200 http://dx.doi.org/10.1186/1472-6831-14-84 Text en Copyright © 2014 Feng et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Feng, Ping
Wang, Xiaojing
Casado, Priscila L
Küchler, Erika C
Deeley, Kathleen
Noel, Jacqueline
Kimm, Hyongsup
Kim, Ji-Hye
Haas, Alex N
Quinelato, Valquiria
Bonato, Leticia L
Granjeiro, Jose M
Susin, Cristiano
Vieira, Alexandre R
Genome wide association scan for chronic periodontitis implicates novel locus
title Genome wide association scan for chronic periodontitis implicates novel locus
title_full Genome wide association scan for chronic periodontitis implicates novel locus
title_fullStr Genome wide association scan for chronic periodontitis implicates novel locus
title_full_unstemmed Genome wide association scan for chronic periodontitis implicates novel locus
title_short Genome wide association scan for chronic periodontitis implicates novel locus
title_sort genome wide association scan for chronic periodontitis implicates novel locus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4096424/
https://www.ncbi.nlm.nih.gov/pubmed/25008200
http://dx.doi.org/10.1186/1472-6831-14-84
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