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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

2p24.2 (rs7552) is a susceptibility locus for nonsyndromic cleft lip with or without cleft palate in the Brazilian population

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Autor(es):
Machado, R. A. [1] ; Nogueira, E. N. [1] ; Martelli-Junior, H. [2, 3] ; Reis, S. R. [4] ; Persuhn, D. C. [5] ; Coletta, R. D. [1]
Número total de Autores: 6
Afiliação do(s) autor(es):
[1] Univ Estadual Campinas, Sch Dent, Dept Oral Diag, Piracicaba, SP - Brazil
[2] Univ Estadual Montes Claros, Dent Sch, Stomatol Clin, Montes Claros, MG - Brazil
[3] Univ Jose Rosario Vellano, Dent Sch, Ctr Rehabil Craniofacial Anomalies, Alfenas, MG - Brazil
[4] Bahiana Sch Med & Publ Hlth, Dept Basic Sci, Salvador, BA - Brazil
[5] Univ Fed Paraiba, Mol Biol Dept, Joao Pessoa, Paraiba - Brazil
Número total de Afiliações: 5
Tipo de documento: Artigo Científico
Fonte: Clinical Genetics; v. 93, n. 6, p. 1199-1204, JUN 2018.
Citações Web of Science: 2
Resumo

The population of Brazil is highly admixed, with each individual showing variable levels of Amerindian, European and African ancestry, which may interfere in the genetic susceptibility of known risk loci to nonsyndromic cleft lip with or without cleft palate (NSCL +/- P). Here, we investigated 5 reported genome-wide loci for NSCL +/- P in an ancestry-structured case-control study containing 1697 Brazilian participants (831 NSCL +/- P and 866 healthy controls). SNPs rs7552 in 2q24.2, rs8049367 in 16p13.3, rs1880646, rs7406226, rs9891446 in 17p13, rs1588366 in 17q23.2 and rs73039426 in 19q13.11 were genotyped using TaqMan allelic discrimination assays and genomic ancestry was estimated using a panel of 40 biallelic short insertion/deletion polymorphic markers informative of the Brazilian population. Logistic regression analysis of the single-markers revealed rs7552 in 2p24.2 as a susceptibility risk marker for NSCL +/- P, yielding an odds ratio (OR) of 1.71 (95% confidence interval (CI): 1.31-2.24, P = 9 x 10(-6)) in the homozygous state. Several SNP-SNP interactions containing rs7552 reached significance after adjustment for multiple tests (both Bonferroni assumption and 1000 permutation test), with the most significant interaction involving the 3-loci among rs7552, rs9891446 and rs73039426 (P = 6.1 x 10(-9) and p(1000 permutation) = 0.001). Our study is the first to support the association of rs7552 in 2p24.2 with NSCL +/- P in the highly admixed Brazilian population. (AU)

Processo FAPESP: 16/02667-0 - Interações entre Fatores Ambientais e Polimorfismos em Genes Relacionados ao Estresse Oxidativo na Suscetibilidade das Fissuras Orais Não-Sindrômicas
Beneficiário:Ricardo Della Coletta
Modalidade de apoio: Auxílio à Pesquisa - Regular