Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/54609
Type: Artigo
Title: Analysis of susceptibility polymorphisms for nonsyndromic cleft lip with or without cleft palate in the brazilian population
Author: De Aquino, S.N.
Messetti, A.C.
Hoshi, R.
Borges, A.
Viena, C.S.
Reis, S.R.A.
Swerts, M.S.O.
Graner, E.
Martelli-Junior, H.
Coletta, R.D.
Abstract: Background: Although genome-wide association studies have identified several susceptibility loci for nonsyndromic cleft lip with or without cleft palate (NSCL/P) in populations around the world, the role of most loci is unknown in the highly heterogeneous Brazilian population. Methods: To determine the association of 7 markers that showed genome-wide significant association in Brazilians with NSCL/P, we conducted a structured association study conditioned upon the individual ancestry proportions to evaluate markers at 1p36 (rs742071), 2p21 (rs7590268), 3p11.1 (rs7632427), 8q21.3 (rs12543318), 13q31.1 (rs8001641), 15q22.2 (rs1873147), and 17q22 (rs227731) in 505 patients with NSCL/P and 594 healthy controls recruited from 2 different geographical regions of Brazil. The polymorphisms were genotyped by TaqMan 5-exonuclease allelic discrimination assay, and each sample was independently typed for 40 biallelic short insertion/deletion markers to characterize the genomic ancestry. Results: After Bonferroni correction for multiple tests, significant associations with NSCL/P were observed for rs742071, rs1873147, and rs227731. However, the frequency of the risk alleles varied between the geographical regions, according to the proportions of European and African genomic ancestry. The group enriched by European ancestry showed significant association with rs227731 (p=0.001), whereas the group with high African ancestry was significantly associated with rs1873147 polymorphism (p=0.005). The significant association with rs742071 was only detected in the combined sample (p=0.005). Conclusion: The findings of the present study revealed the associations of 1p36 (rs742071), 15q22 (rs1873147), and 17p22 (rs227731) with NSCL/P in the Brazilian population, and further confirmed that the genetic heterogeneity of NSCL/P may be related to the different ethnic background of the affected individuals. Birth Defects Research (Part A) 100:36-42, 2014. (c) 2013 Wiley Periodicals, Inc.
Although genome-wide association studies have identified several susceptibility loci for nonsyndromic cleft lip with or without cleft palate (NSCL/P) in populations around the world, the role of most loci is unknown in the highly heterogeneous Brazilian p
Subject: Fenda labial
Polimorfismo de nucleotídeo único
Country: Estados Unidos
Editor: John Wiley & Sons
Citation: Birth Defects Research Part A-clinical And Molecular Teratology. Wiley-blackwell, v. 100, n. 1, n. 36, n. 42, 2014.
Rights: fechado
Fechado
Identifier DOI: 10.1002/bdra.23204
Address: https://onlinelibrary.wiley.com/doi/abs/10.1002/bdra.23204
Date Issue: 2014
Appears in Collections:FOP - Artigos e Outros Documentos

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