Portal de Periódicos da CAPES

Artigo Produção Nacional Revisado por pares

BIBTEX RIS

A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population

2015; Elsevier BV; Volume: 44; Issue: 1 Linguagem: Inglês

10.1016/j.jcms.2015.07.026

1878-4119

Tânia Kawasaki de Araujo, Rodrigo Secolin, Têmis Maria Félix, Liliane Todeschini de Souza, Marshall Ítalo Barros Fontes, Isabella Lopes Monlleó, Josiane Souza, Agnes Cristina Fett‐Conte, Erlane Marques Ribeiro, Ana C. Xavier, Adriana Augusto de Rezende, Milena Simioni, Ândrea Ribeiro‐dos‐Santos, Sidney Emanuel Batista dos Santos, Vera Lúcia Gil‐da‐Silva‐Lopes,

dental development and anomalies

The aim of this study was to use the TaqMan OpenArray system to evaluate associations between 39 genes and the etiology of nonsyndromic cleft lip and palate (NSCLP) in a Brazilian population.This case-control association study was designed with 80.11% statistical power according to logistic regression (GPOWER software). The case group had 182 patients with NSCLP enrolled in the Brazilian Database on Orofacial Clefts. The controls included 355 healthy individuals with no history of oral clefting in the past three generations. All samples were genotyped for 253 tag single nucleotide polymorphisms (tagSNPs) in 39 genes, including two that had recently been associated with this process. The association analysis was performed using logistic regression and stepwise regression. The results were corrected for multiple testing [Bonferroni correction and False Discovery Rate (FDR)].Twenty-four SNPs in 16 genes were significantly associated with the etiology of NSCLP, including MSX1, SPRY1, MSX2, PRSS35, TFAP2A, SHH, VAX1, TBX10, WNT11, PAX9, BMP4, JAG2, AXIN2, DVL2, KIF7, and TCBE3. Stepwise regression analysis revealed that 11 genes contributed to 15.5% of the etiology of NSCLP in the sample.This is the first study to associate KIF7 and TCEB3 with the etiology of NSCLP. New technological approaches using the same design should help to identify further etiological susceptibility variants.