Lack of association between delayed tooth emergence and single nucleotide polymorphisms in estrogen receptors

Autor(es):Mostrar menos -

Isabela Ribeiro Madalena ^[1] ; Caio Luiz Bitencourt Reis ^[2] ; Daniela Silva Barroso de Oliveira ^[3] ; Giovana Daniela Pecharki ^[4] ; Paula Cristina Trevilatto ^[5] ; Kesly Mary Ribeiro Andrades ^[6] ; Julia Carelli ^[7] ; Vinicius Laranjeira Barbosa da Silva ^[8] ; Flares Baratto-Filho ^[9] ; Erika Calvano Küchler ^[10] ; João Armando Brancher ^[11]

Afiliação do(s) autor(es):Mostrar menos -

^[1] University of São Paulo. School of Dentistry of Ribeirão Preto. Department of Pediatric Dentistry - Brasil

^[2] Federal University of Alfenas - Brasil

^[3] Federal University of Alfenas - Brasil

^[4] Federal University of Parana. Department of Community Health - Brasil

^[5] Pontifícia Universidade Católica do Paraná. School of Life Sciences - Brasil

^[6] Univille University. School of Dentistry - Brasil

^[7] Univille University. School of Dentistry - Brasil

^[8] Univille University. School of Dentistry - Brasil

^[9] Univille University. School of Dentistry - Brasil

^[10] University of São Paulo. School of Dentistry of Ribeirão Preto. Department of Pediatric Dentistry - Brasil

^[11] Pontifícia Universidade Católica do Paraná. School of Life Sciences - Brasil

• Tipo de documento: Artigo Científico
• Fonte: Brazilian Dental Journal; v. 32, n. 6, p. 107-114, 2022-01-05.

Resumo

Abstract The purpose of the study was to investigate the association between single nucleotide polymorphisms (SNPs) in genes encoding estrogen receptors (ESR1 and ESR2, respectively) and delayed tooth emergence (DTE). This cross-sectional study was composed of biological unrelated children of both sexes, age ranging from 11 to 13 years old. DTE was defined when the successor primary tooth was still present in the oral cavity after its exfoliation time or the absence of the permanent tooth emergence into the oral cavity. Children were diagnosed with DTE when they had at least one delayed permanent tooth, according to age of exfoliation of each tooth proposed by The American Dental Association. Genomic DNA from saliva was used to evaluate the SNPs in ESR1 (rs9340799 and rs2234693) and ESR2 (rs1256049 and rs4986938) using Real-Time PCR. Chi-square or Fisher exact tests and Logistic Regression adjusted by age and gender were performed. SNP-SNP interaction was accessed by multifactor dimensionality reduction (MDR) analysis also adjusted by gender and age. The established alpha of this study was 5%. Among 537 included children, 296 (55%) were in the “DTE” group and the 241 (45%) were in the “Control” group. Age and gender were not statistically different among the groups (p>0.05). Genotype distribution of the SNPs rs9340799, rs2234693, rs1256049 and rs4986938 were not associated with DTE (p> 0.05). The models elected by MDR were not statistically significant either. Conclusions: The studied SNPs in ESR1 and ESR2 were not associated with permanent DTE. (AU)

• Processo FAPESP: 15/06866-5 - Avaliação do papel do estrógeno no desenvolvimento dentofacial
• Beneficiário: Erika Calvano Kuchler
• Modalidade de apoio: Auxílio à Pesquisa - Jovens Pesquisadores
• Processo FAPESP: 16/08149-1 - Avaliação do papel do estrógeno nos tecidos dentofaciais
• Beneficiário: Erika Calvano Kuchler
• Modalidade de apoio: Bolsas no Brasil - Jovens Pesquisadores