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

Autor:	Madalena IR; Department of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil., Reis CLB; Department of Clinic and Surgery, School of Dentistry, Federal University of Alfenas, Alfenas, MG, Brazil., Oliveira DSB; Department of Clinic and Surgery, School of Dentistry, Federal University of Alfenas, Alfenas, MG, Brazil., Pecharki GD; Department of Community Health, Federal University of Parana, Curitiba, PR, Brazil., Trevilatto PC; School of Life Sciences, Pontifícia Universidade Católica do Paraná, Curitiba, PR, Brazil., Andrades KMR; School of Dentistry, Univille University, Joinville, SC, Brazil., Carelli J; School of Dentistry, Univille University, Joinville, SC, Brazil., Silva VLBD; School of Dentistry, Univille University, Joinville, SC, Brazil., Baratto-Filho F; School of Dentistry, Univille University, Joinville, SC, Brazil., Küchler EC; Department of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil., Brancher JA; School of Life Sciences, Pontifícia Universidade Católica do Paraná, Curitiba, PR, Brazil.
Jazyk:	angličtina
Zdroj:	Brazilian dental journal [Braz Dent J] 2021 Nov-Dec; Vol. 32 (6), pp. 107-114.
DOI:	10.1590/0103-6440202104103
Abstrakt:	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.
Databáze:	MEDLINE
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