Title
Author
DOI
Article Type
Special Issue
Volume
Issue
Association of third molar maturity with estrogen receptors-encoding genes
1Department of Biomaterials, University of Uberaba, 38055-500 Uberaba, MG, Brazil
2School of Dentistry, Presidente Tancredo de Almeida Neves University Center, 36307-251 São João del Rei, MG, Brazil
3Department of Stomatology, Federal University of Paraná, 80060-000 Curitiba, PR, Brazil
4Department of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, 14040-900 Ribeirão Preto, SP, Brazil
5School of Dentistry, University of Tuiuti of Paraná, 82010-210 Curitiba, PR, Brazil
6Postgraduate Program in Dentistry, Health Institute of Nova Friburgo, Fluminense Federal University, 28625-650 Nova Friburgo, RJ, Brazil
7School of Dentistry, University of the Joinville Region, 89219-710 Joinville, SC, Brazil
8Department of Orthodontics, Medical Faculty, University Hospital Bonn, 53111 Bonn, NRW, Germany
DOI: 10.22514/jocpd.2025.097 Vol.49,Issue 5,September 2025 pp.31-37
Submitted: 26 November 2024 Accepted: 12 February 2025
Published: 03 September 2025
*Corresponding Author(s): Erika Calvano Küchler E-mail: Erika.Kuchler@ukbonn.de
Background: Single nucleotide polymorphisms (SNPs) have been linked to variations in dental development, influencing traits such as eruption timing. This study examined the association between third molar maturity and SNPs in genes encoding estrogen receptors alpha (ESR1) and beta (ESR2). Methods: This was a cross-sectional study design using a convenience sample of genomic DNA and orthodontic records of Brazilian children. Third molar maturity was calculated in panoramic radiographs using a dental age estimation method previously developed. A delta value (dental age-chronological age, DA-CA) was calculated in order to show whether the patient has a tendency toward normal third molar maturity, delayed third molar maturity (negative values), or advanced third molar maturity (positive values). DNA isolated from cells in saliva was used for genotyping four SNPs: 2234693 and rs9340799 in ESR1; and rs1256049 and rs4986938 in ESR2. Statistical analysis was made with p-values < 0.05 indicating statistical significance. Results: Eighty-nine children were included in the study, 49 (55.1%) were girls and 40 (44.9%) were boys. There was no statistical difference between sexes and third molar maturity (p > 0.05). For the SNP rs9340799 in the maxilla, patients carrying AA genotype exhibited significantly delayed maxillary third molars maturity (p < 0.05). Conclusions: Third molar maturity is associated with the SNP rs9340799 in ESR1. Our study supports that third molars development time is genetically influenced.
Dental development; Estrogen; Genes
Isabela Ribeiro Madalena,Lhorrany Alves de Souza,Gabriela Fonseca-Souza,Paloma Francia de Carvalho,Mirian Aiko Nakane Matsumoto,Débora Cristina Cardoso Bueno,Livia Azeredo Antunes,Maria Angélica Hueb de Menezes-Oliveira,Flares Baratto-Filho,Christian Kirschneck,César Penazzo Lepri,Erika Calvano Küchler. Association of third molar maturity with estrogen receptors-encoding genes. Journal of Clinical Pediatric Dentistry. 2025. 49(5);31-37.
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