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Genetic polymorphism in the tumour necrosis factor alpha gene (G-308A) is associated with persistent apical periodontitis in Brazilians.
de Castro, Guilherme Assed Piedade; Petean, Igor Bassi Ferreira; de Paula-Silva, Francisco Wanderley Garcia; Kuchler, Erika Calvano; Antunes, Leonardo Dos Santos; Segato, Raquel Assed Bezerra; da Silva, Lea Assed Bezerra; Silva-Sousa, Alice Corrêa; Sousa-Neto, Manoel Damião.
Afiliação
  • de Castro GAP; Department of Restorative Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
  • Petean IBF; Department of Restorative Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
  • de Paula-Silva FWG; Department of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
  • Kuchler EC; Department of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
  • Antunes LDS; Department of Orthodontics, University of Regensburg, Regensburg, Germany.
  • Segato RAB; Research Unit, Fluminense Federal University, Rio de Janeiro, Brazil.
  • da Silva LAB; Specific Formation Department, School of Dentistry of Nova Friburgo, Fluminense Federal University, Rio de Janeiro, Brazil.
  • Silva-Sousa AC; Department of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
  • Sousa-Neto MD; Department of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
Int Endod J ; 56(1): 17-26, 2023 Jan.
Article em En | MEDLINE | ID: mdl-36183324
AIM: To investigate if there was an association between genetic polymorphisms in tumour necrosis factor (TNF)-⍺ and its receptors TNFRSF1A and TNFRSF1B with persistent apical periodontitis (PAP) in Brazilian subjects. METHODOLOGY: Patients who had pulpal necrosis and apical periodontitis at the time of treatment, with at least 1-year of follow-up after non-surgical root canal treatment were recalled. Three hundred and seventy eight subjects were included, 150 subjects with signs/symptoms of PAP and 228 subjects with root canal-treated teeth exhibiting healthy perirradicular tissues (healed). Genomic DNA was extracted from saliva and used for TNF-⍺ (rs1800629), TNFRSF1A (rs1800693) and TNFRSF1B (rs1061622) genotyping by real-time PCR. Genotypes and alleles frequencies were evaluated by c2 or Fisher's exact tests and odds ratios were implemented (α = 5%). RESULTS: The genetic polymorphism in TNF-α (rs1800629) was associated as a protective factor for the development of PAP (p < .05), once subjects who presented at least one allele A (AA+AG X GG), had a higher chance to lesion repair (p < .05). The polymorphisms rs1800693 and rs1061622 in TNF receptors (TNFRSF1A and TNFRSF1B, respectively) were not associated with the development of PAP (p > .05). CONCLUSIONS: The observed results demonstrate that polymorphism in TNF-α but not in its receptors is associated with PAP.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Fator de Necrose Tumoral alfa Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Fator de Necrose Tumoral alfa Idioma: En Ano de publicação: 2023 Tipo de documento: Article