Association between genetic polymorphisms in the promoter region of the defensin beta 1 gene and persistent apical periodontitis.


Journal

International endodontic journal
ISSN: 1365-2591
Titre abrégé: Int Endod J
Pays: England
ID NLM: 8004996

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 22 04 2020
accepted: 26 08 2020
pubmed: 3 9 2020
medline: 30 12 2020
entrez: 3 9 2020
Statut: ppublish

Résumé

To evaluate the association between the promoter region of defensin beta 1 (DEFB1) genetic polymorphisms and persistent apical periodontitis (PAP) in Brazilian patients. Seventy-three patients with post-treatment PAP (PAP group) and 89 patients with root filled teeth with healed and healthy periradicular tissues (healed group) were included (all teeth had apical periodontitis lesions at the beginning of the treatment). Patients who had undergone at least 1 year of follow-up after root canal treatment were recalled, and their genomic DNA was extracted from saliva. Two single nucleotide polymorphisms (SNPs) in DEFB1 at the g. -52G>A (rs1799946) and g. -20G>A (rs11362) positions were analysed using real-time polymerase chain reaction. The chi-squared test was performed, and the odds ratios were calculated using Epi Info 3.5.2. Logistic regression analysis in the codominant model, using the time of follow-up as a variable, was used to evaluate the SNP-SNP interaction. All tests were performed with an established alpha of 0.05 (P = 0.05). For the rs11362 polymorphism in the codominant and recessive models, patients who carried two copies of the T allele had a significantly lower risk of developing PAP (P = 0.040 and P = 0.031, respectively). For the rs1799946 polymorphism in DEFB1 in the codominant and recessive models, carrying one copy of the T allele significantly increased the risk of developing PAP (P = 0.007 and P = 0.031, respectively). In the logistic regression, both polymorphisms were associated with PAP as well as the SNP-SNP interaction (P < 0.0001). Polymorphisms in DEFB1 genes were associated with the development of post-treatment persistent apical periodontitis.

Identifiants

pubmed: 32876967
doi: 10.1111/iej.13401
doi:

Substances chimiques

DEFB1 protein, human 0
beta-Defensins 0

Types de publication

Journal Article

Langues

eng

Pagination

38-45

Informations de copyright

© 2020 International Endodontic Journal. Published by John Wiley & Sons Ltd.

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Auteurs

L S Antunes (LS)

Specific Formation Department, School of Dentistry of Nova Friburgo, Fluminense Federal University, Nova Friburgo, Brazil.
Clinical Research Unit, Fluminense Federal University, Niterói, Brazil.

L Carvalho (L)

Clinical Research Unit, Fluminense Federal University, Niterói, Brazil.
Postgraduate Program, School of Dentistry, Fluminense Federal University, Niterói, Brazil.

I B F Petean (IBF)

Restorative Dentistry Department, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.

L A Antunes (LA)

Specific Formation Department, School of Dentistry of Nova Friburgo, Fluminense Federal University, Nova Friburgo, Brazil.
Clinical Research Unit, Fluminense Federal University, Niterói, Brazil.

J V Freitas (JV)

School of Health and Biological Sciences, Universidade Positivo, Curitiba, Brazil.

A G Salles (AG)

Clinical Research Unit, Fluminense Federal University, Niterói, Brazil.
Postgraduate Program, School of Dentistry, Fluminense Federal University, Niterói, Brazil.

B Olej (B)

Clinical Research Unit, Fluminense Federal University, Niterói, Brazil.

D S B Oliveira (DSB)

Department of Clinic and Surgery, School of Dentistry, Federal University of Alfenas, Minas Gerais, Brazil.

E C Küchler (EC)

School of Health and Biological Sciences, Universidade Positivo, Curitiba, Brazil.
Pediatric Dentistry Department, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.

M D Sousa-Neto (MD)

Restorative Dentistry Department, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.

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