Tumor Necrosis Factor Alpha -308 G/A Single-Nucleotide Polymorphism and Apical Periodontitis: An Updated Systematic Review and Meta-analysis.


Journal

Journal of endodontics
ISSN: 1878-3554
Titre abrégé: J Endod
Pays: United States
ID NLM: 7511484

Informations de publication

Date de publication:
Jul 2021
Historique:
received: 19 01 2021
revised: 10 03 2021
accepted: 15 03 2021
pubmed: 30 3 2021
medline: 29 6 2021
entrez: 29 3 2021
Statut: ppublish

Résumé

This study aimed to perform a more precise estimation of the association between tumor necrosis factor alpha (TNF-α) -308 G/A single-nucleotide polymorphism (SNP) and the risk of development of apical periodontitis (AP) and its phenotypes based on all available published studies. The study was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines and is registered in PROSPERO (CRD42020176190). The literature search was conducted via Clarivate Analytics Web of Science, Scopus, PubMed, Cochrane Central Register of Controlled Trials, and China National Knowledge Infrastructure databases from inception to December 2020 with no language restrictions. Two reviewers were involved independently in the study selection, data extraction, and appraising the studies that were included. The quality of the included studies was evaluated using the Strengthening the Reporting of Genetic Association and the Grading of Recommendations Assessment, Development and Evaluation system. The frequencies of the genotypes and alleles of the TNF-α (G>A 308, rs1800629) gene with 95% odds ratio were used. Four studies met the inclusion criteria with moderate risk of bias. This study revealed no significant association between TNF-α -308 G/A SNP and AP and the risk of AP development. Moreover, there was no significant association between genotype or allele frequency distribution and clinical manifestations (acute vs chronic) of AP. The certainty of evidence per the Grading of Recommendations Assessment, Development and Evaluation system was very low. Because of very low certainty of evidence, whether there is an association between TNF-α -308 G/A SNP and AP warrants further well-designed multicentric studies to adjudicate a better understanding of the role of genetic factors in the etiopathogenesis of AP.

Identifiants

pubmed: 33775731
pii: S0099-2399(21)00193-X
doi: 10.1016/j.joen.2021.03.007
pii:
doi:

Substances chimiques

Tumor Necrosis Factor-alpha 0

Types de publication

Journal Article Meta-Analysis Review Systematic Review

Langues

eng

Pagination

1061-1069

Informations de copyright

Copyright © 2021 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

Auteurs

Aleksandar Jakovljevic (A)

Department of Pathophysiology, School of Dental Medicine, University of Belgrade, Belgrade, Serbia. Electronic address: dr.sasuli@hotmail.com.

Nadja Nikolic (N)

Department of Biology and Human Genetics, School of Dental Medicine, University of Belgrade, Belgrade, Serbia.

Jelena Jacimovic (J)

Central Library, School of Dental Medicine, University of Belgrade, Belgrade, Serbia.

Maja Miletic (M)

Department of Pathophysiology, School of Dental Medicine, University of Belgrade, Belgrade, Serbia.

Miroslav Andric (M)

Department of Oral Surgery, School of Dental Medicine, University of Belgrade, Belgrade, Serbia.

Jelena Milasin (J)

Department of Biology and Human Genetics, School of Dental Medicine, University of Belgrade, Belgrade, Serbia.

Anita Aminoshariae (A)

Department of Endodontics, Case Western Reserve University School of Dental Medicine, Cleveland, Ohio.

Amir Azarpazhooh (A)

Faculty of Dentistry, University of Toronto, Toronto, Ontario, Canada.

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Classifications MeSH