Dental anomalies in individuals with osteogenesis imperfecta

Detalhes bibliográficos
Autor(a) principal: Prado, Heloisa Vieira
Data de Publicação: 2023
Outros Autores: Soares, Enio Cássio Barreto, Carneiro, Natália Cristina Ruy, Vilar, Ivanete Cláudia de Oliveira, Abreu, Lucas Guimarães, Borges-Oliveira, Ana Cristina
Tipo de documento: Conjunto de dados
Título da fonte: SciELO Data
Texto Completo: https://doi.org/10.48331/scielodata.PIOSUG
Resumo: Background: Osteogenesis imperfecta (OI) is a rare genetic disorder primarily caused by mutations in the genes involved in the production of type 1 collagen. OI is also known as brittle bone disease. Objective: To describe the prevalence of dental anomalies (except dentinogenesis imperfecta) in individuals with OI, as well as to compare the prevalence of dental anomalies between individuals with and without OI and between individuals with different types of OI. Search methods: Searches in PubMed, Web of Science, Scopus, Ovid, and gray literature were performed in October 2022. Selection criteria: Observational studies (with or without a comparison group) that evaluated the prevalence of dental anomalies in individuals with OI. Data collection and analysis: Data items were extracted by two authors. Quality assessment employing the Joanna Briggs Institute checklists and meta-analysis were conducted. Results were provided in prevalence values and odds ratio (OR) / 95% confidence interval (CI). Strength of evidence was determined. Results: Eighteen studies were included. Most prevalent dental anomalies in individuals with OI were: pulp obliteration (46.4%), dental impaction (33.5%), dental impaction of second molars (27%), and tooth agenesis (23.9%). Individuals with OI type III/IV had 20.16-fold greater chance of exhibiting tooth discoloration in comparison with individuals with OI type I (CI: 1.10–370.98). In comparison with the group without OI, the individuals with OI had 6.90-fold greater chance of exhibiting dental impaction (CI: 1.54–31.00). High methodological quality was found in 47% of the studies. Strength of evidence was low or very low. Conclusions: Pulp obliteration, dental impaction, and tooth agenesis were the most prevalent dental anomalies in the OI group. Individuals with OI were more likely to have dental impaction than individuals without OI. Individuals with OI type III/IV (severe-moderate) are more likely to have tooth discoloration than individuals with OI type I (mild).
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spelling https://doi.org/10.48331/scielodata.PIOSUGPrado, Heloisa VieiraSoares, Enio Cássio BarretoCarneiro, Natália Cristina RuyVilar, Ivanete Cláudia de OliveiraAbreu, Lucas GuimarãesBorges-Oliveira, Ana CristinaDental anomalies in individuals with osteogenesis imperfectaa systematic review and meta-analysis of prevalence and comparative studiesSciELO DataBackground: Osteogenesis imperfecta (OI) is a rare genetic disorder primarily caused by mutations in the genes involved in the production of type 1 collagen. OI is also known as brittle bone disease. Objective: To describe the prevalence of dental anomalies (except dentinogenesis imperfecta) in individuals with OI, as well as to compare the prevalence of dental anomalies between individuals with and without OI and between individuals with different types of OI. Search methods: Searches in PubMed, Web of Science, Scopus, Ovid, and gray literature were performed in October 2022. Selection criteria: Observational studies (with or without a comparison group) that evaluated the prevalence of dental anomalies in individuals with OI. Data collection and analysis: Data items were extracted by two authors. Quality assessment employing the Joanna Briggs Institute checklists and meta-analysis were conducted. Results were provided in prevalence values and odds ratio (OR) / 95% confidence interval (CI). Strength of evidence was determined. Results: Eighteen studies were included. Most prevalent dental anomalies in individuals with OI were: pulp obliteration (46.4%), dental impaction (33.5%), dental impaction of second molars (27%), and tooth agenesis (23.9%). Individuals with OI type III/IV had 20.16-fold greater chance of exhibiting tooth discoloration in comparison with individuals with OI type I (CI: 1.10–370.98). In comparison with the group without OI, the individuals with OI had 6.90-fold greater chance of exhibiting dental impaction (CI: 1.54–31.00). High methodological quality was found in 47% of the studies. Strength of evidence was low or very low. Conclusions: Pulp obliteration, dental impaction, and tooth agenesis were the most prevalent dental anomalies in the OI group. Individuals with OI were more likely to have dental impaction than individuals without OI. Individuals with OI type III/IV (severe-moderate) are more likely to have tooth discoloration than individuals with OI type I (mild).2023-08-08info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0Medicine, Health and Life SciencesDental anomaliesOral HealthOsteogenesis ImperfectaRare Diseasesinfo:eu-repo/semantics/datasetinfo:eu-repo/semantics/datasetinfo:eu-repo/semantics/publishedVersionDatasetreponame:SciELO Datainstname:Scientific Electronic Library Online (SCIELO)instacron:SCIRepositório de Dados de PesquisaONGhttps://data.scielo.org/oai/requestdata@scielo.orgopendoar:2024-04-11T06:12:59SciELO Data - Scientific Electronic Library Online (SCIELO)falsedoi:10.48331/scielodata.PIOSUG
dc.title.none.fl_str_mv Dental anomalies in individuals with osteogenesis imperfecta
a systematic review and meta-analysis of prevalence and comparative studies
title Dental anomalies in individuals with osteogenesis imperfecta
spellingShingle Dental anomalies in individuals with osteogenesis imperfecta
Prado, Heloisa Vieira
Medicine, Health and Life Sciences
Dental anomalies
Oral Health
Osteogenesis Imperfecta
Rare Diseases
title_short Dental anomalies in individuals with osteogenesis imperfecta
title_full Dental anomalies in individuals with osteogenesis imperfecta
title_fullStr Dental anomalies in individuals with osteogenesis imperfecta
title_full_unstemmed Dental anomalies in individuals with osteogenesis imperfecta
title_sort Dental anomalies in individuals with osteogenesis imperfecta
author Prado, Heloisa Vieira
author_facet Prado, Heloisa Vieira
Soares, Enio Cássio Barreto
Carneiro, Natália Cristina Ruy
Vilar, Ivanete Cláudia de Oliveira
Abreu, Lucas Guimarães
Borges-Oliveira, Ana Cristina
author_role author
author2 Soares, Enio Cássio Barreto
Carneiro, Natália Cristina Ruy
Vilar, Ivanete Cláudia de Oliveira
Abreu, Lucas Guimarães
Borges-Oliveira, Ana Cristina
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Prado, Heloisa Vieira
Soares, Enio Cássio Barreto
Carneiro, Natália Cristina Ruy
Vilar, Ivanete Cláudia de Oliveira
Abreu, Lucas Guimarães
Borges-Oliveira, Ana Cristina
dc.subject.none.fl_str_mv Medicine, Health and Life Sciences
Dental anomalies
Oral Health
Osteogenesis Imperfecta
Rare Diseases
topic Medicine, Health and Life Sciences
Dental anomalies
Oral Health
Osteogenesis Imperfecta
Rare Diseases
description Background: Osteogenesis imperfecta (OI) is a rare genetic disorder primarily caused by mutations in the genes involved in the production of type 1 collagen. OI is also known as brittle bone disease. Objective: To describe the prevalence of dental anomalies (except dentinogenesis imperfecta) in individuals with OI, as well as to compare the prevalence of dental anomalies between individuals with and without OI and between individuals with different types of OI. Search methods: Searches in PubMed, Web of Science, Scopus, Ovid, and gray literature were performed in October 2022. Selection criteria: Observational studies (with or without a comparison group) that evaluated the prevalence of dental anomalies in individuals with OI. Data collection and analysis: Data items were extracted by two authors. Quality assessment employing the Joanna Briggs Institute checklists and meta-analysis were conducted. Results were provided in prevalence values and odds ratio (OR) / 95% confidence interval (CI). Strength of evidence was determined. Results: Eighteen studies were included. Most prevalent dental anomalies in individuals with OI were: pulp obliteration (46.4%), dental impaction (33.5%), dental impaction of second molars (27%), and tooth agenesis (23.9%). Individuals with OI type III/IV had 20.16-fold greater chance of exhibiting tooth discoloration in comparison with individuals with OI type I (CI: 1.10–370.98). In comparison with the group without OI, the individuals with OI had 6.90-fold greater chance of exhibiting dental impaction (CI: 1.54–31.00). High methodological quality was found in 47% of the studies. Strength of evidence was low or very low. Conclusions: Pulp obliteration, dental impaction, and tooth agenesis were the most prevalent dental anomalies in the OI group. Individuals with OI were more likely to have dental impaction than individuals without OI. Individuals with OI type III/IV (severe-moderate) are more likely to have tooth discoloration than individuals with OI type I (mild).
publishDate 2023
dc.date.issued.fl_str_mv 2023-08-08
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