Dental anomalies in individuals with osteogenesis imperfecta
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , |
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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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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info:eu-repo/semantics/dataset |
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info:eu-repo/semantics/publishedVersion |
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https://doi.org/10.48331/scielodata.PIOSUG |
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https://doi.org/10.48331/scielodata.PIOSUG |
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info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/4.0 |
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openAccess |
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http://creativecommons.org/licenses/by/4.0 |
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