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Quality of life of pediatric and adult individuals with osteogenesis imperfecta: a meta-analysis

BACKGROUND: Osteogenesis imperfecta (OI) is a group of rare inheritable disorders of connective tissue. The cardinal manifestations of OI are low bone mass and reduced bone mineral strength, leading to increased bone fragility and deformity that may lead to significant impairment in daily life. The...

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Autores principales: Wehrli, Susanne, Rohrbach, Marianne, Landolt, Markus Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207627/
https://www.ncbi.nlm.nih.gov/pubmed/37226194
http://dx.doi.org/10.1186/s13023-023-02728-z
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author Wehrli, Susanne
Rohrbach, Marianne
Landolt, Markus Andreas
author_facet Wehrli, Susanne
Rohrbach, Marianne
Landolt, Markus Andreas
author_sort Wehrli, Susanne
collection PubMed
description BACKGROUND: Osteogenesis imperfecta (OI) is a group of rare inheritable disorders of connective tissue. The cardinal manifestations of OI are low bone mass and reduced bone mineral strength, leading to increased bone fragility and deformity that may lead to significant impairment in daily life. The phenotypic manifestations show a broad range of severity, ranging from mild or moderate to severe and lethal. The here presented meta-analysis aimed to analyze existing findings on quality of life (QoL) in children and adults with OI. METHODS: Nine databases were searched with predefined key words. The selection process was executed by two independent reviewers and was based on predetermined exclusion and inclusion criteria. The quality of each study was assessed using a risk of bias tool. Effect sizes were calculated as standardized mean differences. Between-study heterogeneity was calculated with the I(2) statistic. RESULTS: Among the studies included two featured children and adolescents (N = 189), and four adults (N = 760). Children with OI had significantly lower QoL on the Pediatric quality of life inventory (PedsQL) with regards to the total score, emotional, school, and social functioning compared to controls and norms. The data was not sufficient to calculate differences regarding OI-subtypes. In the adult sample assessed with Short Form Health Survey Questionnaire, 12 (SF-12) and 36 items (SF-36), all OI types showed significantly lower QoL levels across all physical component subscales compared to norms. The same pattern was found for the mental component subscales namely vitality, social functioning, and emotional role functioning. The mental health subscale was significantly lower for OI type I, but not for type III and IV. All of the included studies exhibited a low risk of bias. CONCLUSIONS: QoL was significantly lower in children and adults with OI compared to norms and controls. Studies in adults comparing OI subtypes showed that the clinical severity of the phenotype is not related to worse mental health QoL. Future research is needed to examine QoL in children and adolescents in more sophisticated ways and to better understand the association between clinical severity of an OI-phenotype/severity and mental health in adults. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-023-02728-z.
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spelling pubmed-102076272023-05-25 Quality of life of pediatric and adult individuals with osteogenesis imperfecta: a meta-analysis Wehrli, Susanne Rohrbach, Marianne Landolt, Markus Andreas Orphanet J Rare Dis Review BACKGROUND: Osteogenesis imperfecta (OI) is a group of rare inheritable disorders of connective tissue. The cardinal manifestations of OI are low bone mass and reduced bone mineral strength, leading to increased bone fragility and deformity that may lead to significant impairment in daily life. The phenotypic manifestations show a broad range of severity, ranging from mild or moderate to severe and lethal. The here presented meta-analysis aimed to analyze existing findings on quality of life (QoL) in children and adults with OI. METHODS: Nine databases were searched with predefined key words. The selection process was executed by two independent reviewers and was based on predetermined exclusion and inclusion criteria. The quality of each study was assessed using a risk of bias tool. Effect sizes were calculated as standardized mean differences. Between-study heterogeneity was calculated with the I(2) statistic. RESULTS: Among the studies included two featured children and adolescents (N = 189), and four adults (N = 760). Children with OI had significantly lower QoL on the Pediatric quality of life inventory (PedsQL) with regards to the total score, emotional, school, and social functioning compared to controls and norms. The data was not sufficient to calculate differences regarding OI-subtypes. In the adult sample assessed with Short Form Health Survey Questionnaire, 12 (SF-12) and 36 items (SF-36), all OI types showed significantly lower QoL levels across all physical component subscales compared to norms. The same pattern was found for the mental component subscales namely vitality, social functioning, and emotional role functioning. The mental health subscale was significantly lower for OI type I, but not for type III and IV. All of the included studies exhibited a low risk of bias. CONCLUSIONS: QoL was significantly lower in children and adults with OI compared to norms and controls. Studies in adults comparing OI subtypes showed that the clinical severity of the phenotype is not related to worse mental health QoL. Future research is needed to examine QoL in children and adolescents in more sophisticated ways and to better understand the association between clinical severity of an OI-phenotype/severity and mental health in adults. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-023-02728-z. BioMed Central 2023-05-24 /pmc/articles/PMC10207627/ /pubmed/37226194 http://dx.doi.org/10.1186/s13023-023-02728-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Wehrli, Susanne
Rohrbach, Marianne
Landolt, Markus Andreas
Quality of life of pediatric and adult individuals with osteogenesis imperfecta: a meta-analysis
title Quality of life of pediatric and adult individuals with osteogenesis imperfecta: a meta-analysis
title_full Quality of life of pediatric and adult individuals with osteogenesis imperfecta: a meta-analysis
title_fullStr Quality of life of pediatric and adult individuals with osteogenesis imperfecta: a meta-analysis
title_full_unstemmed Quality of life of pediatric and adult individuals with osteogenesis imperfecta: a meta-analysis
title_short Quality of life of pediatric and adult individuals with osteogenesis imperfecta: a meta-analysis
title_sort quality of life of pediatric and adult individuals with osteogenesis imperfecta: a meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207627/
https://www.ncbi.nlm.nih.gov/pubmed/37226194
http://dx.doi.org/10.1186/s13023-023-02728-z
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