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

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 m...

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Published in:Orphanet journal of rare diseases 2023-05, Vol.18 (1), p.123-123, Article 123
Main Authors: Wehrli, Susanne, Rohrbach, Marianne, Landolt, Markus Andreas
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description 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. 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 statistic. 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. 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.
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source PubMed (Medline); Publicly Available Content (ProQuest)
subjects Adolescents
Adult
Bias
Bone diseases
Bone mass
Boolean
Children
Collagen
Connective tissues
Databases, Factual
Emotions
Fear & phobias
Fractures
Humans
Intervention
Medical research
Mental Health
Meta-analysis
Mutation
Osteogenesis
Osteogenesis Imperfecta
Pediatrics
Phenotypes
Physical health
Quality of Life
Rare disease
Rare Diseases
Review
Standard deviation
title Quality of life of pediatric and adult individuals with osteogenesis imperfecta: a meta-analysis
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