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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 |
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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. |
doi_str_mv | 10.1186/s13023-023-02728-z |
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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.</description><identifier>ISSN: 1750-1172</identifier><identifier>EISSN: 1750-1172</identifier><identifier>DOI: 10.1186/s13023-023-02728-z</identifier><identifier>PMID: 37226194</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>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</subject><ispartof>Orphanet journal of rare diseases, 2023-05, Vol.18 (1), p.123-123, Article 123</ispartof><rights>2023. The Author(s).</rights><rights>COPYRIGHT 2023 BioMed Central Ltd.</rights><rights>2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c598t-d40827db2839f2c117bc043e55433d4b721dfc992358b1740d9feba6bdd7b2cd3</citedby><cites>FETCH-LOGICAL-c598t-d40827db2839f2c117bc043e55433d4b721dfc992358b1740d9feba6bdd7b2cd3</cites><orcidid>0000-0003-1790-3890</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207627/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2827113332?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,25734,27905,27906,36993,36994,44571,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37226194$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wehrli, Susanne</creatorcontrib><creatorcontrib>Rohrbach, Marianne</creatorcontrib><creatorcontrib>Landolt, Markus Andreas</creatorcontrib><title>Quality of life of pediatric and adult individuals with osteogenesis imperfecta: a meta-analysis</title><title>Orphanet journal of rare diseases</title><addtitle>Orphanet J Rare Dis</addtitle><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.</description><subject>Adolescents</subject><subject>Adult</subject><subject>Bias</subject><subject>Bone diseases</subject><subject>Bone mass</subject><subject>Boolean</subject><subject>Children</subject><subject>Collagen</subject><subject>Connective tissues</subject><subject>Databases, Factual</subject><subject>Emotions</subject><subject>Fear & phobias</subject><subject>Fractures</subject><subject>Humans</subject><subject>Intervention</subject><subject>Medical research</subject><subject>Mental Health</subject><subject>Meta-analysis</subject><subject>Mutation</subject><subject>Osteogenesis</subject><subject>Osteogenesis Imperfecta</subject><subject>Pediatrics</subject><subject>Phenotypes</subject><subject>Physical health</subject><subject>Quality of Life</subject><subject>Rare disease</subject><subject>Rare Diseases</subject><subject>Review</subject><subject>Standard deviation</subject><issn>1750-1172</issn><issn>1750-1172</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkk1v1DAQhiMEoqXwBzigSFzoIcUeO-uEC6qqAitVQnydzcQfW6-SeGs7he2vx0tK6SJkjWx5nve1PZ6ieE7JCaXN4nWkjACr5hDQVDcPikMqalJRKuDhvfVB8STGNSG8ZqR5XBwwAbCgLT8svn-asHdpW3pb9s6a3bwx2mEKTpU46hL11KfSjdpdO53hWP5w6bL0MRm_MqOJLpZu2JhgjUr4psRyMAkrHLHf5tzT4pHNIvPsdj4qvr07_3r2obr4-H55dnpRqbptUqU5aUDoDhrWWlD50p0inJm65oxp3gmg2qq2BVY3HRWc6NaaDhed1qIDpdlRsZx9tce13AQ3YNhKj07-3vBhJTEkp3ojmUCKgFygYBwobyynHLDrCMEGVJu93s5em6kbjFZmTAH7PdP9zOgu5cpfS0qAiAWI7PDq1iH4q8nEJAcXlel7HI2fooSGtiAEMJ7Rl_-gaz-FXL0dBYJSxhj8pVaYX-BG6_PBamcqT_Mv1y0Xi92xJ_-h8tBmcMqPxrq8vyc43hNkJpmfaYVTjHL55fM-CzOrgo8xGHtXEErkriHl3JByjtyQ8iaLXtwv5Z3kTweyX9I42fE</recordid><startdate>20230524</startdate><enddate>20230524</enddate><creator>Wehrli, Susanne</creator><creator>Rohrbach, Marianne</creator><creator>Landolt, Markus Andreas</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-1790-3890</orcidid></search><sort><creationdate>20230524</creationdate><title>Quality of life of pediatric and adult individuals with osteogenesis imperfecta: a meta-analysis</title><author>Wehrli, Susanne ; Rohrbach, Marianne ; Landolt, Markus Andreas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c598t-d40827db2839f2c117bc043e55433d4b721dfc992358b1740d9feba6bdd7b2cd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adolescents</topic><topic>Adult</topic><topic>Bias</topic><topic>Bone diseases</topic><topic>Bone mass</topic><topic>Boolean</topic><topic>Children</topic><topic>Collagen</topic><topic>Connective tissues</topic><topic>Databases, Factual</topic><topic>Emotions</topic><topic>Fear & phobias</topic><topic>Fractures</topic><topic>Humans</topic><topic>Intervention</topic><topic>Medical research</topic><topic>Mental Health</topic><topic>Meta-analysis</topic><topic>Mutation</topic><topic>Osteogenesis</topic><topic>Osteogenesis Imperfecta</topic><topic>Pediatrics</topic><topic>Phenotypes</topic><topic>Physical health</topic><topic>Quality of Life</topic><topic>Rare disease</topic><topic>Rare Diseases</topic><topic>Review</topic><topic>Standard deviation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wehrli, Susanne</creatorcontrib><creatorcontrib>Rohrbach, Marianne</creatorcontrib><creatorcontrib>Landolt, Markus Andreas</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Orphanet journal of rare diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wehrli, Susanne</au><au>Rohrbach, Marianne</au><au>Landolt, Markus Andreas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quality of life of pediatric and adult individuals with osteogenesis imperfecta: a meta-analysis</atitle><jtitle>Orphanet journal of rare diseases</jtitle><addtitle>Orphanet J Rare Dis</addtitle><date>2023-05-24</date><risdate>2023</risdate><volume>18</volume><issue>1</issue><spage>123</spage><epage>123</epage><pages>123-123</pages><artnum>123</artnum><issn>1750-1172</issn><eissn>1750-1172</eissn><abstract>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.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>37226194</pmid><doi>10.1186/s13023-023-02728-z</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-1790-3890</orcidid><oa>free_for_read</oa></addata></record> |
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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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