Social Function and Autism Spectrum Disorder in Children and Adults with Neurofibromatosis Type 1: a Systematic Review and Meta-Analysis
In light of the proliferation of recent research into social function in neurofibromatosis type 1 (NF1), a systematic review and meta-analysis is required to synthesise data and place findings within the context of a theoretical framework. This paper reviews findings from research into social functi...
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Veröffentlicht in: | Neuropsychology review 2018-09, Vol.28 (3), p.317-340 |
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description | In light of the proliferation of recent research into social function in neurofibromatosis type 1 (NF1), a systematic review and meta-analysis is required to synthesise data and place findings within the context of a theoretical framework. This paper reviews findings from research into social function and autism spectrum disorder (ASD) in children and adults with NF1 and integrates these findings with the Socio-Cognitive Integration Abilities Model (SOCIAL). It also critically appraises links between social outcomes, internal and external factors moderating social functioning, cognitive domains implicated in social functioning, and underlying neural pathology in NF1. A systematic literature search conducted in MedLine (Ovid), PsycINFO (Ovid), Embase (Ovid), and PubMed electronic databases yielded 35 papers that met inclusion criteria for the systematic review. Out of these papers, 22 papers provided sufficient data for meta-analysis. Findings from this review and meta-analysis provide evidence that children and adults with NF1 exhibit significantly higher prevalence and severity of social dysfunction and ASD symptomatology. To date, very few studies have examined social cognition in NF1 but results indicate the presence of both perceptual and higher-level impairments in this population. The results of this review also provide support for age, gender, and comorbid ADHD as moderating factors for social outcomes in NF1. Suggestions for future research are offered to further our understanding of the social phenotype in NF1 and to facilitate the development of targeted interventions. |
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This paper reviews findings from research into social function and autism spectrum disorder (ASD) in children and adults with NF1 and integrates these findings with the Socio-Cognitive Integration Abilities Model (SOCIAL). It also critically appraises links between social outcomes, internal and external factors moderating social functioning, cognitive domains implicated in social functioning, and underlying neural pathology in NF1. A systematic literature search conducted in MedLine (Ovid), PsycINFO (Ovid), Embase (Ovid), and PubMed electronic databases yielded 35 papers that met inclusion criteria for the systematic review. Out of these papers, 22 papers provided sufficient data for meta-analysis. Findings from this review and meta-analysis provide evidence that children and adults with NF1 exhibit significantly higher prevalence and severity of social dysfunction and ASD symptomatology. To date, very few studies have examined social cognition in NF1 but results indicate the presence of both perceptual and higher-level impairments in this population. The results of this review also provide support for age, gender, and comorbid ADHD as moderating factors for social outcomes in NF1. Suggestions for future research are offered to further our understanding of the social phenotype in NF1 and to facilitate the development of targeted interventions.</description><identifier>ISSN: 1040-7308</identifier><identifier>EISSN: 1573-6660</identifier><identifier>DOI: 10.1007/s11065-018-9380-x</identifier><identifier>PMID: 30097761</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Autism ; Biomedical and Life Sciences ; Biomedicine ; Children ; Cognitive ability ; Data processing ; Genetic disorders ; Meta-analysis ; Neurofibromatosis ; Neurological disorders ; Neurology ; Neuropsychology ; Neurosciences ; Phenotypes ; Recklinghausen's disease ; Review ; Reviews ; Social interactions ; Systematic review ; Tumors</subject><ispartof>Neuropsychology review, 2018-09, Vol.28 (3), p.317-340</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2018</rights><rights>Neuropsychology Review is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-7edf0d2eda36e10a84e772b57397745607779fae9907db9c8c0a2a3e855d538f3</citedby><cites>FETCH-LOGICAL-c372t-7edf0d2eda36e10a84e772b57397745607779fae9907db9c8c0a2a3e855d538f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11065-018-9380-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11065-018-9380-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30097761$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chisholm, Anita K.</creatorcontrib><creatorcontrib>Anderson, Vicki A.</creatorcontrib><creatorcontrib>Pride, Natalie A.</creatorcontrib><creatorcontrib>Malarbi, Stephanie</creatorcontrib><creatorcontrib>North, Kathryn N.</creatorcontrib><creatorcontrib>Payne, Jonathan M.</creatorcontrib><title>Social Function and Autism Spectrum Disorder in Children and Adults with Neurofibromatosis Type 1: a Systematic Review and Meta-Analysis</title><title>Neuropsychology review</title><addtitle>Neuropsychol Rev</addtitle><addtitle>Neuropsychol Rev</addtitle><description>In light of the proliferation of recent research into social function in neurofibromatosis type 1 (NF1), a systematic review and meta-analysis is required to synthesise data and place findings within the context of a theoretical framework. This paper reviews findings from research into social function and autism spectrum disorder (ASD) in children and adults with NF1 and integrates these findings with the Socio-Cognitive Integration Abilities Model (SOCIAL). It also critically appraises links between social outcomes, internal and external factors moderating social functioning, cognitive domains implicated in social functioning, and underlying neural pathology in NF1. A systematic literature search conducted in MedLine (Ovid), PsycINFO (Ovid), Embase (Ovid), and PubMed electronic databases yielded 35 papers that met inclusion criteria for the systematic review. Out of these papers, 22 papers provided sufficient data for meta-analysis. Findings from this review and meta-analysis provide evidence that children and adults with NF1 exhibit significantly higher prevalence and severity of social dysfunction and ASD symptomatology. To date, very few studies have examined social cognition in NF1 but results indicate the presence of both perceptual and higher-level impairments in this population. The results of this review also provide support for age, gender, and comorbid ADHD as moderating factors for social outcomes in NF1. Suggestions for future research are offered to further our understanding of the social phenotype in NF1 and to facilitate the development of targeted interventions.</description><subject>Autism</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Children</subject><subject>Cognitive ability</subject><subject>Data processing</subject><subject>Genetic disorders</subject><subject>Meta-analysis</subject><subject>Neurofibromatosis</subject><subject>Neurological disorders</subject><subject>Neurology</subject><subject>Neuropsychology</subject><subject>Neurosciences</subject><subject>Phenotypes</subject><subject>Recklinghausen's disease</subject><subject>Review</subject><subject>Reviews</subject><subject>Social interactions</subject><subject>Systematic review</subject><subject>Tumors</subject><issn>1040-7308</issn><issn>1573-6660</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp1kcuOFCEUhitG41z0AdwYEjdu0AM0RZW7TuuMJqMm9rgmNJxymFQVLRdn-g18bJnpVhMTVxD4_h9OvqZ5xuAVA1CvE2PQSgqso73ogN4-aI6ZVIK2bQsP6x4WQJWA7qg5SekaoKY4f9wcCYBeqZYdNz_XwXozkrMy2-zDTMzsyLJknyay3qLNsUzkrU8hOozEz2R15UcX8QC6MuZEbny-Ip-wxDD4TQyTySH5RC53WyTsDTFkvUsZ67G35Av-8Hhzn_6I2dDlbMZdpZ80jwYzJnx6WE-br2fvLlfv6cXn8w-r5QW1QvFMFboBHEdnRIsMTLdApfimDl0HWsgWlFL9YLDvQblNbzsLhhuBnZROim4Qp83Lfe82hu8FU9aTTxbH0cwYStIcOiV7oYSo6It_0OtQYv3vPdVKBpL3lWJ7ysaQUsRBb6OfTNxpBvpOk95r0lWTvtOkb2vm-aG5bCZ0fxK_vVSA74FUr-ZvGP8-_f_WX_wBnj0</recordid><startdate>20180901</startdate><enddate>20180901</enddate><creator>Chisholm, Anita K.</creator><creator>Anderson, Vicki A.</creator><creator>Pride, Natalie A.</creator><creator>Malarbi, Stephanie</creator><creator>North, Kathryn N.</creator><creator>Payne, Jonathan M.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PADUT</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20180901</creationdate><title>Social Function and Autism Spectrum Disorder in Children and Adults with Neurofibromatosis Type 1: a Systematic Review and Meta-Analysis</title><author>Chisholm, Anita K. ; 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This paper reviews findings from research into social function and autism spectrum disorder (ASD) in children and adults with NF1 and integrates these findings with the Socio-Cognitive Integration Abilities Model (SOCIAL). It also critically appraises links between social outcomes, internal and external factors moderating social functioning, cognitive domains implicated in social functioning, and underlying neural pathology in NF1. A systematic literature search conducted in MedLine (Ovid), PsycINFO (Ovid), Embase (Ovid), and PubMed electronic databases yielded 35 papers that met inclusion criteria for the systematic review. Out of these papers, 22 papers provided sufficient data for meta-analysis. Findings from this review and meta-analysis provide evidence that children and adults with NF1 exhibit significantly higher prevalence and severity of social dysfunction and ASD symptomatology. To date, very few studies have examined social cognition in NF1 but results indicate the presence of both perceptual and higher-level impairments in this population. The results of this review also provide support for age, gender, and comorbid ADHD as moderating factors for social outcomes in NF1. Suggestions for future research are offered to further our understanding of the social phenotype in NF1 and to facilitate the development of targeted interventions.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>30097761</pmid><doi>10.1007/s11065-018-9380-x</doi><tpages>24</tpages></addata></record> |
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subjects | Autism Biomedical and Life Sciences Biomedicine Children Cognitive ability Data processing Genetic disorders Meta-analysis Neurofibromatosis Neurological disorders Neurology Neuropsychology Neurosciences Phenotypes Recklinghausen's disease Review Reviews Social interactions Systematic review Tumors |
title | Social Function and Autism Spectrum Disorder in Children and Adults with Neurofibromatosis Type 1: a Systematic Review and Meta-Analysis |
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