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Mapping nonverbal IQ in young boys with fragile X syndrome
This study examines the developmental changes in nonverbal intellectual functioning evident in males with fragile X syndrome (FXS) measured by the Leiter International Performance Scales‐Revised (Leiter‐R). The Leiter‐R provides both IQ scores and associated growth scores which permit the examinatio...
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Published in: | American journal of medical genetics 2005-01, Vol.132A (1), p.25-32 |
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description | This study examines the developmental changes in nonverbal intellectual functioning evident in males with fragile X syndrome (FXS) measured by the Leiter International Performance Scales‐Revised (Leiter‐R). The Leiter‐R provides both IQ scores and associated growth scores which permit the examination of both age‐based IQ scores and overall intellectual growth. Participants were 45 males with full mutation FXS and ranged in age from 4.0 to 13.8 years. Each child was assessed annually using the Leiter‐R as part of a larger longitudinal battery for an average of 3.5 assessments per child and a range of 2–6 assessments, representing a total of 156 assessment occasions. Longitudinal analyzes of Leiter scores consisted primarily of hierarchical linear modeling, with the impact of chronological age, maternal education, fragile X mental retardation 1 protein (FMRP), autistic behaviors also being assessed. Findings revealed a significant linear decline in nonverbal IQ scores, with no effects of maternal education, autistic behaviors, or FMRP on mean level or rate of change in IQ scores over time. The decline slowed significantly around 8 years of age, but scores continued to decline into the 12th year of age. In contrast, a significant linear increase was observed in Leiter‐R growth scores, which was negatively influenced by autistic behaviors. The rate of increase did not change over time, and neither mean level nor rate of increase was influenced by maternal education or FMRP levels. These findings suggest that declines in IQ are the result of steady, but suboptimal intellectual growth, rather than a true deterioration in overall intellectual functioning. © 2004 Wiley‐Liss, Inc. |
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The Leiter‐R provides both IQ scores and associated growth scores which permit the examination of both age‐based IQ scores and overall intellectual growth. Participants were 45 males with full mutation FXS and ranged in age from 4.0 to 13.8 years. Each child was assessed annually using the Leiter‐R as part of a larger longitudinal battery for an average of 3.5 assessments per child and a range of 2–6 assessments, representing a total of 156 assessment occasions. Longitudinal analyzes of Leiter scores consisted primarily of hierarchical linear modeling, with the impact of chronological age, maternal education, fragile X mental retardation 1 protein (FMRP), autistic behaviors also being assessed. Findings revealed a significant linear decline in nonverbal IQ scores, with no effects of maternal education, autistic behaviors, or FMRP on mean level or rate of change in IQ scores over time. The decline slowed significantly around 8 years of age, but scores continued to decline into the 12th year of age. In contrast, a significant linear increase was observed in Leiter‐R growth scores, which was negatively influenced by autistic behaviors. The rate of increase did not change over time, and neither mean level nor rate of increase was influenced by maternal education or FMRP levels. These findings suggest that declines in IQ are the result of steady, but suboptimal intellectual growth, rather than a true deterioration in overall intellectual functioning. © 2004 Wiley‐Liss, Inc.</description><identifier>ISSN: 1552-4825</identifier><identifier>ISSN: 0148-7299</identifier><identifier>EISSN: 1552-4833</identifier><identifier>DOI: 10.1002/ajmg.a.30353</identifier><identifier>PMID: 15551333</identifier><identifier>CODEN: AJMGDA</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adolescent ; Age Factors ; Biological and medical sciences ; Child ; Child, Preschool ; Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...) ; fragile X ; Fragile X Mental Retardation Protein ; Fragile X Syndrome - genetics ; Fragile X Syndrome - psychology ; General aspects. Genetic counseling ; growth curve ; Humans ; Immunohistochemistry ; Intelligence ; Intelligence Tests ; Longitudinal Studies ; Male ; Medical genetics ; Medical sciences ; Mutation ; Nerve Tissue Proteins - analysis ; Nerve Tissue Proteins - genetics ; nonverbal IQ ; RNA-Binding Proteins - analysis ; RNA-Binding Proteins - genetics</subject><ispartof>American journal of medical genetics, 2005-01, Vol.132A (1), p.25-32</ispartof><rights>Copyright © 2004 Wiley‐Liss, Inc.</rights><rights>2005 INIST-CNRS</rights><rights>(c) 2004 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4323-1f45e6f22a5fafc7cea0a4d0ae0edad6d4f95e89e6b78554ff1867b929d5686a3</citedby><cites>FETCH-LOGICAL-c4323-1f45e6f22a5fafc7cea0a4d0ae0edad6d4f95e89e6b78554ff1867b929d5686a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16541472$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15551333$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Skinner, Martie</creatorcontrib><creatorcontrib>Hooper, Stephen</creatorcontrib><creatorcontrib>Hatton, Deborah D.</creatorcontrib><creatorcontrib>Roberts, Jane</creatorcontrib><creatorcontrib>Mirrett, Penny</creatorcontrib><creatorcontrib>Schaaf, Jennifer</creatorcontrib><creatorcontrib>Sullivan, Kelly</creatorcontrib><creatorcontrib>Wheeler, Anne</creatorcontrib><creatorcontrib>Bailey Jr, Donald B.</creatorcontrib><title>Mapping nonverbal IQ in young boys with fragile X syndrome</title><title>American journal of medical genetics</title><addtitle>Am. J. Med. Genet</addtitle><description>This study examines the developmental changes in nonverbal intellectual functioning evident in males with fragile X syndrome (FXS) measured by the Leiter International Performance Scales‐Revised (Leiter‐R). The Leiter‐R provides both IQ scores and associated growth scores which permit the examination of both age‐based IQ scores and overall intellectual growth. Participants were 45 males with full mutation FXS and ranged in age from 4.0 to 13.8 years. Each child was assessed annually using the Leiter‐R as part of a larger longitudinal battery for an average of 3.5 assessments per child and a range of 2–6 assessments, representing a total of 156 assessment occasions. Longitudinal analyzes of Leiter scores consisted primarily of hierarchical linear modeling, with the impact of chronological age, maternal education, fragile X mental retardation 1 protein (FMRP), autistic behaviors also being assessed. Findings revealed a significant linear decline in nonverbal IQ scores, with no effects of maternal education, autistic behaviors, or FMRP on mean level or rate of change in IQ scores over time. The decline slowed significantly around 8 years of age, but scores continued to decline into the 12th year of age. In contrast, a significant linear increase was observed in Leiter‐R growth scores, which was negatively influenced by autistic behaviors. The rate of increase did not change over time, and neither mean level nor rate of increase was influenced by maternal education or FMRP levels. These findings suggest that declines in IQ are the result of steady, but suboptimal intellectual growth, rather than a true deterioration in overall intellectual functioning. © 2004 Wiley‐Liss, Inc.</description><subject>Adolescent</subject><subject>Age Factors</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...)</subject><subject>fragile X</subject><subject>Fragile X Mental Retardation Protein</subject><subject>Fragile X Syndrome - genetics</subject><subject>Fragile X Syndrome - psychology</subject><subject>General aspects. Genetic counseling</subject><subject>growth curve</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Intelligence</subject><subject>Intelligence Tests</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Mutation</subject><subject>Nerve Tissue Proteins - analysis</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>nonverbal IQ</subject><subject>RNA-Binding Proteins - analysis</subject><subject>RNA-Binding Proteins - genetics</subject><issn>1552-4825</issn><issn>0148-7299</issn><issn>1552-4833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFkEtPwzAMgCME4jG4cUa9wImOPJq05TZtMF7jpSG4RW6bjEIfI9kY_fdkbMANTrbsz7b8IbRLcJtgTI_gpRy1oc0w42wFbRLOqR9EjK3-5JRvoC1rXzBmmIdiHW24BieMsU10PIDxOK9GXlVX78okUHjnd15eeU09ddWkbqw3yyfPnjYwygvlPXm2qTJTl2obrWkorNpZxhZ6OD0Zds_8q5v-ebdz5acBo8wnOuBKaEqBa9BpmCrAEGQYFFYZZCILdMxVFCuRhBHngdYkEmES0zjjIhLAWuhgsXds6repshNZ5jZVRQGVqqdWitB9HnPxL0hxFBEeYwceLsDU1NYapeXY5CWYRhIs51LlXKoE-SXV4XvLvdOkVNkvvLTogP0lADaFwqmq0tz-coIHJAip49iCmzmTzZ9HZedi0P8-7y-mcjtRHz9TYF7nr4dcPl735Wnv8vbsvkfkkH0CzBmeaw</recordid><startdate>20050101</startdate><enddate>20050101</enddate><creator>Skinner, Martie</creator><creator>Hooper, Stephen</creator><creator>Hatton, Deborah D.</creator><creator>Roberts, Jane</creator><creator>Mirrett, Penny</creator><creator>Schaaf, Jennifer</creator><creator>Sullivan, Kelly</creator><creator>Wheeler, Anne</creator><creator>Bailey Jr, Donald B.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20050101</creationdate><title>Mapping nonverbal IQ in young boys with fragile X syndrome</title><author>Skinner, Martie ; Hooper, Stephen ; Hatton, Deborah D. ; Roberts, Jane ; Mirrett, Penny ; Schaaf, Jennifer ; Sullivan, Kelly ; Wheeler, Anne ; Bailey Jr, Donald B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4323-1f45e6f22a5fafc7cea0a4d0ae0edad6d4f95e89e6b78554ff1867b929d5686a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adolescent</topic><topic>Age Factors</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...)</topic><topic>fragile X</topic><topic>Fragile X Mental Retardation Protein</topic><topic>Fragile X Syndrome - genetics</topic><topic>Fragile X Syndrome - psychology</topic><topic>General aspects. Genetic counseling</topic><topic>growth curve</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Intelligence</topic><topic>Intelligence Tests</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Mutation</topic><topic>Nerve Tissue Proteins - analysis</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>nonverbal IQ</topic><topic>RNA-Binding Proteins - analysis</topic><topic>RNA-Binding Proteins - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Skinner, Martie</creatorcontrib><creatorcontrib>Hooper, Stephen</creatorcontrib><creatorcontrib>Hatton, Deborah D.</creatorcontrib><creatorcontrib>Roberts, Jane</creatorcontrib><creatorcontrib>Mirrett, Penny</creatorcontrib><creatorcontrib>Schaaf, Jennifer</creatorcontrib><creatorcontrib>Sullivan, Kelly</creatorcontrib><creatorcontrib>Wheeler, Anne</creatorcontrib><creatorcontrib>Bailey Jr, Donald B.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of medical genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Skinner, Martie</au><au>Hooper, Stephen</au><au>Hatton, Deborah D.</au><au>Roberts, Jane</au><au>Mirrett, Penny</au><au>Schaaf, Jennifer</au><au>Sullivan, Kelly</au><au>Wheeler, Anne</au><au>Bailey Jr, Donald B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mapping nonverbal IQ in young boys with fragile X syndrome</atitle><jtitle>American journal of medical genetics</jtitle><addtitle>Am. J. Med. Genet</addtitle><date>2005-01-01</date><risdate>2005</risdate><volume>132A</volume><issue>1</issue><spage>25</spage><epage>32</epage><pages>25-32</pages><issn>1552-4825</issn><issn>0148-7299</issn><eissn>1552-4833</eissn><coden>AJMGDA</coden><abstract>This study examines the developmental changes in nonverbal intellectual functioning evident in males with fragile X syndrome (FXS) measured by the Leiter International Performance Scales‐Revised (Leiter‐R). The Leiter‐R provides both IQ scores and associated growth scores which permit the examination of both age‐based IQ scores and overall intellectual growth. Participants were 45 males with full mutation FXS and ranged in age from 4.0 to 13.8 years. Each child was assessed annually using the Leiter‐R as part of a larger longitudinal battery for an average of 3.5 assessments per child and a range of 2–6 assessments, representing a total of 156 assessment occasions. Longitudinal analyzes of Leiter scores consisted primarily of hierarchical linear modeling, with the impact of chronological age, maternal education, fragile X mental retardation 1 protein (FMRP), autistic behaviors also being assessed. Findings revealed a significant linear decline in nonverbal IQ scores, with no effects of maternal education, autistic behaviors, or FMRP on mean level or rate of change in IQ scores over time. The decline slowed significantly around 8 years of age, but scores continued to decline into the 12th year of age. In contrast, a significant linear increase was observed in Leiter‐R growth scores, which was negatively influenced by autistic behaviors. The rate of increase did not change over time, and neither mean level nor rate of increase was influenced by maternal education or FMRP levels. These findings suggest that declines in IQ are the result of steady, but suboptimal intellectual growth, rather than a true deterioration in overall intellectual functioning. © 2004 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15551333</pmid><doi>10.1002/ajmg.a.30353</doi><tpages>8</tpages></addata></record> |
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subjects | Adolescent Age Factors Biological and medical sciences Child Child, Preschool Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...) fragile X Fragile X Mental Retardation Protein Fragile X Syndrome - genetics Fragile X Syndrome - psychology General aspects. Genetic counseling growth curve Humans Immunohistochemistry Intelligence Intelligence Tests Longitudinal Studies Male Medical genetics Medical sciences Mutation Nerve Tissue Proteins - analysis Nerve Tissue Proteins - genetics nonverbal IQ RNA-Binding Proteins - analysis RNA-Binding Proteins - genetics |
title | Mapping nonverbal IQ in young boys with fragile X syndrome |
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