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Psychiatric Illness and Intellectual Disability in the Prader–Willi Syndrome with Different Molecular Defects - A Meta Analysis

Publication Date: August 14, 2013
Journal: PLOS ONE
Authors: Lin Yang, Guo Dong Zhan, Jun Jie Ding, Hui Jun Wang, et al
Volume: 8
Issue: 8
Pages: e72640
DOI: https://dx.plos.org/10.1371/journal.pone.0072640
Publisher URL: http://journals.plos.org/plosone/article?id=10.1371%2Fjournal.pone.0072640
PubMed: http://www.ncbi.nlm.nih.gov/pubmed/23967326
PubMed Central: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3743792
Europe PMC: http://europepmc.org/abstract/MED/23967326
Web of Science: 000323221500142
Scopus: 84881510247
Mendeley: http://www.mendeley.com/research/psychiatric-illness-intellectual-disability-praderwilli-syndrome-different-molecular-defects-meta-an-1

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{"title"=>"Psychiatric Illness and Intellectual Disability in the Prader-Willi Syndrome with Different Molecular Defects - A Meta Analysis", "type"=>"journal", "authors"=>[{"first_name"=>"Lin", "last_name"=>"Yang", "scopus_author_id"=>"57198987657"}, {"first_name"=>"Guo dong", "last_name"=>"Zhan", "scopus_author_id"=>"55821528500"}, {"first_name"=>"Jun jie", "last_name"=>"Ding", "scopus_author_id"=>"57196527921"}, {"first_name"=>"Hui jun", "last_name"=>"Wang", "scopus_author_id"=>"54942761600"}, {"first_name"=>"Duan", "last_name"=>"Ma", "scopus_author_id"=>"8444245900"}, {"first_name"=>"Guo ying", "last_name"=>"Huang", "scopus_author_id"=>"13309093700"}, {"first_name"=>"Wen hao", "last_name"=>"Zhou", "scopus_author_id"=>"7404516214"}], "year"=>2013, "source"=>"PLoS ONE", "identifiers"=>{"pmid"=>"23967326", "doi"=>"10.1371/journal.pone.0072640", "sgr"=>"84881510247", "scopus"=>"2-s2.0-84881510247", "issn"=>"19326203", "pui"=>"369566645"}, "id"=>"3d467677-771c-3c62-b50b-d9fbea08334a", "abstract"=>"BACKGROUND AND OBJECTIVES: Several studies have suggested a difference in clinical features of intellectual ability and psychiatric illness in the Prader-Willi syndrome (PWS) with the 15q11-q13 paternal deletion and maternal uniparental disomy (mUPD). Our objective was to appraise evidence on this association through a meta-analysis. METHODS: The electronic records PubMed and EMBASE from 1956 to 2012 were extracted for meta-analysis. Meta-analyses were performed by using fixed effect model. Mean difference, odds ratio, and 95% confidence interval were calculated. RESULTS: We retrieved a total of 744 PWS cases from 13 studies. These include 423 cases with paternal 15q11-q13 deletions and 318 cases of mUPD. Compare to the PWS cases with mUPD, PWS patients with the paternal 15q11-q13 deletion associated with significantly lower full scale IQ (FSIQ) [mean difference (MD), -2.69; 95%CI, -4.86 to -0.52; p=0.02] and verbal IQ (VIQ) (MD, -7.5; 95%CI, -9.75 to -5.26; p<0.00001) but higher performance IQ (PIQ) (MD, 4.02; 95%CI, 1.13 to 6.91; p=0.006). In contrast, PWS patients with mUPD are associated with significantly higher risk of psychiatric illness [odds rate (OR), 0.14; 95%CI, 0.08 to 0.23; p<0.00001] and higher risk of bipolar disorder (OR, 0.04; 95%CI, 0.01 to 0.23; p=0.0002). CONCLUSIONS: Significant different clinical features of cognitive development and psychiatric illness are associated with PWS with different molecular defects. These findings provide support for evidence based practice to evaluate and manage the PWS syndrome with different molecular defects.", "link"=>"http://www.mendeley.com/research/psychiatric-illness-intellectual-disability-praderwilli-syndrome-different-molecular-defects-meta-an-1", "reader_count"=>10, "reader_count_by_academic_status"=>{"Student > Doctoral Student"=>1, "Researcher"=>1, "Student > Ph. D. Student"=>3, "Student > Master"=>2, "Student > Bachelor"=>2, "Lecturer"=>1}, "reader_count_by_user_role"=>{"Student > Doctoral Student"=>1, "Researcher"=>1, "Student > Ph. D. Student"=>3, "Student > Master"=>2, "Student > Bachelor"=>2, "Lecturer"=>1}, "reader_count_by_subject_area"=>{"Medicine and Dentistry"=>5, "Agricultural and Biological Sciences"=>1, "Neuroscience"=>1, "Sports and Recreations"=>1, "Psychology"=>2}, "reader_count_by_subdiscipline"=>{"Medicine and Dentistry"=>{"Medicine and Dentistry"=>5}, "Neuroscience"=>{"Neuroscience"=>1}, "Sports and Recreations"=>{"Sports and Recreations"=>1}, "Psychology"=>{"Psychology"=>2}, "Agricultural and Biological Sciences"=>{"Agricultural and Biological Sciences"=>1}}, "reader_count_by_country"=>{"Germany"=>1}, "group_count"=>0}

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Figshare 10529 Apr 04:42 UTC

Figshare

{"files"=>["https://ndownloader.figshare.com/files/1170013"], "description"=>"<div>Background and ObjectivesSeveral studies have suggested a difference in clinical features of intellectual ability and psychiatric illness in the Prader–Willi syndrome (PWS) with the 15q11-q13 paternal deletion and maternal uniparental disomy (mUPD). Our objective was to appraise evidence on this association through a meta-analysis. MethodsThe electronic records PubMed and EMBASE from 1956 to 2012 were extracted for meta-analysis. Meta-analyses were performed by using fixed effect model. Mean difference, odds ratio, and 95% confidence interval were calculated. ResultsWe retrieved a total of 744 PWS cases from 13 studies. These include 423 cases with paternal 15q11-q13 deletions and 318 cases of mUPD. Compare to the PWS cases with mUPD, PWS patients with the paternal 15q11-q13 deletion associated with significantly lower full scale IQ (FSIQ) [mean difference (MD), -2.69; 95%CI, -4.86 to -0.52; p=0.02] and verbal IQ (VIQ) (MD, -7.5; 95%CI, -9.75 to -5.26; p<0.00001) but higher performance IQ (PIQ) (MD, 4.02; 95%CI, 1.13 to 6.91; p=0.006). In contrast, PWS patients with mUPD are associated with significantly higher risk of psychiatric illness [odds rate (OR), 0.14; 95%CI, 0.08 to 0.23; p<0.00001] and higher risk of bipolar disorder (OR, 0.04; 95%CI, 0.01 to 0.23; p=0.0002). ConclusionsSignificant different clinical features of cognitive development and psychiatric illness are associated with PWS with different molecular defects. These findings provide support for evidence based practice to evaluate and manage the PWS syndrome with different molecular defects. </div>", "links"=>[], "tags"=>["molecular", "defects", "meta"], "article_id"=>772736, "categories"=>["Biological Sciences", "Science Policy"], "users"=>["Lin Yang", "Guo-dong Zhan", "Jun-jie Ding", "Hui-jun Wang", "Duan Ma", "Guo-Ying Huang", "Wen-hao Zhou"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0072640", "stats"=>{"downloads"=>2, "page_views"=>8, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Psychiatric_Illness_and_Intellectual_Disability_in_the_Prader_8211_Willi_Syndrome_with_Different_Molecular_Defects_A_Meta_Analysis_/772736", "title"=>"Psychiatric Illness and Intellectual Disability in the Prader–Willi Syndrome with Different Molecular Defects - A Meta Analysis", "pos_in_sequence"=>0, "defined_type"=>3, "published_date"=>"2013-08-14 03:31:08"}
{"files"=>["https://ndownloader.figshare.com/files/1170004"], "description"=>"Flow chart of articles screening and selection process.", "links"=>[], "tags"=>["articles"], "article_id"=>772727, "categories"=>["Biological Sciences", "Science Policy"], "users"=>["Lin Yang", "Guo-dong Zhan", "Jun-jie Ding", "Hui-jun Wang", "Duan Ma", "Guo-Ying Huang", "Wen-hao Zhou"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0072640.g001", "stats"=>{"downloads"=>1, "page_views"=>5, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Flow_chart_of_articles_screening_and_selection_process_/772727", "title"=>"Flow chart of articles screening and selection process.", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2013-08-14 03:31:08"}
{"files"=>["https://ndownloader.figshare.com/files/1170005"], "description"=>"Funnel plot for publication bias about FSIQ.", "links"=>[], "tags"=>[], "article_id"=>772728, "categories"=>["Biological Sciences", "Science Policy"], "users"=>["Lin Yang", "Guo-dong Zhan", "Jun-jie Ding", "Hui-jun Wang", "Duan Ma", "Guo-Ying Huang", "Wen-hao Zhou"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0072640.g002", "stats"=>{"downloads"=>0, "page_views"=>4, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Funnel_plot_for_publication_bias_about_FSIQ_/772728", "title"=>"Funnel plot for publication bias about FSIQ.", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2013-08-14 03:31:08"}
{"files"=>["https://ndownloader.figshare.com/files/1170006"], "description"=>"Meta analysis of the FSIQ in DEL and UPD groups.", "links"=>[], "tags"=>["fsiq", "del", "upd"], "article_id"=>772729, "categories"=>["Biological Sciences", "Science Policy"], "users"=>["Lin Yang", "Guo-dong Zhan", "Jun-jie Ding", "Hui-jun Wang", "Duan Ma", "Guo-Ying Huang", "Wen-hao Zhou"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0072640.g003", "stats"=>{"downloads"=>1, "page_views"=>13, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Meta_analysis_of_the_FSIQ_in_DEL_and_UPD_groups_/772729", "title"=>"Meta analysis of the FSIQ in DEL and UPD groups.", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2013-08-14 03:31:08"}
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PMC Usage Stats 168917 Nov 18:40 UTC

PMC Usage Stats | Further Information

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Relative Metric 8510510 May 17:08 UTC

Relative Metric

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F1000Prime11 Dec 12:26 UTC

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