Disease-related and genetic correlates of psychotic symptoms in Parkinson's disease
Our aim was to examine disease‐related and genetic correlates of the development of psychotic symptoms in a large population of patients with Parkinson's disease. We studied 500 patients with Parkinson's disease from the NeuroGenetics Research Consortium using logistic regression models. P...
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creator | Factor, Stewart A. Steenland, N. Kyle Higgins, Donald S. Molho, Eric S. Kay, Denise M. Montimurro, Jennifer Rosen, Ami R. Zabetian, Cyrus P. Payami, Haydeh |
description | Our aim was to examine disease‐related and genetic correlates of the development of psychotic symptoms in a large population of patients with Parkinson's disease. We studied 500 patients with Parkinson's disease from the NeuroGenetics Research Consortium using logistic regression models. Predictors were demographic, clinical (motor/nonmotor features), and genetic, measured as continuous or dichotomous variables. Continuous measures were divided into population‐based tertiles. Results are given as odds ratios (95% confidence intervals) for dichotomous variables and by ascending tertile for continuous variables. Psychotic symptoms were associated with increasing age: 4.86 (1.62–14.30) and 6.25 (2.09–18.74) (test for trend: P = 0.01); and duration of disease: 3.81 (1.23–11.76) and 5.33 (1.68–16.89) (test for trend: P = 0.03). For nonmotor features, we demonstrated positive trends with depression: 1.31 (0.47–3.61) and 5.01 (2.04–12.33) (test for trend: P < 0.0001); cognitive dysfunction: 0.69 (0.26–1.84) and 2.51 (1.00–6.29) (test for trend: P = 0.03); and an excess for those with sleep disorders: 2.00 (1.03–3.89) (P = 0.04). Psychotic symptoms were not associated with tremor or postural instability scores, but there was an association with freezing of gait: 3.83 (1.67–8.75) (P < 0.002). Psychotic symptoms were not associated with the presence of any examined polymorphisms in the apolipoprotein, alpha‐synuclein, or microtubule associated protein tau genes. This is the largest study to examine correlates of psychotic symptoms in Parkinson's disease. We discovered a novel association with freezing of gait. We demonstrated an association with depression and duration of disease, both of which were inconsistently related in previous studies, and confirmed the association with age, cognitive dysfunction, and sleep disorders. © 2011 Movement Disorder Society |
doi_str_mv | 10.1002/mds.23806 |
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Kyle ; Higgins, Donald S. ; Molho, Eric S. ; Kay, Denise M. ; Montimurro, Jennifer ; Rosen, Ami R. ; Zabetian, Cyrus P. ; Payami, Haydeh</creator><creatorcontrib>Factor, Stewart A. ; Steenland, N. Kyle ; Higgins, Donald S. ; Molho, Eric S. ; Kay, Denise M. ; Montimurro, Jennifer ; Rosen, Ami R. ; Zabetian, Cyrus P. ; Payami, Haydeh</creatorcontrib><description>Our aim was to examine disease‐related and genetic correlates of the development of psychotic symptoms in a large population of patients with Parkinson's disease. We studied 500 patients with Parkinson's disease from the NeuroGenetics Research Consortium using logistic regression models. Predictors were demographic, clinical (motor/nonmotor features), and genetic, measured as continuous or dichotomous variables. Continuous measures were divided into population‐based tertiles. Results are given as odds ratios (95% confidence intervals) for dichotomous variables and by ascending tertile for continuous variables. Psychotic symptoms were associated with increasing age: 4.86 (1.62–14.30) and 6.25 (2.09–18.74) (test for trend: P = 0.01); and duration of disease: 3.81 (1.23–11.76) and 5.33 (1.68–16.89) (test for trend: P = 0.03). For nonmotor features, we demonstrated positive trends with depression: 1.31 (0.47–3.61) and 5.01 (2.04–12.33) (test for trend: P < 0.0001); cognitive dysfunction: 0.69 (0.26–1.84) and 2.51 (1.00–6.29) (test for trend: P = 0.03); and an excess for those with sleep disorders: 2.00 (1.03–3.89) (P = 0.04). Psychotic symptoms were not associated with tremor or postural instability scores, but there was an association with freezing of gait: 3.83 (1.67–8.75) (P < 0.002). Psychotic symptoms were not associated with the presence of any examined polymorphisms in the apolipoprotein, alpha‐synuclein, or microtubule associated protein tau genes. This is the largest study to examine correlates of psychotic symptoms in Parkinson's disease. We discovered a novel association with freezing of gait. We demonstrated an association with depression and duration of disease, both of which were inconsistently related in previous studies, and confirmed the association with age, cognitive dysfunction, and sleep disorders. © 2011 Movement Disorder Society</description><identifier>ISSN: 0885-3185</identifier><identifier>EISSN: 1531-8257</identifier><identifier>DOI: 10.1002/mds.23806</identifier><identifier>PMID: 21714002</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Age Factors ; Aged ; alpha-Synuclein - genetics ; Apolipoproteins E - genetics ; Biological and medical sciences ; Cognition Disorders - etiology ; Community Health Planning ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; depression ; Female ; freezing of gait ; genetics ; Humans ; Logistic Models ; Male ; Medical sciences ; Middle Aged ; Neurology ; Parkinson Disease - complications ; Parkinson Disease - genetics ; Parkinson's disease ; Polymorphism, Single Nucleotide - genetics ; psychosis ; Psychotic Disorders - etiology ; Psychotic Disorders - genetics ; Risk Factors ; Severity of Illness Index ; sleep ; tau Proteins - genetics</subject><ispartof>Movement disorders, 2011-10, Vol.26 (12), p.2190-2195</ispartof><rights>Copyright © 2011 Movement Disorder Society</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Movement Disorder Society.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4826-282ddf88b96bbe7fe6d634f5664fcf913e931351e6e9c060d9c15693affebe43</citedby><cites>FETCH-LOGICAL-c4826-282ddf88b96bbe7fe6d634f5664fcf913e931351e6e9c060d9c15693affebe43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmds.23806$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmds.23806$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24704433$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21714002$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Factor, Stewart A.</creatorcontrib><creatorcontrib>Steenland, N. Kyle</creatorcontrib><creatorcontrib>Higgins, Donald S.</creatorcontrib><creatorcontrib>Molho, Eric S.</creatorcontrib><creatorcontrib>Kay, Denise M.</creatorcontrib><creatorcontrib>Montimurro, Jennifer</creatorcontrib><creatorcontrib>Rosen, Ami R.</creatorcontrib><creatorcontrib>Zabetian, Cyrus P.</creatorcontrib><creatorcontrib>Payami, Haydeh</creatorcontrib><title>Disease-related and genetic correlates of psychotic symptoms in Parkinson's disease</title><title>Movement disorders</title><addtitle>Mov. Disord</addtitle><description>Our aim was to examine disease‐related and genetic correlates of the development of psychotic symptoms in a large population of patients with Parkinson's disease. We studied 500 patients with Parkinson's disease from the NeuroGenetics Research Consortium using logistic regression models. Predictors were demographic, clinical (motor/nonmotor features), and genetic, measured as continuous or dichotomous variables. Continuous measures were divided into population‐based tertiles. Results are given as odds ratios (95% confidence intervals) for dichotomous variables and by ascending tertile for continuous variables. Psychotic symptoms were associated with increasing age: 4.86 (1.62–14.30) and 6.25 (2.09–18.74) (test for trend: P = 0.01); and duration of disease: 3.81 (1.23–11.76) and 5.33 (1.68–16.89) (test for trend: P = 0.03). For nonmotor features, we demonstrated positive trends with depression: 1.31 (0.47–3.61) and 5.01 (2.04–12.33) (test for trend: P < 0.0001); cognitive dysfunction: 0.69 (0.26–1.84) and 2.51 (1.00–6.29) (test for trend: P = 0.03); and an excess for those with sleep disorders: 2.00 (1.03–3.89) (P = 0.04). Psychotic symptoms were not associated with tremor or postural instability scores, but there was an association with freezing of gait: 3.83 (1.67–8.75) (P < 0.002). Psychotic symptoms were not associated with the presence of any examined polymorphisms in the apolipoprotein, alpha‐synuclein, or microtubule associated protein tau genes. This is the largest study to examine correlates of psychotic symptoms in Parkinson's disease. We discovered a novel association with freezing of gait. We demonstrated an association with depression and duration of disease, both of which were inconsistently related in previous studies, and confirmed the association with age, cognitive dysfunction, and sleep disorders. © 2011 Movement Disorder Society</description><subject>Age Factors</subject><subject>Aged</subject><subject>alpha-Synuclein - genetics</subject><subject>Apolipoproteins E - genetics</subject><subject>Biological and medical sciences</subject><subject>Cognition Disorders - etiology</subject><subject>Community Health Planning</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>depression</subject><subject>Female</subject><subject>freezing of gait</subject><subject>genetics</subject><subject>Humans</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Parkinson Disease - complications</subject><subject>Parkinson Disease - genetics</subject><subject>Parkinson's disease</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>psychosis</subject><subject>Psychotic Disorders - etiology</subject><subject>Psychotic Disorders - genetics</subject><subject>Risk Factors</subject><subject>Severity of Illness Index</subject><subject>sleep</subject><subject>tau Proteins - genetics</subject><issn>0885-3185</issn><issn>1531-8257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU9v1DAQxS0EokvhwBdAuaCKQ1o7_hPnglR1oQW1gNQKjpbjjFtDYi-eLLDfnrTZLnDgNNLM771n-RHynNFDRml1NHR4WHFN1QOyYJKzUleyfkgWVGtZcqblHnmC-JVSxiRTj8lexWomJuWCXC4DgkUoM_R2hK6wsSuuIcIYXOFSntdYJF-scONu0u0eN8NqTAMWIRafbP4WIqZ4gEU3ez0lj7ztEZ5t5z65evvm6uSsPP94-u7k-Lx0QleqrHTVdV7rtlFtC7UH1SkuvFRKeOcbxqHhjEsGChpHFe0ax6RquPUeWhB8n7yebVfrdoDOQRyz7c0qh8HmjUk2mH8vMdyY6_TDiIopVdeTwcHWIKfva8DRDAEd9L2NkNZoGkoV1_yOfDWTLifEDH6Xwqi5rcBMFZi7Cib2xd_P2pH3fz4BL7eARWd7n210Af9woqZCcD5xRzP3M_Sw-X-iuVhe3keXsyLgCL92iqkho2peS_Plw6l5_3l5sWzOtJH8Nw0CrnI</recordid><startdate>201110</startdate><enddate>201110</enddate><creator>Factor, Stewart A.</creator><creator>Steenland, N. Kyle</creator><creator>Higgins, Donald S.</creator><creator>Molho, Eric S.</creator><creator>Kay, Denise M.</creator><creator>Montimurro, Jennifer</creator><creator>Rosen, Ami R.</creator><creator>Zabetian, Cyrus P.</creator><creator>Payami, Haydeh</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>201110</creationdate><title>Disease-related and genetic correlates of psychotic symptoms in Parkinson's disease</title><author>Factor, Stewart A. ; Steenland, N. Kyle ; Higgins, Donald S. ; Molho, Eric S. ; Kay, Denise M. ; Montimurro, Jennifer ; Rosen, Ami R. ; Zabetian, Cyrus P. ; Payami, Haydeh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4826-282ddf88b96bbe7fe6d634f5664fcf913e931351e6e9c060d9c15693affebe43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Age Factors</topic><topic>Aged</topic><topic>alpha-Synuclein - genetics</topic><topic>Apolipoproteins E - genetics</topic><topic>Biological and medical sciences</topic><topic>Cognition Disorders - etiology</topic><topic>Community Health Planning</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>depression</topic><topic>Female</topic><topic>freezing of gait</topic><topic>genetics</topic><topic>Humans</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Parkinson Disease - complications</topic><topic>Parkinson Disease - genetics</topic><topic>Parkinson's disease</topic><topic>Polymorphism, Single Nucleotide - genetics</topic><topic>psychosis</topic><topic>Psychotic Disorders - etiology</topic><topic>Psychotic Disorders - genetics</topic><topic>Risk Factors</topic><topic>Severity of Illness Index</topic><topic>sleep</topic><topic>tau Proteins - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Factor, Stewart A.</creatorcontrib><creatorcontrib>Steenland, N. Kyle</creatorcontrib><creatorcontrib>Higgins, Donald S.</creatorcontrib><creatorcontrib>Molho, Eric S.</creatorcontrib><creatorcontrib>Kay, Denise M.</creatorcontrib><creatorcontrib>Montimurro, Jennifer</creatorcontrib><creatorcontrib>Rosen, Ami R.</creatorcontrib><creatorcontrib>Zabetian, Cyrus P.</creatorcontrib><creatorcontrib>Payami, Haydeh</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Movement disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Factor, Stewart A.</au><au>Steenland, N. Kyle</au><au>Higgins, Donald S.</au><au>Molho, Eric S.</au><au>Kay, Denise M.</au><au>Montimurro, Jennifer</au><au>Rosen, Ami R.</au><au>Zabetian, Cyrus P.</au><au>Payami, Haydeh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Disease-related and genetic correlates of psychotic symptoms in Parkinson's disease</atitle><jtitle>Movement disorders</jtitle><addtitle>Mov. Disord</addtitle><date>2011-10</date><risdate>2011</risdate><volume>26</volume><issue>12</issue><spage>2190</spage><epage>2195</epage><pages>2190-2195</pages><issn>0885-3185</issn><eissn>1531-8257</eissn><abstract>Our aim was to examine disease‐related and genetic correlates of the development of psychotic symptoms in a large population of patients with Parkinson's disease. We studied 500 patients with Parkinson's disease from the NeuroGenetics Research Consortium using logistic regression models. Predictors were demographic, clinical (motor/nonmotor features), and genetic, measured as continuous or dichotomous variables. Continuous measures were divided into population‐based tertiles. Results are given as odds ratios (95% confidence intervals) for dichotomous variables and by ascending tertile for continuous variables. Psychotic symptoms were associated with increasing age: 4.86 (1.62–14.30) and 6.25 (2.09–18.74) (test for trend: P = 0.01); and duration of disease: 3.81 (1.23–11.76) and 5.33 (1.68–16.89) (test for trend: P = 0.03). For nonmotor features, we demonstrated positive trends with depression: 1.31 (0.47–3.61) and 5.01 (2.04–12.33) (test for trend: P < 0.0001); cognitive dysfunction: 0.69 (0.26–1.84) and 2.51 (1.00–6.29) (test for trend: P = 0.03); and an excess for those with sleep disorders: 2.00 (1.03–3.89) (P = 0.04). Psychotic symptoms were not associated with tremor or postural instability scores, but there was an association with freezing of gait: 3.83 (1.67–8.75) (P < 0.002). Psychotic symptoms were not associated with the presence of any examined polymorphisms in the apolipoprotein, alpha‐synuclein, or microtubule associated protein tau genes. This is the largest study to examine correlates of psychotic symptoms in Parkinson's disease. We discovered a novel association with freezing of gait. We demonstrated an association with depression and duration of disease, both of which were inconsistently related in previous studies, and confirmed the association with age, cognitive dysfunction, and sleep disorders. © 2011 Movement Disorder Society</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>21714002</pmid><doi>10.1002/mds.23806</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Age Factors Aged alpha-Synuclein - genetics Apolipoproteins E - genetics Biological and medical sciences Cognition Disorders - etiology Community Health Planning Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases depression Female freezing of gait genetics Humans Logistic Models Male Medical sciences Middle Aged Neurology Parkinson Disease - complications Parkinson Disease - genetics Parkinson's disease Polymorphism, Single Nucleotide - genetics psychosis Psychotic Disorders - etiology Psychotic Disorders - genetics Risk Factors Severity of Illness Index sleep tau Proteins - genetics |
title | Disease-related and genetic correlates of psychotic symptoms in Parkinson's disease |
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