K04 Incidence and course of irritability in huntington's disease
BackgroundIrritability is a common neuropsychiatric symptom in patients with Huntington's disease (HD).AimThe objective is to examine incidence, course and predictors of irritablity in subjects with HD.MethodsAt baseline, irritability was measured with the Irritability Scale (IS) in 124 HD muta...
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Veröffentlicht in: | Journal of neurology, neurosurgery and psychiatry neurosurgery and psychiatry, 2012-09, Vol.83 (Suppl 1), p.A42-A42 |
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description | BackgroundIrritability is a common neuropsychiatric symptom in patients with Huntington's disease (HD).AimThe objective is to examine incidence, course and predictors of irritablity in subjects with HD.MethodsAt baseline, irritability was measured with the Irritability Scale (IS) in 124 HD mutation carriers, together with sociodemographic, clinical, and neuropsychiatric characteristics. Follow-up evaluation was performed 2 years later on 92 (74%) subjects. Incident and persistent irritability were examined using logistic regression analysis.ResultsAt follow-up, 16 (18%) of the 87 subjects free of irritability at baseline had developed irritability. Of the 37 subjects with irritability at baseline, 13 (35%) no longer fulfilled the criteria of irritability, whereas 24 (65%) were still irritable. In subjects without irritability at baseline, univariate predictors of incident irritability were lower Total Functional Capacity (TFC; p=0.02), higher Unified Huntington's Disease Rating Scale total motor score (UHDRS-m; p=0.009), use of benzodiazepines (p=0.005), use of antidepressants (p=0.04), low Mini-Mental State Examination score (MMSE; p=0.03), and executive cognitive functioning scores (p=0.02) at baseline. A high UHDRS-m score remained a predictor in multivariate analysis. In subjects with irritability at baseline, univariate baseline predictors of persistent vs remitted irritability after 2 years were executive cognitive functioning (p=0.07) and use of antipsychotics (p=0.08).ConclusionIncident irritability in HD is preceded by higher UHDRS-m scores at baseline, which corresponds with the lower TFC scores at baseline in these subjects. The majority of subjects with irritability at baseline remained irritable at follow-up, although no predictors were found. |
doi_str_mv | 10.1136/jnnp-2012-303524.131 |
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Follow-up evaluation was performed 2 years later on 92 (74%) subjects. Incident and persistent irritability were examined using logistic regression analysis.ResultsAt follow-up, 16 (18%) of the 87 subjects free of irritability at baseline had developed irritability. Of the 37 subjects with irritability at baseline, 13 (35%) no longer fulfilled the criteria of irritability, whereas 24 (65%) were still irritable. In subjects without irritability at baseline, univariate predictors of incident irritability were lower Total Functional Capacity (TFC; p=0.02), higher Unified Huntington's Disease Rating Scale total motor score (UHDRS-m; p=0.009), use of benzodiazepines (p=0.005), use of antidepressants (p=0.04), low Mini-Mental State Examination score (MMSE; p=0.03), and executive cognitive functioning scores (p=0.02) at baseline. A high UHDRS-m score remained a predictor in multivariate analysis. In subjects with irritability at baseline, univariate baseline predictors of persistent vs remitted irritability after 2 years were executive cognitive functioning (p=0.07) and use of antipsychotics (p=0.08).ConclusionIncident irritability in HD is preceded by higher UHDRS-m scores at baseline, which corresponds with the lower TFC scores at baseline in these subjects. The majority of subjects with irritability at baseline remained irritable at follow-up, although no predictors were found.</description><identifier>ISSN: 0022-3050</identifier><identifier>EISSN: 1468-330X</identifier><identifier>DOI: 10.1136/jnnp-2012-303524.131</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd</publisher><subject>Huntingtons disease ; Incidence ; irritability</subject><ispartof>Journal of neurology, neurosurgery and psychiatry, 2012-09, Vol.83 (Suppl 1), p.A42-A42</ispartof><rights>2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><rights>2012 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://jnnp.bmj.com/content/83/Suppl_1/A42.2.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttps://jnnp.bmj.com/content/83/Suppl_1/A42.2.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,776,780,3183,23550,27901,27902,77342,77373</link.rule.ids></links><search><creatorcontrib>Reedeker, N</creatorcontrib><creatorcontrib>Bouwens, J</creatorcontrib><creatorcontrib>Giltay, E</creatorcontrib><creatorcontrib>van der Mast, R</creatorcontrib><creatorcontrib>Roos, R</creatorcontrib><creatorcontrib>van Duijn, E</creatorcontrib><title>K04 Incidence and course of irritability in huntington's disease</title><title>Journal of neurology, neurosurgery and psychiatry</title><addtitle>J Neurol Neurosurg Psychiatry</addtitle><description>BackgroundIrritability is a common neuropsychiatric symptom in patients with Huntington's disease (HD).AimThe objective is to examine incidence, course and predictors of irritablity in subjects with HD.MethodsAt baseline, irritability was measured with the Irritability Scale (IS) in 124 HD mutation carriers, together with sociodemographic, clinical, and neuropsychiatric characteristics. Follow-up evaluation was performed 2 years later on 92 (74%) subjects. Incident and persistent irritability were examined using logistic regression analysis.ResultsAt follow-up, 16 (18%) of the 87 subjects free of irritability at baseline had developed irritability. Of the 37 subjects with irritability at baseline, 13 (35%) no longer fulfilled the criteria of irritability, whereas 24 (65%) were still irritable. In subjects without irritability at baseline, univariate predictors of incident irritability were lower Total Functional Capacity (TFC; p=0.02), higher Unified Huntington's Disease Rating Scale total motor score (UHDRS-m; p=0.009), use of benzodiazepines (p=0.005), use of antidepressants (p=0.04), low Mini-Mental State Examination score (MMSE; p=0.03), and executive cognitive functioning scores (p=0.02) at baseline. A high UHDRS-m score remained a predictor in multivariate analysis. In subjects with irritability at baseline, univariate baseline predictors of persistent vs remitted irritability after 2 years were executive cognitive functioning (p=0.07) and use of antipsychotics (p=0.08).ConclusionIncident irritability in HD is preceded by higher UHDRS-m scores at baseline, which corresponds with the lower TFC scores at baseline in these subjects. The majority of subjects with irritability at baseline remained irritable at follow-up, although no predictors were found.</description><subject>Huntingtons disease</subject><subject>Incidence</subject><subject>irritability</subject><issn>0022-3050</issn><issn>1468-330X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqNkL9OwzAQhy0EEqXwBgyRGJjS-vwvzggVlIoKhFQQm-XEDri0TrFTiW4svChPQqIgZm654b7f3elD6BTwCICK8dL7TUowkJRiygkbAYU9NAAmZEopft5HA4xJN-X4EB3FuMRdyXyALm8x-_78mvnSGetLm2hvkrLehmiTukpcCK7RhVu5Zpc4n7xufeP8S1P785gYF62O9hgdVHoV7clvH6LH66vF5Cad309nk4t5WkCeQVqYglqOBZiK85JyyHWFcZULYwwWmogSGAaQRjMtSyltBQU1IEnGMmYZoUN01u_dhPp9a2Ojlu2fvj2pCIDIORVEtBTrqTLUMQZbqU1wax12CrDqbKnOlupsqd6Wam21sbSPudjYj7-MDm9KZDTj6u5pouYwXdCHBVWy5cc9X6yX_7vwA-kce0w</recordid><startdate>201209</startdate><enddate>201209</enddate><creator>Reedeker, N</creator><creator>Bouwens, J</creator><creator>Giltay, E</creator><creator>van der Mast, R</creator><creator>Roos, R</creator><creator>van Duijn, E</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope></search><sort><creationdate>201209</creationdate><title>K04 Incidence and course of irritability in huntington's disease</title><author>Reedeker, N ; Bouwens, J ; Giltay, E ; van der Mast, R ; Roos, R ; van Duijn, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1971-bdb3e5061df55c3519af00f96ddd06a26c140118da4a8c88ef1b3d1827474e423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Huntingtons disease</topic><topic>Incidence</topic><topic>irritability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reedeker, N</creatorcontrib><creatorcontrib>Bouwens, J</creatorcontrib><creatorcontrib>Giltay, E</creatorcontrib><creatorcontrib>van der Mast, R</creatorcontrib><creatorcontrib>Roos, R</creatorcontrib><creatorcontrib>van Duijn, E</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><jtitle>Journal of neurology, neurosurgery and psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reedeker, N</au><au>Bouwens, J</au><au>Giltay, E</au><au>van der Mast, R</au><au>Roos, R</au><au>van Duijn, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>K04 Incidence and course of irritability in huntington's disease</atitle><jtitle>Journal of neurology, neurosurgery and psychiatry</jtitle><addtitle>J Neurol Neurosurg Psychiatry</addtitle><date>2012-09</date><risdate>2012</risdate><volume>83</volume><issue>Suppl 1</issue><spage>A42</spage><epage>A42</epage><pages>A42-A42</pages><issn>0022-3050</issn><eissn>1468-330X</eissn><abstract>BackgroundIrritability is a common neuropsychiatric symptom in patients with Huntington's disease (HD).AimThe objective is to examine incidence, course and predictors of irritablity in subjects with HD.MethodsAt baseline, irritability was measured with the Irritability Scale (IS) in 124 HD mutation carriers, together with sociodemographic, clinical, and neuropsychiatric characteristics. Follow-up evaluation was performed 2 years later on 92 (74%) subjects. Incident and persistent irritability were examined using logistic regression analysis.ResultsAt follow-up, 16 (18%) of the 87 subjects free of irritability at baseline had developed irritability. Of the 37 subjects with irritability at baseline, 13 (35%) no longer fulfilled the criteria of irritability, whereas 24 (65%) were still irritable. In subjects without irritability at baseline, univariate predictors of incident irritability were lower Total Functional Capacity (TFC; p=0.02), higher Unified Huntington's Disease Rating Scale total motor score (UHDRS-m; p=0.009), use of benzodiazepines (p=0.005), use of antidepressants (p=0.04), low Mini-Mental State Examination score (MMSE; p=0.03), and executive cognitive functioning scores (p=0.02) at baseline. A high UHDRS-m score remained a predictor in multivariate analysis. In subjects with irritability at baseline, univariate baseline predictors of persistent vs remitted irritability after 2 years were executive cognitive functioning (p=0.07) and use of antipsychotics (p=0.08).ConclusionIncident irritability in HD is preceded by higher UHDRS-m scores at baseline, which corresponds with the lower TFC scores at baseline in these subjects. The majority of subjects with irritability at baseline remained irritable at follow-up, although no predictors were found.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd</pub><doi>10.1136/jnnp-2012-303524.131</doi><oa>free_for_read</oa></addata></record> |
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title | K04 Incidence and course of irritability in huntington's disease |
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