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
Hauptverfasser: Reedeker, N, Bouwens, J, Giltay, E, van der Mast, R, Roos, R, van Duijn, E
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container_end_page A42
container_issue Suppl 1
container_start_page A42
container_title Journal of neurology, neurosurgery and psychiatry
container_volume 83
creator Reedeker, N
Bouwens, J
Giltay, E
van der Mast, R
Roos, R
van Duijn, E
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. 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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.</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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subjects Huntingtons disease
Incidence
irritability
title K04 Incidence and course of irritability in huntington's disease
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