Literature DB >> 24828898

Neuropsychiatric symptoms in a European Huntington's disease cohort (REGISTRY).

Erik van Duijn1, David Craufurd2, Anna A M Hubers3, Erik J Giltay3, Raphael Bonelli4, Hugh Rickards5, Karen E Anderson6, Marleen R van Walsem7, Rose C van der Mast3, Michael Orth8, G Bernhard Landwehrmeyer8.   

Abstract

BACKGROUND: The majority of Huntington's disease (HD) mutation carriers experience some psychopathology during their lifetime, varying from irritability to psychosis, but prevalences of particular symptoms vary widely due to diverse study populations in different stages of HD and the use of different assessment methods.
METHODS: The study population consisted of 1993 HD mutation carriers from 15 European countries, all participating in the observational REGISTRY study. The behavioural section of the Unified HD Rating Scale was used to examine the prevalence and correlates of five neuropsychiatric features: depression, irritability/aggression, obsessive/compulsive behaviours, apathy and psychosis.
RESULTS: Twenty-seven per cent of the participants did not have any neuropsychiatric symptom in the last month. Moderate to severe apathy occurred in 28.1% of the participants, whereas moderate to severe depression was found in 12.7%. Irritable/aggressive symptoms were present in 13.9% of the participants, and 13.2% showed obsessive/compulsive behaviours. Moderate to severe psychotic symptoms were found in only 1.2%. Only 54.9% of all participants with moderate to severe depression used antidepressants, suggesting undertreatment of depression. Obsessive/compulsive behaviours and irritability/aggression were inversely correlated with the Total Functional Capacity score, but with apathy showing the strongest inverse association.
CONCLUSIONS: A variety of neuropsychiatric symptoms are highly prevalent in different stages of HD in this European HD population, with apathy as the most frequent symptom. Depression, irritability/aggression and OCBs are prevalent in all stages of HD. Apathy was the key neuropsychiatric symptom occurring most often in advanced HD stages. Due to possible selection of relatively healthy participants, prevalences reported in this study might be an underestimation of prevalence in the entire HD population. 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.

Entities:  

Keywords:  BEHAVIOURAL DISORDER; DEPRESSION; HUNTINGTON'S; MOVEMENT DISORDERS; NEUROPSYCHIATRY

Mesh:

Year:  2014        PMID: 24828898     DOI: 10.1136/jnnp-2013-307343

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  54 in total

1.  Validation of Neuro-QoL and PROMIS Mental Health Patient Reported Outcome Measures in Persons with Huntington Disease.

Authors:  Noelle E Carlozzi; Siera Goodnight; Anna L Kratz; Julie C Stout; Michael K McCormack; Jane S Paulsen; Nicholas R Boileau; David Cella; Rebecca E Ready
Journal:  J Huntingtons Dis       Date:  2019

2.  Vocal emotion processing deficits in HIV-infected individuals.

Authors:  A González-Baeza; J R Arribas; I Pérez-Valero; S Monge; C Bayón; P Martín; S Rubio; F Carvajal
Journal:  J Neurovirol       Date:  2016-12-09       Impact factor: 2.643

Review 3.  Therapeutic Update on Huntington's Disease: Symptomatic Treatments and Emerging Disease-Modifying Therapies.

Authors:  Deepa Dash; Tiago A Mestre
Journal:  Neurotherapeutics       Date:  2020-10       Impact factor: 7.620

4.  Behavioral Changes in Huntington Disease

Authors:  Jason Brandt
Journal:  Cogn Behav Neurol       Date:  2018-03       Impact factor: 1.600

5.  Self-report depressive symptoms are dissociated from tremor severity in essential tremor.

Authors:  Edward D Huey; Stephanie Cosentino; Silvia Chapman; Martina Azar; Brittany Rohl; Kathleen Collins; Sarah Morgan; Xinhua Liu; Elan D Louis
Journal:  Parkinsonism Relat Disord       Date:  2018-02-20       Impact factor: 4.891

6.  Motivational Impairment is Accompanied by Corticoaccumbal Dysfunction in the BACHD-Tg5 Rat Model of Huntington's Disease.

Authors:  Natalie E Zlebnik; Iness Gildish; Thibaut Sesia; Aurelie Fitoussi; Ellen A Cole; Brian P Carson; Roger Cachope; Joseph F Cheer
Journal:  Cereb Cortex       Date:  2019-12-17       Impact factor: 5.357

Review 7.  Neuropalliative Care: A Practical Guide for the Neurologist.

Authors:  K Brizzi; C J Creutzfeldt
Journal:  Semin Neurol       Date:  2018-10-15       Impact factor: 3.420

Review 8.  Huntington's Disease-Update on Treatments.

Authors:  Kara J Wyant; Andrew J Ridder; Praveen Dayalu
Journal:  Curr Neurol Neurosci Rep       Date:  2017-04       Impact factor: 5.081

9.  Resting-state connectivity and modulated somatomotor and default-mode networks in Huntington disease.

Authors:  Cristina Sánchez-Castañeda; Francesco de Pasquale; Chiara Falletta Caravasso; Massimo Marano; Sabrina Maffi; Simone Migliore; Umberto Sabatini; Ferdinando Squitieri
Journal:  CNS Neurosci Ther       Date:  2017-05-02       Impact factor: 5.243

Review 10.  Depressive symptoms in neurodegenerative diseases.

Authors:  Miquel Baquero; Nuria Martín
Journal:  World J Clin Cases       Date:  2015-08-16       Impact factor: 1.337

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