Literature DB >> 25063513

Quality of life in Huntington's disease: a comparative study investigating the impact for those with pre-manifest and early manifest disease, and their partners.

Joy Read1, Rebecca Jones2, Gail Owen1, Blair R Leavitt3, Allison Coleman3, Raymund A C Roos4, Eve M Dumas4, Alexandra Durr5, Damian Justo5, Miranda Say1, Julie C Stout6, Sarah J Tabrizi1, David Craufurd7.   

Abstract

BACKGROUND: Given the multifaceted nature of this inherited neurodegenerative condition, typically affecting adults in mid-life, it is perhaps not surprising that studies indicate poorer Health Related Quality of Life (HrQoL) in those with the gene-expansion and, by association, in their families.
OBJECTIVE: This study aimed to extend the current literature by exploring specific life domains, including at an earlier disease stage than usually reported in the HRQoL literature, and in a subgroup of gene-negative partners.
METHODS: 355 participants from the TRACK-HD cohort (120 Controls, 118 Pre-HD and 117 early-HD) completed standardised self-report measures of HrQoL (SF36 and QoLI), underwent clinical assessments of capacity and motor function (UHDRS), semi structured interviews assessing neuropsychiatric symptoms (PBA-s), completed paper and computerized cognitive tasks and assessment of behaviours associated with damage to frontal brain circuits (FrSBe).
RESULTS: Each gene-expanded group scored statistically significantly lower than gene-negative sibling controls on the SF36 General Health subscale; neuropsychiatric symptoms and executive dysfunction were associated with reduced HrQoL. Those with Stage II disease reported statistically significantly lower HrQoL than gene-negative controls across physical, emotional and social life domains. Those partnered with manifest participants reported lower HrQoL in the social domain compared to those partnered with at-risk participants furthest from disease onset; and perseverative symptoms in manifest partners were found to be related to lower HrQoL in their gene-negative partners. HrQoL in gene-negative partners of pre-manifest individuals was associated with pre-manifest individuals' neuropsychiatric and cognitive function.
CONCLUSIONS: Understanding the nature and timing of disruption to the HrQoL in people who are pre-manifest and diagnosed with HD, and their gene-negative partners, can inform the development of appropriate strategies and interventions.

Entities:  

Keywords:  Huntington's disease; TRACK-HD; cognitive function; life domains; neuropsychiatric function; quality of life

Mesh:

Year:  2013        PMID: 25063513     DOI: 10.3233/JHD-130051

Source DB:  PubMed          Journal:  J Huntingtons Dis        ISSN: 1879-6397


  16 in total

1.  Surface-based morphometry reveals caudate subnuclear structural damage in patients with premotor Huntington disease.

Authors:  Hosung Kim; Ji-Hoon Kim; Katherine L Possin; Joseph Winer; Michael D Geschwind; Duan Xu; Christopher P Hess
Journal:  Brain Imaging Behav       Date:  2017-10       Impact factor: 3.978

2.  Perceptions of the impact of chorea on health-related quality of life in Huntington disease (HD): A qualitative analysis of individuals across the HD spectrum, family members, and clinicians.

Authors:  Carey Wexler Sherman; Ravi Iyer; Victor Abler; Alexandria Antonelli; Noelle E Carlozzi
Journal:  Neuropsychol Rehabil       Date:  2019-03-08       Impact factor: 2.868

3.  Factors influencing the clinical expression of intermediate CAG repeat length mutations of the Huntington's disease gene.

Authors:  Peter K Panegyres; Chen-Chun Shu; Huei-Yang Chen; Jane S Paulsen
Journal:  J Neurol       Date:  2014-11-08       Impact factor: 4.849

4.  Patient-reported outcome measures in Huntington disease: Quality of life in neurological disorders (Neuro-QoL) social functioning measures.

Authors:  Noelle E Carlozzi; Elizabeth A Hahn; Siera M Goodnight; Anna L Kratz; Jane S Paulsen; Julie C Stout; Samuel Frank; Jennifer A Miner; David Cella; Richard C Gershon; Stephen G Schilling; Rebecca E Ready
Journal:  Psychol Assess       Date:  2017-05-29

5.  Understanding the need for assistance with survey completion in people with Huntington disease.

Authors:  Elizabeth A Hahn; Nancy R Downing; Julie C Stout; Jane S Paulsen; Becky Ready; Siera Goodnight; Jin-Shei Lai; Jennifer A Miner; Noelle E Carlozzi
Journal:  Qual Life Res       Date:  2017-12-06       Impact factor: 4.147

6.  Relationships Among Apathy, Health-Related Quality of Life, and Function in Huntington's Disease.

Authors:  Nora E Fritz; Nicholas R Boileau; Julie C Stout; Rebecca Ready; Joel S Perlmutter; Jane S Paulsen; Kimberly Quaid; Stacey Barton; Michael K McCormack; Susan L Perlman; Noelle E Carlozzi
Journal:  J Neuropsychiatry Clin Neurosci       Date:  2018-03-21       Impact factor: 2.198

7.  The development of a new computer adaptive test to evaluate chorea in Huntington disease: HDQLIFE Chorea.

Authors:  N E Carlozzi; N R Downing; S G Schilling; J-S Lai; S M Goodnight; J A Miner; S A Frank
Journal:  Qual Life Res       Date:  2016-05-03       Impact factor: 4.147

8.  Disease Burden of Huntington's Disease (HD) on People Living with HD and Care Partners in Canada.

Authors:  Eileen Shaw; Michelle Mayer; Paul Ekwaru; Suzanne McMullen; Erin Graves; Jennifer W Wu; Nathalie Budd; Bridget Maturi; Tara Cowling; Tiago A Mestre
Journal:  J Huntingtons Dis       Date:  2022

9.  Health-related quality of life and unmet healthcare needs in Huntington's disease.

Authors:  Marleen R van Walsem; Emilie I Howe; Gunvor A Ruud; Jan C Frich; Nada Andelic
Journal:  Health Qual Life Outcomes       Date:  2017-01-07       Impact factor: 3.186

10.  Assistive Technology for Cognition and Health-related Quality of Life in Huntington's Disease.

Authors:  Marleen R van Walsem; Emilie I Howe; Jan C Frich; Nada Andelic
Journal:  J Huntingtons Dis       Date:  2016-10-01
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