Literature DB >> 35978062

Brain, cognitive, and physical disability correlates of decreased quality of life in patients with Huntington's disease.

Estefanía Junca1, Mariana Pino2, Hernando Santamaría-García3,4, Sandra Baez5.   

Abstract

PURPOSE: Following a case-control design, as a primary objective, this study aimed to explore the relationship between quality of life (QoL) scores and gray matter (GM) volumes in patients with Huntington's disease (HD). As a secondary objective, we assessed the relationship between QoL scores and other important behavioral, clinical and demographical variables in patients with HD and HD patients' caregivers.
METHODS: We recruited 75 participants (25 HD patients, 25 caregivers, and 25 controls) and assessed their QoL using the World Health Organization Quality of Life scale-Brief Version (WHOQOL-BREF). Participants were also assessed with general cognitive functioning tests and clinical scales. In addition, we acquired MRI scans from all participants.
RESULTS: Our results showed that patients exhibited significantly lower scores in all four QoL domains (physical health, psychological wellbeing, social relationships, and relationship with the environment) compared to caregivers and controls. Caregivers showed lower scores than controls in the physical health and the environmental domains. In HD patients, lower scores in QoL domains were associated with lower GM volumes, mainly in the precuneus and the cerebellum. Moreover, in HD patients, physical disability and GM volume reduction were significant predictors of QoL decrease in all domains. For caregivers, years of formal education was the most important predictor of QoL.
CONCLUSIONS: HD patients exhibit greater GM volume loss as well as lower QoL scores compared to caregivers and controls. However, caregivers displayed lower scores in QoL scores than controls, with years of education being a significant predictor. Our results reflect a first attempt to investigate the relationships among QoL, GM volumes, and other important factors in an HD and HD caregiver sample.
© 2022. The Author(s).

Entities:  

Keywords:  Brain volumes; Caregivers; Huntington’s disease; Quality of life; WHOQOL-BREF

Year:  2022        PMID: 35978062     DOI: 10.1007/s11136-022-03220-0

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   3.440


  36 in total

1.  Impact of Huntington's disease on quality of life.

Authors:  D I Helder; A A Kaptein; G M van Kempen; J C van Houwelingen; R A Roos
Journal:  Mov Disord       Date:  2001-03       Impact factor: 10.338

2.  The World Health Organization's WHOQOL-BREF quality of life assessment: psychometric properties and results of the international field trial. A report from the WHOQOL group.

Authors:  S M Skevington; M Lotfy; K A O'Connell
Journal:  Qual Life Res       Date:  2004-03       Impact factor: 4.147

3.  Predictors of quality of life in carers for people with a progressive neurological illness: a longitudinal study.

Authors:  Elodie J O'Connor; Marita P McCabe
Journal:  Qual Life Res       Date:  2010-12-02       Impact factor: 4.147

4.  Longitudinal atrophy characterization of cortical and subcortical gray matter in Huntington's disease patients.

Authors:  Gabriel Ramirez-Garcia; Víctor Galvez; Rosalinda Diaz; Leo Bayliss; Juan Fernandez-Ruiz; Aurelio Campos-Romo
Journal:  Eur J Neurosci       Date:  2019-12-18       Impact factor: 3.386

5.  Identification of health-related quality of life (HRQOL) issues relevant to individuals with Huntington disease.

Authors:  Noelle E Carlozzi; David S Tulsky
Journal:  J Health Psychol       Date:  2012-03-16

Review 6.  Caring for the carers: quality of life in Huntington's disease.

Authors:  Aimee Aubeeluck
Journal:  Br J Nurs       Date:  2005 Apr 28-May 11

7.  'All the burden on all the carers': exploring quality of life with family caregivers of Huntington's disease patients.

Authors:  Aimee Victoria Aubeeluck; Heather Buchanan; Edward J N Stupple
Journal:  Qual Life Res       Date:  2011-11-13       Impact factor: 4.147

8.  Meaningful and Measurable Health Domains in Huntington's Disease: Large-Scale Validation of the Huntington's Disease Health-Related Quality of Life Questionnaire Across Severity Stages.

Authors:  Aileen K Ho; Mike C Horton; G Bernhard Landwehrmeyer; Jean-Marc Burgunder; Alan Tennant
Journal:  Value Health       Date:  2019-06       Impact factor: 5.725

9.  Patient and caregiver quality of life in Huntington's disease.

Authors:  Rebecca E Ready; Melissa Mathews; Anne Leserman; Jane S Paulsen
Journal:  Mov Disord       Date:  2008-04-15       Impact factor: 10.338

10.  Assessment of Caregiver Burden in Huntington's Disease.

Authors:  Margaret Yu; Kenny Tan; Kimberly Koloms; Danny Bega
Journal:  J Huntingtons Dis       Date:  2019
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