Predictors of Caregiver Burden in Huntington's Disease

被引:16
|
作者
Hergert, Danielle C. [1 ]
Cimino, Cynthia R. [2 ]
机构
[1] New Mexico Dept Hlth, Dev Disabil Supports Div, 5301 Cent Ave NE,Suite 1100, Albuquerque, NM 87108 USA
[2] Univ S Florida, Dept Psychol, Tampa, FL USA
关键词
Huntington's disease; Movement disorders; Genetic disorders; Genotype studies; Behavioral genetics; COGNITIVE IMPAIRMENT; FUNCTIONAL CONNECTIVITY; ALZHEIMERS-DISEASE; FAMILY CAREGIVERS; SYMPTOMS; DIAGNOSIS; APATHY; SCALE; RELIABILITY; PERFORMANCE;
D O I
10.1093/arclin/acab009
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objective: Huntington's disease (HD) is a genetic neurodegenerative condition that is characterized by cognitive, motor, and psychiatric dysfunction. The purpose of this study was to explore which disease characteristics influence caregiver burden in HD. Methods: Fifty participants with HD and 50 of their caregivers participated in the study at the University of South Florida. Participants were administered a neuropsychological battery, the Unified Huntington's Disease Rating Scale (UHDRS) motor exam, and the Frontal Systems Behavior Scale (FrSBe) self-report. Caregivers completed the Caregiving Appraisal Scale and the FrSBe family-report. Results: There were significant correlations between caregiver burden and caregiver age and sex, UHDRS motor scores, cognitive functioning, and self and caregiver-reported FrSBe scores. The significant variables were entered into a regression model and explained 63.1% of the variance in caregiver burden scores. Caregiver age, cognitive functioning, and caregiverreported FrSBe scores continued to be significant predictors of caregiver burden, whereas the other variables were no longer significant. Conclusions: There were significant relationships between caregiver burden, cognitive functioning, and frontally mediated behaviors, but not motor scores. The results suggest that possible interventions for caregiversmay include education to caregivers on howto cope with apathy/executive dysfunction and cognitive decline. Caregiver agewas associated with burden, with younger age being associated with increased burden when controlling for symptom severity. This has implications for this population in that HD typically has a younger age of onset than other neurodegenerative diseases and therefore, these caregivers may be particularly at risk for caregiver burden.
引用
收藏
页码:1426 / 1437
页数:12
相关论文
共 50 条
  • [21] Predictors of caregiver burden in patients with neurologic Wilson disease
    Wu, Peng
    Zheng, Yanjun
    Fan, Xiaolei
    Wang, Honghao
    Deng, Xiaoxue
    Sun, Bei
    Huang, Peng
    Jin, Shan
    Chen, Yonghua
    Bao, Yuancheng
    JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 2020, 48 (06)
  • [22] Caregiver burden in Parkinson's disease
    Martinez-Martin, Pablo
    Joao Forjaz, Maria
    Frades-Payo, Belen
    Bayes Rusinol, Angels
    Manuel Fernandez-Garcia, Jose
    Benito-Leon, Julian
    Campos Arillo, Victor
    Aguilar Barbera, Miquel
    Pondal Sordo, Margarita
    Jose Catalan, Maria
    MOVEMENT DISORDERS, 2007, 22 (07) : 924 - 931
  • [23] BURDEN OF HUNTINGTON'S DISEASE IN SPAIN
    Dorey, J.
    Trigo, P.
    Garcia de Yebenes, J.
    Toumi, M.
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2012, 83 : A48 - A48
  • [24] Caregiver's burden in Parkinson's disease
    Kerckhofs, E.
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2006, 248 (1-2) : 295 - 295
  • [25] Caregiver Burden in Multiple Sclerosis Is Similar to Caregiver Burden in Alzheimer's Disease
    Phillips, Amy
    Stewart, Michelle
    Gupta, Shaloo
    Edwards, Natalie
    Goren, Amir
    NEUROLOGY, 2011, 76 (09) : A472 - A472
  • [26] Neuropsychiatric Burden in Huntington's Disease
    Paoli, Ricardo Augusto
    Botturi, Andrea
    Ciammola, Andrea
    Silani, Vincenzo
    Prunas, Cecilia
    Lucchiari, Claudio
    Zugno, Elisa
    Caletti, Elisabetta
    BRAIN SCIENCES, 2017, 7 (06)
  • [27] Predictors of types of caregiver burden
    Unson, Christine
    Flynn, Deborah
    Haymes, Elayne
    Sancho, Diane
    Glendon, Mary Ann
    SOCIAL WORK IN MENTAL HEALTH, 2016, 14 (01) : 82 - 101
  • [28] CAREGIVER SUPPORTS FOR FAMILIES OF THOSE WITH HUNTINGTON'S DISEASE
    Ennis, A.
    Gallagher, A.
    Hoblyn, J.
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2014, 85 : A93 - A93
  • [29] Patient and caregiver quality of life in Huntington's disease
    Ready, Rebecca E.
    Mathews, Melissa
    Leserman, Anne
    Paulsen, Jane S.
    MOVEMENT DISORDERS, 2008, 23 (05) : 721 - 726
  • [30] Anosognosia Is Associated With Greater Caregiver Burden and Poorer Executive Function in Huntington Disease
    Wibawa, P.
    Zombor, R.
    Dragovic, M.
    Hayhow, B.
    Lee, J.
    Panegyres, P. K.
    Rock, D.
    Starkstein, S. E.
    JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY, 2020, 33 (01) : 52 - 58