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
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
Background: although health-related quality of life is key for patients with long-term neurodegenerative conditions, measuring this is less straightforward and complex in Huntington’s disease (HD).
Objectives: to refine and validate a fully patient-derived instrument, the Huntington’s Disease health-related Quality of Life questionnaire (HDQoL), and to elucidate health domains that are meaningful to patients’ lived experience.
Methods: five-hundred forty-one participants, from premanifest to end-stage disease, completed the HDQoL, together with generic quality-of-life measures and in-person motor, cognitive, and behavioral assessments. The psychometric properties of the HDQoL were examined using factor analysis and Rasch analysis.
Results: four HDQoL domains emerged, reflecting the classical triad of HD features; they were Physical-Functional, Cognitive, and 2 different behavioral aspects, that is, the Mood-Self domain and a distinct Worries domain. These domains clarify the behavioral sequelae as experienced by patients, and all showed good to excellent internal consistency. Known-groups analyses illustrated significant and graded changes in clinical assessments and corresponding HDQoL domains across disease severity levels. Convergent and discriminant validity was demonstrated by the expected pattern of correlations between specific HDQoL domains and corresponding domain-relevant clinical assessments as well as patient-reported measures. The data demonstrate robust support for the refined HDQoL across disease stages.
Conclusions: the HDQoL, with its 2 distinct behavioral domains of Mood-Self and Worries as well as the Physical-Functional and Cognitive domains, is a relevant, reliable, and valid patient-derived instrument to measure the impact of HD across all severity stages.
Adult, Aged, Female, Humans, Huntington Disease/complications, Male, Middle Aged, Psychometrics/instrumentation, Quality of Life/psychology, Reproducibility of Results, Surveys and Questionnaires/standards
712-720
Ho, Aileen K.
baac5981-eb17-4e08-818c-843ccfad3272
Horton, Mike C.
ccd9c749-7e7e-4ac0-ac54-4ee33b877d94
Landwehrmeyer, G. Bernhard
3ec44cdc-d245-4d9c-aa0f-61c9d9eb7fc7
Burgunder, Jean-Marc
50328902-96ca-46d4-8f44-b727960e948a
Tennant, Alan
d51e5c93-5f17-48c4-a3f3-eeffc63bac06
Kipps, Chris
e43be016-2dc2-45e6-9a02-ab2a0e0208d5
European Huntington’s Disease Network
12 June 2019
Ho, Aileen K.
baac5981-eb17-4e08-818c-843ccfad3272
Horton, Mike C.
ccd9c749-7e7e-4ac0-ac54-4ee33b877d94
Landwehrmeyer, G. Bernhard
3ec44cdc-d245-4d9c-aa0f-61c9d9eb7fc7
Burgunder, Jean-Marc
50328902-96ca-46d4-8f44-b727960e948a
Tennant, Alan
d51e5c93-5f17-48c4-a3f3-eeffc63bac06
Kipps, Chris
e43be016-2dc2-45e6-9a02-ab2a0e0208d5
Ho, Aileen K., Horton, Mike C., Landwehrmeyer, G. Bernhard, Burgunder, Jean-Marc and Tennant, Alan
,
European Huntington’s Disease Network
(2019)
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.
Value in Health, 22 (6), .
(doi:10.1016/j.jval.2019.01.016).
Abstract
Background: although health-related quality of life is key for patients with long-term neurodegenerative conditions, measuring this is less straightforward and complex in Huntington’s disease (HD).
Objectives: to refine and validate a fully patient-derived instrument, the Huntington’s Disease health-related Quality of Life questionnaire (HDQoL), and to elucidate health domains that are meaningful to patients’ lived experience.
Methods: five-hundred forty-one participants, from premanifest to end-stage disease, completed the HDQoL, together with generic quality-of-life measures and in-person motor, cognitive, and behavioral assessments. The psychometric properties of the HDQoL were examined using factor analysis and Rasch analysis.
Results: four HDQoL domains emerged, reflecting the classical triad of HD features; they were Physical-Functional, Cognitive, and 2 different behavioral aspects, that is, the Mood-Self domain and a distinct Worries domain. These domains clarify the behavioral sequelae as experienced by patients, and all showed good to excellent internal consistency. Known-groups analyses illustrated significant and graded changes in clinical assessments and corresponding HDQoL domains across disease severity levels. Convergent and discriminant validity was demonstrated by the expected pattern of correlations between specific HDQoL domains and corresponding domain-relevant clinical assessments as well as patient-reported measures. The data demonstrate robust support for the refined HDQoL across disease stages.
Conclusions: the HDQoL, with its 2 distinct behavioral domains of Mood-Self and Worries as well as the Physical-Functional and Cognitive domains, is a relevant, reliable, and valid patient-derived instrument to measure the impact of HD across all severity stages.
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Published date: 12 June 2019
Keywords:
Adult, Aged, Female, Humans, Huntington Disease/complications, Male, Middle Aged, Psychometrics/instrumentation, Quality of Life/psychology, Reproducibility of Results, Surveys and Questionnaires/standards
Identifiers
Local EPrints ID: 490686
URI: http://eprints.soton.ac.uk/id/eprint/490686
ISSN: 1098-3015
PURE UUID: 0106a303-bdc0-434e-9a78-c5d58c0e385c
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Date deposited: 03 Jun 2024 17:08
Last modified: 04 Jun 2024 01:55
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Contributors
Author:
Aileen K. Ho
Author:
Mike C. Horton
Author:
G. Bernhard Landwehrmeyer
Author:
Jean-Marc Burgunder
Author:
Alan Tennant
Author:
Chris Kipps
Corporate Author: European Huntington’s Disease Network
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