Literature DB >> 31853881

Psychometric properties and responsiveness of Neuro-QoL Cognitive Function in persons with Huntington disease (HD).

Noelle E Carlozzi1,2, Nicholas R Boileau3, Jane S Paulsen4, Nancy R Downing5, Rebecca Ready6, Joel S Perlmutter7,8, David Cella9, Kelvin L Chou10, Michael K McCormack11,12, Stacey Barton7, Jin-Shei Lai9.   

Abstract

PURPOSE: Individuals with Huntington disease (HD) experience progressive cognitive decline that may appear years before motor manifestations of the disease. These declines have a profound effect on health-related quality of life (HRQOL) over the disease course, and thus it is important that self-report measures of cognitive function are validated for use in longitudinal studies.
METHODS: 359 individuals with premanifest or manifest HD completed baseline and at least one follow-up (12- and 24-month) assessment. Neuro-QoL™ Cognitive Function was administered at each time-point. Participants completed a self-reported global rating of cognitive change, as well as performance-based cognitive changes (using the Symbol Digit Modalities Test). Standardized response means (SRMs) and general linear models evaluated whether Neuro-QoL™ Cognitive Function was responsive to change over time with respect to self-reported and performance-based anchors. Test-retest reliability and known-group validity were also examined.
RESULTS: Responsiveness was supported by effect sizes that were small in magnitude, but in the expected direction relative to self-reported and performance-based change. General linear models generally supported 12- and 24-month responsiveness relative to self-reported cognitive change and 12-month responsiveness relative to performance-based change. Test-retest reliability was excellent, and the measure exhibited known-group validity.
CONCLUSION: Longitudinal analyses generally indicate that the Neuro-QoL™ Cognitive Function measure is sensitive to change over time in individuals with HD. Neuro-QoL Cognitive Function changes reflect self-reported cognitive change at 12 and 24 months and performance-based change at 12 months. This measure may be useful in clinical trials or longitudinal observation studies.

Entities:  

Keywords:  Cognition; HDQLIFE; Huntington disease; Longitudinal studies; Outcome assessment (health care); Quality of life

Mesh:

Year:  2019        PMID: 31853881      PMCID: PMC7195233          DOI: 10.1007/s11136-019-02391-7

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  56 in total

1.  Quality criteria were proposed for measurement properties of health status questionnaires.

Authors:  Caroline B Terwee; Sandra D M Bot; Michael R de Boer; Daniëlle A W M van der Windt; Dirk L Knol; Joost Dekker; Lex M Bouter; Henrica C W de Vet
Journal:  J Clin Epidemiol       Date:  2006-08-24       Impact factor: 6.437

2.  Subjective memory complaints with and without objective memory impairment: relationship with risk factors for dementia.

Authors:  Nicola T Lautenschlager; Leon Flicker; Samuel Vasikaran; Peter Leedman; Osvaldo P Almeida
Journal:  Am J Geriatr Psychiatry       Date:  2005-08       Impact factor: 4.105

3.  Huntington disease: functional capacities in patients treated with neuroleptic and antidepressant drugs.

Authors:  I Shoulson
Journal:  Neurology       Date:  1981-10       Impact factor: 9.910

4.  Neuro-QOL: quality of life item banks for adults with neurological disorders: item development and calibrations based upon clinical and general population testing.

Authors:  Richard C Gershon; Jin Shei Lai; Rita Bode; Seung Choi; Claudia Moy; Tom Bleck; Deborah Miller; Amy Peterman; David Cella
Journal:  Qual Life Res       Date:  2011-08-27       Impact factor: 4.147

5.  The use of PROMIS and assessment center to deliver patient-reported outcome measures in clinical research.

Authors:  Richard C Gershon; Nan Rothrock; Rachel Hanrahan; Michael Bass; David Cella
Journal:  J Appl Meas       Date:  2010

Review 6.  The incidence and prevalence of Huntington's disease: a systematic review and meta-analysis.

Authors:  Tamara Pringsheim; Katie Wiltshire; Lundy Day; Jonathan Dykeman; Thomas Steeves; Nathalie Jette
Journal:  Mov Disord       Date:  2012-06-12       Impact factor: 10.338

7.  Patients' perceptions of memory functioning before and after surgical intervention to treat medically refractory epilepsy.

Authors:  Tara T Lineweaver; Richard I Naugle; Alyce M Cafaro; William Bingaman; Hans O Lüders
Journal:  Epilepsia       Date:  2004-12       Impact factor: 5.864

8.  Everyday cognition in prodromal Huntington disease.

Authors:  Janet K Williams; Ji-In Kim; Nancy Downing; Sarah Farias; Deborah L Harrington; Jeffrey D Long; James A Mills; Jane S Paulsen
Journal:  Neuropsychology       Date:  2014-07-07       Impact factor: 3.295

9.  Assessment of cognitive symptoms in prodromal and early huntington disease.

Authors:  Anthony L Vaccarino; Terrence Sills; Karen E Anderson; Beth Borowsky; David Craufurd; Joseph Giuliano; Lavonne Goodman; Mark Guttman; Peter Kupchak; Aileen K Ho; Jane S Paulsen; Julie C Stout; Daniel P van Kammen; Ken Evans
Journal:  PLoS Curr       Date:  2011-10-25

10.  Patterns of consent in epidemiologic research: evidence from over 25,000 responders.

Authors:  Kate M Dunn; Kelvin Jordan; Rosie J Lacey; Mark Shapley; Clare Jinks
Journal:  Am J Epidemiol       Date:  2004-06-01       Impact factor: 4.897

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  1 in total

1.  Meaning and purpose in Huntington's disease: a longitudinal study of its impact on quality of life.

Authors:  Leonard L Sokol; Jonathan P Troost; Benzi M Kluger; Allison J Applebaum; Jane S Paulsen; Danny Bega; Samuel Frank; Joshua M Hauser; Nicholas R Boileau; Colin A Depp; David Cella; Noelle E Carlozzi
Journal:  Ann Clin Transl Neurol       Date:  2021-07-20       Impact factor: 4.511

  1 in total

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