Literature DB >> 25209258

HD-CAB: a cognitive assessment battery for clinical trials in Huntington's disease 1,2,3.

Julie C Stout1, Sarah Queller, Kalyca N Baker, Sean Cowlishaw, Cristina Sampaio, Cheryl Fitzer-Attas, Beth Borowsky.   

Abstract

Cognitive dysfunction is central to Huntington's disease (HD) and undermines quality of life. Clinical trials are now targeting cognitive outcomes in HD; however, no cognitive battery has been optimized for HD clinical trials. We evaluated 16 cognitive tests in a 20-site, five-country, observational study designed to mimic aspects of a clinical trial (e.g., data collection managed by a contract research organization, repeated testing, prespecified statistical analyses). Fifty-five early HD, 103 premanifest HD (pre-HD), and 105 controls were tested at visit 1, visit 2 (1-3 days later), and visit 3 (5-7 weeks after visit 1). For inclusion in a recommended battery, tests were evaluated for sensitivity, practice effects, reliability, domain coverage, feasibility, and tolerability. Most tests differentiated controls from pre-HD and early HD and showed excellent psychometric properties. We selected six tests to constitute the Huntington's Disease Cognitive Assessment Battery (HD-CAB): Symbol Digit Modalities Test, Paced Tapping, One Touch Stockings of Cambridge (abbreviated), Emotion Recognition, Trail Making B, and the Hopkins Verbal Learning Test. These tests demonstrated sensitivity to disease status (Cohen's d effect sizes: early HD= -1.38 to -1.90 and pre-HD= -0.41 to -0.78), and acceptable reliability (r's 0.73-0.93). A composite score yielded large effect sizes (early HD = -2.44 and pre-HD = -0.87) and high reliability (r = 0.95). HD-CAB is the first cognitive battery designed specifically for use in late premanifest and early HD clinical trials. Adoption of the HD-CAB will facilitate evaluation of treatments to improve cognition in HD.
© 2014 International Parkinson and Movement Disorder Society.

Entities:  

Keywords:  cognitive assessment; early Huntington's disease; neuropsychology; practice effects; premanifest Huntington's disease

Mesh:

Year:  2014        PMID: 25209258     DOI: 10.1002/mds.25964

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  18 in total

1.  Feasibility and initial validation of 'HD-Mobile', a smartphone application for remote self-administration of performance-based cognitive measures in Huntington's disease.

Authors:  Brendan McLaren; Sophie C Andrews; Yifat Glikmann-Johnston; Emily-Clare Mercieca; Nicholas W G Murray; Clement Loy; Mark A Bellgrove; Julie C Stout
Journal:  J Neurol       Date:  2020-09-03       Impact factor: 4.849

2.  Does pallidal neuromodulation influence cognitive decline in Huntington's disease?

Authors:  Emily Sanrey; Valérie Macioce; Victoria Gonzalez; Laura Cif; Fabienne Cyprien; Emilie Chan Seng; Philippe Coubes; Gaetan Poulen
Journal:  J Neurol       Date:  2020-09-04       Impact factor: 4.849

Review 3.  Recent Advances in the Treatment of Huntington's Disease: Targeting DNA and RNA.

Authors:  Kathleen M Shannon
Journal:  CNS Drugs       Date:  2020-03       Impact factor: 5.749

4.  Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.HttQ111/+ model of Huntington's disease.

Authors:  Robert M Bragg; Sydney R Coffey; Rory M Weston; Seth A Ament; Jeffrey P Cantle; Shawn Minnig; Cory C Funk; Dominic D Shuttleworth; Emily L Woods; Bonnie R Sullivan; Lindsey Jones; Anne Glickenhaus; John S Anderson; Michael D Anderson; Stephen B Dunnett; Vanessa C Wheeler; Marcy E MacDonald; Simon P Brooks; Nathan D Price; Jeffrey B Carroll
Journal:  Sci Rep       Date:  2017-02-08       Impact factor: 4.379

5.  Motor, cognitive, and functional declines contribute to a single progressive factor in early HD.

Authors:  Scott A Schobel; Giuseppe Palermo; Peggy Auinger; Jeffrey D Long; Shiyang Ma; Omar S Khwaja; Dylan Trundell; Merit Cudkowicz; Steven Hersch; Cristina Sampaio; E Ray Dorsey; Blair R Leavitt; Karl D Kieburtz; Jeffrey J Sevigny; Douglas R Langbehn; Sarah J Tabrizi
Journal:  Neurology       Date:  2017-11-15       Impact factor: 9.910

6.  How to Capitalize on the Retest Effect in Future Trials on Huntington's Disease.

Authors:  Catherine Schramm; Sandrine Katsahian; Katia Youssov; Jean-François Démonet; Pierre Krystkowiak; Frédéric Supiot; Christophe Verny; Laurent Cleret de Langavant; Anne-Catherine Bachoud-Lévi
Journal:  PLoS One       Date:  2015-12-29       Impact factor: 3.240

7.  Stimulating neural plasticity with real-time fMRI neurofeedback in Huntington's disease: A proof of concept study.

Authors:  Marina Papoutsi; Nikolaus Weiskopf; Douglas Langbehn; Ralf Reilmann; Geraint Rees; Sarah J Tabrizi
Journal:  Hum Brain Mapp       Date:  2017-12-13       Impact factor: 5.038

Review 8.  Cognitive-Motor Interference in Neurodegenerative Disease: A Narrative Review and Implications for Clinical Management.

Authors:  Tara L McIsaac; Nora E Fritz; Lori Quinn; Lisa M Muratori
Journal:  Front Psychol       Date:  2018-10-29

9.  Test-Retest Reliability of Measures Commonly Used to Measure Striatal Dysfunction across Multiple Testing Sessions: A Longitudinal Study.

Authors:  Clare E Palmer; Douglas Langbehn; Sarah J Tabrizi; Marina Papoutsi
Journal:  Front Psychol       Date:  2018-01-12

10.  Physical Activity Self-Management and Coaching Compared to Social Interaction in Huntington Disease: Results From the ENGAGE-HD Randomized, Controlled Pilot Feasibility Trial.

Authors:  Monica Busse; Lori Quinn; Cheney Drew; Mark Kelson; Rob Trubey; Kirsten McEwan; Carys Jones; Julia Townson; Helen Dawes; Rhiannon Tudor-Edwards; Anne Rosser; Kerenza Hood
Journal:  Phys Ther       Date:  2017-06-01
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