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PMID: 22019547 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

What is the clinically relevant change on the ADAS-Cog?

Journal of neurology, neurosurgery, and psychiatry ·Vol. 83 ·No. 2 ·2012-02-00 ·Pages 171-3

Schrag A, Schott JM, Alzheimer's Disease Neuroimaging Initiative

Abstract

To establish the minimal clinically relevant change (MCRC) on the Alzheimer's Disease Assessment Scale-Cognitive (ADAS-Cog) for patients with mild Alzheimer's disease (AD). Cohort study. 59 recruiting sites for the Alzheimer's Disease Neuroimaging Initiative. Outpatients with AD in the Alzheimer's Disease Neuroimaging Initiative. The authors applied anchor-based MCRC methodology comparing ADAS-Cog change against clinicians' judgement of clinically relevant worsening between baseline and 6 months in four domains: memory and non-memory cognitive performance; Clinical Dementia Rating Scale; and Functional Assessment Questionnaire. The analysis was repeated for the 6-12-month interval. To support these findings, the authors calculated distribution-based measures including half-baseline SD (1/2 SD) and SEM. 181 patients (baseline ADAS-Cog score 18.5±6.4) had ADAS-Cog data at 0 and 6 months. Those undergoing clinically significant worsening on any of the four anchor questions (n=41-47) had an average ADAS-Cog change of 3.1-3.8 points. Similar results were found for the 177 patients with 6-12-month data. The average 1/2 SD for the baseline ADAS-Cog score was 3.2, and the SEM was 3.7. 3 points decline on the ADAS-Cog may be an appropriate MCRC for clinical trials of patients with early AD. However, further studies assessing the MCRC for improvement on the ADAS-Cog, using patient-based judgement as an anchor, and determining the minimal clinically relevant difference between change on two treatments are required. http://clinicalTrials.gov Identifier: NCT00106899.

MeSH Terms
Aged Alzheimer Disease/diagnosis,psychology Cholinesterase Inhibitors/therapeutic use Cognition/physiology Cognitive Dysfunction Cohort Studies Educational Status Female Humans Longitudinal Studies Male Neuropsychological Tests Nootropic Agents/therapeutic use Surveys and Questionnaires
Chemicals
Cholinesterase Inhibitors Nootropic Agents
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Schrag Anette
Department of Clinical Neurosciences, Institute of Neurology, Royal Free Campus, University College London, London NW3 2PF, UK. [email protected]
Schott Jonathan M
Alzheimer's Disease Neuroimaging Initiative
Article Info
Journal
Journal of neurology, neurosurgery, and psychiatry
Abbr.
J Neurol Neurosurg Psychiatry
ISSN
1468-330X
Published
2012-02-00
Epub
2011-00-21
Pages
171-3
Language
English
Region
England
NLM ID
2985191R
Subset
IM
Grants
NIA NIH HHS · K01 AG030514 · United States
NIA NIH HHS · P30 AG010129 · United States
NIA NIH HHS · U01 AG024904 · United States
Databases
ClinicalTrials.gov
NCT00106899
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