Literature DB >> 23763450

Psychometric evaluation of ADAS-Cog and NTB for measuring drug response.

A Karin1, K Hannesdottir, J Jaeger, P Annas, M Segerdahl, P Karlsson, N Sjögren, T von Rosen, F Miller.   

Abstract

AIMS: To conduct a psychometric analysis to determine the adequacy of instruments that measure cognition in Alzheimer's disease trials.
BACKGROUND: Both the Alzheimer's Disease Assessment Scale - Cognition (ADAS-Cog) and the Neuropsychological Test Battery (NTB) are validated outcome measures for clinical trials in Alzheimer's disease and are approved also for regulatory purposes. However, it is not clear how comparable they are in measuring cognitive function. In fact, many recent trials in Alzheimer's disease patients have failed and it has been questioned if ADAS-Cog still is a sensitive measure.
MATERIALS AND METHODS: The present paper examines the psychometric properties of ADAS-Cog and NTB, based on a post hoc analysis of data from a clinical trial (NCT01024660), which was conducted by AstraZeneca, in mild-to-moderate Alzheimer's disease (AD) patients, with a Mini Mental State Examination (MMSE) Total score 16-24. Acceptability, reliability, different types of validity and ability to detect change were assessed using relevant statistical methods. Total scores of both tests, as well as separate domains of both tests, including the Wechsler Memory Scale (WMS), Rey Auditory Verbal Learning Test (RAVLT) and Delis-Kaplan Executive Function System (D-KEFS) Verbal Fluency Condition, were analyzed.
RESULTS: Overall, NTB performed well, with acceptable reliability and ability to detect change, while ADAS-Cog had insufficient psychometric properties, including ceiling effects in 8 out of a total of 11 ADAS-Cog items in mild AD patients, as well as low test-retest reliability in some of the items. DISCUSSION: Based on a direct comparison on the same patient sample, we see advantages of the NTB compared with the ADAS-Cog for the evaluation of cognitive function in the population of mild-to-moderate AD patients. The results suggest that not all of ADAS-Cog items are relevant for both mild and moderate AD population.
CONCLUSIONS: This validation study demonstrates satisfactory psychometric properties of the NTB, while ADAS-Cog was found to be psychometrically inadequate.
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Alzheimer's Disease Assessment Scale-Cog; Alzheimer's disease; acceptability; ceiling effects; cognitive testing; neuropsychological test battery; psychometric properties; validation

Mesh:

Substances:

Year:  2013        PMID: 23763450     DOI: 10.1111/ane.12153

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  12 in total

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3.  Finding Treatment Effects in Alzheimer Trials in the Face of Disease Progression Heterogeneity.

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Journal:  Alzheimers Dement (Amst)       Date:  2017-12-27

6.  A composite measure of cognitive and functional progression in Alzheimer's disease: Design of the Capturing Changes in Cognition study.

Authors:  Roos J Jutten; John Harrison; Frank Jan de Jong; André Aleman; Craig W Ritchie; Philip Scheltens; Sietske A M Sikkes
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7.  Combining cognitive stimulation therapy and fall prevention exercise (CogEx) in older adults with mild to moderate dementia: a feasibility randomised controlled trial.

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8.  Assessing cognition and daily function in early dementia using the cognitive-functional composite: findings from the Catch-Cog study cohort.

Authors:  Roos J Jutten; John E Harrison; Philippe R Lee Meeuw Kjoe; Silvia Ingala; R Vreeswijk; R A J van Deelen; Frank Jan de Jong; Esther M Opmeer; André Aleman; Craig W Ritchie; Philip Scheltens; Sietske A M Sikkes
Journal:  Alzheimers Res Ther       Date:  2019-05-15       Impact factor: 6.982

9.  What are we trying to prevent in Alzheimer disease?

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10.  Effects of Molecular Hydrogen Assessed by an Animal Model and a Randomized Clinical Study on Mild Cognitive Impairment.

Authors:  Kiyomi Nishimaki; Takashi Asada; Ikuroh Ohsawa; Etsuko Nakajima; Chiaki Ikejima; Takashi Yokota; Naomi Kamimura; Shigeo Ohta
Journal:  Curr Alzheimer Res       Date:  2018-03-14       Impact factor: 3.498

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