Literature DB >> 25022537

Development of a straightforward and sensitive scale for MCI and early AD clinical trials.

Yifan Huang1, Kaori Ito2, Clare B Billing3, Richard J Anziano2.   

Abstract

BACKGROUND: Although the Clinical Dementia Rating Scale-Sum of Boxes score (CDR-SB) is a widely accepted and commonly used global scale, validated clinical endpoints of cognitive changes are unavailable in the predementia stages of Alzheimer's disease (AD), and a new clinical assessment with reliability and sensitivity is needed in the mild cognitive impairment (MCI) population.
METHODS: Using Alzheimer's Disease Neuroimaging Initiative (ADNI)-1/GO data, signal-to-noise ratios (SNRs) were calculated to quantify the sensitivity of a measure for detecting disease progression and hypothetical treatment effects. All possible combinations of selected sensitive measures were assessed for developing composite scores. The analyses were performed in the MCI population and subpopulations enriched by apolipoprotein E4 (APOE ε4), hippocampal volume, and cerebrospinal fluid β-amyloid.
RESULTS: The best composite score was "Word Recall + Delayed Word Recall + Orientation + CDR-SB + FAQ", more sensitive than 13-item Alzheimer's Disease Assessment Scale-cognitive subscale or CDR-SB.
CONCLUSION: The proposed composite score derived from the existing clinical endpoints demonstrated higher sensitivity in the MCI population and is easy to implement and standardize across studies.
Copyright © 2015 The Alzheimer's Association. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Alzheimer's Disease Assessment Scale-cognitive subscale; Alzheimer's disease; Clinical trials; Composite endpoints; Mild cognitive impairment; Signal-to-noise ratio

Mesh:

Substances:

Year:  2014        PMID: 25022537     DOI: 10.1016/j.jalz.2014.03.008

Source DB:  PubMed          Journal:  Alzheimers Dement        ISSN: 1552-5260            Impact factor:   21.566


  6 in total

Review 1.  Recent publications from the Alzheimer's Disease Neuroimaging Initiative: Reviewing progress toward improved AD clinical trials.

Authors:  Michael W Weiner; Dallas P Veitch; Paul S Aisen; Laurel A Beckett; Nigel J Cairns; Robert C Green; Danielle Harvey; Clifford R Jack; William Jagust; John C Morris; Ronald C Petersen; Andrew J Saykin; Leslie M Shaw; Arthur W Toga; John Q Trojanowski
Journal:  Alzheimers Dement       Date:  2017-03-22       Impact factor: 21.566

2.  Endpoints for Pre-Dementia AD Trials: A Report from the EU/US/CTAD Task Force.

Authors:  B Vellas; R Bateman; K Blennow; G Frisoni; K Johnson; R Katz; J Langbaum; D Marson; R Sperling; A Wessels; S Salloway; R Doody; P Aisen
Journal:  J Prev Alzheimers Dis       Date:  2015-06

3.  Efficacy and Safety of MMFS-01, a Synapse Density Enhancer, for Treating Cognitive Impairment in Older Adults: A Randomized, Double-Blind, Placebo-Controlled Trial.

Authors:  Guosong Liu; Jason G Weinger; Zhong-Lin Lu; Feng Xue; Safa Sadeghpour
Journal:  J Alzheimers Dis       Date:  2016       Impact factor: 4.472

Review 4.  The Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog): Modifications and Responsiveness in Pre-Dementia Populations. A Narrative Review.

Authors:  Jacqueline K Kueper; Mark Speechley; Manuel Montero-Odasso
Journal:  J Alzheimers Dis       Date:  2018       Impact factor: 4.472

5.  The importance of endpoint selection: How effective does a drug need to be for success in a clinical trial of a possible Alzheimer's disease treatment?

Authors:  Stephanie Evans; Kevin McRae-McKee; Mei Mei Wong; Christoforos Hadjichrysanthou; Frank De Wolf; Roy Anderson
Journal:  Eur J Epidemiol       Date:  2018-03-23       Impact factor: 8.082

6.  Quantification of cognitive impairment to characterize heterogeneity of patients at risk of developing Alzheimer's disease dementia.

Authors:  Diana L Giraldo; Jan Sijbers; Eduardo Romero
Journal:  Alzheimers Dement (Amst)       Date:  2021-09-14
  6 in total

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