Enrichment of clinical trials in MCI due to AD using markers of amyloid and neurodegeneration
Citation Manager Formats
Make Comment
See Comments
This article requires a subscription to view the full text. If you have a subscription you may use the login form below to view the article. Access to this article can also be purchased.
Abstract
Objective: To investigate the effect of enriching mild cognitive impairment (MCI) clinical trials using combined markers of amyloid pathology and neurodegeneration.
Methods: We evaluate an implementation of the recent National Institute for Aging–Alzheimer's Association (NIA-AA) diagnostic criteria for MCI due to Alzheimer disease (AD) as inclusion criteria in clinical trials and assess the effect of enrichment with amyloid (A+), neurodegeneration (N+), and their combination (A+N+) on the rate of clinical progression, required sample sizes, and estimates of trial time and cost.
Results: Enrichment based on an individual marker (A+ or N+) substantially improves all assessed trial characteristics. Combined enrichment (A+N+) further improves these results with a reduction in required sample sizes by 45% to 60%, depending on the endpoint.
Conclusions: Operationalizing the NIA-AA diagnostic criteria for clinical trial screening has the potential to substantially improve the statistical power of trials in MCI due to AD by identifying a more rapidly progressing patient population.
GLOSSARY
- A+=
- amyloid positive;
- Aβ=
- β-amyloid;
- AD=
- Alzheimer disease;
- ADAS-Cog13=
- Alzheimer's Disease Assessment Scale Cognitive Subscale;
- ADNI=
- Alzheimer's Disease Neuroimaging Initiative;
- FAQ=
- Functional Assessment Questionnaire;
- HV=
- hippocampal volume;
- MCI=
- mild cognitive impairment;
- MMSE=
- Mini-Mental State Examination;
- N+=
- neurodegeneration positive;
- NIA-AA=
- National Institute for Aging–Alzheimer's Association;
- RAVLT=
- Rey Auditory Verbal Learning Test;
- SNR=
- signal-to-noise ratio
Footnotes
Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.
Data used in preparation of this article were obtained from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database (www.loni.usc.edu/ADNI). Therefore, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report. A complete listing of ADNI investigators can be found at Neurology.org.
Supplemental data at Neurology.org
- Received March 1, 2016.
- Accepted in final form June 7, 2016.
- © 2016 American Academy of Neurology
AAN Members
We have changed the login procedure to improve access between AAN.com and the Neurology journals. If you are experiencing issues, please log out of AAN.com and clear history and cookies. (For instructions by browser, please click the instruction pages below). After clearing, choose preferred Journal and select login for AAN Members. You will be redirected to a login page where you can log in with your AAN ID number and password. When you are returned to the Journal, your name should appear at the top right of the page.
AAN Non-Member Subscribers
Purchase access
For assistance, please contact:
AAN Members (800) 879-1960 or (612) 928-6000 (International)
Non-AAN Member subscribers (800) 638-3030 or (301) 223-2300 option 3, select 1 (international)
Sign Up
Information on how to subscribe to Neurology and Neurology: Clinical Practice can be found here
Purchase
Individual access to articles is available through the Add to Cart option on the article page. Access for 1 day (from the computer you are currently using) is US$ 39.00. Pay-per-view content is for the use of the payee only, and content may not be further distributed by print or electronic means. The payee may view, download, and/or print the article for his/her personal, scholarly, research, and educational use. Distributing copies (electronic or otherwise) of the article is not allowed.
Letters: Rapid online correspondence
REQUIREMENTS
You must ensure that your Disclosures have been updated within the previous six months. Please go to our Submission Site to add or update your Disclosure information.
Your co-authors must send a completed Publishing Agreement Form to Neurology Staff (not necessary for the lead/corresponding author as the form below will suffice) before you upload your comment.
If you are responding to a comment that was written about an article you originally authored:
You (and co-authors) do not need to fill out forms or check disclosures as author forms are still valid
and apply to letter.
Submission specifications:
- Submissions must be < 200 words with < 5 references. Reference 1 must be the article on which you are commenting.
- Submissions should not have more than 5 authors. (Exception: original author replies can include all original authors of the article)
- Submit only on articles published within 6 months of issue date.
- Do not be redundant. Read any comments already posted on the article prior to submission.
- Submitted comments are subject to editing and editor review prior to posting.
You May Also be Interested in
Dr. Babak Hooshmand and Dr. David Smith
► Watch
Topics Discussed
Alert Me
Recommended articles
-
Article
Association of blood-based transcriptional risk scores with biomarkers for Alzheimer diseaseYoung Ho Park, Angela Hodges, Andrew Simmons et al.Neurology: Genetics, September 30, 2020 -
Articles
Comparing predictors of conversion and decline in mild cognitive impairmentS.M. Landau, D. Harvey, C.M. Madison et al.Neurology, June 30, 2010 -
Article
Randomized controlled trials in mild cognitive impairmentSources of variabilityRonald C. Petersen, Ronald G. Thomas, Paul S. Aisen et al.Neurology, April 05, 2017 -
Article
Alzheimer disease brain atrophy subtypes are associated with cognition and rate of declineShannon L. Risacher, Wesley H. Anderson, Arnaud Charil et al.Neurology, October 25, 2017