Magnetic resonance imaging measures of brain volumes across the EXPEDITION trials in mild and moderate Alzheimer's disease dementia.

Alzheimer's disease amyloid atrophy magnetic resonance imaging solanezumab volumetric magnetic resonance imaging

Journal

Alzheimer's & dementia (New York, N. Y.)
ISSN: 2352-8737
Titre abrégé: Alzheimers Dement (N Y)
Pays: United States
ID NLM: 101650118

Informations de publication

Date de publication:
2022
Historique:
received: 29 09 2021
revised: 23 03 2022
accepted: 05 05 2022
entrez: 5 7 2022
pubmed: 6 7 2022
medline: 6 7 2022
Statut: epublish

Résumé

Solanezumab is a monoclonal antibody that preferentially binds soluble amyloid beta and promotes its clearance from the brain. The aim of this post hoc analysis was to assess the effect of low-dose solanezumab (400 mg) on global brain volume measures in patients with mild or moderate Alzheimer's disease (AD) dementia quantified using volumetric magnetic resonance imaging (vMRI) data from the EXPEDITION clinical trial program. Patients with mild or moderate AD (EXPEDITION and EXPEDITION2) and mild AD (EXPEDITION3), were treated with either placebo or solanezumab (400 mg) every 4 weeks (Q4W) for 76 weeks. vMRI scans were acquired at baseline and at 80 weeks from 427 MRI facilities using a standardized imaging protocol. Whole brain volume (WBV) and ventricle volume (VV) changes were estimated at 80 weeks using either boundary shift integral (EXPEDITION and EXPEDITION2) or tensor-based morphometry (EXPEDITION3). The pooled cohort used for this study consisted of participants with vMRI at baseline and week 80 across the three trials. Analyzed patient subgroups comprised full patient cohort ( Analysis of patients with mild or moderate AD dementia from baseline to 80 weeks using vMRI measures of WBV and VV changes suggested that low-dose solanezumab was not linked to changes in volumes at 80 weeks. Analysis of the pooled cohort did not demonstrate an effect on brain volumes with treatment. Evaluation of a higher dose of solanezumab in the preclinical stage of AD is currently being undertaken.

Identifiants

pubmed: 35783453
doi: 10.1002/trc2.12313
pii: TRC212313
pmc: PMC9237342
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e12313

Informations de copyright

© 2022 Eli Lilly and Company. Alzheimer's & Dementia: Translational Research & Clinical Interventions published by Wiley Periodicals LLC on behalf of Alzheimer's Association.

Déclaration de conflit d'intérêts

Diana O. Svaldi, Ixavier A. Higgins, Karen C. Holdridge, Roy Yaari, Michael Case, Sergey Shcherbinin, and John R. Sims are all employees and minor shareholders of Eli Lilly and Company. Diana O. Svaldi has received support from Eli Lilly and Company for attending meetings and/or travel. Luc Bracoud and David Scott have nothing to report.

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Auteurs

Diana Otero Svaldi (DO)

Eli Lilly and Company Indianapolis Indiana USA.

Ixavier A Higgins (IA)

Eli Lilly and Company Indianapolis Indiana USA.

Karen C Holdridge (KC)

Eli Lilly and Company Indianapolis Indiana USA.

Roy Yaari (R)

Eli Lilly and Company Indianapolis Indiana USA.

Michael Case (M)

Eli Lilly and Company Indianapolis Indiana USA.

Luc Bracoud (L)

Clario Lyon France.

David Scott (D)

Clario San Mateo California USA.

Sergey Shcherbinin (S)

Eli Lilly and Company Indianapolis Indiana USA.

John R Sims (JR)

Eli Lilly and Company Indianapolis Indiana USA.

Classifications MeSH