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Developing blood-brain barrier arterial spin labelling as a non-invasive early biomarker of Alzheimer's disease (DEBBIE-AD): a prospective observational multicohort study protocol.

Authors :
Padrela B
Mahroo A
Tee M
Sneve MH
Moyaert P
Geier O
Kuijer JPA
Beun S
Nordhøy W
Zhu YD
Buck MA
Hoinkiss DC
Konstandin S
Huber J
Wiersinga J
Rikken R
de Leeuw D
Grydeland H
Tippett L
Cawston EE
Ozturk-Isik E
Linn J
Brandt M
Tijms BM
van de Giessen EM
Muller M
Fjell A
Walhovd K
Bjørnerud A
Pålhaugen L
Selnes P
Clement P
Achten E
Anazodo U
Barkhof F
Hilal S
Fladby T
Eickel K
Morgan C
Thomas DL
Petr J
Günther M
Mutsaerts HJMM
Source :
BMJ open [BMJ Open] 2024 Mar 08; Vol. 14 (3), pp. e081635. Date of Electronic Publication: 2024 Mar 08.
Publication Year :
2024

Abstract

Introduction: Loss of blood-brain barrier (BBB) integrity is hypothesised to be one of the earliest microvascular signs of Alzheimer's disease (AD). Existing BBB integrity imaging methods involve contrast agents or ionising radiation, and pose limitations in terms of cost and logistics. Arterial spin labelling (ASL) perfusion MRI has been recently adapted to map the BBB permeability non-invasively. The DEveloping BBB-ASL as a non-Invasive Early biomarker (DEBBIE) consortium aims to develop this modified ASL-MRI technique for patient-specific and robust BBB permeability assessments. This article outlines the study design of the DEBBIE cohorts focused on investigating the potential of BBB-ASL as an early biomarker for AD (DEBBIE-AD).<br />Methods and Analysis: DEBBIE-AD consists of a multicohort study enrolling participants with subjective cognitive decline, mild cognitive impairment and AD, as well as age-matched healthy controls, from 13 cohorts. The precision and accuracy of BBB-ASL will be evaluated in healthy participants. The clinical value of BBB-ASL will be evaluated by comparing results with both established and novel AD biomarkers. The DEBBIE-AD study aims to provide evidence of the ability of BBB-ASL to measure BBB permeability and demonstrate its utility in AD and AD-related pathologies.<br />Ethics and Dissemination: Ethics approval was obtained for 10 cohorts, and is pending for 3 cohorts. The results of the main trial and each of the secondary endpoints will be submitted for publication in a peer-reviewed journal.<br />Competing Interests: Competing interests: FB is a consultant for Roche, Celltrion, Rewind Therapeutics, Merck, IXICO, Jansen, Combinostics, and has research agreements with Merck, Biogen, GE Healthcare, Roche. All other authors report no disclosures.<br /> (© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)

Details

Language :
English
ISSN :
2044-6055
Volume :
14
Issue :
3
Database :
MEDLINE
Journal :
BMJ open
Publication Type :
Academic Journal
Accession number :
38458785
Full Text :
https://doi.org/10.1136/bmjopen-2023-081635