Non‐hemorrhagic imaging markers of cerebral amyloid angiopathy in memory clinic patients

Author:

Costa Ana Sofia12,Albrecht Milena1,Reich Arno1,Nikoubashman Omid3,Schulz Jörg B.12,Reetz Kathrin12,Pinho João1

Affiliation:

1. Department of Neurology University Hospital RWTH Aachen Aachen Germany

2. JARA Institute Molecular Neuroscience and Neuroimaging (INM‐11) Juelich Research Center GmbH and RWTH Aachen University Aachen Germany

3. Department of Diagnostic and Interventional Neuroradiology University Hospital RWTH Aachen Aachen Germany

Abstract

AbstractINTRODUCTIONThe Boston criteria v2.0 for cerebral amyloid angiopathy (CAA) incorporated non‐hemorrhagic imaging markers. Their prevalence and significance in patients with cognitive impairment remain uncertain.METHODSWe studied 622 memory clinic patients with available magnetic resonance imaging (MRI) and cerebrospinal fluid (CSF) biomarkers. Two raters assessed non‐hemorrhagic markers, and we explored their association with clinical characteristics through multivariate analyses.RESULTSMost patients had mild cognitive impairment; median age was 71 years and 50% were female. Using the v2.0 criteria, possible or probable CAA increased from 75 to 383 patients. Sixty‐eight percent of the sample had non‐hemorrhagic CAA markers, which were independently associated with age (odds ratio [OR] = 1.04, 95% confidence interval [CI] = 1.01–1.07), female sex (OR = 1.68, 95% CI = 1.11–2.54), and hemorrhagic CAA markers (OR = 2.11, 95% CI = 1.02–4.35).DISCUSSIONTwo‐thirds of patients from a memory clinic cohort had non‐hemorrhagic CAA markers, increasing the number of patients meeting the v2.0 CAA criteria. Longitudinal approaches should explore the implications of these markers, particularly the hemorrhagic risk in this population.Highlights The updated Boston criteria for cerebral amyloid angiopathy (CAA) now include non‐hemorrhagic markers. The prevalence of non‐hemorrhagic CAA markers in memory clinic patients is unknown. Two‐thirds of patients in our memory clinic presented non‐hemorrhagic CAA markers. The presence of these markers was associated with age, female sex, and hemorrhagic CAA markers. The hemorrhagic risk of patients presenting these type of markers remains unclear.

Publisher

Wiley

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