Evidence map›Paper›PMID 42862019›Full record

ArticleEuropean journal of neurology2026

Progressive Amyloid-Related Imaging Abnormalities After Discontinuation of Lecanemab in Early Alzheimer Disease in an APOE ε2/ε4 Carrier.

Elisabeth Stögmann, Lukas Haider, Joel Leinkauf, Thomas Nakuz, Helena Untersteiner, Clemens Farr, Sara Silvaieh, Tandis Parvizi, Raphael Wurm, Gregor Kasprian and 3 more

Abstract readCase Reports
In one paragraph

Article in European journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Elisabeth StögmannDepartment of Neurology, Medical University of Vienna, Wien, Austria.ORCID https://orcid.org/0000-0003-4688-8482
Lukas HaiderComprehensive Center for Clinical Neurosciences & Mental Health, Medical University of Vienna, Wien, Austria.ORCID https://orcid.org/0000-0002-1556-1770
Joel LeinkaufComprehensive Center for Clinical Neurosciences & Mental Health, Medical University of Vienna, Wien, Austria.ORCID https://orcid.org/0000-0002-5237-4480
Thomas NakuzComprehensive Center for Clinical Neurosciences & Mental Health, Medical University of Vienna, Wien, Austria.
Helena UntersteinerDepartment of Neurology, Medical University of Vienna, Wien, Austria.ORCID https://orcid.org/0009-0004-5015-4718
Clemens FarrDepartment of Neurology, Medical University of Vienna, Wien, Austria.
Sara SilvaiehDepartment of Neurology, Medical University of Vienna, Wien, Austria.
Tandis ParviziDepartment of Neurology, Medical University of Vienna, Wien, Austria.ORCID https://orcid.org/0000-0001-6989-7539
Raphael WurmDepartment of Neurology, Medical University of Vienna, Wien, Austria.ORCID https://orcid.org/0000-0003-3027-7775
Gregor KasprianComprehensive Center for Clinical Neurosciences & Mental Health, Medical University of Vienna, Wien, Austria.ORCID https://orcid.org/0000-0003-3858-3347
Thomas BergerDepartment of Neurology, Medical University of Vienna, Wien, Austria.ORCID https://orcid.org/0000-0001-5626-1144
Ellen GelpiComprehensive Center for Clinical Neurosciences & Mental Health, Medical University of Vienna, Wien, Austria.ORCID https://orcid.org/0000-0003-2948-4187
Evelyn Berger SieczkowskiDepartment of Neurology, Medical University of Vienna, Wien, Austria.ORCID https://orcid.org/0000-0001-7570-0499

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAmyloid-related imaging abnormalities (ARIA) are the most relevant adverse events associated with anti-amyloid therapies in Alzheimer's disease.

methodsWe report a case of progressive ARIA after discontinuation of lecanemab in a patient with early-onset Alzheimer's disease carrying the rare APOE ε2/ε4 genotype.

resultsAfter two infusions, mild ARIA-edema (ARIA-E) and ARIA-hemorrhage (ARIA-H) were detected on routine MRI, prompting treatment interruption. Despite partial radiologic regression, follow-up MRI 8 weeks after discontinuation demonstrated marked progression with multifocal ARIA-H displaying as superficial siderosis, while the patient remained clinically asymptomatic. Corticosteroid treatment was initiated and lecanemab permanently discontinued.

conclusionThis case highlights that severe ARIA may progress beyond active treatment exposure and emphasizes the importance of continued MRI surveillance even after therapy cessation. Furthermore, the APOE ε2/ε4 genotype may represent a distinct risk factor for cerebral amyloid angiopathy-related vascular fragility and hemorrhagic ARIA.

Indexed as

Alzheimer DiseaseAntibodies, Monoclonal, HumanizedApolipoprotein E2Apolipoprotein E4BrainDisease ProgressionHeterozygoteHumansMagnetic Resonance ImagingAntibodies, Monoclonal, HumanizedApolipoprotein E2Apolipoprotein E4Alzheimer's diseaseAPOE ε2/ε4ARIAcerebral amyloid angiopathylecanemab

Identifiers

PMID42862019
PMCPMC13656894

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.