Evidence map›Paper›PMID 42552750›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2026

Plasma p-tau217 detects Alzheimer's disease co-pathology in cerebral amyloid angiopathy: Comparison to CSF biomarkers in the ANGMAR cohort.

Aida Fernández-Lebrero, Joan Jiménez-Balado, Greta García-Escobar, José Contador, Isabel Estraguès-Gázquez, Laia Peraferrer-Montesinos, Rosa María Manero-Borràs, Laura Ludovica Gramegna, Marc Viles, Ana Rodríguez Campello and 10 more

Abstract readComparative Study
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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5 · Who and what money

Authors and funding

20 authors.

Aida Fernández-LebreroHospital del Mar Research Institute, Barcelona, Spain.ORCID https://orcid.org/0000-0002-2097-4430
Joan Jiménez-BaladoHospital del Mar Research Institute, Barcelona, Spain.
Greta García-EscobarHospital del Mar Research Institute, Barcelona, Spain.
José ContadorBarcelonaβeta Brain Research Center (BBRC), Pasqual Maragall Foundation, Barcelona, Spain.
Isabel Estraguès-GázquezHospital del Mar Research Institute, Barcelona, Spain.
Laia Peraferrer-MontesinosServei de Neurologia, Hospital del Mar, Barcelona, Spain.
Rosa María Manero-BorràsServei de Neurologia, Hospital del Mar, Barcelona, Spain.
Laura Ludovica GramegnaNeuroradiology Department, Hospital del Mar, Barcelona, Spain.
Marc VilesNeuroradiology Department, Hospital del Mar, Barcelona, Spain.
Ana Rodríguez CampelloHospital del Mar Research Institute, Barcelona, Spain.
Paula Ortiz-RomeroBarcelonaβeta Brain Research Center (BBRC), Pasqual Maragall Foundation, Barcelona, Spain.
Marina de DiegoBarcelonaβeta Brain Research Center (BBRC), Pasqual Maragall Foundation, Barcelona, Spain.
Marta Del CampoHospital del Mar Research Institute, Barcelona, Spain.
Javier Torres-TorronterasHospital del Mar Research Institute, Barcelona, Spain.
Esther Jiménez-MoyanoHospital del Mar Research Institute, Barcelona, Spain.
Helena Blasco-ForniésHospital del Mar Research Institute, Barcelona, Spain.
Marc Suárez-CalvetHospital del Mar Research Institute, Barcelona, Spain.
Angel OisHospital del Mar Research Institute, Barcelona, Spain.
Albert Puig-PijoanHospital del Mar Research Institute, Barcelona, Spain.
Irene Navalpotro-GómezHospital del Mar Research Institute, Barcelona, Spain.

Funding

Instituto de Salud Carlos III (ISCIII) PI22/00456"la Caixa" Foundation 847648 (LCF/BQ/PR21/11840004)Miguel Servet program CP25/00015the European Research Area Network on Cardiovascular Diseases AC20/00001the European Research Area Network on Cardiovascular Diseases ERA-CVD_JTC2020-015the European Research Council (ERC) 948677the Fondo de Investigación Sanitaria (FIS) PI21/00194
6 · The paper itself

Abstract

introductionCerebral amyloid angiopathy (CAA) frequently co-occurs with Alzheimer's disease (AD), generating mixed vascular-neurodegenerative phenotypes. Plasma phosphorylated tau (p-tau)217 is a robust biomarker of AD, but its performance in CAA remains unclear.

methodsWe studied 231 participants, including 50 patients with CAA (Boston v2.0), 154 with AD, and 27 cognitively unimpaired controls. Plasma p-tau217 was measured on an automated platform and compared to cerebrospinal fluid (CSF)-defined AD status. Associations with magnetic resonance imaging (MRI) markers of CAA burden were evaluated.

resultsAmong CAA participants, 29 met CSF criteria for AD co-pathology. Plasma p-tau217 discriminated CAA patients with and without AD co-pathology (area under the curve = 0.920) and showed no association with MRI markers of CAA burden. Predefined cut-offs (≥ 0.27 pg/mL and ≥ 0.34 pg/mL) yielded high accuracy for identifying AD co-pathology within CAA.

conclusionsPlasma p-tau217 shows high diagnostic accuracy for identifying AD co-pathology in CAA and is not associated with MRI markers of CAA burden, supporting its specificity for AD-related pathology.

Indexed as

Alzheimer DiseaseCerebral Amyloid Angiopathytau ProteinsAgedAged, 80 and overBiomarkersBrainCohort StudiesFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedPhosphorylationBiomarkersMAPT protein, humantau ProteinsAlzheimer's diseaseamyloid betablood biomarkercerebral amyloid angiopathydiagnosisphosphorylated tau 217

Identifiers

PMID42552750
PMCPMC13438190

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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.