Evidence map›Paper›PMID 42841982›Full record

ArticleActa neuropathologica2026

Amyloid-β plaque diversity across brain regions in Alzheimer's disease and its relation to major clinicopathological traits.

Antonia Neubauer, Paul Feyen, Susanna Pekrun, Sigrun Roeber, Viktoria Ruf, Felix L Strübing, Jochen Herms

Abstract read
In one paragraph

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

0numbers the graph read from it
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

7 authors.

Antonia NeubauerInstitute of Neuropathology, LMU Medizin, Ludwig-Maximilians-Universität München, Munich, Germany. Antonia.Neubauer@med.uni-muenchen.de.ORCID https://orcid.org/0000-0001-9820-3735
Paul FeyenInstitute of Neuropathology, LMU Medizin, Ludwig-Maximilians-Universität München, Munich, Germany.
Susanna PekrunInstitute of Neuropathology, LMU Medizin, Ludwig-Maximilians-Universität München, Munich, Germany.
Sigrun RoeberInstitute of Neuropathology, LMU Medizin, Ludwig-Maximilians-Universität München, Munich, Germany.
Viktoria RufInstitute of Neuropathology, LMU Medizin, Ludwig-Maximilians-Universität München, Munich, Germany.
Felix L StrübingInstitute of Neuropathology, LMU Medizin, Ludwig-Maximilians-Universität München, Munich, Germany.
Jochen HermsInstitute of Neuropathology, LMU Medizin, Ludwig-Maximilians-Universität München, Munich, Germany.

Funding

Deutsche Forschungsgemeinschaft EXC 2145 SyNergy - ID 390857198Deutsche Forschungsgemeinschaft STR 1537/3-1
6 · The paper itself

Abstract

Amyloid beta (Aβ) deposition and tau accumulation are neuropathological hallmarks of Alzheimer's disease (AD). While Aβ deposits present with a wide morphological variety, a comprehensive, cross-regional overview of Aβ plaque composition in AD and associations with clinicopathological traits are missing. In this study, we systematically documented the abundance and morphological diversity of Aβ plaques in up to 23 brain regions of 84 advanced AD cases. Deposits were segmented with a random forest pixel classifier in 4G8 diaminobenzidine stains and classified into six classes using a convolutional neural network (cored, diffuse light, diffuse dense, compact, small dense plaques, cerebral amyloid angiopathy (CAA)). Deposit counts were correlated between classes, regions, and tau load using Pearson correlation. Associations between plaque densities and co-pathologies, sex, ApoE, familial vs. sporadic cases, age at clinical onset, disease duration, and age at death were examined. Our classification model achieved a recall of 81.5% and a precision of 82.4% in the test set. Cortical brain regions showed the highest Aβ plaque loads, predominantly consisting of diffuse light and small dense plaques. Plaque densities correlated within and across the hippocampal and cortical regions. Abundances of diffuse dense, small dense, and compact plaques were positively correlated with one another, while densities of cored plaques and CAA did not correlate with other plaque classes. Only cored plaques were positively correlated with the entorhinal tau load, while other plaque classes, except CAA, showed negative correlations. Notably, female sex was associated with more diffuse plaques, and ApoE4 was associated with diffuse dense and small dense plaques. Earlier age at onset and death were associated with higher densities of diffuse light plaques. Overall, associations varied across brain regions and plaque classes. Cored plaques and CAA stand out statistically from other Aβ deposits, suggesting distinct association patterns in the course of the disease.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesBrainPlaque, AmyloidAgedAged, 80 and overFemaleHumansMaletau ProteinsAmyloid beta-Peptidestau ProteinsAlzheimer’s diseaseAmyloid betaClassificationDigital pathologyMachine learningPlaque morphology

Identifiers

PMID42841982
PMCPMC13645940

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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.