Evidence map›Paper›PMID 39658587›Full record

ArticleCommunications medicine2024

Blood-based quantification of Aβ oligomers indicates impaired clearance from brain in ApoE ε4 positive subjects.

Lara Blömeke, Fabian Rehn, Marlene Pils, Victoria Kraemer-Schulien, Anneliese Cousin, Janine Kutzsche, Tuyen Bujnicki, Silka D Freiesleben, Luisa-Sophie Schneider, Lukas Preis and 32 more

Abstract read
In one paragraph

Article in Communications medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

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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

42 authors.

Lara BlömekeInstitute of Biological Information Processing (Structural Biochemistry: IBI-7), Forschungszentrum Jülich, 52428, Jülich, Germany.ORCID http://orcid.org/0000-0002-8861-9224
Fabian RehnInstitute of Biological Information Processing (Structural Biochemistry: IBI-7), Forschungszentrum Jülich, 52428, Jülich, Germany.ORCID http://orcid.org/0000-0001-8815-0684
Marlene PilsInstitute of Biological Information Processing (Structural Biochemistry: IBI-7), Forschungszentrum Jülich, 52428, Jülich, Germany.ORCID http://orcid.org/0000-0002-1506-3675
Victoria Kraemer-SchulienInstitute of Biological Information Processing (Structural Biochemistry: IBI-7), Forschungszentrum Jülich, 52428, Jülich, Germany.ORCID http://orcid.org/0000-0002-7413-7646
Anneliese CousinInstitute of Biological Information Processing (Structural Biochemistry: IBI-7), Forschungszentrum Jülich, 52428, Jülich, Germany.
Janine KutzscheInstitute of Biological Information Processing (Structural Biochemistry: IBI-7), Forschungszentrum Jülich, 52428, Jülich, Germany.ORCID http://orcid.org/0000-0003-0271-7390
Tuyen BujnickiInstitute of Biological Information Processing (Structural Biochemistry: IBI-7), Forschungszentrum Jülich, 52428, Jülich, Germany.ORCID http://orcid.org/0000-0002-7191-8455
Silka D FreieslebenGerman Center for Neurodegenerative Diseases (DZNE), 10117, Berlin, Germany.ORCID http://orcid.org/0000-0002-2141-8671
Luisa-Sophie SchneiderGerman Center for Neurodegenerative Diseases (DZNE), 10117, Berlin, Germany.ORCID http://orcid.org/0000-0001-5822-1744
Lukas PreisGerman Center for Neurodegenerative Diseases (DZNE), 10117, Berlin, Germany.
Josef PrillerGerman Center for Neurodegenerative Diseases (DZNE), 10117, Berlin, Germany.
Eike J SpruthGerman Center for Neurodegenerative Diseases (DZNE), 10117, Berlin, Germany.
Slawek AltensteinGerman Center for Neurodegenerative Diseases (DZNE), 10117, Berlin, Germany.
Anja SchneiderGerman Center for Neurodegenerative Diseases (DZNE), Bonn, 53127, Bonn, Germany.ORCID http://orcid.org/0000-0001-9540-8700
Klaus FliessbachGerman Center for Neurodegenerative Diseases (DZNE), Bonn, 53127, Bonn, Germany.
Jens WiltfangGerman Center for Neurodegenerative Diseases (DZNE), 37075, Goettingen, Germany.ORCID http://orcid.org/0000-0003-1492-5330
Niels HansenDepartment of Psychiatry and Psychotherapy, University Medical Center Goettingen, University of Goettingen, 37075, Goettingen, Germany.ORCID http://orcid.org/0000-0001-5785-9594
Ayda RostamzadehDepartment of Psychiatry, University of Cologne, Medical Faculty, 50924, Cologne, Germany.
Emrah DüzelGerman Center for Neurodegenerative Diseases (DZNE), 39120, Magdeburg, Germany.
Wenzel GlanzGerman Center for Neurodegenerative Diseases (DZNE), 39120, Magdeburg, Germany.
Enise I IncesoyGerman Center for Neurodegenerative Diseases (DZNE), 39120, Magdeburg, Germany.ORCID http://orcid.org/0000-0003-2014-4098
Katharina BuergerGerman Center for Neurodegenerative Diseases (DZNE, Munich), 81377, Munich, Germany.
Daniel JanowitzInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, 81377, Munich, Germany.
Michael EwersGerman Center for Neurodegenerative Diseases (DZNE, Munich), 81377, Munich, Germany.
Robert PerneczkyGerman Center for Neurodegenerative Diseases (DZNE, Munich), 81377, Munich, Germany.
Boris-Stephan RauchmannDepartment of Psychiatry and Psychotherapy, University Hospital, LMU Munich, 81377, Munich, Germany.
Stefan TeipelGerman Center for Neurodegenerative Diseases (DZNE), 18147, Rostock, Germany.
Ingo KilimannGerman Center for Neurodegenerative Diseases (DZNE), 18147, Rostock, Germany.
Christoph LaskeGerman Center for Neurodegenerative Diseases (DZNE), 72076, Tübingen, Germany.
Matthias H MunkGerman Center for Neurodegenerative Diseases (DZNE), 72076, Tübingen, Germany.
Annika SpottkeGerman Center for Neurodegenerative Diseases (DZNE), Bonn, 53127, Bonn, Germany.
Nina RoyGerman Center for Neurodegenerative Diseases (DZNE), Bonn, 53127, Bonn, Germany.
Michael T HenekaLuxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, L-4367, Belvaux, Luxembourg.ORCID http://orcid.org/0000-0003-4996-1630
Frederic BrosseronGerman Center for Neurodegenerative Diseases (DZNE), Bonn, 53127, Bonn, Germany.ORCID http://orcid.org/0000-0003-3137-7516
Michael WagnerGerman Center for Neurodegenerative Diseases (DZNE), Bonn, 53127, Bonn, Germany.ORCID http://orcid.org/0000-0003-2589-6440
Sandra RoeskeGerman Center for Neurodegenerative Diseases (DZNE), Bonn, 53127, Bonn, Germany.
Alfredo RamirezGerman Center for Neurodegenerative Diseases (DZNE), Bonn, 53127, Bonn, Germany.ORCID http://orcid.org/0000-0003-4991-763X
Matthias SchmidGerman Center for Neurodegenerative Diseases (DZNE), Bonn, 53127, Bonn, Germany.
Frank JessenGerman Center for Neurodegenerative Diseases (DZNE), Bonn, 53127, Bonn, Germany.
Oliver BannachInstitute of Biological Information Processing (Structural Biochemistry: IBI-7), Forschungszentrum Jülich, 52428, Jülich, Germany.
Oliver PetersGerman Center for Neurodegenerative Diseases (DZNE), 10117, Berlin, Germany.
Dieter WillboldInstitute of Biological Information Processing (Structural Biochemistry: IBI-7), Forschungszentrum Jülich, 52428, Jülich, Germany. d.willbold@fz-juelich.de.ORCID http://orcid.org/0000-0002-0065-7366

Funding

Helmholtz Association HVF0079
6 · The paper itself

Abstract

backgroundQuantification of Amyloid beta (Aβ) oligomers in plasma enables early diagnosis of Alzheimer's Disease (AD) and improves our understanding of underlying pathologies. However, quantification necessitates an extremely sensitive and selective technology because of very low Aβ oligomer concentrations and possible interference from matrix components.

methodsIn this report, we developed and validated a surface-based fluorescence distribution analysis (sFIDA) assay for quantification of Aβ oligomers in plasma.

resultsThe blood-based sFIDA assay delivers a sensitivity of 1.8 fM, an inter- and intra-assay variation below 20% for oligomer calibration standards and no interference with matrix components. Quantification of Aβ oligomers in 359 plasma samples from the DELCODE cohort reveals lower oligomer concentrations in subjective cognitive decline and AD patients than healthy Control participants.

conclusionsCorrelation analysis between CSF and plasma oligomer concentrations indicates an impaired clearance of Aβ oligomers that is dependent on the ApoE ε4 status.

Identifiers

PMID39658587
PMCPMC11631981

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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.