Evidence map›Paper›PMID 38666085›Full record

ArticleAlzheimer's & dementia (Amsterdam, Netherlands)

Aβ oligomers peak in early stages of Alzheimer's disease preceding tau pathology.

Lara Blömeke, Fabian Rehn, Victoria Kraemer-Schulien, Janine Kutzsche, Marlene Pils, Tuyen Bujnicki, Piotr Lewczuk, Johannes Kornhuber, Silka D Freiesleben, Luisa-Sophie Schneider and 38 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Alzheimer's & dementia (Amsterdam, Netherlands). The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 3% of its field
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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

48 authors at 15 institutions in 4 countries.

Lara BlömekeInstitute of Biological Information Processing (Structural Biochemistry: IBI-7) Forschungszentrum Jülich GmbH Jülich Germany.
Fabian RehnInstitute of Biological Information Processing (Structural Biochemistry: IBI-7) Forschungszentrum Jülich GmbH Jülich Germany.
Victoria Kraemer-SchulienInstitute of Biological Information Processing (Structural Biochemistry: IBI-7) Forschungszentrum Jülich GmbH Jülich Germany.
Janine KutzscheInstitute of Biological Information Processing (Structural Biochemistry: IBI-7) Forschungszentrum Jülich GmbH Jülich Germany.
Marlene PilsInstitute of Biological Information Processing (Structural Biochemistry: IBI-7) Forschungszentrum Jülich GmbH Jülich Germany.
Tuyen BujnickiInstitute of Biological Information Processing (Structural Biochemistry: IBI-7) Forschungszentrum Jülich GmbH Jülich Germany.
Piotr LewczukDepartment of Psychiatry and Psychotherapy Universitätsklinikum Erlangen and Friedrich-Alexander-Universität Erlangen-Nürnberg Erlangen Germany.
Johannes KornhuberDepartment of Psychiatry and Psychotherapy Universitätsklinikum Erlangen and Friedrich-Alexander-Universität Erlangen-Nürnberg Erlangen Germany.
Silka D FreieslebenDepartment of Psychiatry and Psychotherapy Charité Berlin Germany.
Luisa-Sophie SchneiderDepartment of Psychiatry and Psychotherapy Charité Berlin Germany.
Lukas PreisDepartment of Psychiatry and Psychotherapy Charité Berlin Germany.
Josef PrillerDepartment of Psychiatry and Psychotherapy Charité Berlin Germany.
Eike J SpruthDepartment of Psychiatry and Psychotherapy Charité Berlin Germany.
Slawek AltensteinDepartment of Psychiatry and Psychotherapy Charité Berlin Germany.
Andrea LohseDepartment of Psychiatry and Psychotherapy Charité Berlin Germany.
Anja SchneiderGerman Center for Neurodegenerative Diseases (DZNE) Bonn Germany.
Klaus FliessbachGerman Center for Neurodegenerative Diseases (DZNE) Bonn Germany.
Jens WiltfangGerman Center for Neurodegenerative Diseases (DZNE) Göttingen Germany.
Niels HansenDepartment of Psychiatry and Psychotherapy University Medical Center Göttingen University of Göttingen Göttingen Germany.
Ayda RostamzadehDepartment of Psychiatry Medical Faculty University of Cologne Cologne Germany.
Emrah DüzelGerman Center for Neurodegenerative Diseases (DZNE) Magdeburg Germany.
Wenzel GlanzGerman Center for Neurodegenerative Diseases (DZNE) Magdeburg Germany.
Enise I IncesoyGerman Center for Neurodegenerative Diseases (DZNE) Magdeburg Germany.
Michaela ButrynGerman Center for Neurodegenerative Diseases (DZNE) Magdeburg Germany.
Katharina BuergerGerman Center for Neurodegenerative Diseases (DZNE, Munich) Munich Germany.
Daniel JanowitzInstitute for Stroke and Dementia Research (ISD) University Hospital LMU Munich Munich Germany.
Michael EwersGerman Center for Neurodegenerative Diseases (DZNE, Munich) Munich Germany.
Robert PerneczkyGerman Center for Neurodegenerative Diseases (DZNE, Munich) Munich Germany.
Boris-Stephan RauchmannDepartment of Psychiatry and Psychotherapy University Hospital LMU Munich Munich Germany.
Stefan TeipelGerman Center for Neurodegenerative Diseases (DZNE) Rostock Germany.
Ingo KilimannGerman Center for Neurodegenerative Diseases (DZNE) Rostock Germany.
Doreen GoerssGerman Center for Neurodegenerative Diseases (DZNE) Rostock Germany.
Christoph LaskeGerman Center for Neurodegenerative Diseases (DZNE) Tübingen Germany.
Matthias H MunkGerman Center for Neurodegenerative Diseases (DZNE) Tübingen Germany.
Carolin SanzenbacherGerman Center for Neurodegenerative Diseases (DZNE) Tübingen Germany.
Annika SpottkeGerman Center for Neurodegenerative Diseases (DZNE) Bonn Germany.
Nina Roy-KluthGerman Center for Neurodegenerative Diseases (DZNE) Bonn Germany.
Michael T HenekaLuxembourg Centre for Systems Biomedicine (LCSB) University of Luxembourg Belvaux Luxemburg.
Frederic BrosseronGerman Center for Neurodegenerative Diseases (DZNE) Bonn Germany.
Michael WagnerGerman Center for Neurodegenerative Diseases (DZNE) Bonn Germany.
Steffen WolfsgruberGerman Center for Neurodegenerative Diseases (DZNE) Bonn Germany.
Luca KleineidamGerman Center for Neurodegenerative Diseases (DZNE) Bonn Germany.
Melina StarkDepartment of Neurodegenerative Disease and Geriatric Psychiatry/Psychiatry University of Bonn Medical Center Bonn Germany.
Matthias SchmidGerman Center for Neurodegenerative Diseases (DZNE) Bonn Germany.
Frank JessenGerman Center for Neurodegenerative Diseases (DZNE) Bonn Germany.
Oliver BannachInstitute of Biological Information Processing (Structural Biochemistry: IBI-7) Forschungszentrum Jülich GmbH Jülich Germany.
Dieter WillboldInstitute of Biological Information Processing (Structural Biochemistry: IBI-7) Forschungszentrum Jülich GmbH Jülich Germany.
Oliver PetersDepartment of Psychiatry and Psychotherapy Charité Berlin Germany.
German Center for Neurodegenerative Diseases · DEForschungszentrum Jülich · DEUniversity of Bonn · DECharité - Universitätsmedizin Berlin · DEHeinrich Heine University Düsseldorf · DEUniversitätsklinikum Erlangen · DEUniversity of Göttingen · DEUniversity of Rostock · DEImperial College London · GBLMU Klinikum · DELudwig-Maximilians-Universität München · DEUniversity Hospital Bonn · DEUniversity of Cologne · DEUniversity of Luxembourg · LUUniversity of Sheffield · GB

Funding

USCADRC Diversity Supplement PachicanoP30AG066530 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI HELENA Chang CHUI, ARTHUR W TOGA · 2020 to 2026
$27.8M
NIA NIH HHS P30 AG066530
6 · The paper itself

Abstract

introductionSoluble amyloid beta (Aβ) oligomers have been suggested as initiating Aβ related neuropathologic change in Alzheimer's disease (AD) but their quantitative distribution and chronological sequence within the AD continuum remain unclear.

methodsA total of 526 participants in early clinical stages of AD and controls from a longitudinal cohort were neurobiologically classified for amyloid and tau pathology applying the AT(N) system. Aβ and tau oligomers in the quantified cerebrospinal fluid (CSF) were measured using surface-based fluorescence intensity distribution analysis (sFIDA) technology.

resultsAcross groups, highest Aβ oligomer levels were found in A+ with subjective cognitive decline and mild cognitive impairment. Aβ oligomers were significantly higher in A+T- compared to A-T- and A+T+. DISCUSSION: The accumulation of Aβ oligomers in the CSF peaks early within the AD continuum, preceding tau pathology. Disease-modifying treatments targeting Aβ oligomers might have the highest therapeutic effect in these disease stages. Highlights: Using surface-based fluorescence intensity distribution analysis (sFIDA) technology, we quantified Aβ oligomers in cerebrospinal fluid (CSF) samples of the DZNE-Longitudinal Cognitive Impairment and Dementia (DELCODE) cohortAβ oligomers were significantly elevated in mild cognitive impairment (MCI)Amyloid-positive subjects in the subjective cognitive decline (SCD) group increased compared to the amyloid-negative control groupInterestingly, levels of Aβ oligomers decrease at advanced stages of the disease (A+T+), which might be explained by altered clearing mechanisms.

Indexed as

Alzheimer's diseaseAPOEAT(N) classificationAβcerebrospinal fluidoligomerspreclinicalprodromalsFIDAtau

Identifiers

PMID38666085
PMCPMC11044868
OpenAlexW4395469070

What OpenQuestion holds

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LicenceCC BY-NC
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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.