Evidence map›Paper›PMID 33319314›Full record

ArticleActa neuropathologica2021

A multifactorial model of pathology for age of onset heterogeneity in familial Alzheimer's disease.

Diego Sepulveda-Falla, Lucia Chavez-Gutierrez, Erik Portelius, Jorge I Vélez, Simon Dujardin, Alvaro Barrera-Ocampo, Felix Dinkel, Christian Hagel, Berta Puig, Claudio Mastronardi and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Acta neuropathologica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

44 citing papers in PubMed, 53 citations in OpenAlex.

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  16. Is Alzheimer disease a disease?Nature reviews. Neurology · 2024
    Review
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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

16 authors at 7 institutions in 7 countries.

Diego Sepulveda-FallaInstitute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. dsepulve@uke.de.ORCID http://orcid.org/0000-0003-0176-2042
Lucia Chavez-GutierrezVIB Center for Brain and Disease Research, 3000, Leuven, Belgium.
Erik PorteliusInstitute of Neuroscience and Physiology, Dept. of Psychiatry and Neurochemistry, The Sahlgrenska Academy At the University of Gothenburg, Mölndal, Sweden.
Jorge I VélezDepartment of Genome Sciences, John Curtin School of Medical Research, Australian National University, Canberra, ACT, Australia.
Simon DujardinDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, MassGeneral Institute for Neurodegenerative Disease, Charlestown, USA.
Alvaro Barrera-OcampoInstitute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Felix DinkelInstitute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Christian HagelInstitute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Berta PuigInstitute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Claudio MastronardiDepartment of Genome Sciences, John Curtin School of Medical Research, Australian National University, Canberra, ACT, Australia.
Francisco LoperaNeuroscience Group of Antioquia, Faculty of Medicine, University of Antioquia, Medellín, Colombia.
Bradley T HymanDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, MassGeneral Institute for Neurodegenerative Disease, Charlestown, USA.
Kaj BlennowInstitute of Neuroscience and Physiology, Dept. of Psychiatry and Neurochemistry, The Sahlgrenska Academy At the University of Gothenburg, Mölndal, Sweden.
Mauricio Arcos-BurgosGIPSI Group, Department of Psychiatry, Medical Research Institute, University of Antioquia, Medellín, Colombia.
Bart de StrooperVIB Center for Brain and Disease Research, 3000, Leuven, Belgium.
Markus GlatzelInstitute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. m.glatzel@uke.de.
Universität Hamburg · DEAustralian National University · AUHarvard University · USSahlgrenska University Hospital · SEUniversidad de Antioquia · COUK Dementia Research Institute · GBVIB-KU Leuven Center for Brain & Disease Research · BE

Funding

Are multiple tau species toxic in Alzheimer's Disease?RF1AG059789 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI HYMAN, BRADLEY T. · 2018 to 2018
$2.7M
Synergy between amyloid and tau in Alzheimer's DiseaseRF1AG058674 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI HYMAN, BRADLEY T. · 2018 to 2018
$2.6M
Complexity and Heterogeneity of Alzheimer diseaseR56AG061196 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI HYMAN, BRADLEY T. · 2019 to 2019
$654k
NIA NIH HHS R56 AG061196NIA NIH HHS RF1 AG058674NIA NIH HHS RF1 AG059789NIH HHS RF1AG059789
6 · The paper itself

Abstract

Presenilin-1 (PSEN1) mutations cause familial Alzheimer's disease (FAD) characterized by early age of onset (AoO). Examination of a large kindred harboring the PSEN1-E280A mutation reveals a range of AoO spanning 30 years. The pathophysiological drivers and clinical impact of AoO variation in this population are unknown. We examined brains of 23 patients focusing on generation and deposition of beta-amyloid (Aβ) and Tau pathology profile. In 14 patients distributed at the extremes of AoO, we performed whole-exome capture to identify genotype-phenotype correlations. We also studied kinome activity, proteasome activity, and protein polyubiquitination in brain tissue, associating it with Tau phosphorylation profiles. PSEN1-E280A patients showed a bimodal distribution for AoO. Besides AoO, there were no clinical differences between analyzed groups. Despite the effect of mutant PSEN1 on production of Aβ, there were no relevant differences between groups in generation and deposition of Aβ. However, differences were found in hyperphosphorylated Tau (pTau) pathology, where early onset patients showed severe pathology with diffuse aggregation pattern associated with increased activation of stress kinases. In contrast, late-onset patients showed lesser pTau pathology and a distinctive kinase activity. Furthermore, we identified new protective genetic variants affecting ubiquitin-proteasome function in early onset patients, resulting in higher ubiquitin-dependent degradation of differentially phosphorylated Tau. In PSEN1-E280A carriers, altered γ-secretase activity and resulting Aβ accumulation are prerequisites for early AoO. However, Tau hyperphosphorylation pattern, and its degradation by the proteasome, drastically influences disease onset in individuals with otherwise similar Aβ pathology, hinting toward a multifactorial model of disease for FAD. In sporadic AD (SAD), a wide range of heterogeneity, also influenced by Tau pathology, has been identified. Thus, Tau-induced heterogeneity is a common feature in both AD variants, suggesting that a multi-target therapeutic approach should be used to treat AD.

Indexed as

Age of OnsetAdultAgedAged, 80 and overAlzheimer DiseaseAmyloid beta-Protein PrecursorExome SequencingFemaleGenotypeHeterozygoteHumansMaleMiddle AgedModels, NeurologicalPhenotypePhosphorylationAmyloid beta-Protein PrecursorAPP protein, humanMAPT protein, humanPresenilin-1Proteasome Endopeptidase ComplexPSEN1 protein, humantau Proteins

Identifiers

PMID33319314
PMCPMC7847436
OpenAlexW3112685614

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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.