Evidence map›Paper›PMID 27318146›Full record

ArticleNeurobiology of aging2016

Comparative pathobiology of β-amyloid and the unique susceptibility of humans to Alzheimer's disease.

Rebecca F Rosen, Yasushi Tomidokoro, Aaron S Farberg, Jeromy Dooyema, Brian Ciliax, Todd M Preuss, Thomas A Neubert, Jorge A Ghiso, Harry LeVine, Lary C Walker

Abstract read
In one paragraph

Article in Neurobiology of aging, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
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  8. In-silico structural analysis ofMolecular biology research communications · 2024
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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

10 authors at 3 institutions in 1 country.

Rebecca F RosenYerkes National Primate Research Center, Emory University, Atlanta, GA, USA. Electronic address: rebecca.rosen@nyu.edu.
Yasushi TomidokoroDepartment of Pathology, NYU School of Medicine, New York, NY, USA.
Aaron S FarbergYerkes National Primate Research Center, Emory University, Atlanta, GA, USA.
Jeromy DooyemaYerkes National Primate Research Center, Emory University, Atlanta, GA, USA.
Brian CiliaxDepartment of Neurology, Emory University School of Medicine, Atlanta, GA, USA.
Todd M PreussYerkes National Primate Research Center, Emory University, Atlanta, GA, USA; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, USA.
Thomas A NeubertDepartment of Biochemistry and Molecular Pharmacology, Kimmel Center for Biology and Medicine at the Skirball Institute, NYU School of Medicine, New York, NY, USA.
Jorge A GhisoDepartment of Pathology, NYU School of Medicine, New York, NY, USA; Department of Psychiatry, NYU School of Medicine, New York, NY, USA.
Harry LeVineDepartment of Molecular & Cellular Biochemistry, Center on Aging, Center for Structural Biology, University of Kentucky, Lexington, KY, USA.
Lary C WalkerYerkes National Primate Research Center, Emory University, Atlanta, GA, USA; Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA. Electronic address: lary.walker@emory.edu.
Emory University · USNew York University · USUniversity of Kentucky · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI ALTMAN, JOHN DAVID · 1985 to 2011
$114.0M
The Emory Alzheimer's Disease CenterP50AG025688 · NIA · EMORY UNIVERSITY · PI LEVEY, ALLAN I · 2005 to 2019
$25.7M
SOCIAL COGNITION AND EMOTIONAL AGING IN PRIMATESP01AG026423 · NIA · EMORY UNIVERSITY · PI HERNDON, JAMES G · 2007 to 2011
$11.6M
Protein Mass Spectrometry Core Facility for NeuroscienceP30NS050276 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NEUBERT, THOMAS A · 2005 to 2015
$7.9M
ENNCF - Viral Vector CoreP30NS055077 · NINDS · EMORY UNIVERSITY · PI LEVEY, ALLAN I · 2008 to 2018
$6.8M
Cerebral small vessel disease: Enhancing the diagnostic precision of MRIR21NS077049 · NINDS · EMORY UNIVERSITY · PI WALKER, LARY C · 2011 to 2012
$476k
Insights into the Brain Clearance Mechanisms of Oligomeric Beta-Amyloid SpeciesR21AG051266 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI GHISO, JORGE A · 2015 to 2016
$466k
Probes to differentiate AD brain beta-amyloid from model beta-amyloid systemsR21NS080576 · NINDS · UNIVERSITY OF KENTUCKY · PI LEVINE, HARRY, SPIELMANN, H PETER · 2013 to 2014
$413k
NCRR NIH HHS P51 RR000165NIA NIH HHS P01 AG026423NIA NIH HHS P50 AG025688NIA NIH HHS R21 AG051266NIH HHS P51 OD011132NINDS NIH HHS P30 NS050276NINDS NIH HHS P30 NS055077NINDS NIH HHS R21 NS077049NINDS NIH HHS R21 NS080576
6 · The paper itself

Abstract

The misfolding and accumulation of the protein fragment β-amyloid (Aβ) is an early and essential event in the pathogenesis of Alzheimer's disease (AD). Despite close biological similarities among primates, humans appear to be uniquely susceptible to the profound neurodegeneration and dementia that characterize AD, even though nonhuman primates deposit copious Aβ in senile plaques and cerebral amyloid-β angiopathy as they grow old. Because the amino acid sequence of Aβ is identical in all primates studied to date, we asked whether differences in the properties of aggregated Aβ might underlie the vulnerability of humans and the resistance of other primates to AD. In a comparison of aged squirrel monkeys (Saimiri sciureus) and humans with AD, immunochemical and mass spectrometric analyses indicate that the populations of Aβ fragments are largely similar in the 2 species. In addition, Aβ-rich brain extracts from the brains of aged squirrel monkeys and AD patients similarly seed the deposition of Aβ in a transgenic mouse model. However, the epitope exposure of aggregated Aβ differs in sodium dodecyl sulfate-stable oligomeric Aβ from the 2 species. In addition, the high-affinity binding of (3)H Pittsburgh Compound B to Aβ is significantly diminished in tissue extracts from squirrel monkeys compared with AD patients. These findings support the hypothesis that differences in the pathobiology of aggregated Aβ among primates are linked to post-translational attributes of the misfolded protein, such as molecular conformation and/or the involvement of species-specific cofactors.

Indexed as

Disease SusceptibilityAgingAlzheimer DiseaseAmyloid beta-PeptidesAnimalsBrainDisease Models, AnimalHumansMice, TransgenicSaimiriTauopathiesAmyloid beta-PeptidesAmyloidCerebral amyloid angiopathyPrimatePrionSeedingSenile plaquesTauopathy

Identifiers

PMID27318146
PMCPMC4913040
OpenAlexW2345680808

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.