Evidence map›Paper›PMID 29623063›Full record

ArticleFrontiers in neurology2018

Amyloid-β Plaques in Clinical Alzheimer's Disease Brain Incorporate Stable Isotope Tracer

Norelle C Wildburger, Frank Gyngard, Christelle Guillermier, Bruce W Patterson, Donald Elbert, Kwasi G Mawuenyega, Theresa Schneider, Karen Green, Robyn Roth, Robert E Schmidt and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

22 citing papers in PubMed, 30 citations in OpenAlex.

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  20. A proteomic signature for dementia with Lewy bodies.Alzheimer's & dementia (Amsterdam, Netherlands) · 2019
    Article
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

14 authors at 4 institutions in 1 country.

Norelle C WildburgerDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, United States.
Frank GyngardDepartment of Physics, Washington University in St. Louis, St. Louis, MO, United States.
Christelle GuillermierNanoImaging Center, Division of Genetics, Brigham and Women's Hospital, Cambridge, MA, United States.
Bruce W PattersonDepartment of Medicine, Washington University School of Medicine, St. Louis, MO, United States.
Donald ElbertDepartment of Neurology, The University of Texas at Austin Dell Medical School, Austin, TX, United States.
Kwasi G MawuenyegaDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, United States.
Theresa SchneiderDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, United States.
Karen GreenDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States.
Robyn RothDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, United States.
Robert E SchmidtDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States.
Nigel J CairnsDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, United States.
Tammie L S BenzingerKnight Alzheimer's Disease Research Center, Department of Neurology, Washington University School of Medicine, St Louis, MO, United States.
Matthew L SteinhauserNanoImaging Center, Division of Genetics, Brigham and Women's Hospital, Cambridge, MA, United States.
Randall J BatemanDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, United States.
Washington University in St. Louis · USBrigham and Women's Hospital · USHarvard University · USThe University of Texas at Austin · US

Funding

WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Smartphone-Based "Burst" Cognitive AssessmentsP01AG003991 · NIA · WASHINGTON UNIVERSITY · PI Tammie Lee Smith Benzinger · 1985 to 2026
$69.5M
WASHINGTON UNIVERSITY ALZHEIMERS DISEASE RESEARCH CENTERP50AG005681 · NIA · WASHINGTON UNIVERSITY · PI MORRIS, JOHN · 1985 to 2019
$52.1M
The natural history of AB accumulation in preclinical ADP01AG026276 · NIA · WASHINGTON UNIVERSITY · PI SCHINDLER, SUZANNE ELIZABETH · 2005 to 2025
$49.5M
Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Brian N Finck · 1999 to 2026
$30.2M
THE XNAT IMAGING INFORMATICS PLATFORMR01EB009352 · NIBIB · WASHINGTON UNIVERSITY · PI Daniel Scott Marcus · 2009 to 2026
$9.3M
Quantification of Neuroinflammation inAlzheimer's Disease Using Diffusion BasisSpectrum ImagingR01AG054567 · NIA · WASHINGTON UNIVERSITY · PI BENZINGER, TAMMIE LEE SMITH, WANG, YONG · 2017 to 2021
$3.6M
NINDS CENTER CORE FOR BRAIN IMAGINGP30NS098577 · NINDS · WASHINGTON UNIVERSITY · PI HERSHEY, TAMARA G, MARCUS, DANIEL SCOTT · 2016 to 2019
$2.4M
Expanding Access to Planar Illumination Microscopy in a Neuroimaging CoreR24NS086741 · NINDS · WASHINGTON UNIVERSITY · PI TAGHERT, PAUL H · 2014 to 2017
$814k
WHOLE SLIDE IMAGING SYSTEM FOR TRANSLATIONAL NEUROSCIENCES10RR027552 · NCRR · WASHINGTON UNIVERSITY · PI LEE, JIN-MOO · 2010 to 2010
$275k
NCATS NIH HHS UL1 TR000448NCATS NIH HHS UL1 TR002345NCRR NIH HHS S10 RR027552NIA NIH HHS P01 AG003991NIA NIH HHS P01 AG026276NIA NIH HHS P50 AG005681NIA NIH HHS R01 AG054567NIBIB NIH HHS R01 EB009352NIDDK NIH HHS P30 DK056341NINDS NIH HHS P30 NS098577NINDS NIH HHS R24 NS086741
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a neurodegenerative disorder with clinical manifestations of progressive memory decline and loss of executive function and language. AD affects an estimated 5.3 million Americans alone and is the most common form of age-related dementia with a rapidly growing prevalence among the aging population-those 65 years of age or older. AD is characterized by accumulation of aggregated amyloid-beta (Aβ) in the brain, which leads to one of the pathological hallmarks of AD-Aβ plaques. As a result, Aβ plaques have been extensively studied after being first described over a century ago. Advances in brain imaging and quantitative measures of Aβ in biological fluids have yielded insight into the time course of plaque development decades before and after AD symptom onset. However, despite the fundamental role of Aβ plaques in AD,

Indexed as

Alzheimer’s diseaseAβ plaquesplaque dynamicsSILK–SIMSstable isotope tracer

Identifiers

PMID29623063
PMCPMC5874304
OpenAlexW2789872951

What OpenQuestion holds

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LicenceCC BY
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.