Evidence map›Paper›PMID 35831715›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2022

Introducing a gatekeeping system for amyloid status assessment in mild cognitive impairment.

E Doering, M C Hoenig, G N Bischof, K P Bohn, L M Ellingsen, T van Eimeren, A Drzezga, Alzheimer’s Disease Neuroimaging Initiative

Open access · hybridAbstract read
In one paragraph

Article in European journal of nuclear medicine and molecular imaging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 89% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 5 institutions in 3 countries.

E DoeringGerman Center for Neurodegenerative Diseases (DZNE), Bonn-Cologne, Germany. elena.doering@uk-koeln.de.
M C HoenigGerman Center for Neurodegenerative Diseases (DZNE), Bonn-Cologne, Germany.
G N BischofGerman Center for Neurodegenerative Diseases (DZNE), Bonn-Cologne, Germany.
K P BohnKlinikum Dritter Orden, Department of Radiology and Nuclear Medicine, Munich, Germany.
L M EllingsenDepartment of Electrical and Computer Engineering, Johns Hopkins University, Baltimore, MD, USA.
T van EimerenGerman Center for Neurodegenerative Diseases (DZNE), Bonn-Cologne, Germany.
A DrzezgaGerman Center for Neurodegenerative Diseases (DZNE), Bonn-Cologne, Germany.
Alzheimer’s Disease Neuroimaging Initiative
Forschungszentrum Jülich · DEUniversity Hospital Cologne · DEGerman Center for Neurodegenerative Diseases · DEJohns Hopkins University · USMünchen Klinik · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn patients with mild cognitive impairment (MCI), enhanced cerebral amyloid-β plaque burden is a high-risk factor to develop dementia with Alzheimer's disease (AD). Not all patients have immediate access to the assessment of amyloid status (A-status) via gold standard methods. It may therefore be of interest to find suitable biomarkers to preselect patients benefitting most from additional workup of the A-status. In this study, we propose a machine learning-based gatekeeping system for the prediction of A-status on the grounds of pre-existing information on APOE-genotype

methodsThree hundred and forty-two MCI patients were used to train different machine learning classifiers to predict A-status majority classes among APOE-ε4 non-carriers (APOE4-nc; majority class: amyloid negative (Aβ-)) and carriers (APOE4-c; majority class: amyloid positive (Aβ +)) from

resultsAβ- in APOE4-nc and Aβ + in APOE4-c were predicted with a precision of 87% and a recall of 79% and 51%, respectively. Predicted A-status and gold standard A-status were at least equally indicative of risk of progression to dementia.

conclusionWe developed an algorithm allowing approximation of A-status in MCI with good reliability using APOE-genotype,

Indexed as

Alzheimer DiseaseAmyloidosisCognitive DysfunctionAmyloidAmyloid beta-PeptidesApolipoprotein E4BiomarkersFluorodeoxyglucose F18GatekeepingHumansPositron-Emission TomographyReproducibility of ResultsAmyloidAmyloid beta-PeptidesApolipoprotein E4BiomarkersFluorodeoxyglucose F18Machine learningNeurodegeneration

Identifiers

PMID35831715
PMCPMC9605923
OpenAlexW4285387865

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.