Evidence map›Paper›PMID 35139917›Full record

ArticleTranslational neurodegeneration2022

EEG/ERP evidence of possible hyperexcitability in older adults with elevated beta-amyloid.

Hannes Devos, Kathleen Gustafson, Ke Liao, Pedram Ahmadnezhad, Bradley Estes, Laura E Martin, Jonathan D Mahnken, William M Brooks, Jeffrey M Burns

Open access · goldAbstract read
In one paragraph

Article in Translational neurodegeneration, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Machine learning based on event-related oscillations of working memory differentiates between preclinical Alzheimer's disease and normal aging.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2025
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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

9 authors at 1 institution in 1 country.

Hannes DevosDepartment of Physical Therapy, Rehabilitation Science, and Athletic Training, University of Kansas Medical Center, Kansas City, KS, 66160, USA. hdevos@kumc.edu.ORCID 0000-0002-8853-6840
Kathleen GustafsonDepartment of Neurology, University of Kansas Medical Center, Kansas City, KS, 66160, USA.
Ke LiaoHoglund Biomedical Imaging Center, University of Kansas Medical Center, Kansas City, KS, 66160, USA.
Pedram AhmadnezhadDepartment of Physical Therapy, Rehabilitation Science, and Athletic Training, University of Kansas Medical Center, Kansas City, KS, 66160, USA.
Bradley EstesDepartment of Physical Therapy, Rehabilitation Science, and Athletic Training, University of Kansas Medical Center, Kansas City, KS, 66160, USA.
Laura E MartinHoglund Biomedical Imaging Center, University of Kansas Medical Center, Kansas City, KS, 66160, USA.
Jonathan D MahnkenDepartment of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, KS, 66160, USA.
William M BrooksDepartment of Neurology, University of Kansas Medical Center, Kansas City, KS, 66160, USA.
Jeffrey M BurnsDepartment of Neurology, University of Kansas Medical Center, Kansas City, KS, 66160, USA.
University of Kansas Medical Center · US

Funding

University of Kansas Alzheimer's Disease Research Center (KU ADRC)P30AG072973 · NIA · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Jaime Perales Puchalt · 2021 to 2026
$25.3M
University of Kansas Alzheimer's Disease Core CentersP30AG035982 · NIA · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SWERDLOW, RUSSELL H. · 2011 to 2020
$16.6M
Siemens Magnetom Verio MRI ScannerS10RR029577 · NCRR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BROOKS, WILLIAM M. · 2010 to 2010
$2.9M
Neurophysiological Changes in Pre-clinical Alzheimer's DiseaseK01AG058785 · NIA · UNIVERSITY OF KANSAS MEDICAL CENTER · PI DEVOS, HANNES · 2019 to 2023
$638k
NCRR NIH HHS S10 RR029577NIA NIH HHS K01 AG058785NIA NIH HHS K01AG058785NIA NIH HHS P30 AG035982NIA NIH HHS P30 AG072973
6 · The paper itself

Abstract

backgroundAlthough growing evidence links beta-amyloid (Aβ) and neuronal hyperexcitability in preclinical mouse models of Alzheimer's disease (AD), a similar association in humans is yet to be established. The first aim of the study was to determine the association between elevated Aβ (Aβ+) and cognitive processes measured by the P3 event-related potential (ERP) in cognitively normal (CN) older adults. The second aim was to compare the event-related power between CNAβ+ and CNAβ-.

methodsSeventeen CNAβ+ participants (age: 73 ± 5, 11 females, Montreal Cognitive Assessment [MoCA] score 26 ± 2) and 17 CNAβ- participants group-matched for age, sex, and MOCA completed a working memory task (n-back with n = 0, 1, 2) test while wearing a 256-channel electro-encephalography net. P3 peak amplitude and latency of the target, nontarget and task difference effect (nontarget-target), and event-related power in the delta, theta, alpha, and beta bands, extracted from Fz, Cz, and Pz, were compared between groups using linear mixed models. P3 amplitude of the task difference effect at Fz and event-related power in the delta band were considered main outcomes. Correlations of mean Aβ standard uptake value ratios (SUVR) using positron emission tomography with P3 amplitude and latency of the task difference effect were analyzed using Pearson Correlation Coefficient r.

resultsThe P3 peak amplitude of the task difference effect at Fz was lower in the CNAβ+ group (P = 0.048). Similarly, power was lower in the delta band for nontargets at Fz in the CNAβ+ participants (P = 0.04). The CNAβ+ participants also demonstrated higher theta and alpha power in channels at Cz and Pz, but no changes in P3 ERP. Strong correlations were found between the mean Aβ SUVR and the latency of the 1-back (r =  - 0.69; P = 0.003) and 2-back (r =  - 0.69; P = 0.004) of the task difference effect at channel Fz in the CNAβ+ group.

conclusionsOur data suggest that the elevated amyloid in cognitively normal older adults is associated with neuronal hyperexcitability. The decreased P3 task difference likely reflects early impairments in working memory processes. Further research is warranted to determine the validity of ERP in predicting clinical, neurobiological, and functional manifestations of AD.

Indexed as

Amyloid beta-PeptidesCognitionEvent-Related Potentials, P300Alzheimer DiseaseElectroencephalographyFemaleHumansMaleMemory, Short-TermPositron-Emission TomographyAmyloid beta-PeptidesBeta-amyloidElectro-encephalographyEvent-related potentialsOlder adultsPreclinicalWorking memory

Identifiers

PMID35139917
PMCPMC8827181
OpenAlexW4211021176

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.