Evidence map›Paper›PMID 35974799›Full record

ArticleBrain communications2022

Altered visual entrainment in patients with Alzheimer's disease: magnetoencephalography evidence.

Seth D Springer, Alex I Wiesman, Pamela E May, Mikki Schantell, Hallie J Johnson, Madelyn P Willett, Camilo A Castelblanco, Jacob A Eastman, Nicholas J Christopher-Hayes, Sara L Wolfson and 3 more

Open access · goldAbstract read
In one paragraph

Article in Brain communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

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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

13 authors at 4 institutions in 2 countries.

Seth D SpringerInstitute for Human Neuroscience, Boys Town National Research Hospital, Omaha, NE 68010, USA.ORCID https://orcid.org/0000-0001-6605-398X
Alex I WiesmanCollege of Medicine, University of Nebraska Medical Center, Omaha, NE 68198, USA.ORCID https://orcid.org/0000-0003-0917-1570
Pamela E MayCollege of Medicine, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Mikki SchantellInstitute for Human Neuroscience, Boys Town National Research Hospital, Omaha, NE 68010, USA.ORCID https://orcid.org/0000-0002-2972-1368
Hallie J JohnsonInstitute for Human Neuroscience, Boys Town National Research Hospital, Omaha, NE 68010, USA.
Madelyn P WillettInstitute for Human Neuroscience, Boys Town National Research Hospital, Omaha, NE 68010, USA.
Camilo A CastelblancoInstitute for Human Neuroscience, Boys Town National Research Hospital, Omaha, NE 68010, USA.ORCID https://orcid.org/0000-0003-4102-4714
Jacob A EastmanInstitute for Human Neuroscience, Boys Town National Research Hospital, Omaha, NE 68010, USA.
Nicholas J Christopher-HayesInstitute for Human Neuroscience, Boys Town National Research Hospital, Omaha, NE 68010, USA.
Sara L WolfsonCollege of Medicine, University of Nebraska Medical Center, Omaha, NE 68198, USA.ORCID https://orcid.org/0000-0001-9990-4728
Craig M JohnsonCollege of Medicine, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Daniel L MurmanCollege of Medicine, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Tony W WilsonInstitute for Human Neuroscience, Boys Town National Research Hospital, Omaha, NE 68010, USA.ORCID https://orcid.org/0000-0002-5053-8306
Boys Town · USUniversity of Nebraska Medical Center · USCreighton University · USMontreal Neurological Institute and Hospital · CA

Funding

Stress-Induced Aberrations in the Mitochondrial Redox Environment Impact Developing Neural Circuits Supporting Cognitive ControlP20GM144641 · NIGMS · FATHER FLANAGAN'S BOYS' HOME · PI Giorgia Picci · 2022 to 2026
$15.1M
MULTIMODAL IMAGING OF NEUROHIV DYNAMICS (MIND): AN OMAHA-PITTSBURGH CONSORTIUMR01MH118013 · NIMH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI WILSON, TONY W · 2018 to 2022
$4.9M
THE PROGRESSIVE ELEVATION OF SPONTANEOUS CORTICAL ACTIVITY IN HAND (PESCAH) PROJECTR01MH116782 · NIMH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI WILSON, TONY W · 2018 to 2022
$3.4M
THE IMPACT OF SPONTANEOUS CORTICAL ACTIVITY ON NEURAL OSCILLATIONS AND BEHAVIORAL PERFORMANCE: EVIDENCE FROM HIGH-DEFINITION TDCS AND MEGRF1MH117032 · NIMH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI WILSON, TONY W · 2018 to 2018
$2.4M
Aberrant cortical entrainment in biomarker-confirmed Alzheimer's disease and mild cognitive impairmentF30AG076259 · NIA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Seth D Springer · 2022 to 2026
$208k
Characterizing the interaction between neural attention and somato-motor systems in non-demented patients with Parkinson's diseaseF32NS119375 · NINDS · MCGILL UNIVERSITY · PI WIESMAN, ALEX I · 2020 to 2023
$205k
Oscillatory markers of cognitive deficits in patients with Alzheimer's diseaseF31AG055332 · NIA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI WIESMAN, ALEX I · 2017 to 2019
$119k
NIA NIH HHS F30 AG076259NIA NIH HHS F31 AG055332NIGMS NIH HHS P20 GM144641NIMH NIH HHS R01 MH116782NIMH NIH HHS R01 MH118013NIMH NIH HHS RF1 MH117032NINDS NIH HHS F32 NS119375
6 · The paper itself

Abstract

Recent research has indicated that rhythmic visual entrainment may be useful in clearing pathological protein deposits in the central nervous system of mouse models of Alzheimer's disease. However, visual entrainment studies in human patients with Alzheimer's disease are rare, and as such the degree to which these patients exhibit aberrations in the neural tracking of rhythmic visual stimuli is unknown. To fill this gap, we recorded magnetoencephalography during a 15 Hz visual entrainment paradigm in amyloid-positive patients on the Alzheimer's disease spectrum and compared their neural responses to a demographically matched group of biomarker-negative healthy controls. Magnetoencephalography data were imaged using a beamformer and virtual sensor data were extracted from the peak visual entrainment responses. Our results indicated that, relative to healthy controls, participants on the Alzheimer's disease spectrum exhibited significantly stronger 15 Hz entrainment in primary visual cortices relative to a pre-stimulus baseline period. However, the two groups exhibited comparable absolute levels of neural entrainment, and higher absolute levels of entertainment predicted greater Mini-mental Status Examination scores, such that those patients whose absolute entrainment amplitude was closer to the level seen in controls had better cognitive function. In addition, 15 Hz periodic activity, but not aperiodic activity, during the pre-stimulus baseline period was significantly decreased in patients on the Alzheimer's disease spectrum. This pattern of results indicates that patients on the Alzheimer's disease spectrum exhibited increased visual entrainment to rhythmic stimuli and that this increase is likely compensatory in nature. More broadly, these results show that visual entrainment is altered in patients with Alzheimer's disease and should be further examined in future studies, as changes in the capacity to entrain visual stimuli may prove useful as a marker of Alzheimer's disease progression.

Indexed as

Alzheimer’sdementiaentrainmentmagnetoencephalographyvision

Identifiers

PMID35974799
PMCPMC9374481
OpenAlexW4289261251

What OpenQuestion holds

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Registered trials

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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.