Evidence map›Paper›PMID 36641682›Full record

ArticleJournal of Alzheimer's disease : JAD2023

EEG Entropy in REM Sleep as a Physiologic Biomarker in Early Clinical Stages of Alzheimer's Disease.

Hamed Azami, Sebastian Moguilner, Hector Penagos, Rani A Sarkis, Steven E Arnold, Stephen N Gomperts, Alice D Lam

Open access · greenAbstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 27 citations in OpenAlex.

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  8. Is EEG Entropy a Useful Measure for Alzheimer's Disease?Actas espanolas de psiquiatria · 2024
    Review
  9. Sleep functional connectivity, hyperexcitability, and cognition in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Article
  10. Article
  11. Article
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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

7 authors at 3 institutions in 1 country.

Hamed AzamiMassachusetts Alzheimer's Disease Research Center, Department of Neurology, Massachusetts General Hospital, Charlestown, MA, USA.
Sebastian MoguilnerMassachusetts Alzheimer's Disease Research Center, Department of Neurology, Massachusetts General Hospital, Charlestown, MA, USA.
Hector PenagosPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, MA, USA.
Rani A SarkisDepartment of Neurology, Brigham and Women's Hospital, Boston, MA, USA.
Steven E ArnoldMassachusetts Alzheimer's Disease Research Center, Department of Neurology, Massachusetts General Hospital, Charlestown, MA, USA.
Stephen N GompertsMassachusetts Alzheimer's Disease Research Center, Department of Neurology, Massachusetts General Hospital, Charlestown, MA, USA.
Alice D LamMassachusetts Alzheimer's Disease Research Center, Department of Neurology, Massachusetts General Hospital, Charlestown, MA, USA.
Massachusetts General Hospital · USBrigham and Women's Hospital · USMassachusetts Institute of Technology · US

Funding

Research Education ComponentP30AG062421 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI STEVEN E ARNOLD · 2019 to 2026
$36.5M
Web-based Automated Imaging Differentiation of ParkinsonismU01NS119562 · NINDS · UNIVERSITY OF FLORIDA · PI BARMPOUTIS, ANGELOS, OKUN, MICHAEL S · 2021 to 2025
$4.8M
Neural Circuit Disruption in Freely-Behaving models of Alzheimer's Disease.R01AG077611 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI Stephen N. Gomperts · 2022 to 2026
$3.8M
Elucidating circuit disruptions in Alzheimer's diseaseR01AG066171 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI KASTANENKA, KSENIA V. · 2020 to 2024
$2.9M
Impact of Amyloid Beta on Hippocampal Neurophysiology and Calcium Activity across the Sleep-Wake CycleR01AG054551 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI GOMPERTS, STEPHEN N. · 2017 to 2021
$2.1M
The Contribution of Late Onset Unexplained Epilepsy to Cognitive Decline and its Interaction with Vascular and Alzheimer's Disease PathologiesK23NS119798 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI SARKIS, RANI · 2021 to 2025
$1.1M
Exploring the role of epileptiform activity in Alzheimer's DiseaseK23NS101037 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI LAM, ALICE D · 2018 to 2022
$1.0M
Imaging Epigenetic Mechanisms in the Lewy Body Dementias with [11C]MartinostatR56AG070827 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI GOMPERTS, STEPHEN N., WANG, CHANGNING · 2021 to 2021
$776k
HBI-002 to Treat Parkinson’s DiseaseR41NS122576 · NINDS · HILLHURST BIOPHARMACEUTICALS, INC. · PI GOMPERTS, EDWARD, GOMPERTS, STEPHEN N. · 2021 to 2022
$634k
Investigation of silent mesial temporal lobe hyperexcitability in Alzheimer's diseaseR21AG064413 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI LAM, ALICE D, MARSHALL, GAD ASHER · 2019 to 2020
$409k
NIA NIH HHS P30 AG062421NIA NIH HHS R01 AG054551NIA NIH HHS R01 AG066171NIA NIH HHS R01 AG077611NIA NIH HHS R21 AG064413NIA NIH HHS R56 AG070827NINDS NIH HHS K23 NS101037NINDS NIH HHS K23 NS119798NINDS NIH HHS R41 NS122576NINDS NIH HHS U01 NS119562
6 · The paper itself

Abstract

backgroundAlzheimer's disease (AD) is associated with EEG changes across the sleep-wake cycle. As the brain is a non-linear system, non-linear EEG features across behavioral states may provide an informative physiologic biomarker of AD. Multiscale fluctuation dispersion entropy (MFDE) provides a sensitive non-linear measure of EEG information content across a range of biologically relevant time-scales.

objectiveTo evaluate MFDE in awake and sleep EEGs as a potential biomarker for AD.

methodsWe analyzed overnight scalp EEGs from 35 cognitively normal healthy controls, 23 participants with mild cognitive impairment (MCI), and 19 participants with mild dementia due to AD. We examined measures of entropy in wake and sleep states, including a slow-to-fast-activity ratio of entropy (SFAR-entropy). We compared SFAR-entropy to linear EEG measures including a slow-to-fast-activity ratio of power spectral density (SFAR-PSD) and relative alpha power, as well as to cognitive function.

resultsSFAR-entropy differentiated dementia from MCI and controls. This effect was greatest in REM sleep, a state associated with high cholinergic activity. Differentiation was evident in the whole brain EEG and was most prominent in temporal and occipital regions. Five minutes of REM sleep was sufficient to distinguish dementia from MCI and controls. Higher SFAR-entropy during REM sleep was associated with worse performance on the Montreal Cognitive Assessment. Classifiers based on REM sleep SFAR-entropy distinguished dementia from MCI and controls with high accuracy, and outperformed classifiers based on SFAR-PSD and relative alpha power.

conclusionSFAR-entropy measured in REM sleep robustly discriminates dementia in AD from MCI and healthy controls.

Indexed as

Alzheimer DiseaseCognitive DysfunctionDementiaElectroencephalographyEntropyHumansSleep, REMAlzheimer’s diseaseEEGentropymild cognitive impairmentREM sleepsleep

Identifiers

PMID36641682
PMCPMC10039707
OpenAlexW4316036058

What OpenQuestion holds

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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 OpenQuestion graph.