Evidence map›Paper›PMID 42321332›Full record

ArticleScientific reports2026

Predictability of sleep slow oscillation emergence and spatial extent from pre-onset neural dynamics.

Mahmoud Alipour, Wim van Drongelen, Paola Malerba, Joel Voss, David Satzer

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In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Mahmoud AlipourDepartment of Neurological Surgery, University of Chicago, Chicago, USA. Mahmoud.Alipour@bsd.uchicago.edu.
Wim van DrongelenDepartment of Pediatrics, The University of Chicago, Chicago, USA.
Paola MalerbaCenter for Biobehavioral Health, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, USA.
Joel VossDepartment of Neurology, The University of Chicago, Chicago, USA.
David SatzerDepartment of Neurological Surgery, University of Chicago, Chicago, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Slow oscillations (SOs; ~ 0.5-1.5 Hz) are a hallmark of non-rapid eye movement sleep and are known to support memory consolidation. Although their dynamics are well characterized, processes that precede SO initiation and predict their spatial extent remain largely unknown, despite their potential utility for closed-loop intervention. Using high-density EEG from 29 healthy adults, we examined neural activity in the 2-s interval preceding the SO trough. SOs were classified into Global and Frontal subtypes, which differ in propagation. We quantified instantaneous spectral power, time-frequency dynamics, and cross-frequency coupling including phase-amplitude coupling (PAC). Theta-band power (4-8 Hz) emerged as the strongest individual predictor of SO initiation, although delta-band activity provided complementary predictive information. Spectral parameterization indicated that this pre-onset theta-band elevation primarily reflects broadband shifts in the aperiodic background rather than a modulation of a discrete oscillatory component. Theta-band power exhibited a sustained rise beginning ~ 1.6 s before onset and differentiated SO subtypes with moderate-to-strong effect sizes (Cohen's d = 0.45-0.77). Mechanistically, Global SOs were preceded by enhanced delta-theta PAC and broad low-frequency synchronization, whereas Frontal SOs showed elevated theta/alpha-to-beta/low-gamma coupling, reflecting locally enhanced coupling that restricts propagation. A logistic regression classifier using pre-onset theta power achieved > 95% accuracy distinguishing SOs from surrogate events and ~ 83% accuracy differentiating SO subtypes. These findings demonstrate that pre-onset low-frequency spectral dynamics, particularly theta-band power, can predict SO occurrence and might be leveraged in neuromodulation.

Indexed as

BrainSleepSleep, Slow-WaveAdultElectroencephalographyFemaleHumansMaleTheta RhythmYoung AdultClosed-loop neuromodulationPredictive modelingSleep slow oscillationsSpatiotemporal dynamicsTheta activity

Identifiers

PMID42321332
PMCPMC13550440

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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.