Evidence map›Paper›PMID 41100501›Full record

ArticlePLoS biology2025

Hemispherotomy leads to persistent sleep-like slow waves in the isolated cortex of awake humans.

Michele Angelo Colombo, Jacopo Favaro, Ezequiel Mikulan, Andrea Pigorini, Flavia Maria Zauli, Ivana Sartori, Piergiorgio d'Orio, Laura Castana, Irene Toldo, Stefano Sartori and 4 more

Abstract read
In one paragraph

Article in PLoS biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Structural MRI across lifespan reveals differential thalamic trajectories in Down syndrome.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  3. Review
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

14 authors.

Michele Angelo ColomboDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Jacopo FavaroDepartment of Women's and Children's Health, University of Padua, Padua, Italy.ORCID 0000-0002-4340-2398
Ezequiel MikulanDepartment of Health Sciences, University of Milan, Milan, Italy.
Andrea PigoriniDepartment of Biomedical, Surgical and Dental Sciences, Università degli Studi di Milano, Milan, Italy.
Flavia Maria ZauliDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Ivana SartoriASST GOM Niguarda, "Claudio Munari" Epilepsy Surgery Center, Milan, Italy.
Piergiorgio d'OrioASST GOM Niguarda, "Claudio Munari" Epilepsy Surgery Center, Milan, Italy.
Laura CastanaASST GOM Niguarda, "Claudio Munari" Epilepsy Surgery Center, Milan, Italy.
Irene ToldoDepartment of Women's and Children's Health, University of Padua, Padua, Italy.
Stefano SartoriDepartment of Women's and Children's Health, University of Padua, Padua, Italy.
Simone SarassoDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Tim BayneSchool of Philosophical, Historical and Indigenous Studies Monash University, Melbourne, Australia.
Anil K SethCanadian Institute for Advanced Research (CIFAR), Brain, Mind, and Consciousness Program, Toronto, Ontario, Canada.
Marcello MassiminiDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.

Funding

Canadian Institute for Advanced Research (Brain, Mind, and Consciousness ProgramEuropean Research CouncilMinistero dell’Istruzione, dell’Università e della Ricerca PNRR – EBRAINS-Italy
6 · The paper itself

Abstract

Hemispherotomy is a neurosurgical procedure for treating refractory epilepsy, which entails disconnecting a significant portion of the cortex, potentially encompassing an entire hemisphere, from its cortical and subcortical connections. While this intervention prevents the spread of seizures, it raises important questions. Given the complete isolation from sensory-motor pathways, it remains unclear whether the disconnected cortex retains any form of inaccessible awareness. More broadly, the activity patterns that large portions of the deafferented cortex can sustain in awake humans remain poorly understood. We address these questions by exploring for the first time the electroencephalographic (EEG) state of the isolated cortex during wakefulness before and after surgery in 10 pediatric patients, focusing on non-epileptic background activity. Post-surgery, the isolated cortex exhibited prominent slow oscillations (<2 Hz) and a steeper broad-band spectral decay, reflecting a redistribution of power toward lower frequencies. This broad-band EEG slowing resulted in a marked decrease of the spectral exponent, a validated consciousness marker, reaching values characteristic of deep anesthesia and the vegetative state. When compared with a reference pediatric sample across the sleep-wake cycle, the spectral exponent of the contralateral cortex aligned with wakefulness, whereas that of the isolated cortex was consistent with deep NREM sleep. The findings of prominent slow oscillations and broad-band slowing provisionally support inferences of absent or reduced awareness in the isolated cortex. Moreover, the persistence of unihemispheric sleep-like patterns years after surgery provides unique insights into the long-term electrophysiological effects of cortical disconnections in the human brain.

Indexed as

Cerebral CortexHemispherectomySleepSleep, Slow-WaveWakefulnessAdolescentChildChild, PreschoolDrug Resistant EpilepsyElectroencephalographyEpilepsyFemaleHumansMale

Identifiers

PMID41100501
PMCPMC12530565

What Socratic holds

Textmetadata
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 Socratic graph.