Evidence map›Paper›PMID 42003135›Full record

ArticleJournal of neurophysiology2026

A motor thalamic site in humans that suppresses involuntary breathing without awareness.

Sukhbinder Kumar, Ariane E Rhone, Christopher K Kovach, Md Rakibul Mowla, Aubrey C Chan, Christopher M Garcia, Hiroto Kawasaki, Rashmi N Mueller, Justin D Kuhn, Ryan T Frede and 13 more

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

23 authors.

Sukhbinder KumarDepartment of Neurosurgery, University of Iowa, Iowa City, Iowa, United States.
Ariane E RhoneDepartment of Neurosurgery, University of Iowa, Iowa City, Iowa, United States.ORCID 0000-0002-5699-8733
Christopher K KovachDepartment of Neurosurgery, University of Iowa, Iowa City, Iowa, United States.
Md Rakibul MowlaDepartment of Neurosurgery, University of Iowa, Iowa City, Iowa, United States.ORCID 0000-0001-5765-8856
Aubrey C ChanDepartment of Psychiatry, University of Iowa, Iowa City, Iowa, United States.
Christopher M GarciaDepartment of Neurosurgery, University of Iowa, Iowa City, Iowa, United States.
Hiroto KawasakiDepartment of Neurosurgery, University of Iowa, Iowa City, Iowa, United States.ORCID 0000-0002-7688-9171
Rashmi N MuellerDepartment of Neurosurgery, University of Iowa, Iowa City, Iowa, United States.ORCID 0000-0003-2037-3675
Justin D KuhnDepartment of Respiratory Care, University of Iowa, Iowa City, Iowa, United States.
Ryan T FredeDepartment of Respiratory Care, University of Iowa, Iowa City, Iowa, United States.ORCID 0009-0003-1140-0405
Michael A CilibertoDepartment of Pediatrics, University of Iowa, Iowa City, Iowa, United States.ORCID 0000-0001-8188-7261
Theresa M CzechDepartment of Pediatrics, University of Iowa, Iowa City, Iowa, United States.
Sreenath Thati GangannaDepartment of Pediatrics, University of Iowa, Iowa City, Iowa, United States.
James W M OwensDepartment of Pediatrics, University of Iowa, Iowa City, Iowa, United States.
Ania K DabrowskiDepartment of Pediatrics, University of Iowa, Iowa City, Iowa, United States.
Brittany N SpriggDepartment of Pediatrics, University of Iowa, Iowa City, Iowa, United States.
Matthew A HowardDepartment of Neurosurgery, University of Iowa, Iowa City, Iowa, United States.
Kai HwangIowa Neuroscience Institute, University of Iowa, Iowa City, Iowa, United States.
José L HerreroDepartment of Neurology, Zucker School of Medicine at Hofstra Northwell, Hempstead, New York, United States.ORCID 0000-0001-5969-9678
Kyle T S PattinsonWellcome Centre for Integrative Neuroimaging and Nuffield Division of Anaesthetics, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
George B RichersonDepartment of Neurology, University of Iowa, Iowa City, Iowa, United States.ORCID 0000-0001-5696-1554
John A WemmieDepartment of Psychiatry, University of Iowa, Iowa City, Iowa, United States.
Brian J DlouhyDepartment of Neurosurgery, University of Iowa, Iowa City, Iowa, United States.

Funding

HUMAN AUDITORY CORTEX PHYSIOLOGYR01DC004290 · NIDCD · UNIVERSITY OF IOWA · PI HOWARD, MATTHEW A. · 2000 to 2025
$13.7M
Amygdala modulation of volitional versus automatic breathingK08NS112573 · NINDS · UNIVERSITY OF IOWA · PI DLOUHY, BRIAN J · 2021 to 2025
$925k
HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) K08NS112573HHS | NIH | National Institute on Deafness and Other Communication Disorders (NIDCD) R01DC004290NIDCD NIH HHS R01 DC004290NINDS NIH HHS K08 NS112573VA | Iowa City Veterans Affairs Medical Center (Iowa City VAMC) 5IK2BX006118
6 · The paper itself

Abstract

Breathing is generated by brainstem respiratory networks but can be controlled and modulated by forebrain activity. The recent clinical adoption of thalamic electrode implantation during intracranial electroencephalography (iEEG) provides a rare opportunity to examine the role of the human thalamus in respiratory control. Here, we tested whether thalamic stimulation alters breathing in 11 patients undergoing iEEG for epilepsy monitoring. Across 412 stimulation trials at 108 thalamic sites, thalamic stimulation induced central apnea in every participant. Apnea occurred in isolation without sensory or motor effects and without awareness of breathing cessation. Apnea occurred with stimulation of either the right or left thalamus and was observed across all ages, including participants as young as 22 mo. Volitional breathing and speech were preserved, indicating that respiratory motor pathways remained functional. In contrast, except for the amygdala, stimulation of other forebrain regions, including the hippocampus, insula, cingulate, and frontal, temporal, and parietal cortices, did not affect breathing. Respiratory inhibition depended on thalamic location, occurring most consistently with stimulation of the ventral lateral anterior (VLa) and ventral anterior (VA) nuclei. A machine learning algorithm localized the focal apneic region within the anterior motor thalamus, centered in VLa and extending into VA. Identification of a focal apneic site in the VLa/VA motor thalamus expands thalamic function, revealing a forebrain node capable of overriding brainstem respiratory control. This circuit may coordinate breathing with volitional behaviors such as speech, and dysfunction of this circuit may play a role in central apnea disorders, including sleep apnea, SUDEP, and SIDS.

Indexed as

ApneaAwarenessDeep Brain StimulationRespirationThalamusAdolescentAdultChildChild, PreschoolElectrocorticographyFemaleHumansInfantMaleMiddle AgedYoung Adultapneabreathingintracranial electrical stimulationrespiratory controlthalamus

Identifiers

PMID42003135
PMCPMC13237736

What Socratic holds

Textmetadata
LicenceTDM
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.