Evidence map›Paper›PMID 40674420›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Robust single-trial decoding of physical self-motion from hemodynamic signals in the brain measured by functional ultrasound imaging.

Bingyu Liu, Qingyang Luo, Zhifeng Liang, Hua He, Yong Gu

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 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. Review
  2. A hemispheric decoding principle for vestibular heading perception in the posterior sylvian area.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
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

5 authors.

Bingyu Liu *Chinese Academy of Sciences, Center for Excellence in Brain Science and Intelligence Technology, Key Laboratory of Brain Cognition and Brain-Inspired Intelligence Technology, Institute of Neuroscience, International Center for Primate Brain Research, Chinese Academy of Sciences, Shanghai 200031, China.ORCID 0000-0003-3101-2138
Qingyang Luo *Chinese Academy of Sciences, Center for Excellence in Brain Science and Intelligence Technology, Key Laboratory of Brain Cognition and Brain-Inspired Intelligence Technology, Institute of Neuroscience, International Center for Primate Brain Research, Chinese Academy of Sciences, Shanghai 200031, China.ORCID 0009-0008-9450-714X
Zhifeng LiangChinese Academy of Sciences, Center for Excellence in Brain Science and Intelligence Technology, Key Laboratory of Brain Cognition and Brain-Inspired Intelligence Technology, Institute of Neuroscience, International Center for Primate Brain Research, Chinese Academy of Sciences, Shanghai 200031, China.
Hua HeDepartment of Neurosurgery, Shanghai Eastern Hepatobiliary Surgery Hospital, Shanghai 200438, China.ORCID 0009-0006-9111-9059
Yong GuChinese Academy of Sciences, Center for Excellence in Brain Science and Intelligence Technology, Key Laboratory of Brain Cognition and Brain-Inspired Intelligence Technology, Institute of Neuroscience, International Center for Primate Brain Research, Chinese Academy of Sciences, Shanghai 200031, China.ORCID 0000-0003-4437-8956

Funding

National Science and Technology Major Project () 2022ZD0205000STCSM | Natural Science Foundation of Shanghai Municipality () 2021SHZDZX
6 · The paper itself

Abstract

Physical self-motion frequently happens in daily life, during which our vestibular system is critical in various important functions including balance and visual stability maintenance, postural and motor control, locomotion, spatial perception, and path integration-based navigation. Conventional noninvasive methods for studying vestibular functions include functional MRI (fMRI) that conveniently measures brain-wide signals; however, subjects are required to be physically restricted in the scanner. In such cases, caloric or galvanic vestibular stimulation is applied to stimulate peripheral vestibular organs, suffering a loss of precise stimulation of peripheral vestibular organs as during physical motion conditions. In this study, we adopted functional ultrasound (fUS) imaging, a newly emerging minimally invasive technique with high spatiotemporal resolution, to measure vestibular related signals in primates under passive, physical self-motion conditions that selectively activate vestibular organs. We found that robust fUS signals were evoked in brain-wide regions. While many areas overlapped with those previously reported by fMRI or electrophysiology, significant activations were also seen in areas that were not clearly identified previously including area 5, 1-2, M1, V3A, and 7 m. Importantly, using a linear discriminant analysis algorithm, physical self-motion information, including both translation directions, and translation-vs.-rotation, could be reliably decoded from fUS signals on a single-trial basis. In addition to vestibular-related activity, many areas also exhibited visual-motion response, indicating possible multisensory interactions. Our findings suggest that fUS imaging holds a promising tool for studying vestibular functions in tasks under physical self-motion conditions, as well as interactions with visual or motor systems.

Indexed as

BrainHemodynamicsAnimalsBrain MappingFemaleMacaca mulattaMagnetic Resonance ImagingMaleMotionUltrasonographyVestibule, Labyrinthfunctional ultrasound imagingmacaqueself-motionsensoryvestibular

Identifiers

PMID40674420
PMCPMC12305011

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.