Evidence map›Paper›PMID 38048613›Full record

ArticleBrain : a journal of neurology2024

Integrating direct electrical brain stimulation with the human connectome.

Ludovico Coletta, Paolo Avesani, Luca Zigiotto, Martina Venturini, Luciano Annicchiarico, Laura Vavassori, Sam Ng, Hugues Duffau, Silvio Sarubbo

Abstract read
In one paragraph

Article in Brain : a journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–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

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  5. Review
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  7. Article
  8. Article
  9. Visualization of functional and effective connectivity underlying auditory descriptive naming.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2025
    Article
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  16. Graphs and the idiographic brain.Brain : a journal of neurology · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Ludovico ColettaNeuroinformatics Laboratory (NiLab), Bruno Kessler Foundation (FBK), Trento 38123, Italy.
Paolo AvesaniNeuroinformatics Laboratory (NiLab), Bruno Kessler Foundation (FBK), Trento 38123, Italy.ORCID 0000-0001-8943-8911
Luca ZigiottoDepartment of Neurosurgery, S. Chiara Hospital, Trento 38122, Italy.
Martina VenturiniDepartment of Biotechnology and Life Sciences, Division of Neurosurgery, University of Insubria, Ospedale di Circolo e Fondazione Macchi, Varese 21100, Italy.
Luciano AnnicchiaricoDepartment of Neurosurgery, S. Chiara Hospital, Trento 38122, Italy.
Laura VavassoriCenter for Mind/Brain Sciences - CIMeC, University of Trento, Rovereto 38068, Italy.
Sam NgInstitute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier 34094, France.
Hugues DuffauInstitute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier 34094, France.ORCID 0000-0002-6558-2342
Silvio SarubboDepartment of Neurosurgery, S. Chiara Hospital, Trento 38122, Italy.

Funding

Future AI Research PE00000013NextGenerationEUPAT 764/2021PNRR
6 · The paper itself

Abstract

Neurological and neurodevelopmental conditions are a major public health concern for which new therapies are urgently needed. The development of effective therapies relies on the precise mapping of the neural substrates causally involved in behaviour generation. Direct electrical stimulation (DES) performed during cognitive and neurological monitoring in awake surgery is currently considered the gold standard for the causal mapping of brain functions. However, DES is limited by the focal nature of the stimulation sites, hampering a real holistic exploration of human brain functions at the network level. We used 4137 DES points derived from 612 glioma patients in combination with human connectome data-resting-state functional MRI, n = 1000 and diffusion weighted imaging, n = 284-to provide a multimodal description of the causal macroscale functional networks subtending 12 distinct behavioural domains. To probe the validity of our procedure, we (i) compared the network topographies of healthy and clinical populations; (ii) tested the predictive capacity of DES-derived networks; (iii) quantified the coupling between structural and functional connectivity; and (iv) built a multivariate model able to quantify single subject deviations from a normative population. Lastly, we probed the translational potential of DES-derived functional networks by testing their specificity and sensitivity in identifying critical neuromodulation targets and neural substrates associated with postoperative language deficits. The combination of DES and human connectome data resulted in an average 29.4-fold increase in whole brain coverage compared to DES alone. DES-derived functional networks are predictive of future stimulation points (97.8% accuracy) and strongly supported by the anatomical connectivity of subcortical stimulations. We did not observe any significant topographical differences between the patients and the healthy population at both group and single subject level. Showcasing concrete clinical applications, we found that DES-derived functional networks overlap with effective neuromodulation targets across several functional domains, show a high degree of specificity when tested with the intracranial stimulation points of a different stimulation technique and can be used effectively to characterize postoperative behavioural deficits. The integration of DES with the human connectome fundamentally advances the quality of the functional mapping provided by DES or functional imaging alone. DES-derived functional networks can reliably predict future stimulation points, have a strong correspondence with the underlying white matter and can be used for patient specific functional mapping. Possible applications range from psychiatry and neurology to neuropsychology, neurosurgery and neurorehabilitation.

Indexed as

Brain NeoplasmsConnectomeDeep Brain StimulationBrainHumansWakefulnessintracranial stimulationlesion network mappingneuromodulation targetstranslational neuroscience

Identifiers

PMID38048613
PMCPMC10907080

What OpenQuestion holds

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LicenceCC BY
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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.