Evidence map›Paper›PMID 39822587›Full record

ArticleNeurophotonics2025

Seizure network characterization by functional connectivity mapping and manipulation.

James E Niemeyer, Peijuan Luo, Carmen Pons, Shiqiang Wu, Hongtao Ma, Jyun-You Liou, Daniel Surinach, Suhasa B Kodandaramaiah, Theodore H Schwartz

Abstract read
In one paragraph

Article in Neurophotonics, 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. 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

9 authors.

James E NiemeyerWeill Cornell Medicine, Department of Neurological Surgery, New York, United States.ORCID https://orcid.org/0000-0002-5864-7777
Peijuan LuoThe First Hospital of Jilin University, Department of Neurology, Changchun, China.ORCID https://orcid.org/0009-0003-0007-1909
Carmen PonsWeill Cornell Medicine, Department of Neurological Surgery, New York, United States.
Shiqiang WuWeill Cornell Medicine, Department of Neurological Surgery, New York, United States.ORCID https://orcid.org/0000-0002-3181-3894
Hongtao MaWeill Cornell Medicine, Department of Neurological Surgery, New York, United States.
Jyun-You LiouWeill Cornell Medicine, Department of Anesthesiology, New York, United States.ORCID https://orcid.org/0000-0003-4851-3676
Daniel SurinachUniversity of Minnesota, Department of Mechanical Engineering, Minneapolis, Minnesota, United States.
Suhasa B KodandaramaiahUniversity of Minnesota, Department of Mechanical Engineering, Minneapolis, Minnesota, United States.
Theodore H SchwartzWeill Cornell Medicine, Department of Neurological Surgery, New York, United States.

Funding

Viral Innovation CoreP30DA048742 · NIDA · UNIVERSITY OF MINNESOTA · PI Mark John Thomas · 2020 to 2026
$19.0M
NIDA NIH HHS P30 DA048742
6 · The paper itself

Abstract

Significance: Despite the availability of various anti-seizure medications, nearly 1/3 of epilepsy patients experience drug-resistant seizures. These patients are left with invasive surgical options that do not guarantee seizure remission. The development of novel treatment options depends on elucidating the complex biology of seizures and brain networks. Aim: We aimed to develop an experimental paradigm that uses anatomical network information, functional connectivity, and Approach: Guided by a known anatomical network, we applied widefield calcium imaging to determine how neural activity and seizures spread through the network regions, focusing on the primary somatosensory cortex and secondary motor cortex. We used Results: The microstimulation of the somatosensory cortex propagated in a distinct pattern throughout the bilateral network with sequential reproducible node recruitment. Seizures recapitulated this same pattern, indicating a hijacking of existing pathways. Ablation of a key node in the network in the secondary motor cortex changed contralateral spread. Early chronic cobalt seizure data are presented. Conclusion: Here, we demonstrate a paradigm for combining widefield calcium imaging with microstimulation, cortical ablation, and seizure mapping to determine how anatomical networks inform the propagation patterns of cortical seizures. These experiments can be extended to long-term tracking of epilepsy to study epileptogenesis in other cortical networks. Our proof-of-concept findings suggest that this paradigm may be useful in the development of novel therapies for drug-resistant epilepsy patients and can be extended to the study of other disorders involving brain networks.

Indexed as

bilateral seizure propagationepilepsy networkextra-focal targetingmesoscale imagingseizure models

Identifiers

PMID39822587
PMCPMC11737237

What OpenQuestion holds

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Registered trials

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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.