Evidence map›Paper›PMID 35228583›Full record

ArticleScientific reports2022

Functional network connectivity imprint in febrile seizures.

Ullas V Acharya, Karthik Kulanthaivelu, Rajanikant Panda, Jitender Saini, Arun K Gupta, Bindu Parayil Sankaran, Kenchaiah Raghavendra, Ravindranath Chowdary Mundlamuri, Sanjib Sinha, M L Keshavamurthy and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 16% of its field
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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  4. Febrile temperature-regulated TRPV1 in CD4Journal of neuroinflammation · 2025
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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

11 authors at 2 institutions in 2 countries.

Ullas V Acharya *Department of Neuroimaging and Interventional Radiology, National Institute of Mental Health and Neurosciences, Bengaluru, 560029, Karnataka, India.
Karthik Kulanthaivelu *Department of Neuroimaging and Interventional Radiology, National Institute of Mental Health and Neurosciences, Bengaluru, 560029, Karnataka, India.
Rajanikant Panda *Department of Neuroimaging and Interventional Radiology, National Institute of Mental Health and Neurosciences, Bengaluru, 560029, Karnataka, India.
Jitender SainiDepartment of Neuroimaging and Interventional Radiology, National Institute of Mental Health and Neurosciences, Bengaluru, 560029, Karnataka, India.
Arun K GuptaDepartment of Neuroimaging and Interventional Radiology, National Institute of Mental Health and Neurosciences, Bengaluru, 560029, Karnataka, India.
Bindu Parayil SankaranDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, 560029, Karnataka, India.
Kenchaiah RaghavendraDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, 560029, Karnataka, India.
Ravindranath Chowdary MundlamuriDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, 560029, Karnataka, India.
Sanjib SinhaDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, 560029, Karnataka, India.
M L KeshavamurthyDepartment of Paediatric Medicine, Indira Gandhi Institute of Child Health, Bengaluru, 560029, Karnataka, India.
Rose Dawn BharathDepartment of Neuroimaging and Interventional Radiology, National Institute of Mental Health and Neurosciences, Bengaluru, 560029, Karnataka, India. drrosedawnbharath@gmail.com.
National Institute of Mental Health and Neurosciences · INIndira Gandhi Institute of Child Health · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complex febrile seizures (CFS), a subset of paediatric febrile seizures (FS), have been studied for their prognosis, epileptogenic potential and neurocognitive outcome. We evaluated their functional connectivity differences with simple febrile seizures (SFS) in children with recent-onset FS. Resting-state fMRI (rs-fMRI) datasets of 24 children with recently diagnosed FS (SFS-n = 11; CFS-n = 13) were analysed. Functional connectivity (FC) was estimated using time series correlation of seed region-to-whole-brain-voxels and network topology was assessed using graph theory measures. Regional connectivity differences were correlated with clinical characteristics (FDR corrected p < 0.05). CFS patients demonstrated increased FC of the bilateral middle temporal pole (MTP), and bilateral thalami when compared to SFS. Network topology study revealed increased clustering coefficient and decreased participation coefficient in basal ganglia and thalamus suggesting an inefficient-unbalanced network topology in patients with CFS. The number of seizure recurrences negatively correlated with the integration of Left Thalamus (r = - 0.58) and FC of Left MTP to 'Right Supplementary Motor and left Precentral' gyrus (r = - 0.53). The FC of Right MTP to Left Amygdala, Putamen, Parahippocampal, and Orbital Frontal Cortex (r = 0.61) and FC of Left Thalamus to left Putamen, Pallidum, Caudate, Thalamus Hippocampus and Insula (r 0.55) showed a positive correlation to the duration of the longest seizure. The findings of the current study report altered connectivity in children with CFS proportional to the seizure recurrence and duration. Regardless of the causal/consequential nature, such observations demonstrate the imprint of these disease-defining variables of febrile seizures on the developing brain.

Indexed as

BrainBrain MappingChildHumansMagnetic Resonance ImagingSeizures, Febrile

Identifiers

PMID35228583
PMCPMC8885759
OpenAlexW4221068581

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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.