Evidence map›Paper›PMID 37658249›Full record

ArticleMolecular neurobiology2024

Clinical Correlation of Altered Molecular Signatures in Epileptic Human Hippocampus and Amygdala.

Sayed Mostafa Modarres Mousavi, Fatemeh Alipour, Farshid Noorbakhsh, Maryam Jafarian, Masoud Ghadipasha, Jaber Gharehdaghi, Christoph Kellinghaus, Erwin-Josef Speckmann, Walter Stummer, Maryam Khaleghi Ghadiri and 1 more

Abstract read
In one paragraph

Article in Molecular neurobiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Sayed Mostafa Modarres Mousavi *Shefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran.
Fatemeh Alipour *Shefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran.
Farshid NoorbakhshShefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran.
Maryam JafarianShefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran.
Masoud GhadipashaLegal Medicine Research Center, Legal Medicine Organization, Tehran, Iran.
Jaber GharehdaghiLegal Medicine Research Center, Legal Medicine Organization, Tehran, Iran.
Christoph KellinghausDepartment of Neurology, Klinikum Osnabrück, Osnabrück, Germany.
Erwin-Josef SpeckmannDepartment of Neurosurgery, Westfälische Wilhelms-Universität Münster, Münster, Germany.
Walter StummerDepartment of Neurosurgery, Westfälische Wilhelms-Universität Münster, Münster, Germany.
Maryam Khaleghi GhadiriDepartment of Neurosurgery, Westfälische Wilhelms-Universität Münster, Münster, Germany.
Ali GorjiShefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran. gorjial@uni-muenster.de.ORCID http://orcid.org/0000-0002-4557-3270

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Widespread alterations in the expression of various genes could contribute to the pathogenesis of epilepsy. The expression levels of various genes, including major inhibitory and excitatory receptors, ion channels, cell type-specific markers, and excitatory amino acid transporters, were assessed and compared between the human epileptic hippocampus and amygdala, and findings from autopsy controls. Moreover, the potential correlation between molecular alterations in epileptic brain tissues and the clinical characteristics of patients undergoing epilepsy surgery was evaluated. Our findings revealed significant and complex changes in the expression of several key regulatory genes in both the hippocampus and amygdala of patients with intractable epilepsy. The expression changes in various genes differed considerably between the epileptic hippocampus and amygdala. Different correlation patterns were observed between changes in gene expression and clinical characteristics, depending on whether the patients were considered as a whole or were subdivided. Altered molecular signatures in different groups of epileptic patients, defined within a given category, could be viewed as diagnostic biomarkers. Distinct patterns of molecular changes that distinguish these groups from each other appear to be associated with epilepsy-specific functional consequences.

Indexed as

EpilepsyAmygdalaHippocampusHumansIon ChannelsIon ChannelsBrainEpileptogenesisIntractable epilepsyIon channelsReceptors

Identifiers

PMID37658249
PMCPMC10861640

What Socratic 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 Socratic graph.