Evidence mapPaperPMID 41810643Full record

ArticleBrazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas2026

Exploring the causal impact of mitochondrial dysfunction on epilepsy: a mendelian randomization study.

Lin-Ming Zhang, Fei Wang, Bing-Ran Zhang, Qiu-Juan Zhang, Yan-Lin Zhu, Shu-Ji Gao, Hao Wang, Ming-Wei Liu

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In one paragraph

Article in Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing 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

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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

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No citing paper in PubMed yet.

4 · The record

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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

8 authors.

Lin-Ming ZhangDepartment of Neurology, The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.ORCID http://orcid.org/0000-0001-8373-9131
Fei WangDepartment of Neurosurgery, The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.ORCID http://orcid.org/0000-0002-2315-1042
Bing-Ran ZhangDepartment of Emergency, The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.ORCID http://orcid.org/0009-0009-8579-8464
Qiu-Juan ZhangDepartment of Emergency, The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.ORCID http://orcid.org/0009-0007-6307-8576
Yan-Lin ZhuDepartment of Emergency, The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.ORCID http://orcid.org/0009-0007-9695-7008
Shu-Ji GaoDepartment of Emergency, The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.ORCID http://orcid.org/0009-0006-3867-0407
Hao WangDepartment of Nuclear Medicine, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.ORCID http://orcid.org/0000-0001-7698-5094
Ming-Wei LiuDepartment of Emergency, Dali Bai Autonomous Prefecture People's Hospital, Dali, Yunnan, China.ORCID http://orcid.org/0000-0002-3728-2350

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial dysfunction contributes critically to epileptogenesis. Therefore, identifying key mitochondrial function-associated genes in epilepsy may provide novel insights into its pathogenesis. We employed expression quantitative trait loci (eQTLs) and Mendelian randomization analyses to assess mitochondrial-epilepsy causality, with leave-one-out validation confirming the reliability and directionality of the results. The results revealed that hydroxyacylglutathione hydrolase (HAGH), oxysterol-binding protein-related protein 1A (OSBPL1A) and pantothenate kinase 2 (PANK2) were pivotal epileptogenic genes. HAGH modulates the mechanistic target of rapamycin complex 1 (mTORC1) signaling and fatty acid metabolism pathways. OSBPL1A mediates apoptotic and reactive oxygen species (ROS) pathways. PANK2 regulates phosphatidylinositol 3-kinase (PI3K)/protein kinase B (AKT)/mammalian target of rapamycin (mTOR) signaling and Notch signaling cascades. Additionally, these genes participate in inflammatory pathways, including T cell receptor (TCR), mitogen-activated protein kinase (MAPK), and tumor necrosis factor (TNF) signaling. We demonstrated that HAGH, OSBPL1A, and PANK2 constitute core pathogenic mechanisms in epilepsy. These genes potentially govern epileptogenesis through mitochondrial regulation via neuroinflammatory, immunomodulatory, and apoptotic pathways. Our findings provide a foundation for investigating epileptogenesis, discovering therapeutic targets, and identifying prognostic biomarkers.

Indexed as

EpilepsyMendelian Randomization AnalysisMitochondriaHumansQuantitative Trait LociSignal Transduction

Identifiers

PMID41810643
PMCPMC12971012

What Socratic holds

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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 Socratic graph.