作为癫痫潜在生物标记物的脑脊液代谢物:全基因组关联研究的启示

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY Epilepsia Open Pub Date : 2024-11-18 DOI:10.1002/epi4.13101
Zhenxiang Zhao, Na Xing, Lin Hou
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引用次数: 0

摘要

目的:虽然已观察到癫痫患者体内存在代谢失衡,但对特定代谢物直接参与癫痫发病的研究仍然不足。全面分析脑脊液代谢物(CSF)与癫痫之间的因果关系,对于发现创新性治疗干预措施和预防方法至关重要:方法: 我们分别从脑脊液代谢物和癫痫亚型的全基因组关联研究(GWAS)中获得了汇总数据。共调查了 338 种 CSF 代谢物作为暴露,11 种癫痫表型作为结果。采用双样本孟德尔随机化(MR)方法探讨了这些代谢物对癫痫的因果影响。因果关系主要通过反方差加权(IVW)分析进行估计,并辅以一系列敏感性分析以确保结果的稳定性。此外,还进行了反向 MR 分析,以探讨双向因果关系的可能性:结果:通过敏感性分析,IVW 方法确定了 17 种 CSF 代谢物与六种癫痫表型的因果关系。经过假发现率(FDR)多重检验校正后,发现两个代谢物(甲基丙二酸盐和γ-谷氨酰-α-赖氨酸)与癫痫有很强的因果关系(P 0.05):这项研究强调了脑脊液代谢物可作为有价值的生物标志物,可能对开发有针对性的治疗方法和预防癫痫病至关重要。白话摘要:这项研究探讨了脑液中的某些化学物质如何影响癫痫病的发展,旨在找到治疗或预防癫痫病的新方法。研究人员利用基因数据研究了338种脑脊液代谢物与11种癫痫之间的关系。他们发现,其中 17 种化学物质有可能导致六种类型的癫痫。其中两种化学物质与癫痫密切相关,这表明它们可能对制定特定的治疗或预防策略非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Cerebrospinal fluid metabolites as potential biomarkers for epilepsy: Insights from genome-wide association studies

Objectives

While metabolic imbalances have been observed in individuals with epilepsy, the direct involvement of specific metabolites in the development of the condition remains underexplored. A comprehensive analysis of the causality between cerebrospinal fluid metabolites (CSF) and epilepsy is pivotal in discovering innovative therapeutic interventions and prophylactic approaches.

Methods

Summary data from genome-wide association studies (GWAS) of CSF metabolites and epilepsy subtypes were obtained separately. A total of 338 CSF metabolites were investigated as exposures, and 11 epilepsy phenotypes were examined as the outcomes. A two sample Mendelian randomization (MR) approach was utilized to explore the causal influence of these metabolites on epilepsy. Causality was primarily estimated through inverse variance weighted (IVW) analysis, complemented by a range of sensitivity analyses to ensure result stability. Additionally, reverse MR analysis was performed to explore the possibility of bidirectional causality.

Results

The IVW method, reinforced by sensitivity analyses, pinpointed 17 CSF metabolites with causal implications for six epilepsy phenotypes. After False Discovery Rate (FDR) multiple testing correction, two metabolites (Methylmalonate and Gamma-glutamyl-alpha-lysine) were found to have robust causal links to epilepsy (p < 0.05 and FDR<0.05). The other 15 metabolites exhibited suggestive evidence of a causal association (p < 0.05 and FDR>0.05).

Significance

This study highlights CSF metabolites that could serve as valuable biomarkers and may be critical in developing targeted treatments and preventing epilepsy.

Plain Language Summary

This study explores how certain chemicals in the brain fluid might influence the development of epilepsy, aiming to find new ways to treat or prevent it. Researchers looked at the relationship between 338 cerebrospinal fluid metabolites and 11 types of epilepsy using genetic data. They found that 17 of these chemicals could potentially cause six types of epilepsy. Two of these chemicals were strongly linked to epilepsy, suggesting they could be important for creating specific treatments or prevention strategies.

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来源期刊
Epilepsia Open
Epilepsia Open Medicine-Neurology (clinical)
CiteScore
4.40
自引率
6.70%
发文量
104
审稿时长
8 weeks
期刊最新文献
Efficacy and tolerability of low versus standard daily doses of antiseizure medications in newly diagnosed focal epilepsy. A multicenter, randomized, single-blind, non-inferiority trial (STANDLOW). Three cases of atypical Rasmussen's encephalitis with delayed-onset seizures. GATAD2B-related developmental and epileptic encephalopathy (DEE): Extending the epilepsy phenotype and a literature appraisal. Intrinsic brain network stability during kainic acid-induced epileptogenesis. Diagnostic yield of utilizing 24-72-hour video electroencephalographic monitoring in the diagnosis of seizures presenting as paroxysmal events in resource-limited settings.
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