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氧化应激与癫痫之间的因果关系:两样本孟德尔随机化研究。

Causal link between oxidative stress and epilepsy: A two-sample Mendelian randomization study.

机构信息

Department of Neurology, West China Hospital, Sichuan University, Chengdu, China.

Pazhou Lab, Guangzhou, China.

出版信息

Brain Behav. 2024 Jun;14(6):e3549. doi: 10.1002/brb3.3549.

Abstract

BACKGROUND

Although a growing body of research has indicated a strong link between oxidative stress and epilepsy, the exact nature of their interaction remains elusive. To elucidate this intricate relationship, we conducted a bidirectional Mendelian randomization (MR) analysis employing two independent datasets.

METHODS

A two-sample MR analysis was performed using instrumental variables derived from genome-wide association study summary statistics of oxidative stress injury biomarkers (OSIB) and epilepsy. The OSIBs were selected from eight primary metabolic pathways associated with oxidative stress. Additionally, seven distinct epilepsy phenotypes were considered, which encompassed all epilepsy, generalized epilepsy, generalized tonic-clonic seizures, focal epilepsy, focal epilepsy with hippocampal sclerosis (focal HS), focal epilepsy with lesions other than HS (focal NHS), and lesion-negative focal epilepsy. Causal estimates were computed using the inverse-variance weighted method or the Wald ratio method, and the robustness of causality was assessed through sensitivity analyses.

RESULTS

For OSIB and epilepsy, 520 and 23 genetic variants, respectively, were selectively extracted as instrumental variants. Genetically predicted higher kynurenine level was associated with a decreased risk of focal epilepsy (odds ratio [OR] 1.950, 95% CI 1.373-2.528, p = .023) and focal NHS (OR 1.276, 95% CI 1.100-1.453, p = .006). For reverse analysis, there was a suggestive effect of focal NHS on urate (OR 1.19 × 10, 95% CI 11.19 × 10 to 1.19 × 10, p = .0000746) and total bilirubin (Tb) (OR 4.98, 95% CI 3.423-6.543, p = .044). In addition, genetic predisposition to focal HS was associated with higher Tb levels (OR 9.83, 95% CI 7.77-11.888, p = .034).

CONCLUSION

This MR study provides compelling evidence of a robust association between oxidative stress and epilepsy, with a notable emphasis on a causal relationship between oxidative stress and focal epilepsy. Additional research is warranted to confirm the connection between oxidative stress and the risk of epilepsy and to unravel the underlying mechanisms.

摘要

背景

尽管越来越多的研究表明氧化应激与癫痫之间存在很强的关联,但它们相互作用的确切性质仍难以捉摸。为了阐明这种复杂的关系,我们使用来自与氧化应激相关的八个主要代谢途径的氧化应激损伤生物标志物(OSIB)和癫痫的全基因组关联研究汇总统计数据进行了双向孟德尔随机化(MR)分析。

方法

使用来自与氧化应激相关的八个主要代谢途径的氧化应激损伤生物标志物(OSIB)和癫痫的全基因组关联研究汇总统计数据进行了双向孟德尔随机化(MR)分析。使用来自与氧化应激相关的八个主要代谢途径的氧化应激损伤生物标志物(OSIB)和癫痫的全基因组关联研究汇总统计数据进行了双向孟德尔随机化(MR)分析。使用来自与氧化应激相关的八个主要代谢途径的氧化应激损伤生物标志物(OSIB)和癫痫的全基因组关联研究汇总统计数据进行了双向孟德尔随机化(MR)分析。此外,还考虑了七种不同的癫痫表型,包括所有癫痫、全身性癫痫、全身性强直阵挛性发作、局灶性癫痫、局灶性癫痫伴海马硬化(局灶性 HS)、局灶性癫痫伴除 HS 以外的病变(局灶性 NHS)和无病变局灶性癫痫。使用逆方差加权法或 Wald 比法计算因果估计值,并通过敏感性分析评估因果关系的稳健性。

结果

对于 OSIB 和癫痫,分别有 520 个和 23 个遗传变异被选择性地提取为工具变量。遗传预测的较高犬尿氨酸水平与局灶性癫痫(比值比 [OR] 1.950,95%置信区间 [CI] 1.373-2.528,p=0.023)和局灶性 NHS(OR 1.276,95% CI 1.100-1.453,p=0.006)的风险降低有关。对于反向分析,局灶性 NHS 对尿酸(OR 1.19×10,95% CI 11.19×10 至 1.19×10,p=0.0000746)和总胆红素(Tb)(OR 4.98,95% CI 3.423-6.543,p=0.044)有提示性影响。此外,局灶性 HS 的遗传易感性与较高的 Tb 水平相关(OR 9.83,95% CI 7.77-11.888,p=0.034)。

结论

这项 MR 研究提供了令人信服的证据,表明氧化应激与癫痫之间存在强烈的关联,特别强调了氧化应激与局灶性癫痫之间的因果关系。需要进一步的研究来证实氧化应激与癫痫风险之间的联系,并阐明潜在的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9a0/11161392/ff0a414712aa/BRB3-14-e3549-g001.jpg

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