Heba M Mahdy
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摘要

背景:癫痫是一种广泛存在的神经系统疾病,尤其影响儿童和老年人,给治疗带来了复杂多样的挑战。最近,促红细胞生成素因其在包括癫痫在内的各种神经系统疾病中的实验证明的神经保护作用而备受关注。本综述旨在分析当前有关促红细胞生成素在癫痫发作和癫痫中作用的文献:方法:通过 PubMed、Scopus 和 Web of Science 数据库对截至 2024 年 9 月 30 日的文献进行了全面检索。检索词包括 "癫痫与促红细胞生成素"、"癫痫发作与促红细胞生成素 "和 "癫痫状态与促红细胞生成素",并应用于标题、摘要和关键词:结果:综述强调了目前围绕促红细胞生成素对癫痫影响的争论。虽然促红细胞生成素在减轻癫痫发作引起的脑损伤和调节细胞过程(如抗凋亡和抗炎途径)方面显示出潜力,但其临床应用却因相互矛盾的证据而变得复杂。一些研究表明,促红细胞生成素可能会诱发癫痫发作,而剂量和患者个体特征等因素可能会影响这种风险:实验研究表明,促红细胞生成素对癫痫患者具有神经保护作用。然而,促红细胞生成素可能产生的促惊厥效应--这可能与促红细胞生成素诱发的高血压、血细胞比容水平的快速升高、剂量或患者个体特征有关--引发了安全性问题。这些风险使红细胞生成素的临床应用变得更加复杂,因此完全认可红细胞生成素作为一种治疗手段还为时过早。未来的研究重点应放在非促红细胞生成素衍生物上,这些衍生物能在不刺激红细胞生成的情况下保留神经保护作用,从而降低高血压和血栓形成等风险。精心设计的临床试验和对促红细胞生成素机制的进一步研究对于明确其在癫痫中的作用和优化其治疗潜力至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Erythropoietin for Seizures and Epilepsy: Neuroprotective Effects, Mechanisms, and Contradictory Risks.

Background: Epilepsy is a widespread neurological disorder, particularly affecting children and the elderly, presenting complex and varied challenges in management. Recently, erythropoietin has gained significant attention due to its neuroprotective effects, which have been demonstrated experimentally in various neurological conditions, including epilepsy. This review aims to analyze current literature on the role of erythropoietin in seizures and epilepsy.

Method: A comprehensive literature search was conducted through PubMed, Scopus, and Web of Science databases up to September 30, 2024. The search terms included "Epilepsy AND Erythropoietin", "Seizures AND Erythropoietin," and "Status Epilepticus AND Erythropoietin", applied to titles, abstracts, and keywords.

Results: The review highlights ongoing debates surrounding erythropoietin's effects on epilepsy. While erythropoietin shows potential in mitigating seizure-induced brain damage and modulating cellular processes such as anti-apoptotic and anti-inflammatory pathways, its clinical application is complicated by conflicting evidence. Some studies suggest that erythropoietin may trigger seizures, with factors such as dosage and individual patient characteristics potentially influencing this risk.

Conclusion: Experimental studies suggest that erythropoietin offers neuroprotective benefits in epilepsy. However, its possible pro-convulsant effects-which might be linked to erythropoietin-induced hypertension, rapid increases in hematocrit levels, dosage, or individual patient characteristics-raise safety concerns. These risks complicate its clinical use, making it premature to endorse erythropoietin as a treatment fully. Future research should focus on non-erythropoietic derivatives that retain neuroprotective effects without stimulating red blood cell production, thereby reducing risks, such as hypertension and thrombosis. Well-designed clinical trials and further investigation into erythropoietin's mechanisms are essential to clarify its role and optimize its therapeutic potential in epilepsy.

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