Shnayder Natalia A, Pekarets Nikolai A, Pekarets Natalia I, Dmitrenko Diana V, Grechkina Violetta V, Petrova Marina M, Al-Zamil Mustafa, Nasyrova Regina F
Institute of Personalized Psychiatry and Neurology, V.M. Bekhterev National Medical Research Center for Psychiatry and Neurology, 3 Bekhterev St., 192019 St. Petersburg, Russia.
Shared Core Facilities "Molecular and Cell Technologies", V.F. Voino-Yasenetsky Krasnoyarsk State Medical University, 1 Partizan Zheleznyak St., 660022 Krasnoyarsk, Russia.
J Clin Med. 2025 Apr 2;14(7):2432. doi: 10.3390/jcm14072432.
Antiseizure medication (ASM) induced metabolic syndrome (AIMetS) is a common adverse drug reaction (ADR) of pharmacotherapy for epilepsy and psychiatric disorders. However, the sensitivity and specificity of blood biomarkers may be insufficient due to the influence of combined pathology, concomitant diseases, and the peculiarities of the metabolism of ASMs in patients with epilepsy. : The presented results of experimental and clinical studies of microRNAs (miRs) as epigenetic biomarkers of MetS and AIMetS, which were entered into the different databases, were analyzed for the last decade (2014-2024). : A systematic review demonstrated that miRs can act as promising epigenetic biomarkers of key AIMetS domains. However, the results of the review demonstrated the variable role of various miRs and their paralogs in the pathogenesis of AIMetS. Therefore, as part of this study, an miRs signature was proposed that allows us to assess the risk of developing and the severity of AIMetS as low risk, medium risk, and high risk. : The mechanisms of development and biomarkers of AIMetS are an actual problem of epileptology, which is still far from being resolved. The development of panels (signatures) of epigenetic biomarkers of this widespread ADR may help to increase the safety of pharmacotherapy of epilepsy. However, to increase the sensitivity and specificity of circulating miRs in the blood as biomarkers of AIMetS, it is necessary to conduct "bridge" studies in order to replicate the results of preclinical and clinical studies into real clinical practice.
抗癫痫药物(ASM)诱发的代谢综合征(AIMetS)是癫痫和精神疾病药物治疗中常见的药物不良反应(ADR)。然而,由于合并病理、伴随疾病以及癫痫患者中ASM代谢特性的影响,血液生物标志物的敏感性和特异性可能不足。:对过去十年(2014 - 2024年)纳入不同数据库的作为代谢综合征(MetS)和AIMetS表观遗传生物标志物的微小RNA(miRs)的实验和临床研究结果进行了分析。:一项系统评价表明,miRs可作为有前景的AIMetS关键领域的表观遗传生物标志物。然而,该评价结果表明各种miRs及其旁系同源物在AIMetS发病机制中的作用各不相同。因此,作为本研究的一部分,提出了一种miRs特征,使我们能够将AIMetS发生风险和严重程度评估为低风险、中风险和高风险。:AIMetS的发病机制和生物标志物是癫痫学的一个实际问题,目前仍远未解决。这种广泛存在的ADR的表观遗传生物标志物面板(特征)的开发可能有助于提高癫痫药物治疗的安全性。然而,为了提高血液中循环miRs作为AIMetS生物标志物的敏感性和特异性,有必要进行“桥梁”研究,以便将临床前和临床研究结果复制到实际临床实践中。