Timechko Elena E, Lysova Kristina D, Yakimov Alexey M, Paramonova Anastasia I, Vasilieva Anastasia A, Kantimirova Elena A, Usoltseva Anna A, Yakunina Albina V, Areshkina Irirna G, Dmitrenko Diana V
Department of Medical Genetics, Clinical Neurophysiology of Postgraduate Education, V.F. Voyno-Yasenetsky Krasnoyarsk State Medical University, Russian National Research, Krasnoyarsk 660022, Russia.
Federal State Budgetary Educational Institution, Samara State Medical University, Ministry of Healthcare of the Russian, Samara 443079, Russia.
Med Sci (Basel). 2025 Jan 8;13(1):7. doi: 10.3390/medsci13010007.
: Epilepsy is a group of disorders characterized by a cluster of clinical and EEG signs leading to the formation of abnormal synchronous excitation of neurons in the brain. It is one of the most common neurological disorders worldwide; and is characterized by aberrant expression patterns; both at the level of matrix transcripts and at the level of regulatory RNA sequences. Aberrant expression of a number of microRNAs can mark a particular epileptic syndrome; which will improve the quality of differential diagnosis. : In this work; the expression profile of six microRNAs was analyzed: hsa-miR-106b-5p; hsa-miR-134-5p; hsa-miR-122-5p; hsa-miR-132-3p; hsa-miR-155-5p; and hsa-miR-206-5p in the blood plasma of patients suffering from temporal lobe epilepsy (n = 52) and juvenile myoclonic epilepsy (n = 42); n-amount of participants; in comparison with healthy volunteers. The expression analysis was carried out using RT-PCR. Mathematical processing of the data was carried out according to the Livak method. : A statistically significant change in the expression of hsa-miR-106b-5p; hsa-miR-134-5p; hsa-miR-122-5p; and hsa-miR-132-3p was found. An increase in the expression of hsa-miR-134-5p and hsa-miR-122-5p was registered in the group of patients with temporal lobe epilepsy compared to the control; as well as an increase in the expression of hsa-miR-132-3p and hsa-miR-106b-5p in the juvenile myoclonic epilepsy group compared to the control. hsa-miR-122-5p; 106b-5p; 132-3p are also able to discriminate groups with different syndromes. Additionally; a number of microRNAs are able to discriminate patients with drug-resistant and drug-sensitive forms of epilepsy from the control; as well as patients with hippocampal sclerosis and patients without hippocampal sclerosis from the control. Conclusion. Our data allow us to propose these microRNAs as plasma biomarkers of various epileptic syndromes.
癫痫是一组以一系列临床和脑电图体征为特征的疾病,这些体征导致大脑中神经元形成异常同步兴奋。它是全球最常见的神经系统疾病之一;其特征在于在基质转录本水平和调节性RNA序列水平上的异常表达模式。多种微小RNA的异常表达可标记特定的癫痫综合征,这将提高鉴别诊断的质量。
在这项研究中,分析了六种微小RNA(hsa-miR-106b-5p、hsa-miR-134-5p、hsa-miR-122-5p、hsa-miR-132-3p、hsa-miR-155-5p和hsa-miR-206-5p)在颞叶癫痫患者(n = 52)和青少年肌阵挛癫痫患者(n = 42)血浆中的表达谱,并与健康志愿者进行比较(n为参与者数量)。使用逆转录聚合酶链反应(RT-PCR)进行表达分析。数据的数学处理按照Livak方法进行。
发现hsa-miR-106b-5p、hsa-miR-134-5p、hsa-miR-122-5p和hsa-miR-132-3p的表达有统计学意义的变化。与对照组相比,颞叶癫痫患者组中hsa-miR-134-5p和hsa-miR-122-5p的表达增加;与对照组相比,青少年肌阵挛癫痫组中hsa-miR-132-3p和hsa-miR-106b-5p的表达也增加。hsa-miR-122-5p、106b-5p、132-3p也能够区分不同综合征的组。此外,一些微小RNA能够区分耐药性和药物敏感性癫痫形式的患者与对照组,以及海马硬化患者和无海马硬化患者与对照组。
结论。我们的数据使我们能够提出这些微小RNA作为各种癫痫综合征的血浆生物标志物。