Zahra Mai A, Kamha Eman S, Abdelaziz Hanan K, Nounou Howaida A, Deeb Hany M El
Department of Medical Biochemistry, Faculty of Medicine, University of Alexandria, Alexandria, Alexandria Governorate, Egypt.
Department of Neuropsychiatry, Faculty of Medicine, University of Alexandria, Alexandria, Alexandria Governorate, Egypt.
Ann Neurosci. 2022 Oct;29(4):203-208. doi: 10.1177/09727531221077667. Epub 2022 Aug 8.
Epilepsy is one of the common neurological disorders affecting approximately 50 million people worldwide. Despite the recent introduction of new antiepileptic drugs, about one-third of patients with epilepsy have seizures refractory to pharmacotherapy. Early recognition of patients with drug-resistant epilepsy may help direct these patients to appropriate nonpharmacological treatment.
The possible use of serum microRNAs (miRNAs) as noninvasive biomarkers has been explored in various brain diseases, including epilepsy. In this study, we are aiming at analyzing the expression levels of circulating miRNA-153 and miRNA-199a in patients with generalized epilepsy and their correlation with drug resistance.
Our study comprised 40 patients with generalized epilepsy and 20 healthy controls. 22 patients were drug-resistant and 18 patients were drug-responsive. The expression levels of miRNA-153 and -199a in serum were analyzed using quantitative real-time polymerase chain reaction. Data analysis was done by IBM SPSS Statistics 20.0.
The expression of miRNA-153 and -199a in serum was significantly downregulated in patients with generalized epilepsy compared with that of the healthy control ( < .001). Combined expression level of serum miRNA-153 and -199a had a sensitivity of 85% and a specificity of 90% in the diagnosis of generalized epilepsy. Furthermore, the expression levels of miRNA-153 and -199a were significantly decreased in drug-resistant patients compared to the drug-responsive group, and the combination of both markers gave the best results in differentiating between the two groups.
We suggest that serum miRNAs-153 and -199a expression levels could be potential noninvasive biomarkers supporting the diagnosis of generalized epilepsy. Moreover, they could be used for the early detection of refractory generalized epilepsy.
癫痫是一种常见的神经系统疾病,全球约有5000万人受其影响。尽管最近引入了新的抗癫痫药物,但约三分之一的癫痫患者对药物治疗无效。早期识别耐药性癫痫患者可能有助于指导这些患者接受适当的非药物治疗。
血清微小RNA(miRNA)作为无创生物标志物在包括癫痫在内的各种脑部疾病中的潜在用途已得到探索。在本研究中,我们旨在分析全身性癫痫患者循环miRNA-153和miRNA-199a的表达水平及其与耐药性的相关性。
我们的研究包括40例全身性癫痫患者和20名健康对照者。22例患者耐药,18例患者药物敏感。使用定量实时聚合酶链反应分析血清中miRNA-153和-199a的表达水平。数据分析采用IBM SPSS Statistics 20.0完成。
与健康对照相比,全身性癫痫患者血清中miRNA-153和-199a的表达明显下调(P<0.001)。血清miRNA-153和-199a的联合表达水平在全身性癫痫诊断中的敏感性为85%,特异性为90%。此外,与药物敏感组相比,耐药患者中miRNA-153和-199a的表达水平明显降低,两种标志物的联合使用在区分两组时效果最佳。
我们认为血清miRNAs-153和-199a的表达水平可能是支持全身性癫痫诊断的潜在无创生物标志物。此外,它们可用于难治性全身性癫痫的早期检测。