Neurology Clinic, Aksaray University Training and Research Hospital, Aksaray, Turkey.
Department of Neurology, Medicana Medical Faculty, KTO Karatay University, Konya, Turkey.
Int J Neurosci. 2020 Nov;130(11):1095-1100. doi: 10.1080/00207454.2020.1722662. Epub 2020 Feb 6.
There is a close relationship between systemic inflammation and epileptic seizure. Recently, neutrophil/lymphocyte ratio (NLR) and platelet/lymphocyte ratio (PLR) have been defined as significant inflammation biomarkers. In the present study, it was aimed to determine levels of NLR, PLR, and mean platelet volume (MPV) during generalized tonic clonic epileptic seizures, and to investigate their relationships with epileptic seizures. The present study was conducted on 72 patients with epilepsy who applied with primary and secondary generalized tonic clonic epileptic seizures according to classification of the International League Against Epilepsy (ILAE), and 72 healthy individuals as the control group. Neutrophil and lymphocyte counts, NLR, PLR, and MPV values of patients were evaluated both in acute (in the first hour of epileptic seizure) and subacute (in hour 72 of epileptic seizure) phases by biochemical analysis. Statistically significant differences were determined in laboratory values of white blood cell (WBC) ( < 0.001), neutrophil ( < 0.001), lymphocyte ( < 0.001), NLR ( < 0.001), MPV ( < 0.05), platelet ( < 0.001), C-reactive protein (CRP) ( < 0.05) in acute phase; and in lymphocyte ( < 0.05), NLR ( < 0.05), platelet ( < 0.001), and CRP ( < 0.001) in subacute phase between patients and healthy controls. Statistically significant differences were determined in laboratory values of WBC ( < 0.001), neutrophil ( < 0.001), lymphocyte ( < 0.05), NLR ( < 0.001), CRP ( < 0.001), and PLR ( < 0.05) in patient group between acute and subacute phases. In patient group, mean lymphocyte count was determined lower in acute phase than subacute phase ( < 0.05). The most striking finding of the present study is determination of 1 unit increase in NLR results in 1.95 folds increase in epileptic seizure risk in binary logistic regression analysis. Additionally, it indicates that epileptic seizure is correlated with NLR, PLR, and neutrophil mediated inflammation. To the best of authors knowledge, this is the first report indicating that there is a relationship between epileptic seizure and PLR, neutrophil mediated inflammation, and that 1 unit increase in NLR increases epileptic seizure risk by 1.95 folds.
全身炎症与癫痫发作之间存在密切关系。最近,中性粒细胞/淋巴细胞比值(NLR)和血小板/淋巴细胞比值(PLR)已被定义为重要的炎症生物标志物。本研究旨在确定全身性强直阵挛性癫痫发作期间 NLR、PLR 和平均血小板体积(MPV)的水平,并探讨它们与癫痫发作的关系。本研究纳入了 72 例根据国际抗癫痫联盟(ILAE)分类诊断为原发性和继发性全身性强直阵挛性癫痫发作的癫痫患者,并纳入了 72 例健康个体作为对照组。通过生化分析评估患者在急性(癫痫发作后 1 小时内)和亚急性(癫痫发作后 72 小时内)期的白细胞(WBC)、中性粒细胞、淋巴细胞、NLR、PLR 和 MPV 值。结果发现,在急性期中,白细胞(WBC)( < 0.001)、中性粒细胞( < 0.001)、淋巴细胞( < 0.001)、NLR( < 0.001)、MPV( < 0.05)、血小板( < 0.001)和 C 反应蛋白(CRP)( < 0.05)的实验室值存在显著差异;在亚急性期中,淋巴细胞( < 0.05)、NLR( < 0.05)、血小板( < 0.001)和 CRP( < 0.001)的实验室值存在显著差异。在患者组中,急性期与亚急性期之间的 WBC( < 0.001)、中性粒细胞( < 0.001)、淋巴细胞( < 0.05)、NLR( < 0.001)、CRP( < 0.001)和 PLR( < 0.05)的实验室值存在显著差异。与亚急性期相比,患者组在急性期的平均淋巴细胞计数较低( < 0.05)。本研究最显著的发现是,在二元逻辑回归分析中,NLR 增加 1 个单位,癫痫发作的风险增加 1.95 倍。此外,这表明癫痫发作与 NLR、PLR 和中性粒细胞介导的炎症有关。据作者所知,这是首次表明癫痫发作与 PLR、中性粒细胞介导的炎症有关,并且 NLR 增加 1 个单位可使癫痫发作的风险增加 1.95 倍。