Bartolini Luca, Piras Eleonora, Sullivan Kathryn, Gillen Sean, Bumbut Adrian, Lin Cheng-Te Major, Leibovitch Emily C, Graves Jennifer S, Waubant Emmanuelle L, Chamberlain James M, Gaillard William D, Jacobson Steven
Center for Neuroscience, Children's National Medical Center, George Washington University, Washington, DC, United States.
Clinical Epilepsy Section, National Institute of Neurological Disorders and Stroke, Bethesda, MD, United States.
Front Neurol. 2018 Oct 5;9:834. doi: 10.3389/fneur.2018.00834. eCollection 2018.
One third of children with epilepsy are refractory to medications. Growing data support a role of common childhood infections with neurotropic viruses and inflammation in epileptogenesis. Our objective was to determine the frequency of Human Herpesvirus-6 (HHV-6) and Epstein-Barr Virus (EBV) infection and cytokine levels in saliva from children with seizures compared to healthy controls and to controls with a febrile illness without seizures. In this cross-sectional multi-center study, we collected saliva from 115 consecutive children with acute seizures (cases), 51 children with a fever and no seizures or underlying neurological disease (fever controls) and 46 healthy children (healthy controls). Specimens were analyzed by a novel droplet digital PCR for HHV-6 and EBV viral DNA and a bead-based immunoassay for neuroinflammatory cytokines. Cases included febrile seizures ( = 30), acute seizures without ( = 53) and with fever ( = 4) in chronic epilepsy, new onset epilepsy ( = 13), febrile status epilepticus ( = 3), and first lifetime seizure ( = 12). HHV-6 DNA was found in 40% of cases vs. 37% fever controls and 35% healthy controls, with no statistically significant differences. EBV DNA was also detected with no differences in 17% cases, 16% fever controls, and 28% healthy controls. IL-8 and IL-1β were increased in saliva of 32 random samples from cases compared with 30 fever controls: IL-8 cases mean (SD): 1158.07 pg/mL (1427.41); controls 604.92 (754.04); = 0.02. IL-1β 185.76 (230.57); controls 86.99 (187.39); = 0.0002. IL-1β level correlated with HHV6 viral load ( = 0.007). Increase in inflammatory cytokines may play a role in the onset of acute seizures and saliva could represent an inexpensive and non-invasive method for detection of viral DNA and cytokines.
三分之一的癫痫患儿对药物治疗无效。越来越多的数据支持常见的儿童神经嗜性病毒感染和炎症在癫痫发生过程中发挥作用。我们的目的是确定与健康对照以及无癫痫发作的发热性疾病对照相比,癫痫发作儿童唾液中人类疱疹病毒6型(HHV - 6)和爱泼斯坦 - 巴尔病毒(EBV)感染的频率以及细胞因子水平。在这项横断面多中心研究中,我们收集了115名连续的急性癫痫发作儿童(病例组)、51名发热但无癫痫发作或潜在神经疾病的儿童(发热对照组)以及46名健康儿童(健康对照组)的唾液。通过一种新型的液滴数字PCR检测HHV - 6和EBV病毒DNA,并通过基于微珠的免疫测定法检测神经炎症细胞因子。病例组包括热性惊厥(n = 30)、慢性癫痫中无发热(n = 53)和有发热(n = 4)的急性癫痫发作、新发癫痫(n = 13)、热性癫痫持续状态(n = 3)以及首次终生发作(n = 12)。40%的病例组中检测到HHV - 6 DNA,发热对照组为37%,健康对照组为35%,无统计学显著差异。EBV DNA的检测情况也无差异,病例组为17%,发热对照组为16%,健康对照组为28%。与30名发热对照组相比,病例组32个随机样本的唾液中IL - 8和IL - 1β升高:IL - 8病例组均值(标准差):1158.07 pg/mL(1427.41);对照组604.92(754.04);P = 0.02。IL - 1β 185.76(230.57);对照组86.99(187.39);P = 0.0002。IL - 1β水平与HHV6病毒载量相关(P = 0.007)。炎症细胞因子的增加可能在急性癫痫发作的发病过程中起作用,唾液可能是一种检测病毒DNA和细胞因子的廉价且非侵入性的方法。