van Karnebeek Clara D M, Sayson Bryan, Lee Jessica J Y, Tseng Laura A, Blau Nenad, Horvath Gabriella A, Ferreira Carlos R
Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.
Centre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, BC, Canada.
Front Neurol. 2018 Dec 3;9:1016. doi: 10.3389/fneur.2018.01016. eCollection 2018.
Although inborn errors of metabolism do not represent the most common cause of seizures, their early identification is of utmost importance, since many will require therapeutic measures beyond that of common anti-epileptic drugs, either in order to control seizures, or to decrease the risk of neurodegeneration. We translate the currently-known literature on metabolic etiologies of epilepsy (268 inborn errors of metabolism belonging to 21 categories, with 74 treatable errors), into a 2-tiered diagnostic algorithm, with the first-tier comprising accessible, affordable, and less invasive screening tests in urine and blood, with the potential to identify the majority of treatable conditions, while the second-tier tests are ordered based on individual clinical signs and symptoms. This resource aims to support the pediatrician, neurologist, biochemical, and clinical geneticists in early identification of treatable inborn errors of metabolism in a child with seizures, allowing for timely initiation of targeted therapy with the potential to improve outcomes.
尽管先天性代谢缺陷并非癫痫最常见的病因,但早期识别它们至关重要,因为许多此类疾病需要常规抗癫痫药物以外的治疗措施,以控制癫痫发作或降低神经退行性变的风险。我们将目前已知的关于癫痫代谢病因的文献(21类共268种先天性代谢缺陷,其中74种为可治疗缺陷)转化为一种两级诊断算法,第一层包括尿液和血液中易于获得、价格低廉且侵入性较小的筛查测试,这些测试有可能识别出大多数可治疗的病症,而第二层测试则根据个体的临床体征和症状进行安排。本资源旨在支持儿科医生、神经科医生、生化专家和临床遗传学家早期识别癫痫患儿中可治疗的先天性代谢缺陷,以便及时启动有改善预后潜力的靶向治疗。