Johannesen Katrine M, Nielsen Jimmi, Sabers Anne, Isidor Bertrand, Kattentidt-Mouravieva Anja A, Zieglgänsberger Dominik, Heidlebaugh Alexis R, Oetjens Kathryn F, Vidal Anna Abuli, Christensen Jakob, Tiller Jacob, Freed Amber N, Møller Rikke S, Rubboli Guido
Department of Genetics, University Hospital of Copenhagen, Rigshospitalet, Copenhagen, Denmark.
Department of Epilepsy Genetics and Personalized Treatment, The Danish Epilepsy Centre, Member of the European Reference Network, EpiCARE, Dianalund, Denmark.
Front Neurosci. 2023 Aug 17;17:1216653. doi: 10.3389/fnins.2023.1216653. eCollection 2023.
is one of the most common monogenic causes of epilepsy and is a well-established cause of neurodevelopmental disorders. -neurodevelopmental disorders have a consistent phenotype of mild to severe intellectual disability (ID), epilepsy, language delay and behavioral disorders. This phenotypic description is mainly based on knowledge from the pediatric population.
Here, we sought to describe patients with variants and age above 18 years through the ascertainment of published and unpublished patients. Unpublished patients were ascertained through international collaborations, while previously published patients were collected through a literature search.
A total of 15 adult patients with variants were included. 9/13 patients had moderate to severe ID (data not available in two). Epilepsy was prevalent (11/15) with seizure types such as absence, myoclonic, atonic, and tonic-clonic seizures. Epilepsy was refractory in 7/11, while four patients were seizure free with lamotrigine, valproate, or lamotrigine in combination with valproate. Language development was severely impaired in five patients. Behavioral disorders were reported in and mainly consisted of autism spectrum disorders and aggressive behavior. Schizophrenia was not reported in any of the patients.
The phenotype displayed in the adult patients presented here resembled that of the pediatric cohort with ID, epilepsy, and behavioral disturbances, indicating that the phenotype of -NDD is consistent over time. Seizures were refractory in >60% of the patients with epilepsy, indicating the lack of targeted treatment in -NDDs. With increased focus on repurposing drugs and on the development of new treatments, hope is that the outlook reflected here will change over time. ID appeared to be more severe in the adult patients, albeit this might reflect a recruitment bias, where only patients seen in specialized centers were included or it might be a feature of the natural history of -NDDs. This issue warrants to be explored in further studies in larger cohorts.
是癫痫最常见的单基因病因之一,也是神经发育障碍的确切病因。-神经发育障碍具有从轻度到重度智力残疾(ID)、癫痫、语言发育迟缓及行为障碍的一致表型。这种表型描述主要基于儿科人群的知识。
在此,我们试图通过确定已发表和未发表的患者来描述18岁以上携带变异的患者。未发表的患者通过国际合作确定,而先前发表的患者通过文献检索收集。
共纳入15例携带变异的成年患者。13例患者中有9例存在中度至重度ID(2例数据缺失)。癫痫很常见(15例中有11例),发作类型包括失神发作、肌阵挛发作、失张力发作和强直阵挛发作。11例中有7例癫痫难治,4例患者使用拉莫三嗪、丙戊酸盐或拉莫三嗪联合丙戊酸盐后无癫痫发作。5例患者语言发育严重受损。报告了行为障碍,主要包括自闭症谱系障碍和攻击行为。所有患者均未报告精神分裂症。
此处呈现的成年患者所表现出的表型与儿科队列中具有智力残疾、癫痫和行为障碍的表型相似,表明-NDD的表型随时间是一致的。超过60%的癫痫患者癫痫难治,表明-NDD缺乏针对性治疗。随着对药物重新利用和新治疗方法开发的关注度增加,希望此处反映的前景会随着时间而改变。成年患者的智力残疾似乎更严重,尽管这可能反映了招募偏倚,即仅纳入了在专科中心就诊的患者,或者这可能是-NDD自然史的一个特征。这个问题值得在更大队列的进一步研究中探讨。