Xue Jiao, Yang Zhixian, Wu Ye, Xiong Hui, Zhang Yuehua, Liu Xiaoyan
Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.
Zhonghua Er Ke Za Zhi. 2016 Feb;54(2):141-4. doi: 10.3760/cma.j.issn.0578-1310.2016.02.014.
To analyze clinical characteristics, treatment and prognosis in a cohort of children with vitamin B6 responsive infantile spasms.
Ten patients were diagnosed as vitamin B6 responsive infantile spasms in Peking University First Hospital between January 2012 and May 2015.The clinical manifestations, diagnosis and treatment process, video-electroencephalogram, magnetic resonance imaging (MRI), epilepsy related genes and prognosis were retrospectively analyzed.
Of the 10 patients, 5 were male, and 5 were female. Eight of them were normal at birth, and the other 2 patients had intracranial hemorrhage or anoxia.The age of epilepsy onset was from 3.5 to 8.0 months.All patients presented spasms primarily.Interictal electroencephalogram (EEG) showed hypsarrhythmia at seizures onset. MRI showed normal in 8 patients, and subarachnoid hemorrhage or multiple encephalomalacia foci after hemorrhage respectively in the other 2 patients. The results of blood biochemical, cerebrospinal fluid examination and urinary metabolic screening were negative. Epilepsy related genes including ALDH7A1 gene analysis showed wild type in all patients. Two patients were classified as symptomatic and eight might be idiopathic or cryptogenic. The initial dose of vitamin B6 was 10.0 mg/(kg·d). The interval between seizures onset and taking vitamin B6 was 0 to 4.0 months. Seizures disappeared completely within a week after administration of vitamin B6 in 9 patients and in 1.5 months in one patient.Of the 8 patients whose seizures were controlled completely during the follow-up period, 7 patients' EEG recovered within 1.5 to 4.0 months and then continued to be normal. The EEG of the rest of a patient returned to normal, but showed abnormal discharges after stopping taking vitamin B6. Two patients' EEG continued abnormal and seizures recurred due to vitamin B6 withdrawal. At the last follow-up, seizures were controlled in all patients. Drug treatment in one case had stopped. Vitamin B6 was used in 9 patients at a dose of 0.4 to 10.0 mg/(kg·d). Among them, vitamin B6 monotherapy or coadministration with one low dose antiepileptic drug was applied in 6 or 3 patients respectively. The psychomotor development was normal in 5 patients, mild delay in 3 patients, and severe delay in 2 patients with autism behavior. Of the 2 symptomatic patients, one developed normally and the other showed severe delay.
Vitamin B6 might have effects on both idiopathic or cryptogenic and symptomatic patients, especially for the former. High dose vitamin B6 should be first tried in all patients with infantile spasms. Patients who had response to vitamin B6 could be controlled within a short time and might have better outcomes. Seizures were not easy to relapse in those whose seizures were controlled and EEG recovered completely. Vitamin B6 could be gradually reduced during the course and might be withdrawn in the future. The recurrence of seizures was closely related to EEG abnormality.
分析一组维生素B6反应性婴儿痉挛症患儿的临床特征、治疗及预后情况。
回顾性分析2012年1月至2015年5月在北京大学第一医院确诊为维生素B6反应性婴儿痉挛症的10例患儿的临床表现、诊断及治疗过程、视频脑电图、磁共振成像(MRI)、癫痫相关基因及预后情况。
10例患儿中,男5例,女5例。8例出生时正常,另2例有颅内出血或缺氧史。癫痫起病年龄为3.5至8.0个月。所有患儿均以痉挛发作为主要表现。发作间期脑电图(EEG)在发作起始时显示高峰失律。MRI检查8例正常,另2例分别有蛛网膜下腔出血或出血后多发脑软化灶。血液生化、脑脊液检查及尿代谢筛查结果均为阴性。癫痫相关基因包括ALDH7A1基因分析显示所有患儿均为野生型。2例为症状性,8例可能为特发性或隐源性。维生素B6初始剂量为10.0mg/(kg·d)。发作起始至服用维生素B6的间隔时间为0至4.0个月。9例患儿在服用维生素B6后1周内痉挛完全消失,1例在1.5个月内消失。随访期间痉挛完全控制的8例患儿中,7例EEG在1.5至4.0个月内恢复正常并持续正常。另1例患儿EEG恢复正常,但停用维生素B6后出现异常放电。2例患儿因停用维生素B6,EEG持续异常且痉挛复发。末次随访时,所有患儿痉挛均得到控制。1例患儿已停药。9例患儿使用维生素B6,剂量为0.4至10.0mg/(kg·d)。其中,6例患儿采用维生素B6单药治疗,3例患儿联合一种低剂量抗癫痫药物治疗。5例患儿精神运动发育正常,3例轻度延迟,2例有自闭症行为且严重延迟。2例症状性患儿中,1例发育正常,另1例严重延迟。
维生素B6对特发性或隐源性及症状性患儿均可能有效,尤其是对前者。所有婴儿痉挛症患儿均应首先尝试大剂量维生素B6治疗。对维生素B6有反应的患儿可在短时间内得到控制,且可能有较好的预后。痉挛控制且EEG完全恢复的患儿不易复发。病程中维生素B6可逐渐减量,未来可能停药。痉挛复发与EEG异常密切相关。