Khajezadeh Mohammad-Amin, Zamani Gholamreza, Moazzami Bobak, Nagahi Zahra, Mousavi-Torshizi Mahdie, Ziaee Vahid
Children's Medical Center, Pediatrics Center of Excellence, Tehran, Iran.
Department of Pediatrics, Tehran University of Medical Sciences, Tehran, Iran.
Neurol Res Int. 2018 May 29;2018:2548142. doi: 10.1155/2018/2548142. eCollection 2018.
Systemic lupus erythematosus (SLE) is a complex autoimmune disorder characterized by multisystem involvement, including the nervous system. In the present study, we aimed to assess neuropsychiatric manifestations in juvenile-onset systemic lupus erythematosus (JSLE) in Iran.
One hundred and forty-six pediatric onset patients with SLE who had registered in our pediatric rheumatology database were evaluated prospectively and cross sectionally within 2013-2015. Data including sex, age, age at the time of diagnosis, age at the time of study, physical examination, laboratory review, and neuropsychiatric inventory were extracted from this database. Classification of neuropsychiatric JSLE was according to the 1999 American College of Rheumatology (ACR) neuropsychiatric manifestations of SLE case definitions.
A total number of 41 patients with neuropsychiatric symptoms were selected. The patients' average age was 12.2 years. The most common neuropsychiatric symptoms were seizures, migraine, and depression. The mean age at the onset of symptoms was 10.2 ± 3 years. Mean follow-up period was 57±34 (range: 12-120) months. From 41 SLE patients, 18 (43.9) presented symptoms at the time of diagnosis. In thirteen (31.7%) patients, neurological symptoms were developed more than 1 year after SLE diagnosis. Headache was the most common feature (13%), followed by seizure (9.5%) and chorea (3.4%). Other neurological manifestations included cranial nerve involvement (0.7%), loss of consciousness (2.7%), and impaired deep tendon reflex neuropathy (2.5%). The least common neuropsychiatric JSLE manifestation was aseptic meningitis seen in only one patient (0.7%).
The presence of headache, mood disorders, psychosis, depression, and other neuropsychological manifestations in a patient with JSLE should prompt investigations into diagnosis of the primary nervous system involvement in order to reduce mortality and morbidity.
系统性红斑狼疮(SLE)是一种复杂的自身免疫性疾病,其特征为多系统受累,包括神经系统。在本研究中,我们旨在评估伊朗青少年起病的系统性红斑狼疮(JSLE)的神经精神表现。
对在我们儿科风湿病数据库中登记的146例儿科起病的SLE患者在2013年至2015年期间进行前瞻性和横断面评估。从该数据库中提取包括性别、年龄、诊断时年龄、研究时年龄、体格检查、实验室检查以及神经精神量表等数据。神经精神性JSLE的分类依据1999年美国风湿病学会(ACR)关于SLE神经精神表现的病例定义。
共选取了41例有神经精神症状的患者。患者的平均年龄为12.2岁。最常见的神经精神症状为癫痫发作、偏头痛和抑郁。症状出现的平均年龄为10.2±3岁。平均随访期为57±34(范围:12 - 120)个月。在41例SLE患者中,18例(43.9%)在诊断时出现症状。13例(31.7%)患者在SLE诊断后1年以上出现神经症状。头痛是最常见的特征(13%),其次是癫痫发作(9.5%)和舞蹈症(3.4%)。其他神经表现包括脑神经受累(0.7%)、意识丧失(2.7%)和深部腱反射减退性神经病变(2.5%)。最不常见的神经精神性JSLE表现为无菌性脑膜炎,仅1例患者出现(0.7%)。
JSLE患者出现头痛、情绪障碍、精神病、抑郁及其他神经心理表现时,应促使对原发性神经系统受累的诊断进行调查,以降低死亡率和发病率。