青少年始发系统性红斑狼疮的神经精神参与。

IF 1.7 Q4 NEUROSCIENCES Neurology Research International Pub Date : 2018-05-29 eCollection Date: 2018-01-01 DOI:10.1155/2018/2548142
Mohammad-Amin Khajezadeh, Gholamreza Zamani, Bobak Moazzami, Zahra Nagahi, Mahdie Mousavi-Torshizi, Vahid Ziaee
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引用次数: 26

摘要

目的:系统性红斑狼疮(SLE)是一种复杂的自身免疫性疾病,以包括神经系统在内的多系统受累为特征。在本研究中,我们旨在评估伊朗青少年发病的系统性红斑狼疮(JSLE)的神经精神表现。方法:对2013-2015年在我们的儿童风湿病数据库中登记的146例小儿起病SLE患者进行前瞻性和横断面评估。数据包括性别、年龄、诊断时年龄、研究时年龄、体格检查、实验室检查和神经精神量表。JSLE的神经精神分类依据1999年美国风湿病学会(ACR)对SLE病例的神经精神表现定义。结果:共选入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是癫痫发作、偏头痛和抑郁。平均发病年龄为10.2±3岁。平均随访57±34个月(范围:12 ~ 120个月)。41例SLE患者中,18例(43.9)在诊断时出现症状。在13例(31.7%)患者中,神经系统症状在SLE诊断后超过1年才出现。头痛是最常见的特征(13%),其次是癫痫发作(9.5%)和舞蹈病(3.4%)。其他神经学表现包括颅神经受累(0.7%)、意识丧失(2.7%)和深肌腱反射神经病受损(2.5%)。JSLE最不常见的神经精神表现是无菌性脑膜炎,仅见于1例患者(0.7%)。结论:JSLE患者出现头痛、情绪障碍、精神病、抑郁和其他神经心理表现时,应及时检查原发神经系统受累的诊断,以降低死亡率和发病率。
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Neuropsychiatric Involvement in Juvenile-Onset Systemic Lupus Erythematosus.

Objective: 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.

Methods: 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.

Result: 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%).

Conclusion: 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.

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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
10
审稿时长
17 weeks
期刊介绍: Neurology Research International is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies focusing on diseases of the nervous system, as well as normal neurological functioning. The journal will consider basic, translational, and clinical research, including animal models and clinical trials.
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