Maciel Ricardo Oliveira Horta, Ferreira Gilda Aparecida, Akemy Bárbara, Cardoso Francisco
Movement Disorders Clinic, Department of Neurology, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Rheumatology Clinic, Department of Locomotor System, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
J Neurol Sci. 2016 Jan 15;360:94-7. doi: 10.1016/j.jns.2015.11.052. Epub 2015 Nov 27.
Chorea is well described in a group of patients with Systemic Lupus Erythematosus (SLE). There is less information, however, on other movement disorders as well as non-motor neuropsychiatric features such as obsessive-compulsive symptoms (OCS), executive dysfunction and attention deficit and hyperactivity disorder (ADHD) in subjects with SLE.
Fifty-four subjects with SLE underwent a battery of neuropsychiatric tests that included the Mini Mental State Examination, the Montreal Cognitive Assessment, the Frontal Assessment Battery (FAB), the FAS verbal and the categorical (animals) semantic fluency tests, the Obsessive and Compulsive Inventory - Revised, the Yale-Brown Obsessive and Compulsive Scale and Beck's Anxiety and Depression Scales. ADHD was diagnosed according to DSM-IV criteria. SLE disease activity and cumulative damage were evaluated according to the modified SLE Disease Activity Index 2000 (mSLEDAI-2K) and the SLICC/ACR, respectively.
Six (11.1%) and 33 (61.1%) patients had cognitive impairment according to the MMSE and MoCA, respectively. Eleven (20.4%) had abnormal FAB scores, and 5 (9.3%) had lower semantic fluency scores than expected. The overall frequency of cognitive dysfunction was 72.2% (39 patients) and of neuropsychiatric SLE was 77.8% (42 patients). Two patients (3.7%) had movement disorders. Fifteen (27.8%) had OCS and 17 (31.5%) met diagnostic criteria for ADHD. ADHD and OCS correlated with higher disease activity, p=0.003 and 0.006, respectively. Higher cumulative damage correlated with lower FAB scores (p 0.026).
Executive dysfunction, ADHD, OCS, and movement disorders are common in SLE. Our finding suggests that there is frequent basal ganglia dysfunction in SLE.
系统性红斑狼疮(SLE)患者群体中对舞蹈症已有充分描述。然而,关于SLE患者的其他运动障碍以及非运动性神经精神特征,如强迫症状(OCS)、执行功能障碍和注意力缺陷多动障碍(ADHD)的信息较少。
54名SLE患者接受了一系列神经精神测试,包括简易精神状态检查、蒙特利尔认知评估、额叶评估量表(FAB)、FAS言语和分类(动物)语义流畅性测试、修订版强迫观念及强迫行为量表、耶鲁-布朗强迫量表以及贝克焦虑和抑郁量表。ADHD根据《精神疾病诊断与统计手册》第四版(DSM-IV)标准进行诊断。SLE疾病活动度和累积损伤分别根据改良的2000年SLE疾病活动指数(mSLEDAI-2K)和系统性红斑狼疮国际协作临床/美国风湿病学会(SLICC/ACR)进行评估。
根据简易精神状态检查表(MMSE)和蒙特利尔认知评估量表(MoCA),分别有6名(11.1%)和33名(61.1%)患者存在认知障碍。11名(20.4%)患者FAB评分异常,5名(9.3%)患者语义流畅性得分低于预期。认知功能障碍的总体发生率为72.2%(39名患者),神经精神性SLE的发生率为77.8%(42名患者)。2名患者(3.7%)有运动障碍。15名(27.8%)患者有OCS,17名(31.5%)符合ADHD诊断标准。ADHD和OCS分别与更高的疾病活动度相关,p值分别为0.003和0.006。更高的累积损伤与更低的FAB评分相关(p = 0.026)。
执行功能障碍、ADHD、OCS和运动障碍在SLE中很常见。我们的研究结果表明,SLE中基底神经节功能障碍很常见。