评估系统性红斑狼疮的神经系统表现

Ahmed Abdalrazak Rasheed Al Dulaimy, Ghayath Abd Ali Shalal Al Dulaimy, Sadiq Mahdi Hussein Al Dulaimy
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All patients' demographic and clinical data, including age, gender, disease duration, type and duration of treatment, general signs of the disease, and neurological and psychiatric manifestations of SLE, were collected. Laboratory data comprised plasma anti-phospholipid antibodies (aPL), anti-double stranded DNA (anti-dsDNA), erythrocyte sedimentation rate (ESR), and C-reactive protein (CRP). The cognitive dysfunction was assessed using the six-item cognitive impairment test (6CIT).\nResults: Out of 65 patients, 34 (52.3%) were found to have at least one neuropsychiatric SLE (NPSLE) manifestation. Headache and depression were the most common NPSLE manifestation encountered in 36 patients (55.4%) followed by psychosis (21.5%), neuropathy (16.9%) and stroke and seizure (13.5%). 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引用次数: 0

摘要

摘要背景:神经精神症状是系统性红斑狼疮(SLE)患者的典型症状。目的:确定系统性红斑狼疮患者神经系统表现的发生率及其相关风险:这是一项病例系列研究,由 2022 年 1 月至 2023 年 2 月期间在巴格达教学医院/医疗城风湿病科就诊的 65 名患者组成。研究人员收集了所有患者的人口统计学和临床数据,包括年龄、性别、病程、治疗类型和持续时间、疾病的一般体征以及系统性红斑狼疮的神经和精神表现。实验室数据包括血浆抗磷脂抗体(aPL)、抗双链DNA(anti-dsDNA)、红细胞沉降率(ESR)和C反应蛋白(CRP)。认知功能障碍采用六项认知功能障碍测试(6CIT)进行评估:在65名患者中,34人(52.3%)至少有一种神经精神系统性红斑狼疮(NPSLE)表现。头痛和抑郁是36名患者(55.4%)最常见的NPSLE表现,其次是精神病(21.5%)、神经病变(16.9%)以及中风和癫痫发作(13.5%)。在多变量分析中,年龄大于 35 岁(OR= 2.92,95%CI= 1.12-34.2,p= 0.10)、病程大于 5 年(4.45,95%CI= 1.23-28.43,p= 0.001)、抗磷脂抗体(OR= 4.22,95%CI= 1.17-89.38,p= 0.036)、精神错乱(21.5%)、神经病(16.9%)、中风和癫痫发作(13.5%)各占一半。38,p= 0.036)、狼疮性肾炎(OR= 6.34,95%CI= 1.27- 64.98,p= 0.029)和 6CIT>3(OR= 5.83,95%CI= 1.55- 21.87,p= 0.009)是系统性红斑狼疮患者非系统性红斑狼疮的独立预测因素:结论:在所研究的系统性红斑狼疮病例中,半数以上在病程长达六年的时间内出现了神经精神症状。头痛和抑郁、精神病和神经病是最常见的非系统性红斑狼疮表现。高龄和病程较长是非系统性红斑狼疮发病的危险因素。在临床上,抗磷脂抗体、狼疮肾炎和六项认知障碍测试的高分(>8分)是非系统性红斑狼疮的预测因素:接收:2023年5月接受:2023年9月发表接受:2023年9月发表:2024年1月发表于:2024年1月
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Evaluation of Neurological Manifestations of Systemic Lupus Erythematosus
  Abstract Background: Neuropsychiatric symptoms are typical consequences in patients with systemic lupus erythematosus (SLE). There is no apparent link between the clinical parameters of SLE patients and the development of neuropsychiatric symptoms. Objectives: to determine the incidence of neurological manifestations and the risks associated with them in SLE patients. Patients and Methods: This is a case-series study comprised 65 patients who visited the rheumatology Department at Baghdad Teaching Hospital/Medical City between January 2022 and February 2023. All patients' demographic and clinical data, including age, gender, disease duration, type and duration of treatment, general signs of the disease, and neurological and psychiatric manifestations of SLE, were collected. Laboratory data comprised plasma anti-phospholipid antibodies (aPL), anti-double stranded DNA (anti-dsDNA), erythrocyte sedimentation rate (ESR), and C-reactive protein (CRP). The cognitive dysfunction was assessed using the six-item cognitive impairment test (6CIT). Results: Out of 65 patients, 34 (52.3%) were found to have at least one neuropsychiatric SLE (NPSLE) manifestation. Headache and depression were the most common NPSLE manifestation encountered in 36 patients (55.4%) followed by psychosis (21.5%), neuropathy (16.9%) and stroke and seizure (13.5%). In multivariate analysis, each of age >35 years (OR= 2.92, 95%CI= 1.12-34.2, p= 0.10), disease duration >5 years (4.45, 95%CI=1.23-28.43, p= 0.001), anti-phospholipid Abs (OR= 4.22, 95%CI= 1.17-89.38, p= 0.036), lupus nephritis (OR= 6.34, 95%CI= 1.27- 64.98, p= 0.029) and 6CIT>3 (OR= 5.83, 95%CI= 1.55- 21.87, p= 0.009) are independent predictors for NPSLE in patients with SLE. Conclusions: Neuropsychiatric manifestations developed in more than half of the SLE cases studied within up to six-year of disease duration. Headache and depression, psychosis and neuropathy are the most common NPSLE manifestations. Older age and longer disease duration are risk factors for development of NPSLE. Clinically, anti-phospholipid antibodies, lupus nephritis and a high score of the six-item cognitive impairment test (>8) are predictors for NPSLE. Received: May, 2023 Accepted: Sept., 2023 Published: Jan., 2024  
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