Department of Psychiatry, Université Pierre et Marie Curie and Saint-Antoine Hospital, Paris, France. charles.peretti @ sat.aphp.fr
Psychother Psychosom. 2012;81(5):276-85. doi: 10.1159/000336555. Epub 2012 Jul 20.
Systemic lupus erythematosus (SLE) is known to induce psychiatric disorders, from psychoses to maladaptive coping. Brain autoantibodies were proposed to explain SLE neuropsychiatric disorders and found to be elevated before the onset of clinical symptoms. We assessed cognition in Caucasian SLE women with elevated autoantibodies without overt neuropsychiatric syndromes, in conjunction with single photon emission computerized tomography (SPECT).
31 women meeting SLE criteria of the American College of Rheumatology (ACR) were included. Patients who met the ACR neuropsychiatric definition were excluded. Matched controls were 23 healthy women from the Champagne-Ardenne region, France. Participants completed neuropsychological and autoantibodies measurements, and 19 completed SPECT.
61% (19/31) of women with SLE and 53% (9/17) of those with normal SPECT had significant global cognitive impairment defined as 4 T-scores <40 in cognitive tests, compared to 0% (0/23) of controls. SLE women also had significantly greater cognitive dysfunction (mean T-score) on the Wechsler Adult Intelligence Scale (WAIS) visual backspan, Trail Making Test A and B, WAIS Digit Symbol Substitution Test and Stroop Interference, compared to controls. Elevated antinuclear antibody correlated with impairment in the WAIS visual span, WAIS visual backspan, and cancellation task; elevated anti-double-stranded DNA antibody and anticardiolipin correlated respectively with impairment in the Trail Making Test A and WAIS auditive backspan. Two SLE women had abnormal SPECT.
A high prevalence of cognitive deficits was found in Caucasian SLE women compared to normal women, which included impairment in cognitive domains important for daily activities. Elevated autoantibodies tended to correlate with cognitive dysfunction.
系统性红斑狼疮(SLE)已知可引起精神疾病,从精神病到适应不良的应对方式。脑自身抗体被提出用于解释 SLE 神经精神障碍,并在出现临床症状之前发现升高。我们评估了患有自身抗体升高但无明显神经精神综合征的白种人 SLE 女性的认知能力,并结合单光子发射计算机断层扫描(SPECT)进行评估。
共纳入 31 名符合美国风湿病学会(ACR)SLE 标准的女性患者。排除符合 ACR 神经精神定义的患者。匹配的对照组为来自法国香槟-阿登地区的 23 名健康女性。参与者完成了神经心理学和自身抗体测量,其中 19 人完成了 SPECT。
61%(19/31)的 SLE 女性和 53%(9/17)的 SPECT 正常女性存在显著的整体认知障碍,定义为认知测试中 4 个 T 评分<40,而对照组为 0%(0/23)。SLE 女性在威斯康星卡片分类测试、连线测试 A 和 B、威斯康星数字符号替代测试和斯特鲁普干扰测试中的认知功能障碍也明显更严重。抗核抗体升高与威斯康星卡片分类测试的视觉跨度、威斯康星视觉回溯测试和取消任务的损伤相关;抗双链 DNA 抗体和抗心磷脂抗体升高分别与连线测试 A 和威斯康星听觉回溯测试的损伤相关。两名 SLE 女性的 SPECT 异常。
与正常女性相比,白种人 SLE 女性中发现了较高的认知缺陷患病率,包括对日常活动重要的认知领域的损伤。升高的自身抗体往往与认知功能障碍相关。