Coín M A, Vilar-López R, Peralta-Ramírez I, Hidalgo-Ruzzante N, Callejas-Rubio J L, Ortego-Centeno N, Pérez-García M
Facultad de Psicología, Universidad de Jaén, Spain.
Facultad de Psicología, Universidad de Granada, Spain Centro de Investigación Mente, Cerebro y Comportamiento (CIMCYC), Universidad de Granada, Spain
Lupus. 2015 Jul;24(8):875-9. doi: 10.1177/0961203315572717. Epub 2015 Feb 18.
To analyze the role of the antiphospholipid autoantibodies (aPL) on the neuropsychological deficits in systemic lupus erythematosus (SLE) patients, comparing groups of patients with antiphospholipid syndrome (APS; n = 15), SLE with aPL (n = 12), and SLE without aPL (n = 27), and a healthy control group (n = 31).
Patients fulfilled the American College of Rheumatology SLE classification criteria or the Sydney criteria for APS. All participants were woman, and groups were matched on age and education. A standardized cognitive examination classified patients as cognitively declined or impaired according to the American College of Rheumatology.
Differences between the groups were found in all of the studied variables, comprising attention and executive functions (sustained and selective attention, fluency, and inhibition), and memory (verbal and visual). Post-hoc analyses showed cognitive performance was equivalent between APS and SLE with aPL. Differences between SLE without aPL and control groups were found only in four of the 10 studied variables, while differences in all but two memory variables were found between SLE without aPL and control groups. Furthermore, cognitive deficit was three times more frequent in APS and SLE with aPL patients than for the control group (80%, 75%, and 16%, respectively), and two times more frequent compared to SLE patients without aPL (48%).
Our results support the relationship between aPL and cognitive symptoms in SLE. Also, almost half of the patients with SLE and no aPL showed cognitive problems, pointing to the multifactorial causes of cognitive problems in SLE. Future research with larger sample size is guaranteed to replicate our results.
分析抗磷脂自身抗体(aPL)在系统性红斑狼疮(SLE)患者神经心理缺陷中的作用,比较抗磷脂综合征(APS;n = 15)、伴有aPL的SLE(n = 12)、不伴有aPL的SLE(n = 27)患者组以及健康对照组(n = 31)。
患者符合美国风湿病学会SLE分类标准或APS的悉尼标准。所有参与者均为女性,各患者组在年龄和教育程度上相匹配。一项标准化认知检查根据美国风湿病学会的标准将患者分类为认知功能下降或受损。
在所有研究变量中发现了组间差异,包括注意力和执行功能(持续和选择性注意力、流畅性及抑制能力)以及记忆力(言语和视觉)。事后分析表明,APS组和伴有aPL的SLE组的认知表现相当。不伴有aPL的SLE组与对照组之间仅在10个研究变量中的4个变量上存在差异,而不伴有aPL的SLE组与对照组之间除两个记忆变量外的所有变量均存在差异。此外,APS组和伴有aPL的SLE患者的认知缺陷发生率是对照组的三倍(分别为80%、75% 和16%),是不伴有aPL的SLE患者的两倍(48%)。
我们的结果支持aPL与SLE认知症状之间的关系。此外,几乎一半不伴有aPL的SLE患者存在认知问题,这表明SLE认知问题存在多因素病因。未来有必要进行更大样本量的研究以重复我们的结果。