Division of Rheumatology, Department of Medicine and Pathology, Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada
Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.
Lupus Sci Med. 2022 Jun;9(1). doi: 10.1136/lupus-2022-000668.
Cognitive impairment is common in patients with SLE but the cause is unknown. The current cross-sectional study examined the association between select SLE-related autoantibodies, other serological biomarkers and extensive blood-brain barrier (BBB) leakage in patients with SLE with and without cognitive impairment. In addition, we determined whether the relationship between SLE autoantibodies, other biomarkers and cognitive impairment differed depending on the presence or absence of concurrent extensive BBB leakage.
Consecutive patients with SLE, recruited from a single academic medical centre, underwent formal neuropsychological testing for assessment of cognitive function. On the same day, BBB permeability was determined using dynamic contrast-enhanced MRI scanning. SLE autoantibodies and other serological biomarkers were measured. Regression modelling was used to determine the association between cognitive impairment, extensive BBB leakage and autoantibodies/biomarkers.
There were 102 patients with SLE; 90% were female and 88% were Caucasian, with a mean±SD age of 48.9±13.8 years. The mean±SD SLE disease duration was 14.8±11.0 years. Impairment in one or more cognitive tests was present in 47 of 101 (47%) patients and included deficits in information processing speed (9%), attention span (21%), new learning (8%), delayed recall (15%) and executive abilities (21%). Extensive BBB leakage was present in 20 of 79 (25%) patients and was associated with cognitive impairment (15 of 20 (75%) vs 24 of 59 (41%); p=0.01) and shorter disease duration (median (IQR): 7 (8-24 years) vs 15 (2-16 years); p=0.02). No serological parameters were associated with extensive BBB leakage and there was no statistically significant association between cognitive impairment and circulating autoantibodies even after adjusting for BBB leakage.
Extensive BBB leakage alone was associated with cognitive impairment. These findings suggest that BBB leakage is an important contributor to cognitive impairment, regardless of circulating SLE-related autoantibodies.
认知障碍在系统性红斑狼疮(SLE)患者中很常见,但病因尚不清楚。本横断面研究旨在探讨 SLE 相关自身抗体、其他血清学生物标志物与 SLE 患者伴或不伴认知障碍的广泛血脑屏障(BBB)渗漏之间的关系。此外,我们还确定了 SLE 自身抗体、其他生物标志物与认知障碍之间的关系是否因同时存在广泛 BBB 渗漏而有所不同。
连续招募来自单一学术医疗中心的 SLE 患者,进行正式的神经心理学测试以评估认知功能。同日,通过动态对比增强 MRI 扫描确定 BBB 通透性。测量 SLE 自身抗体和其他血清学生物标志物。回归模型用于确定认知障碍、广泛 BBB 渗漏与自身抗体/生物标志物之间的关系。
共有 102 例 SLE 患者;90%为女性,88%为白种人,平均年龄(±标准差)为 48.9±13.8 岁。平均(±标准差)SLE 病程为 14.8±11.0 年。101 例患者中有 47 例(47%)存在一项或多项认知测试受损,包括信息处理速度受损(9%)、注意力持续时间受损(21%)、新学习受损(8%)、延迟回忆受损(15%)和执行能力受损(21%)。79 例患者中有 20 例(25%)存在广泛 BBB 渗漏,与认知障碍(20 例中的 15 例(75%)与 59 例中的 24 例(41%);p=0.01)和较短的病程(中位数(IQR):7(8-24 年)与 15(2-16 年);p=0.02)相关。没有血清学参数与广泛 BBB 渗漏相关,即使在调整 BBB 渗漏后,认知障碍与循环自身抗体之间也没有统计学显著关联。
单独广泛 BBB 渗漏与认知障碍有关。这些发现表明,无论是否存在循环性 SLE 相关自身抗体,BBB 渗漏都是认知障碍的一个重要原因。