Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore.
Rheumatology (Oxford). 2020 Sep 1;59(9):2534-2543. doi: 10.1093/rheumatology/keaa002.
The impact of glucocorticoids on neurocognitive performance in patients with SLE is not fully addressed. We aimed to study the effect of daily and cumulative glucocorticoid dose on neurocognitive performance in SLE patients.
Consecutive SLE patients and gender- and age-matched healthy controls (HCs) underwent the computer-based Automated Neuropsychological Assessment Matric (ANAM), which evaluates eight neurocognitive domains including learning, recall, visual perception, mental rotation, short-term memory, attention, sustained attention and working memory. The total and individual-domain throughput scores (TPSs) and the presence of cognitive dysfunction (total TPS <1.5 s.d. below the mean TPS of HCs) were compared between SLE patients and HCs. Within the SLE group, univariate and independent associations between prednisolone dose (daily and cumulative) and individual-domain TPS were studied by univariate and multivariable linear regression, respectively.
A total of 96 SLE patients and 96 HCs were studied. SLE patients scored significantly worse across all the neurocognitive domains and had a significantly lower mean total TPS (P < 0.001) and a higher prevalence of cognitive dysfunction compared with HCs (25.0 vs 7.3%, P = 0.001). In SLE patients, daily prednisolone dose was significantly and negatively correlated with mathematical-processing TPS, which probes working memory (P = 0.018). No significant correlation between cumulative prednisolone dose and any of the individual-domain TPSs was found. In multivariable regression, higher daily prednisolone dose and doses >9 mg daily remained independently associated with lower mathematical-processing TPSs (P = 0.031).
Daily prednisolone dose ≥9 mg, but not cumulative glucocorticoid dose, had an independent negative impact on mathematical processing in SLE patients.
糖皮质激素对系统性红斑狼疮(SLE)患者神经认知功能的影响尚未完全阐明。本研究旨在探讨SLE 患者的日剂量和累积剂量糖皮质激素与神经认知功能的关系。
连续纳入 SLE 患者和性别、年龄匹配的健康对照者(HCs),采用计算机化自动化神经心理评估矩阵(ANAM)进行检测,该测试评估 8 个神经认知领域,包括学习、回忆、视觉感知、心理旋转、短期记忆、注意力、持续注意力和工作记忆。比较 SLE 患者与 HCs 的总测试和各领域测试通过率(TPS)以及认知功能障碍的发生情况(总 TPS 低于 HCs 均值的 1.5 个标准差)。在 SLE 组中,通过单变量和多变量线性回归分别研究泼尼松龙剂量(日剂量和累积剂量)与各领域 TPS 的单变量和独立关联。
共纳入 96 例 SLE 患者和 96 例 HCs。与 HCs 相比,SLE 患者在所有神经认知领域的评分均显著降低,总 TPS 明显较低(P<0.001),且认知功能障碍的发生率更高(25.0% vs 7.3%,P=0.001)。SLE 患者的日泼尼松龙剂量与数学处理 TPS 显著负相关,而后者反映工作记忆(P=0.018)。未发现累积泼尼松龙剂量与任何领域 TPS 之间存在显著相关性。多变量回归分析显示,较高的日泼尼松龙剂量和剂量>9mg/d 与较低的数学处理 TPS 独立相关(P=0.031)。
SLE 患者日剂量≥9mg 的泼尼松龙,但不是累积糖皮质激素剂量,与数学处理能力下降有独立的负面影响。