Glucocorticoid toxicity index in patients with systemic lupus erythematosus (preliminary data)

E. V. Ermolaeva, E. Aseeva, N. Nikishina, T. Popkova, A. Lila
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Abstract

Objective: to investigate the contribution of glucocorticoids (GC) to the development of irreversible organ damage in patients with systemic lupus erythematosus (SLE) using the GC toxicity index (GTI).Material and methods. The study included 65 patients with SLE who met the 2012 SLICC classification criteria. GTI, disease activity according to the SLEDAI-2K index and the SLICC damage index (DI) were determined in all patients, and standard laboratory and immunological tests were performed.Results and discussion. Patients were predominantly female (n=56, 86%), median disease duration was 76 [2; 288] months, SLEDAI-2K – 8.8 [0; 26], DI SLICC – 1.0 [0; 5], DI SLICC >0 was found in 28 (43%) patients. The median duration of GC therapy during the disease period was 66.0 [0; 288] months, maximum dose of GC – 32.7 [0; 80] mg, median of total GC dose during intravenous administration was 2942 [0; 17 812.5] mg, GTI at the time of enrolment in the study – 19 [0; 37] points. GTI >0 was present in 47 (72%) of 65 patients. GTI correlated with disease duration (r=0.33; p<0.008); maximum dose of oral GCs (r=0.31; p><0.012); duration of GC use (r=0.35; p><0.005); DI SLICC (r=-0.43; p><0.0001). In patients with an average disease duration of more than 3 years, GTI>˂0.008); maximum dose of oral GCs (r=0.31; p˂0.012); duration of GC use (r=0.35; p˂0.005); DI SLICC (r=-0.43; p˂0.0001). In patients with an average disease duration of more than 3 years, GTI was significantly higher than in patients with a disease duration of 1–3 years (p=0.023).Conclusion. An GTI>0 was found in 72% of SLE patients, which increased significantly with disease duration. The GTI value was influenced by the duration of SLE, the duration of GC treatment and the maximum GC dose during the disease period. A statistically significant correlation was found between the GTI and the SLICC DI, allowing the GTI value to be used as an additional component in the assessment of the contribution of GCs to the development of irreversible organ damage in patients with SLE. It is recommended that GTI is assessed in all patients with SLE receiving long-term GC treatment for the purpose of dose adjustment.
系统性红斑狼疮患者的糖皮质激素毒性指数(初步数据)
目的:使用糖皮质激素毒性指数(GTI)研究糖皮质激素(GC)对系统性红斑狼疮(SLE)患者发生不可逆器官损害的贡献。研究纳入了 65 名符合 2012 SLICC 分类标准的系统性红斑狼疮患者。所有患者的GTI、SLEDAI-2K指数和SLICC损害指数(DI)均已确定,并进行了标准实验室和免疫学检测。患者主要为女性(n=56,86%),中位病程为 76 [2; 288] 个月,SLEDAI-2K - 8.8 [0; 26],SLICC DI - 1.0 [0; 5],28 例(43%)患者的 SLICC DI >0。疾病期间接受 GC 治疗的中位时间为 66.0 [0; 288] 个月,GC 最大剂量为 32.7 [0; 80] 毫克,静脉注射 GC 总剂量的中位数为 2942 [0; 17 812.5] 毫克,加入研究时的 GTI 为 19 [0; 37] 分。65 名患者中有 47 人(72%)的 GTI >0。GTI 与病程(r=0.33;p˂0.008)、口服 GCs 最大剂量(r=0.31;p˂0.012)、GCs 使用时间(r=0.35;p˂0.005)、DI SLICC(r=-0.43;p˂0.0001)相关。在平均病程超过 3 年的患者中,GTI 明显高于病程在 1-3 年的患者(p=0.023)。72%的系统性红斑狼疮患者的GTI>0,且随病程的延长而显著增加。GTI值受系统性红斑狼疮病程、GC治疗时间和病程中最大GC剂量的影响。在统计学上发现,GTI 与 SLICC DI 之间存在明显的相关性,因此在评估 GC 对系统性红斑狼疮患者不可逆器官损伤的发展所起的作用时,可将 GTI 值作为一个额外的组成部分。建议对所有长期接受 GC 治疗的系统性红斑狼疮患者进行 GTI 评估,以便调整剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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