Danza Alvaro, Graña Diego, Soto Evelyn, Silveira Gonzalo, Carlomagno Adriana, Rebella Martín
Facultad de Medicina, Clínica Médica, Hospital Pasteur, 56724Universidad de la República, Montevideo, Uruguay.
Autoimmune Disease Unit, Médica Uruguaya Corporación de Asistencia Médica (MUCAM), Montevideo, Uruguay.
Lupus. 2022 Jun;31(7):880-884. doi: 10.1177/09612033221093485. Epub 2022 Mar 30.
We aimed to study the daily dose of glucocorticoids in the first month associated with damage after 5 years of systemic lupus erythematosus (SLE) diagnosis; and to assess the daily dose of prednisone during the first year, over which damage after 5 years could be predicted.
A retrospective cohort study of SLE patients from the diagnosis and up to 5 years of follow-up was performed. Cumulative prednisone doses in the first month (T1m), at 1 year (T12m), and at 5 years (T5y) were calculated. Damage was estimated using the SLICC index and activity by the SLEDAI-2K. Damage at T5y was categorized as "present" or "absent". To determine the cutoff point of prednisone dose for the first month and for the first year of treatment, related to damage at 5 years, a ROC curve was done. A logistic regression was performed to control damage at 5 years by the activity levels, anti-DNA titers, and the corticosteroid burden between 1 and 5 years.
Forty-eight patients were included with a mean age of 42.4 (12.6) years; 46 (95.8%) were female. The cumulative dose in T1m associated with greater sensitivity and specificity in the ROC curve (1.54; AUC 0.793; 95% CI: 0.66-0.92) to predict glucocorticoid-related damage at 5 years of follow-up was 980mg, which leads to a daily dose for the first month of 32.6 mg/day. The daily dose during the first year associated with damage at 5 years, allowed to calculate an optimal cutoff point of 7.38 mg/day, with a sensitivity of 92.9% (AUC 0.695, 95% CI: 0.52-0.86) to predict damage at 5 years. In the logistic regression, this estimate was maintained, controlling for SLEDAI-2K and for positivity or not of anti-DNA antibodies and for the cumulative dose of prednisone between T5y and T12m.
This pilot study allows to estimate a threshold dose of 32.6 mg/day during the first month and 7.38 mg/day during the first year, over which the risk of permanent damage is high at 5 years, regardless of the activity levels and the glucocorticoid doses considered between the first and the fifth year of follow-up.
我们旨在研究系统性红斑狼疮(SLE)诊断5年后,第一个月糖皮质激素的每日剂量与损伤之间的关系;并评估第一年泼尼松的每日剂量,超过此剂量可预测5年后的损伤情况。
对SLE患者进行了一项回顾性队列研究,从诊断开始直至随访5年。计算了第一个月(T1m)、1年(T12m)和5年(T5y)时的泼尼松累积剂量。使用SLICC指数评估损伤情况,用SLEDAI-2K评估疾病活动度。将T5y时的损伤分为“存在”或“不存在”。为确定与5年后损伤相关的第一个月和第一年治疗的泼尼松剂量的截断点,绘制了ROC曲线。进行了逻辑回归分析,以控制5年时的损伤情况,考虑因素包括活动水平、抗DNA滴度以及1至5年期间的皮质类固醇负荷。
纳入了48例患者,平均年龄为42.4(12.6)岁;46例(95.8%)为女性。在ROC曲线中,与预测随访5年时糖皮质激素相关损伤具有更高敏感性和特异性(1.54;AUC 0.793;95% CI:0.66 - 0.92)的T1m累积剂量为980mg,这导致第一个月的每日剂量为32.6mg/天。与5年后损伤相关的第一年每日剂量,计算出的最佳截断点为7.38mg/天,预测5年后损伤的敏感性为92.9%(AUC 0.695,95% CI:0.52 - 0.86)。在逻辑回归分析中,在控制SLEDAI-2K、抗DNA抗体是否阳性以及T5y和T12m之间泼尼松的累积剂量后,该估计值保持不变。
这项初步研究能够估计出第一个月的阈值剂量为32.6mg/天,第一年为7.38mg/天,超过此剂量,无论随访的第一年至第五年期间的活动水平和糖皮质激素剂量如何,5年后发生永久性损伤的风险都很高。