在开始使用贝利木单抗的同时增加每日泼尼松龙用量,可有效快速减少糖皮质激素用量:一项为期96周的回顾性研究

IF 1.9 4区 医学 Q3 RHEUMATOLOGY
Lupus Pub Date : 2024-05-01 Epub Date: 2024-03-21 DOI:10.1177/09612033241240859
Takashi Yamane, Akira Hashiramoto
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引用次数: 0

摘要

目的:为了适当减少糖皮质激素(GC),我们研究了包括基线因素在内的最佳策略:为了适当减少糖皮质激素(GC),我们研究了最佳策略,包括使用贝利木单抗96周后可将GC减少50%以上的基线因素:这是加古川市中央医院在2019年至2023年进行的一项回顾性队列研究。我们确定了每周皮下注射 200 毫克贝利木单抗并持续 96 周的系统性红斑狼疮患者。我们对基线背景、临床指标的变化趋势以及GC降低的相关因素进行了统计分析。最后,进行了单变量和多变量逻辑分析,以确定与96周时GC下降≥50%相关的基线因素:47名患者入组,中位每日泼尼松龙为5毫克。其中近90%的患者同时服用免疫抑制剂和/或羟氯喹。血清学指标、每日 GC 剂量和 SLEDAI-2K 评分在 96 周内均有显著改善。基线时,GC 的日剂量与发病或最后一次复发的持续时间以及 C4 水平之间存在明显的负相关。在96周时,GC减少率和SLEDAI-2K评分与从发病或最后一次复发到开始使用贝利木单抗的持续时间呈负相关。狼疮肾炎(LN)患者使用霉酚酸酯(Mycophenolate mofetil)的频率很高,这也与既往复发的频率有关。此外,LN的存在与96周时较高的SLEDAI-2K评分有关,基线SLEDAI-2K≥10与96周时较高的GC剂量有关。对96周时实现GC减少≥50%的因素进行的单变量分析表明,较短的病程和基线较高的每日GC剂量是重要的变量。最后,我们将上述两项与年龄结合起来进行了多变量分析,结果发现基线时每日 GC 剂量较高是一个重要变量(OR (95% CI) 1.25 (1.00 to 1.56),p = .047):我们的研究表明,延迟开始使用贝利木单抗会导致SLEDAI-2K评分升高,并且难以在96周时实现GC减少50%的目标。由于GC相关不良事件会随着长期服用GC(尽管每日剂量较小)而增加,因此我们在此建议,开始服用贝利木单抗时应与每日较高剂量的泼尼松龙联合使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Initiation of belimumab with higher daily prednisolone is effective for rapid glucocorticoid reduction: A 96-week retrospective study.

Objectives: For appropriate glucocorticoid (GC) reduction, we investigated the optimal strategy including baseline factors that could reduce GC more than 50% with 96 weeks of belimumab.

Methods: This is a retrospective cohort study of Kakogawa Central City hospital from 2019 to 2023. We identified SLE patients who were receiving 200 mg of belimumab weekly by subcutaneous injection for 96 weeks. The background at baseline, trends in clinical indicators, and factors involved in GC reduction were statistically analyzed. Finally, univariate and multivariate logistic analyses were carried out to identify baseline factors associated ≥50% GC reduction at 96 weeks.

Results: Forty-seven patients were enrolled, with a median daily prednisolone of 5 mg. Almost 90% of them received concomitant immunosuppressants and/or hydroxychloroquine. Serological indices, daily GC dose, and SLEDAI-2K scores showed significant improvement in 96 weeks. At baseline, a significant negative correlation has been shown between the daily dose of GC and the duration from onset or last flare, as well as C4 levels. At 96 weeks, GC reduction rate and SLEDAI-2K scores were negatively correlated with duration from onset or last flare to initiation of belimumab. Mycophenolate mofetil use was significantly frequent in patients with lupus nephritis (LN), which also correlated with the frequency of past flares. In addition, LN presence was associated with higher SLEDAI-2K scores at 96 weeks, and baseline SLEDAI-2K ≥10 was associated with significantly higher GC dose at 96 weeks. Univariate analysis of the factor contributing to achieving ≥50% GC reduction at 96 weeks has pointed shorter disease duration and higher daily GC dose at baseline as significant variables. Finally, we performed a multivariate analysis by combining above two items with age, which extracted the higher daily GC dose at baseline as a significant variable (OR (95% CI) 1.25 (1.00 to 1.56), p = .047).

Conclusions: Our study showed that a delay in belimumab initiation led to higher SLEDAI-2K score and difficulty in achieving a 50% GC reduction at 96 weeks. Since GC-related adverse events increase with long-term administration of GC though with small daily doses, we proposed here that belimumab should be started in combination with higher daily prednisolone.

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来源期刊
Lupus
Lupus 医学-风湿病学
CiteScore
4.20
自引率
11.50%
发文量
225
审稿时长
1 months
期刊介绍: The only fully peer reviewed international journal devoted exclusively to lupus (and related disease) research. Lupus includes the most promising new clinical and laboratory-based studies from leading specialists in all lupus-related disciplines. Invaluable reading, with extended coverage, lupus-related disciplines include: Rheumatology, Dermatology, Immunology, Obstetrics, Psychiatry and Cardiovascular Research…
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