Department of Rheumatology and Systemic Autoinmune Diseases, Hospital Universitari de la Santa Creu i Sant Pau, Barcelona, Spain.
Unit of Systemic Autoimmune Diseases, Department of Internal Medicine, Hospital Universitari Vall d'Hebrón, Barcelona, Spain.
Autoimmun Rev. 2023 Nov;22(11):103441. doi: 10.1016/j.autrev.2023.103441. Epub 2023 Sep 12.
To analyze the effectiveness and safety of intravenous immunoglobulin (IVIG) given in routine care to patients with systemic sclerosis (SSc).
A retrospective multicenter observational study was conducted in SSc patients treated with IVIG. We collected data on epidemiological parameters and clinical outcomes. Firstly, we assessed changes in organ manifestations during IVIG treatment. Secondly, we analyzed the frequency of adverse effects. The following parameters were collected from baseline to the last follow-up: the patient's weight, modified Rodnan Skin Score (mRSS), modified manual muscle strength scale (MRC), laboratory test(creatine kinase(CK), hemoglobin and protein levels), The University of California Los Angeles Scleroderma Clinical Trials Consortium gastrointestinal tract 2.0 (UCLA GIT 2.0) questionnaire, pulmonary function tests, and echocardiography.
Data were collected on 78 patients (82% females; 59% with diffuse SSc). Inflammatory idiopathic myopathy was the most frequent concomitant overlap disease (41%). The time since Raynaud's phenomenon and SSc onset were 8.8 ± 18 and 6.2 ± 6.7 years respectively. The most frequent IVIG indication was myositis (38/78), followed by gastrointestinal (27/78) and cutaneous (17/78) involvement. The median number of cycles given were 5. 54, 53 and 9 patients have been treated previously with glucocorticoids, synthetic disease-modifying antirheumatic drugs and biologic therapies respectively. After IVIG use we found significant improvements in muscular involvement (MRC ≥ 3/5 92% IVIG, p = 0.001 and CK levels from 1149 ± 2026 UI to 217 ± 224 UI, p = 0.02), mRSS (15 ± 12.4 to 13 ± 12.5, p = 0.015) and improvement in total score of UCLA GIT 2.0 (p = 0.05). None Anti-RNA polymerase III patients showed an adequate response in gastrointestinal involvement (0/7) in comparison with other antibodies (0 vs. 25, p = 0,039). Cardiorespiratory involvement remained stable. A total of 12 adverse events were reported with only one withdrawn due to serious adverse effect.
this study suggest that IVIG may improve myositis, gastrointestinal and skin involvement in SSc patients treated in routine care and seems to have a good safety profile.
分析在系统性硬化症(SSc)患者的常规治疗中给予静脉注射免疫球蛋白(IVIG)的有效性和安全性。
对接受 IVIG 治疗的 SSc 患者进行回顾性多中心观察性研究。我们收集了流行病学参数和临床结局的数据。首先,我们评估了 IVIG 治疗期间器官表现的变化。其次,我们分析了不良反应的频率。从基线到最后一次随访收集了以下参数:患者体重、改良罗德曼皮肤评分(mRSS)、改良手动肌肉力量量表(MRC)、实验室检查(肌酸激酶(CK)、血红蛋白和蛋白水平)、加利福尼亚大学洛杉矶分校硬皮病临床试验联合会胃肠道 2.0(UCLA GIT 2.0)问卷、肺功能检查和超声心动图。
共收集了 78 例患者(82%为女性;59%为弥漫性 SSc)的数据。炎症性特发性肌病是最常见的合并重叠疾病(41%)。雷诺现象和 SSc 发病的时间分别为 8.8±18 年和 6.2±6.7 年。IVIG 最常见的适应证是肌炎(38/78),其次是胃肠道(27/78)和皮肤(17/78)受累。中位数给予的周期数为 5.54,53 名患者之前曾接受过糖皮质激素、合成疾病修饰抗风湿药物和生物疗法治疗。使用 IVIG 后,我们发现肌肉受累(MRC≥3/5 92% IVIG,p=0.001 和 CK 水平从 1149±2026 UI 降至 217±224 UI,p=0.02)、mRSS(15±12.4 至 13±12.5,p=0.015)和 UCLA GIT 2.0 总评分的改善(p=0.05)。与其他抗体相比,抗 RNA 聚合酶 III 患者的胃肠道受累(0/7)没有显示出足够的反应(0 与 25,p=0.039)。心肺受累保持稳定。共报告了 12 例不良事件,只有 1 例因严重不良事件而退出。
这项研究表明,IVIG 可能改善常规治疗中 SSc 患者的肌炎、胃肠道和皮肤受累,且似乎具有良好的安全性。