Tang Kuo-Tung, Liao Tsai-Ling, Chen Yi-Hsing, Chen Der-Yuan, Lai Kou-Lung
Division of Allergy, Immunology, and Rheumatology, Taichung Veterans General Hospital, Taichung 407, Taiwan.
Faculty of Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Biomedicines. 2023 Jun 21;11(7):1774. doi: 10.3390/biomedicines11071774.
Fibromyalgia (FM) is a chronic disorder characterized by widespread pain with an enormous symptom burden. Its treatment efficacy is limited. Its pathogenesis involves immune dysregulation, which includes interleukin-6 (IL-6) production.
We herein reported a case series of FM patients receiving subcutaneous tocilizumab at our institution. FM symptoms were evaluated by the revised Fibromyalgia Impact Questionnaire (FIQR), which included pain level, and the fibromyalgianess scale based on the 2016 criteria of the American College of Rheumatology (ACR). FM symptoms were compared using the Wilcoxon signed-rank test. Neutrophils from primary FM patients and matched healthy controls were also isolated for transcriptome analysis.
We presented a total of two primary and four secondary FM patients who had received subcutaneous tocilizumab for a minimum of 12 weeks. All patients had severe symptoms despite standard treatments. Patients' FIQR and fibromyalgianess both dropped at 4 and 12 weeks. Four (67%) of them reached a pain reduction of ≥30% at 4 weeks, and three (50%) reached a pain reduction of ≥30% at 12 weeks. Possible differentially expressed genes were identified in primary FM patients when compared with controls and after tocilizumab treatment.
FM patients likely benefited from subcutaneous tocilizumab therapy. A randomized controlled trial is needed to verify its efficacy.
纤维肌痛(FM)是一种慢性疾病,其特征为广泛疼痛且症状负担极大。其治疗效果有限。其发病机制涉及免疫失调,其中包括白细胞介素-6(IL-6)的产生。
我们在此报告了一系列在我院接受皮下注射托珠单抗的FM患者病例。通过修订的纤维肌痛影响问卷(FIQR)评估FM症状,该问卷包括疼痛程度,以及基于美国风湿病学会(ACR)2016年标准的纤维肌痛程度量表。使用Wilcoxon符号秩检验比较FM症状。还分离了原发性FM患者和匹配的健康对照的中性粒细胞进行转录组分析。
我们共纳入了2例原发性和4例继发性FM患者,他们接受皮下注射托珠单抗至少12周。尽管接受了标准治疗,但所有患者症状都很严重。患者的FIQR和纤维肌痛程度在4周和12周时均有所下降。其中4例(67%)在4周时疼痛减轻≥30%,3例(50%)在12周时疼痛减轻≥30%。与对照组相比以及在托珠单抗治疗后,在原发性FM患者中鉴定出了可能的差异表达基因。
FM患者可能从皮下注射托珠单抗治疗中获益。需要进行随机对照试验来验证其疗效。