Uslu Ugur, Streiff Laura, Sticherling Michael
Friedrich-Alexander-Universität of Erlangen-Nürnberg, Universitätsklinikum Erlangen, Department of Dermatology, Ulmenweg 18, D-91054 Erlangen, Germany.
LVR-Klinik Bonn, Department of Psychiatry and Psychotherapy, Kaiser-Karl-Ring 20, D-53111 Bonn, Germany.
Eur J Dermatol. 2018 Jun 1;28(3):364-369. doi: 10.1684/ejd.2018.3300.
Calcitonin gene-related peptide (CGRP) is a vasodilatory neuropeptide that plays an important role in the blood vessels of heart and peripheral circulation, a lack of which may cause vasculopathies.
In this study, the clinical course of disease, as well as the efficacy, side effects, and patient satisfaction of systemic calcitonin therapy in patients with systemic sclerosis (SSc), was evaluated.
Forty-nine patients received repetitive intravenous calcitonin infusions as first-line treatment. The average number of cycles was 12.2 ± 10.3 over a period of 30 months (each cycle: 100 U/day over 10 days). Clinical examinations, laboratory tests, and organ imaging were performed before the start of, and at regular intervals during therapy in order to evaluate organ manifestations and the clinical course of the disease. In addition, patients' own experiences of the therapy, side effects, and therapy success were evaluated with standardized questionnaires.
Over the course of the treatment, seven patients experienced improvements in their condition with a considerable reduction in digital ulceration and improved movement (14.3%). Pulmonary function in seven patients improved during the therapy (14.3%). With regards to side effects, nausea (41.7%), headaches (33.3%), fluctuations in blood pressure (29.2%), and flushing (29.2%) were observed. Overall, 45.8% of patients evaluated the therapy as good and 58.3% would undergo further courses of therapy with calcitonin.
Systemic calcitonin treatment seems to have positive clinical effects on SSc and contributes to relieving symptoms, especially in patients with cutaneous manifestations. No severe side effects were reported during this study.
降钙素基因相关肽(CGRP)是一种血管舒张神经肽,在心脏血管和外周循环中起重要作用,缺乏该肽可能导致血管病变。
本研究评估了系统性硬化症(SSc)患者疾病的临床病程,以及系统性降钙素治疗的疗效、副作用和患者满意度。
49例患者接受重复静脉输注降钙素作为一线治疗。在30个月的时间内,平均疗程数为12.2±10.3(每个疗程:100U/天,共10天)。在治疗开始前及治疗期间定期进行临床检查、实验室检查和器官成像,以评估器官表现和疾病的临床病程。此外,用标准化问卷评估患者对治疗的自身感受、副作用和治疗效果。
在治疗过程中,7例患者病情改善,指端溃疡明显减少,活动能力改善(14.3%)。7例患者在治疗期间肺功能改善(14.3%)。关于副作用,观察到恶心(41.7%)、头痛(33.3%)、血压波动(29.2%)和面部潮红(29.2%)。总体而言,45.8%的患者对治疗评价良好,58.3%的患者愿意接受进一步的降钙素治疗疗程。
系统性降钙素治疗似乎对SSc有积极的临床效果,有助于缓解症状,尤其是对有皮肤表现的患者。本研究期间未报告严重副作用。