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用5-羟色胺3受体拮抗剂托烷司琼治疗系统性硬化症。

Treatment of systemic sclerosis with the 5-HT3 receptor antagonist tropisetron.

作者信息

Stratz T, Müller W

机构信息

Hochrhein Institute of Rehabilitation Research, Department of Clinical Research, Bad Säckingen, Germany.

出版信息

Scand J Rheumatol Suppl. 2004;119:59-62. doi: 10.1080/03009740410007078.

Abstract

BACKGROUND

There is no known disease-modifying therapy for progressive systemic sclerosis.

OBJECTIVES

It was shown that a patient with secondary fibromyalgia syndrome for whom the development of systemic sclerosis was suspected because of a Raynaud's phenomenon and the presence of SCL-70 antibodies in the serum had experienced a clear pain reduction under treatment with tropisteron, which is the reason why this drug was also used with established systemic sclerosis.

METHOD

Two patients with progressive systemic sclerosis and positive SCL-70 antibodies were treated for 6 weeks with 5 mg tropisetron daily. Both patients had clear skin symptoms, functional impairments of the locomotor system, and a secondary fibromyalgia syndrome. The skin score and joint motion were checked before, during, and after treatment. In addition, the patients filled in the visual analog scale for pain at these times. At the end of the 6 weeks, the patients showed a clear improvement of the skin score and the movability of various joints as well as a clear reduction of pain. The medication was well-tolerated. Constipation developed in the patients; it could be controlled with laxatives. Follow-up questioning of the patients after 3 months showed that their condition had remained stable.

CONCLUSION

Two patients with progressive systemic sclerosis showed an improvement of various symptoms under a blockade of the 5-HT3 receptors via tropisetron. The long-lasting effect pointed to immunomodulation. The two cases give cause for clarifying this by means of clinical studies, which should also investigate the question of dosage (possibly 5 mg tropisetron twice daily).

摘要

背景

目前尚无已知的可改变进行性系统性硬化症病情的治疗方法。

目的

有一名继发性纤维肌痛综合征患者,因雷诺现象及血清中存在SCL - 70抗体而怀疑患有系统性硬化症,该患者在使用曲匹西隆治疗后疼痛明显减轻,这也是该药用于已确诊的系统性硬化症患者的原因。

方法

两名进行性系统性硬化症且SCL - 70抗体阳性的患者,每天服用5毫克曲匹西隆,治疗6周。两名患者均有明显的皮肤症状、运动系统功能障碍及继发性纤维肌痛综合征。在治疗前、治疗期间及治疗后检查皮肤评分和关节活动度。此外,患者在这些时间填写疼痛视觉模拟量表。6周结束时,患者的皮肤评分、各关节活动度明显改善,疼痛明显减轻。药物耐受性良好。患者出现便秘,可用泻药控制。3个月后对患者进行随访询问,结果显示其病情保持稳定。

结论

两名进行性系统性硬化症患者通过曲匹西隆阻断5 - HT3受体后,各种症状均有改善。其持久效果表明存在免疫调节作用。这两例病例促使通过临床研究对此进行阐明,临床研究还应调查剂量问题(可能为每日两次,每次5毫克曲匹西隆)。

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