Suppr超能文献

用内皮素-1受体拮抗剂(波生坦)治疗系统性硬化症中的指端溃疡

[Treatment of digital ulcers in systemtic sclerosis with endothelin-1 receptor antagonist (bosentan)].

作者信息

Riccardi M T, Chialà A, Lannone F, Grattagliano V, Covelli M, Lapadula G

机构信息

DIMIMP, Sezione di Reumatologia, Università degli Studi di Bari, Italia.

出版信息

Reumatismo. 2007 Apr-Jun;59(2):135-9. doi: 10.4081/reumatismo.2007.135.

Abstract

In systemic sclerosis (SSc) occurrence of recurrent digital ulcers (DU) is cause of pain and functional disability of hands. Treatment with vasodilator agents, such as calcium channel blockers, ACE inhibitors, prostanoids, has not shown to be an effective therapy. There is evidence that endotelin-1 (ET-1) is a key mediator in regulation of vascular tone and its enhanced production in SSc is believed to lead to vasoconstriction, vessel remodelling, local ischemia and ulcers of fingertips. Recently, an oral endothelin receptor antagonist, bosentan, has been proved to be effective in the treatment of SSc associated pulmonar arterial hypertension (PAH) and to decrease the development of new DU in patients with SSc. In this study, we assessed the occurrence of new DU in eight patients with SSc associated PAH and one SSc patient with recurrent DU refractory to standard vasodilatation therapy. All patients received bosentan at dosage of 62.5 mg bid for 4 weeks and 125 mg bid thereafter for one year. All patients had 3-4 DU of hands at baseline and one patients had also ulcers at lower limbs. In seven out of nine patients we did not record the occurrence of new DU and we also observed a 50% reduction of existing DU, whereas new DU occurred only in two patients. These data suggest that ET-1 plays a key role in DU induction in SSc patients and that ET-1 inhibition by bosentan can be an effective therapeutic strategy.

摘要

在系统性硬化症(SSc)中,复发性指端溃疡(DU)的出现是手部疼痛和功能障碍的原因。使用血管扩张剂进行治疗,如钙通道阻滞剂、血管紧张素转换酶抑制剂、前列腺素类药物,尚未显示出是一种有效的治疗方法。有证据表明,内皮素-1(ET-1)是调节血管张力的关键介质,并且认为其在SSc中产生增加会导致血管收缩、血管重塑、局部缺血和指尖溃疡。最近,一种口服内皮素受体拮抗剂波生坦已被证明可有效治疗SSc相关的肺动脉高压(PAH),并减少SSc患者新DU的发生。在本研究中,我们评估了8例SSc相关PAH患者和1例对标准血管扩张治疗难治的复发性DU的SSc患者中新DU的发生情况。所有患者先接受波生坦62.5mg,每日两次,治疗4周,之后接受125mg,每日两次,治疗1年。所有患者在基线时手部有3 - 4个DU,1例患者下肢也有溃疡。9例患者中有7例未记录到新DU的发生,并且我们还观察到现有DU减少了50%,而仅2例患者出现了新DU。这些数据表明,ET-1在SSc患者DU的诱发中起关键作用,并且波生坦抑制ET-1可能是一种有效的治疗策略。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验