Ashizuka Shinya, Inatsu Haruhiko, Kita Toshihiro, Kitamura Kazuo
Circulatory and Body Fluid Regulation, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
Dig Dis Sci. 2016 Mar;61(3):872-80. doi: 10.1007/s10620-015-3917-0. Epub 2015 Oct 15.
Adrenomedullin (AM) is a multifunctional biologically active peptide that has an ameliorative effect against inflammatory bowel disease in several experimental models. We reported the first case where AM infusion dramatically improved symptoms and colonoscopy findings in patients with refractory ulcerative colitis (UC). To confirm the reproducibility of the efficacy and safety of AM infusion, this pilot study evaluated the clinical feasibility of intravenous administration of AM in patients with refractory UC.
Seven patients with active refractory UC participated and received intravenous infusion of AM (1.5 pmol/kg/min) for 8 h daily for 14 days, and their Disease Activity Index (DAI) were evaluated before and 2 and 12 weeks after beginning AM administration.
DAI were improved in all patients after AM administration. Within 2 weeks, marked declines in DAI (≥ 3 points and ≥ 30%) were observed in six patients (85.7%), while a more modest decline was observed in one patient (14.3%). Overall mean DAI improved from 9.3 ± 0.6 at baseline to 4.6 ± 0.8 at 2 weeks, and then to 1.2 ± 0.5 at 12 weeks. Endoscopic examination revealed substantial amelioration of ulcers, with mucosal healing and scarring. Four patients remained in clinical remission 12 months after AM treatment. AM administration produced significant increases in plasma AM concentrations (approximately 2.5-fold) that had a mild effect on blood pressure and heart rate, but with no serious adverse effects.
AM is a potentially useful agent that acts via a novel mechanism to safely induce mucosal healing and clinical remission in patients with refractory UC.
肾上腺髓质素(AM)是一种多功能生物活性肽,在多个实验模型中对炎症性肠病具有改善作用。我们报道了首例AM输注显著改善难治性溃疡性结肠炎(UC)患者症状和结肠镜检查结果的病例。为证实AM输注疗效和安全性的可重复性,本前瞻性研究评估了难治性UC患者静脉注射AM的临床可行性。
7例活动性难治性UC患者参与研究,每天接受8小时的AM静脉输注(1.5 pmol/kg/分钟),持续14天,并在开始AM给药前、给药后2周和12周评估其疾病活动指数(DAI)。
AM给药后所有患者的DAI均得到改善。在2周内,6例患者(85.7%)的DAI显著下降(≥3分且≥30%),而1例患者(14.3%)的下降幅度较小。总体平均DAI从基线时的9.3±0.6改善至2周时的4.6±0.8,然后在12周时改善至1.2±0.5。内镜检查显示溃疡明显改善,伴有黏膜愈合和瘢痕形成。4例患者在AM治疗后12个月仍处于临床缓解期。AM给药使血浆AM浓度显著升高(约2.5倍),对血压和心率有轻微影响,但无严重不良反应。
AM是一种潜在的有用药物,通过一种新机制发挥作用,可安全地诱导难治性UC患者的黏膜愈合和临床缓解。