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利那洛肽:用于治疗便秘型肠易激综合征的研究进展。

Linaclotide: a review of its use in the treatment of irritable bowel syndrome with constipation.

机构信息

Adis, 41 Centorian Drive, Private Bag 65901, Mairangi Bay, North Shore, 0754, Auckland, New Zealand,

出版信息

Drugs. 2014 Jan;74(1):53-60. doi: 10.1007/s40265-013-0157-5.

Abstract

Linaclotide (Constella®) is a synthetic 14-amino acid peptide, structurally related to guanylin and uroguanylin, that acts as a potent guanylate cyclase C receptor agonist. It is a first-in-class agent recently approved in the EU for the treatment of adult patients with moderate to severe irritable bowel syndrome with constipation (IBS-C). Linaclotide has very low oral bioavailability and acts locally in the gastrointestinal tract to stimulate fluid secretion, increase colonic transit, and reduce abdominal pain. In phase III trials, once-daily, oral linaclotide significantly increased compared with placebo the proportions of 12-week abdominal pain/discomfort responders and 12-week degree-of-relief responders (co-primary endpoints recommended by the European Medicines Agency). Linaclotide also significantly increased the proportions of responders at 26 weeks compared with placebo, and significantly improved all abdominal symptoms and measures of bowel function at 12 weeks compared with placebo. In addition, linaclotide generally improved health-related quality of life compared with placebo. Linaclotide was generally well tolerated; the most common adverse event was diarrhoea. Thus, linaclotide is a novel and effective single agent for the treatment of IBS-C in adults.

摘要

利那洛肽(Constella®)是一种合成的 14 个氨基酸肽,与鸟苷酸和尿鸟苷酸结构相关,作为一种有效的鸟苷酸环化酶 C 受体激动剂。它是一种新型药物,最近在欧盟被批准用于治疗成年中重度肠易激综合征伴便秘(IBS-C)患者。利那洛肽口服生物利用度非常低,在胃肠道局部发挥作用,刺激液体分泌,增加结肠转运,减少腹痛。在 III 期临床试验中,与安慰剂相比,每日一次口服利那洛肽显著增加了 12 周腹痛/不适缓解者和 12 周缓解程度者的比例(欧洲药品管理局推荐的共同主要终点)。与安慰剂相比,利那洛肽在 26 周时也显著增加了缓解者的比例,与安慰剂相比,在 12 周时显著改善了所有腹部症状和肠功能指标。此外,与安慰剂相比,利那洛肽通常能改善健康相关的生活质量。利那洛肽总体上耐受性良好;最常见的不良事件是腹泻。因此,利那洛肽是治疗成人 IBS-C 的一种新型有效单药。

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