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用胰高血糖素样肽-1受体激动剂治疗胆汁酸腹泻:一种有前景但研究不足的方法。

Treatment of Bile Acid Diarrhea With Glucagon-Like Peptide 1 Receptor Agonists: A Promising Yet Understudied Approach.

作者信息

Ellegaard Anne-Marie, Kårhus Martin L, Winther-Jensen Matilde, Lund Asger B, Knop Filip K

机构信息

Center for Clinical Metabolic Research, Copenhagen University Hospital - Herlev and Gentofte, Hellerup, Denmark.

Center for Clinical Research and Prevention, Copenhagen University Hospital - Bispebjerg and Frederiksberg, Frederiksberg, Denmark.

出版信息

Clin Transl Gastroenterol. 2025 Mar 1;16(3):e00815. doi: 10.14309/ctg.0000000000000815.

Abstract

Bile acid diarrhea (BAD) is a chronic and socially debilitating disease characterized by abdominal pain, diarrhea, urgency, and fecal incontinence. Recently, in a 6-week randomized controlled trial, we showed that the glucagon-like peptide 1 receptor agonist (GLP-1RA) liraglutide is superior to bile acid sequestration (considered standard-of-care) using colesevelam in reducing BAD symptoms. The emergence of new, more potent, and longer-acting GLP-1RAs has spurred an interest in these treatments in BAD management. Here, we review the literature on different GLP-1RAs in BAD treatment and outline their potential mode of actions, highlight knowledge gaps, and outline the need for further clinical evidence generation.

摘要

胆汁酸腹泻(BAD)是一种慢性且会导致社交功能障碍的疾病,其特征为腹痛、腹泻、便急和大便失禁。最近,在一项为期6周的随机对照试验中,我们发现,与使用考来维仑进行胆汁酸螯合(被视为标准治疗方法)相比,胰高血糖素样肽1受体激动剂(GLP-1RA)利拉鲁肽在减轻BAD症状方面更具优势。新型、更高效且作用时间更长的GLP-1RA的出现激发了人们对其在BAD治疗中的兴趣。在此,我们综述了关于不同GLP-1RA用于BAD治疗的文献,概述了它们潜在的作用方式,突出了知识空白,并阐述了进一步生成临床证据的必要性。

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