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超越无麸质饮食:对乳糜泻非饮食性药物治疗2期试验的批判性观点。

Beyond gluten-free diet: a critical perspective on phase 2 trials on non-dietary pharmacological therapies for coeliac disease.

作者信息

Scalvini Davide, Scarcella Chiara, Mantica Giulia, Bartolotta Erica, Maimaris Stiliano, Fazzino Erica, Biagi Federico, Schiepatti Annalisa

机构信息

Department of Internal Medicine and Therapeutics, University of Pavia, Pavia, Italy.

Istituti Clinici Scientifici Maugeri IRCCS, Gastroenterology Unit of Pavia Institute, Pavia, Italy.

出版信息

Front Nutr. 2025 Jan 7;11:1501817. doi: 10.3389/fnut.2024.1501817. eCollection 2024.

Abstract

Coeliac disease is an immune-mediated chronic enteropathy, with a prevalence of around 1% in the general population and occurring in genetically susceptible individuals after the ingestion of gluten proteins present in wheat, rye and barley. Currently, a strict lifelong gluten-free diet is the cornerstone of treatment of coeliac disease. However, maintaining strict dietary adherence is challenging for many patients, due to the high costs, the highly restrictive nature of the diet and the impact on patients' quality of life. Moreover, a tiny minority of coeliac patients can develop pre-malignant/malignant complications of coeliac disease, a group of conditions, that despite being rare, are still burdened by a poor prognosis due to the lack of effective therapies. Therefore, the development of pharmacological treatments as an alternative to or supportive of a gluten-free diet is still an unmet need. The identification of new pathogenetic targets in the last years has enabled the development of several candidates molecules, many of which have been investigated in phase 2/3 clinical trials. In this narrative review we aim to summarise the investigational therapies that have been evaluated in phase 2/3 trials and provide a critical overview on the latest advances in this field.

摘要

乳糜泻是一种免疫介导的慢性肠病,在普通人群中的患病率约为1%,发生于具有遗传易感性的个体在摄入小麦、黑麦和大麦中存在的麸质蛋白之后。目前,严格的终身无麸质饮食是乳糜泻治疗的基石。然而,由于成本高昂、饮食限制极为严格以及对患者生活质量的影响,对许多患者而言,维持严格的饮食依从性具有挑战性。此外,极少数乳糜泻患者会发生乳糜泻的癌前/恶性并发症,这一组病症尽管罕见,但由于缺乏有效治疗方法,预后仍然很差。因此,开发作为无麸质饮食替代方案或支持手段的药物治疗方法仍然是一项未得到满足的需求。近年来新发病机制靶点的确定推动了几种候选分子的开发,其中许多已在2/3期临床试验中进行了研究。在这篇叙述性综述中,我们旨在总结已在2/3期试验中评估的研究性疗法,并对该领域的最新进展进行批判性概述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aece/11748180/7a16647a56d4/fnut-11-1501817-g001.jpg

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