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十二指肠炎症:功能性消化不良的新靶点?

Duodenal inflammation: an emerging target for functional dyspepsia?

机构信息

Translational Research in Gastrointestinal Diseases (TARGID), KU Leuven, Leuven, Belgium.

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.

出版信息

Expert Opin Ther Targets. 2020 Jun;24(6):511-523. doi: 10.1080/14728222.2020.1752181. Epub 2020 Apr 19.

Abstract

: Functional dyspepsia (FD) is one of the most common functional gastrointestinal disorders and is classified into postprandial distress and epigastric pain syndrome. Despite the recognition of duodenal inflammation as a potential trigger of symptoms, only limited anti-inflammatory therapies exist.: This narrative review summarizes the recent advances in the pathophysiology and treatment of FD; it identifies potential therapeutic targets and gaps in the field. An electronic literature search was conducted in Pubmed up to 31st of December 2019.: There is compelling evidence for the role of duodenal inflammation and the eosinophil-mast cell axis in the pathogenesis of dyspeptic symptoms. Traditional prokinetic drugs and neuromodulators target gastric dysmotility and visceral hypersensitivity but are hampered by limited efficacy and side effects. Independent of acid suppression, the anti-inflammatory action of proton pump inhibitors, which remain the first-line therapy in FD, may also explain their therapeutic effect. Other existing and newly established anti-inflammatory drugs should be investigated while trials including probiotics and selective antibiotics should examine the host microbiome and immune activation. Targeted treatments for potential causes of duodenal pathology, such as impaired permeability and dysbiosis, are likely to emerge in the future.

摘要

功能性消化不良(FD)是最常见的功能性胃肠疾病之一,分为餐后不适综合征和上腹疼痛综合征。尽管十二指肠炎症被认为是症状的潜在触发因素,但目前仅有限的抗炎治疗方法。本文对 FD 的病理生理学和治疗的最新进展进行了综述,确定了该领域的潜在治疗靶点和空白。对 Pubmed 数据库截至 2019 年 12 月 31 日的文献进行了电子检索。十二指肠炎症和嗜酸性粒细胞-肥大细胞轴在消化不良症状的发病机制中具有重要作用,这一观点已得到充分证实。传统的促动力药物和神经调节剂针对胃动力障碍和内脏高敏性,但疗效有限,副作用大。质子泵抑制剂(PPI)除了抑制胃酸分泌外,其抗炎作用可能也是其治疗 FD 的机制之一,质子泵抑制剂仍然是 FD 的一线治疗药物。其他现有的和新建立的抗炎药物也应进行研究,同时包括益生菌和选择性抗生素的试验应研究宿主微生物组和免疫激活。针对十二指肠病理的潜在原因(如通透性改变和菌群失调)的靶向治疗可能会在未来出现。

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