Clinical Enteric Neuroscience Translational and Epidemiological Research, Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Am J Physiol Gastrointest Liver Physiol. 2019 Nov 1;317(5):G640-G650. doi: 10.1152/ajpgi.00205.2019. Epub 2019 Aug 28.
The overall objectives of this review are to summarize actionable biomarkers for organic etiology of lower functional gastrointestinal disorders (FGIDs) that lead to individualized treatment for their FGIDs and to assess the pipeline for novel approaches to the management of constipation, diarrhea, and chronic abdominal pain in lower FGIDs. The new approaches to therapy include ion exchangers/transporters for functional constipation (sodium-glucose cotransporter 1, Na/H exchanger 3, and solute carrier family 26 member 3 inhibitors), bile acid modulators for constipation such as ileal bile acid transporter inhibitors and fibroblast growth factor 19 analog for functional constipation, and bile acid sequestrants or farnesoid X receptor agonists for functional diarrhea. Treatment for chronic abdominal pain remains an unmet need in patients with lower FGIDs, and promising novel approaches include delayed-release linaclotide, nonclassical opioid visceral analgesics, and selective cannabinoid receptor agonists. The role of probiotics, fecal microbial transplantation, and possible future microbiome therapies is discussed.
本综述的总体目标是总结导致功能性下胃肠道疾病(FGIDs)的有机病因的可操作生物标志物,以便为其 FGIDs 提供个体化治疗,并评估治疗便秘、腹泻和慢性腹痛的新型方法在 FGIDs 中的应用前景。新的治疗方法包括功能性便秘的离子载体/转运体(钠-葡萄糖共转运蛋白 1、Na/H 交换器 3 和溶质载体家族 26 成员 3 抑制剂)、便秘的胆汁酸调节剂(如回肠胆汁酸转运体抑制剂和纤维母细胞生长因子 19 类似物)以及胆汁酸螯合剂或法尼醇 X 受体激动剂用于治疗功能性腹泻。慢性腹痛的治疗仍然是 FGIDs 患者未满足的需求,有前途的新型方法包括延迟释放利那洛肽、非经典阿片类内脏镇痛药和选择性大麻素受体激动剂。还讨论了益生菌、粪便微生物移植和可能的未来微生物组治疗的作用。