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[胆汁酸腹泻]

[Bile Acid Diarrhea].

作者信息

Kim Hee Jin, Kim Hyun Jin

机构信息

Department of Internal Medicine, Gyeongsang National University Changwon Hospital, Gyeongsang National University College of Medicine, Changwon, Korea.

出版信息

Korean J Gastroenterol. 2024 Apr 25;83(4):133-142. doi: 10.4166/kjg.2023.119.

DOI:10.4166/kjg.2023.119
PMID:38659249
Abstract

Diarrhea is a very common gastrointestinal symptom, and the presence of higher concentrations of bile acid in the colon leads to bile acid diarrhea (BAD). In BAD patients, a portion of bile from the small intestine that is normally controlled by enterohepatic circulation is present at a high concentration in the lumen of the large intestine, resulting in increased motility and secretion of the large intestine. The prevalence of BAD is estimated to be 1-2% of the general population, and it comprises one-third of the instances of diarrhea-predominant irritable bowel syndrome. The clinical symptoms of BAD include chronic diarrhea, increased frequency of defecation, urgency to defecate, fecal incontinence, and cramping abdominal pain. The pathophysiology of BAD has not yet been fully elucidated. However, recent studies have reported increased intestinal permeability, shortened intestinal transit time, and changes in the intestinal microbial community to be the possible causes of BAD. Although fecal and serum bile acid tests are widely used for diagnosis, new test methods that are non-invasive, inexpensive, and have high sensitivity and specificity are needed at various institutions to facilitate the diagnosis. The selenium homo-tauro-cholic acid (SeHCAT) test is the gold standard for BAD diagnosis and severity assessment. The validation of several other serum markers, such as 7-hydroxy-4-cholesten-3-one (serum 7αC4) and the fibroblast growth factor 19 (FGF19) for use in clinical practice is ongoing. Although bile acid sequestrants are the mainstay of treatment, the development of drugs that are more effective and have better compliance is required. Farnesoid X receptor (FXR) agonists are showing promising results.

摘要

腹泻是一种非常常见的胃肠道症状,结肠中胆汁酸浓度升高会导致胆汁酸腹泻(BAD)。在BAD患者中,正常情况下由肠肝循环控制的一部分来自小肠的胆汁在大肠腔内以高浓度存在,导致大肠的蠕动和分泌增加。据估计,BAD在普通人群中的患病率为1%-2%,占以腹泻为主的肠易激综合征病例的三分之一。BAD的临床症状包括慢性腹泻、排便频率增加、排便急迫感、大便失禁和腹部绞痛。BAD的病理生理学尚未完全阐明。然而,最近的研究报告称,肠道通透性增加、肠道转运时间缩短以及肠道微生物群落的变化可能是BAD的病因。尽管粪便和血清胆汁酸检测广泛用于诊断,但各机构需要新的非侵入性、廉价且具有高灵敏度和特异性的检测方法来促进诊断。硒同型牛磺胆酸(SeHCAT)检测是BAD诊断和严重程度评估的金标准。其他几种血清标志物,如7-羟基-4-胆甾烯-3-酮(血清7αC4)和成纤维细胞生长因子19(FGF19)在临床实践中的验证工作正在进行。尽管胆汁酸螯合剂是主要的治疗方法,但仍需要开发更有效且依从性更好的药物。法尼酯X受体(FXR)激动剂显示出有前景的结果。

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