Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Center for Affective, Stress and Sleep Disorders (ZASS), University Psychiatric Clinics (UPK) Basel, University of Basel, Basel, Switzerland.
Aliment Pharmacol Ther. 2023 Jan;57(2):224-236. doi: 10.1111/apt.17256. Epub 2022 Oct 20.
Primary sclerosing cholangitis (PSC) is a progressive bile duct disease associated with inflammatory bowel disease (PSC-IBD).
To investigate whether patients with PSC-IBD benefit from a gluten-free and amylase trypsin inhibitor (ATI)-free diet (GFD).
We performed a prospective clinical pilot study administering an eight-week GFD. The primary outcomes were colonic inflammation assessed by proctosigmoidoscopy, and liver stiffness (surrogate for fibrosis, inflammation and cholestasis) measured by transient elastography before and after GFD. Amongst the secondary (exploratory) outcomes were colonic mucosal and serum cytokine/chemokine changes, the intestinal microbiome and transcriptome dynamics, and shifts in serum markers of hepatic fibrogenesis.
Fifteen patients with PSC-IBD completed the study. The study did not meet its primary outcome: the endoscopic score and liver stiffness remained unchanged. However, the expression of pro-inflammatory mucosal cytokines and chemokines such as IL6, IL8, CCL2, and TNFα was significantly down-regulated. Two critical markers of liver fibrosis and matrix remodelling, thrombospondin-2 and -4, decreased significantly. The microbiota composition changed slightly, including a decrease in the pathogen Romboutsia ilealis. The intestinal transcriptome indicated a gut barrier improvement. Pruritus, fatigue, overall well-being, faecal calprotectin levels, and serum alkaline phosphatase did not change significantly.
This study did not demonstrate a clinical improvement with short-term GFD in patients with PSC-IBD. However, a gluten/ATI-free diet may improve biomarkers of intestinal inflammation and barrier function in these patients with associated changes in the enteric microbiota. Further investigation of the therapeutic potential of the GFD in PSC-IBD is warranted.
原发性硬化性胆管炎(PSC)是一种与炎症性肠病(PSC-IBD)相关的进行性胆管疾病。
研究 PSC-IBD 患者是否从无麸质和淀粉酶胰蛋白酶抑制剂(ATI)饮食(GFD)中获益。
我们进行了一项前瞻性临床试点研究,给予八周的 GFD。主要结局是通过直肠乙状结肠镜检查评估结肠炎症,以及通过瞬态弹性成像在 GFD 前后测量肝硬度(纤维化、炎症和胆汁淤积的替代指标)。次要(探索性)结局包括结肠黏膜和血清细胞因子/趋化因子变化、肠道微生物组和转录组动态以及肝纤维化血清标志物的变化。
15 例 PSC-IBD 患者完成了研究。该研究未达到其主要结局:内镜评分和肝硬度保持不变。然而,促炎黏膜细胞因子和趋化因子的表达如 IL6、IL8、CCL2 和 TNFα 显著下调。两个关键的肝纤维化和基质重塑标志物,血小板反应蛋白-2 和 -4,显著下降。微生物群组成略有变化,包括病原体 Romboutsia ilealis 的减少。肠道转录组表明肠道屏障得到改善。瘙痒、疲劳、整体健康状况、粪便钙卫蛋白水平和血清碱性磷酸酶没有明显变化。
本研究未证明 PSC-IBD 患者短期 GFD 可改善临床症状。然而,无麸质/ATI 饮食可能改善这些患者的肠道炎症和屏障功能的生物标志物,并伴有肠道微生物组的变化。进一步研究 GFD 在 PSC-IBD 中的治疗潜力是必要的。