Immunology, Rheumatology and Infectious Disease Research Area, Human Microbiome Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
GenomeUp SRL, Rome, Italy.
Microbiome. 2024 Oct 23;12(1):217. doi: 10.1186/s40168-024-01927-5.
Crohn's disease (CD) is characterized by chronic intestinal inflammation. Diet is a key modifiable factor influencing the gut microbiome (GM) and a risk factor for CD. However, the impact of diet modulation on GM function in CD patients is understudied. Herein, we evaluated the effect of a high-fiber, low-fat diet (the Mi-IBD diet) on GM function in CD patients. All participants were instructed to follow the Mi-IBD diet for 8 weeks. One group of CD patients received one-time diet counseling only (Gr1); catered food was supplied for the other three groups, including CD patients (Gr2) and dyads of CD patients and healthy household controls (HHCs) residing within the same household (Gr3-HHC dyads). Stool samples were collected at baseline, week 8, and week 36, and analyzed by liquid chromatography-tandem mass spectrometry.
At baseline, the metaproteomic profiles of CD patients and HHCs differed. The Mi-IBD diet significantly increased carbohydrate and iron transport and metabolism. The predicted microbial composition underlying the metaproteomic changes differed between patients with ileal only disease (ICD) or colonic involvement: ICD was characterized by decreased Faecalibacterium abundance. Even on the Mi-IBD diet, the CD patient metaproteome displayed significant underrepresentation of carbohydrate and purine/pyrimidine synthesis pathways compared to that of HHCs. Human immune-related proteins were upregulated in CD patients compared to HHCs.
The Mi-IBD diet changed the microbial function of CD patients and enhanced carbohydrate metabolism. Our metaproteomic results highlight functional differences in the microbiome according to disease location. Notably, our dietary intervention yielded the most benefit for CD patients with colonic involvement compared to ileal-only disease. Video Abstract.
克罗恩病(CD)的特征是慢性肠道炎症。饮食是影响肠道微生物组(GM)的一个关键可改变因素,也是 CD 的一个风险因素。然而,饮食调节对 CD 患者 GM 功能的影响还研究不足。在此,我们评估了高纤维、低脂肪饮食(Mi-IBD 饮食)对 CD 患者 GM 功能的影响。所有参与者均被指示遵循 Mi-IBD 饮食 8 周。一组 CD 患者仅接受一次性饮食咨询(Gr1);为另外三组提供了 Catered 食品,包括 CD 患者(Gr2)以及与 CD 患者同住一个家庭的健康家庭对照者(HHC)的 CD 患者和 HHC 对(Gr3-HHC 对)。在基线、第 8 周和第 36 周采集粪便样本,并通过液相色谱-串联质谱进行分析。
在基线时,CD 患者和 HHC 的代谢组学图谱不同。Mi-IBD 饮食显著增加了碳水化合物和铁的转运和代谢。基于代谢组学变化的微生物组成预测在仅回肠疾病(ICD)或结肠受累的患者中有所不同:ICD 的特征是粪杆菌丰度降低。即使在 Mi-IBD 饮食下,CD 患者的代谢组也明显表现出碳水化合物和嘌呤/嘧啶合成途径的代表性不足,与 HHC 相比。与 HHC 相比,CD 患者的人类免疫相关蛋白上调。
Mi-IBD 饮食改变了 CD 患者的微生物功能,增强了碳水化合物代谢。我们的代谢组学结果根据疾病部位突出了 GM 功能的差异。值得注意的是,与仅回肠疾病相比,我们的饮食干预对结肠受累的 CD 患者最有益。视频摘要。