Zhang Ruonan, Li Zhoulei, Huang Li, Kong Weimiao, Zheng Yidong, Wang Yangdi, Shen Xiaodi, Huang Lili, Wang Xinyue, Zheng Qingzhu, Wu Luyao, Ke Yaoqi, Mao Ren, Peng Zhenpeng, Sun Canhui, Feng Shi-Ting, Lin Shaochun, Wang Yejun, Li Xuehua
Department of Radiology, The First Affiliated Hospital of Sun Yat-Sen University, 58 Zhongshan II Road, Guangzhou 510080, People's Republic of China.
Youth Innovation Team of Medical Bioinformatics, Shenzhen University Medical School, Shenzhen 518060, China.
iScience. 2025 Mar 28;28(5):112310. doi: 10.1016/j.isci.2025.112310. eCollection 2025 May 16.
Altered gut microbiota‒metabolite interactions may result in intestinal inflammation severity variation in Crohn's disease (CD). Magnetic resonance enterography (MRE) advances anti-inflammatory strategy development. We aimed to identify inflammation-related multiomics factors and MRE interactions for CD management, analyzing 425 CD patients and 42 healthy controls undergoing MRE, ileocolonoscopy, and fecal/blood sampling (microbiota/metabolite analyses), with intestinal inflammation categorized by MRE and ileocolonoscopy. species were enriched in CD patients versus healthy controls, while and dominated moderate-severe versus no-mild inflammation groups, suggesting inflammation-level associations. suppressed intestinal inflammation by regulating serum PC(O-34:3), ePE(38:6), and ceramides (all < 0.05). Serum N-acetylneuraminic acid and guanidinoacetic acid correlated with intestinal morphological changes (e.g., MRE-detectable effusion and wall thickness) and inflammation severity ( < 0.05). A link was established between microscopic microbiota-metabolite markers and macroscopic imaging of inflammatory features, which could offer valuable insights into inflammation management.
肠道微生物群与代谢物的相互作用改变可能导致克罗恩病(CD)患者肠道炎症严重程度的差异。磁共振肠造影(MRE)推动了抗炎策略的发展。我们旨在识别与炎症相关的多组学因素以及用于CD管理的MRE相互作用,对425例接受MRE、回结肠镜检查以及粪便/血液采样(微生物群/代谢物分析)的CD患者和42例健康对照进行分析,肠道炎症通过MRE和回结肠镜检查进行分类。与健康对照相比,[具体物种名称1]在CD患者中富集,而[具体物种名称2]和[具体物种名称3]在中度至重度炎症组与无至轻度炎症组中占主导地位,提示与炎症水平相关。[具体物质名称]通过调节血清PC(O-34:3)、ePE(38:6)和神经酰胺抑制肠道炎症(均P<0.05)。血清N-乙酰神经氨酸和胍基乙酸与肠道形态学变化(如MRE可检测到的积液和肠壁厚度)以及炎症严重程度相关(P<0.05)。在微观微生物群-代谢物标志物与炎症特征的宏观成像之间建立了联系,这可为炎症管理提供有价值的见解。