Department of Gastroenterology, the First Affiliated Hospital of Xi'an Jiao Tong University, Xi'an, 710061, China.
BMC Gastroenterol. 2024 Jan 31;24(1):56. doi: 10.1186/s12876-024-03150-w.
The role of the intestinal microbiota in the pathogenesis of inflammatory bowel disease combined with axial spondyloarthritis (axSpA) is gaining widespread interest.
This study was conducted to investigate the clinical and fecal microbiota characteristics of patients with both ulcerative colitis (UC) and axSpA.
Clinical data were collected from patients with UC. Patients were divided into the axSpA and non-axSpA groups according to human leukocyte antigen-B27 serology and sacroiliac joint imaging results. We obtained fecal specimens from 14 axSpA and 26 non-axSpA patients. All samples underwent 16S ribosomal DNA sequencing.
Seventy-three patients with UC were included in this study, and the axSpA incidence was 19.2%. This incidence was significantly higher in patients with C-reactive protein > 10 mg/L. Firmicutes and Faecalibacterium abundances were decreased, and Proteobacteria and Escherichia_Shigella abundances were increased in the axSpA group compared with those of the non-axSpA group. Indicator analysis showed that Escherichia_Shigella was more likely to be an indicator species of axSpA. Additionally, many biosynthetic and metabolic pathways, including glutathione metabolism, fatty acid degradation, geraniol degradation, and biosynthesis of siderophore group nonribosomal peptides, were upregulated in the axSpA group.
Patients with UC have a high axSpA incidence, which may be related to the relative abundances of Escherichia_Shigella in these patients. The abundances of various biosynthetic and metabolic pathways of the fecal flora were upregulated in patients with axSpA.
肠道微生物群在炎症性肠病合并轴性脊柱关节炎(axSpA)发病机制中的作用正引起广泛关注。
本研究旨在探讨溃疡性结肠炎(UC)合并 axSpA 患者的临床和粪便微生物群特征。
收集 UC 患者的临床资料。根据人类白细胞抗原-B27 血清学和骶髂关节影像学结果,将患者分为 axSpA 组和非 axSpA 组。我们从 14 例 axSpA 患者和 26 例非 axSpA 患者中获得粪便标本。所有样本均进行 16S 核糖体 DNA 测序。
本研究共纳入 73 例 UC 患者,axSpA 发病率为 19.2%。C 反应蛋白>10mg/L 的患者 axSpA 发病率明显更高。与非 axSpA 组相比,axSpA 组厚壁菌门和粪杆菌属丰度降低,变形菌门和埃希氏菌属/志贺氏菌属丰度增加。指示菌分析显示,埃希氏菌属/志贺氏菌属更有可能是 axSpA 的指示菌。此外,axSpA 组中许多生物合成和代谢途径,包括谷胱甘肽代谢、脂肪酸降解、香叶醇降解和铁载体族非核糖体肽生物合成等,均上调。
UC 患者 axSpA 发病率较高,这可能与这些患者埃希氏菌属/志贺氏菌属的相对丰度有关。axSpA 患者粪便菌群的各种生物合成和代谢途径丰度上调。