Dai Qiuying, Zhou Yue, Wu Jingjing, Liao Mingjuan
Department of Traditional Chinese Medicine, The Ninth People's Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China.
Department of Breast Surgery, LongHua Hospital Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Front Cell Infect Microbiol. 2025 Jun 10;15:1514315. doi: 10.3389/fcimb.2025.1514315. eCollection 2025.
Granulomatous lobular mastitis (GLM) is a type of non-puerperal mastitis (NPM) associated with autoimmune factors. Previous studies suggest that gut microbiota dysbiosis may play a role in the pathological process of GLM; however, the specific role of gut microbiota metabolites in this process remains unclear. Therefore, this study aimed to investigate the gut metabolic characteristics of short-chain fatty acid (SCFA) in patients with GLM, a type of NPM.
Stool samples were collected from 35 patients with GLM and 26 healthy control (HC) subjects. These samples underwent targeted metabolomic analysis to measure SCFA and 16s rRNA high-throughput sequencing to assess gut microbiota composition and differences between the groups.
Gas chromatography-mass spectrometry(GC-MS) analysis revealed that the content of SCFA-butanoic acid in the feces of patients with GLM was higher than that in the HC group. Notably, significant differences in metabolic pathways were observed between the HC and GLM groups. High-throughput sequencing results showed that the richness and diversity of gut microbiota in patients with GLM were significantly lower than those in healthy individuals. In addition, 53 bacterial species were found to differ significantly in abundance between the two groups. Moreover, the level of isohexanoic acid in the feces of patients with GLM with recurrence disease was significantly higher than that of patients without recurrence.
Patients with GLM exhibit disturbances in gut butanoic acid metabolism and significant differences in gut microbiota structure compared to healthy individuals.
肉芽肿性小叶性乳腺炎(GLM)是一种与自身免疫因素相关的非产褥期乳腺炎(NPM)。先前的研究表明,肠道微生物群失调可能在GLM的病理过程中起作用;然而,肠道微生物群代谢产物在这一过程中的具体作用仍不清楚。因此,本研究旨在调查GLM(一种NPM)患者肠道短链脂肪酸(SCFA)的代谢特征。
收集35例GLM患者和26例健康对照(HC)受试者的粪便样本。对这些样本进行靶向代谢组学分析以测量SCFA,并进行16s rRNA高通量测序以评估肠道微生物群组成及两组之间的差异。
气相色谱-质谱联用(GC-MS)分析显示,GLM患者粪便中SCFA-丁酸的含量高于HC组。值得注意的是,HC组和GLM组之间在代谢途径上观察到显著差异。高通量测序结果表明,GLM患者肠道微生物群的丰富度和多样性显著低于健康个体。此外,发现两组之间有53种细菌的丰度存在显著差异。此外,复发型GLM患者粪便中异己酸水平显著高于未复发患者。
与健康个体相比,GLM患者存在肠道丁酸代谢紊乱和肠道微生物群结构的显著差异。