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口腔菌群变化与食管癌变进程的关联研究

Association Between Alterations in Oral Microbiota and Progression of Esophageal Carcinogenesis

  • 摘要:
    目的 探讨口腔菌群和食管癌变进程的关联。
    方法 采用病例对照研究设计,纳入309名研究对象,包括159例正常对照、32例食管基底细胞增生、32例低级别上皮内瘤变、14例高级别上皮内瘤变以及72例食管鳞癌。采集舌拭子样本进行16S rRNA测序,分析菌群α多样性与β多样性,比较食管癌变进展不同阶段的微生物群落特征。采用比值比OR及其95%置信区间(CI)表示关联强度。
    结果 α多样性分析表明,食管癌病程进展各阶段的观测特征数(Sobs)指数存在显著差异(P<0.001)。在校正年龄、性别、吸烟、饮酒等混杂因素后,辛普森指数和癌变过程正相关(P=0.006)。β多样性分析显示,各组菌群结构存在差异。经有序多分类 logistic回归分析并调整多种混杂因素后发现,消化链球菌属PeptostreptococcusOR: 2.06,95%CI: 1.22~3.60)、髌骨菌门PatescibacteriaOR: 1.31,95%CI: 1.04~1.67)、二氧化碳嗜纤维菌CapnocytophagaOR: 1.24,95%CI: 1.05~1.54)、拟杆菌门BacteroidotaOR: 1.02,95%CI: 1.00~1.05)的相对丰度与癌变进程正相关。口腔杆菌属StomatobaculumOR: 0.57,95%CI: 0.30~1.00)、放线菌门ActinobacteriotaOR: 0.95,95%CI: 0.92~0.98)的相对丰度与癌变进程负相关。
    结论 特定口腔菌群与食管癌变进程显著相关,菌群间可能存在协同或拮抗作用。

     

    Abstract:
    Objective To explore the association between oral microbiota and esophageal carcinogenesis.
    Methods A case-control study design was employed. A total of 309 subjects were recruited, consisting of 159 healthy controls, 32 cases of esophageal basal cell hyperplasia, 32 cases of low-grade intraepithelial neoplasia, 14 cases of high-grade intraepithelial neoplasia, and 72 cases of esophageal squamous cell carcinoma. Tongue swab samples were collected for 16S rRNA sequencing. The α-diversity and β-diversity of the microbiota were analyzed, and the characteristics of the microbial communities at different stages of esophageal carcinogenesis were compared. The strength of the association was expressed by odds ratio (OR) and 95% confidence interval (CI).
    Results α-diversity analysis indicated significant differences in the observed species number (Sobs) index across various stages of esophageal cancer progression (P<0.001). After adjusting for confounding factors such as age, gender, smoking, and alcohol consumption, the Simpson index was positively correlated with carcinogenesis (P=0.006). β-diversity analysis revealed differences in microbiota structure among the groups. After ordered multinomial logistic regression analysis and adjustment for multiple confounding factors, the relative abundance of Peptostreptococcus (OR: 2.06, 95%CI: 1.22–3.60), Patescibacteria (OR: 1.31, 95%CI: 1.04–1.67), Capnocytophaga (OR: 1.24, 95%CI: 1.05–1.54), and Bacteroidota (OR: 1.02, 95%CI: 1.00–1.05) was positively correlated with carcinogenesis. The relative abundance of Stomatobaculum (OR: 0.57, 95%CI: 0.30–1.00) and Actinobacteriota (OR: 0.95, 95%CI: 0.92–0.98) was negatively correlated with carcinogenesis.
    Conclusion Specific oral microbiotas are significantly associated with esophageal carcinogenesis, and synergistic or antagonistic interactions may be observed among the microbiota.

     

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