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胆汁菌群及胆汁酸谱与胆囊结石的相关性分析OA

Correlation of bile microbiota and bile acid profiles with cholecystolithiasis

中文摘要英文摘要

目的 探究胆囊结石与胆汁菌群及胆汁酸谱的相关性,并构建胆囊结石的预测模型.方法 回顾性纳入哈尔滨医科大学附属第二医院与哈尔滨医科大学附属肿瘤医院2024年9月至2025年5月期间行手术切除的35例患者,诊断为胆囊结石并行腹腔镜胆囊切除的患者为胆囊结石组(S组,n=25),诊断为原发性肝癌并行根治性切除的患者为无胆囊结石组(N组,n=10),比较两组患者在临床资料方面的差异.收集两组患者胆汁样本并进行16S rDNA测序和靶向代谢组学测序.对胆汁菌群测序结果进行α与β多样性分析以评估菌群多样性差异,并分析菌群组成变化和代表性差异物种.筛选S组胆汁样本中升高和下降幅度最大的差异代谢物,绘制受试者工作特征(ROC)曲线并计算其曲线下面积(AUC),选取AUC≥0.7的胆汁差异代谢物建立联合预测模型.建立微生物-代谢物网络并采用Spearman秩检验分析胆汁差异代谢物与菌群的相关性.结果 两组在一般资料方面的比较差异无统计学意义(均P>0.05).胆汁菌群多样性分析显示,S组α多样性和β多样性均显著降低(P<0.05);物种组成和差异物种分析显示,胆囊结石与胆汁菌群组成改变显著相关.胆汁代谢物差异分析显示,S组多种胆汁酸水平变化显著,主要表现为次级胆汁酸及其结合物水平升高.熊去氧胆酸-3-硫酸盐、牛磺胆酸-3-硫酸盐、石胆酸、甘氨胆酸-3-硫酸盐、鹅去氧胆酸-24-酰基-β-D-葡糖苷酸这5种胆汁酸预测胆囊结石的ROC曲线AUC≥0.7,根据其建立的联合预测模型AUC=0.926.微生物-代谢物网络相关性分析显示,红微菌属与S组水平升高的胆汁酸显著正相关(均P<0.05).结论 胆囊结石与胆汁菌群和胆汁酸谱改变具有相关性,根据差异胆汁酸构建的联合预测模型效能较好.

Objective To investigate the correlation between cholecystolithiasis and bile microbiota as well as bile acid profiles,and to construct a predictive model for cholecystolithiasis.Methods A retrospective study was conducted involving 35 patients who underwent surgical resection at the Second Affiliated Hospital of Harbin Medical University and The Affiliated Cancer Hospital of Harbin Medical University from September 2024 to May 2025.Patients diagnosed with cholecystolithiasis who underwent laparoscopic cholecystectomy were assigned to the cholecystolithiasis group(Group S,n=25),and patients diagnosed with primary liver cancer who underwent radical resection with no cholecystolithiasis were assigned to the non-cholecystolithiasis group(Group N,n=10).Clinical data were compared between the two groups.Bile samples were collected from both groups for 16S rDNA sequencing and targeted metabolomics analysis.Alpha and beta diversity analyses were performed on the bile microbiota sequencing results to assess differences in microbial diversity,and changes in microbial composition along with representative differential taxa were analyzed.Differential metabolites exhibiting the greatest increase or decrease in bile samples from Group S were screened.Receiver operating characteristic(ROC)curves were generated and the area under the curve(AUC)was calculated.Differential bile metabolites with an AUC≥0.7 were selected to establish a combined predictive model.A microbe-metabolite network was constructed,and Spearman's rank correlation test was used to analyze the correlation between differential bile metabolites and microbial communities.Results No statistically significant differences were observed in baseline clinical characteristics between the two groups(all P>0.05).Analysis of bile microbiota diversity revealed that both alpha diversity and beta diversity were significantly reduced in Group S(P<0.05).Species composition and differential species analysis indicated that cholecystolithiasis was significantly associated with alterations in bile microbiota composition.Differential analysis of bile metabolites showed significant changes in multiple bile acid levels in Group S,primarily characterized by elevated levels of secondary bile acids and their conjugates.Five bile acids including ursodeoxycholic acid-3-sulfate,taurocholic acid-3-sulfate,lithocholic acid,glycocholic acid-3-sulfate,and chenodeoxycholic acid-24-acyl-β-D-glucuronide exhibited an AUC≥0.7 in ROC analysis for predicting cholecystolithiasis.The combined predictive model established based on these metabolites achieved an AUC of 0.926.Microbe-metabolite network correlation analysis revealed that Rubellimicrobium was significantly positively correlated with elevated bile acid levels in Group S(all P<0.05).Conclusion Cholecystolithiasis is correlated with alterations in bile microbiota and bile acid profiles.The combined predictive model constructed based on differential bile acids demonstrates satisfactory diagnostic performance.

荆小伟;吴德海;邰升

哈尔滨医科大学附属第二医院普通外科六病房,黑龙江 哈尔滨 150001哈尔滨医科大学附属第二医院普通外科六病房,黑龙江 哈尔滨 150001哈尔滨医科大学附属肿瘤医院肝胆胰外科,黑龙江 哈尔滨 150081

医药卫生

胆囊结石胆汁菌群胆汁酸16S rDNA测序靶向代谢组学多组学分析

cholecystolithiasisbile microbiotabile acids16S rDNA sequencingtargeted metabolomicsmulti-omics

《肝胆胰外科杂志》 2026 (6)

408-418,11

国家自然科学基金面上项目(82373111).

10.11952/j.issn.1007-1954.2026.06.005

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