Zhang Minghe, Fan Lianhui, Li Jian
Department of Urology, General Hospital of Northern Theater Command, Shenyang, Liaoning Province, China.
Medicine (Baltimore). 2025 Jul 18;104(29):e43103. doi: 10.1097/MD.0000000000043103.
In recent years, the role of the gut microbiome in stone formation has gained increasing attention. Specifically, certain gut microbes that metabolize oxalate may regulate oxalate levels in the body, thereby influencing the occurrence of kidney stones. This study aims to investigate the clinical characteristics of calcium oxalate stone patients, the composition of their gut microbiome, and the relationship between these factors and stone formation. This study included 159 calcium oxalate stone patients (case group) and 141 healthy controls (control group). Clinical data were collected to analyze differences in body mass index, urinary metabolic markers (urinary oxalate, calcium, and pH), and other indicators between the 2 groups. High-throughput 16S rRNA sequencing was used to compare the diversity and composition of the gut microbiome. Further, correlations between the gut microbiome and clinical metabolic indicators were analyzed, and a risk prediction model for calcium oxalate stones was developed based on clinical and gut microbiome characteristics. Significant differences in body mass index, urinary oxalate concentration, urinary calcium concentration, and urinary pH were observed between the case and control groups. Gut microbiome diversity analysis revealed that the Shannon and Chao1 indices were lower in the case group, and significant differences in microbiome composition were found. The abundance of Proteobacteria and Firmicutes changed significantly, with a notable decrease in Oxalobacter formigenes and an increase in Escherichia-Shigella species in the case group. Correlation analysis showed a negative correlation between O formigenes abundance and urinary oxalate concentration, and a negative correlation between Escherichia-Shigella and urinary pH. The random forest prediction model exhibited high predictive accuracy (area under the receiver operating characteristic curve = 0.90). The formation of calcium oxalate stones is closely related to the structure and function of the gut microbiome, particularly with the reduced abundance of the oxalate-degrading bacterium O formigenes. Gut microbiome imbalance may influence stone formation through various mechanisms. This study provides new theoretical insights for the early prediction, prevention, and treatment of calcium oxalate stones.
近年来,肠道微生物群在结石形成中的作用日益受到关注。具体而言,某些代谢草酸盐的肠道微生物可能调节体内草酸盐水平,从而影响肾结石的发生。本研究旨在调查草酸钙结石患者的临床特征、肠道微生物群组成,以及这些因素与结石形成之间的关系。本研究纳入了159例草酸钙结石患者(病例组)和141例健康对照者(对照组)。收集临床数据以分析两组之间体重指数、尿代谢标志物(尿草酸盐、钙和pH值)及其他指标的差异。采用高通量16S rRNA测序比较肠道微生物群的多样性和组成。此外,分析肠道微生物群与临床代谢指标之间的相关性,并基于临床和肠道微生物群特征建立草酸钙结石的风险预测模型。病例组和对照组在体重指数、尿草酸盐浓度、尿钙浓度和尿pH值方面存在显著差异。肠道微生物群多样性分析显示,病例组的香农指数和Chao1指数较低,且微生物群组成存在显著差异。变形菌门和厚壁菌门的丰度发生了显著变化,病例组中产甲酸草酸杆菌明显减少,大肠埃希菌-志贺菌属增加。相关性分析显示,产甲酸草酸杆菌丰度与尿草酸盐浓度呈负相关,大肠埃希菌-志贺菌属与尿pH值呈负相关。随机森林预测模型表现出较高的预测准确性(受试者操作特征曲线下面积=0.90)。草酸钙结石的形成与肠道微生物群的结构和功能密切相关,尤其是与草酸盐降解菌产甲酸草酸杆菌丰度降低有关。肠道微生物群失衡可能通过多种机制影响结石形成。本研究为草酸钙结石的早期预测、预防和治疗提供了新的理论见解。