You Zhiyuan, Zhang Jialin, Xu Yifeng, Lu Junhong, Zhang Renling, Zhu Zhujing, Wang Yiqin, Hao Yiming
Shanghai Key Laboratory of Health Identification and Assessment/Laboratory of TCM Four Diagnostic Information, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, People's Republic of China.
Gastroenterology, Longhua Hospital Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, People's Republic of China.
J Inflamm Res. 2024 Nov 2;17:8027-8045. doi: 10.2147/JIR.S480307. eCollection 2024.
This study aimed to establish a model for identifying chronic gastritis with the traditional Chinese medicine damp phlegm pattern by examining metabolite changes in the tongue coating of patients. It also explored the role of metabolic pathways in the pathogenesis of this condition.
This cross-sectional study involved 300 patients diagnosed with chronic gastritis. Of these, 200 patients exhibited the damp phlegm pattern, while 100 did not. Metabolomic methods employing GC-TOF-MS and UHPLC-QE-MS were utilized to identify various metabolites in the tongue coating of patients. An identification model for chronic gastritis with the damp phlegm pattern was created based on ROC curves derived from differential biomarkers. Additionally, 50 samples not included in model construction were collected for external validation.
Comparison of the damp phlegm pattern group with the non-damp phlegm pattern group revealed a total of 116 differential metabolites. Among these, lipids and lipid-like compounds were most abundant, comprising 27 types, which included four lipid metabolites related to sphingomyelin metabolism. The ROC model, which included phenol, 2.6-diaminoheptanedioic acid, and N-hexadecanoyl pyrrolidine, demonstrated the highest accuracy, with accuracy, sensitivity, and specificity metrics of 94.0%, 91.0%, and 87.0%, respectively. Furthermore, external validation using tongue coating metabolites from 50 patients revealed accuracy, sensitivity, and specificity in the validation set of 93.9%, 90.6%, and 83.3%, respectively.
Differential metabolites between patients with the damp phlegm pattern and those without are primarily lipids and lipid-like compounds. N-hexadecanoyl pyrrolidine, phenol, and 2.6-diaminoheptanedioic acid may serve as potential biomarkers for chronic gastritis characterized by the damp phlegm pattern.
本研究旨在通过检测慢性胃炎患者舌苔中的代谢物变化,建立一种用于识别中医痰湿证型慢性胃炎的模型。同时,探索代谢途径在该病症发病机制中的作用。
本横断面研究纳入了300例被诊断为慢性胃炎的患者。其中,200例患者表现为痰湿证型,100例患者未表现为痰湿证型。采用气相色谱-飞行时间质谱(GC-TOF-MS)和超高效液相色谱-四极杆飞行时间质谱(UHPLC-QE-MS)代谢组学方法,鉴定患者舌苔中的各种代谢物。基于差异生物标志物的ROC曲线,建立了痰湿证型慢性胃炎的识别模型。此外,收集了50个未纳入模型构建的样本进行外部验证。
痰湿证型组与非痰湿证型组比较,共发现116种差异代谢物。其中,脂质和类脂质化合物最为丰富,有27种,包括4种与鞘磷脂代谢相关的脂质代谢物。包含苯酚、2,6-二氨基庚二酸和N-十六烷酰吡咯烷的ROC模型显示出最高的准确性,其准确性、敏感性和特异性指标分别为94.0%、91.0%和87.0%。此外,对50例患者舌苔代谢物进行外部验证,验证集的准确性、敏感性和特异性分别为93.9%、90.6%和83.3%。
痰湿证型患者与非痰湿证型患者之间的差异代谢物主要是脂质和类脂质化合物。N-十六烷酰吡咯烷、苯酚和2,6-二氨基庚二酸可能作为痰湿证型慢性胃炎的潜在生物标志物。