Wang Yu, Li Shu-Min, Li Chao, Yang Wen-Qing, Li Yun-Lun
Affiliated Hospital of Shandong University of Traditional Chinese Medicine Ji'nan 250011, China.
Shandong University of Traditional Chinese Medicine Ji'nan 250355, China.
Zhongguo Zhong Yao Za Zhi. 2021 Jun;46(11):2881-2888. doi: 10.19540/j.cnki.cjcmm.20210323.201.
In this study, patients with prehypertensive liver-fire hyperactivity syndrome(LFHS) were selected as the research objects. The plasma samples of healthy volunteers and patients with prehypertensive LFHS were analyzed by non-targeted metabolomics based on UPLC-Q-Exactive MS. The differential biomarkers and metabolic pathways were screened out by multivariate statistics and metabolic pathway analysis, which revealed the characteristics of metabolic patterns of the syndrome. Thirty-three potential biomarkers such as androsterone and lysophosphatidylcholine and 16 related metabolic pathways such as steroid hormone metabolism and lipid metabolism were identified, and a partial least squares-discriminant analysis(PLS-DA) model of traditional Chinese medicine(TCM) syndromes was preliminarily constructed: Y =-0.070X_(13)-0.006X_8+ 0.040X_5-0.152X_1+0.131X_(10)+0.036X_(11)+0.043X_(23)+0.076X_(16)+0.132X_(20)+0.081X_(19)-0.101X_(31)+0.082X_(15)-0.038X_9+0.079X_(24). The predictive value of the model was 88.1%, and the explanatory power was 88.4%. In this study, the characteristic metabolic pattern of the prehypertensive LFHS was distinguished and revealed by metabolomics. The constructed PLS-DA model is expected to provide an objective basis for the identification of TCM syndromes in prehypertension, and inspiration for exploring the biological basis of TCM syndromes at small-molecular and overall levels.
本研究选取高血压前期肝火亢盛证(LFHS)患者作为研究对象。采用基于超高效液相色谱-四极杆-静电场轨道阱质谱(UPLC-Q-Exactive MS)的非靶向代谢组学方法,对健康志愿者和高血压前期LFHS患者的血浆样本进行分析。通过多元统计和代谢通路分析筛选出差异生物标志物和代谢通路,揭示该证型的代谢模式特征。鉴定出33种潜在生物标志物,如雄酮和溶血磷脂酰胆碱,以及16条相关代谢通路,如类固醇激素代谢和脂质代谢,并初步构建了中医证型的偏最小二乘判别分析(PLS-DA)模型:Y = -0.070X₁₃ - 0.006X₈ + 0.040X₅ - 0.152X₁ + 0.131X₁₀ + 0.036X₁₁ + 0.043X₂₃ + 0.076X₁₆ + 0.132X₂₀ + 0.081X₁₉ - 0.101X₃₁ + 0.082X₁₅ - 0.038X₉ + 0.079X₂₄。该模型的预测值为88.1%,解释力为88.4%。本研究通过代谢组学区分并揭示了高血压前期LFHS的特征性代谢模式。构建的PLS-DA模型有望为高血压前期中医证型的识别提供客观依据,并为从小分子和整体水平探索中医证型的生物学基础提供启示。