Serum Metabolomic Analysis of Coronary Heart Disease Patients with Stable Angina Pectoris Subtyped by Traditional Chinese Medicine Diagnostics Reveals Biomarkers Relevant to Personalized Treatments

被引:6
|
作者
Guo, Na [1 ,2 ]
Wang, Peili [3 ]
Yang, Jiaying [4 ]
Yang, Xiaofang [1 ]
van der Voet, Monique [5 ]
Wildwater, Marjolein [5 ]
Wei, Junying [6 ]
Tang, Xuan [7 ]
Wang, Mei [8 ]
Yang, Hongjun [1 ]
机构
[1] China Acad Chinese Med Sci, Expt Res Ctr, Beijing, Peoples R China
[2] China Acad Chinese Med Sci, Ctr Postdoctoral Res, Natl Resource Ctr Chinese Mat Med, State Key Lab Breeding Base Daodi Herbs, Beijing, Peoples R China
[3] China Acad Chinese Med Sci, Xiyuan Hosp, Beijing, Peoples R China
[4] Heilongjiang Univ Tradit Chinese Med, Coll Pharm, Harbin, Peoples R China
[5] Vivaltes BV, Heerhugowaard, Netherlands
[6] China Acad Chinese Med Sci, Inst Chinese Mat Med, Beijing, Peoples R China
[7] Tianjin Univ Tradit Chinese Med, Sch Chinese Mat Med, Tianjin, Peoples R China
[8] Leiden Univ, Inst Biol, LU European Ctr Chinese Med & Nat Cpds, Leiden, Netherlands
基金
中国国家自然科学基金;
关键词
angina pectoris; coronary heart disease; traditional Chinese medicine subtypes; metabolomics; vascular endothelial damage; ARTERY-DISEASE; BILE-ACIDS; RISK; ATHEROSCLEROSIS; ELEVATIONS; GENETICS; STEROLS; SEX;
D O I
10.3389/fphar.2021.664320
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To improve the treatment of patients with coronary heart disease (CHD), personalized treatments based on potential biomarkers could make a difference. To investigate if such potential biomarkers could be found for CHD inhomogeneous, we combined traditional Chinese medicine based diagnosis with untargeted and targeted metabolomics analyses. Shi and Xu patient subtype groups of CHD with angina pectoris were identified. Different metabolites including lipids, fatty acids and amino acids were further analyzed with targeted metabolomics and mapped to disease-related pathways. The long-chain unsaturated lipids ceramides metabolism, bile acid metabolism were differentially affected in the Xu subtype groups. While, Shi-subtype patients seemed to show inflammation, anomalous levels of bioactive phospholipids and antioxidant molecules. Furthermore, variations in the endothelial damage response and energy metabolism found based on ELISA analysis are the key divergence points between different CHD subtypes. The results showed Xu subtype patients might benefit from long-chain unsaturated lipids ceramides as therapeutic targets. Shi subtype patients might benefit more from levels of polyunsaturated fatty acid consumption and treatments that help in restoring energy balance. Metabolic differences can be essential for treatment protocols. Thus, patient group specific differences can serve as important information to refine current treatment approaches in a personalized manner.
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页数:14
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