Analysis of Differential Metabolites in Serum Metabolomics of Patients with Aortic Dissection

Author:

Gong Yun1,Li Tangzhiming1,Liu Qiyun1,Wang Xiaoyu1,Deng Zixian1,Liu Huadong1,Yu Biao2,Cheng Lixin3

Affiliation:

1. Shenzhen People’s Hospital (The Second Clinical Medical College, Jinan University; )

2. Luohu People’s Hospital (Shenzhen Luohu Hospital Group, The Third Affiliated Hospital of Shenzhen University)

3. Shenzhen People’s Hospital, First Affiliated Hospital of Southern University of Science and Technology,

Abstract

Abstract Background Pathogenesis and diagnostic biomarkers of aortic dissection (AD) can be classified by analysis of the serum differential metabolites. Analysis of differential metabolites in serum provides new methods for exploring the early diagnosis and treatment of aortic dissection Objectives This study examined affected metabolic pathways to assess the diagnostic value of metabolomics biomarkers in clients with AD. Method The serum from 30 patients with AD and 30 healthy people was collected. The most diagnostic metabolite markers were determined using metabolomic analysis and related metabolic pathways were explored. Results A total of 71 differential metabolites were identified. The altered metabolic pathways included reduced phospholipid catabolism and four different metabolites considered of most diagnostic value including N2-gamma-glutamylglutamine, PC(phocholines) (20:4(5Z,8Z,11Z,14Z)/15:0), propionyl carnitine, and taurine. These four predictive metabolic biomarkers accurately classified AD patient and healthy control (HC) samples with an area under the curve (AUC) of 0.9875. Based on the value of the four different metabolites, a formula was created to calculate the risk of aortic dissection. Risk score = N2-gamma-glutamylglutamine × -0.684 ་ PC(20:4(5Z,8Z,11Z,14Z)/15:0) × 0.427 ་ propionyl carnitine × 0.523 ་ taurine × -1.242. An additional metabolic pathways model related to aortic dissection was explored. Conclusion Metabolomics can help to explore the metabolic disorders of AD and aid a further search for potential metabolic biomarkers.

Publisher

Research Square Platform LLC

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