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Lipid metabolism and identification of biomarkers in asthma by lipidomic analysis

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ELSEVIER
DOI: 10.1016/j.bbalip.2020.158853

关键词

Asthma; Biomarkers; Lipid metabolism; Lipidomics

资金

  1. National Natural Science Foundation of China [U1904142, 81800891]
  2. Scientific and technological projects of Science and Technology Department of Henan Province [182102410010]
  3. Key Scientific Research Project of Colleges and Universities in Henan Province [18A320056]

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The study characterized the plasma lipid profile of asthmatic patients and healthy controls, identifying significant changes in ten lipid species in the asthmatic patients. Some lipids were positively correlated with the severity of asthma, while others were negatively correlated. PE (38:1) was identified as a potential lipid biomarker for asthma, while PE (20:0/18:1) and TG (16:0/16:0/18:1) may be related to IgE levels in asthmatic patients.
Background: Lipids participate in many important biological functions through energy storage, material transport, signal transduction, and molecular recognition processes. Studies have reported that asthmatic patients have abnormal lipid metabolism. However, there are limited studies on the characterization of lipid metabolism in asthmatic patients by lipidomics. Methods: We characterized the plasma lipid profile of 28 healthy controls and 33 outpatients with asthma (18 mild, 15 moderate) by liquid chromatography mass spectrometry/mass spectrometry-based lipidomics. Results: We determined 1338 individual lipid species in the plasma. Significant changes were identified in ten lipid species in asthmatic patients than in healthy controls (all P < 0.05). Phosphatidylethanolamine (PE) (18:1p/22:6), PE (20:0/18:1), PE (38:1), sphingomyelin (SM) (d18:1/18:1), and triglyceride (TG) (16:0/16:0/18:1) positively correlated with the severity of asthma (all P < 0.05). Phosphatidylinositol (PI) (16:0/20:4), TG (17:0/18:1/18:1), phosphatidylglycerol (PG) (44:0), ceramide (Cer) (d16:0/27:2), and lysophosphatidylcholine (LPC) (22:4) negatively correlated with the severity of asthma (all P < 0.05). Correlation analysis showed a significant correlation between all ten lipid species (all P < 0.05). From the area under the curve of the receiver operating characteristic curve analysis, PE (38:1) was the major lipid metabolite that distinguished asthmatic patients from healthy controls, and may be considered a potential lipid biomarker. PE (20:0/18:1) and TG (16:0/16:0/18:1) might be related to IgE levels in asthmatic patients. Conclusions: Our results indicated the presence of abnormal lipid metabolism, which correlated with the severity and IgE levels in asthmatic patients.

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