4.2 Article

A software-assisted untargeted liquid chromatography-mass spectrometry method for lipidomic profiling of human plasma samples

期刊

INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS
卷 37, 期 4, 页码 368-376

出版社

SAGE PUBLICATIONS LTD
DOI: 10.1177/03936155221132291

关键词

Clinical and molecular epidemiology; epidemiology; mass spectrometry methods; metabolomics methods

资金

  1. Italian Ministry of Health (MoH) [708392]
  2. MRC-PHE Centre for Environment and Health [MR/L019744/1]
  3. Italian Ministry of Health Ricerca Corrente funds
  4. Horizon 2020 Marie Sklodowska-Curie fellowship EXACT [708392]
  5. Marie Curie Actions (MSCA) [708392] Funding Source: Marie Curie Actions (MSCA)

向作者/读者索取更多资源

This paper proposes an analytical pipeline for untargeted lipidomic profiling in human plasma, which is particularly suitable for large case-control epidemiologic studies. The method involves isopropanol protein precipitation, reverse phase liquid chromatography coupled to high resolution mass spectrometry, and software-assisted data processing. It can detect and identify a wide range of lipids.
Introduction In this paper, an analytical pipeline designed for untargeted lipidomic profiling in human plasma is proposed. The analytical pipeline was developed for case-control studies nested in prospective cohorts. Methods The procedure consisted of isopropanol protein precipitation followed by reverse phase liquid chromatography coupled to high resolution mass spectrometry and software-assisted data processing. The compounds are putatively annotated by matching experimental mass spectrometry data with spectral library data using LipidSearch software. The lipid profile of a pool of plasma samples from 10 healthy volunteers was detected in both positive and negative polarity modes. The impact of the chosen polarity on the number and quality of the lipid identification has been evaluated. Results More than 1000 lipids from 12 different classes were detected, 1150 in positive mode and 273 in negative mode. Nearly half of them were unambiguously identified by the software in positive mode, and about one-third in negative mode. The method repeatability was assessed on the plasma pool samples by means of variance components analysis. The intra- and inter-assay precision was measured for 10 lipids chosen among the most abundant found within the different lipid classes. The intra-assay coefficients of variation ranged from 2.56% to 4.56% while intra- and inter-day coefficients of variance never exceeded the 15% benchmark adopted. The lipidomic profiles of the 10 healthy volunteers were also investigated. Discussion This method detects a wide range of lipids and reports their degree of identification. It is particularly fit and well-designed for large case-control epidemiologic studies.

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