Deep mining of oxysterols and cholestenoic acids in human plasma and cerebrospinal fluid: Quantification using isotope dilution mass spectrometry.

Bile acid Cholestenoic acid Cholesterol Derivatisation Hydroxycholesterol Isotope-labelled standard LC-MS

Journal

Analytica chimica acta
ISSN: 1873-4324
Titre abrégé: Anal Chim Acta
Pays: Netherlands
ID NLM: 0370534

Informations de publication

Date de publication:
15 Apr 2021
Historique:
received: 22 12 2020
accepted: 25 01 2021
entrez: 19 3 2021
pubmed: 20 3 2021
medline: 15 5 2021
Statut: ppublish

Résumé

Both plasma and cerebrospinal fluid (CSF) are rich in cholesterol and its metabolites. Here we describe in detail a methodology for the identification and quantification of multiple sterols including oxysterols and sterol-acids found in these fluids. The method is translatable to any laboratory with access to liquid chromatography - tandem mass spectrometry. The method exploits isotope-dilution mass spectrometry for absolute quantification of target metabolites. The method is applicable for semi-quantification of other sterols for which isotope labelled surrogates are not available and approximate quantification of partially identified sterols. Values are reported for non-esterified sterols in the absence of saponification and total sterols following saponification. In this way absolute quantification data is reported for 17 sterols in the NIST SRM 1950 plasma along with semi-quantitative data for 8 additional sterols and approximate quantification for one further sterol. In a pooled (CSF) sample used for internal quality control, absolute quantification was performed on 10 sterols, semi-quantification on 9 sterols and approximate quantification on a further three partially identified sterols. The value of the method is illustrated by confirming the sterol phenotype of a patient suffering from ACOX2 deficiency, a rare disorder of bile acid biosynthesis, and in a plasma sample from a patient suffering from cerebrotendinous xanthomatosis, where cholesterol 27-hydroxylase is deficient.

Identifiants

pubmed: 33736801
pii: S0003-2670(21)00085-4
doi: 10.1016/j.aca.2021.338259
pmc: PMC7988461
pii:
doi:

Substances chimiques

Oxysterols 0
Sterols 0
Cholesterol 97C5T2UQ7J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

338259

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: WJG and YW are listed as inventors on the patent “Kit and method for quantitative detection of steroids” US9851368B2. WJG, EY and YW are shareholders in CholesteniX Ltd.

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Auteurs

Eylan Yutuc (E)

Swansea University Medical School, ILS1 Building, Singleton Park, Swansea, SA2 8PP, Wales, UK.

Alison L Dickson (AL)

Swansea University Medical School, ILS1 Building, Singleton Park, Swansea, SA2 8PP, Wales, UK.

Manuela Pacciarini (M)

Swansea University Medical School, ILS1 Building, Singleton Park, Swansea, SA2 8PP, Wales, UK.

Lauren Griffiths (L)

Swansea University Medical School, ILS1 Building, Singleton Park, Swansea, SA2 8PP, Wales, UK.

Paul R S Baker (PRS)

Avanti Polar Lipids Inc, Alabaster, AL, USA.

Lisa Connell (L)

Avanti Polar Lipids Inc, Alabaster, AL, USA.

Anders Öhman (A)

Department of Integrative Medical Biology, Umeå University, SE-901 87, Umeå, Sweden.

Lars Forsgren (L)

Department of Clinical Science, Neurosciences, Umeå University, SE-901 85, Umeå, Sweden.

Miles Trupp (M)

Department of Clinical Science, Neurosciences, Umeå University, SE-901 85, Umeå, Sweden.

Sílvia Vilarinho (S)

Departments of Internal Medicine, Section of Digestive Diseases, and of Pathology, Yale University School of Medicine, New Haven, CT, USA.

Youssef Khalil (Y)

Inborn Errors of Metabolism, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, UK.

Peter T Clayton (PT)

Inborn Errors of Metabolism, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, UK.

Sinan Sari (S)

Department of Pediatrics, Division of Gastroenterology, Gazi University Faculty of Medicine, Ankara, Turkey.

Buket Dalgic (B)

Department of Pediatrics, Division of Gastroenterology, Gazi University Faculty of Medicine, Ankara, Turkey.

Philip Höflinger (P)

Department of Neurology and Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.

Ludger Schöls (L)

Department of Neurology and Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany; German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.

William J Griffiths (WJ)

Swansea University Medical School, ILS1 Building, Singleton Park, Swansea, SA2 8PP, Wales, UK. Electronic address: w.j.griffiths@swansea.ac.uk.

Yuqin Wang (Y)

Swansea University Medical School, ILS1 Building, Singleton Park, Swansea, SA2 8PP, Wales, UK.

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