Towards an SI-Traceable Reference Measurement System for Seven Serum Apolipoproteins Using Bottom-Up Quantitative Proteomics: Conceptual Approach Enabled by Cross-Disciplinary/Cross-Sector Collaboration

Author:

Cobbaert Christa M1ORCID,Althaus Harald2,Begcevic Brkovic Ilijana34,Ceglarek Uta34,Coassin Stefan5ORCID,Delatour Vincent6,Deprez Liesbet7ORCID,Dikaios Ioannis7ORCID,Dittrich Julia34,Hoofnagle Andrew N8,Kostner Gerhard M9ORCID,Kronenberg Florian5ORCID,Kuklenyik Zsusanna10,Prinzing Urban11,Vesper Hubert W10,Zegers Ingrid6,Ruhaak L Renee1ORCID,

Affiliation:

1. Department of Clinical Chemistry and Laboratory Medicine, Leiden University Medical Center, Leiden, The Netherlands

2. Siemens Healthcare Diagnostics Products GmbH, Marburg, Germany

3. Institute of Laboratory Medicine, Clinical Chemistry and Molecular Diagnostics, University Hospital Leipzig, Leipzig,Germany

4. LIFE-Leipzig Research Center for Civilization Diseases, University of Leipzig, Leipzig, Germany

5. Institute of Genetic Epidemiology, Department of Genetics and Pharmacology, Medical University of Innsbruck, Innsbruck, Austria

6. Laboratoire National de Métrologie et d’Essais, Paris, France

7. European Commission, Joint Research Centre (JRC), Geel, Belgium

8. Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA

9. Gottfried Schatz Research Center (for Cell Signaling, Metabolism and Aging), Division of Molecular Biology and Biochemistry, Medical University of Graz, Graz, Austria

10. Division of Laboratory Sciences, Centers for Disease Control and Prevention, Atlanta, GA

11. Roche Diagnostics GmbH, Penzberg, Germany

Abstract

Abstract Current dyslipidemia management in patients with atherosclerotic cardiovascular disease (ASCVD) is based on traditional serum lipids. Yet, there is some indication from basic research that serum apolipoproteins A-I, (a), B, C-I, C-II, C-III, and E may give better pathophysiological insight into the root causes of dyslipidemia. To facilitate the future adoption of clinical serum apolipoprotein (apo) profiling for precision medicine, strategies for accurate testing should be developed in advance. Recent discoveries in basic science and translational medicine set the stage for the IFCC Working Group on Apolipoproteins by Mass Spectrometry. Main drivers were the convergence of unmet clinical needs in cardiovascular disease (CVD) patients with enabling technology and metrology. First, the residual cardiovascular risk after accounting for established risk factors demonstrates that the current lipid panel is too limited to capture the full complexity of lipid metabolism in patients. Second, there is a need for accurate test results in highly polymorphic and atherogenic apolipoproteins such as apo(a). Third, sufficient robustness of mass spectrometry technology allows reproducible protein quantification at the molecular level. Fourth, several calibration hierarchies in the revised ISO 17511:2020 guideline facilitate metrological traceability of test results, the highest achievable standard being traceability to SI. This article outlines the conceptual approach aimed at achieving a novel, multiplexed Reference Measurement System (RMS) for seven apolipoproteins based on isotope dilution mass spectrometry and peptide-based calibration. This RMS should enable standardization of existing and emerging apolipoprotein assays to SI, within allowable limits of measurement uncertainty, through a sustainable network of Reference Laboratories.

Funder

German Society for Clinical Chemistry and Laboratory Medicine

NIDDK/NIH

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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