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Meeting abstract

https://doi.org/10.15836/ccar2023.281

Biomarker Potential of Plasma Protein N-glycans in Coronary Artery Disease

Aleksandar Blivajs orcid id orcid.org/0000-0003-3404-3837 ; Dubrava University Hospital, Zagreb, Croatia
Barbara Radovani ; Department of Biotechnology, University of Rijeka, Rijeka, Croatia
Lovorka Đerek orcid id orcid.org/0000-0002-3041-7718 ; Dubrava University Hospital, Zagreb, Croatia
Diana Rudan orcid id orcid.org/0000-0001-9473-2517 ; Dubrava University Hospital, Zagreb, Croatia
David Visentin ; Department of Biotechnology, University of Rijeka, Rijeka, Croatia
Gordan Lauc orcid id orcid.org/0000-0003-1840-9560 ; Genos Glycoscience Research Laboratory, Zagreb, Croatia
Ivan Gudelj orcid id orcid.org/0000-0003-0624-7170 ; Department of Biotechnology, University of Rijeka, Rijeka, Croatia


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Abstract

Keywords

plasma proteins; N-glycans; coronary artery disease

Hrčak ID:

310172

URI

https://hrcak.srce.hr/310172

Publication date:

28.11.2023.

Visits: 474 *



Introduction: Coronary artery disease (CAD) is the most common cardiovascular disease (CVD), resulting from chronic inflammation of the coronary arteries due to the formation of atherosclerotic plaques, and its presence is a significant marker of adverse cardiovascular events. A growing body of research suggests that alterations in protein N-glycosylation are involved in the development of CVD through various mechanisms and have significant biomarker potential because of their sensitivity to changes that occur in the organism during inflammation-related conditions such as CVD (1-3). Our aim was to determine whether the N-glycome of total plasma proteins is associated with CAD, because N-glycans are known to alter the effector functions of proteins, which may enhance their inflammatory response in CAD.

Patients and Methods: In this study, we analysed the N-glycome of plasma proteins isolated from patients who underwent coronary angiography and classified into patients with confirmed coronary atherosclerosis and patients with clean coronaries. Proteins were denatured and enzymatically deglycosylated, and the released and fluorescently labelled N-glycans were analysed by ultra-high performance liquid chromatography based on hydrophilic interactions with fluorescence detection (HILIC-UHPLC-FLR) (Figure 1). Because previous studies have shown evidence of sexual dimorphism in CVD and significant sex differences in the association of N-glycans with CVD risk, we performed sex-stratified analysis of plasma N-glycans.

FIGURE 1 Representative chromatogram of 2-AB labelled plasma protein N-glycans separated by HILIC–UHPLC-FLR. The integration areas together with a major structure presented in each glycan peak are shown.
CC202318_11-12_281-f1

Results: The results showed significant differences in plasma N-glycome composition in CAD. Lower abundance of complex biantennary galactosylated N-glycans with core fucose and, conversely, a higher abundance of highly branched (tri- and tetra-antennary) sialylated N-glycan structures with terminal fucose was shown to be associated with CAD.

Conclusion: The obtained chromatograms shed light on the composition of plasma protein N-glycans in CAD and provided new insights into N-glycosylation changes in CAD. Overall, because of their sensitivity to changes that occur in an organism, protein N-glycosylation emerges as a significant factor in CAD and holds potential as a diagnostic tool, with glycan-based biomarkers showing promise for predicting cardiovascular health.

LITERATURE

1 

Wittenbecher C, Štambuk T, Kuxhaus O, Rudman N, Vučković F, Štambuk J, et al. Plasma N-Glycans as Emerging Biomarkers of Cardiometabolic Risk: A Prospective Investigation in the EPIC-Potsdam Cohort Study. Diabetes Care. 2020 March;43(3):661–8. https://doi.org/10.2337/dc19-1507 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/31915204

2 

Birukov A, Plavša B, Eichelmann F, Kuxhaus O, Hoshi RA, Rudman N, et al. Immunoglobulin G N-Glycosylation Signatures in Incident Type 2 Diabetes and Cardiovascular Disease. Diabetes Care. 2022 November 1;45(11):2729–36. https://doi.org/10.2337/dc22-0833 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/36174116

3 

Plavša B, Szavits-Nossan J, Blivajs A, Rapčan B, Radovani B, Šesto I, et al. The N-Glycosylation of Total Plasma Proteins and IgG in Atrial Fibrillation. Biomolecules. 2023 March 28;13(4):605. https://doi.org/10.3390/biom13040605 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/37189353


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