Biomarker profiles of endothelial activation and dysfunction in rare systemic autoimmune diseases: implications for cardiovascular risk

Rheumatology (Oxford). 2021 Feb 1;60(2):785-801. doi: 10.1093/rheumatology/keaa270.

Abstract

Objectives: Vasculopathy is an important hallmark of systemic chronic inflammatory connective tissue diseases (CICTD) and is associated with increased cardiovascular risk. We investigated disease-specific biomarker profiles associated with endothelial dysfunction, angiogenic homeostasis and (tissue) inflammation, and their relation to disease activity in rare CICTD.

Methods: A total of 38 serum proteins associated with endothelial (dys)function and inflammation were measured by multiplex-immunoassay in treatment-naive patients with localized scleroderma (LoS, 30), eosinophilic fasciitis (EF, 8) or (juvenile) dermatomyositis (34), 119 (follow-up) samples during treatment, and 65 controls. Data were analysed by unsupervised clustering, Spearman correlations, non-parametric t test and ANOVA.

Results: The systemic CICTD, EF and dermatomyositis, had distinct biomarker profiles, with 'signature' markers galectin-9 (dermatomyositis) and CCL4, CCL18, CXCL9, fetuin, fibronectin, galectin-1 and TSP-1 (EF). In LoS, CCL18, CXCL9 and CXCL10 were subtly increased. Furthermore, dermatomyositis and EF shared upregulation of markers related to interferon (CCL2, CXCL10), endothelial activation (VCAM-1), inhibition of angiogenesis (angiopoietin-2, sVEGFR-1) and inflammation/leucocyte chemo-attraction (CCL19, CXCL13, IL-18, YKL-40), as well as disturbance of the Angiopoietin-Tie receptor system and VEGF-VEGFR system. These profiles were related to disease activity, and largely normalized during treatment. However, a subgroup of CICTD patients showed continued elevation of CXCL10, CXCL13, galectin-9, IL-18, TNFR2, VCAM-1, and/or YKL-40 during clinically inactive disease, possibly indicating subclinical interferon-driven inflammation and/or endothelial dysfunction.

Conclusion: CICTD-specific biomarker profiles revealed an anti-angiogenic, interferon-driven environment during active disease, with incomplete normalization under treatment. This warrants further investigation into monitoring of vascular biomarkers during clinical follow-up, or targeted interventions to minimize cardiovascular risk in the long term.

Keywords: autoimmune diseases; biomarkers; cardiovascular disease; dermatomyositis; disease activity; endothelial dysfunction; eosinophilic fasciitis; localized scleroderma.

MeSH terms

  • Autoimmunity
  • Biomarkers / blood*
  • Chemokine CXCL10 / blood
  • Chemokine CXCL13 / blood
  • Dermatomyositis* / blood
  • Dermatomyositis* / diagnosis
  • Endothelium, Vascular / immunology*
  • Eosinophilia* / blood
  • Eosinophilia* / diagnosis
  • Fasciitis* / blood
  • Fasciitis* / diagnosis
  • Female
  • Galectins / blood
  • Heart Disease Risk Factors
  • Humans
  • Male
  • Middle Aged
  • Monitoring, Immunologic / methods
  • Netherlands
  • Patient Acuity
  • Receptors, Tumor Necrosis Factor, Type II / blood
  • Scleroderma, Localized* / blood
  • Scleroderma, Localized* / diagnosis
  • Vascular Cell Adhesion Molecule-1 / blood

Substances

  • Biomarkers
  • CXCL13 protein, human
  • Chemokine CXCL10
  • Chemokine CXCL13
  • Galectins
  • LGALS9 protein, human
  • Receptors, Tumor Necrosis Factor, Type II
  • Vascular Cell Adhesion Molecule-1

Supplementary concepts

  • Eosinophilic Fasciitis