Progranulin, sICAM-1, and sVCAM-1 May Predict an Increased Risk for Ventricular Arrhythmias in Patients with Systemic Sclerosis

Author:

Sebestyén Veronika12,Ratku Balázs13ORCID,Ujvárosy Dóra1,Lőrincz Hajnalka4ORCID,Tari Dóra5,Végh Lilla12,Majai Gyöngyike6,Somodi Sándor13,Páll Dénes3ORCID,Szűcs Gabriella5ORCID,Harangi Mariann34ORCID,Szabó Zoltán1

Affiliation:

1. Department of Emergency Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary

2. Doctoral School of Health Sciences, University of Debrecen, 4032 Debrecen, Hungary

3. Institute of Health Studies, Faculty of Health Sciences, University of Debrecen, 4032 Debrecen, Hungary

4. Division of Metabolism, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary

5. Department of Rheumatology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary

6. Division of Clinical Immunology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary

Abstract

In systemic sclerosis (SSc), fibrosis of the myocardium along with ongoing autoimmune inflammation can alter the electric function of the cardiac myocytes, which may increase the risk for ventricular arrhythmias and sudden cardiac death. We analyzed the electrocardiographic (ECG) variables describing ventricular repolarization such as QT interval, QT dispersion (QTd), T wave peak-to-end interval (Tpe), and arrhythmogeneity index (AIX) of 26 patients with SSc and 36 healthy controls. Furthermore, echocardiographic and laboratory parameters were examined, with a focus on inflammatory proteins like C-reactive ptotein (CRP), soluble intracellular adhesion molecule-1 (sICAM-1), soluble vascular adhesion molecule-1 (sVCAM-1), and progranulin (PGRN). The CRP, sICAM-1, and sVCAM-1 levels were positively correlated with the length of the QT interval. Although the serum PGRN levels were not increased in the SSc group compared to the controls, in SSc patients, the PGRN levels were positively correlated with the QT interval and the AIX. According to our results, we conclude that there may be a potential association between autoimmune inflammation and the risk for ventricular arrhythmias in patients with SSc. We emphasize that the measurement of laboratory parameters of inflammatory activity including CRP, PGRN, sVCAM-1, and sICAM-1 could be helpful in the prediction of sudden cardiac death in patients with SSc.

Funder

Ministry of Culture and Innovation of Hungary

Publisher

MDPI AG

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