Progranulin, sICAM-1, and sVCAM-1 May Predict an Increased Risk for Ventricular Arrhythmias in Patients with Systemic
Veronika Sebestyén1,2, Balázs Ratku1,3, Dóra Ujvárosy1
1Department of Emergency Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Insights
Systemic sclerosis (SSc) patients show altered heart electrical function due to inflammation, increasing arrhythmia risk. Inflammatory markers like CRP and PGRN correlate with ECG changes, aiding sudden cardiac death prediction in SSc.
Area of Science:
- Cardiology
- Immunology
- Electrophysiology
Background:
- Systemic sclerosis (SSc) involves cardiac fibrosis and autoimmune inflammation, potentially affecting heart electrical function.
- This can elevate the risk of ventricular arrhythmias and sudden cardiac death in SSc patients.
Purpose of the Study:
- To investigate the association between autoimmune inflammation and cardiac electrical abnormalities in SSc.
- To analyze electrocardiographic (ECG) variables of ventricular repolarization and their correlation with inflammatory markers.
Main Methods:
- Compared ECG parameters (QT interval, QT dispersion, Tpe, AIX) in 26 SSc patients and 36 controls.
- Measured echocardiographic and laboratory parameters, including C-reactive protein (CRP), sICAM-1, sVCAM-1, and progranulin (PGRN).
Main Results:
- CRP, sICAM-1, and sVCAM-1 levels positively correlated with QT interval length in SSc patients.
- In SSc patients, progranulin (PGRN) levels correlated positively with QT interval and arrhythmogeneity index (AIX).
Conclusions:
- Autoimmune inflammation may be linked to ventricular arrhythmia risk in SSc.
- Measuring inflammatory markers (CRP, PGRN, sVCAM-1, sICAM-1) could help predict sudden cardiac death in SSc.
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.
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