Endocan and Circulating Progenitor Cells in Women with Systemic Sclerosis: Association with Inflammation and Pulmonary Hypertension

• Published in: Biomedicines Vol. 9; no. 5; p. 533
• Main Authors: Lo Gullo, Alberto, Mandraffino, Giuseppe, Rodríguez-Carrio, Javier, Scuruchi, Michele, Sinicropi, Davide, Postorino, Maria, Morace, Carmela, Giuffrida, Clemente, Sciortino, Davide, Gallizzi, Romina, Loddo, Saverio, Zito, Concetta, Squadrito, Giovanni
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 11-05-2021; MDPI
• Subjects: Biomarkers; Blood pressure; Bone marrow; CD34 antigen; Cell number; Chronic obstructive pulmonary disease; circulating progenitor cells; Disease; Echocardiography; endocan; Endothelial cells; Fibrinogen; Fibrosis; Flow cytometry; Heart rate; Hypertension; Inflammation; Inflammatory diseases; Laboratories; Plasma levels; Progenitor cells; Proteoglycans; Pulmonary artery; Pulmonary hypertension; Stem cells; Systemic sclerosis; Ulcers; Ultrasonic imaging; Vascular diseases; Vitamin D; Walking
• ISSN: 2227-9059; 2227-9059
• DOI: 10.3390/biomedicines9050533

Background: Systemic sclerosis (SSc) is characterized by early vasculopathy and fibrosis in the skin, lungs, and other tissues. Vascular manifestations of SSc include Raynaud’s phenomenon, digital ulcers, and pulmonary artery hypertension (PAH). PAH is the second most common cause of mortality in SSc. Circulating CD34+ cells associated with cardiovascular health status in several conditions, including chronic immune-inflammatory disease. CD34+ cell numbers have been found inconstantly reduced in SSc. Endocan, a proteoglycan expressed by endothelial cells, was recently suggested as a marker of vascular stress. We tested the relationships among CD34+ cells, endocan, inflammatory markers, vitamin D levels, and clinical parameters in SSc patients with PAH. METHODS: Standard echocardiography was performed. Vitamin D levels, CD34+ cells, inflammatory markers, endocan plasma levels were determined in 36 female SSc patients (24 diffuse/12 limited) and 36 matched controls (HC). RESULTS: We found no difference in CD34+ and vitamin D levels in SSc as compared to controls; ESR, CRP, fibrinogen, endocan, sPAP were higher in SSc with respect to controls. We found a correlation between endocan and: CD34+ cells (r: −0.540, p = 0.002), pulmonary arterial pressure (sPAP) (r: 0.565, p < 0.001), tricuspid annular plane excursion (TAPSE) (r: −0.311, p < 0.01), and E/A ratio (r: −0.487, p < 0.001), but not with ejection fraction (r: −0.057, p = 0.785) in SSc. CD34+ cells correlate with fibrinogen (r: −0.619, p < 0.001), sPAP (r: −0.404, p = 0.011), E/A (r: 0.470, p < 0.005 in SSc. CONCLUSION: CD34+ cell number was significantly correlated with endocan levels and with sPAP in SSc; endocan and CD34+ progenitor cells might be suggested as a potential marker of disease status.