TY - JOUR
T1 - Serum levels of vascular dysfunction markers reflect disease severity and stage in systemic sclerosis patients
AU - Cossu, Marta
AU - Andracco, Romina
AU - Santaniello, Alessandro
AU - Marchini, Maurizio
AU - Severino, Adriana
AU - Caronni, Monica
AU - Radstake, Timothy
AU - Beretta, Lorenzo
PY - 2016/6/1
Y1 - 2016/6/1
N2 - Objective. To improve knowledge of vasculopathy in SSc through the assessment of serum levels of circulating angiogenetic and endothelial dysfunction markers in patients at different stages of the disease. Methods. Sera from 224 subjects were obtained and concentrations of angiopoietin-2, chemokine (C-X-C motif) ligand (CXCL)-16 (CXCL16), E-selectin, soluble intercellular adhesion molecule-1, IL-8 (CXCL8), soluble vascular adhesion molecule-1 and VEGF were determined by a Luminex assay. Subjects included healthy controls, 47 early SSc patients according to LeRoy and Medsger without other signs and symptoms of evolutive disease, 48 definitive SSc (defSSc) patients according to the 2013 ACR/EULAR criteria without skin or lung fibrosis, 51 lcSSc subjects and 35 dcSSc subjects. Results. The four groups of patients showed well-distinct clinical and laboratory characteristics, with a linear decreasing trend in forced vital capacity and diffusing capacity for carbon monoxide % predicted values from early SSc to defSSc to lcSSc and to dcSSc, and a linear increasing trend in ESR, and in the prevalence of abnormal CRP, serum gamma globulins and lung fibrosis (all P
AB - Objective. To improve knowledge of vasculopathy in SSc through the assessment of serum levels of circulating angiogenetic and endothelial dysfunction markers in patients at different stages of the disease. Methods. Sera from 224 subjects were obtained and concentrations of angiopoietin-2, chemokine (C-X-C motif) ligand (CXCL)-16 (CXCL16), E-selectin, soluble intercellular adhesion molecule-1, IL-8 (CXCL8), soluble vascular adhesion molecule-1 and VEGF were determined by a Luminex assay. Subjects included healthy controls, 47 early SSc patients according to LeRoy and Medsger without other signs and symptoms of evolutive disease, 48 definitive SSc (defSSc) patients according to the 2013 ACR/EULAR criteria without skin or lung fibrosis, 51 lcSSc subjects and 35 dcSSc subjects. Results. The four groups of patients showed well-distinct clinical and laboratory characteristics, with a linear decreasing trend in forced vital capacity and diffusing capacity for carbon monoxide % predicted values from early SSc to defSSc to lcSSc and to dcSSc, and a linear increasing trend in ESR, and in the prevalence of abnormal CRP, serum gamma globulins and lung fibrosis (all P
KW - Adhesion molecules
KW - Angiogenesis
KW - Early disease
KW - Systemic sclerosis
UR - http://www.scopus.com/inward/record.url?scp=84974829727&partnerID=8YFLogxK
U2 - 10.1093/rheumatology/kew017
DO - 10.1093/rheumatology/kew017
M3 - Article
C2 - 26989111
AN - SCOPUS:84974829727
SN - 1462-0324
VL - 55
SP - 1112
EP - 1116
JO - Rheumatology (Oxford, England)
JF - Rheumatology (Oxford, England)
IS - 6
M1 - kew017
ER -