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Circulating angiostatin serum level in patients with systemic sclerosis

INTRODUCTION: Systemic sclerosis (SSc) is achronic connective tissue disease characterized by microangiopathy with inadequate angiogenesis. Angiostatin (AS) is a potent antiangiogenic factor specifically inhibiting proliferation and inducing apoptosis of vascular endothelial cells. AIM: To evaluate...

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Detalles Bibliográficos
Autores principales: Gerlicz-Kowalczuk, Zofia, Dziankowska-Zaborszczyk, Elzbieta, Dziankowska-Bartkowiak, Bożena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5799757/
https://www.ncbi.nlm.nih.gov/pubmed/29422818
http://dx.doi.org/10.5114/ada.2017.72459
Descripción
Sumario:INTRODUCTION: Systemic sclerosis (SSc) is achronic connective tissue disease characterized by microangiopathy with inadequate angiogenesis. Angiostatin (AS) is a potent antiangiogenic factor specifically inhibiting proliferation and inducing apoptosis of vascular endothelial cells. AIM: To evaluate the level of angiostatin in the serum of patients with SSc. MATERIAL AND METHODS: Serum levels of AS were measured in 20 SSc patients and 12 healthy controls. RESULTS: A statistically significant difference in the serum levels of AS in SSc patients was observed compared to the control group (636.51 vs. 869.20 ng/ml; p = 0.012). Significant correlations between limited and disseminated SSc (lSSc/dSSc) were not found, however, a difference between lSSc and the control group was demonstrated (620.00 vs. 869.20 ng/ml; p = 0.011). The serum level of AS was not associated positively with organ changes caused by SSc. However, a statistically significant lower serum level of AS was observed in patients with SSc and no esophageal (p = 0.008) or pulmonary changes (p = 0.007) compared to the control group. CONCLUSIONS: Our results reveal significant differences in AS level in SSc patients compared to the healthy controls, and suggest that a low level of AS may occur as a result of impaired angiogenesis.