| Literature DB >> 29600562 |
Antonietta Gigante1, Domenico Margiotta2, Luca Navarini2, Biagio Barbano1, Maria L Gasperini1, Claudia D'Agostino3, Antonio Amoroso1, Antonella Afeltra2, Edoardo Rosato1.
Abstract
Patients with systemic sclerosis (SSc) are at a high risk of the development of ischaemic digital ulcers (DUs) that can be complicated with infections, gangrene, and osteomyelitis. The aim of this study is to evaluate the role of endostatin in scleroderma DUs.In total, 90 SSc patients were enrolled in this study. Serum endostatin levels and DU assessment were determined in all SSc patients. The serum levels of endostatin significantly increased with progression of capillaroscopic damage (P < .01). The serum levels of endostatin are significantly (P < .05) higher in SSc patients with new DUs than in SSc patients without new DUs (127 ± 31.1 ng/mL vs 116.3 ± 39.7 ng/mL). The Receiver Operating Characteristic (ROC) curves demonstrated good accuracy of new DU prediction for the serum level of endostatin (0.70, P < .01 [95% confidence interval (CI) 0.59-0.81]). Using a cut-off value of 116 ng/mL, the odds ratio was 2.609 (CI 1.075-6.330, P < .05). The serum levels of endostatin are significantly (P < .01) higher in SSc patients with infected DUs than in SSc patients without infected DUs (139.2 [114.6-340.91] ng/mL vs 117.5 [64.3-163.9] ng/mL). Serum levels of endostatin are higher in patients with DUs, especially in those with infected DUs.Entities:
Keywords: angiogenesis; digital ulcers; endostatin; systemic sclerosis; vasculopathy
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Year: 2018 PMID: 29600562 PMCID: PMC7950077 DOI: 10.1111/iwj.12882
Source DB: PubMed Journal: Int Wound J ISSN: 1742-4801 Impact factor: 3.315