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Serum resistin is predictive marker of development of new digital ulcers in systemic sclerosis.

Authors :
Pellicano C
Leodori G
Colalillo A
Navarini L
Gigante A
Rosato E
Source :
Clinical and experimental medicine [Clin Exp Med] 2022 Aug; Vol. 22 (3), pp. 421-426. Date of Electronic Publication: 2021 Aug 30.
Publication Year :
2022

Abstract

Systemic sclerosis (SSc) is autoimmune disease characterized by endothelial dysfunction and microvascular damage. Resistin has been implied in microvascular dysfunction. Objective of this study is to evaluate the association between baseline resistin and development of new digital ulcers (DUs) in SSc patients. At baseline, serum resistin has been assessed in 70 female SSc patients and 26 healthy controls (HC). In SSc patients, clinical assessment was performed at baseline and after a 52-weeks follow-up. Serum resistin level was increased in SSc patients compared to HC [5.89 ng/ml (2.5 ng/ml-8.1 ng/ml) vs 2.3 ng/ml (0.4 ng/ml-2.4 ng/ml), p = 0.0004)]. Resistin was lower (p = 0.005) in SSc patients with early capillaroscopic pattern than patients with active or late capillaroscopic pattern [2.49 ng/ml (0.89 ng/ml-5.81 ng/ml) vs 7.11 ng/ml (3.48 ng/ml-11.35 ng/ml) and 6.49 ng/ml (3.35 ng/ml-8.87 ng/ml), respectively]. After a 52-weeks follow-up, 34 (48.6%) patients developed new DUs. Median serum resistin was significantly higher in patients with new DUs than in patients without new DUs [6.54 ng/ml (3.35 ng/ml-11.02 ng/ml) vs 4.78 ng/ml (1.06 ng/ml-7.6 ng/ml), p = 0.019]. Kaplan-Meier curves show a significantly reduced free survival from DUs in patients with increased resistin (p = 0.002). In multivariate analysis, resistin is associated with the development of new DUs. Increased serum resistin level is a predictive marker of new DUs in SSc.<br /> (© 2021. The Author(s).)

Details

Language :
English
ISSN :
1591-9528
Volume :
22
Issue :
3
Database :
MEDLINE
Journal :
Clinical and experimental medicine
Publication Type :
Academic Journal
Accession number :
34462844
Full Text :
https://doi.org/10.1007/s10238-021-00756-2