IL33 and sST2 serum level in systemic sclerosis microvascular involvement

Aim: Endothelial dysfunction and microvascular damage are hallmarks of systemic sclerosis (SSc). Objective of this study was to evaluate IL33 and ST2 serum levels in SSc patients and healthy controls (HC). Secondary aim was to evaluate the IL33 axis in the SSc microvascular manifestation. Methods: IL33 and sST2 have been assessed in 46 SSc patients and 24 HC matched for sex and age. Main clinimetric indexes were assessed. Skin perfusion of hands was evaluated by Laser Speckle Contrast Analysis (LASCA) and echocolordoppler ultrasound of renal arteries was performed to evaluate subclinical renal involvement. Results: SSc patients had higher serum level of IL33 and sST2 than HC. IL33 and sST2 were significantly higher in SSc patient with digital ulcers (DUs) compared to SSc patients without DUs. SSc patients with late nailfold videocapillaroscopy (NVC) pattern had higher serum levels of sST2 than SSc patients with active NVC pattern. SSc patients without proximal-distal gradient (PDG) at LASCA had significantly higher sST2 serum level compared to SSc patients with PDG. SSc patients with renal resistive index (RRI) >= 0.70 had higher serum levels of sST2 than SSc patients with RRI < 0.70. A positive linear correlation was shown between sST2 and RRI, between sST2 and intrarenal S/D and between sST2 and PI. Kaplan-Meier curves show a significantly reduced free survival from DUs in patients with increased sST2 (p = 0.025). In multivariate analysis, sST2 is associated with the development of new DUs. Conclusion: IL33 and sST2 are increased in SSc patients and ST2 might be a marker of microvascular damage.

Automated summary

The aim of this study was to evaluate IL33 and ST2 serum levels in systemic sclerosis (SSc) patients and healthy controls (HC), and to investigate their association with microvascular damage in SSc. The results showed that SSc patients had higher levels of IL33 and sST2 compared to HC, and these levels were positively correlated with the presence of digital ulcers, nailfold videocapillaroscopy pattern, LASCA proximal-distal gradient, and renal resistive index in SSc patients. The study suggests that ST2 might be a marker of microvascular damage in SSc.