Micro- and Macro-Vascular Disease in Systemic Sclerosis and Very Early SSc (VEDOSS): Results from a Monocentric Observational Study

医学 观察研究 内科学 内皮功能障碍 心脏病学 大血管病 疾病 血管疾病 硬皮病(真菌) 病理生理学 全身性疾病 病理 代理终结点 冲程(发动机) 风险因素 冠状动脉疾病 生物标志物 疾病严重程度 风险评估 结缔组织病 内皮 激光多普勒测速 系统性硬皮病 内皮细胞活化 多发性硬化 全身炎症 胃肠病学
作者
Vincenzo Zaccone,S. Contegiacomo,Silvia Agarbati,Chiara Paolini,Carolina Clementi,Matteo Mozzicafreddo,Silvia Svegliati,Lorenzo Falsetti,Devis Benfaremo,Gianluca Moroncini
出处
期刊:Biomedicines [Multidisciplinary Digital Publishing Institute]
卷期号:14 (3): 607-607
标识
DOI:10.3390/biomedicines14030607
摘要

Background: Systemic sclerosis (SSc) is characterized by endothelial dysfunction leading to progressive vascular injury and fibrosis. While microvascular involvement is well established as an early disease feature, macrovascular disease has been historically underrecognized and poorly investigated in very early disease stages. Integrated assessments across the SSc spectrum, including very early diagnosis of systemic sclerosis (VEDOSS), remain limited. Methods: In this cross-sectional observational study, patients with established SSc, VEDOSS, and primary Raynaud’s phenomenon (PRP) were prospectively enrolled between October 2023 and April 2025. Participants underwent comprehensive microvascular and macrovascular evaluation, including nailfold videocapillaroscopy, multisegmental arterial Doppler ultrasound (carotid, aortic, and lower limb districts), flow-mediated dilation, and measurement of endothelial biomarkers (vascular cell adhesion molecule 1 (VCAM-1), intercellular adhesion molecule 1 (ICAM-1), and circulating endothelial cells (CECs)). Traditional cardiovascular risk was estimated using Systematic Coronary Risk Estimation 2 (SCORE2). Results: Sixty-two female subjects were included (34 SSc, 14 VEDOSS, and 14 PRP). Microvascular abnormalities followed the expected disease continuum, with capillaroscopic changes present in 57% of VEDOSS and 91% of SSc patients. Although SCORE2 estimates and carotid intima–media thickness were comparable across groups, macrovascular abnormalities were more frequent in SSc (52.9%) and VEDOSS (50%) compared with PRP (21.4%). VCAM-1, ICAM-1, and CEC levels were significantly increased in SSc compared with PRP, whereas no significant differences were observed between VEDOSS and PRP. Conclusions: These findings support a unified micro- and macro-vascular disease model in SSc and demonstrate that macrovascular involvement is detectable already in the VEDOSS phase. Conventional cardiovascular risk scores underestimate the true vascular burden, highlighting the need for disease-specific risk stratification tools integrating vascular imaging and endothelial biomarkers.
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