Tas Marine, Lecigne Romain, Belhomme Nicolas, Robin François, Louis Thibaut, Perlat Antoinette, Cazalets Claire, Coiffier Guillaume, Lescoat Alain
Department of Radiology, CHU Rennes, Univ Rennes, Rennes, France.
Department of Internal Medicine, CHU Rennes, Univ Rennes, Rennes, France.
Rheumatology (Oxford). 2025 May 1;64(5):2756-2765. doi: 10.1093/rheumatology/keae602.
The objective of this study was to explore the aetiologies and contributing factors of synovial and tenosynovial involvement in SSc, as well as to assess the phenotype of patients with these synovial and tenosynovial features.
One hundred and seventy-one SSc patients with hand manifestations (either vascular, skin or joint manifestations) who underwent standard X-rays of both hands and hand US, were included. Two independent evaluators recorded the presence or absence of acro-osteolysis, calcinosis, microcrystalline and degenerative rheumatisms, including osteophytosis on X-rays. The presence of synovitis and tenosynovitis (active or fibrotic) was assessed through US by a third evaluator, blinded for X-ray parameters.
In multivariate analysis, the characteristics associated with active synovitis and tenosynovitis were CRP > 10 mg/l (P = 0.013), fibrotic tenosynovitis on US (P = 0.005), anti-RNA polymerase III antibodies (P = 0.043) and poly-osteophytosis on hand X-rays (P = 0.001). After exclusion of patients with RA (n = 5) and/or poly-osteophytosis (n = 53), 14 remaining patients (12.7%) had active synovitis and/or tenosynovitis on US. In multivariate analyses, parameters associated with active synovitis and/or tenosynovitis in this selected population were scleroderma renal crisis (P = 0.012) and fibrotic tenosynovitis on US (P < 0.001).
Our study confirms that osteophytosis is a significant contributor of joint involvement in SSc patients based on real life data. After exclusion of potential confounders, >10% of SSc patients still had active synovitis and/or tenosynovitis on US, providing indirect evidence for the existence of a specific SSc-related synovial and/or tenosynovial involvement.
本研究的目的是探讨硬皮病中滑膜和腱鞘受累的病因及相关因素,并评估具有这些滑膜和腱鞘特征的患者的表型。
纳入171例有手部表现(血管、皮肤或关节表现)并接受双手标准X线检查和手部超声检查的硬皮病患者。两名独立评估者记录双手X线片上有无肢端骨质溶解、钙质沉着、微晶和退行性风湿病,包括骨赘形成。由第三位对X线参数不知情的评估者通过超声评估滑膜炎和腱鞘炎(活动期或纤维化期)的存在情况。
在多因素分析中,与活动期滑膜炎和腱鞘炎相关的特征为CRP>10 mg/l(P=0.013)、超声显示纤维化腱鞘炎(P=0.005)、抗RNA聚合酶III抗体(P=0.043)和手部X线片上多发骨赘形成(P=0.001)。排除类风湿关节炎患者(n=5)和/或多发骨赘形成患者(n=53)后,其余14例患者(12.7%)超声显示有活动期滑膜炎和/或腱鞘炎。在多因素分析中,该选定人群中与活动期滑膜炎和/或腱鞘炎相关的参数为硬皮病肾危象(P=0.012)和超声显示纤维化腱鞘炎(P<0.001)。
我们的研究基于实际生活数据证实,骨赘形成是硬皮病患者关节受累的一个重要因素。排除潜在混杂因素后,超过10%的硬皮病患者超声仍显示有活动期滑膜炎和/或腱鞘炎,为存在特定的硬皮病相关滑膜和/或腱鞘受累提供了间接证据。