Department of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Graf Biostatistics, Winterthur, Switzerland.
Arthritis Res Ther. 2024 Oct 31;26(1):187. doi: 10.1186/s13075-024-03418-2.
Patients with diffuse cutaneous systemic sclerosis (dcSSc) frequently show spontaneous improvement of skin fibrosis. Our aim was to examine whether an improvement in skin fibrosis predicts lower likelihood of visceral organ progression and better survival.
Patients from the European Scleroderma Trials and Research (EUSTAR) cohort with dcSSc, baseline modified Rodnan skin score (mRSS) ≥7, and valid mRSS at 12±3 months follow up were included. Regression/progression of skin fibrosis was defined as a decrease/increase in mRSS >5 points and ≥25% from baseline to follow up. The outcomes included progression of lung, renal, cardiac and gastrointestinal manifestations using consensus derived definitions and all-cause death. Regressive, stable and progressive patients were compared by univariate, Kaplan-Meier survival curve and Cox regression analysis.
Of 1257 included patients, 883 (70.2%) were stable, 282 (22.4%) regressive, and 92 (7.3%) progressive. Regressive patients, adjusted for baseline mRSS, baseline immunosuppression, baseline FVC, and disease duration, showed a significantly lower probability of FVC decline ≥10% than progressive patients (p=0.00003), lower probability of all-cause mortality during follow up (p=0.035) compared to progressive patients. .Improvement of skin fibrosis was not associated with progression of other organ manifestations.
We found that regression of skin fibrosis is associated with a lower probability of lung progression and better survival at follow up. The link between the disease course of skin and lung fibrosis in SSc can help to better stratify patients in clinical practice and enrich for ILD progressive patients in clinical trials.
弥漫性皮肤系统性硬化症(dcSSc)患者的皮肤纤维化常自发改善。本研究旨在探讨皮肤纤维化的改善是否预示着内脏器官进展的可能性降低和生存率提高。
纳入来自欧洲硬皮病试验和研究(EUSTAR)队列的 dcSSc 患者,基线改良 Rodnan 皮肤评分(mRSS)≥7,且 12±3 个月随访时 mRSS 有效。皮肤纤维化的进展/消退定义为 mRSS 较基线下降/增加>5 分且≥25%。使用共识定义的肺、肾、心脏和胃肠道表现以及全因死亡的进展作为结局。通过单变量、Kaplan-Meier 生存曲线和 Cox 回归分析比较退行性、稳定和进展性患者。
在纳入的 1257 例患者中,883 例(70.2%)病情稳定,282 例(22.4%)退行性,92 例(7.3%)进展性。与进展性患者相比,调整基线 mRSS、基线免疫抑制、基线 FVC 和疾病持续时间后,退行性患者 FVC 下降≥10%的概率显著降低(p=0.00003),且在随访期间全因死亡率也较低(p=0.035)。皮肤纤维化的改善与其他器官表现的进展无关。
我们发现皮肤纤维化的消退与肺进展的可能性降低和随访时的生存率提高相关。SSc 中皮肤和肺纤维化的病程之间的联系有助于更好地对患者进行临床分层,并在临床试验中富集ILD 进展患者。