Di Donato Stefano, Ross Rebecca, Karanth Ranjitha, Kakkar Vishal, De Lorenzis Enrico, Bissell Lesley-Anne, Clark Kristina, Yee Philip, Denton Christopher P, Del Galdo Francesco
Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds and Leeds Biomedical Research Centre, National Institute for Health Research, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom.
Arthritis Rheumatol. 2025 Jul;77(7):929-941. doi: 10.1002/art.43120. Epub 2025 Mar 3.
To assess the value of serum type I interferon (IFN) score in predicting clinically meaningful progression in limited cutaneous systemic sclerosis (lcSSc) using a novel composite endpoint adopted from the MINIMISE clinical trial.
A retrospective, longitudinal lcSSc cohort was identified within a national, multicenter observational cohort. The MINIMISE trial combined Morbi-mortality endpoint was used as the clinical outcome for a time to clinical worsening (TTCW) design. The IFN score was calculated from the serum concentration of chemokine C-C motif ligand (CCL) 2, CCL8, CCL19, C-X-C motif chemokine ligand (CXCL) 9, CXCL10, and CXCL11 on patients and age- and sex-matched healthy controls (HCs). A "high" IFN score was defined as 2 SDs above the HC mean. The association of the IFN score with TTCW was assessed using Cox proportional hazard regressions and Kaplan-Meier curves. The potential improvement in risk stratification when combining IFN score with lcSSc clinical features was explored.
A total of 149 patients were included in the analysis: 67 "high" IFN and 82 "low." High IFN patients presented a shorter TTCW (74.7 months [95% confidence interval (CI) 70.1-79.3] vs 110.6 months [95% CI 107.2-114.0]; P < 0.001) and met the endpoint in higher proportion compared with low IFN (55% vs 12%; P < 0.001). A high IFN score conferred hazard ratio (HR) 5.5 (95% CI 2.7-11.3) for TTCW compared with low IFN, and IFN score as a continuous variable conferred HR 2.38 (95% CI 1.4-4.0) for TTCW independently of clinical variables. Pulmonary arterial hypertension, interstitial lung disease, digital ulcers, and modified Rodnan skin score were associated with TTCW. An exploratory analysis showed that these clinical features improve risk stratification over time in combination with IFN score.
Serum assessment of type I IFN activity is a valuable predictor of clinically meaningful outcomes in lcSSc. The combination of serum IFN score with sentinel clinical features can improve stratification strategies in clinical trials and patient management.
采用一项源自MINIMISE临床试验的新型复合终点,评估血清I型干扰素(IFN)评分在预测局限性皮肤系统性硬化症(lcSSc)临床意义上的病情进展方面的价值。
在一项全国性多中心观察性队列中确定了一个回顾性纵向lcSSc队列。MINIMISE试验的联合病残死亡率终点被用作临床恶化时间(TTCW)设计的临床结局。根据患者以及年龄和性别匹配的健康对照(HC)中趋化因子C-C基序配体(CCL)2、CCL8、CCL19、C-X-C基序趋化因子配体(CXCL)9、CXCL10和CXCL11的血清浓度计算IFN评分。“高”IFN评分定义为高于HC平均值2个标准差。使用Cox比例风险回归和Kaplan-Meier曲线评估IFN评分与TTCW的关联。探讨了将IFN评分与lcSSc临床特征相结合时风险分层的潜在改善情况。
共有149例患者纳入分析:67例“高”IFN患者和82例“低”IFN患者。高IFN患者的TTCW较短(74.7个月[95%置信区间(CI)70.1 - 79.3]对110.6个月[95%CI 107.2 - 114.0];P < 0.001),与低IFN患者相比达到终点的比例更高(55%对12%;P < 0.001)。与低IFN相比,高IFN评分使TTCW的风险比(HR)为5.5(95%CI 2.7 - 11.3),IFN评分作为连续变量独立于临床变量使TTCW的HR为2.38(95%CI 1.4 - 4.0)。肺动脉高压、间质性肺病、指端溃疡和改良Rodnan皮肤评分与TTCW相关。一项探索性分析表明,这些临床特征与IFN评分相结合可随时间改善风险分层。
血清I型IFN活性评估是lcSSc临床意义结局的有价值预测指标。血清IFN评分与标志性临床特征相结合可改善临床试验和患者管理中的分层策略。