Kinetic changes in serum KL-6 levels predict disease progression in patients with systemic sclerosis-associated interstitial lung disease

医学 内科学 间质性肺病 危险系数 胃肠病学 肺活量 比例危险模型 生物标志物 置信区间 单变量分析 扩散能力 多元分析 肺功能 生物化学 化学
作者
Satoshi Watanabe,Kazumasa Kase,Keigo Saeki,Noriyuki Ohkura,Akari Murata,Yuko Waseda,Hazuki Takato,Yukari Ichikawa,Masahide Yasui,Kazuo Kasahara
出处
期刊:Respiratory Medicine [Elsevier BV]
卷期号:191: 106689-106689 被引量:7
标识
DOI:10.1016/j.rmed.2021.106689
摘要

The clinical course of patients with systemic sclerosis-associated interstitial lung disease (SSc-ILD) is highly variable. The Krebs von den Lungen-6 (KL-6) glycoprotein is a promising biomarker for reflecting epithelial injury. However, serum KL-6 and its association with the progression of SSc-ILD have been understudied.We reviewed 77 consecutive patients with SSc-ILD seen from 2004 to 2016. A longitudinal study of forced vital capacity (FVC), serum KL-6 levels, and changes in KL-6 levels from baseline (ΔKL-6) was conducted. The progression of ILD was defined as ≥10% relative decline in FVC predicted or 5%-10% decline in FVC predicted along with radiological progression on chest computed tomography. The risk factors for ILD progression were assessed by univariate and multivariate regression.During a 5-year follow-up period, 10 (13%) patients showed rapid progression of ILD within 2 years, 39 (51%) showed overall progression during the 5 years, and 28 (36%) had stable disease. Most patients with progressive ILD showed elevations in serum KL-6 levels over the initial 1-year follow-up period. The best cut-off value for ΔKL-6 that predicted progression of ILD was 193 U/mL (sensitivity 81.6%, specificity 92.9%). Multivariate analysis adjusted by age, sex, smoking status, and immunosuppressant use found that diffuse cutaneous SSc (hazard ratio [HR] 4.51; 95% confidence interval [CI] 1.56-13.04) and ΔKL-6 > 193 U/mL from baseline (HR 7.19; 95% CI 3.30-15.69) were independent predictors for progression of SSc-ILD.Changes in the KL-6 level can be useful for predicting disease progression in patients with SSc-ILD.
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