Kuwana Masataka, Shirai Yuichiro, Takeuchi Tsutomu
From the Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine; Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.M. Kuwana, MD, PhD, Professor, Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine; Y. Shirai, MD, PhD, Instructor, Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine; T. Takeuchi, MD, PhD, Professor, Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine.
J Rheumatol. 2016 Oct;43(10):1825-1831. doi: 10.3899/jrheum.160339. Epub 2016 Aug 1.
To identify predictors of poor prognosis in patients with systemic sclerosis (SSc) associated with interstitial lung disease (ILD).
Fifty patients with early-stage SSc-ILD who had never received disease-modifying drugs and were either observed for ≥ 10 years or died from ILD-related causes were enrolled. The baseline variables of patients who developed endstage lung disease (ESLD) were compared with those of patients who remained ESLD-free, and the Cox proportional hazard model was used to identify initial factors that correlated with ESLD development.
Sixteen patients (32%) developed ESLD during 173.5 ± 64.7 months of followup. Elevated serum Krebs von den Lungen-6 (KL-6) at initial assessment was highly correlated with ESLD development (p = 0.0002). Receiver-operating characteristic curve analysis revealed that a KL-6 value of 1273 U/ml effectively discriminated patients who developed ESLD from those who did not. Patients with KL-6 > 1273 U/ml were less likely to remain ESLD-free compared with those with lower KL-6 levels (p < 0.0001). Multivariate analysis showed that KL-6 > 1273 U/ml was the most reliable predictor of ESLD development (OR 51.2, 95% CI 7.6-343, p < 0.0001). Finally, the initial KL-6 level correlated with the forced vital capacity (FVC) decline rate (r = 0.58, p < 0.0001).
The natural course of SSc-ILD is highly variable. Baseline serum KL-6 is a biomarker potentially useful for predicting FVC decline.
确定系统性硬化症(SSc)相关间质性肺疾病(ILD)患者预后不良的预测因素。
纳入50例从未接受过改善病情药物治疗、观察时间≥10年或死于ILD相关原因的早期SSc-ILD患者。将发生终末期肺病(ESLD)的患者的基线变量与未发生ESLD的患者进行比较,并使用Cox比例风险模型确定与ESLD发生相关的初始因素。
16例患者(32%)在173.5±64.7个月的随访期间发生了ESLD。初始评估时血清克雷伯斯-冯-登-伦根-6(KL-6)升高与ESLD发生高度相关(p=0.0002)。受试者工作特征曲线分析显示,KL-6值为1273 U/ml可有效区分发生ESLD的患者和未发生ESLD的患者。与KL-6水平较低的患者相比,KL-6>1273 U/ml的患者保持无ESLD的可能性较小(p<0.0001)。多变量分析显示,KL-6>1273 U/ml是ESLD发生最可靠的预测因素(OR 51.2,95%CI 7.6-343,p<0.0001)。最后,初始KL-6水平与用力肺活量(FVC)下降率相关(r=0.58,p<0.0001)。
SSc-ILD的自然病程差异很大。基线血清KL-6是一种可能有助于预测FVC下降的生物标志物。