Center for Interstitial and Rare Lung Diseases, Pneumology, Thoraxklinik Heidelberg, University Hospital Heidelberg and German Center for Lung Research (DZL), Heidelberg, Germany,
Center for Interstitial and Rare Lung Diseases, Pneumology, Thoraxklinik Heidelberg, University Hospital Heidelberg and German Center for Lung Research (DZL), Heidelberg, Germany.
Respiration. 2023;102(8):591-600. doi: 10.1159/000531945. Epub 2023 Aug 16.
As fibrosing interstitial lung diseases (fILDs) are associated with high mortality, monitoring of disease activity under treatment is highly relevant. Krebs von den Lungen-6 (KL-6) is associated with the presence and severity of different fILDs, mainly in Asian patient populations.
Our aim was to evaluate KL-6 as a predictive biomarker in fILDs in Caucasian patients.
Consecutive patients with fILDs were recruited prospectively and serum concentrations of KL-6 were measured at baseline (BL), after 6 and 12 months (6 Months, 12 Months). Clinical characteristics including pulmonary function tests were assessed at 6-monthly visits and correlated with KL-6 BL levels as well as with KL-6 level changes.
A total of 47 fILD patients were included (mean age: 65 years, 68% male). KL-6 levels at BL were significantly higher in fILD patients than in healthy controls (n = 44, mean age: 45, 23% male) (ILD: 1,757 ± 1960 U/mL vs. control: 265 ± 107 U/mL, p < 0.0001). However, no differences were noted between ILD subgroups. KL-6 decreased significantly under therapy (6M∆BL-KL6: -486 ± 1,505 mean U/mL, p = 0.032; 12M∆BL-KL6: -547 ± 1,782 mean U/mL, p = 0.041) and KL-6 level changes were negatively correlated with changes in pulmonary function parameters (forced vital capacity [FVC]: r = -0.562, p < 0.0001; DLCOSB: r = -0.405, p = 0.013). While neither absolute KL-6 levels at BL nor KL-6 level changes were associated with ILD progression (FVC decline ≥10%, DLCOSB decline ≥15% or death), patients with a stable FVC showed significantly decreasing KL-6 levels (p = 0.022).
A decline of KL-6 under therapy correlated with a clinically relevant stabilization of lung function. Thus, KL-6 might serve as a predictive biomarker, which however must be determined by larger prospective cohorts.
由于纤维性间质性肺病(fILDs)与高死亡率相关,因此治疗下的疾病活动监测非常重要。KL-6 与不同 fILDs 的存在和严重程度相关,主要在亚洲患者人群中。
我们旨在评估 KL-6 作为高加索患者 fILDs 的预测生物标志物。
连续招募了 fILD 患者进行前瞻性研究,并在基线(BL)、6 个月和 12 个月时测量血清 KL-6 浓度。每 6 个月进行一次临床特征评估,包括肺功能检查,并与 KL-6 BL 水平以及 KL-6 水平变化相关联。
共纳入 47 名 fILD 患者(平均年龄:65 岁,68%为男性)。fILD 患者的 KL-6 水平明显高于健康对照组(n=44,平均年龄:45 岁,23%为男性)(ILD:1757±1960 U/mL 比对照组:265±107 U/mL,p < 0.0001)。然而,ILD 亚组之间没有差异。治疗后 KL-6 显著下降(6M∆BL-KL6:-486±1505 平均 U/mL,p=0.032;12M∆BL-KL6:-547±1782 平均 U/mL,p=0.041),KL-6 水平变化与肺功能参数变化呈负相关(用力肺活量 [FVC]:r=-0.562,p < 0.0001;DLCOSB:r=-0.405,p=0.013)。尽管 BL 时的绝对 KL-6 水平或 KL-6 水平变化均与 ILD 进展无关(FVC 下降≥10%,DLCOSB 下降≥15%或死亡),但 FVC 稳定的患者 KL-6 水平显著下降(p=0.022)。
治疗下 KL-6 的下降与肺功能的临床相关稳定相关。因此,KL-6 可能作为一种预测生物标志物,但必须通过更大的前瞻性队列来确定。