Department of Respiratory Medicine, Beijing Ditan Hospital, Capital Medical University, China.
Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chaoyang Hospital, Capital Medical University, Beijing, China.
Ther Adv Respir Dis. 2024 Jan-Dec;18:17534666241250332. doi: 10.1177/17534666241250332.
Different types of inflammatory processes and fibrosis have been implicated in the pathogenesis of interstitial lung disease (ILD), a heterogeneous, diffuse, parenchymal lung disease. Acute exacerbation (AE) of ILD is characterized by significant respiratory deterioration and is associated with high mortality rates. Several serum oncomarkers have been used to determine the prognosis of ILD; however, the prognostic value of serum oncomarker levels in patients with AE-ILD remains unclear.
To evaluate the prognostic value of serum oncomarker levels in patients with AE-ILD and its main subtypes.
Retrospective study.
The serum levels of 8 oncomarkers in 281 patients hospitalized with AE-ILD at our institution between 2017 and 2022 were retrospectively reviewed. The baseline characteristics and serum oncomarker levels were compared between the survival and non-survival groups of AE-ILD and its main subtypes. Multivariate logistic regression analysis was performed to identify independent prognosis-related markers, and the best prognostic predictor was analyzed using receiver operating characteristic curve (ROC) analysis.
Idiopathic pulmonary fibrosis (IPF; = 65), idiopathic nonspecific interstitial pneumonia (iNSIP; = 26), and connective tissue disease-associated interstitial lung disease (CTD-ILD; = 161) were the three main subtypes of ILD. The in-hospital mortality rate among patients with AE-ILD was 21%. The serum oncomarker levels of most patients with AE-ILD and its main subtypes in the non-survival group were higher than those in the survival group. Multivariate analysis revealed that ferritin and cytokeratin 19 fragments (CYFRA21-1) were independent prognostic risk factors for patients hospitalized with AE-ILD or AE-CTD-ILD. CYFRA21-1 was identified as an independent prognostic risk factor for patients hospitalized with AE-IPF or AE-iNSIP.
CYFRA21-1 may be a viable biomarker for predicting the prognosis of patients with AE-ILD, regardless of the underlying subtype of ILD. Ferritin has a prognostic value in patients with AE-ILD or AE-CTD-ILD.
不同类型的炎症过程和纤维化被认为与间质性肺病(ILD)的发病机制有关,ILD 是一种异质性、弥漫性、实质肺疾病。ILD 的急性加重(AE)以显著的呼吸恶化为特征,与高死亡率相关。已经有几种血清肿瘤标志物被用于确定ILD 的预后;然而,AE-ILD 患者的血清肿瘤标志物水平的预后价值尚不清楚。
评估 AE-ILD 及其主要亚型患者的血清肿瘤标志物水平的预后价值。
回顾性研究。
回顾性分析了 2017 年至 2022 年期间我院收治的 281 例 AE-ILD 患者的 8 种血清肿瘤标志物水平。比较了 AE-ILD 及其主要亚型的生存组和非生存组的基线特征和血清肿瘤标志物水平。采用多变量 logistic 回归分析确定独立的预后相关标志物,并通过受试者工作特征曲线(ROC)分析分析最佳预后预测指标。
特发性肺纤维化(IPF;=65)、特发性非特异性间质性肺炎(iNSIP;=26)和结缔组织疾病相关间质性肺疾病(CTD-ILD;=161)是 ILD 的三个主要亚型。AE-ILD 患者的住院死亡率为 21%。AE-ILD 及其主要亚型中,非生存组患者的血清肿瘤标志物水平多数高于生存组。多变量分析显示,铁蛋白和细胞角蛋白 19 片段(CYFRA21-1)是 AE-ILD 或 AE-CTD-ILD 患者住院的独立预后危险因素。CYFRA21-1 是 AE-IPF 或 AE-iNSIP 患者住院的独立预后危险因素。
CYFRA21-1 可能是预测 AE-ILD 患者预后的一种可行的生物标志物,无论 ILD 的潜在亚型如何。铁蛋白在 AE-ILD 或 AE-CTD-ILD 患者中有预后价值。