Role of serum surfactant protein-D as a prognostic predictor in fibrotic hypersensitivity pneumonitis

医学 内科学 过敏性肺炎 胃肠病学 蜂窝状 入射(几何) 队列 间质性肺病 比例危险模型 危险系数 回顾性队列研究 表面活性蛋白D 特发性肺纤维化 置信区间 物理 受体 先天免疫系统 光学
作者
Masaru Ejima,Tsukasa Okamoto,Takafumi Suzuki,Yasunari Miyazaki
出处
期刊:Respiratory investigation [Elsevier BV]
标识
DOI:10.1016/j.resinv.2021.12.003
摘要

Serum Krebs von den Lungen-6 (KL-6) and surfactant protein-D (SP-D) are candidate diagnostic and activity markers for fibrotic hypersensitivity pneumonitis (HP), although their correlation with prognosis remains unclear. We aimed to evaluate the prognostic usefulness of serum KL-6 and SP-D in patients with fibrotic HP.This was a retrospective medical record review of 185 patients with fibrotic HP at a single center from 2005 to 2019. The baseline and minimum serum KL-6 and SP-D levels over two years were recorded. The contribution of KL-6 and SP-D levels to the incidence of progressive fibrosing interstitial lung disease (PF-ILD) and mortality were evaluated using multivariate analysis.The respective baseline and minimum levels were 1441 and 808 U/ml for KL-6 and 254 and 132 ng/mL for SP-D. A high minimum SP-D level was significantly associated with a high incidence of PF-ILD by logistic regression, independent of baseline forced vital capacity and honeycombing. Similarly, a high minimum SP-D level was significantly associated with high mortality by Cox proportional hazard model analysis. The stratified minimum SP-D levels of <100, 100-200, and >200 revealed significantly distinct groups in the entire cohort, with PF-ILD incidence rates of 28%, 48%, and 74% and median survival times of 120, 74, and 45 months, respectively.High minimum SP-D levels over two years were correlated with an unfavorable prognosis in our cohort. Patient with consistently high SP-D levels during the clinical course may have a poor prognosis and be a candidate for early treatment intensification.

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