Change in serum surfactant protein (SP)-A, SP-D and KL-6 predict the therapeutic effect of antifibrotic drugs in IPF

Takumi Yoshikawa, M. Otsuka, Kimiyuki Ikeda, Yuki Mori, Yasuaki Umeda, Hirotaka Nishikiori, Satsuki Miyajima, Mamoru Takahashi, K. Kuronuma, H. Chiba, Hiroki Takahashi
{"title":"Change in serum surfactant protein (SP)-A, SP-D and KL-6 predict the therapeutic effect of antifibrotic drugs in IPF","authors":"Takumi Yoshikawa, M. Otsuka, Kimiyuki Ikeda, Yuki Mori, Yasuaki Umeda, Hirotaka Nishikiori, Satsuki Miyajima, Mamoru Takahashi, K. Kuronuma, H. Chiba, Hiroki Takahashi","doi":"10.1183/13993003.congress-2019.pa4704","DOIUrl":null,"url":null,"abstract":"Background: Serum surfactant protein (SP)-A, SP-D, and KL-6 are prognostic biomarkers of patients with idiopathic pulmonary fibrosis (IPF), however, the relationship with the therapeutic effect of antifibrotic drugs has not been investigated. Aim: To clarify whether serum SP-A, SP-D and KL-6 are therapeutic predictive markers of pirfenidone and nintedanib in patients with IPF. Methods: We retrospectively investigated patients with IPF who started pirfenidone or nintedanib between January 2014 and June 2018 at our hospital. The change in clinical parameters and serum SP-A, SP-D and KL-6 levels were evaluated. Patients with a > 10% decline in forced vital capacity (FVC) or a > 15% decline in diffusing capacity of the lung for carbon monoxide (DLco) from baseline to 6 months were classified as a deterioration group and the other was classified as an effective group. Results: Forty-nine patients were included (pirfenidone; 23, nintedanib; 26). Thirty-two patients were the effective group and 17 patients were the deterioration group. In the effective group, the change in serum SP-A, SP-D, and KL-6 from baseline to 3 and/or 6 months significantly decreased compared with the deterioration group. The change in serum SP-A and SP-D showed significant negative correlations with the change in %FVC and %DLCO. According to the logistic regression analysis, the decrease in SP-A from baseline to 3 months was a predictor of the effect at 6 months (odd’ ratio 0.88). Conclusions: Change in SP-A, SP-D and KL-6 represent the therapeutic effect of antifibrotic drugs. These may be therapeutic predictive biomarkers of antifibrotic drugs.","PeriodicalId":13242,"journal":{"name":"Idiopathic interstitial pneumonias","volume":"54 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Idiopathic interstitial pneumonias","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1183/13993003.congress-2019.pa4704","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Serum surfactant protein (SP)-A, SP-D, and KL-6 are prognostic biomarkers of patients with idiopathic pulmonary fibrosis (IPF), however, the relationship with the therapeutic effect of antifibrotic drugs has not been investigated. Aim: To clarify whether serum SP-A, SP-D and KL-6 are therapeutic predictive markers of pirfenidone and nintedanib in patients with IPF. Methods: We retrospectively investigated patients with IPF who started pirfenidone or nintedanib between January 2014 and June 2018 at our hospital. The change in clinical parameters and serum SP-A, SP-D and KL-6 levels were evaluated. Patients with a > 10% decline in forced vital capacity (FVC) or a > 15% decline in diffusing capacity of the lung for carbon monoxide (DLco) from baseline to 6 months were classified as a deterioration group and the other was classified as an effective group. Results: Forty-nine patients were included (pirfenidone; 23, nintedanib; 26). Thirty-two patients were the effective group and 17 patients were the deterioration group. In the effective group, the change in serum SP-A, SP-D, and KL-6 from baseline to 3 and/or 6 months significantly decreased compared with the deterioration group. The change in serum SP-A and SP-D showed significant negative correlations with the change in %FVC and %DLCO. According to the logistic regression analysis, the decrease in SP-A from baseline to 3 months was a predictor of the effect at 6 months (odd’ ratio 0.88). Conclusions: Change in SP-A, SP-D and KL-6 represent the therapeutic effect of antifibrotic drugs. These may be therapeutic predictive biomarkers of antifibrotic drugs.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
血清表面活性蛋白(SP)-A、SP- d和KL-6的变化预测抗纤维化药物对IPF的治疗效果
背景:血清表面活性蛋白(SP)-A、SP- d和KL-6是特发性肺纤维化(IPF)患者的预后生物标志物,但其与抗纤维化药物治疗效果的关系尚未研究。目的:阐明血清SP-A、SP-D和KL-6是否为IPF患者吡非尼酮和尼达尼布治疗的预测指标。方法:回顾性调查2014年1月至2018年6月在我院开始使用吡非尼酮或尼达尼布的IPF患者。观察两组临床指标及血清SP-A、SP-D、KL-6水平的变化。从基线到6个月,用力肺活量(FVC)下降> 10%或肺一氧化碳弥散量(DLco)下降> 15%的患者归为恶化组,另一组归为有效组。结果:纳入49例患者(吡非尼酮;23日,nintedanib;26)。有效组32例,恶化组17例。与恶化组相比,有效组血清SP-A、SP-D和KL-6从基线到3和/或6个月的变化显著降低。血清SP-A、SP-D的变化与FVC %、DLCO %的变化呈显著负相关。根据logistic回归分析,SP-A从基线到3个月的下降是6个月效果的预测因子(奇数比0.88)。结论:SP-A、SP-D和KL-6的变化反映了抗纤维化药物的治疗效果。这些可能是抗纤维化药物的治疗预测性生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Differential expression of PD-1/PD-L1 axis in mediastinal lymph nodes of experimental and human lung fibrosis Systematic review and meta-analysis of interstitial lung disease transcriptomics Myeloid cells immunomodulate tissue niches and promotes idiopathic pulmonary fibrosis Profibrotic and proinflammatory pulmonary response to bleomycin in a Swiss nude mice model Mitochondrial iron regulates AEC2 dysfunction, senescence and senescent associated secretory phenotype in response to bleomycin challenge.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1