医学
间质性肺病
特发性肺纤维化
病理
表型
临床试验
肺纤维化
重症监护医学
梅德林
生物信息学
基因检测
临床表型
纤维化
肺
治疗方法
遗传异质性
作者
Amornpun Wongkarnjana,Ciaran Scallan,Martin Kolb
标识
DOI:10.1097/mcp.0000000000000712
摘要
Recent evidence supports the use of antifibrotic therapy in the management of the phenotype progressive non-IPF ILD. Ongoing studies exploring genetic and other molecular biomarkers could identify at-risk individuals or predict treatment response and prognosis (endotypes). This would support the concept of 'treatable traits' in the field of ILD.
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