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特发性肺纤维化与端粒

Idiopathic Pulmonary Fibrosis and Telomeres.

作者信息

Mulet Alba, Signes-Costa Jaime

机构信息

Department of Pulmonology, Hospital Clínico, 46010 Valencia, Spain.

Respiratory Diseases Research Group, INCLIVA, 46010 Valencia, Spain.

出版信息

J Clin Med. 2022 Nov 22;11(23):6893. doi: 10.3390/jcm11236893.

Abstract

Idiopathic pulmonary fibrosis is an interstitial lung disease of unknown etiology with a highly compromised prognosis and a significant mortality rate within a few years of diagnosis. Despite being idiopathic, it has been shown that telomeric shortening could play an important role in its etiopathogenesis. Mutations in telomere-related genes have been identified, but they are not always present despite telomere shortening. On the other hand, this telomeric shortening has been linked to a worse prognosis of the disease independently of other clinical factors, implying it may serve as a biomarker.

摘要

特发性肺纤维化是一种病因不明的间质性肺病,预后极差,确诊后几年内死亡率很高。尽管病因不明,但研究表明端粒缩短可能在其发病机制中起重要作用。已发现端粒相关基因的突变,但尽管存在端粒缩短,这些突变并不总是出现。另一方面,这种端粒缩短与疾病的不良预后相关,独立于其他临床因素,这意味着它可能作为一种生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bcf/9740997/6ff018e0a1bd/jcm-11-06893-g001.jpg

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