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Biomarkers of cellular senescence in idiopathic pulmonary fibrosis

特发性肺纤维化 衰老 生物标志物 疾病 医学 肺纤维化 肺功能测试 免疫学 内科学 生物信息学 病理 生物 遗传学
作者
Zaira Aversa,Elizabeth J. Atkinson,Eva M. Carmona,Thomas A. White,Amanda A. Heeren,Sarah K. Jachim,Xu Zhang,Steven R. Cummings,Sergio E. Chiarella,Andrew H. Limper,Nathan K. LeBrasseur
出处
期刊:Respiratory Research [BioMed Central]
卷期号:24 (1) 被引量:36
标识
DOI:10.1186/s12931-023-02403-8
摘要

Abstract Background Cellular senescence is a cell fate in response to diverse forms of age-related damage and stress that has been implicated in the pathogenesis of idiopathic pulmonary fibrosis (IPF). The associations between circulating levels of candidate senescence biomarkers and disease outcomes have not been specifically studied in IPF. In this study we assessed the circulating levels of candidate senescence biomarkers in individuals affected by IPF and controls and evaluated their ability to predict disease outcomes. Methods We measured the plasma concentrations of 32 proteins associated with senescence in Lung Tissue Research Consortium participants and studied their relationship with the diagnosis of IPF, parameters of pulmonary and physical function, health-related quality of life, mortality, and lung tissue expression of P16 , a prototypical marker of cellular senescence. A machine learning approach was used to evaluate the ability of combinatorial biomarker signatures to predict disease outcomes. Results The circulating levels of several senescence biomarkers were significantly elevated in persons affected by IPF compared to controls. A subset of biomarkers accurately classified participants as having or not having the disease and was significantly correlated with measures of pulmonary function, health-related quality of life and, to an extent, physical function. An exploratory analysis revealed senescence biomarkers were also associated with mortality in IPF participants. Finally, the plasma concentrations of several biomarkers were associated with their expression levels in lung tissue as well as the expression of P16 . Conclusions Our results suggest that circulating levels of candidate senescence biomarkers are informative of disease status, pulmonary and physical function, and health-related quality of life. Additional studies are needed to validate the combinatorial biomarkers signatures that emerged using a machine learning approach.
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