Pulmonary Function Modulates Epigenetic Age in Subjects with Cystic Fibrosis
Alice Castaldo, Mariella Cuomo, Paola Iacotucci, Vincenzo Carnovale, Lorenzo Chiariotti, Giuseppe Castaldo, Monica Gelzo

TL;DR
This study shows that lung function in cystic fibrosis patients influences their epigenetic age, and treatment with a specific therapy can improve both.
Contribution
The study links epigenetic age with lung function in CF patients treated with ETI and suggests its potential as a biomarker.
Findings
Half of the subjects had accelerated epigenetic age and worse lung function at baseline.
ETI therapy improved lung function and tended to increase epigenetic age in some patients.
Epigenetic age may serve as a potential biomarker for therapy outcomes in CF.
Abstract
Cystic fibrosis (CF) is the most common severe autosomal recessive disease among Caucasians. Modulators of cystic fibrosis transmembrane conductance regulator (CFTR) mutated protein significantly improved the outcome of subjects with CF. In the present study, we studied epigenetic age, applying the Horvath clock model, in 52 adult subjects with CF, all treated with elexacaftor/tezacaftor/ivacaftor (ETI). At baseline (T0), we found that half of the subjects have a significantly accelerated epigenetic age and a worse lung function, evaluated by forced expiratory volume in one second (FEV1). One year of ETI therapy (T1) impacted both the parameters, indicating that therapy with modulators must be started early, particularly in CF subjects with impaired lung function. The second group of CF subjects had an epigenetic age lower than the chronological one at T0 and lung function was better…
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Taxonomy
TopicsCystic Fibrosis Research Advances · Neonatal Respiratory Health Research · Child Nutrition and Feeding Issues
