Abstract

BackgroundChronic obstructive pulmonary disease (COPD) has been proposed as a disease of accelerated aging. Several cross-sectional studies have related a shorter telomere length (TL), a marker of biological aging, with COPD outcomes. Whether accelerated telomere shortening over time relates to worse outcomes in COPD patients, is not known.MethodsRelative telomere length (T/S) was determined by qPCR in DNA samples from peripheral blood in 263 patients at baseline and up to 10 years post enrolment. Yearly clinical and lung function data of 134 patients with at least two-time measures of T/S over this time were included in the analysis.ResultsAt baseline, T/S inversely correlated with age (r = − 0.236; p < 0.001), but there was no relationship between T/S and clinical and lung function variables (p > 0.05). Over 10 years of observation, there was a median shortening of TL of 183 bp/year for COPD patients. After adjusting for age, gender, active smoking and mean T/S, patients that shortened their telomeres the most over time, had worse gas exchange, more lung hyperinflation and extrapulmonary affection during the follow-up, (PaO2 p < 0.0001; KCO p = 0.042; IC/TLC p < 0.0001; 6MWD p = 0.004 and BODE index p = 0.009). Patients in the lowest tertile of T/S through the follow-up period had an increased risk of death [HR = 5.48, (1.23–24.42) p = 0.026].ConclusionsThis prospective study shows an association between accelerated telomere shortening and progressive worsening of pulmonary gas exchange, lung hyperinflation and extrapulmonary affection in COPD patients. Moreover, persistently shorter telomeres over this observation time increase the risk for all-cause mortality.

Highlights

  • Chronic obstructive pulmonary disease (COPD) has been proposed as a disease of accelerated aging

  • Chronic obstructive pulmonary disease (COPD), one of the leading causes of morbidity and mortality worldwide, is a disease characterized by a persistent reduction of airflow that frequently progresses over time [1, 2]

  • There was no relationship between telomere length and clinical and lung function parameters (p > 0.05) cross-sectionally

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Summary

Introduction

Chronic obstructive pulmonary disease (COPD) has been proposed as a disease of accelerated aging. Several cross-sectional studies have related a shorter telomere length (TL), a marker of biological aging, with COPD outcomes. Whether accelerated telomere shortening over time relates to worse outcomes in COPD patients, is not known. Chronic obstructive pulmonary disease (COPD), one of the leading causes of morbidity and mortality worldwide, is a disease characterized by a persistent reduction of airflow that frequently progresses over time [1, 2]. Patients with COPD develop 10 or 20 years earlier, COPD has been described as a disease of accelerated aging and shorter telomere length as a surrogate marker of biological aging [5, 6].

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