Telomere Length but Not Mitochondrial DNA Copy Number Is Altered in Both Young and Old COPD

Accelerated ageing is implicated in the pathogenesis of respiratory diseases as chronic obstructive pulmonary disease (COPD), but recent evidence indicates that the COPD can have roots early in life. Here we hypothesise that the accelerated ageing markers might have a role in the pathobiology of you...

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Autores principales: Sandra Casas-Recasens, Nuria Mendoza, Alejandra López-Giraldo, Tamara Garcia, Borja G. Cosio, Sergi Pascual-Guardia, Ady Acosta-Castro, Alicia Borras-Santos, Joaquim Gea, Gloria Garrabou, Alvar Agusti, Rosa Faner
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Publicado: Frontiers Media S.A. 2021
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spelling oai:doaj.org-article:21328096c5dc4b70aabf06761fa0ba5a2021-11-30T18:13:46ZTelomere Length but Not Mitochondrial DNA Copy Number Is Altered in Both Young and Old COPD2296-858X10.3389/fmed.2021.761767https://doaj.org/article/21328096c5dc4b70aabf06761fa0ba5a2021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fmed.2021.761767/fullhttps://doaj.org/toc/2296-858XAccelerated ageing is implicated in the pathogenesis of respiratory diseases as chronic obstructive pulmonary disease (COPD), but recent evidence indicates that the COPD can have roots early in life. Here we hypothesise that the accelerated ageing markers might have a role in the pathobiology of young COPD. The objective of this study was to compare two hallmarks of ageing, telomere length (TL), and mitochondrial DNA copy number (mtDNA-CN, as a surrogate marker of mitochondrial dysfunction) in young (≤ 50 years) and old (>50 years) smokers, with and without COPD. Both, TL and mtDNA-CN were measured in whole blood DNA by quantitative PCR [qPCR] in: (1) young ever smokers with (n = 81) or without (n = 166) COPD; and (2) old ever smokers with (n = 159) or without (n = 29) COPD. A multivariable linear regression was used to assess the association of TL and mtDNA-CN with lung function. We observed that in the entire study population, TL and mtDNA-CN decreased with age, and the former but not the latter related to FEV1/FVC (%), FEV1 (% ref.), and DLCO (% ref.). The short telomeres were found both in the young and old patients with severe COPD (FEV1 <50% ref.). In addition, we found that TL and mtDNA-CN were significantly correlated, but their relationship was positive in younger while negative in the older patients with COPD, suggesting a mitochondrial dysfunction. We conclude that TL, but not mtDNA-CN, is associated with the lung function impairment. Both young and old patients with severe COPD have evidence of accelerated ageing (shorter TL) but differ in the direction of the correlation between TL and mtDNA-CN in relation to age.Sandra Casas-RecasensNuria MendozaAlejandra López-GiraldoAlejandra López-GiraldoAlejandra López-GiraldoTamara GarciaBorja G. CosioBorja G. CosioBorja G. CosioSergi Pascual-GuardiaSergi Pascual-GuardiaSergi Pascual-GuardiaAdy Acosta-CastroAdy Acosta-CastroAlicia Borras-SantosAlicia Borras-SantosJoaquim GeaJoaquim GeaJoaquim GeaGloria GarrabouGloria GarrabouGloria GarrabouGloria GarrabouAlvar AgustiAlvar AgustiAlvar AgustiAlvar AgustiRosa FanerRosa FanerFrontiers Media S.A.articletelomeresmitochondrial DNAchronic bronchitisemphysemaageingMedicine (General)R5-920ENFrontiers in Medicine, Vol 8 (2021)
institution DOAJ
collection DOAJ
language EN
topic telomeres
mitochondrial DNA
chronic bronchitis
emphysema
ageing
Medicine (General)
R5-920
spellingShingle telomeres
mitochondrial DNA
chronic bronchitis
emphysema
ageing
Medicine (General)
R5-920
Sandra Casas-Recasens
Nuria Mendoza
Alejandra López-Giraldo
Alejandra López-Giraldo
Alejandra López-Giraldo
Tamara Garcia
Borja G. Cosio
Borja G. Cosio
Borja G. Cosio
Sergi Pascual-Guardia
Sergi Pascual-Guardia
Sergi Pascual-Guardia
Ady Acosta-Castro
Ady Acosta-Castro
Alicia Borras-Santos
Alicia Borras-Santos
Joaquim Gea
Joaquim Gea
Joaquim Gea
Gloria Garrabou
Gloria Garrabou
Gloria Garrabou
Gloria Garrabou
Alvar Agusti
Alvar Agusti
Alvar Agusti
Alvar Agusti
Rosa Faner
Rosa Faner
Telomere Length but Not Mitochondrial DNA Copy Number Is Altered in Both Young and Old COPD
description Accelerated ageing is implicated in the pathogenesis of respiratory diseases as chronic obstructive pulmonary disease (COPD), but recent evidence indicates that the COPD can have roots early in life. Here we hypothesise that the accelerated ageing markers might have a role in the pathobiology of young COPD. The objective of this study was to compare two hallmarks of ageing, telomere length (TL), and mitochondrial DNA copy number (mtDNA-CN, as a surrogate marker of mitochondrial dysfunction) in young (≤ 50 years) and old (>50 years) smokers, with and without COPD. Both, TL and mtDNA-CN were measured in whole blood DNA by quantitative PCR [qPCR] in: (1) young ever smokers with (n = 81) or without (n = 166) COPD; and (2) old ever smokers with (n = 159) or without (n = 29) COPD. A multivariable linear regression was used to assess the association of TL and mtDNA-CN with lung function. We observed that in the entire study population, TL and mtDNA-CN decreased with age, and the former but not the latter related to FEV1/FVC (%), FEV1 (% ref.), and DLCO (% ref.). The short telomeres were found both in the young and old patients with severe COPD (FEV1 <50% ref.). In addition, we found that TL and mtDNA-CN were significantly correlated, but their relationship was positive in younger while negative in the older patients with COPD, suggesting a mitochondrial dysfunction. We conclude that TL, but not mtDNA-CN, is associated with the lung function impairment. Both young and old patients with severe COPD have evidence of accelerated ageing (shorter TL) but differ in the direction of the correlation between TL and mtDNA-CN in relation to age.
format article
author Sandra Casas-Recasens
Nuria Mendoza
Alejandra López-Giraldo
Alejandra López-Giraldo
Alejandra López-Giraldo
Tamara Garcia
Borja G. Cosio
Borja G. Cosio
Borja G. Cosio
Sergi Pascual-Guardia
Sergi Pascual-Guardia
Sergi Pascual-Guardia
Ady Acosta-Castro
Ady Acosta-Castro
Alicia Borras-Santos
Alicia Borras-Santos
Joaquim Gea
Joaquim Gea
Joaquim Gea
Gloria Garrabou
Gloria Garrabou
Gloria Garrabou
Gloria Garrabou
Alvar Agusti
Alvar Agusti
Alvar Agusti
Alvar Agusti
Rosa Faner
Rosa Faner
author_facet Sandra Casas-Recasens
Nuria Mendoza
Alejandra López-Giraldo
Alejandra López-Giraldo
Alejandra López-Giraldo
Tamara Garcia
Borja G. Cosio
Borja G. Cosio
Borja G. Cosio
Sergi Pascual-Guardia
Sergi Pascual-Guardia
Sergi Pascual-Guardia
Ady Acosta-Castro
Ady Acosta-Castro
Alicia Borras-Santos
Alicia Borras-Santos
Joaquim Gea
Joaquim Gea
Joaquim Gea
Gloria Garrabou
Gloria Garrabou
Gloria Garrabou
Gloria Garrabou
Alvar Agusti
Alvar Agusti
Alvar Agusti
Alvar Agusti
Rosa Faner
Rosa Faner
author_sort Sandra Casas-Recasens
title Telomere Length but Not Mitochondrial DNA Copy Number Is Altered in Both Young and Old COPD
title_short Telomere Length but Not Mitochondrial DNA Copy Number Is Altered in Both Young and Old COPD
title_full Telomere Length but Not Mitochondrial DNA Copy Number Is Altered in Both Young and Old COPD
title_fullStr Telomere Length but Not Mitochondrial DNA Copy Number Is Altered in Both Young and Old COPD
title_full_unstemmed Telomere Length but Not Mitochondrial DNA Copy Number Is Altered in Both Young and Old COPD
title_sort telomere length but not mitochondrial dna copy number is altered in both young and old copd
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/21328096c5dc4b70aabf06761fa0ba5a
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