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ACE and response to pulmonary rehabilitation in COPD: two observational studies

INTRODUCTION: Skeletal muscle impairment is an important feature of chronic obstructive pulmonary disease (COPD). Renin–angiotensin system activity influences muscle phenotype, so we wished to investigate whether it affects the response to pulmonary rehabilitation. METHODS: Two studies are described...

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Autores principales: Kon, Samantha S C, Jolley, Caroline J, Shrikrishna, Dinesh, Montgomery, Hugh E, Skipworth, James R A, Puthucheary, Zudin, Moxham, John, Polkey, Michael I, Man, William D-C, Hopkinson, Nicholas S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5353252/
https://www.ncbi.nlm.nih.gov/pubmed/28321311
http://dx.doi.org/10.1136/bmjresp-2016-000165
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author Kon, Samantha S C
Jolley, Caroline J
Shrikrishna, Dinesh
Montgomery, Hugh E
Skipworth, James R A
Puthucheary, Zudin
Moxham, John
Polkey, Michael I
Man, William D-C
Hopkinson, Nicholas S
author_facet Kon, Samantha S C
Jolley, Caroline J
Shrikrishna, Dinesh
Montgomery, Hugh E
Skipworth, James R A
Puthucheary, Zudin
Moxham, John
Polkey, Michael I
Man, William D-C
Hopkinson, Nicholas S
author_sort Kon, Samantha S C
collection PubMed
description INTRODUCTION: Skeletal muscle impairment is an important feature of chronic obstructive pulmonary disease (COPD). Renin–angiotensin system activity influences muscle phenotype, so we wished to investigate whether it affects the response to pulmonary rehabilitation. METHODS: Two studies are described; in the first, the response of 168 COPD patients (mean forced expiratory volume in one second 51.9% predicted) to pulmonary rehabilitation was compared between different ACE insertion/deletion polymorphism genotypes. In a second, independent COPD cohort (n=373), baseline characteristics and response to pulmonary rehabilitation were compared between COPD patients who were or were not taking ACE inhibitors or angiotensin receptor antagonists (ARB). RESULTS: In study 1, the incremental shuttle walk distance improved to a similar extent in all three genotypes; DD/ID/II (n=48/91/29) 69(67)m, 61 (76)m and 78 (78)m, respectively, (p>0.05). In study 2, fat free mass index was higher in those on ACE-I/ARB (n=130) than those who were not (n=243), 17.8 (16.0, 19.8) kg m(−2) vs 16.5 (14.9, 18.4) kg/m(2) (p<0.001). However change in fat free mass, walking distance or quality of life in response to pulmonary rehabilitation did not differ between groups. CONCLUSIONS: While these data support a positive association of ACE-I/ARB treatment and body composition in COPD, neither treatment to reduce ACE activity nor ACE (I/D) genotype influence response to pulmonary rehabilitation.
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spelling pubmed-53532522017-03-20 ACE and response to pulmonary rehabilitation in COPD: two observational studies Kon, Samantha S C Jolley, Caroline J Shrikrishna, Dinesh Montgomery, Hugh E Skipworth, James R A Puthucheary, Zudin Moxham, John Polkey, Michael I Man, William D-C Hopkinson, Nicholas S BMJ Open Respir Res Chronic Obstructive Pulmonary Disease INTRODUCTION: Skeletal muscle impairment is an important feature of chronic obstructive pulmonary disease (COPD). Renin–angiotensin system activity influences muscle phenotype, so we wished to investigate whether it affects the response to pulmonary rehabilitation. METHODS: Two studies are described; in the first, the response of 168 COPD patients (mean forced expiratory volume in one second 51.9% predicted) to pulmonary rehabilitation was compared between different ACE insertion/deletion polymorphism genotypes. In a second, independent COPD cohort (n=373), baseline characteristics and response to pulmonary rehabilitation were compared between COPD patients who were or were not taking ACE inhibitors or angiotensin receptor antagonists (ARB). RESULTS: In study 1, the incremental shuttle walk distance improved to a similar extent in all three genotypes; DD/ID/II (n=48/91/29) 69(67)m, 61 (76)m and 78 (78)m, respectively, (p>0.05). In study 2, fat free mass index was higher in those on ACE-I/ARB (n=130) than those who were not (n=243), 17.8 (16.0, 19.8) kg m(−2) vs 16.5 (14.9, 18.4) kg/m(2) (p<0.001). However change in fat free mass, walking distance or quality of life in response to pulmonary rehabilitation did not differ between groups. CONCLUSIONS: While these data support a positive association of ACE-I/ARB treatment and body composition in COPD, neither treatment to reduce ACE activity nor ACE (I/D) genotype influence response to pulmonary rehabilitation. BMJ Publishing Group 2017-03-08 /pmc/articles/PMC5353252/ /pubmed/28321311 http://dx.doi.org/10.1136/bmjresp-2016-000165 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
spellingShingle Chronic Obstructive Pulmonary Disease
Kon, Samantha S C
Jolley, Caroline J
Shrikrishna, Dinesh
Montgomery, Hugh E
Skipworth, James R A
Puthucheary, Zudin
Moxham, John
Polkey, Michael I
Man, William D-C
Hopkinson, Nicholas S
ACE and response to pulmonary rehabilitation in COPD: two observational studies
title ACE and response to pulmonary rehabilitation in COPD: two observational studies
title_full ACE and response to pulmonary rehabilitation in COPD: two observational studies
title_fullStr ACE and response to pulmonary rehabilitation in COPD: two observational studies
title_full_unstemmed ACE and response to pulmonary rehabilitation in COPD: two observational studies
title_short ACE and response to pulmonary rehabilitation in COPD: two observational studies
title_sort ace and response to pulmonary rehabilitation in copd: two observational studies
topic Chronic Obstructive Pulmonary Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5353252/
https://www.ncbi.nlm.nih.gov/pubmed/28321311
http://dx.doi.org/10.1136/bmjresp-2016-000165
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