TY - JOUR
T1 - Distinct skeletal muscle molecular responses to pulmonary rehabilitation in chronic obstructive pulmonary disease
T2 - a cluster analysis
AU - Kneppers, Anita E. M.
AU - Haast, Roy A. M.
AU - Langen, Ramon C. J.
AU - Verdijk, Lex B.
AU - Leermakers, Pieter A.
AU - Gosker, Harry R.
AU - van Loon, Luc J. C.
AU - Lainscak, Mitja
AU - Schols, Annemie M. W. J.
N1 - Publisher Copyright:
© 2019 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of the Society on Sarcopenia, Cachexia and Wasting Disorders
PY - 2019/4
Y1 - 2019/4
N2 - Background Pulmonary rehabilitation (PR) is a cornerstone in the management of chronic obstructive pulmonary disease (COPD), targeting skeletal muscle to improve functional performance. However, there is substantial inter-individual variability in the effect of PR on functional performance, which cannot be fully accounted for by generic phenotypic factors. We performed an unbiased integrative analysis of the skeletal muscle molecular responses to PR in COPD patients and comprehensively characterized their baseline pulmonary and physical function, body composition, blood profile, comorbidities, and medication use. Methods Musculus vastus lateralis biopsies were obtained from 51 COPD patients (age 64 +/- 1 years, sex 73% men, FEV1, 34 (26-41) %pred.) before and after 4 weeks high-intensity supervised in-patient PR. Muscle molecular markers were grouped by network-constrained clustering, and their relative changes in expression values-assessed by qPCR and western blot-were reduced to process scores by principal component analysis. Patients were subsequently clustered based on these process scores. Pre-PR and post-PR functional performance was assessed by incremental cycle ergometry and 6 min walking test (6MWT). Results Eight molecular processes were discerned by network-constrained hierarchical clustering of the skeletal muscle molecular rehabilitation responses. Based on the resulting process scores, four clusters of patients were identified by hierarchical cluster analysis. Two major patient clusters differed in PR-induced autophagy (P <0.001), myogenesis (P = 0.014), glucocorticoid signalling (P <0.001), and oxidative metabolism regulation (P <0.001), with Cluster 1 (C1; n = 29) overall displaying a more pronounced change in marker expression than Cluster 2 (C2; n = 16). General baseline characteristics did not differ between clusters. Following PR, both 6 min walking distance (+26.5 +/- 8.3 m, P = 0.003) and peak load on the cycle ergometer test (+9.7 +/- 1.9 W, P <0.001) were improved. However, the functional improvement was more pronounced in C1, as a higher percentage of patients exceeded the minimal clinically important difference in peak workload (61 vs. 21%, P = 0.022) and both peak workload and 6 min walking test (52 vs. 8%, P = 0.008) upon PR. Conclusions We identified patient groups with distinct skeletal muscle molecular responses to rehabilitation, associated with differences in functional improvements upon PR.
AB - Background Pulmonary rehabilitation (PR) is a cornerstone in the management of chronic obstructive pulmonary disease (COPD), targeting skeletal muscle to improve functional performance. However, there is substantial inter-individual variability in the effect of PR on functional performance, which cannot be fully accounted for by generic phenotypic factors. We performed an unbiased integrative analysis of the skeletal muscle molecular responses to PR in COPD patients and comprehensively characterized their baseline pulmonary and physical function, body composition, blood profile, comorbidities, and medication use. Methods Musculus vastus lateralis biopsies were obtained from 51 COPD patients (age 64 +/- 1 years, sex 73% men, FEV1, 34 (26-41) %pred.) before and after 4 weeks high-intensity supervised in-patient PR. Muscle molecular markers were grouped by network-constrained clustering, and their relative changes in expression values-assessed by qPCR and western blot-were reduced to process scores by principal component analysis. Patients were subsequently clustered based on these process scores. Pre-PR and post-PR functional performance was assessed by incremental cycle ergometry and 6 min walking test (6MWT). Results Eight molecular processes were discerned by network-constrained hierarchical clustering of the skeletal muscle molecular rehabilitation responses. Based on the resulting process scores, four clusters of patients were identified by hierarchical cluster analysis. Two major patient clusters differed in PR-induced autophagy (P <0.001), myogenesis (P = 0.014), glucocorticoid signalling (P <0.001), and oxidative metabolism regulation (P <0.001), with Cluster 1 (C1; n = 29) overall displaying a more pronounced change in marker expression than Cluster 2 (C2; n = 16). General baseline characteristics did not differ between clusters. Following PR, both 6 min walking distance (+26.5 +/- 8.3 m, P = 0.003) and peak load on the cycle ergometer test (+9.7 +/- 1.9 W, P <0.001) were improved. However, the functional improvement was more pronounced in C1, as a higher percentage of patients exceeded the minimal clinically important difference in peak workload (61 vs. 21%, P = 0.022) and both peak workload and 6 min walking test (52 vs. 8%, P = 0.008) upon PR. Conclusions We identified patient groups with distinct skeletal muscle molecular responses to rehabilitation, associated with differences in functional improvements upon PR.
KW - Chronic obstructive pulmonary disease
KW - Peripheral muscle dysfunction
KW - Exercise training
KW - Muscle plasticity
KW - Cluster analysis
KW - MITOCHONDRIAL ADAPTATION
KW - COPD
KW - EXERCISE
KW - SARCOPENIA
KW - COMORBIDITIES
KW - DISUSE
KW - AGE
KW - REGENERATION
KW - PREDICTORS
KW - ACTIVATION
U2 - 10.1002/jcsm.12370
DO - 10.1002/jcsm.12370
M3 - Article
C2 - 30657653
SN - 2190-5991
VL - 10
SP - 311
EP - 322
JO - Journal of cachexia, sarcopenia and muscle
JF - Journal of cachexia, sarcopenia and muscle
IS - 2
ER -