Literature DB >> 24480322

Chronic inflammation and infection associate with a lower exercise training response in cystic fibrosis adolescents.

Pauline B van de Weert-van Leeuwen1, Hendrikus J Hulzebos2, Maarten S Werkman2, Sabine Michel3, Lodewijk A W Vijftigschild4, Marit A van Meegen4, Cornelis K van der Ent3, Jeffrey M Beekman4, Hubertus G M Arets3.   

Abstract

Considerable heterogeneity among training-induced effects is observed in patients with cystic fibrosis (CF). We previously showed that longitudinal changes in exercise capacity in adolescents with CF were negatively associated with Pseudomonas aeruginosa (P. aeruginosa) colonization and total immunoglobulin G (IgG) levels, independent of age, pulmonary function and bodyweight. This is the first study investigating whether chronic inflammation and infection also associate with the exercise training response in adolescents with CF. Participants performed a home-based exercise training program for 12 weeks. Pulmonary function, anthropometrics, exercise capacity, markers of inflammation and P. aeruginosa colonization status were measured at baseline. Exercise training-induced changes in pulmonary function and exercise capacity were compared between patients with a low and high inflammation-infection status. Participants with CF with high total IgG levels and P. aeruginosa colonization improved significantly less from the exercise training program, with regard to maximal oxygen consumption. These observations support the hypothesis that chronic systemic inflammation and infection leads to devastating effects on skeletal muscles, hampering skeletal muscle tissue to improve from regular physical exercise. Data further suggest that patients with CF should preferentially be encouraged to engage in regular physical exercise when inflammation and infection status is low (e.g. at a young age).
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Cystic fibrosis; Exercise; Immunoglobulin; Inflammation; Oxygen consumption; Pseudomonas aeruginosa

Mesh:

Substances:

Year:  2013        PMID: 24480322     DOI: 10.1016/j.rmed.2013.08.012

Source DB:  PubMed          Journal:  Respir Med        ISSN: 0954-6111            Impact factor:   3.415


  5 in total

1.  CrossTalk opposing view: Skeletal muscle oxidative capacity is not altered in cystic fibrosis patients.

Authors:  H J Erik Hulzebos; Jeroen A L Jeneson; Cornelis K van der Ent; Tim Takken
Journal:  J Physiol       Date:  2017-03-01       Impact factor: 5.182

2.  Exercise performance and quality of life in children with cystic fibrosis and mildly impaired lung function: relation with antibiotic treatments and hospitalization.

Authors:  Kristof Vandekerckhove; Michiel Keyzer; Jasper Cornette; Ilse Coomans; Filip Pyl; Frans De Baets; Petra Schelstraete; Filomeen Haerynck; Daniel De Wolf; Sabine Van Daele; Jan Boone
Journal:  Eur J Pediatr       Date:  2017-09-30       Impact factor: 3.183

3.  Physical Activity Regulates TNFα and IL-6 Expression to Counteract Inflammation in Cystic Fibrosis Patients.

Authors:  Ersilia Nigro; Rita Polito; Ausilia Elce; Giuseppe Signoriello; Paola Iacotucci; Vincenzo Carnovale; Monica Gelzo; Federica Zarrilli; Giuseppe Castaldo; Aurora Daniele
Journal:  Int J Environ Res Public Health       Date:  2021-04-28       Impact factor: 3.390

4.  Pseudomonas aeruginosa Quorum Sensing Molecule Alters Skeletal Muscle Protein Homeostasis by Perturbing the Antioxidant Defense System.

Authors:  Arunava Bandyopadhaya; A Aria Tzika; Laurence G Rahme
Journal:  mBio       Date:  2019-10-01       Impact factor: 7.867

5.  High-intensity interval training accelerates oxygen uptake kinetics and improves exercise tolerance for individuals with cystic fibrosis.

Authors:  Ronen Reuveny; Fred J DiMenna; Cedric Gunaratnam; Avigdor D Arad; Gerry N McElvaney; Davide Susta; Michael Peled; Niall M Moyna
Journal:  BMC Sports Sci Med Rehabil       Date:  2020-04-13
  5 in total

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