Predictors and changes of physical activity in idiopathic pulmonary fibrosis


Por: Badenes-Bonet, D, Rodo-Pin, A, Castillo-Villegas, D, Vicens-Zygmunt, V, Bermudo, G, Hernandez-Gonzalez, F, Portillo, K, Martinez-Llorens, J, Chalela, R, Caguana, O, Sellares, J, Molina-Molina, M, Duran, X, Gea, J, Rodriguez-Chiaradia, DA, Balcells, E

Publicada: 9 sep 2022
Resumen:
Background Different clinical predictors of physical activity (PA) have been described in idiopathic pulmonary fibrosis (IPF), but studies are lacking evaluating the potential role of muscle strength and anxiety and depression symptoms in PA limitation. Moreover, little is known about the impact of changes in PA in the course of the disease. The aim of the present study was to investigate the relationship between baseline PA and a wide range of variables in IPF, to assess its longitudinal changes at 12 months and its impact on progression free-survival. Methods PA was assessed by accelerometer and physiological, clinical, psychological factors and health-related quality of life were evaluated in subjects with IPF at baseline and at 12 month follow-up. Predictors of PA were determined at baseline, evolution of PA parameters was described and the prognostic role of PA evolution was also established. Results Forty participants with IPF were included and 22 completed the follow-up. At baseline, subjects performed 5765 (3442) daily steps and spent 64 (44) minutes/day in moderate to vigorous PA. Multivariate regression models showed that at baseline, a lower six-minute walked distance, lower quadriceps strength (QMVC), and a higher depression score in the Hospital Anxiety and Depression scale were associated to lower daily step number. In addition, being in (Gender-Age-Physiology) GAP III stage, having a BMI >= 25 kg/m(2) and lower QMVC or maximum inspiratory pressure were factors associated with sedentary behaviour. Adjusted for age, gender and forced vital capacity (FVC) (%pred.) a lower progression-free survival was evidenced in those subjects that decreased PA compared to those that maintained, or even increased it, at 12 months [HR 12.1 (95% CI, 1.9-78.8); p = 0.009]. Conclusion Among a wide range of variables, muscle strength and depression symptoms have a predominant role in PA in IPF patients. Daily PA behaviour and its evolution should be considered in IPF clinical assessment and as a potential complementary indicator of disease prognosis.

Filiaciones:
Badenes-Bonet, D:
 Hosp Mar, Resp Med Dept, Interstitial Lung Dis Unit, Barcelona 08003, Spain

 Univ Pompeu Fabra UPF, Dept Med & Life Sci, Barcelona, Spain

 IMIM Hosp Mar Med Res Inst, Barcelona, Spain

Rodo-Pin, A:
 Hosp Mar, Resp Med Dept, Interstitial Lung Dis Unit, Barcelona 08003, Spain

Castillo-Villegas, D:
 Hosp Santa Creu & Sant Pau, Resp Med Dept, Barcelona, Spain

Vicens-Zygmunt, V:
 Hosp Univ Bellvitge, Resp Med Dept, IDIBELL, Barcelona, Spain

Bermudo, G:
 Hosp Univ Bellvitge, Resp Med Dept, IDIBELL, Barcelona, Spain

Hernandez-Gonzalez, F:
 Hosp Clin Barcelona, Resp Med Dept, Barcelona, Spain

Portillo, K:
 Hosp Badalona Germans Trias & Pujol, Resp Med Dept, Barcelona, Spain

Martinez-Llorens, J:
 Hosp Mar, Resp Med Dept, Interstitial Lung Dis Unit, Barcelona 08003, Spain

 Univ Pompeu Fabra UPF, Dept Med & Life Sci, Barcelona, Spain

 Inst Salud Carlos III ISCIII, Ctr Invest Red Enfermedades Respiratorias, CIBERES, Barcelona, Spain

 IMIM Hosp Mar Med Res Inst, Barcelona, Spain

Chalela, R:
 Hosp Mar, Resp Med Dept, Interstitial Lung Dis Unit, Barcelona 08003, Spain

 Univ Pompeu Fabra UPF, Dept Med & Life Sci, Barcelona, Spain

 IMIM Hosp Mar Med Res Inst, Barcelona, Spain

Caguana, O:
 Hosp Mar, Resp Med Dept, Interstitial Lung Dis Unit, Barcelona 08003, Spain

Sellares, J:
 Hosp Clin Barcelona, Resp Med Dept, Barcelona, Spain

Molina-Molina, M:
 Inst Salud Carlos III ISCIII, Ctr Invest Red Enfermedades Respiratorias, CIBERES, Barcelona, Spain

 Hosp Univ Bellvitge, Resp Med Dept, IDIBELL, Barcelona, Spain

Duran, X:
 Hosp Mar IMIM, Sci Stat & Tech Dept, Barcelona, Spain

Gea, J:
 Hosp Mar, Resp Med Dept, Interstitial Lung Dis Unit, Barcelona 08003, Spain

 Univ Pompeu Fabra UPF, Dept Med & Life Sci, Barcelona, Spain

 Inst Salud Carlos III ISCIII, Ctr Invest Red Enfermedades Respiratorias, CIBERES, Barcelona, Spain

 IMIM Hosp Mar Med Res Inst, Barcelona, Spain

Rodriguez-Chiaradia, DA:
 Hosp Mar, Resp Med Dept, Interstitial Lung Dis Unit, Barcelona 08003, Spain

 Univ Pompeu Fabra UPF, Dept Med & Life Sci, Barcelona, Spain

 Inst Salud Carlos III ISCIII, Ctr Invest Red Enfermedades Respiratorias, CIBERES, Barcelona, Spain

 IMIM Hosp Mar Med Res Inst, Barcelona, Spain

Balcells, E:
 Hosp Mar, Resp Med Dept, Interstitial Lung Dis Unit, Barcelona 08003, Spain

 Univ Pompeu Fabra UPF, Dept Med & Life Sci, Barcelona, Spain

 Inst Salud Carlos III ISCIII, Ctr Invest Red Enfermedades Respiratorias, CIBERES, Barcelona, Spain

 IMIM Hosp Mar Med Res Inst, Barcelona, Spain
ISSN: 14712466
Editorial
BMC, CAMPUS, 4 CRINAN ST, LONDON N1 9XW, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 22 Número: 1
Páginas:
WOS Id: 000852438000002
ID de PubMed: 36085057
imagen Green Published, gold, All Open Access, Gold, Green

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