Your browser doesn't support javascript.
Predictors and changes of physical activity in idiopathic pulmonary fibrosis.
Badenes-Bonet, Diana; Rodó-Pin, Anna; Castillo-Villegas, Diego; Vicens-Zygmunt, Vanesa; Bermudo, Guadalupe; Hernández-González, Fernanda; Portillo, Karina; Martínez-Llorens, Juana; Chalela, Roberto; Caguana, Oswaldo; Sellarés, Jacobo; Molina-Molina, Maria; Duran, Xavier; Gea, Joaquim; Rodríguez-Chiaradia, Diego Agustín; Balcells, Eva.
  • Badenes-Bonet D; Interstitial Lung Disease Unit, Respiratory Medicine Department, Hospital del Mar, Passeig Marítim 25, 08003, Barcelona, Spain.
  • Rodó-Pin A; Department of Medicine and Life Sciences, Universitat Pompeu Fabra (UPF), Barcelona, Spain.
  • Castillo-Villegas D; IMIM (Hospital del Mar Medical Research Institute), Barcelona, Spain.
  • Vicens-Zygmunt V; Interstitial Lung Disease Unit, Respiratory Medicine Department, Hospital del Mar, Passeig Marítim 25, 08003, Barcelona, Spain.
  • Bermudo G; Respiratory Medicine Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Hernández-González F; Respiratory Medicine Department, IDIBELL, Hospital Universitari de Bellvitge, Barcelona, Spain.
  • Portillo K; Respiratory Medicine Department, IDIBELL, Hospital Universitari de Bellvitge, Barcelona, Spain.
  • Martínez-Llorens J; Respiratory Medicine Department, Hospital Clínic, Barcelona, Spain.
  • Chalela R; Respiratory Medicine Department, Hospital Germans Trias i Pujol, Barcelona, Spain.
  • Caguana O; Interstitial Lung Disease Unit, Respiratory Medicine Department, Hospital del Mar, Passeig Marítim 25, 08003, Barcelona, Spain.
  • Sellarés J; Department of Medicine and Life Sciences, Universitat Pompeu Fabra (UPF), Barcelona, Spain.
  • Molina-Molina M; Centro de Investigación en Red de Enfermedades Respiratorias, (CIBERES), Instituto de Salud Carlos III (ISCIII), Barcelona, Spain.
  • Duran X; IMIM (Hospital del Mar Medical Research Institute), Barcelona, Spain.
  • Gea J; Interstitial Lung Disease Unit, Respiratory Medicine Department, Hospital del Mar, Passeig Marítim 25, 08003, Barcelona, Spain.
  • Rodríguez-Chiaradia DA; Department of Medicine and Life Sciences, Universitat Pompeu Fabra (UPF), Barcelona, Spain.
  • Balcells E; IMIM (Hospital del Mar Medical Research Institute), Barcelona, Spain.
BMC Pulm Med ; 22(1): 340, 2022 Sep 09.
Article in English | MEDLINE | ID: covidwho-2038720
ABSTRACT

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/m2 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.
Subject(s)
Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: Idiopathic Pulmonary Fibrosis Type of study: Cohort study / Experimental Studies / Prognostic study Limits: Humans / Infant Language: English Journal: BMC Pulm Med Year: 2022 Document Type: Article Affiliation country: S12890-022-02134-4

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Main subject: Idiopathic Pulmonary Fibrosis Type of study: Cohort study / Experimental Studies / Prognostic study Limits: Humans / Infant Language: English Journal: BMC Pulm Med Year: 2022 Document Type: Article Affiliation country: S12890-022-02134-4