Patients with chronic obstructive lung disease (COPD) suffer from a progressive loss of lung function that leads to poor quality of life, and often invalidity and early death. Regular exercise can improve quality of life in these patients, but there is a lack in understanding the underlying mechanism of exercise-induced improvement in COPD and it is widely thought not to have any effect on the lung as such. In the present study, the investigators aim to investigate the impact of an extensive high-intensity interval training (HIIT)-based exercise scheme on the regenerative capacity of the lung in patients with COPD on waiting list for lung volume reduction surgery. Design: Prospective randomized controlled clinical trial. Intervention: 24 persons with COPD referred for lung volume reduction surgery will randomly be allocated (1:1) to prehabilitation with high intensity interval training (HIIT) or non-exercise control. Outcomes: The primary outcome is differences in change in differential protein composition in distal lung tissue between HIIT and control groups post-intervention using spatial multimodal proteomics. Furthermore, lung tissue mass, protein composition (mass spectrometry and spatial omics e.g. MACSima), pulmonary blood volume, blood protein profile (biomarkers), diffusion capacity at rest and during exercise, oxygen consumption tests, body composition scan, distal airspace radii and physical functional tests will be measured before and after the intervention. Perspective: This study may fundamentally change the view on the regenerative potential of the lungs in COPD.
Patients with chronic obstructive pulmonary disease (COPD) suffer from a progressive loss of lung function that leads to low physical performance, poor quality of life, and early death. Pulmonary rehabilitation, including exercise training, is considered the most effective non-pharmacological intervention for improving quality of life in patients with COPD. However, its use is halted by the lack of understanding of the mechanism of exercise-induced improvement in COPD, and is widely thought not to have any effect on lung function, at least as measured by dynamic spirometry and diffusion capacity measured at rest in the upright position. It is thus mainly considered a mean to alleviate symptoms, primarily by improving skeletal muscle function, but without the potential to reverse any structural changes within the pulmonary system which are seen in patients with COPD. The rationale for recommending exercise as a way to reduce symptom burden and increase quality of life, is based on the finding from the most recent Cochrane review. The authors stated that no additional studies comparing exercise with control were warranted, as exercise per se leads to improvements, regardless of the type of exercise. The reasoning for not prescribing exercise more widely to patients with COPD is based on two assumptions: 1) new tissue cannot be formed in the adult lung, and 2) no consistent exercise training-induced changes in lung function have previously been documented. However, de novo tissue formation has repeatedly been demonstrated in the adult lung, both in animals and humans, primarily in response to prolonged hypoxia and pneumonectomy. It has recently been reported that interval-based training counteracts the progressive loss of lung tissue in animal models of experimental COPD. The most likely stimulus is the mechanical strain, and if any measurable changes are to be induced by training, a high-intensity interval training (HIIT) scheme is preferable to be initiated in pulmonary rehabilitation. An aspect of the progressive lung tissue loss in COPD that sets in from the very early stages of disease, seemingly before any ventilatory disturbance can be observed, is pulmonary vascular dysfunction and loss of pulmonary capillaries, driven by a seemingly disease-specific imbalance between angiogenetic and angiostatic processes in the pulmonary vasculature. Indeed, this is likely a mechanism that drives the concomitant loss of lung tissue, and also limits exercise capacity as the ability to expand the alveolar-capillary membrane though pulmonary capillary recruitment and distension becomes limited, thus critically attenuating oxygen uptake during exercise. It is now well-established that the human lung conceals a diverse population of mechanosensitive progenitor and stem cells that appear to be dormant in COPD. Their reactivation by the stretch and strain as well as high vascular pressures associated with for example physical activity may likely explain why interval-based training has been found to counteract the progressive loss of lung tissue in animal models of experimental COPD. The investigators have developed in vitro protocols for assessing the regenerative capacity of the lung, and the next step will be to develop similar protocols for the human lung, both in the healthy state and from patients with COPD. In the present pilot study, the investigators will investigate the effects of an extensive high-intensity interval training (HIIT) on the regenerative capacity of the lung as determined by in vitro lung organoid culture and vascular tissue engineering 3D methods on patients with COPD on waiting list for lung volume reduction surgery. Primary objective: To investigate whether prehabilitation with supervised HIIT while on waiting list for lung volume reduction surgery affects regenerative pathways in the lung. The investigators aim to determine if these effects can be detected non-invasively using blood biomarkers and spatial omics technologies to map region-specific molecular changes, cellular composition, and structural remodelling in lung tissue. Secondary objectives: To determine whether an increase in blood volume is associated with an increased lung tissue mass (LTM), pulmonary blood volume (PBV), reduced symptom severity, and pulmonary diffusing capacity at rest and during exercise. To use explanted tissue to develop ex vivo models for disease and repair mechanisms. Research hypotheses: Primary: Prehabilitation while on waiting list for lung volume reduction surgery is superior to a non-exercise control group for increasing activating regenerative pathways in the lung with concomitant changes in LTM and PBV. Secondary: Diffusing capacity during exercise and quality of life increases following prehabilitation with HIIT compared to a non-exercise control group. Finally, it is hypothesized that functional outcomes, V̇O2peak, body composition and cardiac output will be improved despite no/or limited changes in lung function in the HIIT group.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
24
The HIIT intervention consist of 4 intervals with each lasting 4 minutes (4x4min). If a participant reports discomfort related to the length of the intervals or start to feel unmotivated by performing the same exercise, we will use another HIIT protocol: 10x1min. The 4x4min HIIT consists of a warm-up period of 10 minutes with a target heart rate at 60-70% of HRmax, followed by 4 HIIT intervals with a target HR ≥85%. The intervals are separated by three minutes of active rest, in which the HR should drop to 60% of maximum. Following this, a cool down period of three minutes at warm up intensity is performed. The 10x1min HIIT consists of a 10-minute warm-up period.The warm-up is followed by 10 intervals, each lasting 1 min at 100% of maximal workload, separated by three minutes of active rest, in which the HR should drop to 60% of maximum. Following the intervals, a cool down period of three minutes at warm up intensity is performed.
Centre for Physical Activity Research, Copenhagen University Hospital
Copenhagen, Denmark
Differential protein composition
Differences in change in differential protein composition in distal lung tissue between HIIT and control group post-intervention using spatial multimodal proteomics.
Time frame: At surgery
Differential protein composition
Differences in change in differential protein composition in distal lung tissue between HIIT and control group post-intervention using mass spectrometry.
Time frame: At surgery
Lung tissue protein composition
Differences in change in distal lung tissue protein composition pre- and post-HIIT intervention via mass spectrometry.
Time frame: At surgery
Serum protein profiles
Differences in change in serum protein profiles between HIIT and control groups after intervention using mass spectrometry.
Time frame: At surgery
Tissue niche and cellular composition
Tissue niche and cellular composition in the lung will be determined
Time frame: At surgery
Translational regions
Healthy, diseased and transitional (''border zones'') regions in the lung will be deliniated/identified by using spation omic analysis. This will be done both at a gene level, protein level and glycosaminoglycan level.
Time frame: At surgery
Inflammatory and remodelling factors (blood samples)
Difference in change from baseline to follow-up between groups in inflammatory and remodelling factor proteins in blood samples measured by mass spectrometry
Time frame: From time of inclusion in the study and until surgery (up to 8 months)
Protein markers
Protein markers will be identified by mass spectrometry and the difference in the spatial localisation of these will be identified between the groups after the intervention. This will be done using Pentachrome and/or multiplexed inmunofluorescence stainings.
Time frame: At surgery
Lung cell population
Difference in change from baseline to follow-up between groups in lung cell populations by single cell-RNA sequencing.
Time frame: At surgery
Lung tissue mass
Difference in change from baseline to follow-up between groups in total LTM (g)
Time frame: From inclusion in the study and until surgery (up to 8 months)
Pulmonary blood volume at rest
Difference in change from baseline to follow-up between groups in pulmonary blood volume (mL) at rest
Time frame: From inclusion in the study and until surgery (up to 8 months)
DLNO at rest and during exercise
Difference in change from baseline to follow-up between groups in DL,NO (mmol/(min kPa)) as a function of V̇O2 measured at rest, 60% of current maximal workload (relative), and at follow-up including 60% of maximal workload at baseline (absolute)
Time frame: From inclusion in the study and until surgery (up to 8 months)
DLNO during exercise
Difference in change from baseline to follow-up between groups in DL,NO (mmol/(min kPa)) during exercise at 60% of current maximal workload (relative)
Time frame: From inclusion in the study and until surgery (up to 8 months)
DLNO during exercise
Difference in change from baseline to follow-up between groups in DL,NO (mmol/(min kPa)) during exercise at 60% of the maximal workload measured at baseline (absolute)
Time frame: From inclusion in the study and until surgery (up to 8 months)
Pulmonary blood volume / total blood volume ratio
Difference in change from baseline to follow-up between groups in pulmonary blood volume / total blood volume ratio
Time frame: From inclusion in the study and until surgery (up to 8 months)
Health related quality of life
Difference in change from baseline to follow-up between groups in health-related quality of life - COPD Assessment Test (CAT) score, and St. George's Respiratory Questionnaire (SGRQ)
Time frame: From enrollment until 3 months post-surgery
Extra cellular matrix structure
Extracellular matrix structure
Time frame: At surgery
Inflammatory and remodelling factors (lung tissue)
Difference in change from baseline to follow-up between groups in inflammatory and remodelling factor proteins in lung tissue measured by mass spectrometry
Time frame: At surgery
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