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Factors Associated with Reduction of Sedentary Time Following Tiotropium/Olodaterol Therapy in Treatment-Naïve Chronic Obstructive Pulmonary Disease

Authors Takahashi K , Tashiro H, Tajiri R, Takamori A, Uchida M , Kato G, Kurihara Y, Sadamatsu H, Kinoshita T, Yoshida M , Kawaguchi A, Kimura S, Sueoka-Aragane N, Kawayama T

Received 13 September 2021

Accepted for publication 23 November 2021

Published 6 December 2021 Volume 2021:16 Pages 3297—3307

DOI https://doi.org/10.2147/COPD.S338560

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Richard Russell



Koichiro Takahashi,1 Hiroki Tashiro,1 Ryo Tajiri,2 Ayako Takamori,2 Masaru Uchida,3 Go Kato,4 Yuki Kurihara,1 Hironori Sadamatsu,1 Takashi Kinoshita,5 Makoto Yoshida,6 Atsushi Kawaguchi,2,7 Shinya Kimura,1 Naoko Sueoka-Aragane,1 Tomotaka Kawayama5 On behalf of Saga-naïve COPD Physical Activity Evaluation (SCOPE) Study Investigator Group

1Division of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan; 2Clinical Research Center, Saga University Hospital, Faculty of Medicine, Saga University, Saga, Japan; 3Division of Internal Medicine, Japan Community Health Care Organization Saga Central Hospital, Saga, Japan; 4Division of Respiratory Medicine, Saga Prefectural Medical Center Koseikan, Saga, Japan; 5Division of Respirology, Neurology, and Rheumatology, Department of Medicine, Kurume University School of Medicine, Fukuoka, Japan; 6Division of Respiratory Medicine, National Hospital Organization Fukuoka Hospital, Fukuoka, Japan; 7Education and Research Center for Community Medicine, Faculty of Medicine, Saga University, Saga, Japan

Correspondence: Koichiro Takahashi
Division of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, 5-1-1 Nabeshima, Saga, 849-8501, Japan
Email [email protected]

Background: Prolonged sedentary behavior is associated with worse prognosis in patients with chronic obstructive pulmonary disease (COPD). Our previous study found that first-line dual therapy with tiotropium/olodaterol significantly reduces sedentary time compared to tiotropium monotherapy in Japanese patients with treatment-naïve COPD, although the characteristics of responders to dual-therapy versus monotherapy for COPD are still unclear.
Methods: Patients with treatment-naïve COPD were randomized to receive either tiotropium or tiotropium/olodaterol treatment for 12 weeks. Physical activity was assessed using a triaxle accelerometer for 2 weeks before and after treatment. This analysis focused on the change in sedentary time, indicated by physical activity of 1.0– 1.5 metabolic equivalents (METs), with stratification for the following factors: age, body mass index (BMI), pulmonary function, COPD assessment test (CAT), the 6-minute walk distance (6MWD), and physical activity level at study entry.
Results: Thirty-five patients received tiotropium/olodaterol and 34 patients received tiotropium. In patients with lower inspiratory capacity at study entry, a significant reduction in sedentary time was observed in the tiotropium/olodaterol group compared with the tiotropium group (Tio: − 12.8 ± 13.5 min, Tio/Olo: − 65.1 ± 21.0 min, mean difference, − 52.2 min, 95% CI − 103.6 to 0.88, p = 0.046). In patients with a shorter duration of physical activity of ≥ 2 METs at study entry, a significant reduction of sedentary time was observed in the tiotropium/olodaterol group compared with the tiotropium group (Tio: − 3.3 ± 17.5 min, Tio/Olo: − 72.9 ± 23.1 min, mean difference, − 69.7 min, 95% CI − 128.7 to − 10.6, p = 0.02). There were no differences in terms of age, BMI, CAT score, 6MWD, FEV1, FVC, VC, and physical activity of 1.0– 1.5 METs and ≥ 3.0 METs.
Conclusion: This study showed that COPD patients with lower inspiratory capacity or shorter active time of ≥ 2.0 METs at study entry are likely to exhibit significantly greater reduction in sedentary time with tiotropium/olodaterol treatment.

Keywords: chronic obstructive pulmonary disease, physical activity, sedentary time, long-acting muscarinic antagonist, long-acting beta 2 agonist

Introduction

In patients with chronic obstructive pulmonary disease (COPD), airflow limitation causes dyspnea, decreasing quality of life (QOL) and physical activity.1 Physical inactivity has been shown to be associated with increased risks of exacerbation of COPD and mortality.2,3 Long-acting bronchodilator therapy results in an improvement in lung function, along with reduction of symptoms and exacerbations.4–6 The dual bronchodilator combination of a long-acting muscarinic antagonist (LAMA) and a long-acting beta 2 agonist (LABA) reportedly provides greater improvement in pulmonary function and QOL compared with LAMA monotherapy.7,8

Physical activity is defined as any bodily movement produced by skeletal muscles that leads to energy expenditure.9 Physical activity includes all activities in daily life, such as indoor activities, walking, and exercise.10 A step count is one of the indicators of physical activity in daily life, while the tri-axial accelerometer is used to assess physical activity in clinical research.11,12 The intensity of physical activity is measured in terms of metabolic equivalents (METs).13 Patients with COPD have been reported to have a decreased level of physical activity compared with healthy adults, even at an early stage of the disease.14–16

The global initiative for chronic obstructive lung disease (GOLD) has recommended regular physical activity for COPD patients.17 A previous study showed that increasing not only high-intensity physical activity, but also low-intensity physical activity, including sedentary behavior, was essential as a COPD treatment strategy.18 The Saga-naïve COPD Physical Activity Evaluation (SCOPE) Study reported that dual-therapy with tiotropium/olodaterol resulted in significantly greater improvement in forced expiratory volume in 1 s (FEV1) and dyspnea, and reduction in sedentary time as compared to tiotropium monotherapy, although the baseline clinical characteristics of the responders to such therapy among Japanese patients with treatment-naïve COPD receiving dual-therapy could not be investigated.19 The aim of the present study was to clarify the baseline characteristics of responders to first-line dual-therapy as compared to monotherapy by performing a stratified analysis of data from the SCOPE study.

Materials and Methods

Study Subjects

This was a prospective, randomized, multicenter, open-labeled, and parallel intervention study that was conducted at 9 public hospitals located in Japan described in a previous report (UMIN; UMIN000027190).19 In brief, 80 patients (age ≥40 and <85 years old) with treatment-naïve COPD were randomized 1:1, using electronic data capture system, according to 3 factors: %FEV1, age, and smoking history to receive either tiotropium alone or tiotropium/olodaterol treatment for 12 weeks. Entry period of this study was July 2017 to February 2019. Sixty-nine of the 80 patients were included in the study, among whom 34 received tiotropium monotherapy and 35 received dual-therapy with tiotropium and olodaterol (Table 1). A diagnosis of COPD was made based on a post-bronchodilator (short acting beta 2 agonist) forced expiratory volume in 1 s (FEV1)/forced vital capacity (FVC) ratio of less than 70% and presence of a smoking history of ≥10 pack years. However, current and ex-smokers with a post-bronchodilator less than 80% of predicted normal and FEV1 were accepted at the screening visit. Treatment-naïve COPD patients were defined as those who had not received inhaled corticosteroids (ICS), LABA and/or LAMA in the previous 12 months (the full study protocol is described in a previous report).19

Table 1 Characteristics of the Patients at the Baseline

Ethics Approval

Written informed consent was obtained from all patients. This study was approved by the institutional review board of each participating center (approval number: 2016-12-01, Supplementary Table 1). The SCOPE study was conducted according to the principles of the International Conference on Harmonization and Good Clinical Practice, Declaration of Helsinki, and Japanese Good Clinical Practice, and complied with all relevant local regulatory, legal, and ethical requirements (the Japan Registry of Clinical Trials approval no.; jRCTs071180021). The inclusion criteria are described in full in the primary report.19

Study Protocol

To clarify the baseline characteristics of responders to first-line dual-therapy (tiotropium/olodaterol group) versus those receiving monotherapy (tiotropium group) in terms of improvement in physical activity, analyses of the change in physical activity levels after 12 weeks treatments were performed in groups stratified according to age, body mass index (BMI), total COPD assessment test (CAT) scores, the 6-minute walk distance (6MWD), respiratory functions such as FEV1, FVC, vital capacity (VC), and inspiratory capacity (IC) at baseline, and the amount of baseline physical activity, assessed as the daily duration (in minutes) spent doing activity of ≥3, ≥2, and 1.0–1.5 metabolic equivalents (METs) intensity, using the data obtained in the SCOPE study.20,21 In each of the tiotropium/olodaterol and tiotropium treatment groups, patients were divided into two sub-groups based on the median values of each confounding factor, ie, age, BMI, total CAT scores, 6MWD and respiratory function, and longer and shorter duration of physical activity before treatment (baseline).

The average duration of daily physical activity from 8 a.m. to 8 p.m. of three valid days with evaluable data for 12 hours of the day was assessed before and after treatment using a tri-axis accelerometer (Active style PRO HJA-750C, OMRON, Kyoto, Japan).20 Physical activity of 1.0–1.5 METs was considered representative of sedentary time and changes in sedentary time were compared before and after treatment.

Statistical Analysis

The data are presented as mean and standard deviation (SD). Differences between the two treatment groups and the two sub-groups stratified according to each characteristic in each treatment group were evaluated using the Student’s t-test or χ2 test.

First, the correlation coefficient matrix was calculated to examine the correlation between each factor. Figure 1 shows a graphical representation of the correlation coefficient matrix using the graph theory. In the graph theory, connecting lines (edges) are used to show the relationship between factors (nodes). In this figure, factors with an absolute value of correlation coefficients of 0.2–0.4 are linked by thin lines, and those with correlation coefficients greater than 0.4 are linked by thick lines, thus graphically showing the strength of the correlation between each factor. The Plotly Python graphing library was used to create this figure.

Figure 1 Graphical representation of the factors related to reduction of sedentary time created using a graphical model. Factors with a direct link are connected by lines. The thickness of the line represents the strength of the relationship. The thick lines indicate an absolute value of the correlation coefficient of > 0.4, and the thin line represents a correlation coefficient of 0.2–0.4. The red circle stands for changes in physical activity of 1.0–1.5 METs. The green circle shows treatment with tiotropium/olodaterol, the Orange circles show pulmonary function, the blue circles show clinical characteristics, and the yellow circles represent baseline physical activities.

Abbreviations: IC, inspiratory capacity; FEV1, forced expiratory volume in 1 s; BMI, body mass index; 6MWD, 6-minute walk distance; CAT, COPD assessment test; Tio/Olo, tiotropium/olodaterol; PA 1.0–1.5, baseline physical activity of 1.0–1.5 METs intensity; PA ≥2.0, baseline physical activity of ≥ 2.0 METs intensity; METs, metabolic equivalents.

Next, mean changes in daily sedentary time after treatment were compared between tiotropium/olodaterol and tiotropium treatment groups stratified according to the median baseline value of each confounding factor (ie, higher and lower than the median value), or shorter and longer daily physical activity of ≥3, ≥2, and 1.0–1.5 METs at baseline using Welch’s t-tests. Confounding factors and duration of physical activity of different intensities in patients with a significant reduction of daily sedentary time following tiotropium/olodaterol treatment were identified as baseline characteristics possibly predictive of treatment responders in terms of improvement in sedentary time with dual-therapy compared to tiotropium monotherapy.

Finally, the decision tree method was used to identify baseline factors associated with changes in activity time for each treatment group. The classification and regression tree (CART) algorithm was used to create this decision tree, and mean squared error (MSE) was used as the loss function. The CART algorithm calculates the MSE when the data are divided by a certain factor and cut-off value, and then applies this operation to all candidate factors and cut-off values to find the pair of factors and cut-off values with the minimum MSE. This pair of factors and cut-off values divides the data into two sub-groups, and this operation is repeated recursively to generate further sub-groups. The results can be illustrated as a dendrogram, creating a profile for changes in activity time.

Statistical significance was indicated by a p-value of <0.05, and the missing values were excluded. Data were analyzed with R 3.6.1 software (The R Project for Statistical Computing).

Results

First, graphical representation of the correlation coefficient matrix was used to investigate the association between baseline patient characteristics, pulmonary function, physical activity, treatment, and reduction of sedentary time. Reduction of sedentary time was found to have a direct correlation with treatment with tiotropium/olodaterol, duration of physical activity at baseline of 1.0–1.5 METs and >2.0 METs, IC, FEV1, and BMI. Other factors also showed a correlation with reduction of sedentary time, although the correlation was indirect (Figure 1).

Next, the effect of patient characteristics at study entry on the reduction of sedentary time with treatment was analyzed by subdividing the two treatment groups into two groups stratified by the median value of the characteristic (Supplemental Figure 1). Subgroup analyses found no correlation between age, BMI, CAT score, or 6MWD and reduction of sedentary time.

Changes in daily sedentary time following treatment in terms of pulmonary function parameters at baseline are shown in Figure 2. In the subgroup of patients with lower baseline IC, but not those with higher IC, tiotropium/olodaterol treatment (−65.1 ± 21.0 min) significantly reduced daily sedentary time compared with tiotropium monotherapy (−12.8 ± 13.5 min) (Mean difference, −52.2 min [95% CI −103.6 to 0.88], p = 0.046) (Figure 2A). On the other hand, there were no significant differences in changes in sedentary time between tiotropium/olodaterol and tiotropium treatment groups in the sub-groups of patients with lower and higher baseline FEV1 (Figure 2B), FVC (Figure 2C), and VC (Figure 2D).

Figure 2 Changes in sedentary time before and after treatment stratified according to pulmonary function. Patients were stratified into two groups by a median IC of 1970 mL (A), FEV1 of 1510 mL (B), median FVC of 2840 mL (C), and median VC of 3010 mL (D), for stratified analysis of a reduction in sedentary time with Tio or Tio/Olo treatment. The error bars represent standard errors. p values show differences between two groups. In the subgroup of patients with lower baseline IC, Tio/Olo treatment significantly reduced sedentary time compared with Tio treatment.

Abbreviations: METs, metabolic equivalents; Tio, tiotropium; Tio/Olo, tiotropium/olodaterol; FEV1, forced expiratory volume in 1 s; FVC, forced vital capacity; VC, vital capacity; IC, inspiratory capacity.

Comparison of reduction of sedentary time with treatment in terms of the intensity of physical activity at baseline (Figure 3) showed that a significant reduction of sedentary time was observed in the tiotropium/olodaterol treatment group (−72.9 ± 23.1 min) compared with the tiotropium treatment group (−3.3 ± 17.5 min) in patients with a shorter, but not longer, duration of baseline physical activity of ≥2 METs intensity (Mean difference −69.7 min [95% CI −128.7 to −10.6], p = 0.02) (Figure 3B). There were no significant differences in changes in sedentary time between tiotropium/olodaterol and tiotropium treatment groups in the subgroup of patients with shorter and longer baseline physical activity of 1.0–1.5 (Figure 3A) and ≥3.0 METs (Figure 3C).

Figure 3 Changes in sedentary time before and after treatment stratified by the duration and intensity of physical activity at study entry. Patients were divided into two groups based on a median duration of PA of 1.0–1.5 METs intensity of 282.7 min (A), median duration of PA of ≥ 2.0 METs intensity of 125.1 min (B), and median duration of PA of ≥ 3.0 METs intensity of 31.1 min (C), for stratified analysis of reduction in sedentary time with Tio or Tio/Olo treatment. The error bars represent standard errors. p values show differences between two groups. In the subgroup of patients with a shorter duration of baseline physical activity of ≥2 METs, Tio/Olo treatment significantly reduced sedentary time compared with Tio treatment.

Abbreviations: METs, metabolic equivalents; Tio, tiotropium; Tio/Olo, tiotropium/olodaterol; PA, physical activity; METs, metabolic equivalents.

Decision tree analyses were performed to show the most influential factors among patient characteristics, pulmonary function, and physical activity at baseline for reduction of sedentary time with tiotropium (Figure 4A) and tiotropium/olodaterol treatment (Figure 4B). Tiotropium monotherapy was found to be most effective for reduction of sedentary time in patients in whom the daily duration of physical activity of 1.0–1.5 METs at study entry was more than 339.4 min. On the other hand, tiotropium/olodaterol was most effective in patients in whom the duration of physical activity of ≥2.0 METs intensity at study entry was shorter than 111.0 min. Therapeutic efficacy was also observed in the group with baseline daily activity of ≥2.0 METs intensity for more than 111.0 min and in those with a CAT score of <6.5.

Figure 4 Decision tree about treatment with Tio or Tio/Olo in treatment-naïve COPD patients. The decision tree was obtained by statistical analysis including patient characteristics (age, BMI, CAT, and 6MWD), pulmonary functions (FEV1, FVC, VC, and IC), and baseline physical activity of 1.0–1.5 METs, PA ≥ 2.0 METs, and PA ≥ 3.0 METs intensity as confounding factors. The decision trees show treatment with Tio (A), and Tio/Olo (B). Tio treatment was most effective for reduction of sedentary time in patients in whom the daily duration of baseline PA of 1.0–1.5 METs was more than 339.4 min. Tio/Olo treatment was most effective in patients in whom the duration of baseline PA of ≥ 2.0 METs was shorter than 111.0 min.

Abbreviations: METs, metabolic equivalents; BMI, body mass index; CAT, COPD assessment test; 6MWD, 6-minute walk distance; FEV1, forced expiratory volume in 1 s; FVC, forced vital capacity; VC, vital capacity; IC, inspiratory capacity; PA, physical activity; Tio, tiotropium; Tio/Olo, tiotropium/olodaterol.

Discussion

The SCOPE study demonstrated that tiotropium/olodaterol treatment improves physical activity, especially in terms of reduction of sedentary time, in treatment-naïve COPD patients. The present study showed that COPD patients with lower IC and shorter active time (≥2.0 METs) at study entry experience a significantly greater reduction of sedentary time with tiotropium/olodaterol treatment. This is the first report to show patient characteristics that are likely associated with reduced sedentary time following treatment with dual bronchodilator therapy. Elucidation of the characteristics of patients in whom tiotropium/olodaterol treatment is likely to be more effective will help tailor the pharmacological treatment strategy in patients with COPD.

Patients with COPD are known to have significantly lower levels of physical activity as compared with healthy subjects.21 The duration of walking is significantly shorter in COPD patients compared with healthy, age-matched subjects.22 Even if patients with mild COPD decreased a level of physical activity, since dyspnea is known to lead to diminished activity levels.9,14 Furthermore, physical inactivity is an essential predictor of mortality in chronic diseases, including diabetes mellitus and cardiovascular disease.23,24 In patients with COPD, physical activity is known to be the strongest prognostic factor for survival compared with pulmonary function.3

Sedentary behavior represents physical activity of 1.0–1.5 METs intensity, standing or walking at a pace of less than 55 m/min is considered physical activity of 2 METs intensity, and walking faster than 55 m/min is considered physical activity of 3 METs intensity.25 Sedentary behavior has also been reported to be an independent predictor of mortality in COPD, even adjusting for moderate-to-vigorous physical activity. Mortality was higher in patients with COPD who spend ≥8.5 h per day in activities requiring <1.5 METs.26

The World Health Organization (WHO) published guidelines on physical activity and sedentary behavior in 2020.27 The guidelines provide general recommendations to reduce sedentary time, which accords with the growing concern regarding the negative health effects of sedentary behavior.28 The recommendations also state that older adults should limit the amount of sedentary time, since replacing sedentary time with physical activity of any intensity (including light intensity) provides health benefits.27 Hence, improving physical activity levels is one of the management goals of COPD guidelines.29 Further, pulmonary rehabilitation programs, including patient education, have been reported to be effective in improving physical activity.30 In the SCOPE study, however, since only a simple leaflet was used to provide a basic explanation of COPD, reduction of sedentary time was considered to be the pure effect of tiotropium/olodaterol rather than patient education.

Stratified analysis showed significant reduction of sedentary time in the low IC group with tiotropium/olodaterol treatment. IC is an index of pulmonary hyperinflation, and the effect of reduction in sedentary time with treatment was probably because the low IC is related to dyspnea and decreased exercise tolerance.31–33 Dynamic hyperinflation is also reported to have an effect on physical activity, regardless of the severity of COPD.34 In the VESUTO study of patients treated with tiotropium/olodaterol, a reduction of sedentary time was observed in the group with higher pulmonary function at baseline, which was contrary to the results observed in our study.35,36 However, baseline pulmonary function of patients in the VESUTO study (%FEV1 52.6%) was lower than in patients in the SCOPE study (%FEV1 62.9%), and the difference in the results could have been due to differences in patient characteristics and COPD treatment at the time of study entry. Furthermore, a significant reduction of sedentary time was observed in patients with a shorter duration of physical activity of above 2.0 METs with tiotropium/olodaterol treatment in the SCOPE study. These data show that tiotropium/olodaterol is more effective in COPD patients with reduced activity levels. These data suggest the efficacy of tiotropium/olodaterol treatment in reducing sedentary time in inactive COPD patients.

A decrease in physical activity time of above 2.5 METs has been reported even in mild COPD patients.22 The previous study showed that replacing sedentary time with other physical activity leads to significant improvements in lung function in COPD patients, suggesting that physicians should pay more attention to the physical activity levels of patients with mild COPD.37 The time spent watching television is also reportedly longer in patients with COPD as compared to healthy older subjects.38 Our results suggest that patients might benefit from even low-intensity exercise, such as standing up during television commercials. Further, since LAMA monotherapy might not be enough to reduce sedentary time in patients with treatment-naïve COPD, treatment with dual-bronchodilator therapy should be considered in patients with low inspiratory capacity and shorter durations of physical activity.

The present study has certain limitations. First, this study included a small sample size and was limited to Japanese patients, which limits its generalizability to other populations. Second, since the duration of treatment was only 12 weeks, we could not show the effects of therapy for more than 12 weeks. Third, this study did not involve intensive patient education regarding COPD and the need for increased physical activity. In clinical settings, pulmonary rehabilitation might result in further behavior modification.

Conclusions

Dual bronchodilator therapy with tiotropium/olodaterol treatment reduced sedentary time in patients with treatment-naïve COPD. Patients with a lower inspiratory capacity and shorter active time of ≥2.0 METs intensity are more likely to benefit from dual tiotropium/olodaterol treatment rather than tiotropium monotherapy.

Data Sharing Statement

The data of this study are stored and managed at the Saga University Clinical Research Center. Any requests for sharing of this data should be addressed to the corresponding author.

Author Contributions

K.T. is the guarantor and takes responsibility for the content of this manuscript, including the data and analysis. H.T., M.U., G.K., Y. K., H.S., T.K., M.Y., and T.K. contributed to study conception and design, data acquisition, and interpretation of the data. R.T., A.T., and A.K. contributed to data acquisition, analysis and interpretation. S.K. and N.S-A. contributed to study conception and design and interpretation of the data. All authors made substantial contributions to conception and design, acquisition of data, or analysis and interpretation of data; took part in drafting the article or revising it critically for important intellectual content; agreed to submit to the current journal; gave final approval of the version to be published; and agree to be accountable for all aspects of the work.

Funding

This study was financially supported by Nippon Boehringer Ingelheim Co., Ltd. as an independent investigator study.

Disclosure

Dr. Koichiro Takahashi received lecture fees from Nippon Boehringer Ingelheim and AstraZeneca. Dr. Takashi Kinoshita received grants from Daiichi Sankyo. Dr. Makoto Yoshida received lecture fees from AstraZeneca, GlaxoSmithKline, and Novartis Pharma. Dr. Tomotaka Kawayama received grants from Novartis, and lecture fees from AstraZeneca, GlaxoSmithKline, Boehringer Ingelheim, Novartis Pharma, Teijin Pharma and Home Healthcare, Sanofi, Kyorin Pharmaceutical, and MeijiSeika Pharma. Dr. Hiroki Tashiro, Dr. Masaru Uchida, Dr. Go Kato, Dr. Yuki Kurihara, Dr. Ayako Takamori, Dr. Ryo Tajiri, Dr. Hironori Sadamatsu, Dr. Atsushi Kawaguchi, Dr. Shinya Kimura, and Dr. Naoko Sueoka-Aragane did not have any conflicts of interests.

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