Introduction
Chronic obstructive pulmonary disease (COPD) is a common, preventable, and treatable disease that is characterized by persistent respiratory symptoms and airflow limitation [
1], and its morbidity and mortality rates are on the rise. Globally, the COPD burden is projected to increase in the future owing to the continued exposure to COPD risk factors and population aging [
2]. Other important factors contributing to the burden are patients’ lack of knowledge of COPD, their denial of pulmonary function testing and reasonable standard treatments, and poor patient compliance to prescribed medications in the stable period. Therefore, the treatment of COPD, especially the management of stable COPD, is particularly important.
In 2011, the global initiative for chronic obstructive lung disease (GOLD) guidelines proposed that stable COPD patients should be divided into four groups (A, B, C, and D) according to the clinical symptoms and risk of future acute exacerbation [
3]. The symptom scores of patients in groups B and D were higher than those in groups A and C, which indicates that the former COPD group patients have more prominent respiratory symptoms, such as chronic cough, sputum production and dyspnea. Moreover, several studies have suggested that the proportion of COPD patients in groups B and D are higher than in groups A and C [
4‐
7]. The GOLD 2017 guidelines recommend long-acting anticholinergic agents (LAMAs) as the preferred treatment in different groups of stable COPD [
1]. Previous studies have shown that inhaled tiotropium relieves symptoms and improves the pulmonary function and quality of life [
8‐
10]. There have been numerous reports on the use of tiotropium in COPD patients in China, but few are randomized controlled clinical trials with a large sample size.
Oral slow-release theophylline is widely used as a bronchodilator. Kanehara et al. found low-dose theophylline not only improved forced vital capacity (FVC), forced expiratory volume in 1 s (FEV
1), and forced expiratory volume in 1 s% predicted (FEV
1% pred), but also improved the small airway function [
11]. However, Berger and Smith, showed that theophylline could not improve the small airway function [
12]. Because of the differences noted by the aforementioned studies, the effects of low-dose theophylline on the small airway function in patients with stable COPD remain controversial. In addition, limited research has been performed using the combination of tiotropium bromide and theophylline in China and abroad. Thus, the efficacy of this combination needs to be further clinically evaluated.
Therefore, we conducted a prospective randomized controlled trial to investigate the effects of tiotropium alone and tiotropium combined with low-dose theophylline in patients with stable COPD of groups B and D.
Methods
The study was performed at the West China Hospital of Sichuan University. The protocol was designed in accordance with good clinical practice and the latest revisions to the Declaration of Helsinki. The study was approved by the institutional ethics committees of the West China Hospital of Sichuan University, and it has been registered at
http://www.chictr.org.cn/(ChiCTR1800019027). All participants gave informed consent, and all work was conducted in accordance with the Declaration of Helsinki (1964).
Patients
Outpatients with a clinical diagnosis of stable COPD were recruited from March 2015 to June 2016 in the West China Hospital of Sichuan University, China. The inclusion criteria were as follows: confirmed COPD of groups B and D by pulmonary physicians based on the 2015 GOLD guidelines [
13], age ≥ 40 years, aand bsence of exacerbations [
13] for at least 1 month. Exclusion criteria: patients used LAMAs, long-acting β
2-adrenergic agonists (LABAs), inhaled glucocorticoids, oral or intravenous glucocorticoid in the previous 1 month, with any infection in the previous 1 month before study entry, with proved prostatic hyperplasia, bladder neck stenosis or narrow angle glaucoma, or with other clinically significant lung diseases (e.g., asthma, bronchiectasis, cancer or tuberculosis). We used group design mean comparison to estimate sample size, and the calculation formula was
n = 2
(Zα+
Zβ)2σ2/δ2,
Zα/2 = 1.96,
Zβ = 0.842, σ = 3.08,
δ =
π2 −
π1 = 1.45; each group needed 56 cases, a total of 142 cases in the two groups, plus 20% of the withdrawal cases (about 142 × 0.2 = 28 cases), and the total estimated sample size was 170 patients.
Study Design
We conducted a 6-month, randomized, controlled, parallel-group open-label trial. Eligible participants were then randomly assigned (1:1) using a computer-generated randomization list to one of two arms: Group I: tiotropium 18 µg once daily by Handihaler (Boehringer Ingelheim Pharma, Ingelheim, Germany) plus slow-release theophylline 100 mg twice daily by oral (Maite Xing Hua Pharmaceutical Factory, Guangzhou, China) group; Group II: tiotropium 18 µg once-daily group. None of the patients was treated with oral prednisolone, LABAs, antihistamines, antileukotrienes, or cromolyn throughout the study.
The treatment duration was 6 months, with clinical visits at the end of the first month (visit 2), the third month (visit 3) and the sixth month (visit 4). During the treatment, subjects with any of the following conditions were removed from the study: combined with acute exacerbations; poor compliance (taking < 80% or > 120% of the dosage); occurring serious adverse events; combined with any one of the above exclusion criteria.
Pulmonary Function Test
The spirometry was performed before and after inhalation of a bronchodilator. We recorded the following indicators: FVC, FEV1, FEV1% pred, FEV1/FVC, peak expiratory flow% predicted (PEF% pred), forced expiratory flow after 75% of the FVC% predicted (MEF75% pred), MEF50% pred, MEF25% pred, maximal mid-expiratory flow% predicted (MMEF% pred). PEF% pred and MEF75% pred are the indicators of airflow in large airways; MEF50% pred, MEF25% pred, and MMEF% pred are the indicators of airflow in small airways.
Outcome Measurements
The primary outcomes included COPD assessment test (CAT) score, the modified British Medical Research Council (mMRC) dyspnea scale score and pulmonary function test indicators at baseline and each visit. According to COPD-related minimal clinically important differences, lung function of FEV
1 should increase 100 ml, while modified Medical Research Council (mMRC) dyspnea scores should decrease 1 unit [
14]. The secondary outcomes were acute exacerbations and adverse events.
Statistical Analysis
All statistical analysis was performed using SPSS 20.0 (IBM, Chicago, IL, USA), and a p value < 0.05 was considered statistically significant. Means and standard derivations (SD) are used for those variables with normal distributions. Other variables are expressed as medians and inter-quartile ranges. Dichotomous variables (COPD exacerbations, complications, adverse events) were reported as frequencies and proportions.
The demographic data, clinical data, and outcome indexes were compared between the two groups at baseline and each visit. For variables with normal distribution, we used the independent sample t test, while for non-normal data, we used the independent samples Mann–Whitney U test. When comparing the symptom scores and lung function of the two arms between baseline and each visit, we used the paired sample t test if the data had normal distribution, otherwise we used the Wilcoxon signed-rank test. The Chi squared test was used to compare the rates of complications and adverse events of the two groups.
Discussion
Our study was a prospective randomized controlled trial. We innovatively selected patients with groups B and D COPD with severe symptoms as research participants. We used LAMA, which is recommended by GOLD 2017 for each group of stable COPD patients, as the control therapy. This is the first study to explore the effect of low-dose theophylline combined with tiotropium bromide on small airway function in patients with COPD. We demonstrated that add-on therapy with low-dose theophylline significantly improved the symptom scores and pulmonary function, especially small airway function in patients with stable COPD of groups B and D who are already on tiotropium treatment.
Previous studies have shown that inhaled tiotropium relieves symptoms and improves the pulmonary function and quality of life in COPD patients [
8,
15,
16]. The 1-year Prevention Of Exacerbations with Tiotropium in COPD (POET-COPD) trial [
17] showed that tiotropium was more effective than salmeterol in preventing exacerbations in 7376 patients with moderate-to-very-severe COPD. A meta-analysis comparing the relative clinical effects of tiotropium and LABAs revealed that, although both were similar in symptom improvement and changes in lung function, tiotropium was more effective than LABAs as a group in preventing COPD exacerbations and disease-related hospitalizations [
18]. Recently, Suissa et al. showed that COPD treatment initiation with tiotropium compared with LABAs does not increase cardiovascular risk in the first year of treatment [
19]. The above studies tend to show that tiotropium is superior to LABAs; therefore, we chose tiotropium as the control therapy.
The 1-month short-term follow-up results showed that the CAT scores and mMRC dyspnea scores decreased significantly in both groups, suggesting that both combination therapy and tiotropium alone could improve the symptoms of COPD patients. We also found that the changes of CAT and mMRC scores between the two groups after treatment were significant. It is suggested that the combined treatment could alleviate the symptoms of COPD patients in a short time, which is consistent with the results of several studies. A randomized controlled study conducted by Kawayama et al. compared effects of tiotropium combined with theophylline versus theophylline alone on lung function (including FVC, FEV
1, and PEF) and mMRC scores in stable COPD patients; the combination treatment was superior to the latter in all respects [
20].
A previous study showed that therapy with tiotropium improved the absolute value of FVC and FEV
1 during a 4-year follow-up period in patients with COPD [
8]. Our results indicated that the combination of low-dose theophylline and tiotropium could not improve the lung function in stable COPD patients in the short term, but improved the absolute values of FVC and FEV
1 in the long term. Kohansal et al. found that high airway mucus secretion is related to the FEV
1 decline [
21]. Therefore, we have a reason to believe that tiotropium improves FEV
1 by antagonizing the cholinergic receptor and reducing airway mucus secretion. Compared with tiotropium monotherapy, adding theophylline (200 mg twice daily) did not improve FVC and FEV
1 in patients with stable COPD. This was different from Cazzola and Matera’s findings, which may be related to several factors [
23]. First, their study added formoterol on tiotropium. Second, the follow-up period of 8 weeks was short, while our follow-up was for 6 months. Third, the sample size was small (36 cases). Therefore, further clinical research is required to investigate whether adding oral low-dose theophylline on tiotropium can improve lung function.
Pathological changes characteristic of COPD is found in the airways, lung parenchyma, and pulmonary vasculature [
22]. Small airway dysfunction in COPD patients is significant. Our study showed that oral low-dose theophylline added on tiotropium could not significantly improve the small airway function in COPD patients in the short term, but it could alleviate the patient’s small airway flow limitation in the long term. Our results were consistent with an 8-week randomized controlled study that showed low-dose theophylline significantly improved lung function in patients with stable COPD [
11]. Theophylline can dilate both the central airways and peripheral small airways. A previous study has shown that oral theophylline can reduce gas trapping in COPD patients, which suggests its impact on the peripheral airways [
23]. Recent studies have shown that low-dose theophylline (150–300 mg/day) has an airway anti-inflammatory effect, it inhibits oxidative stress, and regulates immunity [
24‐
27]. Therefore, the mechanism of low-dose theophylline in improving small airway function may be related to its ability to control airway inflammation and relieve airway smooth muscle spasm; however, the specific mechanism remains to be further researched.
The common adverse effects of tiotropium are dry mouth, COPD exacerbation, and respiratory tract infection [
28]. The main adverse reactions to oral theophylline are gastrointestinal discomfort, tachycardia, and nervous system symptoms [
11], and patients present with nausea, palpitations, and headaches. Our study showed low-dose theophylline combined with tiotropium was relatively safe in the treatment of patients with stable COPD of groups B and D.
Our study had several limitations. First, we did not have a placebo control group. This is because the selected subjects were stable COPD of groups B and D with severe symptoms and (or) poor lung function; it was not possible to ethically have a placebo control group. Second, the study was an open-label experiment without blinding due to technical conditions and therefore prone to bias. Third, the relationship between therapies and the reduction in COPD exacerbations was not analyzed due to the limitation of follow-up time. Fourth, some subjects had poor compliance, changed treatment themselves and adjusted the drug doses, which resulted in the observations not being comprehensive.
Acknowledgements
We sincerely thank all the patients who participated in this study.