Academic Editors: Kazuhiro P. Izawa and Peter H. Brubaker
Objective: To assess the clinical effectiveness of Yangxinshi (YXS)
tablets on exercise capacity and symptoms of anxiety and depression in patients
with coronary heart disease (CHD). Methods and Results: A randomized,
double-blind, placebo-controlled, multicenter clinical trial was performed to
assess the effects of YXS tablets on exercise capacity and quality of life in
patients with CHD. A total of 82 patients were included in this trial. Compared
with the placebo group, the YXS group showed significant improvement in peak
VO
Coronary heart disease (CHD) is the leading cause of death worldwide [1]. CHD
includes all heart diseases caused by coronary atherosclerosis or spasm,
resulting in blood vessel stenosis or obstruction, leading to myocardial
ischemia, angina, and myocardial infarction [2]. The traditional treatments
recommended by the guidelines include anti-inflammatory, anti-platelet, and
lipid-lowering agents,
Exercise-based cardiac rehabilitation (CR) significantly improves exercise capacity for patients with CHD, and is considered a Class Ia recommendation by international guidelines [7, 8]. Previous studies had reported that CR is a safe and effective intervention to improve exercise capacity and quality of life in patients with CHD [9, 10, 11]. Improvements in exercise capacity significantly reduce all-cause and cardiovascular mortality by up to 20%–25%. The benefits of reducing cardiovascular risk factors on quality of life have also been established for CHD patients [12, 13]. Despite these well-known benefits, participation in CR programs remains low [14, 15]. Traditional Chinese medicine (TCM) has recently been shown to be advantageous in treating CHD. Hence, integrated Chinese and Western medicine treatments combined with exercise-based CR may improve exercise capacity in patients with CHD.
According to the theory of TCM, Qi deficiency and blood stasis (QDBS) is the most common syndrome in patients with CHD [16]. Many herbal formulas and extracts are used to tonify Qi and nourish Yin in the clinic, such as Astragalus membranaceus Ginseng, and Codonopsis pilosula. Yangxinshi (YXS) tablet, which consists of thirteen kinds of chemical compounds, is widely used to treat patients with CHD and heart failure based on the theory of Reinforcing Qi and Activating Blood [17]. Since limited research is available for TCM in improving exercise capacity for patients with CHD, we conducted a randomized, double-blind, placebo-controlled, multicenter trial to demonstrate whether the YXS tablets can be a suitable adjunct to exercise-based CR for improving exercise capacity and quality of life in patients with CHD.
The design, criteria, and study procedure has been described in the published protocol (Trial registration:ClinicalTrials.gov with the ID NCT03478332) [18]. Patients were recruited from Three-Grade A-level hospitals in mainland China, including the Affiliated Hospital of Changchun University of Traditional Chinese Medicine, Tongji Hospital Affiliated with Shanghai Tongji University, and Jinqiu Hospital in Liaoning Province. CHD was rated by the Canadian Cardiovascular Society grading of angina pectoris (CSS). In order to obtain a significant difference between groups (a = 0.05, power of 80%), a minimum of 30 patients in each group was needed.
All eligible patients signed an informed consent and were then randomly allocated to the intervention group (YXS group) and control group (placebo group) at a ratio of 1:1 with blinding to both patients and investigators. All patients received standard treatment for CHD, including angiotensin-converting enzyme inhibitor (ACEI) or angiotensin receptor blocker (ARB), beta-blockers, calcium antagonistsand, anti-platelet aggregation, and or statins, combined with exercise-based CR in the hospital for 12 weeks. Other similar Chinese patent medicines were prohibited during the trial period. Eligible patients receive three tablets of YXS or placebo (sponsored by Qingdao Growful Pharmaceutical Co.Ltd. Qingdao, Shandong Province, China) three times a day for 12 consecutive weeks.
Aerobic exercise training included in the CR program was performed three days per week for 12 weeks. Each session lasted for 30 minutes, and all participants were instructed to exercise on a cycle ergometer or treadmill. The target heart rate was obtained by cardiopulmonary exercise testing (CPET). A trained physiotherapist closely supervised the CPET. The training intensity was determined based on the recorded during the CPET examination. Warm-up and cool-down periods were performed in accordance with American College of Sports Medicine guidelines [19]. All the participants were supervised by the CR team consisting of cardiologists, trained physiotherapists, and nurses.
At the first visit, all patients had their medical history, physical
examination, concomitant medicine, 12-lead electrocardiography (ECG), CPET, 6
minutes walking test (6MWT), Hamilton anxiety rating scale (HAM-A), and Hamilton
depression rating scale (HAM-D) taken. Blood samples were taken for urinalysis,
blood count, lipid levels, liver, and renal function. Follow-up visits were
conducted every week (with a window of
CPET and 6MWT evaluated exercise capacity. CPET was performed in accordance with
the Exercise Standards for Testing and Training from the American Heart
Association [20, 21]. 6MWT was performed in a 30 m corridor, following the
guidelines of The American Thoracic Society [22]. The primary expression of
exercise capacity is peak oxygen uptake (VO
Peak VO
A 14-item version of the HAM-A and a 17-item version of the HAM-D were used to assess anxious and depressive symptoms, which were commonly used in clinical practice for cardiac patients [28]. Higher HAM-A and HAM-D scores indicate more anxiety and depression.
Patients’ weight and height were measured with a calibrated scale to calculate the body mass index (BMI) value. An automatic sphygmomanometer measured blood pressure and heart rate from the non-dominant arm (J750L, Omron, Osaka, Japan). All participants were instructed to remain at a stabilization time of at least 10 min before the test. We performed the measurement twice and then calculated the mean value as the measurement value.
The definition of AE was the appearance or deterioration of any syndrome, symptom, or disease that may affect participants’ health during the trial period. This may be a new disease, degeneration of symptoms, treatment, or a combination of one or more factors. The supervisor carefully recorded all the details, such as manifestation, occurrence time, duration, and degree of AE. Once an AE occurreds, researchers immediately provided optimal medical treatment. Any AE was submitted to the ethics committee within 24 hours.
Data were analyzed by SAS software Version 9.4 (SAS Institute, Cary, NC, USA).
Categorical variables were expressed as a percentage, while distributed
continuous variables were expressed as mean
Eighty-two patients were included in the trial. Thirty-seven patients were randomly assigned to the YXS group, and 45 patients were assigned to the control group (Fig. 1). The baseline characteristics of the two groups are shown in Table 1. There was no significant difference between these two groups except for the height.
Flowchart of the study.
Placebo group (n = 45) | YXS group (n = 37) | t/ |
p-value | ||
Height (cm) | 166.51 |
172.78 |
–4.051 | ||
Weight (kg) | 70.57 |
73.72 |
–1.394 | 0.167 | |
BMI (kg/m |
25.39 |
24.61 |
1.329 | 0.188 | |
Age, yr | 60.20 |
59.57 |
0.297 | 0.767 | |
Sex | 9.927 | 0.002 | |||
Male | 26 (57.8%) | 33 (89.2%) | |||
Female | 19 (42.2%) | 4 (10.8%) | |||
Angina class | 0.122 | 0.727 | |||
CCS I | 30 (66.7%) | 26 (70.3%) | |||
CCS II | 15 (33.3%) | 11 (29.7%) | |||
Therapy, no. (%) | |||||
Aspirin | 40 (88.9%) | 35 (94.6%) | 0.274 | 0.601 | |
Clopidogrel | 16 (35.6%) | 8 (21.6%) | 1.904 | 0.168 | |
Statin | 42 (93.3%) | 34 (91.9%) | 0.000 | 1.000 | |
Beta adrenergic blockers | 28 (62.2%) | 22 (59.5%) | 0.065 | 0.799 | |
Calcium channel blocker | 8 (17.8%) | 7 (18.9%) | 0.018 | 0.894 | |
ACE inhibitors (or ARB) | 15 (33.3%) | 10 (27.0%) | 0.381 | 0.537 | |
Nitrates | 9 (20.0%) | 6 (16.2%) | 0.194 | 0.659 | |
BMI, body mass index; ACE, angiotensin converting enzyme; ARB, angiotensin II receptor blocker; CCS, Canadian Cardiovascular Society grading of angina pectoris. |
Table 2 presents the exercise capacity results from baseline to 3 months between
the groups. Treatment with YXS tablets was associated with a significant
improvement in the distance of 6MWT compared to placebo (mean difference 29.92,
95% CI 18.78–41.07, p
Placebo group | p-value | YXS group | p-value | Changes (95% CI) | between-group p-value | |||||
Baseline | 3 months | Change | Baseline | 3 months | Change | |||||
Distance (m) | 470.44 |
482.36 |
11.91 |
0.079 | 472.19 |
522.24 |
50.05 |
29.92 (18.78–41.07) | ||
AT VO |
0.85 |
0.89 |
0.04 |
0.229 | 0.90 |
1.14 |
0.23 |
0.12 (0.07–0.18) | ||
AT MET | 3.30 |
3.46 |
0.16 |
0.088 | 3.34 |
3.96 |
0.62 |
0.35 (0.20–0.50) | 0.001 | |
PeakVO |
1.19 |
1.19 |
0.01 |
0.774 | 1.24 |
1.46 |
0.22 |
0.10 (0.04–0.16) | ||
Peak MET | 4.59 |
4.68 |
0.09 |
0.405 | 4.67 |
5.25 |
0.58 |
0.30 (0.12–0.47) | 0.005 | |
Peak WR (w) | 94.16 |
97.09 |
2.93 |
0.300 | 93.28 |
105.19 |
11.92 |
6.87 (3.13–10.61) | 0.014 | |
AT, anaerobic threshold; MET, metabolic equivalents; WR, work rate. |
The YXS-CR combination increased the peak VO
There was no significant difference in anxiety and depression scores between the
two groups (p
Placebo group | P1 | YXS group | P2 | Changes (95% CI) | p-value | |||||
Baseline | 3 months | Change | Baseline | 3 months | change | |||||
HAM-A | 6.98 |
4.91 |
2.07 |
0.007 | 5.63 |
3.00 |
1.97 |
0.012 | 2.03 (0.99–3.06) | 0.926 |
HAM-D | 8.18 |
6.48 |
1.70 |
0.062 | 6.17 |
4.76 |
1.06 |
0.155 | 1.42 (0.24–2.60) | 0.592 |
There were no patients who had adverse events during the period of the trial. There were no significant ECG or physical examination findings or changes in laboratory parameters associated with the experimental drugs.
This trial was designed to evaluate the effect of adjunctive YXS tablets on exercise-based CR in patients with CHD and the underlying mechanisms of TCM in improving exercise capacity.
Our findings demonstrated that YXS tablets significantly increased exercise capacity in patients with CHD.
Previous studies have shown that mitochondrial biogenesis and mitochondrial adenosine triphosphate (ATP) production supply energy for cellular biosynthesis, and mitochondrial dysfunction is a characteristic of exercise intolerance [29, 30, 31]. As a traditional patent Chinese medicine, YXS tables consist of thirteen compounds: Astragalus membranaceus, Codonopsis pilosula, Salvia miltiorrhiza, Pueraria, epimedium, hawthorn, Rehmannia glutinosa, angelica, Coptis Chinensis, corydalis, Ganoderma lucidum, ginseng, and licorice. A network pharmacology-based study has shown that YXS tables could increase myocardial mitochondrial membrane potential, expiratory chain I activity, and ATP levels in rat models, thereby promoting mitochondrial biogenesis and aerobic metabolism. Previous animal studies also showed that YXS tablets improved energy metabolism in rats, thus increasing exercise tolerance [32]. Other studies have confirmed its antioxidant and anti-depression properties [33, 34].
According to the theory of TCM, Qi, which includes oxygen and nutrition, flows through the whole body, promotes blood circulation, and induces ATP synthase in the mitochondria [35]. Qi deficiency may lead to blood stasis, eventually leading to a decline in exercise tolerance. From the perspective of TCM, the primary mechanism of improving exercise capacity lies in regulating Qi, activating blood, and then improving mitochondrial energy metabolism. Previous investigations have demonstrated some tonic herbs with the effects of Qi-invigorating and increasing mitochondrial ATP generation, which may enhance exercise capacity [36]. YXS tablets, Ginseng, Astragalus membranaceus, Coptis Chinensis, and puerarin are all related to modulating energy metabolism. Moreover, salvia miltiorrhiza could also regulate energy metabolism via the phosphorylated-Jun N-terminal kinase-kappaB transient receptor potential cation channel, subfamily C, member 6 (p-JNK-NF-kappaB-TRPC6) pathway, and Rho kinase (ROCK) dependent ATP5D modulation [37, 38, 39].
It is well known that (GLU) is the primary energy source for the heart; GLUT4
transports glucose to the mitochondria for utilization [40]. Ginseng and Salvia
miltiorrhiza can increase glucose uptake via the GLUT4 and Adenosine
5’monophosphate-activated protein kinase (AMPK) signaling pathways in
vivo [41, 42]. The active compound of Coptis Chinensis, Berberine can moderate
glucose metabolism via the AMPK/peroxisome proliferator-activated receptor
coactivator (PGC)-1ɑ/GLUT4 pathway [43]. The compounds in the YXS tablets are
involved in glucose metabolism, which suggests that this is a potential
therapeutic strategy for exercise intolerance. Multiple mechanisms contribute to
the benefits of the YXS tablets in improving exercise capacity. A significant
difference in peak VO
However, no difference was found in anxiety and depression between groups, indicating that the improvement of exercise capacity by YXS tablets might not be necessarily related to an improvement in psychological parameters. There are several possible reasons for this. First, the population included in both the YXS and placebo groups had lower baseline HAM-A (5.63 vs 6.98) and HAM-D (6.17 vs 8.18) scores, indicating no/minimal anxiety and depression. Second, our trial was only conducted for three months, which may not be a sufficient time to notice improvements in anxiety and depression. Additionally, the lack of psychological rehabilitation intervention, including patient education, may contribute to these outcomes during the intervention period.
This trial demonstrates the unique advantages of TCM in improving exercise capacity and provides the theoretical basis for herbal medicine in rehabilitating patients with CHD. The CR program has studied many methods from TCM to improve exercise capacities, such as Taiji and Ba Duanjin. We and others have found that YXS tablets significantly improved exercise capacity in patients with CHD. In our study, CR was delivered via a supervised center-based program. Due to the advances in telemedicine technology, home-based cardiac rehabilitation could be seen as a safe and suitable alternative to center-based CR in patients, especially for the elderly, disabled, and patients in rural areas [47]. Based on the results of our study, we propose incorporating YXS tablets and home-based CR as a potential alternative to improve exercise capacity in patients with CHD.
The moderate sample size and the single ethnic patient group are recognized as limitations of this study and will need to be verified in larger studies enlisting multiple ethnic populations.
Compared with placebo, adding YXS tablets to exercise-based cardiac rehabilitation programs could improve exercise capacity in patients with CHD. However, there were no improvements in anxiety and depression. Further larger studies with longer follow-up and multiethnic patient populations are necessary to further assess the benefits of YXS tablets to improve exercise capacity in patients with CHD.
The limitations of this study include the differences between groups at the baseline, such as sex and height. A randomized controlled trial with a larger sample size could help eliminate such biases in the future.
XPM, and DYH designed the research study. YQS and PLL performed the research. SSZ analyzed the data and wrote the manuscript. All authors contributed to editorial changes in the manuscript. All authors read and approved the final manuscript.
All subjects gave their informed consent for inclusion before participating in the study. The study was conducted in accordance with the Declaration of Helsinki, and the Ethics Committee approved the protocol of the Affiliated Hospital of Changchun University of Traditional Chinese Medicine (2015R002089), Tongji Hospital Affiliated with Shanghai Tongji University (No.427), and Jinqiu Hospital in Liaoning Province.
The authors thank the patients for participating in this trial and all the research staff at each hospital site for data collection and analysis.
This research received no external funding.
The authors declare no conflict of interest.
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