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. 2015 Dec 24;17:380. doi: 10.1186/s13075-015-0893-x

The beneficial effects of Tai Chi exercise on endothelial function and arterial stiffness in elderly women with rheumatoid arthritis

Jeong-Hun Shin 1, Yonggu Lee 2, Soon Gil Kim 1, Bo Youl Choi 3, Hye-Soon Lee 4, So-Young Bang 4,
PMCID: PMC4718020  PMID: 26702640

Abstract

Background

Rheumatoid arthritis (RA) has been known to be associated with increased risk of cardiovascular disease (CVD). The aim of this study was to investigate the effects of Tai Chi exercise on CVD risk in elderly women with RA.

Method

In total, 56 female patients with RA were assigned to either a Tai Chi exercise group (29 patients) receiving a 3-month exercise intervention once a week or a control group (27 patients) receiving general information about the benefits of exercise. All participants were assessed at baseline and at 3 months for RA disease activity (Disease Activity Score 28 and Routine Assessment of Patient Index Data 3), functional disability (Health Assessment Questionnaire), CVD risk factors (blood pressure, lipids profile, body composition, and smoking), and three atherosclerotic measurements: carotid intima-media thickness, flow-mediated dilatation (FMD), and brachial-ankle pulse wave velocity (baPWV).

Results

FMD, representative of endothelial function, significantly increased in the Tai Chi exercise group (initial 5.85 ± 2.05 versus 3 months 7.75 ± 2.53 %) compared with the control group (initial 6.31 ± 2.12 versus 3 months 5.78 ± 2.13 %) (P = 1.76 × 10−3). Moreover, baPWV, representative of arterial stiffness, significantly decreased in the Tai Chi exercise group (initial 1693.7 ± 348.3 versus 3 months 1600.1 ± 291.0 cm/s) compared with the control group (initial 1740.3 ± 185.3 versus 3 months 1792.8 ± 326.1 cm/s) (P = 1.57 × 10−2). In addition, total cholesterol decreased significantly in the Tai Chi exercise group compared with the control group (−7.8 ± 15.5 versus 2.9 ± 12.2 mg/dl, P = 2.72 × 10−2); other changes in RA-related characteristics were not significantly different between the two groups. Tai Chi exercise remained significantly associated with improved endothelial function (FMD; P = 4.32 × 10−3) and arterial stiffness (baPWV; P = 2.22 × 10−2) after adjustment for improvement in total cholesterol level.

Conclusion

Tai Chi exercise improved endothelial dysfunction and arterial stiffness in elderly women with RA, suggesting that it can be a useful behavioral strategy for CVD prevention in patients with RA.

Electronic supplementary material

The online version of this article (doi:10.1186/s13075-015-0893-x) contains supplementary material, which is available to authorized users.

Keywords: Rheumatoid arthritis, Tai Chi, Cardiovascular risk

Background

Rheumatoid arthritis (RA) (MIM 180300) is a chronic systemic inflammatory disease characterized by articular and extra-articular involvement. It associates with high cardiovascular disease (CVD) morbidity, which is not fully explained by the presence of traditional CVD risk factors [14]. Recently, there has been growing interest in the prevention of CVD in patients with RA. Because many patients with RA have below-average levels of physical activity with a sedentary lifestyle, appropriate exercise training should be included as an important treatment modality of RA. Moreover, given that the main cause of reduced life expectancy in RA is CVD-related, the probable cardioprotective benefit of regular exercise to patients with RA cannot be ignored. To date, however, most studies of the beneficial effects of exercise training in RA have focused on improvements in functional ability and other RA-related disease activity. Few studies have explored the cardiovascular benefits of exercise for RA patients, who already have higher cardiovascular risk as well as lower baseline levels of activity [5].

Several studies have suggested that the development of atherosclerosis, the underlying process of CVD, is increased in RA [69]. Atherosclerosis is a dynamic inflammatory process that begins with the activation of the vascular endothelium, immigration of leukocytes, and lipid oxidation and culminates with plaque destabilization and thrombosis. Striking similarities have been noted between the inflammatory pathways in atherosclerosis and those in RA [10, 11]. In patients with RA, the result of increased systemic inflammation leads to a pro-atherogenic profile, namely, endothelial dysfunction and increased arterial stiffness [6]. Endothelial dysfunction is a pivotal early step in atherosclerosis and is measured non-invasively by brachial artery flow-mediated dilatation (FMD). Arterial stiffness is also an important indicator of vascular disease and is measured non-invasively by brachial ankle pulse wave velocity (baPWV). Previous studies demonstrated that endothelial dysfunction and arterial stiffness were predictors of adverse cardiovascular events [12, 13], which were improved by medical therapy [14] or exercise [1517]. Moreover, improvement in endothelial function after aerobic exercise has been recently shown in patients with RA [18].

Tai Chi, a set of Chinese systematic callisthenic exercises, combines deep breathing and relaxation with slow, relaxed, continuous movements and is officially supported by the Arthritis Foundation of Australia as a complementary therapy for RA. As a form of physical exercise, Tai Chi enhances cardiovascular fitness, muscular strength, balance, and physical function. It also appears to be associated with reduced stress, anxiety, and depression as well as improved quality of life [19]. In patients with RA, a randomized controlled trial pilot study showed that Tai Chi reduced RA symptoms, disease activity, and improved quality of life [20].

However, the effect of Tai Chi exercise on endothelial function and arterial stiffness in RA has not been studied. The aim of the present study was to investigate the effects of Tai Chi exercise on CVD risk, including arterial stiffness and endothelial function, in elderly women with RA.

Methods

Participants

Female patients with RA were consecutively recruited from the rheumatology department of Hanyang University Guri Hospital, and all satisfied the American College of Rheumatology 1987 revised classification criteria for RA [21]. Inclusion criteria were more than 50 years old, sedentary lifestyle (no participation in structured exercise for the preceding 6 months), and stable disease (no changes in disease-modifying anti-rheumatic drugs (DMARDs) or steroid in the last 3 months). Patients with an inability to bear weight on the lower extremities, recent or ongoing disease flare, unstable heart conditions (including atrial fibrillation and heart failure), or serious comorbidities such as terminal malignancy were excluded. During the study period, medical treatments for RA such as DMARDs or steroid administration at baseline were maintained without any change.

Figure 1 presents a consort flow diagram with the details of enrollment, allocation, and analyses. In total, 70 patients with RA were first recruited into the study. Fourteen patients dropped out: one from the Tai Chi exercise group and 13 from the control group after the baseline assessment (Fig. 1). The 56 patients with RA were assigned to two groups by their willingness to participate, for which age and body mass index were matched; 29 patients in the Tai Chi exercise group and 27 patients in the control group that were given information about lifestyle modification, including smoking cessation and weight reduction. Patients in control group also received advice about appropriate regular exercises.

Fig. 1.

Fig. 1

Flow diagram of study subject recruitment

This study was approved by the ethics committee of Hanyang University Guri Hospital (2012-024). The procedures were fully explained to all subjects, and written informed consent was obtained.

Exercise program

Patients participated in a Tai Chi exercise program “Twelve Movement Tai Chi for arthritis” [22]. This style applies small to large degrees of motion; knee flexion; straight and extended head and trunk; combined rotation of head, trunk, and extremities; and symmetrical diagonal arm and leg movements [23]. The program allows adjustment for movements to the functional level of the participant and within the comfort zone of either standing or sitting. The intervention was implemented as a group exercise once a week for 60 min over the course of 3 months at the hospital gymnasium.

Assessments

Demographic and anthropometric data

Demographic data were collected by using a self-administered questionnaire. Eligible patients attended a rheumatology unit to undergo assessment by a trained nurse in the following standardized sequence: self-completed patient questionnaire, height, weight, and waist and hip circumference.

RA assessment

Clinical data were collected by means of interviews and clinical examination. The practitioners who performed clinical assessment were blinded to exercise group and study phase. Laboratory data to identify characteristics of RA were obtained. Anti-cyclic citrullinated peptide antibody (anti-CCP) was assayed by using the ImmuLisa CCP ELISA test (IMMCO Diagnostics Inc., Buffalo, NY, USA). A level of more than 25 units/ml of anti-CCP was considered positive. Contemporary inflammation was evaluated by the erythrocyte sedimentation rate (ESR) and C-reactive protein. The routine assessment of patient index data 3 (RAPID3)—remission (<3) and low (3.1–12) and high (>12) activity—and Disease Activity Score-28 (DAS-28) from visual analogue scale score of the patient’s global health, ESR, and number of swollen and tender joints—remission (<2.6) and low (2.6–5.1) or high (>5.1) activity—were calculated to assess disease activity. The Health Assessment Questionnaire (HAQ) was used to assess functional disability [24]. General clinical and RA medication information was also obtained.

Individual cardiovascular disease risk factors

Blood pressure was assessed following at least 5 min of rest, on either arm with the patient in a seated position. A venous blood sample was drawn after overnight fast to determine the following parameters: glucose, creatinine, total cholesterol, high-density lipoprotein cholesterol, triglyceride, and HbA1c. Smoking and comorbidity status were obtained from all patients via questionnaire.

Carotid intima-media thickness

Ultrasonographic evaluations for carotid intima-media thickness (cIMT) were achieved with an 11.3-MHz high-resolution linear probe and with simultaneous electrocardiographic recording. cIMT was measured at the T wave of the cardiac cycle on the common carotid wall at 1 cm from the bifurcation, calculating the distance between the intima-lumen interface and the media-adventitia interface. cIMT was measured bilaterally, and the average was determined for statistical analyses.

Flow-mediated dilatation

Brachial artery FMD was measured by using two-dimensional ultrasonography (iE33; Philips Medical Systems, Bothell, WA, USA) with a linear 11.3-MHz high-resolution probe. Measurements were taken with the patient supine for at least 10 min in a quiet room after an overnight fast; morning medications were not taken. The brachial artery was visualized in a longitudinal section, and baseline B-mode and Doppler images were obtained and diameter measurements were made. Subsequently, an adult blood pressure cuff was placed on the upper arm and inflated to 50 mm Hg above the systolic blood pressure for 5 min. Vasodilatory capacity was expressed as the percentage of change in the brachial artery diameter from baseline to 60 seconds post-cuff deflation. All images were digitized and recorded for study measurements, and techniques followed published guidelines [25]; these measures were interpreted by a single reader blinded to treatment and study phase. All patients abstained from smoking and drinking alcohol and coffee for at least 12 hours.

Brachial-ankle pulse wave velocity

After the subjects had rested in a supine position for more than 5 min, the measurement of baPWV was conducted by using a wave form analyzer (VP-2000; Colin Co Ltd., Komaki, Japan). Pulse waves were recorded automatically by sensors in the cuffs. The transmission times and distances between the cuffs on arms and legs were recorded, and the baPWV was produced as an output. The mean of the baPWVs in the left and right side was used for analysis.

Statistical analysis

Normality of data distribution was evaluated with the Kolmogorov-Smirnov test. Accordingly, either a Student t test or a Mann-Whitney U test was used to compare continuous variables between groups (Tai Chi exercise versus control) at baseline. Chi-square tests were used to compare categorical variables between the two groups at baseline. The differences between values of the variables at baseline and those at the end of the 3-month Tai Chi exercise intervention were also compared by using either a Student t test or a Mann-Whitney U test. Analysis of covariance (ANCOVA) was employed to estimate the effect of Tai-Chi exercise on the changes of FMD and baPWV (dependent variables), independent of covariates which had also significantly changed over the period. To estimate the direct effects of Tai Chi exercise on outcome variables that changed significantly over time, we also performed mediation analysis by using a bootstrapping technique with bias-corrected confidence interval estimates. Mediation analysis using a bootstrapping technique is a statistical method that can effectively generate confidence interval estimates of the regression coefficients of independent variables that allow estimation of the direct and indirect effect of an independent variable on a dependent variable [26]. All statistical analyses were performed by using SPSS Statistics 21.0 (IBM SPSS 21.0; IBM Corporation, Chicago, IL, USA). Mediation analysis was performed with a set of 1,000 bootstrap resamples by using the PROCESS module incorporated in the SPSS software (model type 4, by Andrew F. Hayes, downloadable at http://www.afhayes.com).

Results

Among the initial allocated 56 patients, 13 patients in the control group dropped out due to losing interest in the study. In total, 43 patients were further analyzed: Tai chi exercise group (n = 29) and control group (n = 14). Participants’ baseline characteristics are shown Table 1. The demographic, anthropometric characteristics between groups were similar. The mean ages ± standard deviations (SDs) (the mean disease duration, age ± SD) of the Tai Chi exercise group and control group were 64.0 ± 5.4 years (10.3 ± 9.4) and 60.9 ± 7.2 years (15.3 ± 7.8), respectively. There was a relatively high prevalence of medical history of metabolic disorders in each of these groups, and mean prevalence rates were 53.5 % (23/43) for hypertension, 7.0 % (3/43) for diabetes, and 46.5 % (20/43) for dyslipidemia. Anti-CCP positivity was 90.7 % in total patients with RA. According to their DAS-28 and RAPID3, in both groups, most patients with RA had low disease activity—mean DAS-28-ESR and RAPID3 scores of 3.8 and 9.4 (Tai Chi exercise group) and 3.5 and 9.0 (control group)—which were similar in the two groups. However, the number of tender joints (4.5 ± 5.5 versus 1.6 ± 1.5, P = 1.23 × 10−2) and functional disability score (HAQ) (0.63 ± 0.50 versus 0.35 ± 0.29, P = 2.43 × 10−2) were significantly higher in the Tai Chi exercise group compared with the control group, respectively. There were no significant differences between groups at baseline in any of the assessed atherosclerosis markers (cIMT, FMD, or baPWV).

Table 1.

Baseline demographic, anthropometric, RA-related, and CVD characteristics, and atherosclerotic measurements for the total RA population as well as the exercise and control groups

Total (n = 43) Tai Chi group (n = 29) Control group (n = 14) P
Demographic, mean ± SD
 Age, years 63.6 ± 5.53 64.0 ± 5.4 62.7 ± 5.9 0.469
Anthropometric, mean ± SD
 Height, cm 153.8 ± 5.6 154.2 ± 5.7 153.0 ± 5.6 0.506
 Weight, kg 54.0 ± 7.8 53.7 ± 7.6 54.6 ± 8.4 0.725
 BMI, kg/m2 22.8 ± 2.9 22.5 ± 2.7 23.4 ± 3.2 0.388
 Waist circumference, cm 79.3 ± 8.4 78.3 ± 8.5 81.4 ± 8.1 0.259
 Waist-hip ratio 0.86 ± 0.53 0.85 ± 0.01 0.87 ± 0.05 0.142
Medical history, n (%)
 Hypertension 23 (53.5) 15 (51.7) 8 (57.1) 0.739
 Diabetes mellitus 3 (7.0) 1 (3.4) 2 (14.3) 0.191
 Dyslipidemia 20 (46.5) 12 (41.4) 8 (57.1) 0.331
 Coronary artery disease 2 (4.6) 1 (3.4) 1 (7.1) 0.590
 Cerebrovascular disease 4 (9.3) 2 (6.9) 2 (14.3) 0.434
 Smoking 6 (13.9) 2 (6.9) 4 (28.6) 0.133
RA medication, n (%)
 Methotrexate 36 (83.7) 24 (82.8) 12 (85.7) 0.806
 Hydroxychloroquine 17 (39.5) 11 (37.9) 6 (42.9) 0.757
 Sulfasalazine 5 (11.6) 3 (10.3) 2 (14.3) 0.706
 Leflunomide 11 (25.6) 7 (24.1) 4 (28.6) 0.755
 Glucocorticoids 31 (72.1) 21 (72.4) 10 (71.4) 0.946
 Dosage, median, mg/day 2.5 2.5 2.5 0.168
RA characteristics, mean ± SD
 Disease duration, years 12.0 ± 9.2 10.3 ± 9.4 15.4 ± 8.0 0.092
 anti-CCP, n (%) 38 (88.4) 24 (82.8) 14 (100) 0.307
 Swollen joint count, 0–69 joints 1.2 ± 2.4 1.5 ± 2.9 0.6 ± 0.9 0.237
 Tender joint count, 0–69 joints 3.6 ± 4.7 4.5 ± 5.5 1.6 ± 1.5 0.012
 DAS-28-ESR 3.7 ± 1.0 3.8 ± 1.1 3.5 ± 0.6 0.229
 RAPID3 9.4 ± 4.5 9.4 ± 4.7 9.2 ± 4.0 0.895
 HAQ 0.54 ± 0.46 0.63 ± 0.50 0.35 ± 0.29 0.024
 ESR 31.7 ± 21.9 31.4 ± 22.7 32.2 ± 21.0 0.908
 CRP 0.44 ± 0.44 0.48 ± 0.49 0.36 ± 0.34 0.384
CVD, mean ± SD
 Systolic BP, mm Hg 130.5 ± 11.6 129.2 ± 12.1 133.1 ± 10.5 0.313
 Diastolic BP, mm Hg 77.6 ± 5.2 77.0 ± 4.8 78.7 ± 6.0 0.331
 Heart rate 72.0 ± 6.1 72.5 ± 5.4 71.0 ± 7.5 0.473
 Total cholesterol, mg/dl 184.6 ± 35.8 187.3 ± 36.1 179.0 ± 35.6 0.480
 Triglycerides, mg/dl 112.2 ± 47.4 108.7 ± 36.6 122.14 ± 54.3 0.343
 HDL, mg/dl 61.6 ± 12.0 63.9 ± 12.1 56.8 ± 10.5 0.070
 LDL, mg/dl 97.9 ± 31.1 96.6 ± 31.4 100.7 ± 31.7 0.689
 Fasting glucose, mg/dl 91.5 ± 11.1 89.8 ± 9.3 95.1 ± 13.9 0.141
 Creatinine, mg/dl 0.74 ± 0.12 0.72 ± 0.12 0.76 ± 0.11 0.300
Atherosclerosis, mean ± SD
 cIMT, mm 0.68 ± 0.13 0.69 ± 0.13 0.66 ± 0.13 0.596
 FMD, % 6.00 ± 2.06 5.85 ± 2.05 6.31 ± 2.12 0.494
 baPWV, cm/s 1708.8 ± 303.3 1693.7 ± 348.3 1740.3 ± 185.3 0.643

Values are presented as mean ± standard deviation (SD). anti-CCP anti-cyclic citrullinated peptide antibody, BMI body-mass index, DAS-28 disease activity score-28, ESR erythrocyte sedimentation rate, CRP C-reactive protein, RAPID3 routine assessment of patient index data 3, HAQ Health Assessment Questionnaire, BP blood pressure, HDL high-density lipoprotein, LDL low-density lipoprotein, cIMT carotid intima-media thickness, FMD flow-mediated dilatation, baPWV brachial-ankle pulse wave velocity

Effects of Tai Chi exercise on disease activity of RA and CVD characteristics

Results of change in body composition, RA-related characteristics, and cardiovascular risk factors after the 3-month follow-up are summarized in Table 2. All changes (Δ: initial – at 3 months) of RA characteristics, including disease activity (mean ΔDAS-28-ESR and ΔRAPID3) and functional disability (mean ΔHAQ), related to RA over time were not significantly different between the two groups. Blood pressure and heart rate were not significantly changed in the two groups. Interestingly, total cholesterol after the 3-month follow-up significantly decreased in the Tai Chi exercise group compared with the control group: mean Δ total cholesterol −7.8 (Tai Chi group) and 2.9 (control group) mg/dl, P = 2.72 × 10−2.

Table 2.

Changes in body composition, rheumatoid arthritis-related characteristics and cardiovascular risk factors at 3-month follow-up

Tai Chi group (n = 29) Control group (n = 14) P
Anthropometric, mean ± SD
 ΔBMI, kg/m2 0.0 ± 0.63 −0.1 ± 1.52 0.530
 ΔWaist circumference, cm −0.2 ± 3.7 0.1 ± 4.0 0.537
RA characteristics, mean ± SD
 ΔSwollen joint count, 0 ~ 69 joints −0.6 ± 3.3 0.0 ± 1.7 0.834
 ΔTender joint count, 0 ~ 69 joints −2.5 ± 4.5 0.1 ± 3.0 0.107
 ΔDAS-28-ESR −0.4 ± 1.1 −0.0 ± 1.1 0.247
 ΔRAPID3 −2.2 ± 4.7 −1.0 ± 3.9 0.404
 ΔHAQ −0.13 ± 0.29 0.00 ± 0.20 0.274
 ΔESR 2.0 ± 18.0 −1.1 ± 12.4 0.569
 ΔCRP 0.2 ± 0.8 0.1 ± 0.6 0.399
CVD, mean ± SD
 ΔSystolic BP, mm Hg −0.9 ± 10.5 1.8 ± 14.4 0.496
 ΔDiastolic BP, mm Hg 0.2 ± 6.8 −0.1 ± 6.3 0.910
 ΔHeart rate 1.3 ± 4.9 3.4 ± 4.4 0.238
 ΔTotal cholesterol, mg/dl −7.8 ± 15.5 2.9 ± 12.2 2.72 × 10−2
 ΔTriglycerides, mg/dl −2.48 ± 32.99 6.58 ± 36.18 0.078
 ΔHDL, mg/dl 6.91 ± 12.82 0.53 ± 8.73 0.053
 ΔLDL, mg/dl −9.2 ± 13.2 −4.8 ± 12.6 0.337
 ΔFasting glucose, mg/dl 2.3 ± 13.6 −5.6 ± 12.7 0.227
Atherosclerotic measurements, mean ± SD
 ΔcIMT, mm −0.02 ± 0.08 −0.02 ± 0.08 0.746
 ΔFMD, % 1.90 ± 2.00 −0.54 ± 2.49 1.76 × 10−3
 ΔbaPWV, cm/s −93.6 ± 152.2 52.6 ± 224.1 1.57 × 10−2

Values are presented as mean ± standard deviation (SD). BMI body-mass index, DAS-28 disease activity score-28, ESR erythrocyte sedimentation rate, CRP C-reactive protein, RAPID3 routine assessment of patient index data 3, HAQ Health Assessment Questionnaire, BP blood pressure, HDL high-density lipoprotein, LDL low-density lipoprotein, cIMT carotid intima-media thickness, FMD flow-mediated dilatation, baPWV brachial-ankle pulse wave velocity

Effects of Tai Chi on endothelial function and arterial stiffness

Changes in FMD over time were significantly different between the two groups (P = 1.76 × 10 − 3), with a significant increment in the Tai Chi exercise group—initial versus 3 months (5.85 ± 2.05 versus 7.75 ± 2.53 %), mean ΔFMD 1.90 %—but not in the control group: initial versus 3 months (6.31 ± 2.12 versus 5.78 ± 2.13 %), mean ΔFMD −0.50 % (Table 2 and Fig. 2a). Changes in baPWV over time were significantly different between the two groups (P = 1.57 × 10−2), with a significant reduction in the Tai Chi exercise group (1693.7 ± 348.3 versus 1600.1 ± 291.0 cm/s, mean Δ baPWV −93.6 cm/s) but not in the control group (1740.3 ± 185.3 versus 1792.8 ± 326.1 cm/s, mean Δ baPWV 52.6 cm/s) (Table 2 and Fig. 2b). In addition, these changes in FMD and baPWV were significantly negatively correlated (r = −0.33, P = 0.031) (Additional file 1). However, the change in cIMT was not significantly different between the Tai Chi exercise and control groups (P = 0.746).

Fig. 2.

Fig. 2

Change in flow-mediated dilatation (FMD) (a) and brachial-ankle pulse wave velocity (baPWV) (b) from baseline to 3 months for Tai Chi exercise group (red) versus control group (blue)

Tai Chi exercise was associated with a significant improvement in FMD and baPWV as well as total cholesterol. We examined the significance of Tai Chi exercise regarding ΔFMD and ΔPWV as dependent variables by using an ANCOVA model that included Δtotal cholesterol. After adjustment for Δtotal cholesterol, Tai Chi exercise was associated with ΔFMD (P = 4.32 × 10−3) and ΔbaPWV (P = 2.22 × 10−2) (Table 3). Moreover, since the improvement in total cholesterol level could have positively impacted on the change of FMD and baPWV, we performed mediation analysis by using the bootstrapping method with bias-corrected confidence interval estimates to evaluate whether the change in total cholesterol level was associated with ΔFMD and ΔbaPWV. Tai Chi exercise modestly correlated with Δtotal cholesterol (r = 0.27, P = 7.76 × 10−2), but mediation analysis showed that the indirect effects of Tai Chi exercise on ΔFMD and ΔbaPWV through Δtotal cholesterol were not significant (β coefficient, 95 % CI = 0.13, −0.19 to 0.82 for ΔFMD and −1.0, −53.1 to 25.6 for ΔbaPWV), whereas the direct effects of Tai Chi exercise were significant (β coefficient, 95 % CI = 2.31, 0.77 to 3.86, P = 4.32 × 10−3 for ΔFMD and −145.1, −268.4 to −21.8, P = 2.22 × 10−2 for ΔbaPWV) (Additional file 2).

Table 3.

Analysis of covariance analysis for the determinants of ∆FMD and ∆baPWV

Independent variables β coefficient S.E. P value
∆FMD Intercept −0.525 0.604
Tai Chi 2.312 0.764 4.32 × 10−3
∆Cholesterol −0.015 0.024 0.532
∆baPWV Intercept 52.456 48.456
Tai Chi −145.121 61.018 2.22 × 10−2
∆Cholesterol 0.117 1.9 0.951

FMD flow-mediated dilatation, baPWV brachial-ankle pulse wave velocity, S.E. standard error

Discussion

Our findings show that Tai Chi exercise in elderly women with RA significantly improves endothelial dysfunction and arterial stiffness, which are known atherosclerosis precursors, useful indexes for early detection of CVD, and predictors for increased cardiovascular mortality [2730]. To the best of our knowledge, this study is the first evidence of a possible reduction of cardiovascular risk through Tai Chi exercise by improving endothelial dysfunction and arterial stiffness in patients with RA.

The increased risk of CVD in patients with RA has recently become the focus of intense investigations. In RA, disease-related inflammation and traditional risk factors, such as hypertension, diabetes, dyslipidemia, and smoking, are widely assumed to contribute to the elevated CVD risk [79]. Moreover, physical inactivity is likely a notable risk factor in RA. Therefore, exercise can be an important behavioral strategy for CVD prevention in patients with RA as well as in the general population [31]. Moreover, exercise is a cost-effective intervention that may significantly improve cardiorespiratory fitness, CVD risk factors, and 10-year CVD event probability in RA [3133].

Recently, there has been increasing interest in the promotion of aerobic exercise or increasing physical activity for patients with RA, although many clinicians still discourage such activity because of concerns about exacerbating joint damage [34]. Because many patients with RA have below-average physical capacity and lead a sedentary lifestyle, low-intensity exercise tailored to individual needs is recommended for patients with RA [35]. During the past several years, multiple trials have been completed to examine the effect of exercise on RA, but most focus on pain, disease activity, functional ability, quality of life, structural damage, and aerobic capacity [2, 32, 34, 3639]. Although one study found that an individualized exercise training program, which consisted of a 6-month tailored aerobic and resistance exercise intervention, improved endothelial function in patients with RA [18], there are limited data available regarding the optimal dose and types of exercise as well as the cardioprotective effects of exercise in RA.

Tai Chi is a Chinese martial art that combines meditation with slow, gentle, graceful movements as well as deep breathing and relaxation [40]. Intensity in Tai Chi is low and equivalent to walking 6 km/h and provides a moderate increase in heart rate [41]. Significant improvement in cardiopulmonary function has been found in Tai Chi practitioners when compared with sedentary control subjects of middle age and older [4244]. Tai Chi training can also improve cardiopulmonary function in patients with CVD, such as chronic heart failure [45, 46] and myocardial infarction [47]. Recent studies have reported that Tai Chi has been found to improve arterial compliance in elderly subjects [48, 49]. Recently, Tai Chi has been applied with substantial benefits in patients with RA. Tai Chi leads to reduced disability and fatigue [20, 50] and is considered safe in patients with RA, especially long-standing and dramatically physically inactive individuals [51]. A Cochrane review on Tai Chi exercise concluded that there were positive effects on a selected range of motion outcomes as well as increased level of participation and enjoyment of exercise for patients with RA [52]. Moreover, recent systematic reviews have shown that Tai Chi can reduce blood pressure and increase cardiovascular exercise capacity in patients with CVD and cardiovascular risk factors [53]. Despite encouraging evidence suggesting that Tai Chi has multiple benefits for patients with RA, few studies have reported relationships between Tai Chi exercise and any other cardiovascular risk factors or surrogate markers of atherosclerosis. In the present study, we demonstrated that Tai Chi exercise significantly improved endothelial function, arterial stiffness, and lipid profile, suggesting that Tai Chi exercise can be a useful behavioral strategy for CVD prevention as well as for promotion of aerobic exercise and physical activity in patients with RA.

Aerobic exercise has been shown to improve endothelial dysfunction [54, 55] and arterial stiffness [16, 56], but the mechanism by which Tai Chi exercise improves these functions remains unclear. One suggestion is that the meditative components of Tai Chi have the potential to reduce stress levels, which can mediate a range of effects by attenuating the sympathoadrenal axis. Reductions in catecholamine levels can improve the lipid profile, the hemodynamic profile, including blood pressure, and the coagulation profile [57, 58]. Similarly, stress can activate the hypothalamic-pituitary-adrenal axis, increasing hypothalamic release of multiple corticotrophin secretagogues, corticotrophin-releasing hormone, and arginine vasopressin. Cortisol hypersecretion has been associated with hypertension and the development of the constellation of cardiovascular risk factors, including diabetes, hypertension, and dyslipidemia, termed the metabolic syndrome, and associated cardiovascular comorbidities [59]. Another suggestion is that Tai Chi decreased sympathetic nervous system activity in older adults [60] and could improve baroreflex sensitivity and heart rate variability in patients with coronary heart disease [61], which are closely associated with endothelial dysfunction and arterial stiffness and are predictors of mortality in patients with coronary heart disease.

Interestingly, participants in the Tai Chi exercise group showed an improvement in their lipid profile, possibly indicating a favorable effect of Tai Chi exercise on the lipid metabolism. Our findings are in line with previous studies that examined changes in lipid profile as a result of Tai Chi exercise [58, 62]. As all participants were informed of their higher risk profile and were given general information about lifestyle modification and exercise, dietary change or lifestyle modification during the exercise training period would be expected to have favorable effects on total cholesterol, but the mechanisms by which Tai Chi exercise may improve lipid profiles remain uncertain. The possibility that the change in body fat ratio and insulin resistance might have an influence on lipid profile should be considered. Favorable changes in lipid profile after Tai Chi exercise likely play a role in improving endothelial dysfunction and arterial stiffness. To examine the mediation effect of Δtotal cholesterol on ΔFMD and ΔPWV after Tai Chi exercise, we constructed a bootstrapping mediation analysis. As expected, these data further support the notion that Tai Chi exercise may lower cardiovascular risk in RA patients via a beneficial effect on the arterial wall, independently of the improvement in lipid profile.

There are a few limitations in our study. The sample size was small, and there were a considerable number of control-group participants who were lost to follow-up. In this prospective observational study, we recruited only elderly women with RA and so the results may not be applicable to men or all patients with RA. Only short-term follow-up assessment was performed and so no long-term effects could be established. The present data indicate that, for the cohort studied, the positive profiles of change in arterial stiffness and endothelial function were not significantly related to improvements in RA disease activity or blood pressure. We are unable to specify whether these improvements in vascular function are the direct consequence of the Tai Chi exercise since no assessments about physical activity, which was also known to reduce cardiovascular risk factors and associated mortality in patients with sedentary lifestyle, were included in the study. We are also unable to document whether perceived benefits from the Tai Chi exercise related to the improved cardiovascular outcome. It is recommended that such measures be included in future studies to elucidate the mechanism for improvements resulting from Tai Chi exercise. Moreover, further large-scale, long-term randomized clinical trials should be needed to determine whether and to what extent improvement of endothelial dysfunction and arterial stiffness by Tai Chi exercise affects disease activity as well as clinical cardiovascular events in patients with RA. Despite these limitations, positive outcomes reported in the present study provide the rationale for the wider adoption of Tai Chi exercise as a health-promoting activity in patients with RA and to help overcome individual barriers to exercise, especially among long-standing and elderly patients with RA.

Conclusions

This study demonstrated that Tai Chi exercise significantly contributed to improvement in endothelial function and arterial stiffness, independently of the traditional CVD risk factors, including lipid profile. Tai Chi exercise may be a useful treatment strategy for RA as a complementary and alternative medical approach to preventing CVD.

Ethics approval

This study was approved by the institutional review board of Hanyang University.

Patient consent

Consents were obtained from all patients who participated in this study.

Acknowledgments

This study was supported by the research fund of Hanyang University (HY-201200000000560-N).

Abbreviations

ANCOVA

Analysis of covariance

anti-CCP

Anti-cyclic citrullinated peptide antibody

baPWV

Brachial-ankle pulse wave velocity

cIMT

Carotid intima-media thickness

CVD

Cardiovascular disease

DAS-28

Disease activity score-28

DMARD

Disease-modifying anti-rheumatic drug

ESR

Erythrocyte sedimentation rate

FMD

Flow-mediated dilatation

HAQ

Health Assessment Questionnaire

RA

Rheumatoid arthritis

RAPID3

Routine assessment of patient index data 3

SD

Standard deviation

Additional files

Additional file 1: (337.3KB, jpg)

Correlation plot of change in flow-mediated dilatation (FMD) versus change in brachial-ankle pulse wave velocity (baPWV) after 3 months of Tai Chi exercise. (JPG 337 kb)

Additional file 2: (481.2KB, jpg)

Mediation analysis to evaluate whether the change in total cholesterol level was associated with the change in flow-mediated dilatation (FMD) and brachial-ankle pulse wave velocity (baPWV) after Tai Chi exercise. (JPG 481 kb)

Footnotes

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

J-HS carried out most of the study and drafted and revised the manuscript. YL made substantial contributions to analysis, interpretation of the data, and participated in the drafting and revising the manuscript. SGK made substantial contributions to acquisition of study sujbects and generation of clinical data and helped to draft the article. BYC participated in the design of the study, analysis the data and helped to revise the manuscript. H-SL made substantial contributions to study design, acquisition of study subjects, generation of clinical data and helped to draft and revise the manuscript. S-YB conceived of the study, participated in its design and coordination, participated in draft the manuscript and helped to revise the manuscript. All authors read and approved the final manuscript.

Contributor Information

Jeong-Hun Shin, Email: cardio.hyapex@gmail.com.

Yonggu Lee, Email: hmedi97@naver.com.

Soon Gil Kim, Email: kimsg@hanyang.ac.kr.

Bo Youl Choi, Email: bychoi@hanyang.ac.kr.

Hye-Soon Lee, Email: lhsberon@hanyang.ac.kr.

So-Young Bang, Phone: +82-31-560-2637, Email: sybang@hanyang.ac.kr.

References

  • 1.Panoulas VF, Metsios GS, Pace A, John H, Treharne G, Banks M, et al. Hypertension in rheumatoid arthritis. Rheumatology. 2008;47:1286–98. doi: 10.1093/rheumatology/ken159. [DOI] [PubMed] [Google Scholar]
  • 2.Metsios GS, Stavropoulos-Kalinoglou A, van Zanten JV, Treharne G, Panoulas VF, Douglas KM, et al. Rheumatoid arthritis, cardiovascular disease and physical exercise: a systematic review. Rheumatology. 2008;47:239–48. doi: 10.1093/rheumatology/kem260. [DOI] [PubMed] [Google Scholar]
  • 3.Toms TE, Panoulas VF, Smith JP, Douglas KM, Metsios GS, Stavropoulos-Kalinoglou A, et al. Rheumatoid arthritis susceptibility genes associate with lipid levels in patients with rheumatoid arthritis. Ann Rheum Dis. 2011;70:1025–32. doi: 10.1136/ard.2010.144634. [DOI] [PubMed] [Google Scholar]
  • 4.Liao KP, Solomon DH. Traditional cardiovascular risk factors, inflammation and cardiovascular risk in rheumatoid arthritis. Rheumatology. 2013;52:45–52. doi: 10.1093/rheumatology/kes243. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Cooney JK, Law RJ, Matschke V, Lemmey AB, Moore JP, Ahmad Y, et al. Benefits of exercise in rheumatoid arthritis. J Aging Res. 2011;2011:681640. doi: 10.4061/2011/681640. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Ozbalkan Z, Efe C, Cesur M, Ertek S, Nasiroglu N, Berneis K, et al. An update on the relationships between rheumatoid arthritis and atherosclerosis. Atherosclerosis. 2010;212:377–82. doi: 10.1016/j.atherosclerosis.2010.03.035. [DOI] [PubMed] [Google Scholar]
  • 7.Soltesz P, Kerekes G, Der H, Szucs G, Szanto S, Kiss E, et al. Comparative assessment of vascular function in autoimmune rheumatic diseases: considerations of prevention and treatment. Autoimmun Rev. 2011;10:416–25. doi: 10.1016/j.autrev.2011.01.004. [DOI] [PubMed] [Google Scholar]
  • 8.Gonzalez-Gay MA, Gonzalez-Juanatey C, Martin J. Rheumatoid arthritis: a disease associated with accelerated atherogenesis. Semin Arthritis Rheum. 2005;35:8–17. doi: 10.1016/j.semarthrit.2005.03.004. [DOI] [PubMed] [Google Scholar]
  • 9.Sattar N, McCarey DW, Capell H, McInnes IB. Explaining how “high-grade” systemic inflammation accelerates vascular risk in rheumatoid arthritis. Circulation. 2003;108:2957–63. doi: 10.1161/01.CIR.0000099844.31524.05. [DOI] [PubMed] [Google Scholar]
  • 10.Pasceri V, Yeh ET. A tale of two diseases: atherosclerosis and rheumatoid arthritis. Circulation. 1999;100:2124–6. doi: 10.1161/01.CIR.100.21.2124. [DOI] [PubMed] [Google Scholar]
  • 11.Skeoch S, Bruce IN. Atherosclerosis in rheumatoid arthritis: is it all about inflammation? Nat Rev Rheumatol. 2015;11:390–400. doi: 10.1038/nrrheum.2015.40. [DOI] [PubMed] [Google Scholar]
  • 12.Kullo IJ, Malik AR. Arterial ultrasonography and tonometry as adjuncts to cardiovascular risk stratification. J Am Coll Cardiol. 2007;49:1413–26. doi: 10.1016/j.jacc.2006.11.039. [DOI] [PubMed] [Google Scholar]
  • 13.Sugamata W, Nakamura T, Uematsu M, Kitta Y, Fujioka D, Saito Y, et al. Combined assessment of flow-mediated dilation of the brachial artery and brachial-ankle pulse wave velocity improves the prediction of future coronary events in patients with chronic coronary artery disease. J Cardiol. 2014;64:179–84. doi: 10.1016/j.jjcc.2014.01.004. [DOI] [PubMed] [Google Scholar]
  • 14.Mordi I, Tzemos N. Is reversal of endothelial dysfunction still an attractive target in modern cardiology? World J Cardiol. 2014;6:824–35. doi: 10.4330/wjc.v6.i8.824. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Yang SJ, Hong HC, Choi HY, Yoo HJ, Cho GJ, Hwang TG, et al. Effects of a three-month combined exercise programme on fibroblast growth factor 21 and fetuin-A levels and arterial stiffness in obese women. Clin Endocrinol (Oxf) 2011;75:464–9. doi: 10.1111/j.1365-2265.2011.04078.x. [DOI] [PubMed] [Google Scholar]
  • 16.Collier SR, Kanaley JA, Carhart R, Jr, Frechette V, Tobin MM, Hall AK, et al. Effect of 4 weeks of aerobic or resistance exercise training on arterial stiffness, blood flow and blood pressure in pre- and stage-1 hypertensives. J Hum Hypertens. 2008;22:678–86. doi: 10.1038/jhh.2008.36. [DOI] [PubMed] [Google Scholar]
  • 17.Currie KD, McKelvie RS, Macdonald MJ. Flow-mediated dilation is acutely improved after high-intensity interval exercise. Med Sci Sports Exerc. 2012;44:2057–64. doi: 10.1249/MSS.0b013e318260ff92. [DOI] [PubMed] [Google Scholar]
  • 18.Metsios GS, Stavropoulos-Kalinoglou A, Veldhuijzen van Zanten JJ, Nightingale P, Sandoo A, Dimitroulas T, et al. Individualised exercise improves endothelial function in patients with rheumatoid arthritis. Ann Rheum Dis. 2014;73:748–51. doi: 10.1136/annrheumdis-2013-203291. [DOI] [PubMed] [Google Scholar]
  • 19.Wang C. Role of Tai Chi in the treatment of rheumatologic diseases. Curr Rheumatol Rep. 2012;14:598–603. doi: 10.1007/s11926-012-0294-y. [DOI] [PubMed] [Google Scholar]
  • 20.Wang C. Tai Chi improves pain and functional status in adults with rheumatoid arthritis: results of a pilot single-blinded randomized controlled trial. Med Sport Sci. 2008;52:218–29. doi: 10.1159/000134302. [DOI] [PubMed] [Google Scholar]
  • 21.Arnett FC, Edworthy SM, Bloch DA, McShane DJ, Fries JF, Cooper NS, et al. The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum. 1988;31:315–24. doi: 10.1002/art.1780310302. [DOI] [PubMed] [Google Scholar]
  • 22.Lam P. New horizons. developing tai chi for health care. Aust Fam Physician. 1998;27:100–1. [PubMed] [Google Scholar]
  • 23.Wolf SL, Coogler C, Xu T. Exploring the basis for Tai Chi Chuan as a therapeutic exercise approach. Arch Phys Med Rehabil. 1997;78:886–92. doi: 10.1016/S0003-9993(97)90206-9. [DOI] [PubMed] [Google Scholar]
  • 24.Bae SC, Cook EF, Kim SY. Psychometric evaluation of a Korean Health Assessment Questionnaire for clinical research. J Rheumatol. 1998;25:1975–9. [PubMed] [Google Scholar]
  • 25.Corretti MC, Anderson TJ, Benjamin EJ, Celermajer D, Charbonneau F, Creager MA, et al. Guidelines for the ultrasound assessment of endothelial-dependent flow-mediated vasodilation of the brachial artery: a report of the International Brachial Artery Reactivity Task Force. J Am Coll Cardiol. 2002;39:257–65. doi: 10.1016/S0735-1097(01)01746-6. [DOI] [PubMed] [Google Scholar]
  • 26.Preacher KJ, Hayes AF. SPSS and SAS procedures for estimating indirect effects in simple mediation models. Behav Res Methods Instrum Comput. 2004;36:717–31. doi: 10.3758/BF03206553. [DOI] [PubMed] [Google Scholar]
  • 27.Stamatelopoulos KS, Kitas GD, Papamichael CM, Chryssohoou E, Kyrkou K, Georgiopoulos G, et al. Atherosclerosis in rheumatoid arthritis versus diabetes: a comparative study. Arterioscler Thromb Vasc Biol. 2009;29:1702–8. doi: 10.1161/ATVBAHA.109.190108. [DOI] [PubMed] [Google Scholar]
  • 28.Tanaka H, Safar ME. Influence of lifestyle modification on arterial stiffness and wave reflections. Am J Hypertens. 2005;18:137–44. doi: 10.1016/j.amjhyper.2004.07.008. [DOI] [PubMed] [Google Scholar]
  • 29.Weber T, Auer J, O’Rourke MF, Kvas E, Lassnig E, Berent R, et al. Arterial stiffness, wave reflections, and the risk of coronary artery disease. Circulation. 2004;109:184–9. doi: 10.1161/01.CIR.0000105767.94169.E3. [DOI] [PubMed] [Google Scholar]
  • 30.Schachinger V, Britten MB, Zeiher AM. Prognostic impact of coronary vasodilator dysfunction on adverse long-term outcome of coronary heart disease. Circulation. 2000;101:1899–906. doi: 10.1161/01.CIR.101.16.1899. [DOI] [PubMed] [Google Scholar]
  • 31.Stavropoulos-Kalinoglou A, Metsios GS, Veldhuijzen van Zanten JJ, Nightingale P, Kitas GD, Koutedakis Y. Individualised aerobic and resistance exercise training improves cardiorespiratory fitness and reduces cardiovascular risk in patients with rheumatoid arthritis. Ann Rheum Dis. 2013;72:1819–25. doi: 10.1136/annrheumdis-2012-202075. [DOI] [PubMed] [Google Scholar]
  • 32.de Jong Z, Munneke M, Zwinderman AH, Kroon HM, Jansen A, Ronday KH, et al. Is a long-term high-intensity exercise program effective and safe in patients with rheumatoid arthritis? Results of a randomized controlled trial. Arthritis Rheum. 2003;48:2415–24. doi: 10.1002/art.11216. [DOI] [PubMed] [Google Scholar]
  • 33.Metsios GS, Stavropoulos-Kalinoglou A, Panoulas VF, Wilson M, Nevill AM, Koutedakis Y, et al. Association of physical inactivity with increased cardiovascular risk in patients with rheumatoid arthritis. Eur J Cardiovasc Prev Rehabil. 2009;16:188–94. doi: 10.1097/HJR.0b013e3283271ceb. [DOI] [PubMed] [Google Scholar]
  • 34.Cairns AP, McVeigh JG. A systematic review of the effects of dynamic exercise in rheumatoid arthritis. Rheumatol Int. 2009;30:147–58. doi: 10.1007/s00296-009-1090-5. [DOI] [PubMed] [Google Scholar]
  • 35.Panel O. Ottawa Panel evidence-based clinical practice guidelines for therapeutic exercises in the management of rheumatoid arthritis in adults. Phys Ther. 2004;84:934–72. [PubMed] [Google Scholar]
  • 36.Hakkinen A, Pakarinen A, Hannonen P, Kautiainen H, Nyman K, Kraemer WJ, et al. Effects of prolonged combined strength and endurance training on physical fitness, body composition and serum hormones in women with rheumatoid arthritis and in healthy controls. Clin Exp Rheumatol. 2005;23:505–12. [PubMed] [Google Scholar]
  • 37.Stenstrom CH, Minor MA. Evidence for the benefit of aerobic and strengthening exercise in rheumatoid arthritis. Arthritis Rheum. 2003;49:428–34. doi: 10.1002/art.11051. [DOI] [PubMed] [Google Scholar]
  • 38.Hurkmans E, van der Giesen FJ, Vliet Vlieland TP, Schoones J, Van den Ende EC. Dynamic exercise programs (aerobic capacity and/or muscle strength training) in patients with rheumatoid arthritis. Cochrane Database Syst Rev. 2009;4:CD006853. doi: 10.1002/14651858.CD006853.pub2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Baillet A, Zeboulon N, Gossec L, Combescure C, Bodin LA, Juvin R, et al. Efficacy of cardiorespiratory aerobic exercise in rheumatoid arthritis: meta-analysis of randomized controlled trials. Arthritis Care Res (Hoboken) 2010;62:984–92. doi: 10.1002/acr.20146. [DOI] [PubMed] [Google Scholar]
  • 40.Wang C, Schmid CH, Rones R, Kalish R, Yinh J, Goldenberg DL, et al. A randomized trial of tai chi for fibromyalgia. N Engl J Med. 2010;363:743–54. doi: 10.1056/NEJMoa0912611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Jin P. Efficacy of Tai Chi, brisk walking, meditation, and reading in reducing mental and emotional stress. J Psychosom Res. 1992;36:361–70. doi: 10.1016/0022-3999(92)90072-A. [DOI] [PubMed] [Google Scholar]
  • 42.Lai JS, Lan C, Wong MK, Teng SH. Two-year trends in cardiorespiratory function among older Tai Chi Chuan practitioners and sedentary subjects. J Am Geriatr Soc. 1995;43:1222–7. doi: 10.1111/j.1532-5415.1995.tb07397.x. [DOI] [PubMed] [Google Scholar]
  • 43.Lan C, Lai JS, Chen SY, Wong MK. 12-month Tai Chi training in the elderly: its effect on health fitness. Med Sci Sports Exerc. 1998;30:345–51. doi: 10.1097/00005768-199803000-00003. [DOI] [PubMed] [Google Scholar]
  • 44.Hong Y, Li JX, Robinson PD. Balance control, flexibility, and cardiorespiratory fitness among older Tai Chi practitioners. Br J Sports Med. 2000;34:29–34. doi: 10.1136/bjsm.34.1.29. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Yeh GY, Wood MJ, Lorell BH, Stevenson LW, Eisenberg DM, Wayne PM, et al. Effects of tai chi mind-body movement therapy on functional status and exercise capacity in patients with chronic heart failure: a randomized controlled trial. Am J Med. 2004;117:541–8. doi: 10.1016/j.amjmed.2004.04.016. [DOI] [PubMed] [Google Scholar]
  • 46.Barrow DE, Bedford A, Ives G, O’Toole L, Channer KS. An evaluation of the effects of Tai Chi Chuan and Chi Kung training in patients with symptomatic heart failure: a randomised controlled pilot study. Postgrad Med J. 2007;83:717–21. doi: 10.1136/pgmj.2007.061267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Channer KS, Barrow D, Barrow R, Osborne M, Ives G. Changes in haemodynamic parameters following Tai Chi Chuan and aerobic exercise in patients recovering from acute myocardial infarction. Postgrad Med J. 1996;72:349–51. doi: 10.1136/pgmj.72.848.349. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Lu X, Hui-Chan CW, Tsang WW. Tai Chi, arterial compliance, and muscle strength in older adults. Eur J Prev Cardiol. 2013;20:613–9. doi: 10.1177/2047487312443483. [DOI] [PubMed] [Google Scholar]
  • 49.Lu X, Hui-Chan CW, Tsang WW. Effects of Tai Chi training on arterial compliance and muscle strength in female seniors: a randomized clinical trial. Eur J Prev Cardiol. 2013;20:238–45. doi: 10.1177/2047487311434233. [DOI] [PubMed] [Google Scholar]
  • 50.Wang C, Roubenoff R, Lau J, Kalish R, Schmid CH, Tighiouart H, et al. Effect of Tai Chi in adults with rheumatoid arthritis. Rheumatology (Oxford) 2005;44:685–7. doi: 10.1093/rheumatology/keh572. [DOI] [PubMed] [Google Scholar]
  • 51.Kirsteins AE, Dietz F, Hwang SM. Evaluating the safety and potential use of a weight-bearing exercise, Tai-Chi Chuan, for rheumatoid arthritis patients. Am J Phys Med Rehabil. 1991;70:136–41. doi: 10.1097/00002060-199106000-00005. [DOI] [PubMed] [Google Scholar]
  • 52.Han A, Robinson V, Judd M, Taixiang W, Wells G, Tugwell P. Tai chi for treating rheumatoid arthritis. Cochrane Database Syst Rev. 2004;3:CD004849. doi: 10.1002/14651858.CD004849. [DOI] [PubMed] [Google Scholar]
  • 53.Yeh GY, Wang C, Wayne PM, Phillips R. Tai chi exercise for patients with cardiovascular conditions and risk factors: a systematic review. J Cardiopulm Rehabil Prev. 2009;29:152–60. doi: 10.1097/HCR.0b013e3181a33379. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Higashi Y, Sasaki S, Kurisu S, Yoshimizu A, Sasaki N, Matsuura H, et al. Regular aerobic exercise augments endothelium-dependent vascular relaxation in normotensive as well as hypertensive subjects: role of endothelium-derived nitric oxide. Circulation. 1999;100:1194–202. doi: 10.1161/01.CIR.100.11.1194. [DOI] [PubMed] [Google Scholar]
  • 55.Hambrecht R, Fiehn E, Weigl C, Gielen S, Hamann C, Kaiser R, et al. Regular physical exercise corrects endothelial dysfunction and improves exercise capacity in patients with chronic heart failure. Circulation. 1998;98:2709–15. doi: 10.1161/01.CIR.98.24.2709. [DOI] [PubMed] [Google Scholar]
  • 56.Hayashi K, Sugawara J, Komine H, Maeda S, Yokoi T. Effects of aerobic exercise training on the stiffness of central and peripheral arteries in middle-aged sedentary men. Jpn J Physiol. 2005;55:235–9. doi: 10.2170/jjphysiol.S2116. [DOI] [PubMed] [Google Scholar]
  • 57.Anfossi G, Trovati M. Role of catecholamines in platelet function: pathophysiological and clinical significance. Eur J Clin Invest. 1996;26:353–70. doi: 10.1046/j.1365-2362.1996.150293.x. [DOI] [PubMed] [Google Scholar]
  • 58.Thomas GN, Hong AW, Tomlinson B, Lau E, Lam CW, Sanderson JE, et al. Effects of Tai Chi and resistance training on cardiovascular risk factors in elderly Chinese subjects: a 12-month longitudinal, randomized, controlled intervention study. Clin Endocrinol (Oxf) 2005;63:663–9. doi: 10.1111/j.1365-2265.2005.02398.x. [DOI] [PubMed] [Google Scholar]
  • 59.Rosmond R. Role of stress in the pathogenesis of the metabolic syndrome. Psychoneuroendocrinology. 2005;30:1–10. doi: 10.1016/j.psyneuen.2004.05.007. [DOI] [PubMed] [Google Scholar]
  • 60.Motivala SJ, Sollers J, Thayer J, Irwin MR. Tai Chi Chih acutely decreases sympathetic nervous system activity in older adults. J Gerontol A Biol Sci Med Sci. 2006;61:1177–80. doi: 10.1093/gerona/61.11.1177. [DOI] [PubMed] [Google Scholar]
  • 61.Sato S, Makita S, Uchida R, Ishihara S, Masuda M. Effect of Tai Chi training on baroreflex sensitivity and heart rate variability in patients with coronary heart disease. Int Heart J. 2010;51:238–41. doi: 10.1536/ihj.51.238. [DOI] [PubMed] [Google Scholar]
  • 62.Tsai JC, Wang WH, Chan P, Lin LJ, Wang CH, Tomlinson B, et al. The beneficial effects of Tai Chi Chuan on blood pressure and lipid profile and anxiety status in a randomized controlled trial. J Altern Complement Med. 2003;9:747–54. doi: 10.1089/107555303322524599. [DOI] [PubMed] [Google Scholar]

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