Synergistic effects of drug and aerobic exercise on endothelial function and epicardial fat thickness in patients with hypertension and dyslipidemia

Article information

Kosin Med J. 2025;40(1):31-40
Publication date (electronic) : 2025 February 17
doi : https://doi.org/10.7180/kmj.24.137
1Department of Sports Science, Pusan National University, Busan, Korea
2Division of Cardiology, Department of Internal Medicine, Kosin University Gospel Hospital, Kosin University College of Medicine, Busan, Korea
Corresponding Author: Jung-Ho Heo, MD, PhD Division of Cardiology, Department of Internal Medicine, Kosin University Gospel Hospital, Kosin University College of Medicine, 262 Gamcheon-ro, Seo-gu, Busan 49267, Korea Tel: +82-51-990-3421 Fax: +82-51-241-5458 E-mail: duggymdc@kosinmed.or.kr
Received 2024 August 29; Revised 2024 October 26; Accepted 2024 November 13.

Abstract

Background

Aerobic exercise training and drug therapy are well-established interventions for the prevention and treatment of hypertension and dyslipidemia. We investigated the synergistic effects of aerobic exercise and olmesartan/rosuvastatin on epicardial fat thickness (EFT) and endothelial function in patients with hypertension and dyslipidemia.

Methods

A sample of 75 participants with hypertension and dyslipidemia was evaluated for multifactorial cardiovascular risk at baseline and at 6 months of intervention according to anthropometric and hemodynamic components, lipid profile, glycemia, brachial artery flow-mediated dilation (FMD), and EFT. After 3 months of drug therapy only, participants were allocated to one of three conditions: treadmill (n=22), exergame (n=29), or control (n=24).

Results

After 12 weeks of drug therapy only, systolic and diastolic blood pressure (3% and 2%, both p<0.05), total cholesterol (6.3%, p<0.01), low-density lipoprotein cholesterol (4.9%, p<0.05), triglycerides (11.1%, p<0.05), fasting blood glucose (10.2%, p<0.01), and glycosylated hemoglobin (3%, p<0.01) were significantly reduced. After 12 weeks of combined aerobic exercise and drug therapy, both the treadmill and exergame groups showed a significant improvement in FMD (both p<0.001) and reduction in EFT (both p<0.001). Systolic and diastolic blood pressures decreased in the treadmill group only (1.9% and 2.7%, respectively, p<0.05).

Conclusions

Incorporating aerobic exercise into drug therapy regimens can yield synergistic effects, particularly in improving endothelial function and reducing EFT, providing a comprehensive approach to managing cardiovascular risk in patients with hypertension and dyslipidemia.

Introduction

Cardiovascular disease (CVD) stands as the foremost cause of death and illness globally [1]. In 2020, it was responsible for over 10 million fatalities worldwide [2]. Research has shown that hypertension and dyslipidemia play critical roles in the development of CVD [3], with a substantial number of individuals with high blood pressure (BP) also exhibiting dyslipidemia [1,2,4]. The combined presence of hypertension and dyslipidemia significantly increases the risk of coronary heart disease beyond the additive risks of each condition alone [5]. Given the interconnected nature of cardiovascular risk factors such as elevated BP and abnormal lipid levels, it is essential to address both conditions to minimize the risk of future cardiovascular incidents [6,7].

Endothelial dysfunction is a crucial early factor in the onset of atherosclerosis and is considered a major predictor of CVD risk [8]. In terms of cardiometabolic parameters, epicardial adipose tissue plays a significant role in endocrine and inflammatory processes [9]. Its proximity to the atrial myocardium indicates it may contribute to the development of cardiac diseases related to metabolic disorders [9]. Epicardial adipose tissue has also been implicated in insulin resistance and promotes a pro-inflammatory milieu, further linking its pathophysiological role to metabolic disorders such as type 2 diabetes and coronary artery disease [10].

Managing hypertension and dyslipidemia has primarily involved aerobic exercise and medication. Aerobic exercise has consistently been effective in lowering the incidence and mortality rates associated with cardiovascular complications. Recently, a novel approach to physical activity has emerged with advanced gaming technology, known as exergaming or active video gaming. Exergames are video games that necessitate physical activity as part of gameplay [11]. This form of exercise is gaining traction in both the entertainment sector and rehabilitation settings [12], showing promise in enhancing physical activity levels and cardiovascular fitness [12,13], particularly among older adults [14].

However, medication will be needed if normal BP and lipidemia cannot be achieved through exercise and lifestyle changes. Rosuvastatin/olmesartan showed good efficacy and safety profiles in patients with both hypertension and dyslipidemia [15,16]. Nevertheless, no studies so far have examined the actions of rosuvastatin/olmesartan in combination with aerobic exercise on endothelial function and epicardial adipose tissue in patients with hypertension and dyslipidemia.

In this study, we sought to (1) evaluate the effects of olmesartan/rosuvastatin alone or in combination with aerobic exercise programs on endothelial function and epicardial fat thickness (EFT) and (2) compare the effects of exercise programs on endothelial function and EFT in patients with hypertension and dyslipidemia.

Methods

Ethical statements: This study was approved by the Institutional Review Board of Kosin University Gospel Hospital (IRB No. 2016-06-029). Written informed consent was obtained from the patients to participate in the study.

1. Study design and population

This single-center study was conducted from February 2017 to August 2017. Ninety-nine patients with hypertension and dyslipidemia who had been sedentary and had not engaged in any type of regular exercise training for at least 3 months prior to this study were enrolled. If patients were taking medications, they were required to undergo a wash-out period of at least 2 weeks for antihypertensive medications and 4 weeks for statins before participating in this study. Patients who were pregnant; current smokers; alcohol users; and those with uncontrolled hypertension, renal failure, established CVD, chronic obstructive pulmonary disease, or musculoskeletal disease were excluded.

The subjects were randomly assigned to the treadmill or exergame or control group. This study period lasted 6 months, during which the first 3 months were dedicated to evaluating the effects of medication alone, while from months 3 to 6, the combined effects of medication and exercise were assessed (Fig. 1). Subjects attended a total of three visits for measurements. At each visit, venous blood was drawn to measure glucose and lipids profiles after an 8-hour overnight fast, and BP, height, and weight were recorded. Additionally, flow-mediated dilation (FMD) and EFT were measured. In premenopausal women, blood sampling was performed at the follicular phase of the menstrual cycle.

Fig. 1.

Study flow diagram.

The numbers and reasons for early withdrawal from the study are presented in Fig. 1. During the medication treatment period, six participants were unable to complete the training program: five for tracking fail and one for withdraw consent (scheduling difficult). During the medication and exercise treatment period, 18 participants were unable to complete the training program: six for tracking failed, 12 for withdraw consent (seven owing to insufficient attendance, three for scheduling difficult, two for fatigue one for personal reasons). Thus, a total of 75 participants were included in our data analysis.

2. Measurement FMD and EFT

FMD was assessed in the brachial artery following established guidelines. A two-dimensional ultrasound system (Vivid 7; General Electric) equipped with a 10-MHz linear-array transducer was used for the measurements. After obtaining baseline readings, reactive hyperemia was triggered by inflating a pneumatic cuff on the forearm to 180 to 200 mmHg, which is 50 mmHg above the systolic BP, and maintaining this pressure for 5 minutes. The brachial artery’s peak diameter was recorded 40 to 60 seconds after the cuff was rapidly deflated. The percentage change in FMD due to reactive hyperemia was calculated relative to the baseline diameter (%FMD=100×[diameter post-hyperemia–baseline diameter]/baseline diameter). Each diameter was measured three times during two heartbeats at the peak of the R wave on the surface electrocardiogram, with the average value used for the final analysis.

The echocardiographic measurement of EFT was defined as the echo-free region between the myocardium's outer wall and the visceral pericardium [15]. Standard echocardiography was performed with the participant in the left lateral decubitus position using a 3.5 MHz transducer (Philips iE33; Philips Medical Systems). The EFT was measured vertically from the free wall of the right ventricle at the end-systolic phase over three cardiac cycles. The recorded EFT value was determined by averaging measurements from the parasternal long-axis view, the parasternal short-axis view at the level of the papillary muscles, and the apical four-chamber view at the right ventricular free wall to ensure consistent evaluation. To reduce observational bias during both initial and follow-up analyses, the researcher conducting the measurement was blinded to the baseline values. A reliability analysis using intra-class correlation coefficient was performed to obtain the intra-observer variability. The intra-observer variability of the EFT was 3.2%.

3. Exercise program

Exercise training was carried out at the Kosin University Convergence Medicine & Exercise Science Research Institute under the close supervision of a qualified director. Both the exergame and treadmill groups followed an exercise regimen that included a 5-minute warm-up, a 40-minute main session, and a 5-minute cool-down. Participants who completed less than 80% of the 12-week exercise program were excluded from the study. The control group was instructed to maintain their usual level of physical activity over the 12-week period.

For the treadmill group, the exercise involved 40 minutes of walking or jogging at an intensity of 60% to 80% of the heart rate (HR) reserve. Exercise intensity was calculated using the Karvonen formula: target HR=(exercise intensity×[HR max–resting HR])+resting HR. HR was monitored during each session using a HR monitor (Polar RS400sd, Pola).

The exergame group exercised with the Exerheart device (D&J Humancare), which included a running/jumping platform connected to a screen (Fig. 2A). The exercise sessions involved playing the exergame “Alchemist's Treasure,” where the player's movements on the platform controlled an avatar in the game. The game required the user to run with the avatar, avoid obstacles, and collect items by utilizing sensors on the front, back, left, and right of the exercise platform (Fig. 2B).

Fig. 2.

Components of exergame. (A) The exergaming group performed exercise using Exerheart devices with the permission of D&J Humancare, which is the copyright holder of Exerheart. (B) Features of the video game “Alchemist's Treasure.”

One of the primary benefits of exergaming is the enjoyment it provides. In this study, exercise intensity was not strictly controlled to enhance participants' enjoyment of the exergame. Thus, during the training period, the population exercised at a self-selected pace for 40 minutes per day. Individual exercise intensity was monitored using a HR monitor (Polar RS400s), and data on resting, minimum, maximum, and average HRs were collected throughout the exergame sessions. The participants' resting HR averaged 79±12 beats per minute (bpm), with a minimum of 98±26 bpm, a maximum of 153±28 bpm, and a mean HR of 120±19 bpm. Based on American College of Sports Medicine guidelines [17], the exercise intensity for exergaming typically falls within 42% to 82% of HR reserve.

4. Statistical analysis

Baseline characteristics across the groups were assessed using a one-way analysis of variance (ANOVA) for continuous variables. To compare variables both between and within groups, a two-way ANOVA (group×time) with repeated measures was employed. Bonferroni post hoc tests were conducted to determine the significance of any findings identified by the one-way or two-way ANOVA. All values are expressed as mean±standard deviation, and statistical significance was defined as p<0.05. Statistical analyses were performed using IBM SPSS ver. 21.0 (IBM Corp.).

Results

1. Baseline characteristics of study participants

Ninety-nine patients enrolled for the study and run-in drug therapy. Among these, 93 patients were randomized to one of the treatment groups (31 to the treadmill group, 31 to exergame group, and 31 to the control group), and 75 completed the study (22 in the treadmill group, 29 in the exergame group, 24 in the control group). The numbers and reasons for early withdrawal from the study are presented in Fig. 1. Patient demographics and baseline characteristics showed no differences between the three groups (Table 1). The mean patient age was 61.3 years, and 26.7% were male.

Baseline characteristics

2. Primary outcomes

FMD levels significantly improved in both the treadmill and exergame groups between weeks 12 and 24 (both p<0.01). However, no changes in FMD were observed at week 12 compared to baseline levels. Compared to the control group, significant improvements in FMD were noted in the treadmill and exergame groups from week 12 to week 24 (both p<0.05). There were no significant differences in FMD between the treadmill and exergame groups (Fig. 3A).

Fig. 3.

A combined intervention of aerobic exercise with drug therapy effectively improved flow-mediated dilation (FMD) and reduced epicardial fat thickness (EFT). (A) Changes in FMD from baseline to week 24. (B) Changes in EFT from baseline to week 24. a)p<0.01 (mean values were significantly different from week 12), b)p<0.05 (mean values were significantly different from control).

The EFT levels were significantly decreased in treadmill and exergame groups from week 12 to week 24 (both p<0.01). However, at week 12, there were no changes in EFT compared with baseline levels. Compared with the control group, a significant improvement in EFT was observed for treadmill and exergame groups from week 12 to week 24 (both p<0.05). There were no differences between treadmill and exergame groups (Fig. 3B).

3. Other clinical outcomes

At week 12, systolic BP, diastolic BP, total cholesterol, low-density lipoprotein cholesterol (LDL-C), triglycerides, fasting blood glucose (FBG), and glycosylated hemoglobin (HbA1c) levels were significantly decreased compared with baseline (both p<0.01). At week 12, alanine aminotransferase levels were significantly increased compared with baseline (p<0.05). Systolic BP and diastolic BP had additionally decreased only in the treadmill group from week 12 to week 24 (both p<0.05, with no group differences). However, there were no additional changes in total cholesterol, LDL-C, triglycerides, FBG, and HbA1c levels in any of groups from week 12 to week 24 (Tables 2,3).

Parameters after 12 weeks of drug therapy only

Parameters after 24 weeks of combined of aerobic exercise and drug therapy

Discussion

In this study, while the reduction in BP, lipid profiles, and glucose levels was primarily due to the effects of medication, we found that exercise had a greater impact on improving endothelial function and decreasing EFT in patients with hypertension and dyslipidemia. This study was designed to evaluate the effects of treadmill exercise and exergaming on these parameters. The results showed that both exercise programs significantly improved FMD and EFT, while systolic BP decreased only in the treadmill group, supporting previous findings that exercise positively impacts cardiovascular health.

The effects of angiotensin Ⅱ receptor blocker (ARB)/statin combination on lipid profiles and BP reduction have been verified. The study by Naya et al. [18] provides evidence that treatment with an ARB (olmesartan medoxomil) has a beneficial effect on the coronary microcirculation and improves endothelium-dependent coronary dilation independent of lowering BP. In addition, statin therapy significantly improved endothelial function, as assessed by FMD [19] and reduced epicardial fat [20]. However, the effects of these drugs on endothelial function and epicardial fat remain unclear. We found that medical therapy with these drugs did not significantly reduce FMD and EFT, but a significant reduction was observed when the drugs were combined with exercise.

The effectiveness of conventional exercise in enhancing endothelial function among patients with cardiovascular or chronic diseases is well-established [21]. However, there is limited research on how exergaming impacts endothelial function. In this study, both the treadmill and exergame groups demonstrated significant improvements in FMD, with no notable differences between them. This finding implies that exergaming can offer similar benefits to traditional aerobic exercise in terms of improving endothelial function. Exercise is known to lower BP through various mechanisms, with enhanced endothelial function playing a crucial role in its antihypertensive effects [22]. Nonetheless, only the treadmill group exhibited further reductions in BP, with no significant changes observed in other clinical measures. This suggests that treadmill exercise may be more effective for long-term management of BP.

Recent studies have indicated that EFT may serve as a better indicator of visceral fat and a more significant cardiometabolic risk factor than overall fat accumulation disorders [23]. While physical exercise is widely recognized as the primary intervention for metabolic syndrome associated with increased adipose tissue [24], there is still limited research on how exercise impacts EFT. In this study, although there was no significant difference compared to the control group, both the treadmill and exergame groups demonstrated reductions in EFT by 11.8% and 18.4%, respectively. Previous research has reported that exercise can reduce EFT in postmenopausal women with metabolic syndrome [25] and in obese individuals [26]. However, other studies have found no significant reduction in EFT among patients with type 2 diabetes mellitus following 6 months of exercise training [27].

Several mechanisms have been suggested to explain the reduction in visceral adipose tissue, including the release of hormones that promote fat breakdown [28], increased energy expenditure following exercise [29], and enhanced fat oxidation that contributes to a more substantial negative energy balance [30]. Although the mechanisms involved in epicardial adipose tissue are not well-known, epicardial adipose tissue is an indicator of visceral adipose tissue [31]. Therefore, it can be inferred that the same mechanisms led to the reduction in EFT in the treadmill and exergame groups in this study.

Exergaming showed higher exercise adherence compared to the treadmill group. The drop-out rate was 13.9% in the treadmill group, while it was 4.5% in the exergame group. Although this study did not measure enjoyment directly, it is believed that exergaming offered greater enjoyment and motivation than treadmill exercise. Research suggests that exergaming can produce higher levels of enjoyment compared to traditional exercise activities. Enjoyment in an activity can enhance attendance and adherence, leading to increased physical activity and improved health benefits. This suggests that exergaming may be a more enjoyable and engaging form of exercise. Additionally, new exercise forms like exergaming can provide health benefits similar to those of traditional aerobic exercise.

Although no statistical difference was observed for high sensitivity C-reactive protein (HS-CRP), the improvement in HS-CRP appears slightly more pronounced in the control group that received only drug treatment compared to the exercise groups. However, it is considered to have minimal or no clinical impact on patient care. We believe it is not clinically significant and does not affect the interpretation of the main findings. Further research may be required to confirm whether this difference has any clinical relevance.

We acknowledge several limitations in our study that may have impacted our outcomes. First, measurement of EFT using ultrasound. While ultrasound is a widely used method for assessing EFT, it may be subject to operator dependency and variability in measurements. Second, our study only evaluated the “Alchemist's Treasure” game with the Exerheart, so the results cannot be generalized to all exergame exercise programs. Third, we observed low adherence and high drop-out rates in both the treadmill and control groups. This reflects real-world challenges, as patients with no prior exercise experience may struggle to maintain traditional aerobic treadmill exercises. Finally, our findings highlight the importance of enjoyment and motivation in exercise. Future research should focus on the enjoyment levels of different exercise types, generalizing findings across various exergame programs, incorporating direct measurements of cardiorespiratory fitness, and examining the impact of exercise enjoyment on adherence and health outcomes. By addressing these areas, we can gain a better understanding of the potential benefits of innovative exercise forms, such as exergaming, in improving cardiovascular health and managing chronic diseases.

This study demonstrates that both treadmill exercise and exergaming significantly improve endothelial function and reduce EFT in patients with hypertension and dyslipidemia. While the reduction in BP, lipid profiles, and glucose levels was primarily attributed to medication, exercise was shown to have a greater impact on enhancing cardiovascular health markers, such as FMD and EFT. These findings support the notion that exercise, whether traditional or exergame-based, plays a crucial role in cardiovascular health management. Notably, exergaming both produced similar improvements in endothelial function and epicardial fat reduction as traditional treadmill exercise and exhibited higher exercise adherence and lower drop-out rates. This suggests that exergaming may be a more engaging and sustainable form of exercise for patients, potentially leading to better long-term health outcomes.

Notes

Conflicts of interest

No potential conflict of interest relevant to this article was reported.

Funding

None.

Author contributions

Conceptualization: JHH. Data curation: EAJ. Formal analysis: EAJ. Funding acquisition: JHH. Investigation: EAJ, SSW, HRH. Methodology: EAJ, SSW, HRH, JJP. Project administration: EAJ. Resources: JHH. Software: EAJ. Supervision: JHH. Validation: EAJ. Visualization: EAJ. Writing – original draft: EAJ. Writing – review & editing: SSW, HRH, JJP, JHH. All authors read and approved the final manuscript.

References

1. GBD 2019 Diseases and Injuries Collaborators. Global burden of 369 diseases and injuries in 204 countries and territories, 1990-2019: a systematic analysis for the Global Burden of Disease Study 2019. Lancet 2020;396:1204–22. 10.1016/S0140-6736(20)30925-9. 33069326.
2. Wong ND, Lopez V, Tang S, Williams GR. Prevalence, treatment, and control of combined hypertension and hypercholesterolemia in the United States. Am J Cardiol 2006;98:204–8. 10.1016/j.amjcard.2006.01.079. 16828593.
3. Borghi C, Fogacci F, Agnoletti D, Cicero AF. Hypertension and dyslipidemia combined therapeutic approaches. High Blood Press Cardiovasc Prev 2022;29:221–30. 10.1007/s40292-022-00507-8. 35334087.
4. O'Meara JG, Kardia SL, Armon JJ, Brown CA, Boerwinkle E, Turner ST. Ethnic and sex differences in the prevalence, treatment, and control of dyslipidemia among hypertensive adults in the GENOA study. Arch Intern Med 2004;164:1313–8. 10.1001/archinte.164.12.1313. 15226165.
5. Egan BM, Li J, Qanungo S, Wolfman TE. Blood pressure and cholesterol control in hypertensive hypercholesterolemic patients: national health and nutrition examination surveys 1988-2010. Circulation 2013;128:29–41. 10.1161/circulationaha.112.000500. 23817481.
6. Jackson R, Lawes CM, Bennett DA, Milne RJ, Rodgers A. Treatment with drugs to lower blood pressure and blood cholesterol based on an individual's absolute cardiovascular risk. Lancet 2005;365:434–41. 10.1016/s0140-6736(05)70240-3. 15680460.
7. Trimarco V, Izzo R, Morisco C, Mone P, Virginia Manzi M, Falco A, et al. High HDL (high-density lipoprotein) cholesterol increases cardiovascular risk in hypertensive patients. Hypertension 2022;79:2355–63. 10.1161/hypertensionaha.122.19912. 35968698.
8. Celermajer DS, Sorensen KE, Bull C, Robinson J, Deanfield JE. Endothelium-dependent dilation in the systemic arteries of asymptomatic subjects relates to coronary risk factors and their interaction. J Am Coll Cardiol 1994;24:1468–74. 10.1016/0735-1097(94)90141-4. 7930277.
9. Iacobellis G. Epicardial adipose tissue in endocrine and metabolic diseases. Endocrine 2014;46:8–15. 10.1007/s12020-013-0099-4. 24272604.
10. Yang T, Li G, Wang C, Xu G, Li Q, Yang Y, et al. Insulin resistance and coronary inflammation in patients with coronary artery disease: a cross-sectional study. Cardiovasc Diabetol 2024;23:79. 10.1186/s12933-024-02159-5. 38402392.
11. Nurkkala V-M, Kalermo J, Jarvilehto T. Development of exergaming simulator for gym training, exercise testing and rehabilitation. J Commun Comput 2014;11:403–11.
12. Bond S, Laddu DR, Ozemek C, Lavie CJ, Arena R. Exergaming and virtual reality for health: implications for cardiac rehabilitation. Curr Probl Cardiol 2021;46:100472. 10.1016/j.cpcardiol.2019.100472. 31606141.
13. Blasco-Peris C, Fuertes-Kenneally L, Vetrovsky T, Sarabia JM, Climent-Paya V, Manresa-Rocamora A. Effects of exergaming in patients with cardiovascular disease compared to conventional cardiac rehabilitation: a systematic review and meta-analysis. Int J Environ Res Public Health 2022;19:3492. 10.3390/ijerph19063492. 35329177.
14. Kappen DL, Mirza-Babaei P, Nacke LE. Older adults’ physical activity and exergames: a systematic review. Int J Hum Comput Interact 2019;35:140–67. 10.1080/10447318.2018.1441253.
15. Kim W, Chang K, Cho EJ, Ahn JC, Yu CW, Cho KI, et al. A randomized, double-blind clinical trial to evaluate the efficacy and safety of a fixed-dose combination of amlodipine/rosuvastatin in patients with dyslipidemia and hypertension. J Clin Hypertens (Greenwich) 2020;22:261–9. 10.1111/jch.13774. 32003938.
16. Jin X, Kim MH, Han KH, Hong SJ, Ahn JC, Sung JH, et al. Efficacy and safety of co-administered telmisartan/amlodipine and rosuvastatin in subjects with hypertension and dyslipidemia. J Clin Hypertens (Greenwich) 2020;22:1835–45. 10.1111/jch.13893. 32937023.
17. Thomas DT, Erdman KA, Burke LM. Nutrition and athletic performance. Med Sci Sports Exerc 2016;48:543–68. 10.1249/mss.0000000000000852. 26891166.
18. Naya M, Tsukamoto T, Morita K, Katoh C, Furumoto T, Fujii S, et al. Olmesartan, but not amlodipine, improves endothelium-dependent coronary dilation in hypertensive patients. J Am Coll Cardiol 2007;50:1144–9. 10.1016/j.jacc.2007.06.013. 17868805.
19. Arabi SM, Chambari M, Bahrami LS, Hadi S, Sahebkar A. Statin therapy and flow-mediated dilation: a systematic review and dose-response meta-analysis using the GRADE of data from randomized controlled trials. Curr Hypertens Rev 2024;20:90–100. 10.2174/0115734021280797240212091416. 38385489.
20. Raggi P, Gadiyaram V, Zhang C, Chen Z, Lopaschuk G, Stillman AE. Statins reduce epicardial adipose tissue attenuation independent of lipid lowering: a potential pleiotropic effect. J Am Heart Assoc 2019;8e013104. 10.1161/jaha.119.013104. 31190609.
21. Valenzuela PL, Ruilope LM, Santos-Lozano A, Wilhelm M, Krankel N, Fiuza-Luces C, et al. Exercise benefits in cardiovascular diseases: from mechanisms to clinical implementation. Eur Heart J 2023;44:1874–89. 10.1093/eurheartj/ehad170. 37005351.
22. Ashor AW, Lara J, Siervo M, Celis-Morales C, Oggioni C, Jakovljevic DG, et al. Exercise modalities and endothelial function: a systematic review and dose-response meta-analysis of randomized controlled trials. Sports Med 2015;45:279–96. 10.1007/s40279-014-0272-9. 25281334.
23. Sengul C, Duman D. The association of epicardial fat thickness with blunted heart rate recovery in patients with metabolic syndrome. Tohoku J Exp Med 2011;224:257–62. 10.1620/tjem.224.257. 21737994.
24. Hu FB, Manson JE, Stampfer MJ, Colditz G, Liu S, Solomon CG, et al. Diet, lifestyle, and the risk of type 2 diabetes mellitus in women. N Engl J Med 2001;345:790–7. 10.1056/nejmoa010492. 11556298.
25. Fornieles Gonzalez G, Rosety Rodriguez MA, Rodriguez Pareja MA, Diaz Ordonez A, Rosety Rodriguez J, Pery Bohorquez MT, et al. A home-based treadmill training reduced epicardial and abdominal fat in postmenopausal women with metabolic syndrome. Nutr Hosp 2014;30:609–13. 10.3305/nh.2014.30.3.7129. 25238838.
26. Kim MK, Tomita T, Kim MJ, Sasai H, Maeda S, Tanaka K. Aerobic exercise training reduces epicardial fat in obese men. J Appl Physiol (1985) 2009;106:5–11. 10.1152/japplphysiol.90756.2008. 18927266.
27. Jonker JT, de Mol P, de Vries ST, Widya RL, Hammer S, van Schinkel LD, et al. Exercise and type 2 diabetes mellitus: changes in tissue-specific fat distribution and cardiac function. Radiology 2013;269:434–42. 10.1148/radiol.13121631. 23801768.
28. El-Zayat SR, Sibaii H, El-Shamy KA. Physiological process of fat loss. Bull Natl Res Cent 2019;43:208. 10.1186/s42269-019-0238-z.
29. Kolnes KJ, Petersen MH, Lien-Iversen T, Hojlund K, Jensen J. Effect of exercise training on fat loss-energetic perspectives and the role of improved adipose tissue function and body fat distribution. Front Physiol 2021;12:737709. 10.3389/fphys.2021.737709. 34630157.
30. Kuo CH, Harris MB, Jensen J, Alkhatib A, Ivy JL. Editorial: possible mechanisms to explain abdominal fat loss effect of exercise training other than fatty acid oxidation. Front Physiol 2021;12:789463. 10.3389/fphys.2021.789463. 34867489.
31. Fernandez Munoz MJ, Basurto Acevedo L, Cordova Perez N, Vazquez Martinez AL, Tepach Gutierrez N, Vega Garcia S, et al. Epicardial adipose tissue is associated with visceral fat, metabolic syndrome, and insulin resistance in menopausal women. Rev Esp Cardiol (Engl Ed) 2014;67:436–41. 10.1016/j.rec.2013.10.011. 24863591.

Article information Continued

Fig. 1.

Study flow diagram.

Fig. 2.

Components of exergame. (A) The exergaming group performed exercise using Exerheart devices with the permission of D&J Humancare, which is the copyright holder of Exerheart. (B) Features of the video game “Alchemist's Treasure.”

Fig. 3.

A combined intervention of aerobic exercise with drug therapy effectively improved flow-mediated dilation (FMD) and reduced epicardial fat thickness (EFT). (A) Changes in FMD from baseline to week 24. (B) Changes in EFT from baseline to week 24. a)p<0.01 (mean values were significantly different from week 12), b)p<0.05 (mean values were significantly different from control).

Table 1.

Baseline characteristics

Characteristic Treadmill (n=22) Exergame (n=29) Control (n=24) p-value
Age (yr) 60.6±11.4 60.1±8.9 62.9±12.0 0.443
Male sex 6 (27.2) 7 (24.1) 7 (29.1) 0.536
Height (cm) 159.3±8.3 157.8±8.4 160.0±8.2 0.633
Weight (kg) 68.6±9.9 72.2±17.0 67.4±10.7 0.793
BMI (kg/m2) 27.2±3.1 28.6±4.6 27.6±4.1 0.324
Systolic BP (mmHg) 132.4±18.2 133.2±13.5 131.5±19.1 0.953
Diastolic BP (mmHg) 79.0±13.2 76.3±10.3 76.3±14.5 0.624
Total cholesterol (mg/dL) 160.6±42.6 152.0±36.5 153.8±30.6 0.849
LDL-C (mg/dL) 84.8±33.7 80.9±33.0 82.6±28.3 0.932
HDL-C (mg/dL) 49.9±12.9 47.2±11.3 48.6±12.6 0.537
Triglyceride (mg/dL) 130.7±84.7 170.8±120.8 153.0±117.9 0.285
FBG (mg/dL) 124.4±39.2 130.0±40.1 129.0±38.9 0.844
HbA1c (%) 6.8±1.3 6.9±1.3 6.8±1.0 0.705
HS-CRP (mg/dL) 1.157±5.050 0.394±1.045 0.180±0.253 0.329
AST (IU/L) 25.4±8.7 26.9±10.3 26.8±11.9 0.564
ALT (IU/L) 25.3±12.9 30.7±20.4 24.5±14.2 0.590
γ-GTP (IU/L) 37.4±30.0 32.3±21.0 28.1±22.3 0.221
FMD (%) 5.2±4.0 7.2±6.9 7.2±5.2 0.366
EFT (mm) 6.9±2.9 7.6±3.6 8.3±2.6 0.129

Values are presented as mean±standard deviation or number (%).

BMI, body mass index; BP, blood pressure; LDL-C, low-density lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol; FBG, fasting blood glucose; HbA1c, glycosylated hemoglobin; HS-CRP, high sensitivity C-reactive protein; AST, aspartate aminotransferase; ALT, alanine aminotransferase; γ-GTP, gamma-glutamyl transferase; FMD, flow-mediated dilation; EFT, epicardial fat thickness.

Table 2.

Parameters after 12 weeks of drug therapy only

Parameter Baseline (n=75) Visit 2 (n=75) p-value
BMI (kg/m2) 27.7±4.0 27.6±4.6 0.359
Systolic BP (mmHg) 132.3±16.9 130.2±16.7a) 0.020
Diastolic BP (mmHg) 77.2±12.7 75.4±10.1a) 0.017
Total cholesterol (mg/dL) 155.5±36.6 145.7±29.4b) 0.006
LDL-C (mg/dL) 83.1±31.4 79.0±26.8a) 0.203
HDL-C (mg/dL) 48.1±11.2 48.4±12.9 0.576
Triglyceride (mg/dL) 148.2±112.3 131.7±94.7a) 0.030
FBG (mg/dL) 128.4±40.5 114.9±22.7b) 0.001
HbA1c (%) 6.7±1.1 6.5±0.6b) 0.004
HS-CRP (mg/dL) 0.596±3.180 0.314±1.650 0.467
AST (IU/L) 26.7±10.8 28.0±10.8 0.139
ALT (IU/L) 26.8±17.0 30.1±16.0a) 0.039
γ-GTP (IU/L) 34.1±25.7 35.9±31.3 0.361
FMD (%) 6.7±5.3 6.7±5.9 0.864
EFT (mm) 79.5±31.8 80.7±27.6 0.477

Values are presented as mean±standard deviation.

BMI, body mass index; BP, blood pressure; LDL-C, low-density lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol; FBG, fasting blood glucose; HbA1c, glycosylated hemoglobin; HS-CRP, high sensitivity C-reactive protein; AST, aspartate aminotransferase; ALT, alanine aminotransferase; γ-GTP, gamma-glutamyl transferase; FMD, flow-mediated dilation; EFT, epicardial fat thickness.

Different from before and after at same group

a)

p<0.05;

b)

p<0.01.

Table 3.

Parameters after 24 weeks of combined of aerobic exercise and drug therapy

Variable Treadmill (n=22) Exergame (n=29) Control (n=24)
Visit 2 Visit 3 Visit 2 Visit 3 Visit 2 Visit 3
BMI (kg/m2) 27.0±3.0 26.7±2.8a) 27.7±3.0 27.4±3.0 27.3±4.6 27.0±4.7
Systolic BP (mmHg) 132.4±19.3 129.9±17.6a) 134.4±11.3 132.9±18.3 126.8±13.7 133.1±19.5
Diastolic BP (mmHg) 77.6±12.5 75.5±10.5a) 79.3±8.4 77.8±10.5 72.8±9.1 77.7±14.3
Total cholesterol (mg/dL) 144.9±27.5 144.2±28.5 146.8±29.9 141.6±25.1 150.0±34.8 143.6±30.8
LDL-C (mg/dL) 75.6±22.2 74.9±23.6 78.5±22.6 77.2±22.2 82.7±34.4 75.7±25.5
HDL-C (mg/dL) 49.2±10.7 50.8±10.8 46.1±11.1 48.1±10.8 51.6±15.3 51.5±14.6
Triglyceride (mg/dL) 130.6±93.7 114.4±59.6 152.5±111.7 136.2±9.8 136.0±90.1 127.5±59.2
FBG (mg/dL) 114.0±24.8 115.6±26.0 120.3±22.1 114.3±21.6 114.7±22.9 124.6±35.9
HbA1c (%) 6.5±0.7 6.5±0.7 6.7±0.8 6.7±0.7 6.5±0.6 6.5±0.5
HS-CRP (mg/dL) 0.124±0.229 0.294±1.076 0.189±0.298 0.182±0.308 0.615±2.566 0.131±0.221
AST (IU/L) 27.2±10.7 23.8±9.8 28.35±9.4 28.5±10.9 27.4±10.9 28.9±13.6
ALT (IU/L) 30.3±14.5 25.4±11.1 33.2±17.4 32.5±17.4 25.8±11.9 28.9±19.1
γ-GTP (IU/L) 33.9±28.4 32.7±24.3 37.9±35.7 38.9±33.8 30.1±23.5 31.9±23.7
FMD (%) 5.9±4.6 15.6±18.4b),c) 6.9±8.6 17.8±7.0b),c) 7.3±6.4 9.3±6.6
EFT (mm) 6.8±2.2 6.0±1.6b) 7.6±2.6 6.2±1.7b) 8.1±2.8 8.0±2.8

Values are presented as mean±standard deviation.

BMI, body mass index; BP, blood pressure; LDL-C, low-density lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol; FPG, fasting plasma glucose; HbA1c, glycosylated hemoglobin; HS-CRP, high sensitivity C-reactive protein; AST, aspartate aminotransferase; ALT, alanine aminotransferase; γ-GTP, gamma-glutamyl transferase; FMD, flow-mediated dilation; EFT, epicardial fat thickness.

Different from before and after at same group

a)

p<0.05;

b)

p<0.01;

different from control at the same period

c)

p<0.05.