Warning: mkdir(): Permission denied in /home/virtual/lib/view_data.php on line 81

Warning: fopen(upload/ip_log/ip_log_2024-11.txt): failed to open stream: No such file or directory in /home/virtual/lib/view_data.php on line 83

Warning: fwrite() expects parameter 1 to be resource, boolean given in /home/virtual/lib/view_data.php on line 84
The Synergy Effect of Weight‐Bearing Circuit Training and Aloe QDM Complex on Obese Middle Aged Women: a Randomized Double‐Blind Controlled Trial

The Synergy Effect of Weight‐Bearing Circuit Training and Aloe QDM Complex on Obese Middle Aged Women: a Randomized Double‐Blind Controlled Trial

Article information

Korean J Health Promot. 2014;14(2):59-66
Publication date (electronic) : 2014 January 20
doi : https://doi.org/10.15384/kjhp.2014.14.2.59
1Health and Exercise Science Laboratory, Institute of Sports Science, Department of Physical Education, College of Education, Seoul National University, Seoul, Korea
2Univera Inc., Seoul, Korea
Corresponding author:Wook Song, PhD Health and Exercise Science Laboratory, Institute of Sports Science, Department of Physical Education, College of Education, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 151-748, Korea Tel: +82-2-880-7804, Fax: +82-2-886-7804 E-mail: songw3@snu.ac.kr
Received 2014 January 16; Accepted 2014 June 10.

Abstract

Abstract

Background

Obesity is a major health problem and leads to metabolic diseases such as type 2 diabetes, insulin resistance and hyperlipidemia. Recently, it was reported that aloe QDM complex, composed of processed aloe vera gel, aloesin and chromiun could improve insulin sensitivity by enhancing 5' adenosine monophosphate-activated protein (AMPK) activity and has an anti-inflammatory effect by reducing the level of pro-inflammatory cytokines. It is also known that aloe QDM complex can reduce body weight, body fat mass and insulin resistance in type 2 diabetes patients. The purpose of this study was to assess for possible synergistic effects of weight-bearing circuit training and aloe QDM complex supplementation on body composition, physical fitness, blood profile and diabetes risk factors.

Methods

Study subjects included 19 participants randomly assigned to the Exercise group (Ex, n=9) and to the Exercise with aloe QDM complex group (Q-Ex, n=10). Both groups participated in weight-bearing circuit training 3 times a week for 4 weeks and took a capsule composed of either aloe (aloe QDM complex) or soy bean (placebo), 1100 mg/day for 4 weeks. Body composition was measured by dual-energy x-ray absorptiometry. Grip strength, flexibility, curl-up, balance, agility, Sargent jump and VO2max were measured, as well as fasting blood samples taken.

Results

After 4 weeks of weight-bearing circuit training and aloe QDM complex supplementation, the significant interactions (time × intervention) between the groups regarding body fat percentage (F=7.024, P=0.017) and body fat mass (F=5.243, P=0.035) were calculated. There were significant differences in body fat percentage (P=0.029) and body fat mass (P=0.039). No significant interaction was observed in physical fitness, blood profile and diabetes risk factors.

Conclusions

In this study, the combination of weight-bearing circuit training and aloe QDM complex supplementation showed a positive effect for reducing body fat mass, and could be an effective intervention for managing obesity.

Keywords: Obesity; Exercise; Aloe
Figure 1.

Study population and design

Exercise program

Basal characteristics of study subjects at ‘intention-to-treat' (ITT) and ‘per-protocol' (PP)a

Changes in body composition measured by DXA after 4 weeks of weight bearing circuit training and aloe QDMC supplementation (n=19)a

Changes in physical fitness after 4 weeks of weight bearing circuit training and aloe QDMC supplementation (n=19)a,b

Changes in blood lipids and diabetes risk factors after 4 weeks of weight bearing circuit training and aloe QDMC supplementation (n=19)a,b

References

1. Statistics Korea. National Health and Nutrition Survey 2011. Korea Health Statistics 2011: Korea National Health and Nutrition Examination Survey(KNHANESV‐2) Reston: Ministry of Health and Welfare; 2012. [Accessed January 2, 2013]. https://knhanes.cdc.go.kr/knhanes/sub04/sub04_03.do?classType=7.
2. Klein S, Sheard NF, Pi-Sunyer X, Daly A, Wylie-Rosett J, Kulkarni K, et al. Weight management through lifestyle modification for the prevention and management of type 2 diabetes: rationale and strategies: a statement of the American Diabetes Association, the North American Association for the Study of Obesity, and the American Society for Clinical Nutrition. Diabetes Care 2004;27(8):2067–73.
3. American College of Sports Medicine; Whaley MH, Brubaker PH, Otto RM, Armstrong LE. ACSM's Guidelines for Exercise Testing and Prescription 7th ed.th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006. p. 19–54. 216–9.
4. Hunter GR, Bryan DR, Wetzstein CJ, Zuckerman PA, Bamman MM. Resistance training and intraabdominal adipose tissue in older men and women. Med Sci Sports Exerc 2002;34(6):1023–8.
5. Booth FW, Tseng BS. America needs to exercise for health. Med Sci Sports Exerc 1995;27(3):462–5.
6. Most J, Goossens GH, Jocken JW, Blaak EE. Short-term supplementation with a specific combination of dietary polyphenols increases energy expenditure and alters substrate metabolism in overweight subjects. Int J Obes (Lond) 2014;38(5):698–706.
7. Capasso F, Borrelli F, Capasso R, Di Carlo G, Izzo AA, Pinto L, et al. Aloe and its therapeutic use. Phytother Res 1998;12(S1):S124–7.
8. Heggers JP, Kucukcelebi A, Stabenau CJ, Ko F, Broemeling LD, Robson MC, et al. Wound healing effects of Aloe gel and other topical antibacterial agents on rat skin. Phytother Res 1995;9(6):455–7.
9. Koo MW. Aloe vera: antiulcer and antidiabetic effects. Phytother Res 1994;8(8):461–4.
10. Winters WD, Benavides R, Clouse WJ. Effects of aloe extracts on human normal and tumor cells in vitro. Econ Bot 1981;35(1):89–95.
11. Ngo MQ, Nguyen NN, Shah SA. Oral aloe vera for treatment of diabetes mellitus and dyslipidemia. Am J Health Syst Pharm 2010;67(21):1804–11.
12. Langmead L, Feakins RM, Goldthorpe S, Holt H, Tsironi E, De Silva A, et al. Randomized, double-blind, placebocontrolled trial of oral aloe vera gel for active ulcerative colitis. Aliment Pharmacol Ther 2004;19(7):739–47.
13. Yongchaiyudha S, Rungpitarangsi V, Bunyapraphatsara N, Chokechaijaroenporn O. Antidiabetic activity of Aloe vera L. juice. I. Clinical trial in new cases of diabetes mellitus. Phytomedicine 1996;3(3):241–3.
14. Bunyapraphatsara N, Yongchaiyudha S, Rungpitarangsi V, Chokechaijaroenporn O. Antidiabetic activity of Aloe vera L. juice II. Clinical trial in diabetes mellitus patients in combination with glibenclamide. Phytomedicine 1996;3(3):245–8.
15. Misawa E, Tanaka M, Nomaguchi K, Yamada M, Toida T, Takase M, et al. Administration of phytosterols isolated from Aloe vera gel reduce visceral fat mass and improve hyperglycemia in Zucker diabetic fatty (ZDF) rats. Obes Res Clin Pract 2008;2(4):239–45.
16. Choi HC, Kim SJ, Son KY, Oh BJ, Cho BL. Metabolic effects of aloe vera gel complex in obese prediabetes and early non-treated diabetic patients: randomized controlled trial. Nutrition 2013;29(9):1110–4.
17. Shin E, Shin S, Kong H, Lee S, Do SG, Jo TH, et al. Dietary aloe reduces adipogenesis via the activation of AMPK and suppresses obesity-related inflammation in obese mice. Immune Netw 2011;11(2):107–13.
18. Mu J, Brozinick JT Jr, Valladares O, Bucan M, Birnbaum MJ. A role for AMP-activated protein kinase in contraction- and hypoxia-regulated glucose transport in skeletal muscle. Mol Cell 2011;7(5):1085–94.
19. Reznick RM, Shulman GI. The role of AMP-activated protein kinase in mitochondrial biogenesis. J Physiol 2006;574(Pt 1):33–9.
20. O'Neill HM, Holloway GP, Steinberg GR. AMPK regulation of fatty acid metabolism and mitochondrial biogenesis: implications for obesity. Mol Cell Endocrinol 2013;366(2):135–51.
21. American College of Sports Medicine; Pescatello LS. ACSM's Guidelines for Exercise Testing and Prescription 9th ed.th ed. Philadelphia, PA: Lippincott Williams & Wilkins Health; 2014. p.320.
22. Shin E, Shim KS, Kong H, Lee S, Shin S, Kwon J, et al. Dietary aloe improves insulin sensitivity via the suppression of obesity-induced inflammation in obese mice. Immune Netw 2011;11(1):59–67.
23. So WY, Choi DH. Effects of walking and resistance training on the body composition, cardiorespiratory function, physical fitness, and blood profiles of middle-aged obese women. Exerc Sci 2007;16(2):85–94.
24. Kwon YI, Park TG, Park GH, Park CH, Jeon JY, Choi MG, et al. Effects of combined exercise training on physical fitness and metabolic syndrome in obese middle school boys. Korean J Phys Educ-Nat Sci 2006;45(6):611–21.
25. Watts K, Jones TW, Davis EA, Green D. Exercise training in obese children and adolescents: current concepts. Sports Med 2005;35(5):375–92.
26. Swain DP. Moderate or vigorous intensity exercise: which is better for improving aerobic fitness? Prev Cardiol 2005;8(1):55–8.
27. Olson TP, Dengel DR, Leon AS, Schmitz KH. Changes in inflammatory biomarkers following one-year of moderate resistance training in overweight women. Int J Obes (Lond) 2007;31(6):996–1003.
28. Ibáñez J, Izquierdo M, Martínez-Labari C, Ortega F, Grijalba A, Forga L, et al. Resistance training improves cardiovascular risk factors in obese women despite a significative decrease in serum adiponectin levels. Obesity (Silver Spring) 2010;18(3):535–41.

Article information Continued

Figure 1.

Study population and design

Table 1.

Exercise program

Type Intensity Duration, wk Frequency Contents
Weight bearing circuit training (HRmax – HRrest) × 40% to 60% + HRrest 4 3 times/wk, 20–30 repetition, 2 sets Hip circles, push up, lateral squat, long lever crunches, squat, arm & leg raise, calf raise

Abbreviations: HRmax, maximum heart rate; HRrest, resting heart rate.

Table 2.

Basal characteristics of study subjects at ‘intention-to-treat' (ITT) and ‘per-protocol' (PP)a

Variables ITT PP P
Ex (n=12) Q‐Ex (n=16) Ex (n=9) Q‐Ex (n=10) ITT PP
Age, y 51.0±2.0 50.0±2.3 50.7±2.4 50.7±2.4 N.S. N.S.
Height, cm 155.3±1.8 157.8±1.4 153.7±2.1 156.2±1.3 N.S. N.S.
Weight, kg 64.6±2.4 63.5±2.1 65.0±2.7 59.9±1.7 N.S. N.S.
WHR 0.92±0.008 0.90±0.014 0.93±0.009 0.88±0.013 N.S. 0.013b
BMI, kg/m2 26.8±0.8 25.5±0.7 27.4±0.7 24.6±0.7 N.S. 0.010c
Body fat, % 37.2±0.8 37.6±0.9 38.2±0.7 36.5±1.0 N.S. N.S.
Lean body, % 62.8±0.8 62.4±0.9 61.8±0.7 63.5±1.0 N.S. N.S.
VO2max, mL/kg/min 21.9±1.5 22.9±0.6 20.0±1.3 22.68±0.9 N.S. N.S.
FBG, mg/dL 94.8±3.4 104.1±11.4 95.3±4.4 91.6±3.1 N.S. N.S.
Insulin, mlU/L 6.6±1.0 7.3±1.1 7.3±1.2 6.5±1.7 N.S. N.S.
HbA1c, % 6.1±0.1 5.9±0.2 6.0±0.1 5.6±0.1 N.S. 0.004d
HOMA‐IR 1.6±0.2 1.9±0.3 1.7±0.3 1.5±0.5 N.S. N.S.
Total cholesterol, mg/dL 208.0±8.6 192.2±5.8 216.9±9.6 197.1±8.1 N.S. N.S.
HDL‐C, mg/dL 49.8±2.3 55.6±3.8 49.0±2.7 57.6±5.8 N.S. N.S.
Triglyceride, mg/dL 131.0±25.6 112.6±23.2 145.6±33.0 124.0±36.8 N.S. N.S.

Abbreviations: Ex, exercise group; Q‐Ex, aloe QDM complex group; WHR, waist hip ratio; BMI, body mass index; VO2max, maximum oxygen consumption; FBG, fasting blood glucose; HbA1c, hemoglobin A1c; HOMA-IR, homeostatic model assessment-insulin resistance; HDL-C, high-density lipoprotein cholesterol.

a

Values are presented as mean±SEM.

b

Calculated by independent t-test in PP group, P=0.013.

c

Calculated by independent t-test in PP group, P=0.010.

d

Calculated by independent t-test in PP group, P=0.004.

Table 3.

Changes in body composition measured by DXA after 4 weeks of weight bearing circuit training and aloe QDMC supplementation (n=19)a

Variables Pre Post F P
Ex Q‐Ex Ex Q‐Ex
Body fat, % 38.2±2.1 36.5±3.1 37.7±2.3 34.9±2.9b,c 7.024 0.017d
Body fat mass, kg 24.8±3.6 22.0±3.5 24.2±3.6e 20.6±3.5f,g 5.243 0.035h
Lean body mass, kg 40.1±4.9 37.9±2.8 39.9±5.1 38.3±3.3 1.929 0.183

Abbeviations: Ex, exercise group; Q‐Ex, aloe QDM complex group; DXA, dual-energy x-ray absorptiometry.

a

Values are presented as mean±SEM.

b

Calculated by paired t-test, P=0.001, compared with Pre Q-Ex.

c

Calculated by independent t-test, P=0.029, compared with Post Ex group.

d

Calculated by repeated measures ANOVA, P=0.017, time × intervention interaction.

e

Calculated by paired t-test, P=0.032, compared with Pre Ex group.

f

Calculated by paired t-test, P<0.001, compared with Pre Q-Ex group.

g

Calculated by independent t-test, P=0.039, compared with Post Ex group.

h

Calculated by repeated measures ANOVA, P=0.035, time × intervention interaction.

Table 4.

Changes in physical fitness after 4 weeks of weight bearing circuit training and aloe QDMC supplementation (n=19)a,b

Variables Pre Post F P
Ex Q-Ex Ex Q-Ex
Grip strength, kg 26.4±1.6 25.5±1.5 29.0±1.3 27.6±1.1 0.116 0.738
Flexibility, cm 16.8±2.3 13.7±2.3 18.1±2.4 17.5±2.0 2.638 0.123
Curl-up, times/60 s
Sargent jump, cm
12.8±1.7
20.1±1.1
13.4±1.5
20.6±1.6
14.8±1.7
22.1±1.1
17.3±1.3
23.7±1.6
2.771
0.437
0.114
0.517
Agility, msec 334±32.5 302±31.1 287±55.3 272±32.1 0.064 0.803
Balance, s 21.4±5.9 15.5±5.8 27.0±5.9 53.5±16.9 4.176 0.057
VO2max, mL/kg/min 20.0±1.3 22.7±0.9 21.8±1.2 25.9±1.5 0.509 0.485

Abbeviations: Ex, exercise group; Q‐Ex, aloe QDM complex group; VO2max, maximum oxygen consumption.

a

Values are presented as mean±SEM.

b

Calculated by repeated measures ANOVA.

Table 5.

Changes in blood lipids and diabetes risk factors after 4 weeks of weight bearing circuit training and aloe QDMC supplementation (n=19)a,b

Variables Pre Post F P
Ex Q‐Ex Ex Q‐Ex
Lipid profile
 Triglyceride, mL/dL 145.6±33.0 124.0±36.8 111.1±19.6 75.0±13.5 0.211 0.652
 Total cholesterol, mg/dL 216.9±9.5 197.1±8.0 219.4±7.8 192.1±6.0 0.765 0.394
 HDL‐C, mL/dL 49.0±2.2 57.6±5.8 43.8±1.5 57.8±5.3 0.049 0.828
Diabetes risk factors            
 FBG, mg/dL 95.3±4.3 91.6±3.0 97.7±4.4 90.8±1.6 0.419 0.526
 Insulin, mIU/L
 HbA1c, %
7.3±3.6
6.1±0.12
6.5±1.7
5.6±0.0
6.0±2.0
6.01±0.08
4.7±0.3
5.6±0.0
0.056
2.342
0.816
0.144
 HOMA‐IR 1.71±0.27 1.54±0.47 1.42±0.16 1.06±0.08 0.140 0.713

Abbreviations: Ex, exercise group; Q‐Ex, aloe QDM complex group; HDL-C, high-density lipoprotein cholesterol; FBG, fasting blood glucose; HbA1c, hemoglobin A1c; HOMA-IR, homeostatic model assessment-insulin resistance.

a

Values are presented as mean±SEM.

b

Calculated by repeated measures ANOVA.