CC BY
123
14. Nazarenko L.D., Anisimova E.A. Vospitanie v sporte [Upbringing in sport]. Moscow: "Theory and practice of physical culture and sport". 2015: 80.
15. Prokhodovskiy R.Y. Physical readiness structure and new volleyball players' motor skills development. Candidate's thesis. Malakhovka. 2004: 25.
16. Rodin A.V. The skill of run-up and jump formation during a direct attacking strike fulfillment on the basis of new volleyball players' dynamic and kinematic structure of motor action. Candidate's thesis. Smolensk. 2006: 22.
Submitted: 24.07.2018
17. Kuznetsova Z., Kuznetsov A., Mutaeva I., Khalikov G., Zakharova A., 2015. Athletes training based on a complex assessment of functional state. In
Proceedings of the 3rd International Congress on Sport Sciences Research and Technology support. SCITEPRESS. P. 156-160 (Scopus).
18. Kuznetsov A., Mutaeva I., Kuznetsova Z., 2017. Diagnostics of Functional State and Reserve Capacity of young Athletes' Organism. In Proceedings of the 5th International Congress on Sport Sciences Research and Technology support. SCITEPRESS. P. 111-115 (Scopus).
Author's information:
Tinyukov A.B. - senior Lecturer, Federal State Budgetary Educational Establishment of Higher Education "Ulyanovsk State Pedagogical University Named After I.N. Ulyanov", Ulyanovsk, Russia, e-mail: [email protected]
DOI 10.14526/2070-4798-2018-13-3-82-90
EFFECT OF CAFFEINE CONSUMPTION PRIOR TO WALKING EXERCISE ON BODY COMPOSITION IN OVERWEIGHT INDIVIDUALS
Chee Keong Chen1'2 and Mohd Afieq Mohd Rosli2
1Sports Science Unit, School of Medical Sciences, Universiti Sains Malaysia, 16150, Kubang Kerian, Kelantan, Malaysia, 2Exercise and Sports Science Programme, School of Health Sciences, Universiti Sains Malaysia, 16150, Kubang Kerian, Kelantan, Malaysia,
Abstract. Introduction: Caffeine has been shown to increase the amount of available energy, in form of circulating free fatty acid via lipolysis. Thus, caffeine consumption increases oxidation of lipid oxidation in individuals performing exercise. Aim: The purpose of the study was to investigate the effect of caffeine consumption on body composition in overweight individuals. Methods: Thirty overweight individuals from the campus of Universiti Sains Malaysia, with body mass index (BMI) between 25.1 to 29.0 kg/m2 were recruited for this study. The participants were randomly assigned into three groups: control (C) group (n=10), exercise (E) group (n=10), and exercise with caffeine consumption (CE) group (n=10). The E and CE groups participated in a prescribed brisk walking program for six weeks. In addition, participants in the CE group were required to consume caffeine (50-100mg) one hour prior to each exercise session. The C group was requested not to participate in any exercise program during the study period. Results: There were no significant differences in body weight between the 3 groups at pre- and post- intervention. However, body weight was significantly lower (p<0.05) after the intervention program in the E and CE groups compared to their respective pre-intervention values. BMI was significantly lower (p<0.05) in CE group compared to C group at post-intervention. BMI was also significantly lower (p<0.05) after the intervention program in E and CE groups compared to their respective pre-intervention values. Furthermore, % body fat in E and CE groups were significantly lower (p<0.05) than C group at post-intervention. Conclusion: Both the intervention programs resulted in a small but significantly
lower body weight, BMI and percent body fat among the participants but consuming caffeine (50-100mg) one hour prior to exercise did not result in any further weight loss compared to exercise alone.
Key words: caffeine, brisk walking, body composition, obese, BMI.
For citations: Chee Keong Chen, Mohd Afieq Mohd Rosli. Effect of caffeine consumption prior to walking exercise on body composition in overweight individuals. The Russian Journal of Physical Education and Sport (Pedagogico-Phycological and Medico-Biological Problems of Physical Culture and Sports). 2018; 13(3): 62-69. DOI 10.14526/2070-4798-2018-13-3-82-90.
INTRODUCTION
Caffeine and 3 dimethylxanthines (theophylline, theobromine, paraxanthine) are biologically active, and the putative impact of methylxantines on metabolism has received considerable attention in sports (Graham et al. , 2008). Coffee is certainly the most common mode of caffeine ingestion, and it can also provide caffeine in a more concentrated form than do other foodstuffs (Arnaud, 1993). Caffeine also has many pharmacological effects in humans, including increase in heart rate variability during rest as well as during aerobic exercise (Nishijima et al., 2002). Athletes are among the group of people who are interested in the effects of caffeine on endurance and exercise capacity (Burke, 2008). To date, many research trials have demonstrated caffeine to be an ergogenic aid for exercise of varying intensities, durations and modalities in an athletic population (Bruce et al., 2000; Graham, 2001; Bell and McLellan, 2002; Stuart et al., 2005; Ping et al., 2010). The ability to perform more work after caffeine ingestion, as demonstrated in athletic populations, can result in greater caloric expenditure and the possibility of improved fitness if the exercise is maintained over an extended period of time (Wallman et al., 2010).
Overweight and obesity represent a threat to the health of populations in an increasing number of countries (WHO, 2000). Obesity is the outcome of a prolonged positive energy balance, due to an excess energy intake over energy expenditure. A negative energy balance is needed to produce weight loss and can be achieved by either decreasing intake or increasing energy expenditure. Nutritional agents like caffeine, ephedrine, capsaicin, and green tea have been
proposed as strategies for weight loss and weight maintenance, since they may increase energy expenditure and have been proposed to counteract the decrease in metabolic rate that is present during weight loss (Diepvens et al., 2007). Bracco et al. (1995) observed that compared with lean women, obese women had increased lipid oxidation the day after caffeine ingestion. There was also increased fat oxidation in obese women who consumed a restricted diet and a mixture of ephedrine and caffeine over an eight weeks period (Astrup et al., 1992). The increase in energy expenditure and changes in plasma substrates after caffeine ingestion resemble those caused by increased activity of the sympathetic nervous system (Acheson et al., 2004).
To our knowledge, information about effect of caffeine consumption prior to exercise on body composition in overweight individuals in Malaysia is scarce. Thus the present study was carried out to investigate the effect of caffeine consumption prior to walking exercise for six weeks on body composition in overweight individuals. METHODS Participants
Thirty healthy individuals from the campus in Universiti Sains Malaysia were recruited as participants for this study. They were age-matched and randomly assigned into two interventions groups and a control group. Intervention groups were named exercise group (E) and combined exercise plus caffeine group (CE). Each group consisted of ten participants. All the participants had body mass index (BMI) between 25.1 kg/m2 to 29.9 kg/m2 and were classified as overweight according to World Health Organization (WHO). They were instructed not to be involved in any other exercise program during
the study period. The nature and risk of the experimental procedures were explained to them and a written informed consent was obtained from each of the participants. This study was approved by the Human Research Ethics Committee, Universiti Sains Malaysia. Research Design
All participants in both interventions group were requested to participate in a prescribed exercise program three times per week for six weeks. The walking exercise
suggested by the National Heart, Lung, and Blood Institute (NHLB). For the first week, participants were requested to complete three sessions of 15 minutes of brisk walking exercise. The 15 minutes sessions consisted of warm up for five minutes, walk briskly for five minutes and cool down for five minutes. For next five weeks, the duration of brisk walking was increased two minutes each week. The prescribed exercise is shown in Table 1.
Warm-up Exercising Cool down Total time
Week 1 Walk 5 min. Then walk briskly 5 min Then walk more slowly 5 min 15 min
Session A Repeat pattern above
Session B Repeat pattern above
Session C Repeat pattern above
Continue at least three exercise sessions during each week of the program.
Week 2 Walk 5 min. Walk briskly 7 min Walk 5 min. 17 min.
Week 3 Walk 5 min. Walk briskly 9 min Walk 5 min. 19 min.
Week 4 Walk 5 min. Walk briskly 11 min Walk 5 min. 21 min.
Week 5 Walk 5 min. Walk briskly 13 min Walk 5 min. 23 min.
Week 6 Walk 5 min. Walk briskly 15 min Walk 5 min. 25 min
(Adapted from walking program by National Heart, Lung and Blood Institute, USA, 2006)
Table 1: Intervention Brisk Walking Program
In addition, participants in the caffeine + exercise group were required to consume caffeine an hour before the exercise sessions. Caffeine was consumed in the form of a Nescafe® drink (3 in 1, Rich). Amount of caffeine in each sachet (20g) was between 50-100mg. Participants in the control group were requested not to participate or involve in any exercise program for six weeks. Anthropometric, body composition and waist-to-hip ratio assessment were carried out on the control group at the same interval as for the intervention groups which were done before and after six weeks of the prescribed exercise program. Procedures
A stadiometer (Seca Corporation, Germany) was used to measure standing height of each participant to the nearest 0.1 centimeter (cm). Participants were requested
to stand with foot together and with their shoes removed. A weighing scale (Seca Corporation, Germany) was used to measure body mass of each participant to the nearest 0.1 kilogram (kg). A body composition analyzer (Omron Healthcare Corporation, Japan) was used to measure the body composition of the participants. After keying in the data of the participants such as height, gender and age, they were requested to step onto the body composition analyzer until the measurements were recorded. For measurement of the waist to hip ratio, a non-elastic measuring tape was used to measure the circumference of the waist and hip of the participants. The circumference of hip was measured at the widest part of the buttocks and the circumference of waist was measured at the narrowest point of the natural waist, just above the belly button. To determine the ratio,
waist measurement was divided by the hip
measurement.
Statistical Analysis
Statistical Package for Social Sciences (SPSS) version 20.0 was used for the analytical procedure. All the data were expressed as means ± standard deviation
used to analyze and compare differences of body weight, BMI, WHR, and percentage of body fat between groups. Statistical significance was accepted at p < 0.05. RESULTS
The participants' physical characteristics are presented in Table 2.
N = 30 Control(C) Exercise(E) Caffeine + Exercise(C+E)
N 10 10 10
Age (years) 21.6 ± 1.3 21.6 ± 1.4 21.5 ± 1.2
Height (cm) 168.3 ± 6.9 168.2 ± 7.0 166.2 ± 6.3
Weight (kg) 79.3 ± 9.5 76.9 ± 9.9 75.3 ± 8.0
Values shown as means ± standard deviation (SD)
Table 2: Physical characteristics of the participants.
Body Weight
Body weight of the participants in all three groups during pre and post intervention is shown in Fig. 1. ANOVA with repeated measures revealed that there was no interaction between all groups and time on body weight. However, there was a
significant difference (p<0.05) in body weight between pre and post for both intervention groups. Body weight was significantly lower in the Exercise and Caffeine + Exercise groups compared to their respective baseline values after the 6 weeks walking program.
Figure 1: Mean body weight at pre and post intervention. * Significantly different from respective pre intervention values (p<0.05)
Body Mass Index (BMI)
BMI of participants in all three groups at pre and post intervention is shown in Fig. 2. At post intervention, BMI of CE and E groups were significantly lower than the control C group. Body mass index was significantly (p<0.05) lower in the Exercise and Caffeine + Exercise groups compared to their respective pre-intervention values after the 6 weeks
walking program. BMI was also significantly (p<0.05) lower in the Exercise and Caffeine group compared to the control group at posttest.
Figure 2: Mean Body Mass Index at pre and post intervention.
* Significantly different from respective pre intervention values (p<0.05)
# Significantly different from control group (p< 0.05)
Percent Body Fat
Percent of body fat of participants in all three groups during pre and post is shown in Fig. 3. ANOVA with repeated measures revealed that there was an interaction (p<0.05) between both intervention groups and time on percent body fat. At post
Figure 3: Mean percent body fat at pre and post intervention.
* Significantly different from respective pre intervention values (p<0.05)
# Significantly different from control group (p< 0.05)
intervention, BMI of E group and CE group were significantly lower than C group. Furthermore, paired-sample T tests revealed a lower percent body fat between pre and post intervention values in both CE and E groups.
Waist-to-Hip Ratio (WHR)
WHR of participants in all three groups during pre and post intervention is shown in Fig. 4. ANOVA with repeated measures revealed that there was no interaction between all groups and time on WHR. Furthermore, there was also no significant main effect of time on WHR. A paired-sample T test revealed that there were no differences between pre and post WHR for all the 3 groups.
Figure 4: Mean waist-to-hip at pre and post intervention.
Heart Rate of Participants at the End of Brisk Walking Exercise
Mean heart rate of the participants in both intervention groups at the end of brisk walking sessions are shown in Table 3. These
DISCUSSION
The 6-week brisk walking exercise program resulted in a significant (p<0.05) 0.7 kg mean weight loss in E group and 1.3 kg in CE group compared to the respective pre intervention body weights. This finding of weight reduction following a walking program has also been reported in other studies. For example, brisk walking exercise for 16 weeks without caffeine consumption has reported a mean weight loss of 5.7 kg (Leon et al.., 1979). Bergman et al. (1996) reported that body weight decreased significantly during an 8-week walking program without caffeine consumption. In a study by Racette el al. (1995), 12-weeks of aerobic exercise program, resulted in a higher mean weight losses in the exercise group (10.8 ± 3.2 kg) compared to non-exercise group (8.1 ± 2.3 kg).
There were no significant differences between body weight in both intervention groups and these data indicated that caffeine consumption did not have any addictive effect when compared to the weight loss by just brisk walking alone. This finding was in agreement with another study by Astrup et al. (1992) who reported that caffeine had no effect on body weight loss after participants were treated by diet (4.2 MJ/day) and caffeine (200 mg) three times a day for 24 weeks. Pasman et al. (1997) also reported that supplementation of caffeine has no beneficial effect on body weight loss and weight maintenance in the long-term. One of possible explanations for these results is the
the intervention program were walking at the prescribed intensity during these brisk walking sessions.
Table 3: Mean heart rate of the participants in intervention groups at the end of brisk
development of insensitivity to caffeine effects (Diepvens et al., 2007).
In the present study, six weeks of prescribed intervention brisk walking training resulted in significant changes in BMI for both intervention groups compared to pre intervention values, (27.1 ± 1.4 kg/m2 vs. 26.8 ± 1.2 kg/m2, p<0.05) in the E group and (27.9 ± 1.7 kg/m2 vs. 27.5 ± 1.6 kg/m2, p<0.05) in the CE group. Thus, BMI of E and CE groups reduced 0.3 kg/m2 and 0.4 kg/m2 after the prescribed intervention. CE group also had a significantly lower in BMI when compared to Control group at post intervention (26.8 ± 1.9 kg/m2 vs. 27.9 ± 1.6 kg/m2, p<0.05).
Reduction of BMI after a prescribed exercise program was supported by the suggestion of Okita et al. (2004), who found that after two months of aerobic exercise program ( 60% to 80% of the maximum heart rate) without caffeine supplementation resulted in a significant reduction of BMI (1.2 kg/m2). Another study demonstrated that BMI decreased significantly (from 28.7 ± 6.4 kg/m2 to 28.2 ± 6.4 kg/m2) after the participants participated in eight weeks of walking exercise program (Bergman et al., 1996). A change in BMI is directly proportionate with changes in body weight, i. e., a decrease in body weight will result in a reduction in BMI.
There were no significant differences in percent body fat between the 3 groups at pre intervention but after 6 weeks of the prescribed intervention brisk walking program, percent of body fat in the E and CE groups were significantly lower (p<0.05) than
data indicated that the participants involved in
walking sessions
Exercise (E) Caffeine + Exercise (C+E)
Mean Heart Rate (beats.min-1) 149 144
the control group (23.0 ± 3.2 % vs 25.6 ± 3.4 %, p<0.05 and 21.9 ± 4.1 % vs. 25.6 ± 3.4 %, p<0.05) respectively. At post intervention, there was also a significant reduction (p<0.05) of 0.6 % and 1.5 % of percent body fat in the E and CE groups compared to their respective pre intervention values. These data indicated that the brisk walking program may have resulted in increased mobilization of fat stores to supply activity energy requirements which resulted in reduction of fat stores with the continuous lipolysis demanded. A previuos study also revealed that percent body fat decreased significantly during the 8 weeks walking program (Bergman et al., 1996). Lewis et al. (1976) combined a walk-jog program with moderate calorie restriction in obese adult women and showed 5% decreased of percentage of body fat in 17 weeks.
Caffeine is commonly proposed to enhance exercise capacity by promoting fat oxidation and inhibiting carbohydrate oxidation via feedback mechanisms in the active muscle (Graham et al., 2008; Ping et al., 2010). It also act as a thermogenic agent that in combination with slimming regimens could be use in promoting the loss of body energy (Miller et al., 1974). Caffeine alone has several important metabolic effects. Caffeine stimulates fat utilization in muscle tissue during exercise (Spriet et al., 1992). Van Soeren and Graham (1998) suggested that caffeine is an adenosine-receptor antagonist and all tissues with adenosine receptors can be affected by caffeine exposure. This will increase the lipolysis process and result in a higher amount of free fatty acids in the blood that will be available as a substrate for continuous muscular contractions during prolonged exercise. However, there was no significant effect of caffeine consumption on extra weight loss when compared to the E group in the present study. Although CE group showed a higher percentage of body fat loss, it was not statistically significant. The probable reason for this finding was that the dosage of caffeine given to the participants was not adequate to elicit a more discernable effect on percent body fat loss.
After 6 weeks of intervention, the results showed that there were no significant differences in WHR between groups at pre and post intervention and no significant changes after the intervention programme in all three groups. Bergman et al. (1996) also failed to demonstrate any significant changes in hip circumference after an 8-week of exercise. Both findings might be partially explained by a possible increase of lean tissue in the measured areas although there was a decrease in body weight and percent of body fat. Walking could increase the strength and muscle size, masking any reduction in fat stores when circumference measures are taken (Bergman et al., 1996). CONCLUSIONS
Both intervention program (brisk walking and brisk walking + caffeine consumption) resulted in a small but significantly lower body weight, BMI and percent of body fat among the overweight male participants. Our results also indicated that consuming caffeine (50-100mg) one hour prior to exercise did not result in any further weight loss compared to exercise alone. In addition, the prescribed brisk walking program did not have any effect on the waist to hip ratio among the participants.
References
1. Acheson K. J., Gremaud G., Meirim I., Montigon F., Krebs Y. & Fay L. B. Metabolic effects of caffeine in humans: lipid oxidation or futile cycling? Am J Clin Nutr.2004; 79: 40-46.
2. Arnaud M. J. Metabolism of caffeine and other components of coffee. In: Caffeine, Coffee, and Health, ed Garattini S. New York: Riven. 1993: 43-96.
3. Astrup A., Breum L., Toubro S., Hein P. & Quaade F. The effect and safety of an ephedrine/caffeine compound compared to ephedrine, caffeine and placebo in obese participants on an energy-restricted diet. A double blind trial. Int J Obes, 1992; 16: 269-277.
4. Bell D. G. & McLellan T. M. Exercise endurance 1, 3, and 6 h after caffeine ingestion in caffeine users and nonusers. J Appl Physiol. 2002; 93: 1227-1234.
5. Bergman, E. A., Boyungs, J. C. & Joseph, E. Walking, fitness, body composition and inch loss. Nutr Res. 1996; 16(6): 907-914.
6. Bracco D., M., F. J., Arnaud M. J., Jequier E. & Schutz Y. Effects of caffeine on energy metabolism, heart rate, and methylxanthine metabolism
in lean and obese women. Am J Physiol Endocrinol Metab. 1995; 269: E671-E678.
7. Bruce C. R., Anderson M. E., Fraser S. F., Stepto N. K., Klein R., Hopkins W. G. & Hawley J. A. Enhancement of 2000-m rowing performance after caffeine ingestion. MedSci Sports Exerc. 2000; 32(11): 1958 - 1963.
8. Burke L. M. Caffeine and sport performance. Appl Physiol NutrMetab. 2008; 33: 1319 - 1334.
9. Diepvens K., Westerterp K. R. & Westerterp-Plantenga M. S. Obesity and thermogenesis related to the consumption of caffeine ephedrine, capsaicin, and green tea. Am J Physiol Regul Integr Comp Physiol. 2007; 292(1): 77-85.
10. Graham T. E. Caffeine and exercise: metabolic, endurance and performance. Sports Med. 2001; 31(11): 785 - 807.
11. Graham T. E., Battram D. S., Dela F., El-Sohemy A. & Thong F. S. L. Does caffeine alter muscle carbohydrate and fat metabolism during exercise? Appl Physiol Nutr Metab. 2008; 33: 13111318.
12. Leon A., Conrad J. S. & Hunninghake D. M. Effects of a vigorous walking program on body composition, and carbohydrate and lipid metabolism of obese young men. Am J Clin Nutr. 1979; 2: 1776-1787.
13. Lewis S., Haskell W. L., Wood P. D., Manoogian N., Bailey J. E. & Pereira M. B. Effects of physical activity on weight reduction in obese middle-aged women. Am. J. Clin. Nutr. 1976; 29: 151-156.
14. Miller D. S., Stock M. J. & Stuart J. A. The effects of caffeine and carnitine on the oxygen consumption of fed and fasted participants. Proc Nutr Soc. 1974; 33: 28A-29A.
15. Nishijima Y., Ikeda, T., Takamatsu M., Kiso Y., Shibata H., Fushiki T. & Moritani T. Influence of caffeine ingestion on autonomic nervous activity during endurance exercise in humans. Eur J Appl Physiol. 2002; 87(6): 475-480.
16. Okita K., Nishijima H., Murakami T., Nagai T., Morita N., Yonezawa K., Iizuka K., Kawaguchi H. & Kitabatake A. Can exercise training with weight loss lower serum C-reactive protein levels? Arterioscler Thromb Vasc Biol. 2004; 24: 1868-1873.
Submitted: 03.08.2018
17. Pasman W. J., Westerterp-Plantenga M. S. & Saris W. H. M. The effectiveness of long-term supplementation of carbohydrate, chromium, fibre and caffeine on weight maintenance. Int J Obes. 1997; 21: 1143-1151.
18. Ping W. C., Keong C. C. & Bandyopadhyay A. Effect of acute supplementation of caffeine on cardiorespiratory responses during endurance running in a hot and humid climate. Indian J. Med. Res. 2010; 132: 36 - 41.
19. Racette S. B., Schoeller D. A., Kushner R. F. & Neil K.M. Exercise enhances dietary compliance during moderate energy restriction in obese women. Am J Clin Nutr. 1995; 62: 345-349.
20. Spriet L. L., MacLean D. A., Dyck D. J., Hultman E., Cederblad G. & Graham T. E. Caffeine ingestion and muscle metabolism during prolonged exercise in humans. Am J Physiol. 1992; 262: E891-E898.
21. Stuart G. R., Hopkins W. G., Cook C. & Cairns S. P. Multiple effects of caffeine on stimulated high-intensity team-sport performance. Med Sci Sports Exerc. 2005; 37(11): 1998 - 2005.
22. Van Soeren M. H. & Graham T. E. (1998). Effect of caffeine on metabolism, exercise endurance, and catecholamine responses after withdrawal. J Appl Physiol. 1998; 85: 1493-1501.
23. Wallman K. E., Goh J. W. & Guelfi K. J. Effects of caffeine on exercise performance in sedentary females. J Sports Sci Med. 2010; 9: 183-189.
24. World Health Organization. Obesity: preventing and managing the global epidemic. Report of a WHO consultation. World Health Organ Tech Rep Ser 894: i-xii. 2000: 1-253.
25. Kuznetsova Z., Kuznetsov A., Mutaeva I., Khalikov G., Zakharova A., 2015. Athletes training based on a complex assessment of functional state. In Proceedings of the 3rd International Congress on Sport Sciences Research and Technology support. SCITEPRESS. P. 156-160 (Scopus).
26. Kuznetsov A., Mutaeva I., Kuznetsova Z., 2017. Diagnostics of Functional State and Reserve Capacity of young Athletes' Organism. In Proceedings of the 5th International Congress on Sport Sciences Research and Technology support. SCITEPRESS. P. 111-115 (Scopus).
Chee Keong Chen - Sports Science Unit, School of Medical Sciences, Universiti Sains Malaysia, 16150, Kubang Kerian, Kelantan, Malaysia, ckchen@ usm.my, Exercise and Sports Science Programme, School of Health Sciences, Universiti Sains Malaysia, 16150, Kubang Kerian, Kelantan, Malaysia
Mohd Afieq Mohd Rosli - Exercise and Sports Science Programme, School of Health Sciences, Universiti Sains Malaysia, 16150, Kubang Kerian, Kelantan, Malaysia
