Abstract
Background:
High intensity interval training (HIIT) and circuit resistance training (CRT) have been introduced as useful strategies for weight management in overweight and obese individuals. However, little is known about their effects on inducing anti-inflammatory cytokine response, and improving body composition and metabolic profile (lipid profile and insulin resistance index (HOMA-IR)) in overweight adolescents.Objectives:
This study aimed at examining the effects of HIIT and CRT on serum levels of interleukin-10 (IL-10), lipid profile, body composition and insulin resistance index (HOMA-IR) in overweight male adolescents.Methods:
Twenty overweight male adolescents were divided into two groups of HIIT and CRT. The blood samples were drawn from all participants before the beginning of exercise protocols and after one day the last session of the exercise protocols.Results:
Following 6 weeks of both HIIT and CRT protocols, serum levels of IL-10 increased insignificantly in both groups (P > 0.05). However, that of IL-10 showed a much more increase in HIIT group. Furthermore, unlike CRT protocol, six weeks of HIIT improved body composition, lipid profile and HOMA-IR in overweight male adolescents.Conclusions:
By this study, it seems that HIIT has more potent impact than CRT on inducing an anti-inflammatory cytokine response. Moreover, HIIT is a more appropriate exercise modality than CRT to improve body composition and metabolic profile (lipid profile and HOMA-IR) in overweight male adolescents.Keywords
HIIT CRT Obesity Interleukin-10 Metabolic Profile Body Composition Adolescents
1. Background
The outbreak of overweight and obesity among adolescents is a global challenge (1). Obesity-induced systemic low-grade inflammation is characterized by the alterations of circulating concentrations of pro- and anti-inflammatory cytokines (2). Interleukin-10 (IL-10), a powerful anti-inflammatory peptide, plays a beneficial role in human metabolism (3) and insulin sensitivity (4). In the condition of obesity, the number of cells secreting interleukin-10 is decreased; consequently, resulting in the decreased circulating levels of IL-10. Such alterations in cytokine secretion are thought to cause a systemic low grade inflammation contributing to the increase of insulin resistance and metabolic syndrome (5). It has been proved that weight-loss exercise programs are accompanied by increased circulating levels of IL-10 in obese individuals; thereby creating improved metabolic disorders (3). Physical activity is recommended for the management of overweight among adolescents (6), and its anti-inflammatory effects on a regular basis are well demonstrated (7). Basically, aerobic workouts are used for overweight and obese adolescents (8-10); nonetheless, high-intensity interval training (HIIT) (11-14) and resistance training (RT) (15-19) also offer a number of physical health-related benefits such as reducing fatness, improved blood glucose, insulin sensitivity, lipid profile, and improved body composition, which are recommended for the weight management of overweight/obese population (14, 20). However, there is a paucity of information on the efficacy of both HIIT and CRT in inducing an anti-inflammatory cytokine response, and in improving metabolic health profile (lipid profile and HOMA-IR) and body composition in overweight male adolescents. Hence, this study was designed to evaluate the anti-inflammatory cytokine response, and to evaluate the metabolic profile and body composition in overweight male adolescents subjected to HIIT and CRT.
2. Methods
2.1. Study Design
Twenty overweight sedentary male adolescents participated voluntarily in this trial. All of the participants were high school students with the 17-19 age range and the body mass index (BMI) range of 25-30 kg/m2. Subjects were equally and randomly assigned into two groups of HIIT (N = 10) and CRT (N = 10). The percentage of the body fat was also calculated using Caliper (Lafayette made in America) and Jackson and Pollack’s three points formula (21) by measuring the subcutaneous fat of three muscles (triceps brachii, abdomen, and thigh). Body weight, BMI, and body fat percent of each group at baseline are depicted in Table 1.
Exercises | %1RM | Numbers of Repetitions | Length of Each Exercise, s |
---|---|---|---|
Chest press (free weights) | 60 | 8 - 12 | 30 |
Leg press (machine) | 60 | 8 - 12 | 30 |
Shoulder press (free weights) | 60 | 8 - 12 | 30 |
Seated rows (machine) | 60 | 8 - 12 | 30 |
Leg extension (machine) | 60 | 8 - 12 | 30 |
Triceps extension (machine) | 60 | 8 - 12 | 30 |
Leg curl (machine) | 60 | 8 - 12 | 30 |
Biceps curl (machine) | 60 | 8 - 12 | 30 |
2.2. HIIT Protocol
Participants in the HIIT group performed a sprint interval training (SIT) three times a week for six weeks. This protocol, also known as a shuttle-run test, was carried out in a gym. Each participant performed a 20-meters sprint for 30 seconds (Figure 1). Three cones were placed 10 meters apart. Each participant was required to sprint from the middle cone to the first cone, turning and sprinting in the reverse direction to the second cone, turning and sprinting again through the middle cone. After 30 seconds rest, the participants repeated this method for other 3 times. The overload principle was applied by increasing the number of repeats from four frequencies during weeks 1 and 2 to 5 frequencies during weeks 3 and 4 to 6 frequencies during weeks 5 and 6. Heart rate (HR) response was measured in all participants after completing each repetition via the use of heart rate monitor watch (Beurer, PM80, Germany) with a belt connected to the subject’s chest. Throughout the training protocol, the HIIT intensity was considered above 90% of peak heart rate and calculated by Karvonen formula. The peak heart rate was calculated by the equation, HRmax= 207 - 0.7 × age (y).
Course outline showing distance and direction taken by the participants during the 30-s HIIT protocol. A = 10 m, B = 20 m, C = 10 m.
2.3. CRT Protocol
Participants in the RT group performed nine different exercises targeting the principal muscles. The exercises consisted of chest press, leg press, shoulder press, seated rows, leg extension, triceps extension, leg curl, biceps curl, and sit-up (Table 1). Each exercise included 8 - 12 frequencies at the workload of 60% of the subject's one repetition maximum (1 RM). The subjects underwent training for 6 weeks, 3 sessions per week. Each session consisted of three circuits and in each circuit 9 movements, previously mentioned were done one after another. The duration of each movement was 30 seconds (8 - 12 repeats), the duration of resting between two consecutive movements was 30 seconds, and the duration of resting between the two circuits was considered to be 120 seconds. Each session took a total time of 50 - 55 minutes. The principle of overload was designed after each four weeks of training. In this study, the Brzycki formula was used to calculate the 1RM (22).
Blood samples were drawn from all participants one day before the start of protocols and one day after the last session of the exercise protocols. The volume of each blood sample was 10 mL of the whole blood that was centrifuged at 3,000 rpm for 8 minutes at 4°C to separate the serum, and then stored at -80°C for future analysis. Analysis of IL-10 was performed by Enzyme immunoassay ELISA (enzyme-linked immunosorbent assay). The analysis of IL-10 (Cat No. 950.060.096, Diaclone, France) concentrations was performed using the kits purchased from Diaclone Company with the minimum detectable concentration of 4.9 pg/mL. The intra-assay and inter-assay variations were 3.5% and 7.5%, respectively. Analysis of insulin concentrations was performed by ELISA kit (Monobind Inc., Lake Forest, CA, USA) with a sensitivity of 0.75 µlU/mL, and intra-assay variability was 4.3% to 8.3%. Serum concentrations of total cholesterol (TC) high-density lipoprotein (HDL), low-density lipoprotein (LDL), triglycerides (TG), and glucose were measured by photometric method (Pars Azmun Company Kits, Iran). Insulin resistance index (IRI) was calculated using the homeostasis model assessment (HOMA). IRI = (fasting insulin [µU/mL] × fasting glucose [mmol/L])/22.5 (23).
The normality of the data was assessed by the Kolmogorov-Smirnov test. The paired t-test was applied for determining the possible changes in each group after 6 weeks of exercise interventions. Moreover, the independent t-test was used to verify possible differences between pre-training, as well as the magnitude of the variations (Δ) after training among the two groups. The SPSS version
16.0 was used to analyze the data and the significance level was considered < 5%.
3. Results
The pre-training and post-training values of the body weight, BMI, and body fat percent for each group are presented in Table 2. The HIIT significantly reduced body mass, BMI, and body fat percent of the participants; however, the RT increased the body weight, BMI, while reduced body fat percent insignificantly. The changes of the body weight and BMI were only significant between the groups. Serum concentrations of IL-10, lipid profile, insulin, and glucose are presented in Table 3. Serum concentrations of IL-10 were insignificantly increased in both groups; however, the concentration of IL-10 showed a more tendency to increase after HIIT (P = 0.060) than CRT (P = 0.60). There was no significant difference in the serum concentrations of IL-10 between the groups. The HIIT protocol significantly increased the serum concentration of HDL-C and decreased significantly serum concentrations of LDL-C, total cholesterol (TC), triglyceride (TG) in contrast to the RT protocol that had no effect on lipid profile of adolescent overweight boys. There were significant differences in terms of HDL-C, TC, and TC between the groups. The HIIT group, in contrast to the RT group, promoted significant changes in insulin resistance index in which the fasting serum concentration of glucose and insulin were significantly decreased. Furthermore, there were significant differences in terms of serum concentration of glucose and homeostasis model assessment of insulin resistance (HOMA-IR) between the groups.
Anthropometric Characteristic of the Subjects in Each Group Before and After 6 Weeks of Exercise Interventionsa
Variables/Group | Pre-Test | Pre-Test | ∆b | P Valuec |
---|---|---|---|---|
BW, kg | ||||
CRT | 82.27 ± 4.06 | 83.10 ± 4.14 | 0.83 ± 0.25 | 0.071 |
HIIT | 82.70 ± 3.6 | 80.40 ± 3.6d | -2.3 ± 0.4e | 0.001 |
P valuef | 0.418 | 0.659 | 0.001 | - |
BMI, kg/m2 | ||||
CRT | 27.89 ± 0.73 | 28.56 ± 0.72 | 0.67 ± 0.1 | 0.117 |
HIIT | 27.80 ± 1 | 26.50 ± 1d | -1.3 ± 0.1e | 0.000 |
P valuef | 0.778 | 0.535 | 0.021 | - |
BFP, % | ||||
CRT | 22.56 ± 2.54 | 21.56 ± 2.53 | -1 ± 0.008 | 0.096 |
HIIT | 22.5 ± 3 | 21.3 ± 3d | -1.2 ± 0.01 | 0.001 |
P valuef | 0.987 | 0.977 | 0.516 | - |
Serum Variables, the Calculation of Homeostasis Model, and the Assessment of Insulin Resistance in Each Groupa
Variables/Group | Pre-Test | Post-Test | ∆b | P Valuec |
---|---|---|---|---|
IL-10, pg/mL | ||||
CRT | 5.8 ± 1.38 | 5.9 ± 1.79 | 0.1 ± 0.67 | 0.60 |
HIIT | 5.04 ± 1.07 | 5.7 ± 1.26 | 0.7 ± 0.98 | 0.06 |
P valued | 0.168 | 0.731 | 0.16 | |
HDL, mg/dL | ||||
CRT | 39.5 ± 5.5 | 41.3 ± 7.40 | 1.8 ± 4.78 | 0.264 |
HIIT | 41.9 ± 5.91 | 48.9 ± 7.68e | 7 ± 4.05f | 0.000 |
P valued | 0.360 | 0.037 | 0.017 | |
LDL, mg/dL | ||||
CRT | 122.2 ± 24.09 | 119.7 ± 24.48 | -2.5 ± 13.45 | 0.571 |
HIIT | 140.7 ± 30.7 | 127.3 ± 27.33e | -13.4 ± 9.98 | 0.002 |
P valued | 0.152 | 0.521 | 0.056 | |
TC, mg/dL | ||||
CRT | 163.2 ± 28.42 | 162.2 ± 31.45 | -1 ± 11.47 | 0.789 |
HIIT | 172.4 ± 22.07 | 157.1 ± 19.95e | -15.30 ± 14.22f | 0.008 |
P valued | 0.430 | 0.671 | 0.024 | |
Glucose, mg/dL | ||||
CRT | 87.10 ± 6.08 | 88.60 ± 6.38 | 1.5 ± 4.62 | 0.332 |
HIIT | 89 ± 5.41 | 85.7 ± 6.63e | -3.3 ± 4.6f | 0.049 |
P valued | 0.470 | 0.332 | 0.032 | |
Insulin, µL U/mL | ||||
CRT | 7.75 ± 4.63 | 7.76 ± 4.46 | 0.019 ± 0.90 | 0.948 |
HIIT | 7.72 ± 4.0 | 6.96 ± 4.16e | -0.76 ± 0.96 | 0.034 |
P valued | 0.989 | 0.681 | 0.079 | |
HOMA-IR | ||||
CRT | 1.64 ± 0.93 | 1.67 ± 0.91 | 0.033 ± 0.21 | 0.632 |
HIIT | 1.68 ± 0.86 | 1.45 ± 0.86e | -0.22 ± 0.25f | 0.022 |
P valued | 0.926 | 0.587 | 0.025 |
4. Discussion
Our study demonstrated that (a) HIIT had more effect on inducing an anti-inflammatory cytokine response via increasing the basal serum levels of IL-10 to a greater extent than CRT, and (b) HIIT is superior to CRT in improving body composition, lipid profile and insulin resistance index in overweight male adolescents. The present investigation failed to find a significant change in resting circulating level of IL-10 following 6 weeks of HIIT in overweight male adolescents. Two studies of Leggate et al. (24) and Kelly et al. (25) showed that a 2-week HIIT did not change the circulating levels of IL-10 in the overweight/obese males. Moreover, Zwetsloot et al. (26) showed that two weeks of HIIT did not make any difference in the resting circulating levels of IL-10 in recreationally active young males. However, we observed a considerable increase in the circulating level of IL-10 (+0.4 ± 0.87Δ, P = 0.060) in response to HIIT after six weeks of training in overweight adolescents.
The reasons for these discrepancies can be due to the type, duration and intensity of HIIT protocols, and also the subjects involved in the trials. The studies addressing the anti-inflammatory response to HIIT in overweight/obese population is scarce that warrants more researches should be carried out to understand the mechanisms by which HIIT stimulates an anti-inflammatory response in the overweight/obese population. Similar to the HIIT group, six weeks of CRT did not change the resting serum level of IL-10 in overweight male adolescents with the difference that HIIT produced more considerable changes in the resting serum level of IL-10 in overweight male adolescents. A study using a 10-week RT protocol showed no change in the resting circulating level of IL-10 in sedentary females (27). However, it is concluded that 12 weeks of RT improves resting circulatory levels of IL-10 in obese women (28). Two studies have claimed that exercise intensity has a profound effect on the inflammatory response, resulting in higher anti-inflammatory cytokine responses (29, 30). However, the intensity of workloads in our protocol was considered moderate and fixed. Therefore, it is likely that the intensity used in our protocol is one of the determining factors for not inducing an anti-inflammatory response in the overweight adolescent cohort. Another variable that should be considered is the duration of the protocol. A longer period of training would probably allow further physiological adaptations that might show more robust effects on cytokine responses. The beneficial anti-inflammatory effect of RT has not been consistent between all studies. The mixed findings of the effects of RT could be due to a large number of utilized training protocols (31-33). The mode, intensity, and duration of exercise can be modified and all these factors have been shown to affect the response in terms of inflammatory markers (32). We also observed an improved body composition, lipid profile, and insulin resistance index (HOMA-1IR) in response to HIIT in overweight male adolescents. Contrary to the present findings, the results of a meta-analysis study (34) suggest that short term HIIT (< 12 weeks) has no effect on the body weight, percent of body fat, fasting insulin, lipid profile, and fasting insulin, but reduces fasting glucose by a small effect on overweight/obese populations. The reasons for this contradiction may be due to the baseline activity level (recreationally active), age conditions (≥ 18 years) and gender (female) of the overweight population investigated in the aforementioned meta-analysis study, whereas the subjects participating in our study were sedentary overweight adolescents ranging from 16 to 19 years. However, there are some studies showing the efficacy of the HIIT among the protocols in improving the body composition (10, 35, 36), lipid profile (13, 36, 37), and HOMA-IR (10, 38, 39) in healthy, overweight, and obese adolescents (36, 37) included 30-s sprints interspersed with 30-s rest bouts are of effective protocols to improve metabolic profile. Further studies are needed to be done to support these findings in overweight male adolescents. Contrarily, 6 weeks of resistance training did not improve the body composition, lipids profile, and insulin resistance condition in overweight male adolescents. There are few trials with conflicting results examining the effects of resistance exercise training on the body composition in overweight and obese adolescents (18, 40-43). Some studies have shown decreases (18), whereas others reported no difference (40) or increases (41) in the body fat percent of obese adolescents following a resistance exercise training program. Shaibi et al. study (18) showed that resistance training decreased significantly the body fat percentage of male adolescents. However, Davis et al. study (41) revealed no change in the body composition after 16 weeks of strength training. Benson et al. observed that 8 weeks of high-intensity resistance exercise training induced useful results in overweight/obese adolescents (43). When designing the resistance training, the intensity of a workout is essential as the higher intensity of resistance exercise training would also be beneficial in overweight/obese adolescents (44). The intensity applied to our resistance protocol was considered fix and moderate (60% 1RM), which may be one of the factors contributing to the achieved results. Besides the exercise intensity, the protocol duration (6 weeks) and the small numbers of subjects (n = 10) could be the other factors affecting the achieved results. Another variable analyzed was HOMA-IR. Our study showed that 6 weeks of circuit resistance training did not decrease fasting serum glucose and insulin in overweight male adolescents. A meta-analysis study emphasizes the efficacy of exercise in reducing fasting insulin and improving insulin resistance in adolescents (45). Moreover, van der Heijden et al. found that 12 weeks of resistance training in obese Hispanic adolescents induced an increase in hepatic insulin sensitivity (9). Shaibi et al. study (18) showed that 16 weeks of resistance training significantly increased insulin sensitivity in overweight or obese male adolescents. Another variable analyzed was lipid profile. In this study, a 6-weeks resistance training program did not improve lipid profile in sedentary overweight male adolescents. Results of other studies indicate that regular exercise decreases lipid profile (46, 47). However, some studies did not find any changes in lipids within overweight/obese adolescents (42, 43, 48). Altogether, six weeks of moderate intensity resistance training had no effect on anthropometric parameters and metabolic health in overweight male adolescents.
4.1. Conclusions
In conclusion, it seems that HIIT has more potent impact than CRT on inducing an anti-inflammatory cytokine response. Moreover, HIIT is a more appropriate exercise modality than CRT to improve body composition and metabolic profile (lipid profile and HOMA-IR) in overweight male adolescents. More studies are needed to support these findings in overweight adolescents' cohort.
References
-
1.
Ogden CL, Carroll MD, Kit BK, Flegal KM. Prevalence of childhood and adult obesity in the United States, 2011-2012. JAMA. 2014;311(8):806-14. [PubMed ID: 24570244]. [PubMed Central ID: PMC4770258]. https://doi.org/10.1001/jama.2014.732.
-
2.
Bruunsgaard H. Physical activity and modulation of systemic low-level inflammation. J Leukoc Biol. 2005;78(4):819-35. [PubMed ID: 16033812]. https://doi.org/10.1189/jlb.0505247.
-
3.
Agha Alinejad H, Molanouri SM. [Exercise induced release of cytokines from skeletal muscle: Emphasis on IL-6]. Iran J Endocrinol Metab. 2010;12(2):181-90. Persian.
-
4.
Cintra DE, Pauli JR, Araujo EP, Moraes JC, de Souza CT, Milanski M, et al. Interleukin-10 is a protective factor against diet-induced insulin resistance in liver. J Hepatol. 2008;48(4):628-37. [PubMed ID: 18267346]. https://doi.org/10.1016/j.jhep.2007.12.017.
-
5.
Wisse BE. The inflammatory syndrome: The role of adipose tissue cytokines in metabolic disorders linked to obesity. J Am Soc Nephrol. 2004;15(11):2792-800. [PubMed ID: 15504932]. https://doi.org/10.1097/01.ASN.0000141966.69934.21.
-
6.
Lipnowski S, Leblanc CM, Canadian Paediatric Society HAL, Sports Medicine C. Healthy active living: Physical activity guidelines for children and adolescents. Paediatr Child Health. 2012;17(4):209-12. [PubMed ID: 23543633]. [PubMed Central ID: PMC3381667]. https://doi.org/10.1093/pch/17.4.209.
-
7.
Beavers KM, Brinkley TE, Nicklas BJ. Effect of exercise training on chronic inflammation. Clin Chim Acta. 2010;411(11-12):785-93. [PubMed ID: 20188719]. [PubMed Central ID: PMC3629815]. https://doi.org/10.1016/j.cca.2010.02.069.
-
8.
Nassis GP, Papantakou K, Skenderi K, Triandafillopoulou M, Kavouras SA, Yannakoulia M, et al. Aerobic exercise training improves insulin sensitivity without changes in body weight, body fat, adiponectin, and inflammatory markers in overweight and obese girls. Metabolism. 2005;54(11):1472-9. [PubMed ID: 16253636]. https://doi.org/10.1016/j.metabol.2005.05.013.
-
9.
van der Heijden GJ, Wang ZJ, Chu ZD, Sauer PJ, Haymond MW, Rodriguez LM, et al. A 12-week aerobic exercise program reduces hepatic fat accumulation and insulin resistance in obese, Hispanic adolescents. Obesity (Silver Spring). 2010;18(2):384-90. [PubMed ID: 19696755]. https://doi.org/10.1038/oby.2009.274.
-
10.
Tjonna AE, Stolen TO, Bye A, Volden M, Slordahl SA, Odegard R, et al. Aerobic interval training reduces cardiovascular risk factors more than a multitreatment approach in overweight adolescents. Clin Sci (Lond). 2009;116(4):317-26. [PubMed ID: 18673303]. https://doi.org/10.1042/CS20080249.
-
11.
Talanian JL, Galloway SD, Heigenhauser GJ, Bonen A, Spriet LL. Two weeks of high-intensity aerobic interval training increases the capacity for fat oxidation during exercise in women. J Appl Physiol (1985). 2007;102(4):1439-47. [PubMed ID: 17170203]. https://doi.org/10.1152/japplphysiol.01098.2006.
-
12.
Cornish AK, Broadbent S, Cheema BS. Interval training for patients with coronary artery disease: A systematic review. Eur J Appl Physiol. 2011;111(4):579-89. [PubMed ID: 20972578]. https://doi.org/10.1007/s00421-010-1682-5.
-
13.
Little JP, Gillen JB, Percival ME, Safdar A, Tarnopolsky MA, Punthakee Z, et al. Low-volume high-intensity interval training reduces hyperglycemia and increases muscle mitochondrial capacity in patients with type 2 diabetes. J Appl Physiol (1985). 2011;111(6):1554-60. [PubMed ID: 21868679]. https://doi.org/10.1152/japplphysiol.00921.2011.
-
14.
Boutcher SH. High-intensity intermittent exercise and fat loss. J Obes. 2011;2011:868305. [PubMed ID: 21113312]. [PubMed Central ID: PMC2991639]. https://doi.org/10.1155/2011/868305.
-
15.
Bell LM, Watts K, Siafarikas A, Thompson A, Ratnam N, Bulsara M, et al. Exercise alone reduces insulin resistance in obese children independently of changes in body composition. J Clin Endocrinol Metab. 2007;92(11):4230-5. [PubMed ID: 17698905]. https://doi.org/10.1210/jc.2007-0779.
-
16.
Lau PWC, Kong Z, Choi CR, Yu CCW, Chan DFY, Sung RYT, et al. Effects of short-term resistance training on serum leptin levels in obese adolescents. Journal of Exercise Science & Fitness. 2010;8(1):54-60. https://doi.org/10.1016/s1728-869x(10)60008-1.
-
17.
McGuigan MR, Tatasciore M, Newton RU, Pettigrew S. Eight weeks of resistance training can significantly alter body composition in children who are overweight or obese. J Strength Cond Res. 2009;23(1):80-5. [PubMed ID: 19130639]. https://doi.org/10.1519/JSC.0b013e3181876a56.
-
18.
Shaibi GQ, Cruz ML, Ball GD, Weigensberg MJ, Salem GJ, Crespo NC, et al. Effects of resistance training on insulin sensitivity in overweight Latino adolescent males. Med Sci Sports Exerc. 2006;38(7):1208-15. [PubMed ID: 16826016]. https://doi.org/10.1249/01.mss.0000227304.88406.0f.
-
19.
Lee S, Bacha F, Hannon T, Kuk JL, Boesch C, Arslanian S. Effects of aerobic versus resistance exercise without caloric restriction on abdominal fat, intrahepatic lipid, and insulin sensitivity in obese adolescent boys: A randomized, controlled trial. Diabetes. 2012;61(11):2787-95. [PubMed ID: 22751691]. [PubMed Central ID: PMC3478522]. https://doi.org/10.2337/db12-0214.
-
20.
Thomas GA, Kraemer WJ, Comstock BA, Dunn-Lewis C, Volek JS, Denegar CR, et al. Effects of resistance exercise and obesity level on ghrelin and cortisol in men. Metabolism. 2012;61(6):860-8. [PubMed ID: 22146097]. https://doi.org/10.1016/j.metabol.2011.10.015.
-
21.
Lohman TG. Advances in body composition assessment. Champaign, Ill: Human Kinetics Publishers; 1992.
-
22.
Nascimento MA, Cyrino ES, Nakamura FY, Romanzini M, Pianca HJC, Queiróga MR. Validation of the Brzycki equation for the estimation of 1-RM in the bench press. Revi Brasi Med Esp. 2007;13(1):47-50. https://doi.org/10.1590/s1517-86922007000100011.
-
23.
Wallace TM, Levy JC, Matthews DR. Use and abuse of HOMA modeling. Diabetes Care. 2004;27(6):1487-95. [PubMed ID: 15161807]. https://doi.org/10.2337/diacare.27.6.1487.
-
24.
Leggate M, Carter WG, Evans MJ, Vennard RA, Sribala-Sundaram S, Nimmo MA. Determination of inflammatory and prominent proteomic changes in plasma and adipose tissue after high-intensity intermittent training in overweight and obese males. J Appl Physiol (1985). 2012;112(8):1353-60. [PubMed ID: 22267387]. [PubMed Central ID: PMC3331586]. https://doi.org/10.1152/japplphysiol.01080.2011.
-
25.
Kelly BM, Xenophontos S, King JA, Nimmo MA. An evaluation of low volume high-intensity intermittent training (HIIT) for health risk reduction in overweight and obese men. BMC Obes. 2017;4:17. [PubMed ID: 28435687]. [PubMed Central ID: PMC5395873]. https://doi.org/10.1186/s40608-017-0151-7.
-
26.
Zwetsloot KA, John CS, Lawrence MM, Battista RA, Shanely RA. High-intensity interval training induces a modest systemic inflammatory response in active, young men. J Inflamm Res. 2014;7:9-17. [PubMed ID: 24520199]. [PubMed Central ID: PMC3920540]. https://doi.org/10.2147/JIR.S54721.
-
27.
Ferreira FC, de Medeiros AI, Nicioli C, Nunes JE, Shiguemoto GE, Prestes J, et al. Circuit resistance training in sedentary women: body composition and serum cytokine levels. Appl Physiol Nutr Metab. 2010;35(2):163-71. [PubMed ID: 20383226]. https://doi.org/10.1139/H09-136.
-
28.
Phillips MD, Patrizi RM, Cheek DJ, Wooten JS, Barbee JJ, Mitchell JB. Resistance training reduces subclinical inflammation in obese, postmenopausal women. Med Sci Sports Exerc. 2012;44(11):2099-110. [PubMed ID: 22874536]. https://doi.org/10.1249/MSS.0b013e3182644984.
-
29.
Peake JM, Suzuki K, Hordern M, Wilson G, Nosaka K, Coombes JS. Plasma cytokine changes in relation to exercise intensity and muscle damage. Eur J Appl Physiol. 2005;95(5-6):514-21. [PubMed ID: 16151834]. https://doi.org/10.1007/s00421-005-0035-2.
-
30.
Izquierdo M, Ibanez J, Calbet JA, Navarro-Amezqueta I, Gonzalez-Izal M, Idoate F, et al. Cytokine and hormone responses to resistance training. Eur J Appl Physiol. 2009;107(4):397-409. [PubMed ID: 19649649]. https://doi.org/10.1007/s00421-009-1139-x.
-
31.
Ara I, Perez-Gomez J, Vicente-Rodriguez G, Chavarren J, Dorado C, Calbet JA. Serum free testosterone, leptin and soluble leptin receptor changes in a 6-week strength-training programme. Br J Nutr. 2006;96(6):1053-9. [PubMed ID: 17181880]. https://doi.org/10.1017/BJN20061956.
-
32.
Libardi CA, De Souza GV, Cavaglieri CR, Madruga VA, Chacon-Mikahil MP. Effect of resistance, endurance, and concurrent training on TNF-alpha, IL-6, and CRP. Med Sci Sports Exerc. 2012;44(1):50-6. [PubMed ID: 21697747]. https://doi.org/10.1249/MSS.0b013e318229d2e9.
-
33.
Rall LC, Roubenoff R, Cannon JG, Abad LW, Dinarello CA, Meydani SN. Effects of progressive resistance training on immune response in aging and chronic inflammation. Med Sci Sports Exerc. 1996;28(11):1356-65. [PubMed ID: 8933485]. https://doi.org/10.1097/00005768-199611000-00003.
-
34.
Batacan RB Jr, Duncan MJ, Dalbo VJ, Tucker PS, Fenning AS. Effects of high-intensity interval training on cardiometabolic health: A systematic review and meta-analysis of intervention studies. Br J Sports Med. 2017;51(6):494-503. [PubMed ID: 27797726]. https://doi.org/10.1136/bjsports-2015-095841.
-
35.
Baquet G, Berthoin S, Gerbeaux M, Van Praagh E. High-intensity aerobic training during a 10 week one-hour physical education cycle: effects on physical fitness of adolescents aged 11 to 16. Int J Sports Med. 2001;22(4):295-300. [PubMed ID: 11414674]. https://doi.org/10.1055/s-2001-14343.
-
36.
Buchan DS, Ollis S, Young JD, Thomas NE, Cooper SM, Tong TK, et al. The effects of time and intensity of exercise on novel and established markers of CVD in adolescent youth. Am J Hum Biol. 2011;23(4):517-26. [PubMed ID: 21465614]. https://doi.org/10.1002/ajhb.21166.
-
37.
Buchan DS, Ollis S, Young JD, Cooper SM, Shield JP, Baker JS. High intensity interval running enhances measures of physical fitness but not metabolic measures of cardiovascular disease risk in healthy adolescents. BMC Public Health. 2013;13:498. [PubMed ID: 23705968]. [PubMed Central ID: PMC3666892]. https://doi.org/10.1186/1471-2458-13-498.
-
38.
Corte de Araujo AC, Roschel H, Picanco AR, do Prado DM, Villares SM, de Sa Pinto AL, et al. Similar health benefits of endurance and high-intensity interval training in obese children. PLoS One. 2012;7(8). e42747. [PubMed ID: 22880097]. [PubMed Central ID: PMC3412799]. https://doi.org/10.1371/journal.pone.0042747.
-
39.
Racil G, Ben Ounis O, Hammouda O, Kallel A, Zouhal H, Chamari K, et al. Effects of high vs. moderate exercise intensity during interval training on lipids and adiponectin levels in obese young females. Eur J Appl Physiol. 2013;113(10):2531-40. [PubMed ID: 23824463]. https://doi.org/10.1007/s00421-013-2689-5.
-
40.
Davis JN, Kelly LA, Lane CJ, Ventura EE, Byrd-Williams CE, Alexandar KA, et al. Randomized control trial to improve adiposity and insulin resistance in overweight Latino adolescents. Obesity (Silver Spring). 2009;17(8):1542-8. [PubMed ID: 19247280]. [PubMed Central ID: PMC2846423]. https://doi.org/10.1038/oby.2009.19.
-
41.
Davis JN, Tung A, Chak SS, Ventura EE, Byrd-Williams CE, Alexander KE, et al. Aerobic and strength training reduces adiposity in overweight Latina adolescents. Med Sci Sports Exerc. 2009;41(7):1494-503. [PubMed ID: 19516150]. [PubMed Central ID: PMC2836768]. https://doi.org/10.1249/MSS.0b013e31819b6aea.
-
42.
Lau PW, Yu CW, Lee A, Sung RY. The physiological and psychological effects of resistance training on Chinese obese adolescents. J Exerc Sci Fitness. 2004;2(2):115-20.
-
43.
Benson AC, Torode ME, Fiatarone Singh MA. The effect of high-intensity progressive resistance training on adiposity in children: A randomized controlled trial. Int J Obes (Lond). 2008;32(6):1016-27. [PubMed ID: 18283282]. https://doi.org/10.1038/ijo.2008.5.
-
44.
Alberga AS, Sigal RJ, Kenny GP. A review of resistance exercise training in obese adolescents. Phys Sportsmed. 2011;39(2):50-63. [PubMed ID: 21673485]. https://doi.org/10.3810/psm.2011.05.1895.
-
45.
Fedewa MV, Gist NH, Evans EM, Dishman RK. Exercise and insulin resistance in youth: A meta-analysis. Pediatrics. 2014;133(1):e163-74. [PubMed ID: 24298011]. https://doi.org/10.1542/peds.2013-2718.
-
46.
Bouchard C, Shephard RJ, Stephens T, Sutton JR, McPherson BD. Exercise, fitness, and health: the consensus statement. Exercise, fitness, and health: a consensus of current knowledge: proceedings of the International Conference on Exercise, fitness and health, May 29-June 3, 1988. Toronto, Canada. Human Kinetics Publishers; 1990. p. 3-28.
-
47.
Balas-Nakash M, Benitez-Arciniega A, Perichart-Perera O, Valdes-Ramos R, Vadillo-Ortega F. The effect of exercise on cardiovascular risk markers in Mexican school-aged children: comparison between two structured group routines. Salud Publica Mex. 2010;52(5):398-405. [PubMed ID: 21031246]. https://doi.org/10.1590/S0036-36342010000500007.
-
48.
Watts K, Beye P, Siafarikas A, Davis EA, Jones TW, O'Driscoll G, et al. Exercise training normalizes vascular dysfunction and improves central adiposity in obese adolescents. J Am Coll Cardiol. 2004;43(10):1823-7. [PubMed ID: 15145107]. https://doi.org/10.1016/j.jacc.2004.01.032.