Resting Metabolic Rate Does Not Change in Response to Different Types of Training in Subjects with Type 2 Diabetes

Kristian Karstoft, Cecilie Fau Brinkløv, Ida Kær Thorsen, Jens Steen Nielsen, Mathias Ried-Larsen, Kristian Karstoft, Cecilie Fau Brinkløv, Ida Kær Thorsen, Jens Steen Nielsen, Mathias Ried-Larsen

Abstract

Background and objectives: Ambiguous results have been reported regarding the effects of training on resting metabolic rate (RMR), and the importance of training type and intensity is unclear. Moreover, studies in subjects with type 2 diabetes (T2D) are sparse. In this study, we evaluated the effects of interval and continuous training on RMR in subjects with T2D. Furthermore, we explored the determinants for training-induced alterations in RMR.

Methods: Data from two studies, both including T2D subjects, were encompassed in this manuscript. Study 1 was a randomized, crossover study where subjects (n = 14) completed three, 2-week interventions [control, continuous walking training (CWT), interval-walking training (IWT)] separated by washout periods. Training included 10 supervised treadmill sessions, 60 min/session. CWT was performed at moderate walking speed [aiming for 73% of walking peak oxygen uptake (VO2peak)], while IWT was performed as alternating 3-min repetitions at slow (54% VO2peak) and fast (89% VO2peak) walking speed. Study 2 was a single-arm training intervention study where subjects (n = 23) were prescribed 12 weeks of free-living IWT (at least 3 sessions/week, 30 min/session). Before and after interventions, RMR, physical fitness, body composition, and glycemic control parameters were assessed.

Results: No overall intervention-induced changes in RMR were seen across the studies, but considerable inter-individual differences in RMR changes were seen in Study 2. At baseline, total body mass (TBM), fat-free mass (FFM), and fat mass were all associated with RMR. Changes in RMR were associated with changes in TBM and fat mass, and subjects who decreased body mass and fat mass also decreased their RMR. No associations were seen between changes in physical fitness, glycemic control, or FFM and changes in RMR.

Conclusion: Neither short-term continuous or interval-type training, nor longer term interval training affects RMR in subjects with T2D when no overall changes in body composition are seen. If training occurs concomitant with a reduction in fat mass, however, RMR is decreased.

Clinical trials registration wwwclinicaltrialsgov: NCT02320526 and NCT02089477.

Keywords: body composition; diabetes type 2; exercise interventions; exercise training; glycemic control; physical fitness; resting metabolic rate.

Figures

Figure 1
Figure 1
The effect of training interventions on resting metabolic rate (RMR). Subjects with type 2 diabetes underwent three 2-week interventions (A–C); no training [control (CON)], continuous walking training (CWT), interval-walking training [IWT or 12 weeks of IWT training (D–F)]. RMR was measured before and after interventions and is reported as total RMR (A,D), RMR relative to total body mass [TBM (B,E)] and RMR relative to fat-free mass [FFM (C,F)]. Data are shown as mean ± SEM (A–C) and mean + individual data (D–F). Statistical analyses [two-way repeated-measures ANOVA in Panels (A–C)] and Student’s paired t-test (D–F) did not result in any significant changes within interventions (p > 0.05 for all comparisons).
Figure 2
Figure 2
Baseline associations between resting metabolic rate (RMR) and potential determinants of RMR. Simple regression analyses were performed between baseline values of potential determinants of RMR (x-axis) and baseline RMR (y-axis). The potential determinants were VO2max [absolute, relative to total body mass (TBM), and relative to fat-free mass (FFM) (A–C)], body composition [body mass, FFM, and fat mass (D–F)] and glycemic control [fasting glucose, mean oral glucose tolerance test (OGTT) glucose, and 2 h OGTT glucose (G–I)]. Data from both Study 1 (open circles) and Study 2 (black circles) were included in the regression analyses and results (β-coefficients, r2-, and p-values) are given in each panel.
Figure 3
Figure 3
Associations between delta (post minus pre intervention) values of resting metabolic rate (RMR) and delta values of potential determinants of RMR. Simple regression analyses were performed between delta values of potential determinants of RMR (x-axis) and delta values of RMR (y-axis). The potential determinants were VO2max [absolute, relative to total body mass (TBM) and relative to fat-free mass (FFM) (A–C)], body composition [body mass, FFM and fat mass (D–F)] and glycemic control [fasting glucose, mean oral glucose tolerance test (OGTT) glucose, and 2 h OGTT glucose (G–I)]. Data from Study 2 were included in the regression analyses and results (β-coefficients, r2-, and p-values) are given in each panel.
Figure 4
Figure 4
Stratified analyses of potential determinants for resting metabolic rate (RMR). Subjects included in Study 2 were stratified according to their change in RMR as increased RMR (≥10%, n = 7), unchanged RMR (n = 9), or decreased RMR (≥10%, n = 7). Delta (post minus pre intervention) values ± SEM of potential determinants for RMR {VO2max [absolute, relative to total body mass (TBM), and relative to fat free mass (FFM); panel (A–C)], body composition [body mass, fat free mass, and fat mass; panel (D–F)], and glycemic control [fasting glucose, mean OGTT glucose, and 2 h OGTT glucose; panel (G–I)]} are shown for the different strata. Within-strata changes in potential determinants of RMR were analyzed by two-way (strata × time) repeated-measures (RM) ANOVA (significant changes indicated by an asterisk above the bar) and between-strata differences were analyzed by one-way RM ANOVA of the delta values (significant changes indicated by a connecting line and an asterisk).

References

    1. Lyssenko V, Almgren P, Anevski D, Perfekt R, Lahti K, Nissen M, et al. Predictors of and longitudinal changes in insulin sensitivity and secretion preceding onset of type 2 diabetes. Diabetes (2005) 54:166–74.10.2337/diabetes.54.1.166
    1. Goldstein DJ. Beneficial health effects of modest weight loss. Int J Obes Relat Metab Disord (1992) 16:397–415.
    1. 7. Obesity management for the treatment of type 2 diabetes. Diabetes Care (2017) 40:S57–63.10.2337/dc17-S010
    1. Ravussin E, Lillioja S, Anderson TE, Christin L, Bogardus C. Determinants of 24-hour energy expenditure in man. Methods and results using a respiratory chamber. J Clin Invest (1986) 78:1568–78.10.1172/JCI112749
    1. Caron N, Peyrot N, Caderby T, Verkindt C, Dalleau G. Energy expenditure in people with diabetes mellitus: a review. Front Nutr (2016) 3:56.10.3389/fnut.2016.00056
    1. Borsheim E, Bahr R. Effect of exercise intensity, duration and mode on post-exercise oxygen consumption. Sports Med (2003) 33:1037–60.10.2165/00007256-200333140-00002
    1. Weyer C, Walford RL, Harper IT, Milner M, MacCallum T, Tataranni PA, et al. Energy metabolism after 2 y of energy restriction: the biosphere 2 experiment. Am J Clin Nutr (2000) 72:946–53.
    1. Speakman JR, Selman C. Physical activity and resting metabolic rate. Proc Nutr Soc (2003) 62:621–34.10.1079/PNS2003282
    1. Van Pelt RE, Jones PP, Davy KP, Desouza CA, Tanaka H, Davy BM, et al. Regular exercise and the age-related decline in resting metabolic rate in women. J Clin Endocrinol Metab (1997) 82:3208–12.10.1210/jc.82.10.3208
    1. Tremblay A, Fontaine E, Poehlman ET, Mitchell D, Perron L, Bouchard C. The effect of exercise-training on resting metabolic rate in lean and moderately obese individuals. Int J Obes (1986) 10:511–7.
    1. Sjodin AM, Forslund AH, Westerterp KR, Andersson AB, Forslund JM, Hambraeus LM. The influence of physical activity on BMR. Med Sci Sports Exerc (1996) 28:85–91.10.1097/00005768-199601000-00018
    1. Potteiger JA, Kirk EP, Jacobsen DJ, Donnelly JE. Changes in resting metabolic rate and substrate oxidation after 16 months of exercise training in overweight adults. Int J Sport Nutr Exerc Metab (2008) 18:79–95.10.1123/ijsnem.18.1.79
    1. Santa-Clara H, Szymanski L, Ordille T, Fernhall B. Effects of exercise training on resting metabolic rate in postmenopausal African American and Caucasian women. Metabolism (2006) 55:1358–64.10.1016/j.metabol.2006.06.006
    1. Wilmore JH, Stanforth PR, Hudspeth LA, Gagnon J, Daw EW, Leon AS, et al. Alterations in resting metabolic rate as a consequence of 20 wk of endurance training: the HERITAGE Family Study. Am J Clin Nutr (1998) 68:66–71.
    1. Poehlman ET, Melby CL, Badylak SF, Calles J. Aerobic fitness and resting energy expenditure in young adult males. Metabolism (1989) 38:85–90.10.1016/0026-0495(89)90185-6
    1. Araiza P, Hewes H, Gashetewa C, Vella CA, Burge MR. Efficacy of a pedometer-based physical activity program on parameters of diabetes control in type 2 diabetes mellitus. Metabolism (2006) 55:1382–7.10.1016/j.metabol.2006.06.009
    1. Mourier A, Gautier JF, De KE, Bigard AX, Villette JM, Garnier JP, et al. Mobilization of visceral adipose tissue related to the improvement in insulin sensitivity in response to physical training in NIDDM. Effects of branched-chain amino acid supplements. Diabetes Care (1997) 20:385–91.10.2337/diacare.20.3.385
    1. Jennings AE, Alberga A, Sigal RJ, Jay O, Boule NG, Kenny GP. The effect of exercise training on resting metabolic rate in type 2 diabetes mellitus. Med Sci Sports Exerc (2009) 41:1558–65.10.1249/MSS.0b013e31819d6a6f
    1. Alawad AO, Merghani TH, Ballal MA. Resting metabolic rate in obese diabetic and obese non-diabetic subjects and its relation to glycaemic control. BMC Res Notes (2013) 6:382.10.1186/1756-0500-6-382
    1. Weyer C, Bogardus C, Pratley RE. Metabolic factors contributing to increased resting metabolic rate and decreased insulin-induced thermogenesis during the development of type 2 diabetes. Diabetes (1999) 48:1607–14.10.2337/diabetes.48.8.1607
    1. Shaw K, Gennat H, O’Rourke P, Del MC. Exercise for overweight or obesity. Cochrane Database Syst Rev (2006) (4):CD003817.10.1002/14651858.CD003817.pub3
    1. Karstoft K, Winding K, Knudsen SH, Nielsen JS, Thomsen C, Pedersen BK, et al. The effects of free-living interval-walking training on glycemic control, body composition, and physical fitness in type 2 diabetes patients. Diabetes Care (2013) 36:228–36.10.2337/dc12-0658
    1. Karstoft K, Wallis GA, Pedersen BK, Solomon TP. The effects of interval- vs. continuous exercise on excess post-exercise oxygen consumption and substrate oxidation rates in subjects with type 2 diabetes. Metabolism (2016) 65:1316–25.10.1016/j.metabol.2016.05.017
    1. Byrne HK, Wilmore JH. The relationship of mode and intensity of training on resting metabolic rate in women. Int J Sport Nutr Exerc Metab (2001) 11:1–14.10.1123/ijsnem.11.1.1
    1. 2. Classification and diagnosis of diabetes. Diabetes Care (2016) 39(Suppl 1):S13–22.10.2337/dc16-S005
    1. Pedersen BK, Saltin B. Exercise as medicine – evidence for prescribing exercise as therapy in 26 different chronic diseases. Scand J Med Sci Sports (2015) 25(Suppl 3):1–72.10.1111/sms.12581
    1. Brinklov CF, Thorsen IK, Karstoft K, Brons C, Valentiner L, Langberg H, et al. Criterion validity and reliability of a smartphone delivered sub-maximal fitness test for people with type 2 diabetes. BMC Sports Sci Med Rehabil (2016) 8:31.10.1186/s13102-016-0056-7
    1. Karstoft K, Clark MA, Jakobsen I, Muller IA, Pedersen BK, Solomon TP, et al. The effects of 2 weeks of interval vs continuous walking training on glycaemic control and whole-body oxidative stress in individuals with type 2 diabetes: a controlled, randomised, crossover trial. Diabetologia (2017) 60:508–17.10.1007/s00125-016-4170-6
    1. Ried-Larsen M, Thomsen RW, Berencsi K, Brinklov CF, Brons C, Valentiner LS, et al. Implementation of interval walking training in patients with type 2 diabetes in Denmark: rationale, design, and baseline characteristics. Clin Epidemiol (2016) 8:201–9.10.2147/CLEP.S97303
    1. Levine JA. Measurement of energy expenditure. Public Health Nutr (2005) 8:1123–32.10.1079/PHN2005800
    1. Weir JB. New methods for calculating metabolic rate with special reference to protein metabolism. J Physiol (1949) 109:1–9.10.1113/jphysiol.1949.sp004363
    1. Ashcraft CM, Frankenfield DC. Validity test of a new open-circuit indirect calorimeter. JPEN J Parenter Enteral Nutr (2015) 39:738–42.10.1177/0148607114526242
    1. Byrne HK, Wilmore JH. The effects of a 20-week exercise training program on resting metabolic rate in previously sedentary, moderately obese women. Int J Sport Nutr Exerc Metab (2001) 11:15–31.10.1123/ijsnem.11.1.15
    1. Bacchi E, Negri C, Zanolin ME, Milanese C, Faccioli N, Trombetta M, et al. Metabolic effects of aerobic training and resistance training in type 2 diabetic subjects: a randomized controlled trial (the RAED2 study). Diabetes Care (2012) 35:676–82.10.2337/dc11-1655
    1. Hirsch KR, Smith-Ryan AE, Blue MN, Mock MG, Trexler ET. Influence of segmental body composition and adiposity hormones on resting metabolic rate and substrate utilization in overweight and obese adults. J Endocrinol Invest (2017) 40(6):635–43.10.1007/s40618-017-0616-z
    1. Westerterp KR, Meijer GA, Janssen EM, Saris WH, Ten HF. Long-term effect of physical activity on energy balance and body composition. Br J Nutr (1992) 68:21–30.10.1079/BJN19920063
    1. Muller MJ, Enderle J, Bosy-Westphal A. Changes in energy expenditure with weight gain and weight loss in humans. Curr Obes Rep (2016) 5:413–23.10.1007/s13679-016-0237-4
    1. Thorp AA, Schlaich MP. Relevance of sympathetic nervous system activation in obesity and metabolic syndrome. J Diabetes Res (2015) 2015:341583.10.1155/2015/341583
    1. Muller MJ, Enderle J, Pourhassan M, Braun W, Eggeling B, Lagerpusch M, et al. Metabolic adaptation to caloric restriction and subsequent refeeding: the Minnesota Starvation Experiment revisited. Am J Clin Nutr (2015) 102:807–19.10.3945/ajcn.115.109173
    1. Leibel RL, Rosenbaum M, Hirsch J. Changes in energy expenditure resulting from altered body weight. N Engl J Med (1995) 332:621–8.10.1056/NEJM199503093321001
    1. Straznicky NE, Lambert EA, Lambert GW, Masuo K, Esler MD, Nestel PJ. Effects of dietary weight loss on sympathetic activity and cardiac risk factors associated with the metabolic syndrome. J Clin Endocrinol Metab (2005) 90:5998–6005.10.1210/jc.2005-0961
    1. Hulmi JJ, Isola V, Suonpaa M, Jarvinen NJ, Kokkonen M, Wennerstrom A, et al. The effects of intensive weight reduction on body composition and serum hormones in female fitness competitors. Front Physiol (2016) 7:689.
    1. Johannsen DL, Knuth ND, Huizenga R, Rood JC, Ravussin E, Hall KD. Metabolic slowing with massive weight loss despite preservation of fat-free mass. J Clin Endocrinol Metab (2012) 97:2489–96.10.1210/jc.2012-1444
    1. Gentile CL, Orr JS, Davy BM, Davy KP. Modest weight gain is associated with sympathetic neural activation in nonobese humans. Am J Physiol Regul Integr Comp Physiol (2007) 292:R1834–8.10.1152/ajpregu.00876.2006
    1. Gram B, Christensen R, Christiansen C, Gram J. Effects of Nordic walking and exercise in type 2 diabetes mellitus: a randomized controlled trial. Clin J Sport Med (2010) 20:355–61.10.1227/NEU.0b013e3181e56e0a
    1. Negri C, Bacchi E, Morgante S, Soave D, Marques A, Menghini E, et al. Supervised walking groups to increase physical activity in type 2 diabetic patients. Diabetes Care (2010) 33:2333–5.10.2337/dc10-0877

Source: PubMed

3
Abonnieren