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Diabetes Research and Clinical Practice 72 (2006) 271–276

www.elsevier.com/locate/diabres

The effect of resistance versus aerobic training on metabolic control


in patients with type-1 diabetes mellitus
Ana Claudia Ramalho a,*, Maria de Lourdes Lima a, Fabiana Nunes b,
Zanine Cambuı́ b, Cynara Barbosa b, Aline Andrade b, Adriana Viana b,
Marlene Martins b, Valter Abrantes c, Crésio Aragão b, Marcos Temı́stocles c
a
Department of Endocrinology, Bahian School of Medicine, Salvador, Bahia, Brazil
b
Department of Endocrinology, Roberto Santos Hospital, Salvador, Bahia, Brazil
c
Department of Exercise Science, Bahia State University, Salvador, Bahia, Brazil
Received 25 April 2005; received in revised form 4 November 2005; accepted 11 November 2005
Available online 6 January 2006

Abstract
This study evaluated the effect of aerobic versus resistance training on metabolic control in type-1 diabetes patients. Thirteen
non-active patients, ranging in age from 13–30, were submitted to a 12-week aerobic exercise (Group A, n = 7) or resistance training
(Group B, n = 6) period. Group A training consisted of a 40 min walk or run and Group B training consisted of resistance exercises
three times a week. Blood samples were obtained before and after the 12-week training period. When these samples were compared,
results showed that in Group A there were no changes in glycated hemoglobin, lipid profile, fast glucose level or body mass index
(BMI). There was, however, a reduction in waist circumference and in average self-monitored blood glucose levels, measured after
each exercise session. In Group B, there were no changes in the parameters evaluated. In both groups the total insulin dosage was
reduced. As other authors have shown, resistance/aerobic training did not improve glycated hemoglobin in type-1 diabetes patients.
# 2005 Elsevier Ireland Ltd. All rights reserved.

Keywords: Diabetes; Aerobic exercise; Resistance exercise; Glycated hemoglobin

1. Introduction 12-week period of both aerobic exercise and resistance


training [2]. Similar beneficial results were also
Although physical activity has been associated with demonstrated by Campaigne et al. in adolescents with
a reduction in cardiovascular mortality in type-1 type-1 diabetes after 12 weeks of vigorous games and
diabetes patients [1], contradictory data have been recreational activities [3]. In contrast, no decrease in
reported regarding the benefits of physical activity on glycated hemoglobin levels was reported by Laaksonen
metabolic control in these patients. et al. after a 12-week training program in twenty type-1
Mosher et al. showed beneficial effects on glycated diabetes patients, compared to a control group [4].
hemoglobin in eleven type-1 diabetes patients after a Improvements in maximal oxygen uptake (VO2 max)
with no associated changes in glycemic control have
been reported by Rowland [5] and Zinman et al. [6] after
12 weeks of bicycle and treadmill exercise, respectively.
* Corresponding author. Rua Altino Seberto de Barros 119 sala
1501, Itaigara, Salvador, Bahia, Brazil. Tel.: +55 71 33599831;
Apart from the controversy surrounding the bene-
fax: +55 71 33599831. ficial effects of exercise on glycemic control in type-1
E-mail address: acrramalho@superig.com.br (A.C. Ramalho). diabetes patients, the question remains about which type

0168-8227/$ – see front matter # 2005 Elsevier Ireland Ltd. All rights reserved.
doi:10.1016/j.diabres.2005.11.011
272 A.C. Ramalho et al. / Diabetes Research and Clinical Practice 72 (2006) 271–276

of activity is better: aerobic exercise or resistance estimate maximal oxygen consumption (VO2 max),
training. Studies that evaluated the effect of exercise on using the Bruce protocol [8].
metabolic control in type-1 diabetes patients used
aerobic training or aerobic exercise associated with 2.4. Blood chemistry
resistance training [2–4]. Information is lacking about
the effect of resistance training without aerobic exercise Venous blood samples were collected after a 12 h
on metabolic control in type-1 diabetes. Taking into overnight fast. Samples were taken before and after the
account that today type-1 diabetes is more prevalent in 12-week exercise program of: glycated hemoglobin
young people who frequent gyms for resistance (HbA1c) (enzymatic colorimetry, Biorad, reference
training, this evaluation becomes even more important. range 4.0–6.3%), plasma glucose and lipid profile
The unanswered question as to whether exercise (total cholesterol and fractions-HDL, VLDL, triglycer-
should be encouraged in subjects with type-1 diabetes in ide) (enzymatic colorimetry, Merck-selectra ll). LDL
order to achieve better glycemic control has important was calculated according to Friedewald’s formula [9],
implications for these patients. Better glycemic control is which has been validated in type-1 diabetes [10].
associated with a reduced risk of diabetic complications,
as shown in the DCCT trial [7]. At present, the 2.5. Pre- and post-exercise self-monitored blood
relationship between physical activity and glycemic glucose levels
control in type-1 diabetes patients has yet to be fully
established. The aim of this study was to evaluate the Self-monitored blood glucose levels were deter-
effect of 12 weeks of aerobic exercise and resistance mined using a Roche glucometer (Active) before and
training on metabolic control in type-1 diabetes patients. after each exercise session, using blood drawn from a
finger prick. Subjects with pre-exercise self-moni-
2. Materials and methods tored blood glucose levels higher than 250 mg/dl, had
their urine examined for the presence of ketosis, and if
2.1. Subjects positive, the exercise session was canceled as
recommended [11]. The session was also canceled
Sixteen patients with type-1 diabetes mellitus ranging if self-monitored blood glucose levels were higher
in ages from 13 to 30, who exercised less than twice a than 300 mg/dl even without ketosis, if the subject had
week, were chosen from outpatients at a public hospital in measured this glucose level over the previous 2-day
Salvador, Bahia, Brazil. Patients with ketosis, chronic period. When the subject began the exercise session
complications, such as proliferative retinopathy and with a self-monitored blood glucose level of
peripheral neuropathy, as determined by the monofila- >250 mg/dl, the level was monitored again after
ment test (Semmes–Weinstein 5.07/10 g), were 20 min; if the level increased, the session was
excluded. At baseline, treatments were administered in interrupted.
the morning and at bedtime using NPH insulin and Subjects consumed a carbohydrate supplement
regular, lispro or aspart insulin, before meals. The study based on pre-exercise self-monitored blood glucose
was approved by the Hospital Ethics Committee and all levels. If the level was between 70 and 140 mg/dl,
patients gave their informed written consent. they consumed 15–20 g of carbohydrates before
exercising. If the level was between 140 and
2.2. Anthropometric measurements 180 mg/dl, no carbohydrates were consumed before
exercise. Subjects who had a self-monitored blood
The anthropometric measurements consisted of glucose level of less than 70 mg/dl during or after
weight (calibrated scale-Filizola), height (nearest cm- training, stopped the exercise and received 30 g of
stadiometers-Standard), waist circumference measured carbohydrates, and the dose of regular, lispro or aspart
at the level of umbilicus and the waist/hip ratio was cal- insulin for the pre-exercise meal was reduced by 2
culated. The body mass index (BMI) was calculated as the units. If patients experienced hypoglycemia in the
ratio of weight (kg) to the square of height (m) (kg/m2). evening after the exercise session, the insulin NPH
night dose was reduced by 20%. At the end of the
2.3. Exercise testing study, each patient’s final insulin dose was compared
to the dose used before the study began, and the
Before and after 12 weeks of training, all subjects percentage change in NPH, regular, aspart and lispro
underwent a maximal treadmill-graded exercise test to insulin was verified.
A.C. Ramalho et al. / Diabetes Research and Clinical Practice 72 (2006) 271–276 273

2.6. Exercise training 3. Results

Patients were randomized into two groups: Group One patient in Group A and two in Group B did not
A patients participated in an aerobic exercise complete the study, the former because of an infectious
program (n = 8) and Group B patients in a resistance disease, and the latter two because of personal
training program (n = 8). Both groups trained three problems. Group A consisted of seven patients (five
times a week for 12 weeks, doing either aerobic women and two men), with an average age of
exercise or resistance training, supervised by a 19.8  5.1 years who had had diabetes for 7.0  5.9
physical trainer and an endocrinologist. Each exer- years. Group B consisted of six patients (five women
cise session began and finished with a 10 min and one man) with an average age of 20.8  4.7 who
warm-up or cool-down and stretching period. The had had diabetes for 7.8  4.8 years.
intensity and duration of the exercise program were After the exercise program, five in Group A (5/7) and
progressively increased throughout the 12-week five in Group B (5/6) showed a reduction in the NPH
period, according to the tolerance of each individual insulin dose. The rapid and ultra-rapid insulin dose was
patient. reduced in one patient (1/7) in Group A and in four (4/6)
in Group B. The average pre- and post-training program
2.7. Aerobic training total insulin doses are shown in Table 1.
There was a slight increase in cardio-respiratory
Patients in Group A were submitted to a 40 min endurance in both groups, based on VO2 max (ml/kg/
aerobic session on a treadmill, either walking or min): 34.5–36.5 in Group A and 31.7–36.8 in Group B.
running, based on heart rate, until the target heart rate A significant reduction in waist/hip ratio ( p = 0.017)
was reached, according to American College of Sport and in waist circumference ( p = 0.009) was observed in
Medicine guidelines [12]. The program began with Group A, while no difference was observed in these
10 min of stretching and was conducted using the parameters in Group B (Fig. 1). Nor was there any
maximal heart rate index (HRmax) estimated by: 220- alteration in BMI for either of the groups (22.2  2.3 to
age [13]. First 2 weeks = 60–70% of HRmax, 3rd to 6th 22.15  2.2 kg/m2 in Group A and 20.6  1.4 to
weeks = 70–80% of HRmax, 7th to 12th weeks = 70– 20.6  1.8 kg/m2 in Group B).
90% of HRmax. In Group A there was no difference in lipid profile or
fasting blood sugar before and after the exercise
2.8. Resistance training program, while the HbA1c increased. In Group B there
were no significant alterations in these parameters.
Patients in Group B were submitted to a 40 min (Table 2).
session of resistance training. The program began with
10 min of stretching and was conducted with exercises Table 1
done on nine resistance machines. The resistance Pre- and post-training daily insulin dosages in Groups A and B
machines used were: chest press, bicep curl, triceps
Daily insulin dosage (units/kg/day)
extension, lower back, abdominals, leg press, leg curl
and leg extension. Subjects performed three sets of 8–12 Pre-training Post-training
repetitions, with 60 s of rest between each set. Group A 0.84 0.65
Resistance was increased by five pounds after the 0.78 0.62
subject was able to complete three sets of eight 0.59 0.50
1.30 1.27
repetitions on three consecutive days. Subjects were 0.89 0.56
trained using between 60 and 80% of their one maximal 0.75 0.88
repetition weight (1-RM). 0.98 1.05
Group B 1.70 1.11
2.9. Statistical methodology 1.01 0.83
1.20 1.16
The Student’s t-test was used to compare means, and, 1.20 0.51
0.46 0.64
when necessary, Wilcoxon statistical significance was
0.60 0.48
defined at p < 0.05 with a 95% confidence interval.
SPSS/PC Windows software version 9.0 was used for Total mean 0.95  0.34 0.79  0.28*
*
statistical analyses. p < 0.05.
274 A.C. Ramalho et al. / Diabetes Research and Clinical Practice 72 (2006) 271–276

Fig. 2. Average self-monitored blood glucose levels in Groups A and


B, measured immediately before and after exercise training.

Fig. 1. Waist circumference measurements before and after 12 weeks


of exercise training. exercise. Some of them showed an improvement in
metabolic control [2,6], but others did not [14–17]. Few
Self-monitored blood glucose levels, measured studies exist that evaluate the effect of resistance
before and after each session, showed a significant training on metabolic control in type-1 diabetes, and
reduction in Group A and a less significant reduction in most of those that do exist evaluated resistance
Group B (Fig. 2). The average number of hypoglycemic associated with aerobic exercise in the same patient
episodes during the 12-week training program was 3.4 [2]. In this study, no improvement in glycated
in Group A and 3.8 in Group B. hemoglobin was found after either aerobic exercise
or resistance training programs. In fact, in the aerobic
4. Discussion exercise group there was a slight increase in glycated
hemoglobin.
Evidence that regular exercise can improve metabolic The lack of improvement in glycated hemoglobin
control in type-1 diabetes is lacking. As is the case with can, in part, be explained by the reduction of insulin
non-diabetic subjects, the insulin sensitivity of type-1 doses related to the hypoglycemic episodes that
diabetic patients improves [14], but this does not translate frequently occur in these patients. As no generally
into an improvement in long-term glucose control, accepted guidelines to adapt insulin and food intake to
according to glycated hemoglobin levels [14–17]. exercise exist, the insulin dose was reduced based on
Most studies that evaluated the effect of exercise on each patient’s response to exercise, as determined by
metabolic control in type-1 diabetes used aerobic self monitoring blood glucose levels. The American

Table 2
Blood chemistry before and after 12 weeks of exercise training in Groups A and B
Group A Group B
Pre-training Post-training Pre-training Post-training
Fasting glycemia (mg/dl) 229.8  118.0 270.0  109.0 141.5  117.0 180.6  87.2
HbA1c (%) 8.7  1.6 9.8  1.8* 8.2  2.9 7.6  1.6
Frutosamine (mmol/L) 4.0  0.7 3.8  0.4 3.6  0.8 3.4  0.5
Total cholesterol (mg/dl) 176.4  35.0 181.0  36.1 156.6  29.9 165.0  44.2
HDL-c (mg/dl) 62.6  9.1 64.4  8.2 53.5  9.2 54.3  10.9
LDL-c (mg/dl) 98.1  33.4 100.7  31.8 89.3  23.1 94.8  40.6
Triglycerides (mg/dl) 81.4  26.2 75.8  17.5 69.2  15.9 79.0  23.2
*
p < 0.05.
A.C. Ramalho et al. / Diabetes Research and Clinical Practice 72 (2006) 271–276 275

Diabetes Association [18], based on Wasserman and the training program and the lack of guidelines to adapt
Zima’s general recommendations [11], states that these the insulin dose.
adaptations are based on blood glucose monitoring in Although this study provides no evidence that
order to avoid hypoglycemia and does not provide regular exercise improves glycemic control in type-1
specific values. diabetes patients, insulin sensitivity and muscle glucose
After 12 weeks, patients in both aerobic exercise and uptake are altered by exercise training [19]. Re-
resistance training programs showed a reduction in their assessment of the insulin dose, diet and prescriptive
NPH insulin dose, which was related to hypoglycemic exercise characteristics (frequency, duration, intensity
episodes. Probably, the 20% reduction in the NPH dose and mode) should be done to obtain more conclusive
was higher than necessary, and this could explain the results.
fact that there was no reduction in glycated hemoglobin The lack of an improvement in glycemic control
in either group, and that there was even a slight increase shown in this and other studies should not discourage
in the aerobic group. type-1 diabetes patients from exercising. A reduction in
In patients with type-1 diabetes, as in individuals waist circumference in the aerobic exercise group
without diabetes, exercise increases insulin sensitivity associated with a tendency for increased HDL-c levels
and muscle glucose uptake [14]. This effect can last shown in this study may indicate a reduction of visceral
more than 12 h after exercise, as shown by Mikines et al. fat, with an improvement in insulin resistance, which
[19] and could explain the hypoglycemic episodes and could have an impact on cardiovascular risk, thereby
the subsequent reduction in insulin doses observed in reducing mortality.
the patients in the present study.
Ligtenberg et al. [20] showed a significant decrease Acknowledgements
in glycated hemoglobin in type-2 diabetes patients, but
only after 1 year of training, and not within 6 months. We would like to thank the group who helped us with
This suggests that a longer period of regular activity is the patients at the gym: Luciano Vidal, João Marcelo,
necessary before any difference in glycemic control David Teixeira, Fábio Castro, Humberto Santos, João
can be observed. In the present study, a 3-month Paulo, Marcos Paulo, Marli Batista, Paulo Cezar,
training program was carried out, which may have Tiago Neto, Vinicius David, Flávia Costa and Nixon
been too short to modify metabolic control, although Fernandes.
some authors found no improvement, even when
evaluating a long-term training program in type-1 References
women [16].
The effect of exercise on the lipid profile is [1] C.S. Moy, T.J. Songer, R. La Porte, J.S. Dorman, A.M. Kriska,
controversial. Mosher et al. showed a reduction of T.J. Orchard, et al., Insulin-dependent diabetes mellitus, physical
LDLc in adolescents with type-1 diabetes, who activity and death, Am. J. Epidemiol. 137 (1993) 74–81.
[2] P.E. Mosher, M.S. Nash, A.C. Perry, A.R. La Pierriere, B.B.
underwent endurance and resistance training [2]. Goldberg, Aerobic circuit training: effect on adolescents with
Conversely, no alterations of lipoprotein profiles were well-controlled insulin-dependent diabetes mellitus, Arch. Phys.
observed after 10 weeks of either running, weight Med. Rehabil. 79 (1998) 652–657.
training or a combination of both in adolescent men [3] B.N. Campaigne, T.B. Gilliam, M.L. Spencer, R.M. Lampman,
M.A. Stork, Effects of a physical activity program on metabolic
[21].
control and cardiovascular fitness in children with insulin-depen-
The lipid profile did not change in this type-1 dent diabetes mellitus, Diab. Care 7 (1984) 57–62.
diabetes group. In fact, they had normal pre-training [4] D.E. Laaksonen, M. Attala, L.K. Insane, J. Mudstone, C.K. Sen,
lipid levels, and the greatest improvement was observed T.A. Lake, et al., Aerobic exercise and the lipid profile in type-1
in individuals with the highest lipid levels [22]. A diabetic men: a randomized controlled trial, Med. Sci. Sports
tendency was observed for an increase in HDL-c levels Exerc. 32 (2000) 1541–1548.
[5] T. Rowland, Physical fitness in children: implications for the
in both groups, which could be considered significant if prevention of coronary artery disease, Curr. Prob. Pediatr. 11
the number of subjects were higher. Furthermore, this (1981) 1–5.
study did not evaluate other lipid parameters such as [6] B. Zinman, S. Zuniga-Guajardo, D. Kelly, Comparison of the
LDL-a or Apo B levels, which may have changed as acute and long-term effects of exercise on glucose control in
shown by Laaksonen et al. [4]. type-1 diabetes, Diab. Care 7 (1984) 515–519.
[7] The Diabetes Control and Complication Trial Research Group,
The present study has some limitations. It is possible The effect of intensive treatment of diabetes on the development
that no significant difference in metabolic control was and progression of long term complications in insulin-dependent
detected because of the small sample size, the length of diabetes mellitus, N. Engl. J. Med. 329 (1993) 977–986.
276 A.C. Ramalho et al. / Diabetes Research and Clinical Practice 72 (2006) 271–276

[8] R.A. Bruce, F. Kusumi, D. Hosmer, Maximal oxygen intake glycemic control in type-1 diabetes patients: a cross-sectional
and monographic assessment of functional aerobic impair- study, Neth. J. Med. 2 (1999) 59–63.
ment in cardiovascular disease, Am. Heart J. 85 (1973) 546– [16] H. Wallberg-Henriksson, R. Gurnasson, S. Rossner, J. Wahren,
562. Long term physical training in female type-1 (insulin-dependent)
[9] W. Friedewald, R. Levy, D. Fredrikson, Estimation of the con- diabetic patients: absence of significant effect on glycemic
centration of low-density lipoprotein cholesterol in plasma, control and lipoprotein levels, Diabetologia 7 (1986) 515–519.
without use of the preparative ultracentrifuge, Clin. Chem. 18 [17] K.W. Landt, B.N. Campaigne, F.W. James, M.A. Sperling,
(1972) 499–502. Effects of exercise training on insulin sensitivity in adolescents
[10] M. Whitting, M. Shephard, G. Tallis, Measurement of plasma with type-1 diabetes, Diab. Care 8 (1985) 461–465.
LDL cholesterol in patients with diabetes, Diab. Care 20 (1997) [18] American Diabetes Association, Standards of medical care in
12–14. diabetes, Diab. Care 28 (2005) S4–S36.
[11] D.H. Wasserman, B. Ziman, Exercise in individual with IDDM, [19] K.J. Mikines, B. Sonne, P.A. Farrel, B. Tronier, H. Galbo, Effect
Diab. Care 17 (1994) 914–937. of physical exercise on sensitivity and responsiveness to insulin
[12] American College of Sport Medicine, ACSM’s Guidelines for in humans, Am. J. Physiol. 254 (1988) E248–E259.
Exercise Testing and Prescription, 6th ed., Lippincott, Williams [20] P.C. Ligtenberg, J.B. Hoekstra, M.L. Zonderland, E. Bol, D.W.
& Wilkins, Baltimore, MD, 2000. Erkelens, The effect of physical training on glucose tolerance
[13] A.R. Robert, R. Landwehr, The Surprising History of the ‘‘220– and lipid profile and in obese, elderly NIDDM patients, Clin. Sci.
age’’ Equation, J. Exerc. Physiol. 05 (2002) 1–10. 93 (1997) 127–135.
[14] H. Wallberg-Henriksson, R. Gurnasson, J. Henriksson, R. [21] A. Lee, B.W. Craig, J. Lucas, R. Pohlman, H. Stelling, The effect
Defronzo, P. Felig, J. Ostman, et al., Increased peripheral insulin of endurance training and weight training upon the blood lipid
sensitivity and mitochondrial enzymes but unchanged blood profiles of young male subjects, J. Appl. Sport Sci. Res. 4 (1990)
glucose control in type-1 diabetics after physical training, Dia- 68–75.
betes 31 (1983) 1044–1050. [22] R.P. Fripp, J.L. Hodgson, Effects of resistance training on plasma
[15] P.C. Ligtenberg, M. Blans, J.B. Hoekstra, I. Van der Tweel, lipid and lipoprotein levels in male adolescent, J. Pediatr. 111
D.W. Erkelens, No effect of long term physical activity on the (1987) 926–931.

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