Services on Demand
- Cited by Google
- Similars in SciELO
- Similars in Google
On-line version ISSN 1678-4170
Arq. Bras. Cardiol. vol.92 no.1 São Paulo Jan. 2009
Denise Maria Martins VanceaI; José Nelson VanceaII; Maria Izabel Fernandes PiresIII; Marco Antonio ReisIV; Rafael Brandão MouraV; Sergio Atala DibI
Federal de São Paulo
IIIUniversidade de São Paulo
IVColégio Estadual Salime Mudeh
VColégio Estadual Marechal Carlos Machado Bitencourt, São Paulo, SP - Brazil
Diabetes and cardiovascular disease have emerged as key threats to human health,
and the risk is increased in individuals with visceral obesity. The consensus
is that physical exercise should be part of the treatment of diabetes mellitus
OBJECTIVE: To compare the influence of guided and structured physical exercise programs (SPEP), three to five times per week, during a period of 20 weeks, on glycemic control and body composition of type 2 diabetic patients (DM2).
METHODS: The research was conducted at the Universidade Federal de São Paulo (Federal University School of Medicine in São Paulo). At the clinical visit, patients from the Control Group (CG) n=17, mean age 55.8 years, were encouraged to engage in a physical exercise program. Patients from Group 3x (G3), n=14, mean age 57.4 years, were to engage in 1 hour of physical exercise, 3x/week, and Group 5x (G5), n=9, mean age 58.8 years, followed the same protocol but 5x/week. Mean of 5 years since diagnosis in all groups. Classes consisted of a 5-minute warm-up, 30-minute treadmill walk at 70% of maximum heart rate, and 10-minute relaxation. BMI, abdominal circumference (AC), percentage of body fat (BF), capillary glycemia (CG), fasting glycemia (FG), and glycated hemoglobin (HbA1c) were assessed.
RESULTS: A comparison was made between the baseline time point (B) and the 20th week (20th). BMI in G3 (B:29.5±2.9 vs. 20th: 28.3 ± 2.2 Kg/sqm, p=0.005) and G5 (B:29.7±4.4 vs. 20th: 29.1 ± 4.3 Kg/sqm, p=0.025); abdominal circumference in G5 (B:100.5±11.9 vs. 20th: 933 ± 11.7 cm, p=0.001); BF in G3 (B:31±5.1 vs 20th: 26±5%, p=0.001) and G5 (B:32.4 ± 5.4 vs. 20th: 30.3 ± 6.9%, p=0.001); FG, G5 (B:150.8 ± 47.5 vs. 20th: 109.2± 30.5 mg/dL, p=0.034), showed statistically significant differences. CG did not show statistically significant differences for these variables. CG showed a tendency to drop after physical exercise in G5. HbA1c showed no statistically significant differences in the three groups.
CONCLUSION: G5 did better than G3 in most parameters assessed. However, results failed to show a decrease of HbA1c in DM2 patients.
Key Words: Diabetes mellitus, type 2; exercise; blood glucose; control; body compostion.
Atherosclerosis is the most important cause of mortality and great morbidity among diabetic patients. Endothelial dysfunction is thought to play a key role in the initial lesion of atherosclerosis. Endothelial dysfunction has been documented in type 2 diabetes mellitus (DM2), where hyperglycemia is associated with increased oxidative stress, leading to increased formation of oxygen radicals such as superoxide that reacts with nitric oxide and causes its breakdown1.
Diabetes and cardiovascular disease have emerged as key threats to human health, and the risk is increased in individuals with visceral obesity2,3.
The consensus is that physical exercise should be part of diabetes mellitus (DM) treatment, as well as diet and medication. Unfortunately, this is not common practice, according to routine clinical visits. This is likely due to the lack of understanding and/or motivation in some of these individuals and their assistants. The very frequency of such recommendations by healthcare professionals is deficient4.
Among participating factors are genetic determinants, age differences, biotype, patient' physical fitness, duration, and modality of exercise5-8.
Studies have shown that the effects of physical exercise on glycemic control can be temporary, with a post-exercise drop in glycemia that is soon restored to pre-exercise values once physical activity is discontinued9,10.
Most studies conducted with the objective of obtaining good control levels of glycated hemoglobin (HbA1c) were not effective. One possible reason could be related to the frequency of exercise sessions (3x per week). It is known that the increase in insulin sensitivity levels associated with physical exercise lasts no longer than 72 hours5. One suggestion for avoiding this would be to increase the frequency of exercises so that the interval between sessions does not exceed this period.
On the other hand, reports of the impact of physical exercise frequency on DM2 body composition are scarce.
The aim of this study was to compare the effect that the frequency of a physical exercise program has on body composition and glycemic control in DM2 patients.
This is a randomized prospective study conducted to evaluate 40 individuals with Type 2 diabetes mellitus (DM2). Patients signed Informed Consent Forms in order to participate in the research.
Inclusion criteria were: 1) diagnosis of DM2, according to the American Diabetes Association criteria11; 2) less than 10 years since diagnosis of DM; 3) both genders; 4) age between 40 and 65 years; 5) Body Mass Index (BMI): 25-35 kg/sqm; 6) fasting glycemia < 250 mg/dL; 7) arterial blood pressure (AP): systolic <160 mmHg and diastolic <100 mmHg; and 8) absence of chronic clinical DM complications which could be harmful or be impaired by the physical exercise program.
Patients enrolled in the study were divided into three groups: Control Group = CG (n=17): during the routine visits with the multidisciplinary team, these patients received orientation and were encouraged to engage in spontaneous regular physical exercising; Group 3x = G3 (n=14), patients who participated in three workout sessions per week, and group 5x = G5 (n=9) patients who participated in five workout sessions during 20 weeks (Table 1).
The study protocol was previously approved by the Research Ethics Committee of the Universidade Federal de São Paulo (CEP Protocol number 1293/00).
Physical exercise program
The structured physical exercise program (SPEP) was conducted at the Respiratory Physiology Unit of the Pneumology Department under the supervision of physical education teachers.
At the start of the SPEP program, G3 and G5 patients attended a lecture when the program was explained, including its benefits, risks and recommendations to be followed to assure that physical exercises were performed safely.
SPEP was conducted in the morning after a routine meal in a workout room equipped with treadmills and stretching mats.
Classes were divided as follows: 1) warm-up (5 minutes): stretching exercises; 2) main exercises (30 minutes): walking on the treadmill, and 3) back to relaxation (10 minutes): stretching, relaxation and body consciousness.
At the beginning of the program, intensity of the physical exercise was kept at 60% of the maximum heart rate (max HR) predicted for the age (220 - age) for both groups (G3 and G5), and gradually increased until reaching the 70% of max HR target12.
Clinical and metabolic parameters
Capillary glycemia (Roche and Abbott meters for capillary glucose testing were used) and heart rate were measured before and after each SPEP session.
All patients enrolled in our study displayed glycemia levels within the recommended range (<250 mg/dL) before beginning each exercise session. Approximately 1,608 capillary glycemia tests were performed in G3, and 1,800 in G5.
Abdominal circumference (AC) was measured with a measuring tape placed around the smallest perimeter of the abdominal area with the patient standing and after normal expiration.
Body weight was measured to the nearest 0.1 kg using a calibrated scale, with subjects wearing light clothing and no shoes. Height was measured to the nearest 0.5 cm using a stadiometer, with subjects barefoot. BMI (kg/sqm) was calculated dividing the individual's weight (Kg) by the squared height in meters.
Percentage of body fat was calculated using the Pollock and Jackson protocol and measuring the following skin folds: triceps, suprailiac and thigh for women, and thorax, abdomen and thigh for men13.
Abdominal waist (AW) and BMI were measured by the same professional at all data collection time points.
Fasting glycemia and glycated hemoglobin were measured after a period of 8-12 hours, and postprandial glycemia 2 hours after a standardized 300 kcal snack (50g CHO).
Plasma glucose was determined using the GOD-PAP method, considering 70-100 mg/dL as the reference values. Measurement of HbA1c was performed using high-performance liquid chromatography (TOSOH automated analysis of glycated hemoglobin, Shiba, Mianto-ku, Tokyo, Japan), with nominal values between 3.6 and 6.8%.
Over the period of the study, patients continued to take their regular medications, which are indicated on Table 2.
Variable averages were compared using repeated measurement analysis of variance. Multiple comparisons were carried out in order to consider Fisher's significant smallest difference, as well as the Kruskal-Wallis non-parametric test. An a = 0.05 significance level was adopted for all tests.
The baseline evaluation of the study groups showed no significant difference among demographic, clinical, and metabolic characteristics (Table 1).
Intragroup evaluation BMI, abdominal waist, and percentage of fat
A significant BMI reduction in G3 was recorded starting at the 8th week of SPEP (B: 29.5 vs. 2.9, 8th week: 29.0 ± 2.7 kg/sqm, p=0.013), and continuing through the 16th week (8th week: 29.0 vs. 2.7, 16th week: 28.8, 2.6, kg/sqm, p=0.023). In the 20th week of SPEP, BMI showed a statistically significant difference as compared to baseline BMI of G3 patients (B: 29.5 vs. 2.9, 20th week: 28.3 ± 2.2 kg/sqm, p= 0.005) and in G5 patients (B: 29.7 ± 4.4 vs. 20th week = 29.1 ± 4.3 kg/sqm, p=0.025). CG patients showed no statistically significant differences in BMI over that period.
No significant differences were observed in patients' ACs (Control and G3 groups) over the entire period of the study. On the other hand, G5 patients' AC dropped after the 8th week of SPEP (B: 100.5 vs. 11.9, 8th week: 93.0 ± 10.8 cm, p=0.001), and showed no difference from the baseline value in the 16th week, but dropped again in the 20th week (B: 100.5 ± 11.9 vs. 20th week = 93.3 ± 11.7 cm. p=0.001).
Systolic arterial pressure (SAP) and diastolic arterial pressure (DAP) showed no statistically significant changes in the CG and G3 groups. The G5 group showed a tendency towards a reduction, although not statistically significant (SAP - B: 12.8 ± 2.0 mmHg vs. 20th = 12.5 ± 2.0 mmHg, and DAP - B: 8.0 ± 2.0 mmHg vs. 20th = 7.6 ± 3.0 mmHg).
The percentage of body fat showed a significant reduction in the G3 and G5 groups as compared to the baseline values in the 20th week (G3 - B: 31.0 vs. 5.1 x 20th week: 26.0 ± 5.0 %, p= 0.001 and G5 - B: 32.4 ± 5.4 vs. 20th week = 30.3 ± 6.9%, p = 0.001). The CG showed no statistically significant changes in the percentage of body fat over the period of study.
Capillary glycemia monitored during the Physical Exercise Program
There was a tendency towards a drop in capillary glycemia levels monitored after SPEP sessions in G5. These data are displayed on Figure 1.
Fasting and Postprandial Glycemia, and HbA1c
Fasting glycemia values (B: 150.8 vs. 47.5 vs. 20th: 109.2 ± 30.5 mg/dl), p= 0.034) and postprandial values (B: 214.5 ± 81.7 vs. 20th week: 194.4 ± 53.4 mg/dL p=0.028) showed a significant reduction compared to baseline only for the G5 evaluation performed at the 20th week. These data are displayed on Figures 2 and 3. The CG showed no statistically significant changes in fasting and postprandial glycemia values over the study period.
Glycated hemoglobin in the 20th week of SPEP showed no significant differences as to baseline values in the two SPEP groups (G3 - B: 8.2 ± 1.9 vs. 20th week: 7.4 ± 1.2 % and G5 -: B: 7.7 vs. 1.8 vs. 20th week: 7.4 ± 0.7%), and in the control group (CG - B: 9.0 vs. 3.1 x 20th week: 8.7 ± 2.6%).
The intergroup evaluation showed no statistically significant difference in the three groups. Table 3 displays data obtained on the variables for the 3 groups in the study periods.
This study has shown that a structured program of moderate intensity physical exercise (SPEP) can lead to a drop in BMI and in the percentage of body fat for a group of DM2 patients as of the 8th week of exercise. However, with an increased frequency to 5x per week, there may be additional effects such as reduction in abdominal circumference, mean capillary glycemic values, and fasting and postprandial glycemic values. The addition of twenty weeks of SPEP to a group of DM2 patients who were following a stable anti-hyperglycemic treatment was not enough to reduce HbA1c values.
Therefore, these data corroborate the controversies observed in studies that analyzed just the effect of regular physical exercise on the metabolic control of DM2 patients5-8.
As per baseline BMI classification13, CG, G3, and G5 individuals were considered overweight. Despite the statistically significant drop observed in G3 and G5, the comparison between the baseline and 20th week values showed that individuals were still overweight at the end of the study.
One of the interesting findings in our study was that a reduction in BMI was observed as of the 8th week of SPEP in G3, which remained through the 16th and 20th weeks. As to G5, the reduction was observed only when baseline and 20th week values were compared. This delay in BMI reduction in this latter group may be due to an unconscious increase of calorie intake to compensate for the increase in physical activity.
We should take into consideration that physical exercise improves the metabolic profile and has anti-inflammatory effects in DM2 patients, even when no significant loss of body weight is achieved14.
A reduction in AC occurred only in G5. G5 baseline AC was greater than that recorded for G3, what can account for the greater drop in G5. Riddell (2007)15 explains that DM2 patients lose visceral fat even when they do not lose body weight, thus explaining the reduction in abdominal circumference. It is known that a reduction in abdominal circumference is a strong indicator of a drop in cardiovascular risk16.
A study by Boulé et al.7 also showed a reduction in abdominal circumference after a series of exercises. We know that a reduction in this variable is very important for diabetes patients, because there is a positive relationship among abdominal circumference, central obesity, insulin resistance, metabolic syndrome, and cardiovascular disease7.
The positive relationship between AC, central obesity, insulin resistance, metabolic syndrome, and cardiovascular disease17 makes the reduction in this variable one of the important objectives in the treatment of DM2.
Systolic and diastolic arterial pressures showed no statistically significant changes. In the G5 group, a tendency towards a drop in SAP and DAP was recorded. Arterial hypertension is one of the leading risk factors for the onset and progress of chronic complications of DM2. Physical exercise is one of the pillars in the treatment of hypertension in diabetic patients, and a positive influence on the drop of arterial pressure in DM2 patients18. In our study, arterial pressure values were not very different from the reference values (SAP = 120-129 mmHG and DAP = 80-84 mmHg)19. Therefore, this could be one reason why no significant reduction in these values was observed.
As to percentage of body fat, a significant drop was recorded for groups 3 and 5. In his 2007 study of changes in the level of physical activity and body composition of DM2 patients after an interventionist program, Mathieu et al18 also reported a reduction in body fat percentage calculated from skin folds, and an improvement in patient fitness, thus reducing cardiovascular risks.
A drop in capillary glycemia right after the workout sessions indicated the acute effect of physical exercise. It was also possible to detect a smaller variation in capillary glycemic levels of G5 patients after physical exercise, but this variation was not statistically significant. In our study, the intensity or duration of the sessions may not have been enough to ensure significant acute changes in capillary glucose levels in this group of patients.
After the 13th week, a better control of glycemic levels measured before physical exercise sessions in both groups was recorded, indicating a residual effect of SPEP on baseline glycemia. Nevertheless, data in our study on the topic suggest that G5 had lower and more stable capillary glycemic levels than G3 (Figure 1). However, these differences were not statistically significant. Frequency of physical exercise seems to be an important factor in controlling baseline glycemia. These findings add to those of other studies reporting the acute effect of physical exercise, but the long-term effect was not as clear20-22.
The relationship between fasting glycemia and physical exercise programs is controversial. A recent study7 showed that FG increases within 24 to 72 hours after a workout session (60% of max. VO2, one-hour long, 3x week). In this program, patients with Type 2 diabetes were on a diet and used oral agents. In our study, a drop in fasting glycemia was observed only in G5.
A further discrepancy among these studies and in ours as well, may involve medication, particularly insulin and oral hypoglycemic agents taken by DM2 patients. For instance, there are studies17 in which the oral hypoglycemic medications were interrupted 7 days before the beginning of the study. Since our patients did not interrupt the use of medication prescribed by their doctors, there may be different effects on fasting and postprandial glycemia.
In the groups evaluated, we found a reduction in HbA1c ranging from 0.3 to 0.8 percentage points. Despite being aware of the clinical importance of such a reduction, considering that a 1% drop in HbA1c value is associated with a 15%-20% reduction in cardiovascular events and a 37% reduction in microvascular complications3, in our sample this difference was not significant. Nevertheless, it is important to stress that by the 20th week, patients in groups G3 and G5 had reached HbA1c values close to suggested disease-control levels5.
Studies in medical literature7 about the influence of physical exercise on HbA1c have reported heterogeneous results. A recent meta-analysis considered data from 14 studies, which reported a reduction of approximately 10% in HbA1c concentrations with physical exercise23.
The effect on insulin sensitivity is triggered by the physical exercise session itself, and remains for a relatively short time (no longer than 72 hours). Here we have a clear example of an acute and non-chronic effect leading to an important methodological issue, as some studies have retested their patients at different times elapsed since the last workout session and may have found, therefore, different effects23.
It is important to analyze that the effect on insulin sensitivity of one single workout session remains for 24-72 hours, depending on the duration and intensity of the exercise. That is because the duration of the increase in insulin sensitivity generally does not last longer than 72 hours. It is recommended that the interval between sessions does not exceed 72 hours5.
Reduced insulin resistance and increased sensitivity can be, above all, a response to each exercise session, rather than the long-term result associated with exercise training24.
Nonetheless, in the two experimental groups (G3 and G5), the interval between sessions was less than 72 hours including weekends. Even then, in our study, no improvement in HbA1c values (chronic effect on physical exercise) was observed.
Ligtenberg et al25 reported a significant reduction of glycated hemoglobin in type 2 diabetes, but only with one year of training and not within 6 months. This suggests that a difference in glycemic control can only be achieved with regular physical exercising over a longer period.
Moreover, exercise intensity is also important to reduce HbA1c values. There are studies showing that it is important to encourage type 2 diabetes patients who already are engaged in physical exercise to consider increasing the intensity from moderate to high, which could result in additional benefits, especially concerning glycemic control.5, 26
Non-optimized dieting and therapeutic plans, added by physical exercise performed at only 70% of maximum heart rate due to the limitations of this group of patients may account for the non-reduction in HbA1c and the lack of continuous control of glycemia in DM2 patients.
Baseline HbA1c values should also be considered. It seems that the higher the HbA1c levels at the beginning of the treatment, the greater the drop of these levels will be. In our study, HbA1c values in G3 and G5 were not very different (0.9 to 1.3%) from the reference values. Therefore, this could be another reason why no significant reduction in these values was observed in our study. The small size of our sample may also account for the statistically non-significant drop in HbA1c.
Our results show that the ideal frequency of a moderate intensity physical exercise program for DM2 patients, in the great majority of parameters evaluated, is five times per week (5x). However, results did not show a decrease of HbA1c values in patients with DM2.
Potential Conflict of Interest
No potential conflict of interest relevant to this article was reported.
Sources of Funding
This study was partially funded by Roche and Abbott.
This article is part of the thesis of Doctoral submitted by Denise Maria Martins Vancea, from Escola Paulista de Medicina - Universidade Federal de São Paulo.
1. Wajchenberg BL. Disfunção endotelial no DM2. Arq Bras Endocrinol Metab. 2002; 46 (5): 514-9. [ Links ]
2. Després JP. Cardiovascular disease under the influence of excess visceral fat. Crit Pathw Cardiol. 2007; 6 (2): 51-9. [ Links ]
3. Selvin E, Marinopoulos S, Berkenblit G, Rami T, Brancati FL, Powe NR, et al. Meta-analysis: glycosylated hemoglobin and cardiovascular disease in diabetes mellitus. Ann Intern Med. 2004; 141: 421-31. [ Links ]
4. Sociedade Brasileira de Diabetes. Novas diretrizes da SBD para o controle glicêmico do diabetes tipo 2 - Posicionamento oficial SBD 2007; nº 4 (on line). [acesso em 2008 jan 10]. Disponível em http://www.diabetesebook.org.br/capitulo/novas-diretrizes-da-sbd. [ Links ]
5. Sigal RJ, Kenny GP, Wasserman DH, Castaneda-Sceppa C. Physical activity/exercise and type 2 diabetes. Diabetes Care. 2004; 27(10): 2518-39. [ Links ]
6. Tokmakidis SP, Zois CE, Volaklis KA, Kotsa K, Touvra AM. The effects of a combined strength and aerobic exercise program on glucose control and insulin action in women with type 2 diabetes. Eur J Appl Physiol. 2004; 92: 437-42. [ Links ]
7. Boulé NG, Weisnagel SJ, Lakka TA, Tremblay A, Bergman RN, Rankinen T, et al. Effects of exercise training on glucose homeostasis. Diabetes Care. 2005; 28: 108-14. [ Links ]
8. Poirier P, Tremblay A, Catellier C, Tancrede G, Garneau C, Nadeau A. Impact of time interval from the last meal on glucose response to exercise in subjects with type 2 diabetes. J Clin Endocrinol Metabol. 2000; 85: 2860-4. [ Links ]
9. Burstein RC, Polychronakos CJ, Tows JD, Toews CJ, MacDougall JD, Guyda HJ, et al. Acute reversal of the enhanced insulin action in trained athletes: association with insulin receptor changes. Diabetes. 1985; 34: 756-60. [ Links ]
10. Heath GW, Gavin JR, Hinderliter JM, Hagberg JM, Bloomfield SA, Holloszy JO. Effects of exercise and lack of exercise on glucose tolerance and insulin sensitivity. J Appl Physiol. 1983; 55: 512-17. [ Links ]
11. The Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Diabetes Care. 2000; 23 (Suppl. 1): S4-19. [ Links ]
12. Fox EL, Bowers RW, Foss ML. Bases fisiológicas da educação física e dos desportos. Rio de Janeiro: Guanabara Koogan, 1991. p. 209-10. [ Links ]
13. Pollock ML, Wilmore JH. Exercícios na saúde e na doença. Rio de Janeiro: MEDSI, 1993; p. 55, 329-33. [ Links ]
14. Kadoglou NP, Iliadis F, Angelopoulou N, Perrea D, Ampatzidis G, Liapis CD, et al. The anti-inflammatory effects of exercise training in patients with type 2 diabetes mellitus. Eur J Cardiovasc Prev Rehabil. 2007; 14 (6): 837-43. [ Links ]
15. Riddell M. Diabetes tipo 1 e a atividade física 2007. In: 16º Congresso Brasileiro de Diabetes. Campinas/São Paulo, 2007. [ Links ]
16. Bianchini C. Treating the metabolic syndrome. Expert Rev Cardiovasc Ther. 2007; 5 (3): 491-506. [ Links ]
17. Duncan BB, Schmidt MI. Chronic activation of the innate immune system may underlie the metabolic syndrome. São Paulo Med J. 2001; 119 (3): 122-7. [ Links ]
18. Mathieu ME, Brochu M, Beliveau L. DiabetAction: changes in physical activity practice, fitness, and metabolic syndrome in type 2 diabetic and at-risk individuals. Clin J Sport Med. 2008; 18 (1): 70-5. [ Links ]
19. American College of Sports Meddicine (ACSM). Manual do ACSM para avaliação da aptidão física relacionada à saúde. Rio de Janeiro: Guanabara Koogan, 2006. [ Links ]
20. Martins DM, Thiago DDBS, Borges PSS. Efeito do exercício físico regular sobre o controle da glicemia capilar de mulheres diabéticas não insulino-dependentes. Rev Bras Ativ Fis Saúde. 1997; 2 (2): 17-23. [ Links ]
21. Martins DM, Duarte MFS. Efeito do exercício físico sobre o comportamento da glicemia em indivíduos diabéticos. Rev Bras Ativ Fis Saúde. 1998; 3 (3): 32-44. [ Links ]
22. Martins DM, Duarte MFS. Exercise chronic effects on non insulin-dependent diabetes mellitus. In : 26 World Congress of Sports Medicine. 30/05 a 06/06; Orlando / Florida, 1998. [ Links ]
23. Araújo CGE. Exercício físico no tratamento do paciente diabético. In: Oliveira JEP (ed.) Diabetes melito tipo 2: terapêutica clínica prática. Rio da Janeiro: Diagraphic. 2003, p. 73-113 [ Links ]
24. Wilmore JH, Costill DL. Fisiologia do exercício e do esporte. São Paulo: Manole, 2001. [ Links ]
25. Lee BW, Craig J, Lucas R, Pohlman and Stelling H. The effect of endurance training and weight training upon the blood lipid profiles of young male subjects. J Appl Sports Sci Res. 1990; 4: 68-75. [ Links ]
26. Di Loreto C, Fanelli C, Lucidi P, Murdolo G, De Cicco A, Parlanti N, et al. Long-term impact of different amounts of physical activity on type 2 diabetes. Diabetes Care. 2005; 28: 1295-302. [ Links ]
Mailing address: Manuscript received
January 31, 2008; revised manuscript received March 07, 2008; accepted March
Denise Maria Martins Vancea
Rua Cruz e Souza, 514 - 88101-040
Campinas - São José, SC - Brazil
Manuscript received January 31, 2008; revised manuscript received March 07, 2008; accepted March 19, 2008.