Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1
Milena Raffi
 -- 4489 2023-11-15 12:18:46 |
2 layout
Camila Xu
 Meta information modification 4489 2023-11-16 01:22:16 |

Video Upload Options

Do you have a full video?
Send video materials Upload full video

Confirm

Are you sure to Delete?
Yes No
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Piras, A.; Raffi, M. Exercise Training in Managing Diabetes Mellitus. Encyclopedia. Available online: https://encyclopedia.pub/entry/51607 (accessed on 04 May 2024).
Piras A, Raffi M. Exercise Training in Managing Diabetes Mellitus. Encyclopedia. Available at: https://encyclopedia.pub/entry/51607. Accessed May 04, 2024.
Piras, Alessandro, Milena Raffi. "Exercise Training in Managing Diabetes Mellitus" Encyclopedia, https://encyclopedia.pub/entry/51607 (accessed May 04, 2024).
Piras, A., & Raffi, M. (2023, November 15). Exercise Training in Managing Diabetes Mellitus. In Encyclopedia. https://encyclopedia.pub/entry/51607
Piras, Alessandro and Milena Raffi. "Exercise Training in Managing Diabetes Mellitus." Encyclopedia. Web. 15 November, 2023.
Exercise Training in Managing Diabetes Mellitus
Edit
This entry is adapted from the peer-reviewed paper 10.3390/healthcare11222947

Diabetes mellitus (DM) is a metabolic disease characterized by chronic hyperglycemia associated with impaired carbohydrate, lipid, and protein metabolism, with concomitant absence of insulin secretion or reduced sensitivity to its metabolic effects. Physical activity (PA) is normally suggested in the management of type 1 (T1DM) and type 2 (T2DM) diabetes mellitus and can improve glucose uptake by increasing insulin sensitivity, glucose transportation into the cells, and lowering body adiposity.

resistance training aerobic training physical exercise exercise guidelines

1. Introduction

Physical activity (PA) is normally suggested in the management of type 1 (T1DM) and type 2 (T2DM) diabetes mellitus and can improve glucose uptake by increasing insulin sensitivity, glucose transportation into the cells, and lowering body adiposity. In T2DM, the practice of PA, both alone and when combined with diet and drug therapy (e.g., oral hypoglycemic agents), can result in improved glycemic control [1]. In addition, PA can also help to prevent the onset of T2DM and has an important role in reducing the significant worldwide problem of this pathology. Different studies have enhanced the understanding of the acute and long-term physiological benefits of PA, although the precise duration, intensity, and type have yet to be fully elucidated [1][2][3]. In T1DM, however, the expected improvements in glycemic control with PA have not been clearly established. Instead, significant physical and psychological benefits of physical exercise can be achieved while careful education, screening, and planning allow the metabolic, microvascular, and macrovascular risks to be predicted and diminished [4].
The probable hypoglycemic advantage associated with PA was initially observed by Aristotle and later promoted by Allen and Joslin in 1920 [2]. Even though PA is considered one of the main solutions for diabetes management, indications about the exercise protocols for diabetes are scarce. Notwithstanding, different results have highlighted that many characteristics of the pathology can be improved and probably avoided following regular PA [2][3][4].
It has been estimated that more than 600 million individuals will suffer from T2DM by 2035 [5]. Increasing attention has been paid to people at increased risk of developing T2DM, such as those living with impaired fasting glucose (i.e., prediabetes) [6]. PA is beneficial for preventing the progression of impaired fasting glucose to diabetes [7][8], but people at high risk of developing diabetes often fail to meet the PA guidelines of 150 min of moderate-to-vigorous aerobic exercise per week [9]. Innovative trials, such as the Diabetes Prevention Program (DPP), have demonstrated that a lifestyle intervention that comprises 150 min of moderate-intensity PA per week can reduce the progression of impaired fasting glucose by up to 58% compared to a non-exercise group and is almost twice as effective as the leading pharmaceutical intervention [10]. This represents a valid procedure designed to assess the potency of lifestyle modification for the prevention of T2DM [6]. Nowadays, even though the benefits of PA as a therapeutic measure for diabetic patients are well known and accepted, it is difficult to put exercise recommendations into action for several reasons. Insufficient knowledge among diabetologists and exercise professionals and a lack of dedicated facilities are indicated as important limitations [2]. Moreover, to provide effective PA support to people with diabetes, research is required to develop clinically effective, cost-effective, scalable interventions that bridge the gap between supervised PA advice. Print-based materials [11] and technology-based support, such as websites [12][13][14], smartphone apps [15][16], and telephone helplines [11][17], have also been shown to be effective in supporting people with diabetes to increase their level of PA. However, such interventions would have better efficacy if grounded in health behavior change theory [14]. For this reason, wearable technologies, offering biometric data to patients and healthcare professionals, bridging the gap between supervised PA advice, and enabling patients to engage in regular, long-term, physically active lifestyles [18][19], seem to be very helpful in diabetes prevention and management. It has been shown that professional exergames, as well as mobile app-based programs [20], have the potential to be effective treatment options, especially because they seem to at least partly solve the adherence problem [21]. Prescribing physical exercise is not generally undertaken, either by the general practitioner or by the diabetologist. This may be because there is insufficient awareness of the benefits of physical exercise or because there is a lack of specific knowledge regarding current recommendations. Thus, prescriptions, when suggested, are generic and more oriented towards ‘physical activity’ rather than ‘exercise therapy’, without appropriate indication about type, intensity, frequency, timing, progression, and precautions [2]. Furthermore, barriers to, and discriminations in, PA and exercise adoption and maintenance must be addressed to maximize participation [3].

2. Acute Effect of Exercise on Sugar Metabolism

PA allows for improving the glucose-tolerance curve by ameliorating insulin sensitivity in any subject, either with T2DM or T1DM [22]. Traditionally, physical exercise is promoted in T2DM, where insulin action is scarce in the context of insulin resistance and/or inappropriate insulin secretion. Nevertheless, even in the dysregulation of immune system function found in T1DM, the β-cell toxicity is facilitated by a complex interaction between oxidative stress and inflammation, for which the chronic exercise effect could be protective. During physical exercise, large changes in energy utilization require fine adjustments of glucose and fatty acid concentrations present in the blood. During the first 5–10 min of moderate-intensity exercise, a mixture of fatty acid and glucose provides the major fuel source for skeletal muscle. As exercise duration is prolonged and maintained at a moderate intensity, the contribution of fatty acid becomes more significant, thanks to hormonal responses, such as increased levels of norepinephrine and glucagon that promote the release of fatty acids from adipose tissue (fat stores) into the bloodstream (lipolysis) [23]. The liberated fatty acids circulate in the blood and are available for uptake by muscle cells. There is also an upregulation of fatty acid transporters in muscle cells. This increased expression of transport proteins facilitates the uptake of fatty acids from the bloodstream into the muscle fibers, making them available for energy production. The oxidation of fatty acids produces a larger amount of ATP compared to glucose metabolism. By relying more on fatty acids for energy, the body can conserve its limited glycogen stores [24]. Preserving glycogen is crucial for sustaining exercise performance, especially during endurance activities or when exercise intensity increases. Glycogen is the primary fuel source for high-intensity exercise, and by sparing its usage, it helps delay the onset of fatigue. There is a direct relationship between exercise intensity and glucose utilization: when the exercise intensity increases, an augmented glucose utilization via the glycogen deposit from muscles and liver was observed [24]. A complex hormonal and autonomic response allows an intensification in hepatic glucose production and tissue uptake by the mobilization of non-esterified fatty acid from adipose tissue deposits [23]. This is produced both by a fall in circulating insulin concentrations and a wide variety of counterregulatory hormones (glucagon, adrenaline, cortisol, and growth hormone) that counteract the hypoglycemic action of insulin [25]. Elevations in the blood concentrations of these hormones promote both increased glucose production and mobilization of non-esterified fatty acids from adipose storage sites. In addition, the production of new glucose in the liver (gluconeogenesis) from substrates such as lactate is enhanced [26]. Direct sympathetic stimulation of the pancreas and liver after muscle contraction may also bypass initial hormonal control and additional fuel supplies are provided by ketone formation and mobilization of lactate from inactive muscle glycogen. Glucose transport into muscle is again provided by the transporter protein GLUT4, which is recruited to the membrane surface in large quantities in contracting muscle, independently of insulin. Altogether, these changes maintain the increased fuel supply for exercising muscles and prevent hypoglycemia from excessive utilization [26].
Higher-intensity exercise or shorter-duration activities primarily rely on glycogen as the predominant fuel source, while lower-intensity or longer-duration exercise shifts towards a greater reliance on fatty acids for energy [24]. When exercise is ended, the body goes into a fasted state in which glycogen stores in muscle and liver are low and hepatic glucose production is enhanced. The level of the counter-regulatory hormones could remain higher for a long time with an associated hyperglycemic and hyperinsulinaemic response [27]. Improved GLUT4 transport and insulin sensitivity produce augmented glycogen resynthesis at the muscle level. Thereafter, when glycogen, glucose, and hormone levels return to normal levels, and homoeostasis is reached, insulin can produce supplementary glucose uptake and glycogen resynthesis in muscle and liver. When insulin is scarce, or the body is in a resistant state, glucose storage could be reduced within muscle as a consequence of the inadequate transport with an associated decrement in glycogen synthase activity [25][28].

3. Exercise Benefits for People with Diabetes

PA, sports, and exercise should be encouraged in people with T1DM for the same reasons as it should be promoted in people with T2DM or in the general population. The prescription of physical exercise for diabetic control should be considered for a variety of associated and independent health benefits. The full scope of these benefits can be seen in a number of reviews and include weight loss, weight loss maintenance, lipid profiles, reduction in blood pressure, good psychological profile, and the regulation of symptoms implicated in the metabolic syndrome [1][29]. It would appear that the combined effect of PA and diet provides the first and possibly most effective intervention in improving cardiovascular risk [30].
It has become evident that the most important effect of physical exercise is the improvement of blood sugar control, weight loss, and weight loss maintenance. PA helps in lowering blood sugar levels by increasing the uptake of glucose into muscles, even without the need for insulin. It enhances insulin sensitivity, making the body more efficient at using insulin to regulate blood sugar. Regular exercise can contribute to better long-term glycemic control. Moreover, physical exercise plays a crucial role in weight management, which is particularly important for individuals with T2DM. Regular PA reduces body fat, increases muscle mass, and improves overall body composition. Maintaining a healthy weight can enhance insulin sensitivity, allowing for more efficient glucose utilization. This can lead to decreased insulin resistance, which is a key factor in T2DM. By improving insulin sensitivity, physical exercise can reduce the reliance on medication or insulin therapy in managing diabetes [28][31][32].
PA can also improve cardiovascular health by strengthening the heart, reducing blood pressure, lowering LDL cholesterol levels, increasing HDL cholesterol levels, and improving blood circulation, significantly reducing the risk of heart disease and stroke. Cardiovascular complications are also worsened by stress, and PA is an excellent stress reliever [33]. Managing stress is important for individuals with diabetes because stress hormones can raise blood sugar levels. Physical exercise reduces stress levels, improves mood, and promotes overall mental well-being. By improving blood sugar control, weight management, cardiovascular health, and overall well-being, regular exercise can lower the risk of diabetes-related complications such as heart disease, stroke, nerve damage, kidney disease, and eye problems [28][31][32][33][34].

4. Exercise and Diabetes: General Recommendations

All levels of PA, including leisure activities, recreational sports, and competitive professional performance, can be performed by people with DM who do not have complications and are in good blood glucose control. A recent systematic review and meta-analysis of eight randomized controlled trials (5190 participants) reported that effective exercise interventions have the potential to reduce the personal and economic costs associated with diabetes [11][35]. They questioned the efficacy and cost-effectiveness of exercise referral schemes, increasing the exercise level and recommending further trials, especially those that are theory-driven [36]. It should be noted that many of the referral schemes used leisure centers for group-based programs, which did not provide expert supervision. James et al. [17] demonstrated a significant increase in PA among insufficiently active primary care patients who were provided a referral to receive five sessions from an exercise specialist. It has been suggested that those who potentially have the most to gain from exercise are often the ones who find it most difficult to engage in healthy behavior [35][37]. The effectiveness of PA as a therapeutic intervention is also seriously hampered by uncertainty concerning how clinical care teams should support people with diabetes to meet and maintain exercise guidelines [38].
It has been largely confirmed that daily PA has different implications in improving people's lifestyles by improving insulin sensitivity, reducing exogenous insulin injection, managing body weight and lipid profiles, boosting self-confidence, improving psychological problems associated with the pathology, reducing systemic inflammation, and most importantly, enhancing long-term protection against cardiovascular disease. Chronic hyperglycemia is supposed to be the mechanism by which coronary artery disease, stroke, nephropathy, retinopathy, and neuropathy occur over decades after disease onset. Moreover, hyperglycemia is related to increased inflammation, as reflected by activation of immune cells and increased systemic concentrations of proinflammatory cytokines/chemokines [39]. This inflammatory status persists for several hours or days after hyperglycemia has been resolved [40]. Preventing hyperglycemia is the main aim of DM treatment and may eliminate the excess inflammation caused by physical exercise. When this occurs, the subject can (i) postpone or cancel the planned exercise activity until the pro-inflammatory effects are reduced, (ii) perform physical exercise in a pro-inflammatory status, or (iii) reduce physical exercise-associated inflammation via medical treatment. Given that prior hyperglycemia alone (without ketosis) is not currently included in the contraindications to physical exercise, the second option is good [41]. General guidelines that may prove helpful in regulating the glycemic response to PA are presented below [2][42].

5. Metabolic Control before Exercise

I.
Avoid physical exercise if the fasting glucose level is >250 mg/dL and ketosis is present, and take care if the glucose level is >300 mg/dL and no ketosis is present.
II.
Ingest additional carbohydrates if glucose levels are <100 mg/dL.
Blood glucose monitoring before, during, and after physical exercise
I.
Identify when changes in medication (insulin/hypoglycemic agent) or food intake are necessary.
II.
Learn the glycemic response to different PA conditions.

5.1. Food Intake the Physical Exercise Day

I.
Consume additional carbohydrates as required to avoid hypoglycemia.
II.
Carbohydrate-based foods should be readily available during and after PA.

5.2. Food Intake the Rest Day

I.
Reduce carbohydrate intake (<50 g/day).
II.
A low carbohydrate diet has been shown to be effective for weight loss due to its effect on decreasing appetite and calorie intake.
III.
Lowering dietary carbohydrate intake has demonstrated benefits for insulin resistance, the underlying cause of T2DM, by independently promoting both weight loss and a reduction in insulin levels.

6. Exercise in Managing T1DM

The ability to adjust the therapeutic regimen (insulin administration and timing, type and quantity of food ingestion before and after physical exercise) that allows safe participation and high performance has recently been recognized as an important management strategy in individuals with T1DM. In particular, the important role played by the patient in collecting self-monitored blood glucose data related to physical exercise responses to improve performance and enhance safety is now fully accepted [1][2][43].
When amateurs exercise at 50–60% of VO2max, which is below their anaerobic threshold, glucose levels rise following the increased uptake of skeletal muscle. The level of glycemia is generally reduced 30/45 min after PA, and it is preserved within the physiological range by two processes: a rapid increase in endogenous glucose production and a reduction in systemic insulin levels [41]. Patients should reduce or stop insulin infusion before exercise. This is to avoid the hypoglycemic effect due to the increase in glucose uptake at the skeletal muscle and to suppress endogenous glucose production.
Different is the situation in which the subject is involved in physical exercise above the anaerobic threshold and close to the VO2max. In this condition, the body produces a higher adrenergic activation that facilitates, beyond cardiovascular response, an endogenous increase in glucose level, exceeding the metabolic need at the peripheral level. This creates a state of moderate, transient hyperglycemia that does not exceed 140 mg/dL in healthy people. In T1DM, given that insulin cannot be secreted in response to this hyperglycemic response, the hyperglycemia value often continues to increase after exercise, sometimes becoming dangerous (>400 mg/dL) [41].
Hypoglycemia, which can occur during, immediately after, or many hours after PA, can be avoided. Indeed, during physical exercise, the body requires approximately 30–50% less insulin than in resting conditions to transport glucose across the cell membrane of myocytes. This is due to a considerable fraction of exercise-stimulated transmembrane glucose transport that occurs via noninsulin-dependent mechanisms [44]. In this case, it is important that the patient has both an adequate knowledge of the metabolic and hormonal responses to PA and well-tuned self-management skills. The increasing use of intensive insulin therapy has provided patients with the flexibility to make appropriate insulin dose adjustments for various activities. Moreover, in T1DM, after 2–4 years of disease onset, the ability to increase glucagon secretion (the main counterregulatory hormone) in response to hypoglycemia is permanently and completely abolished. However, in T1DM, hypoglycemia is caused by excessive exogenous insulin injection, involving low glycemia and high insulinemia that blocks glucagon release [41].
Aerobic performance is reduced in T1DM because of cardiovascular, muscular, and metabolic impairments. When compared to their nondiabetic counterparts, young patients with T1DM showed a reduction in VO2max despite insulin therapy [45], a difference exacerbated in adults with neuropathic complications or sedentary lifestyles [46]. Different is the situation in which athletes with T1DM are compared to their nondiabetic counterparts, where VO2peak was found to be similar [47]. Moreover, in T1DM, various cardiovascular parameters, such as end-diastolic volume and left ventricular ejection fraction, do not show a normal increment due to exercise, meaning that exercise can lead to normal aerobic and cardiovascular parameters [41].
The general recommendations for PA in adults with T1DM, free of complications, are the same for children, considering that kids are more subjected to a greater variability in glycemic level. For this reason, attention should be focused on glycemic fluctuation during exercise so that parents, teachers, and athletic coaches are properly trained. When dealing with adolescents, hormonal variations can increase the difficulty in managing glycemic levels. Notwithstanding these additional difficulties, it is out of the question that following the useful recommendations to avoid hypoglycemia, PA is a safe and satisfying practice for most children and adolescents with T1DM [42].

7. Exercise in Managing T2DM

A standard recommendation for people with and without diabetes is to start PA with a warm-up and end with a cool-down phase. The warm-up involves 5–10 min of aerobic exercises (walking, cycling, etc.) at low intensity. The aim is to prepare the skeletal muscles, heart, and lungs for a progressive increase in exercise intensity. Then, muscles can be gradually stretched for an additional 5–10 min to maintain a good range of motion in the joints [48]. After the main training session, a 5–10 min cool-down should be organized similarly to the warm-up. The aim of the cool-down is to gradually bring the heart rate back to its pre-exercise value. There are some recommendations that are particularly important and specific for people with T2DM. Moderate weight training exercises with light weights and high repetitions can be suggested for maintaining or enhancing upper body strength in people with diabetes. Different long-term studies have established long-lasting beneficial effects of regular PA on carbohydrate metabolism and insulin sensitivity, which can be maintained for at least 5 years. They suggested PA programs with an intensity in the range of 50–80% of VO2max, three to four times a week, for 30–60 min a session. Aerobic exercise should be suggested, considering safety measures for PA involving the feet, which are essential for many patients with diabetes [1][2][48][49][50][51]. High-resistance exercise using weights may be acceptable for young individuals with diabetes but not for older individuals with long-standing diabetes.
Good hydration is also crucial, as dehydration can adversely affect glycemic levels and heart function. Through PA, fluid should be frequently consumed to compensate for losses in sweat reflected in body weight loss or the maximal amount of fluid tolerated (e.g., 0.5 L of fluid consumed 2 h before PA) [52]. Precautions should be taken when exercising in extremely hot or cold environments.
It has been shown that improvements in glycated hemoglobin (HbA1c) are generally 10–20% of the baseline and are most marked in patients with mild T2DM and in those who are likely to show insulin resistance [53]. It remains true, unfortunately, that most of these studies suffer from inadequate randomization and controls and are confounded by associated lifestyle changes. The general agreement is that regular exercise should not be expected to dramatically affect HbA1c values; other variables, such as increased food intake or reduced insulin dosages, compensate for any increases in glucose disposal. Nonetheless, epidemiological evidence confirmed that being physically active, rather than sedentary, can lower mortality and morbidity for any given level of HbA1c [54].
It seems that long-lasting programs of PA are good enough and demonstrate a higher rate of adherence in patients with prediabetes or uncomplicated T2DM. In this kind of study, researchers started their training programs with initial supervision, followed by home-training programs with follow-up to assess the level of adherence [4]. A lot of them have shown good results in the maximum oxygen consumption with few complications for patients [55].

8. Psychological Profile, Muscular, and Cardiovascular Evaluations

Other important aspects to consider when prescribing an exercise program are the evaluation of motor responses and the consideration of the psychological profile. Evaluations represent a fundamental moment for understanding the real capabilities of an individual, setting up protocols and assessing results over time. People with diabetes show both impaired exercise tolerance and an excessive risk of developing heart failure, which are not entirely explained by known cardiovascular risk factors or coronary artery disease [56]. The risk for cardiovascular disease and other diabetes-related complications, including neuropathy, retinopathy, and nephropathy in persons with long-standing disease, is high, and care should be taken to properly screen individuals before recommending a new exercise program. Caution is warranted for those with advanced disease complications and medical screening; before initiating any new vigorous exercise program, a graded exercise stress test with ECG and blood pressure monitoring should be performed. The main assessments that should be made before carrying out any type of physical exercise are, in order: (i) the Health Assessment Questionnaire; (ii) assessment of balance level and risk of falls; (iii) cardiopulmonary exercise testing; (iv) the assessment of muscle strength.
Health assessment questionnaires [57]. While several tools are available to measure health-related quality of life (HRQoL) for patients with diabetes, the design and, therefore, duration of these measurements may limit their feasibility in the daily routine of a sports facility. Furthermore, these measures do not distinguish items for diabetes-specific quality of life. Thus, a specific questionnaire on the diabetics’ quality of life (DMQoL) was developed with only 10 questions, sensitive to the change related to the progression of diabetes compared to the initial stages (e.g., glycemic changes). The combination of the DMQoL and the WHOQOL-BREF (the shortened version of the quality of life questionnaire designed by WHO) provides a comprehensive picture of overall health-related quality of life in patients with diabetes and improves the ability to detect changes clinically significant to the pathology.
Tests that determine the level of balance and the risk of falls. Patients with T2DM, particularly those ≥65 years old, exhibit an increased rate of falls. It is, therefore, important to assess the risk of falling before the prescription of an exercise intervention. The most used tests are the Timed Up and Go Test (TUG), the Functional Reach Test, (FRT), the Berg Balance Scale (BBS), and the Dynamic Gait Index (DGI). Among those tests, the TUG showed the greatest sensitivity (90%) and specificity (88%) to the phenomenon [58]. In this assessment, the patient gets up from a chair, walks 3 m, turns around, returns to the chair, and sits down again. This task must be completed within 10.6 s. Times between 11 and 20 s are within the normal range for frail elderly and disabled patients; times ≥20 s indicate that the person needs external assistance. A score ≥30 s predicts a higher risk of falling.
Cardiopulmonary exercise testing (CPET). Measurements of ventilation, gas exchange, and electrocardiography during an incremental exercise test are noninvasive protocols that provide an assessment of pulmonary, cardiovascular, and muscle function during exercise (see Table 1). The addition of echocardiographic monitoring (“imaging-CPET”), mainly used in patients with heart failure, may provide further insight into different aspects of cardiac function during exercise and their impact on exercise intolerance [59]. Even though guidelines recommend the application of objective exercise prescriptions using CPET data [59], it is common to find programs without CPET information or with limited resources to establish exercise intensity on the basis of resting heart rate (e.g., exercising heart rate threshold set 20 or 30 beats/min above the resting heart rate). This simple method has been criticized and demonstrated to be inadequate by several researchers. Moreover, it should be noted that performing this test routinely and its cost mean that specific criteria must be defined regarding patients for whom it would be imperative to perform the test.
Table 1. Physiological variables measured during CPET.
Physiological Mechanism Direct Measurement Indirect Measurement
General VO2; peak power VO2%
Cardiovascular system HR; BP VO2/HR
Cardiac electrical system ECG Chronotropic insufficiency; change in heart rate of recovery
Ventilation Ventilation; Tidal volume VE/VO2; VE/VCO2
Gases exchange SpO2; PETO2; PETCO2 Anaerobic threshold
Skeletal muscles Scala di Borg Δ(a − v)O2; Anaerobic threshold
Metabolism RER Anaerobic threshold
Systolic function LVEF; TAPSE Systolic reserve
Diastolic function E/A; DT Systolic reserve
Legend: VO2%, percentage of peak oxygen uptake; HR, heart rate; BP, blood pressure; ECG, electrocardiography; VE/VO2; VE/VCO2, ventilator equivalents of oxygen and carbon dioxide; SpO2, arterial oxygen saturation; PETO2 and PETCO2, end-expiratory pressure of oxygen and carbon dioxide; Δ(a − v)O2, arteriovenous difference in oxygen; RER, respiratory exchange ratio; LVEF, left ventricular ejection fraction; TAPSE, tricuspid annular plane systolic excursion; E/A, transmittal flow velocity; DT, deceleration time.
Assessment of muscle strength. A significant percentage of T2DM patients (prevalence 16%, mean age 58 years old) are sarcopenic compared to age-matched healthy individuals [34]. Considering that 80% of insulin-mediated glucose uptake occurs in skeletal muscle (lean mass) [60], the importance of increasing lean mass for improving glycemic control in these individuals should be considered [61]. Furthermore, muscle strength is reduced by 30% to 50% in T2DM patients compared to their healthy counterparts. Dynamometry is considered the gold standard for examining muscle strength. However, considering the cost of this device and the technical skills required, this test is not feasible for those working in private and home care settings. There are different types of tests, such as handgrip strength and sit-to-stand tests. Handgrip strength shows moderate to high correlations with extremity muscle strength. The patient sits in a chair with their elbow flexed to 90 degrees and a force device in one hand. Subsequently, the patient grips the device as tightly as possible for 3 s. This test is performed three times, alternating hands. Another strength test that could be considered to assess muscle strecngth in T2DM patients is the sit-to-stand test, although the validity of this test is currently under intense debate. Briefly, in this test, the person, without the help of the hands and arms, but with only the work of the legs, must perform, in 1 min, as many reps as possible and sit with legs bent at 90 degrees. Another version foresees a 30 s duration (30s-STS) [62], and another comprises five reps executed as quickly as possible (FTSST) [63].

References

  1. Sigal, R.J.; Kenny, G.P.; Wasserman, D.H.; Castaneda-Sceppa, C. Physical activity/exercise and type 2 diabetes: A consensus statement from the American Diabetes Association. Diabetes Care 2004, 29, 1433–1438.
  2. Peirce, N.S. Diabetes and exercise. Br. J. Sports Med. 1999, 33, 161–172.
  3. Kanaley, J.A.; Colberg, S.R.; Corcoran, M.H.; Malin, S.K.; Rodriguez, N.R.; Crespo, C.J.; Kirwan, J.P.; Zierath, J.R. Exercise/Physical Activity in Individuals with Type 2 Diabetes: A Consensus Statement from the American College of Sports Medicine. Med. Sci. Sports Exerc. 2022, 54, 353–368.
  4. Zinman, B.; Ruderman, N.; Campaigne, B.N.; Devlin, J.T.; Schneider, S.H. Diabetes mellitus and exercise. Diabetes Care 2002, 25, S64.
  5. Guariguata, L.; Whiting, D.R.; Hambleton, I.; Beagley, J.; Linnenkamp, U.; Shaw, J.E. Global estimates of diabetes prevalence for 2013 and projections for 2035. Diabetes Res. Clin. Pract. 2014, 103, 137–149.
  6. Bourne, J.E.; Little, J.P.; Beauchamp, M.R.; Barry, J.; Singer, J.; Jung, M.E. Brief exercise counseling and high-intensity interval training on physical activity adherence and cardiometabolic health in individuals at risk of type 2 diabetes: Protocol for a randomized controlled trial. JMIR Res. Protoc. 2019, 8, e11226.
  7. Gillies, C.L.; Abrams, K.R.; Lambert, P.C.; Cooper, N.J.; Sutton, A.J.; Hsu, R.T.; Khunti, K. Pharmacological and lifestyle interventions to prevent or delay type 2 diabetes in people with impaired glucose tolerance: Systematic review and meta-analysis. BMJ 2007, 334, 299.
  8. Warburton, D.E.R.; Charlesworth, S.; Ivey, A.; Nettlefold, L.; Bredin, S.S.D. A systematic review of the evidence for Canada’s Physical Activity Guidelines for Adults. Int. J. Behav. Nutr. Phys. Act. 2010, 7, 39.
  9. Mynarski, W.; Cholewa, J.; Rozpara, M.; Borek, Z.; Strojek, K.; Nawrocka, A. Recommendations for health-enhancing physical activities in type 2 diabetes patients. J. Phys. Ther. Sci. 2015, 27, 2419–2422.
  10. Iabetes, D.; Revention, P.; Rogram, P.; Esearch, R.; Roup, G. Reduction of the incidence of type 2 diabetes with lifestyle intervention or metformin. Int. Urol. Nephrol. 2002, 34, 162–163.
  11. Plotnikoff, R.C.; Courneya, K.S.; Sigal, R.J.; Johnson, J.A.; Birkett, N.; Lau, D.; Raine, K.; Johnson, S.T.; Karunamuni, N. Alberta Diabetes and Physical Activity Trial (ADAPT): A randomized theory-based efficacy trial for adults with type 2 diabetes—Rationale, design, recruitment, evaluation, and dissemination. Trials 2010, 11, 4.
  12. Liebreich, T.; Plotnikoff, R.C.; Courneya, K.S.; Boulé, N. Diabetes NetPLAY: A physical activity website and linked email counselling randomized intervention for individuals with type 2 diabetes. Int. J. Behav. Nutr. Phys. Act. 2009, 6, 18.
  13. Sazlina, S.G.; Browning, C.; Yasin, S. Interventions to promote physical activity in older people with type 2 diabetes mellitus: A systematic review. Front. Public Health 2013, 1, 71.
  14. Webb, T.L.; Joseph, J.; Yardley, L.; Michie, S. Using the internet to promote health behavior change: A systematic review and meta-analysis of the impact of theoretical basis, use of behavior change techniques, and mode of delivery on efficacy. J. Med. Internet Res. 2010, 12, e4.
  15. Aguiar, E.J.; Morgan, P.J.; Collins, C.E.; Plotnikoff, R.C.; Young, M.D.; Callister, R. The PULSE (Prevention Using LifeStyle Education) trial protocol: A randomised controlled trial of a Type 2 Diabetes Prevention programme for men. Contemp. Clin. Trials 2014, 39, 132–144.
  16. Middelweerd, A.; Mollee, J.S.; van der Wal, C.N.; Brug, J.; te Velde, S.J. Apps to promote physical activity among adults: A review and content analysis. Int. J. Behav. Nutr. Phys. Act. 2014, 11, 97.
  17. James, E.L.; Ewald, B.D.; Johnson, N.A.; Stacey, F.G.; Brown, W.J.; Holliday, E.G.; Jones, M.; Yang, F.; Hespe, C.; Plotnikoff, R.C. Referral for Expert Physical Activity Counseling: A Pragmatic RCT. Am. J. Prev. Med. 2017, 53, 490–499.
  18. Hesketh, K.; Low, J.; Andrews, R.; Jones, C.A.; Jones, H.; Jung, M.E.; Little, J.; Mateus, C.; Pulsford, R.; Singer, J.; et al. Mobile health biometrics to enhance exercise and physical activity adherence in type 2 diabetes (MOTIVATE-T2D): Protocol for a feasibility randomised controlled trial. BMJ Open 2021, 11, e052563.
  19. Höchsmann, C.; Walz, S.P.; Schäfer, J.; Holopainen, J.; Hanssen, H.; Schmidt-Trucksäss, A. Mobile Exergaming for Health-Effects of a serious game application for smartphones on physical activity and exercise adherence in type 2 diabetes mellitus-study protocol for a randomized controlled trial. Trials 2017, 18, 103.
  20. Fukuoka, Y.; Gay, C.L.; Joiner, K.L.; Vittinghoff, E. A Novel Diabetes Prevention Intervention Using a Mobile App A Randomized Controlled Trial With Overweight Adults at Risk. Am. J. Prev. Med. 2015, 49, 223–237.
  21. Lieberman, D.A. Video games for diabetes self-management: Examples and design strategies. J. Diabetes Sci. Technol. 2012, 6, 802–806.
  22. Kahn, S.E.; Prigeon, R.L.; McCulloch, D.K.; Boyko, E.J.; Bergman, R.N.; Schwartz, M.W.; Neifing, J.L.; Ward, W.K.; Beard, J.C.; Palmer, J.P.; et al. Quantification of the relationship between insulin sensitivity and β-cell function in human subjects: Evidence for a hyperbolic function. Diabetes 1993, 42, 1663–1672.
  23. Stokie, J.R.; Abbott, G.; Howlett, K.F.; Hamilton, D.L.; Shaw, C.S. Intramuscular lipid utilization during exercise: A systematic review, meta-analysis, and meta-regression. J. Appl. Physiol. 2023, 134, 581–592.
  24. Coyle, E.F. Substrate utilization during exercise in active people. Am. J. Clin. Nutr. 1995, 61, 968S–979S.
  25. Frid, A.; Ostman, J.; Linde, B. Hypoglycemia risk during exercise after intramuscular injection of insulin in thigh in IDDM. Diabetes Care 1990, 13, 473–477.
  26. Berger, M.; Assal, J.P.; Jorgens, V. Physical exercise in the diabetic. The importance of understanding endocrine and metabolic responses. Diabete Metab. 1980, 6, 59–69.
  27. Wasserman, D.H.; Vranic, M. Interaction between insulin and counterregulatory hormones in control of substrate utilization in health and diabetes during exercise. Diabetes. Metab. Rev. 1986, 1, 359–384.
  28. Wasserman, D.H.; Abuad, N.N. Physiological Bases for the Treatment of the Physically Active Individual with Diabetes. Sport. Med. 1989, 7, 376–392.
  29. Sato, Y. Overview of Exercise Prescription for Diabetes Patients and Its Application in Japan. J. Sci. Sport Exerc. 2020, 2, 226–235.
  30. Anderssen, S.; Holme, I.; Urdal, P.; Hjermann, I. Diet and exercise intervention have favourable effects on blood pressure in mild hypertensives: The Oslo diet and exercise study (ODES). Blood Press. 1995, 4, 343–349.
  31. Roglic, G. WHO Global report on diabetes: A summary. Int. J. Noncommun. Dis. 2016, 1, 3.
  32. Wasserman, D.H.; Zinman, B. Exercise in individuals with IDDM. Diabetes Care 1994, 17, 924–937.
  33. Gracia-Sánchez, A.; López-Pineda, A.; Chicharro-Luna, E.; Gil-Guillén, V.F. A delphi study protocol to identify recommendations on physical activity and exercise in patients with diabetes and risk of foot ulcerations. Int. J. Environ. Res. Public Health 2021, 18, 10988.
  34. Purnamasari, D.; Tetrasiwi, E.N.; Kartiko, G.J.; Astrella, C.; Husam, K.; Laksmi, P.W. Sarcopenia and Chronic Complications of Type 2 Diabetes Mellitus. Rev. Diabet. Stud. 2022, 18, 157–165.
  35. Plotnikoff, R.C.; Costigan, S.A.; Karunamuni, N.D.; Lubans, D.R. Community-based physical activity interventions for treatment of type 2 diabetes: A systematic review with meta-analysis. Front. Endocrinol. 2013, 4, 3.
  36. Pavey, T.G.; Taylor, A.H.; Fox, K.R.; Hillsdon, M.; Anokye, N.; Campbell, J.L.; Foster, C.; Green, C.; Moxham, T.; Mutrie, N.; et al. Effect of exercise referral schemes in primary care on physical activity and improving health outcomes: Systematic review and meta-analysis. BMJ 2011, 343, 980.
  37. Eves, N.D.; Plotnikoff, R.C. Resistance training and type 2 diabetes: Considerations for implementation at the population level. Diabetes Care 2006, 29, 1933–1941.
  38. Murphy, M.L.; Lubans, D.R.; Cohen, K.E.; Robards, S.L.; Wilczynska, M.; Kennedy, S.G.; James, E.L.; Brown, W.J.; Courneya, K.S.; Sigal, R.J.; et al. Preliminary efficacy and feasibility of referral to exercise specialists, psychologists and provision of a technology-based behavior change support package to promote physical activity in school teachers “at risk” of, or diagnosed with, type 2 diabetes: T. Contemp. Clin. Trials 2019, 78, 53–62.
  39. Gordin, D.; Forsblom, C.; Rönnback, M.; Parkkonen, M.; Wadén, J.; Hietala, K.; Groop, P.H. Acute hyperglycaemia induces an inflammatory response in young patients with type 1 diabetes. Ann. Med. 2008, 40, 627–633.
  40. El-Osta, A.; Brasacchio, D.; Yao, D.; Pocai, A.; Jones, P.L.; Roeder, R.G.; Cooper, M.E.; Brownlee, M. Transient high glucose causes persistent epigenetic changes and altered gene expression during subsequent normoglycemia. J. Exp. Med. 2008, 205, 2409–2417.
  41. Galassetti, P.; Riddell, M.C. Exercise and type 1 diabetes (T1DM). Compr. Physiol. 2013, 3, 1309–1336.
  42. Sonnenberg, G.E.; Kemmer, F.W.; Berger, M. Exercise in Type 1 (insulin-dependent) diabetic patients treated with continuous subcutaneous insulin infusion—Prevention of exercise induced hypoglycaemia. Diabetologia 1990, 33, 696–703.
  43. AlShorman, O.; AlShorman, B.; Alkahtani, F. A review of wearable sensors based monitoring with daily physical activity to manage type 2 diabetes. Int. J. Electr. Comput. Eng. 2021, 11, 646–653.
  44. Hayashi, T.; Wojtaszewski, J.F.P.; Goodyear, L.J. Exercise regulation of glucose transport in skeletal muscle. Am. J. Physiol.—Endocrinol. Metab. 1997, 273, E1039–E1051.
  45. Komatsu, W.R.; Lima Gabbay, M.A.; Castro, M.L.; Saraiva, G.L.; Chacra, A.R.; Leite de Barros Neto, T.; Dib, S.A. Aerobic exercise capacity in normal adolescents and those with type 1 diabetes mellitus. Pediatr. Diabetes 2005, 6, 145–149.
  46. Veves, A.; Saouaf, R.; Donaghue, V.M.; Mullooly, C.A.; Kistler, J.A.; Giurini, J.M.; Horton, E.S.; Fielding, R.A. Aerobic exercise capacity remains normal despite impaired endothelial function in the micro- and macrocirculation of physically active IDDM patients. Diabetes 1997, 46, 1846–1852.
  47. Komatsu, W.R.; Neto, T.L.B.; Chacra, A.R.; Dib, S.A. Aerobic exercise capacity and pulmonary function in athletes with and without type 1 diabetes. Diabetes Care 2010, 33, 2555–2557.
  48. Colberg, S.R.; Sigal, R.J.; Fernhall, B.; Regensteiner, J.G.; Blissmer, B.J.; Rubin, R.R.; Chasan-Taber, L.; Albright, A.L.; Braun, B. Exercise and type 2 diabetes: The American College of Sports Medicine and the American Diabetes Association: Joint position statement. Diabetes Care 2010, 33, e147–e167.
  49. Warburton, D.E.R.; Katzmarzyk, P.T.; Rhodes, R.E.; Shephard, R.J. Evidence-informed physical activity guidelines for Canadian adults. Appl. Physiol. Nutr. Metab. 2007, 32, S16–S68.
  50. Tuomilehto, J.; Lindström, J.; Eriksson, J.G.; Valle, T.T.; Hämäläinen, H.; Ilanne-Parikka, P.; Keinänen-Kiukaanniemi, S.; Laakso, M.; Louheranta, A.; Rastas, M.; et al. Prevention of Type 2 Diabetes Mellitus by Changes in Lifestyle among Subjects with Impaired Glucose Tolerance. N. Engl. J. Med. 2001, 344, 1343–1350.
  51. Samuelson, G. Global strategy on diet, physical activity and health. Scand. J. Nutr. 2004, 48, 57.
  52. Convertino, V.A.; Armstrong, L.; Coyle, E.; Mack, G.; Sawka, M.; Senay, L.; Sherman, W. Exercise and fluid replacement. Med. Sci. Sport. Exerc 1999, 28, 1–7.
  53. Sherwani, S.I.; Khan, H.A.; Ekhzaimy, A.; Masood, A.; Sakharkar, M.K. Significance of HbA1c test in diagnosis and prognosis of diabetic patients. Biomark. Insights 2016, 11, 95–104.
  54. Jansson, A.K.; Chan, L.X.; Lubans, D.R.; Duncan, M.J.; Plotnikoff, R.C. Effect of resistance training on HbA1c in adults with type 2 diabetes mellitus and the moderating effect of changes in muscular strength: A systematic review and meta-analysis. BMJ Open Diabetes Res. Care 2022, 10, e002595.
  55. Najafipour, F.; Mobasseri, M.; Yavari, A.; Nadrian, H.; Aliasgarzadeh, A.; Abbasi, N.M.; Niafar, M.; Gharamaleki, J.H.; Sadra, V. Effect of regular exercise training on changes in HbA1c, BMI and VO 2 max among patients with type 2 diabetes mellitus: An 8-year trial. BMJ Open Diabetes Res. Care 2017, 5, e000414.
  56. Johnston, C.A.; Moreno, J.P.; Foreyt, J.P. Cardiovascular Effects of Intensive Lifestyle Intervention in Type 2 Diabetes. Curr. Atheroscler. Rep. 2014, 16, 145–154.
  57. Lin, C.Y.; Lee, T.Y.; Sun, Z.J.; Yang, Y.C.; Wu, J.S.; Ou, H.T. Development of diabetes-specific quality of life module to be in conjunction with the World Health Organization quality of life scale brief version (WHOQOL-BREF). Health Qual. Life Outcomes 2017, 15, 167.
  58. Dominguez-Muñoz, F.J.; Hernández-Mocholi, M.A.; Manso, L.J.; Collado-Mateo, D.; Villafaina, S.; Adsuar, J.C.; Gusi, N. Test-retest reliability of kinematic parameters of timed up and go in people with type 2 diabetes. Appl. Sci. 2019, 9, 4709.
  59. Guazzi, M.; Bandera, F.; Ozemek, C.; Systrom, D.; Arena, R. Cardiopulmonary Exercise Testing: What Is its Value? J. Am. Coll. Cardiol. 2017, 70, 1618–1636.
  60. DeFronzo, R.A.; Tripathy, D. Skeletal muscle insulin resistance is the primary defect in type 2 diabetes. Diabetes Care 2009, 32 (Suppl. 2), S157–S163.
  61. Kobayashi, Y.; Long, J.; Dan, S.; Johannsen, N.M.; Talamoa, R.; Raghuram, S.; Chung, S.; Kent, K.; Basina, M.; Lamendola, C.; et al. Strength training is more effective than aerobic exercise for improving glycaemic control and body composition in people with normal-weight type 2 diabetes: A randomised controlled trial. Diabetologia 2023, 66, 1897–1907.
  62. Alfonso-Rosa, R.M.; Del Pozo-Cruz, B.; Del Pozo-Cruz, J.; Sañudo, B.; Rogers, M.E. Test-retest reliability and minimal detectable change scores for fitness assessment in older adults with type 2 diabetes. Rehabil. Nurs. 2014, 39, 260–268.
  63. Vaz, M.M.; Costa, G.C.; Reis, J.G.; Junior, W.M.; De Paula, F.J.A.; Abreu, D.C. Postural control and functional strength in patients with type 2 diabetes mellitus with and without peripheral neuropathy. Arch. Phys. Med. Rehabil. 2013, 94, 2465–2470.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.
Upload a video for this entry
Information
Subjects: Sport Sciences
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Alessandro Piras
,
Milena Raffi
View Times: 86
Revisions: 2 times (View History)
Update Date: 16 Nov 2023
Table of Contents
    1000/1000
    Hot Most Recent
    Feedback