Sunteți pe pagina 1din 11

Sports Med (2013) 43:39–49

DOI 10.1007/s40279-012-0004-y

REVIEW ARTICLE

Exercise Prescription in the Treatment


of Type 2 Diabetes Mellitus
Current Practices, Existing Guidelines and Future Directions

Ciara O’Hagan • Giuseppe De Vito •

Colin A. G. Boreham

Published online: 28 November 2012


Ó Springer International Publishing Switzerland 2012

Abstract Exercise is an effective treatment for type 2 1 Introduction


diabetes mellitus, resulting in stabilization of plasma glu-
cose in the acute phase and improvements in body com- Diabetes mellitus is a chronic disease affecting 171 million
position, insulin resistance and glycosylated haemoglobin adults globally (2.8%); this is estimated to increase to 366
with chronic exercise training. However, the most appro- million (4.4%) by 2030 [1]. Between 90 and 95% of
priate exercise prescription for type 2 diabetes has not yet patients have type 2 diabetes, the form of the disease
been established, resulting from insufficient evidence to previously known as ‘adult onset diabetes’ or ‘non-insulin
determine the optimum type, intensity, duration or fre- dependent diabetes mellitus’ [2].
quency of exercise training. Furthermore, patient engage- The aim of treatment for type 2 diabetes is to prevent or
ment in exercise is suboptimal. There are many likely slow progression of the disease and the development of
reasons for low engagement in exercise; one possible micro- and macro-vascular complications including car-
contributory factor may be a tendency for expert bodies to diovascular disease, retinopathy, neuropathy and kidney
prioritize the roles of diet and medication over exercise in disease. This is typically approached with a combination of
their treatment guidelines. Published treatment guidelines medication, dietary modification and exercise prescription
vary in their approach to exercise training, but most to reduce blood glucose concentrations and blood pressure,
agencies suggest that people with type 2 diabetes engage in induce weight loss and modify blood lipid levels.
150 min of moderate to vigorous aerobic exercise per However, while most patients and practitioners under-
week. This prescription is similar to the established stand the benefits of medication and dietary control in the
guidelines for cardiovascular health in the general popu- treatment of type 2 diabetes, the specific benefits of exer-
lation. Future possibilities in this area include investigation cise may be less well understood and, as such, the potential
of the physiological effects and practical benefits of exer- of exercise prescription may not be fully exploited [3]. In
cise training of different intensities in type 2 diabetes, and this review we briefly outline current understanding of the
the use of individualized prescription to maximize the beneficial effects of exercise training for people with type 2
health benefits of training. diabetes, discuss trends for patient participation in exercise
training, review the available guidelines for exercise pre-
scription, and suggest some future directions for research
and practice in this area.
Articles for inclusion in Sect. 4, ‘Existing guidelines for
prescription of exercise in type 2 diabetes’, were selected
C. O’Hagan (&)
Academy of Sport and Physical Activity, Sheffield Hallam using a search of the MEDLINE database. The search was
University, Collegiate Crescent, Sheffield S10 2BP, UK restricted to articles published between 1998 and 2011, and
e-mail: c.ohagan@shu.ac.uk which were categorized as one of the following article
types: guideline, practice guideline, consensus develop-
C. O’Hagan  G. De Vito  C. A. G. Boreham
Institute for Sport and Health, University College Dublin, ment conference, government publication or patient edu-
Dublin, Ireland cation handout. The search terms ‘type 2 diabetes’,
40 C. O’Hagan et al.

‘physical activity’, ‘exercise’, ‘guidelines’ and ‘consensus [15]). A later meta-analysis included a larger number of
statement’ were used, and the resulting articles were then studies, (27 studies, including all 14 included in the Boule
screened to remove guidelines relating solely or primarily et al. meta-analysis [15]) with training studies being sub-
to pharmacological or dietary treatments, diagnosis of type divided into aerobic training (17 studies, 622 subjects)
2 diabetes, diagnosis or management of secondary com- resistance training (6 studies, 202 subjects) and combined
plications of type 2 diabetes or management of type 2 training (5 studies, 251 subjects; [16]). The authors
diabetes in children. Lastly, the reference lists of the reported that all three forms of training resulted in small
selected articles were hand searched to identify any addi- but clear improvements in HbA1c, and small to moderate
tional relevant publications. This search process resulted in improvements in fasting glucose, postprandial glucose,
the 13 guidelines listed in Table 1. fasting insulin and insulin sensitivity. A 2008 Cochrane
review of exercise training studies involving people with
type 2 diabetes drew similar conclusions [17]. Employing
2 Effects of Exercise Training in Type 2 Diabetes stringent inclusion criteria, this latter meta-analysis of 14
Mellitus studies (377 subjects) supported the findings of the two
previous meta-analyses. A 2011 meta-analysis confined to
Exercise induces glucose uptake in skeletal muscle by an studies with HbA1c as an outcome measure confirmed
insulin-independent pathway and enhances glucose uptake earlier findings, reporting a 0.67% decrease in HbA1c from
by the insulin-dependent pathway, and this exercise- 23 studies of structured exercise interventions [14]. A 1%
induced increase is maintained in the insulin resistant state reduction in HbA1c has been associated with a 21%
of type 2 diabetes [4]. A single bout of exercise has been reduction in risk of diabetic complications (microvascular
shown to induce an increased glucose uptake (and conse- disease, stroke and myocardial infarction), and thus a
quent reduction in blood glucose) in people with type 2 training-induced reduction of 0.66% can be considered
diabetes that persists for at least 24 h post exercise [4]. clinically significant [18]. Importantly, in three of the four
Furthermore, the single bout stabilizes plasma glucose meta-analyses, the reduction in HbA1c was independent of
response for the subsequent 24 h, reducing the appearance body weight changes, indicating that exercise can have
of postprandial hyperglycaemic ‘spikes’ that are known to beneficial effects for people with type 2 diabetes without
be a significant precursor in the development of diabetic concomitant weight loss [15–17]. The meta-analyses of
complications [5]. Snowling and Hopkins [16], and of Thomas and co-
The cumulative effect of repeated exercise bouts (i.e. the workers [17] also sought to examine the moderating effects
training effect), can thus be exploited for disease therapy. of some study characteristics on outcome measures. A key
Exercise training programmes for people with type 2 dia- finding of the Snowling and Hopkins [16] review was that
betes have been shown to have beneficial effects on body there is a substantial influence of training programme
weight [6], fasting glucose [7], fasting insulin and insulin duration on HbA1c changes, with programmes longer than
resistance [8], rate of fat oxidation [9], blood cholesterol 12 weeks resulting in a mean HbA1c reduction of 0.8%,
[10] and blood pressure [11]. Importantly, several long- compared with only 0.4% for those studies shorter than
term exercise training studies have shown a reduction in gly- 12 weeks. In contrast, Thomas et al. reported a greater
cosylated haemoglobin (HbA1c), used clinically as a key marker change in HbA1c after shorter training studies (-0.8% for
of long-term glycaemic control, and therefore frequently con- periods shorter than 3 months, -0.5% for 3–12 month
sidered as an indicator of treatment efficacy [12–14]. studies). While Thomas and co-workers suggest that this
However, there are still relatively few well controlled, discrepancy may be accounted for by differences in exer-
large-group exercise intervention studies in this area, and cise intensity, training volume and patient compliance [17],
those that have been published display considerable variety it is also important to note that the methods used in the two
in group sizes, intervention duration, exercise training meta-analyses differ with respect to pooling of aerobic,
parameters (mode, intensity and volume [bout duration and resistance and mixed-exercise training programmes and, as
frequency]) and reported outcome measures. To address such, any comparisons must be made with caution. Such
this issue, several authors have conducted meta-analyses on variation in analytical approaches and results has important
the available data, concluding that there is sufficient evi- implications for researchers designing studies in this area,
dence to support the use of exercise as a treatment but also for clinicians, as it illustrates the difficulty of
modality. A 2001 meta-analysis of 14 exercise intervention prescribing exercise programmes based on currently
studies involving a total of 504 subjects confirmed that available literature. Most recently, Hansen and co-workers
exercise training periods longer than 8 weeks had a sta- [19] concluded in their review that the impact of training
tistically significant effect on HbA1c (mean HbA1c 0.66% frequency, duration or volume on clinical outcomes in type
lower post-exercise intervention compared with control; 2 diabetes is not yet clear.
Prescription of Exercise Training in T2DM
Table I Published guidelines for the prescription of exercise in the treatment of type 2 diabetes mellitus
Guideline Prescription guidelines Specific recommendations
Type Intensity Frequency Duration Volume Progression

General treatment guidelines, no exercise recommendations


American Association of Clinical – – – – – – Aggressively implement all
Endocrinologists Medical Guidelines appropriate components of care
for Clinical Practice for the (medical nutrition therapy,
Management of Diabetes Mellitus [37] physical activity, weight
management regimen,
pharmacological interventions,
diabetes self-management
education) at the time of
diagnosis
American Association of Clinical – – – – – – Advise lifestyle modification
Endocrinologists Road Maps to
Achieve Glycaemic Control in Type 2
Diabetes Mellitus [35]
The Royal College of General – – – – – – Encourage increased physical
Practitioners and Diabetes UK; activity
Clinical Guidelines for Type 2
Diabetes [36]
General treatment guidelines, including exercise recommendations
International Diabetes Federation; – – 3–5 days/ 30–45 150 minutes/ – Introduce physical activity
Global Guidelines for Type 2 Diabetes week minutes week gradually. Advanced care could
[38] include exercise testing and
individualized testing and
education by exercise specialists
Diabetes Australia; Diabetes Aerobic 60–70% MHR, 3–4 days/ 30 minutes 150 minutes/ – Exercise professional included in
Management in General Practice [41] moderate week week care team
Institute for Clinical Systems Aerobic 50–70% MHR, 3 days/week – 150 minutes/ Start by incorporating
Improvement; Diagnosis and moderate week 10 min into each day
Management of Type 2 Diabetes and then progress to
Mellitus in Adults [42] meet guidelines

41
42
Table I continued
Guideline Prescription guidelines Specific recommendations
Type Intensity Frequency Duration Volume Progression

Canadian Diabetes Association; 2008 Aerobic Moderate to 3 days/week – 150 minutes/ – Initial instruction and periodic
Clinical Practice Guidelines for the vigorous (50 % to week supervision by an exercise
Prevention and Management of [70% MHR) specialist are recommended
Diabetes in Canada [40] (resistance training). An exercise
electrocardiogram stress test
should be considered for
previously sedentary individuals
with diabetes at high risk for
cardiovascular disease who wish
to undertake exercise more
vigorous than brisk walking
Resistance Moderate 3 days/week – 1 set of 10–15 Start with one set of
progressing to repetitions 10–15 repetitions at
heavier weights moderate weight
Progress to 2 sets of
10–15 repetitions
Progress to 3 sets of 8
repetitions at heavier
weight
American Diabetes Association; Aerobic Moderate (50–70% – – 150 minutes/ –
Standards of Medical Care in Diabetes MHR) week
2011 [39] Resistance – 3 days/week – – –
Specific exercise guidelines
American College of Sports Medicine Aerobic Moderate (40–60% 3 days/week C10 min 150 min/week Gradual No more than two consecutive
and American Diabetes Association; (large _ 2max) to
VO days between bouts of activity
Joint Position Statement: Exercise and muscle vigorous
Type 2 Diabetes [43] group)
Resistance Moderate (50–80% 2–3 days/ – 5–10 Progressing to 4 sets of
1RM) to vigorous week (non- exercises, 1 8–10 repetitions
consecutive) set of 10–15
repetitions
American Diabetes Association; Aerobic Moderate to 3 days/week – 150 min or –
Consensus Statement: Physical vigorous (40-60%
Activity/Exercise and Type 2 Diabetes _ 2max or 50-70%
VO
[46] MHR) or
Vigorous ([60% 90 min

C. O’Hagan et al.
_ 2max or [70%
VO
MHR)
Prescription of Exercise Training in T2DM 43

3 Current Trends in Patient Engagement in Exercise

and periodic reassessments by a


Recommend initial supervision
Programmes

qualified exercise specialist


Specific recommendations

Despite the substantial body of evidence supporting the


beneficial role of exercise in the treatment of type 2 dia-
betes, it appears that patients are still not engaging in
sufficient physical activity. Between 1988 and 1994, the
Third National Health and Nutrition Examination Survey
(NHANES III) examined physical activity habits of 1,480
adults with type 2 diabetes in the US [20]. Only 31% of
respondents reported engaging in sufficient physical

Progress intensity and


activity to meet the minimum recommendations of the US
volume over initial
Surgeon General’s report, with a further 38% reporting
2–3 weeks of some physical activity but not enough to meet the recom-
programme
Progression

mendations and 31% self-reporting as inactive. In contrast,


among all adults surveyed, the corresponding figure for
self-reported inactivity was only 23% [21]. More recently,

similarly low levels of engagement in physical activity


rest 1–2 min

among people with type 2 diabetes were reported in two


_ 2max maximal oxygen consumption
repetitions,
150 min or

2–4 sets of

further large-scale studies that also reported lower physical


Volume

90 min

8–10

activity in people with type 2 diabetes compared with non-


diabetics. In the 2003 Scottish Health Survey of 8,148

adults, 58% of male and 74% of female people with type 2


repetitions

diabetes reported engaging in less than 30 minutes per


C10 min
Duration

3 sets of

30 min
8–10

week of physical activity but in the general population,


participation rates were significantly higher with only 36%

of men and 41% of women in this category [22]. Similarly,


3 days/week

3 days/week

3 days/week

of the 481,251 respondents surveyed between 2001 and


Frequency

3–7 days/

MAP maximal aerobic power, MHR maximum heart rate, RM repetitions maximum, VO

2005 for the Behavioural Risk Factor Surveillance System


week

survey from the Centers for Disease Control and Preven-


tion in the US, 5.9% self-reported as diabetic and only
39.7% of these people with type 2 diabetes met the
American Diabetes Association recommendations for
_ 2max
progressing to

physical activity. In contrast, 48% of the non-diabetic


40–50% VO

70% MAP
Moderate or
Prescription guidelines

population met the guidelines. Furthermore, while there


Vigorous
8–10RM

8–10RM
Intensity

was a significant trend for an increase in physical activity


among non-diabetics from 2001 to 2005, the same was not
seen in people with type 2 diabetes, with physical activity
Resistance

Resistance

participation remaining unchanged [23].


Aerobic

Aerobic
Type

Engagement in physical activity also appears to be lower


than adherence to other self-care behaviours in type 2
diabetes. The US-based TRIAD (Translating Research Into
l’Association de Langue Française pour
Training for Type 2 Diabetes Mellitus
American Heart Association; Exercise

l’Etude du Diabète et des Maladies


Métaboliques; Activité Physique et

Action for Diabetes) study analysed a range of self-repor-


ted health behaviours in 8,763 people with type 2 diabetes.
Only 46% of respondents reported taking part in regular
physical activity, but compliance with other health pro-
moting behaviours was significantly higher, with 68%
performing daily foot examination and 75% reporting daily
Table I continued

blood glucose self-monitoring [24]. The Diabetes Atti-


Diabète [44]

tudes, Wishes and Needs study of 5,104 patients across 13


Guideline

countries used a self-reported 1–4 scale to assess adherence


[45]

to ‘lifestyle recommendations’ (result: 3.06) and medica-


tion schedules (result: 3.48) [25]. While it is not possible to
44 C. O’Hagan et al.

interpret the clinical significance of this difference as no nutritional therapy, but physical activity recommendations
supporting data is provided, the results are suggestive of a are seldom afforded the same degree of promotion.
similar trend to that observed in the TRIAD study. An Table 1 outlines the range of published guidelines that
earlier WHO review of available data also suggested lower are currently available to practitioners. These guidelines
adherence to physical activity recommendations than die- can be categorized into three groups: general management
tary advice or medication prescriptions [26]. guidelines with no specific exercise recommendations [35–
As a result of this suboptimal engagement with exercise 37], general management guidelines that do include exer-
in people with type 2 diabetes, the role of the physician in cise recommendations [38–42] and statements or guide-
advising or prescribing exercise has been examined. Of the lines that specifically relate to physical activity or exercise
26,878 US adults surveyed for the 2002 Medical Expen- recommendations for type 2 diabetes [43–46].
diture Panel Survey, 1,972 self-reported as diabetic [27, While there are some differences in specific elements of the
28]. While only 38% of diabetic respondents reported prescription guidelines, most statements recommend that
taking part in moderate or vigorous physical activity three patients accumulate 150 min of moderate to vigorous inten-
or more times per week, 73% reported that they had been sity aerobic exercise each week [38–43, 45, 46]. Selected
advised by their healthcare professional to exercise more. guidelines provide detail on recommended session duration
In the non-diabetic population, just 31% had received this [38, 43–45], frequency [38, 43–46], distribution [43] and
advice, yet 58% took part in regular physical activity. progression [43, 44], and several agencies also recommend a
Furthermore, no significant association was seen between programme of resistance training [39, 43, 45, 46].
engagement in physical activity and physician advice to It appears that the 150-min recommendation is drawn from
take part. The trend for type 2 diabetic patients to receive the traditional guidelines for health in the general population
more physical activity advice than other adults was sup- (US Department of Health and Human Services Physical
ported by the findings of the US National Health Interview Activity Guidelines for Americans [47] and the US Surgeon
Survey and a survey of a sample population of Medicare General’s report [48]). The American Diabetes Association
members in California [20, 29]. and American College of Sports Medicine report that their
These large scale studies show that although healthcare adoption of the US Surgeon General’s ‘150 minutes, moder-
professionals do advise exercise for people with type 2 dia- ate intensity’ guidelines is based on the evidence presented in
betes, often patients do not comply with this advice and par- the meta-analysis performed by Boule and colleagues [15],
ticipation rates are low. The reasons for these discrepancies which indicated that interventions which matched these
are unclear, with several possibilities suggested: financial and guidelines had beneficial effects on HbA1c [15, 39, 43].
environmental barriers, time limitations, the physical limita- These guidelines and statements provide a template for
tions imposed by secondary complications of type 2 diabetes the physician to suggest exercise training programmes to
and co-morbidities, low self-efficacy and motivation, low the type 2 diabetic patient and, in many cases, adherence to
levels of family support and lack of patient understanding of these recommendations may successfully ameliorate the
the benefits of exercise [26, 30, 31]. The role of healthcare patient’s disease state. This traditional approach is gener-
professionals’ support in promoting adherence has also been ally aimed at producing improvements in cardiovascular
examined. A review authored by Kirk and colleagues suggests and muscular fitness and, thus, prevention of the develop-
that specific physical activity consultations improve adher- ment of cardiovascular and other chronic diseases [47].
ence [32], while mixed-method studies of barriers to exercise These changes are undoubtedly of benefit to the diabetic
among people with type 2 diabetes highlighted a lack of patient, and may be accompanied by improvements in
specificity in exercise advice given, and a perception of a low HbA1c, the traditional marker of blood glucose control and
priority of exercise as treatment [33, 34]. thus of the disease state. However, in many patients, HbA1c
targets are achieved through medication regimens and
therefore the beneficial effects of exercise on glucose
4 Existing Guidelines for Prescription of Exercise control may be masked. Furthermore, as type 2 diabetes is
in Type 2 Diabetes characterized by disorders in overall substrate metabolism
and not only glucose control, it is likely that further ben-
Published guidelines for the management of type 2 diabetes efits could be gained from exercise programmes targeting
all include the common triad of medication, medical the pathogenic mechanisms at the origin of the disease.
nutrition therapy and engagement in physical activity. Secondly, and perhaps critically, just as pharmacological
These guidelines generally provide extensive discussion of therapies and dietary modifications are individualized to
the evidence bases, mechanisms of action and recom- the patient, the same approach could be adopted for exer-
mended dosage regimens for pharmacological therapies as cise treatment, with the prescription of an individualized
well as comprehensive recommendations for medical programme for physical activity.
Prescription of Exercise Training in T2DM 45

5 Future Possibilities in Exercise Prescription time-efficient method of cardiorespiratory training in


young healthy people, more recently it has also been pro-
The current guidelines for the prescription of exercise in posed for use in clinical populations [59–61]. While data
type 2 diabetes discussed above are based on analysis of relating to the use of HIIT in people with type 2 diabetes is
the clinical outcomes of exercise intervention research limited, two recently published studies show beneficial
studies. However, it is important also to ensure the prac- effects on glycaemic control after a single bout [62] and 6
ticality of the prescribed programmes, particularly with bouts [63] of HIIT, suggesting that this may be a promising
respect to patient compliance. As such, a parameter of line of investigation.
interest is exercise training intensity, as it has previously However, perhaps as important as consideration of
been suggested that training intensity is inversely related to clinical benefits of differing exercise intensities in type 2
adherence to prescribed programmes in sedentary [49] and diabetes is the need to improve patient adherence. The
clinical populations [50, 51]. suggested inverse relationship between intensity and
A comparison of low-to-moderate intensity (50% peak adherence [49–51] could be used to support a shift towards
oxygen uptake [VO _ 2peak]) and moderate-to-high intensity lower intensities of continuous aerobic training. Never-
(75% VO _ 2peak) training programmes in people with type 2 theless, in a study involving young, healthy adults, HIIT
diabetes showed similar improvements in clinical out- was reported to be more enjoyable than continuous aerobic
comes of low-density lipoprotein cholesterol, cardiovas- training, a finding which the authors postulate may result in
cular fitness and skeletal muscle oxidative capacity from improved adherence [64]. ‘Lack of time’ is frequently cited
both regimens, with no difference between groups [52]. as a barrier to engagement in exercise in sedentary popu-
Importantly, there was also no difference in improvements lations [65], and as it is likely that both time constraints and
in HbA1c, suggesting that the beneficial effects of exercise low enjoyment of exercise contribute to low adherence in
training on glucose metabolism are not intensity dependent. people with type 2 diabetes, the benefits of low-volume,
However, one recent study of acute exercise effects in high-intensity exercise programmes for this population
people with type 2 diabetes proposed a greater benefit of warrant further investigation.
low-intensity exercise; the authors found that a single low- Coupled with the need to develop exercise training
intensity exercise bout (35% maximal workload capacity) programmes that target specific metabolic outcomes in type
reduced subsequent 24-h blood glucose more than a high- 2 diabetes are the potential benefits of individualizing the
intensity bout (75% maximal workload capacity), and also exercise prescription based on exercise test results. The
decreased the prevalence of hyperglycaemic spikes [5]. ‘FATmax’ training protocols mentioned above rely on
As well as changes in glucose metabolism, people with matching prescribed training intensity (walking speed or
type 2 diabetes exhibit disturbances in lipid metabolism cycling power) for each patient to their optimal substrate
during exercise relative to healthy, sedentary people [53, use; in contrast, traditional exercise prescription relies on
54]. It has been suggested that in treating type 2 diabetes, generalized heart rate zones or subjective ratings. While
continuous exercise training at the intensity corresponding this ‘one size fits all’ approach is suitable for large-scale
to an individual’s maximal rate of fat oxidation (so-called disease prevention programmes and health guidelines for
‘FATmax’ training), may result in greater improvements in the general population, it is likely that patients will benefit
substrate utilization compared with traditional higher more from exercise programmes tailored to their own
intensities, where the principal benefits seen are in blood disease status. Individualized prescription of exercise pro-
pressure reduction and weight loss [55]. Programmes of grammes based on laboratory exercise testing has long
‘FATmax’ training for 4 weeks in obese healthy people been advocated in cardiac disease populations [66] and,
[56], 12 weeks in obese healthy males [57] and 10 weeks more recently, in chronic low back pain [67], fall-preven-
in middle-aged men with type 2 diabetes [9] resulted in tion exercise programmes in the elderly [68], chronic heart
improvements in lipid oxidation rates during exercise, failure [69], spinal cord injured patients [70], hypertension
compared with higher-intensity training programmes. The [71], chronic fatigue syndrome [72], fibromyalgia [73],
authors suggest that this may specifically relate to coronary artery disease [74] and cancer-related fatigue
increased oxidation of intramuscular triglycerides [9, 56], [75], and has be shown to be effective in increasing aerobic
the excess accumulation of which contributes to the capacity in cancer patients [76], and exercise capacity in
development of insulin resistance [58]. cardiac rehabilitation [77]. In type 2 diabetes, individual-
In parallel with this recent interest in low-intensity ized prescription has been recommended [78–81] but the
continuous exercise, there has been an increased focus on proposed benefits have not yet been thoroughly investi-
the use of low-volume, high-intensity interval training gated. A small number of studies have investigated the
(HIIT). While HIIT training was originally proposed as a efficacy of this approach. Five months of individualized
46 C. O’Hagan et al.

mixed resistance and aerobic (high-intensity interval intervention of Brun and co-workers reduced hospital
training) training induced improvements in fasting blood admissions and medication use in people with type 2 dia-
glucose, HbA1c and body composition in 11 people with betes, leading to estimated healthcare cost savings of 50%
type 2 diabetes, although no control group (non-exercise or [8]. Thus, while implementation of exercise programmes
non-individualized exercise prescription) was included in may be expensive in the short term, the resultant delay of
this study [82]. In a 1-year study of obese, middle-aged disease progression and development of complications may
males with type 2 diabetes, twice weekly aerobic exercise more than offset this initial outlay. An area of some current
at the intensity of ventilatory threshold improved exercise attention is the use of financial incentives to leverage
capacity and insulin resistance compared with non-exer- greater adherence to treatment schedules in people with
cising controls [8]. However, in a study comparing an chronic diseases. This approach has been successfully
individualized medical fitness prescription with generic implemented in smoking cessation programmes [89], and
brisk walking, similar results were obtained in the two has mixed results in weight loss programmes in obese
groups [83], although high dropout figures for both arms of populations [90–92]. While research investigating the
the study suggest that a key element of any exercise pre- possible health benefits and long-term financial viability of
scription may be continued supervision. This proposal was incentive-based programmes in type 2 diabetes would be
substantiated by the results of a 2-year intervention from welcome, due consideration must be given to the need to
the same researchers, who showed that prescribed but promote adherence to guidelines for sustainable, long-term
unsupervised exercise programmes did not significantly lifestyle change, rather than short-term intensive exercise
improve markers of disease state [84]. However, in this programmes.
study, the exercise prescription was ‘personalized’ based
on patient habits, preferences, motivation and ‘tolerance’
rather than a specific prescription describing exercise 6 Conclusions
duration, intensity and frequency based on clinical testing.
Thus, the initial evidence in this area is mixed, and further The benefits of exercise training in the treatment of type 2
work is required to establish whether individualized pre- diabetes are well established, but physician implementation
scription of exercise is more beneficial than prescription of and patient engagement are low. Current guidelines for the
training based on general guidelines and, furthermore, prescription of exercise as treatment in type 2 diabetics are
whether supervision of exercise is required. generic in nature, and most do not specifically target the
If individualized exercise prescription is to be promoted, metabolic disturbances that contribute to disease progres-
due consideration must be given to the associated costs. sion and development of secondary complications. The
Successful exercise interventions in type 2 diabetes tend to development of prescription guidelines that both target the
require intensive counselling and supervision from medical specific metabolic disturbances of the type 2 diabetes and
or exercise professionals, with some of the success of these incorporate individualization of prescription for the
programmes related to higher patient compliance than non- patients may improve adherence, improve clinical out-
supervised programmes. Regarding the implementation of comes and contribute to reducing the economic burden of
generalized or individualized prescriptions, the latter the disease.
requires initial and repeated laboratory testing that is
expensive and time consuming. However, current treat- Acknowledgements Funding sources, previous publication and
conflicts of interest: This review was supported by a grant from the
ment of diabetes and its associated complications is a Irish Research Council for Science, Engineering and Technology.
significant global economic burden. Previous studies have This review has not been previously published and the authors have
estimated the daily healthcare cost for each diabetic patient no conflicts of interest that are directly relevant to the content of this
in France was $US15 in 2000, and $US36 in the US in review.
2002 [85–87]. Recently published estimates from the
International Diabetes Federation for 2010 are that the
References
international average annual expenditure for diabetes-
related healthcare costs is $US1,330 per patient; with 1. Wild S, Roglic G, Green A, et al. Global prevalence of diabetes:
values of $US3,574 and $US7,382 for the UK and US, estimates for the year 2000 and projections for 2030. Diabetes
respectively [88]. The estimated average percentage of Care. 2004;27(5):1047–53.
healthcare budget spend on the treatment of type 2 diabetes 2. Centers for Disease Control and Prevention. National diabetes
fact sheet: general information and national estimates on diabetes
and its complications is 12%, increasing to 21% in coun- in the United States. Atlanta (GA): U.S. Department of Health
tries with a high prevalence of the disease [88]. While and Human Services; 2005.
evidence supporting the long-term cost-saving effects of 3. Hordern MD, Dunstan DW, Prins JB, et al. Exercise prescription
exercise interventions is sparse, a 1-year exercise for patients with type 2 diabetes and pre-diabetes: a position
Prescription of Exercise Training in T2DM 47

statement from exercise and sport science Australia. J Sci Med 22. Joint Health Surveys Unit. University College London and
Sport. 2011;15(1):25–31. Medical Research Council. Scottish Health Survey. Essex: Social
4. Henriksen EJ. Effects of acute exercise and exercise training on and Public Health Sciences Unit; 2005.
insulin resistance. J Appl Physiol. 2002;93(2):788–96. 23. Zhao G, Ford ES, Li C, et al. Compliance with physical activity
5. Manders RJ, Van Dijk JW, van Loon LJ. Low-intensity exercise recommendations in US adults with diabetes. Diabet Med.
reduces the prevalence of hyperglycemia in type 2 diabetes. Med 2008;25(2):221–7.
Sci Sports Exerc. 2010;42(2):219–25. 24. Karter AJ, Stevens MR, Brown AF, et al. Educational disparities
6. Cuff DJ, Meneilly GS, Martin A, et al. Effective exercise in health behaviors among patients with diabetes: the Translating
modality to reduce insulin resistance in women with type 2 dia- Research Into Action for Diabetes (TRIAD) Study. BMC Public
betes. Diabetes Care. 2003;26(11):2977–82. Health. 2007;7:308.
7. Dunstan DW, Puddey IB, Beilin LJ, et al. Effects of a short-term 25. Rubin RR, Peyrot M, Siminerio LM. Health care and patient-
circuit weight training program on glycaemic control in NIDDM. reported outcomes: results of the cross-national Diabetes Atti-
Diabetes Res Clin Pract. 1998;40(1):53–61. tudes, Wishes and Needs (DAWN) study. Diabetes Care.
8. Brun JF, Bordenave S, Mercier J, et al. Cost-sparing effect of 2006;29(6):1249–55.
twice-weekly targeted endurance training in type 2 diabetics: a 26. Sabate E, World Health O, Project WHOAtLTT, Global Adher-
one-year controlled randomized trial. Diabetes Metab. ence Interdisciplinary N. Adherence to long-term therapies: evi-
2008;34(3):258–65. dence for action. Geneva: World Health Organization; 2003.
9. Bordenave S, Metz L, Flavier S, et al. Training-induced 27. Morrato EH, Hill JO, Wyatt HR, et al. Are health care profes-
improvement in lipid oxidation in type 2 diabetes mellitus is sionals advising patients with diabetes or at risk for developing
related to alterations in muscle mitochondrial activity: effect of diabetes to exercise more? Diabetes Care. 2006;29(3):543–8.
endurance training in type 2 diabetes. Diabetes Metab. 28. Morrato EH, Hill JO, Wyatt HR, et al. Physical activity in U.S.
2008;34(2):162–8. adults with diabetes and at risk for developing diabetes, 2003.
10. Verity LS, Ismail AH. Effects of exercise on cardiovascular Diabetes Care. 2007;30(2):203–9.
disease risk in women with NIDDM. Diabetes Res Clin Pract. 29. Damush TM, Stewart AL, Mills KM, et al. Prevalence and cor-
1989;6(1):27–35. relates of physician recommendations to exercise among older
11. Schneider SH, Khachadurian AK, Amorosa LF, et al. Ten-year adults. J Gerontol A Biol Sci Med Sci. 1999;54(8):M423–7.
experience with an exercise-based outpatient life-style modifi- 30. Kirk JK, Raggio GA, Nesbit BA, et al. Individualized enhanced
cation program in the treatment of diabetes mellitus. Diabetes adherence intervention study in adults with diabetes. J Diabetes
Care. 1992;15(11):1800–10. Sci Technol. 2007;1(4):L1–2.
12. Sigal RJ, Kenny GP, Boule NG, et al. Effects of aerobic training, 31. Delamater A. Improving patient adherence. Clin Diabetes.
resistance training, or both on glycemic control in type 2 diabe- 2006;24(2):71–7.
tes: a randomized trial. Ann Intern Med. 2007;147(6):357–69. 32. Kirk AF, Barnett J, Mutrie N. Physical activity consultation for
13. Church TS, Blair SN, Cocreham S, et al. Effects of aerobic and people with Type 2 diabetes: evidence and guidelines. Diabet
resistance training on hemoglobin A1c levels in patients with Med. 2007;24(8):809–16.
type 2 diabetes: a randomized controlled trial. JAMA. 33. Armstrong Shultz J, Sprague MA, Branen LJ, et al. A comparison
2010;304(20):2253–62. of views of individuals with type 2 diabetes mellitus and diabetes
14. Umpierre D, Ribeiro PA, Kramer CK, et al. Physical activity educators about barriers to diet and exercise. J Health Commun.
advice only or structured exercise training and association with 2001;6(2):99–115.
HbA1c levels in type 2 diabetes: a systematic review and meta- 34. Ary DV, Toobert D, Wilson W, et al. Patient perspective on
analysis. JAMA. 2011;305(17):1790–9. factors contributing to nonadherence to diabetes regimen. Dia-
15. Boule NG, Haddad E, Kenny GP, et al. Effects of exercise on betes Care. 1986;9(2):168–72.
glycemic control and body mass in type 2 diabetes mellitus: a 35. Jellinger PS, Davidson JA, Blonde L, et al. Road maps to achieve
meta-analysis of controlled clinical trials. JAMA. 2001;286(10): glycemic control in type 2 diabetes mellitus: ACE/AACE Dia-
1218–27. betes Road Map Task Force. Endocr Pract. 2007;13(3):260–8.
16. Snowling NJ, Hopkins WG. Effects of different modes of exer- 36. McIntosh A, Hutchinson A, Home PD, et al. Clinical guidelines and
cise training on glucose control and risk factors for complications evidence review for Type 2 diabetes: blood glucose management.
in type 2 diabetic patients: a meta-analysis. Diabetes Care. Sheffield: ScHARR, University of Sheffield: Royal College of
2006;29(11):2518–27. General Practitioners Effective Clinical Practice Programme; 2001.
17. Thomas DE, Elliott EJ, Naughton GA. Exercise for type 2 dia- 37. Rodbard HW, Blonde L, Braithwaite SS, et al. American Asso-
betes mellitus. Cochrane Database Syst Rev. 2006;3:CD002968. ciation of Clinical Endocrinologists medical guidelines for clin-
18. Stratton IM, Cull CA, Adler AI, et al. Additive effects of ical practice for the management of diabetes mellitus. Endocr
glycaemia and blood pressure exposure on risk of complications Pract. 2007;13(Suppl 1):1–68.
in type 2 diabetes: a prospective observational study (UKPDS 38. IDF Clinical Guidelines Task Force. Global Guideline for type 2
75). Diabetologia. 2006;49(8):1761–9. diabetes: recommendations for standard, comprehensive, and
19. Hansen D, Dendale P, van Loon LJ, et al. The impact of training minimal care. Diabet Med. 2006;23(6):579–93.
modalities on the clinical benefits of exercise intervention in 39. American Diabetes Association. Standards of medical care in
patients with cardiovascular disease risk or type 2 diabetes mel- diabetes. Diabetes Care. 2011;34(Suppl 1):S11–61.
litus. Sports Med. 2010;40(11):921–40. 40. Canadian Diabetes Association Clinical Practice Guidelines
20. Nelson KM, Reiber G, Boyko EJ. Diet and exercise among adults Expert Committee. Canadian Diabetes Association 2008 clinical
with type 2 diabetes: findings from the third national health and practice guidelines for the prevention and management of dia-
nutrition examination survey (NHANES III). Diabetes Care. betes in Canada. Can J Diabetes. 2008;32(S1):S1–S201.
2002;25(10):1722–8. 41. Harris P, editor. Diabetes management in general practice. Can-
21. Crespo CJ, Ainsworth BE, Keteyian SJ, et al. Prevalence of berra: Diabetes Australia; 2009.
physical inactivity and its relation to social class in U.S. adults: 42. Institute for Clinical Systems Improvement. Diagnosis and
results from the Third National Health and Nutrition Examination management of type 2 diabetes mellitus in adults. Bloomington
Survey, 1988–1994. Med Sci Sports Exerc. 1999;31(12):1821–7. (MN): Institute for Clinical Systems Improvement; 2010.
48 C. O’Hagan et al.

43. Colberg SR, Albright AL, Blissmer BJ, et al. Exercise and type 2 prevalence of hyperglycaemia in patients with type 2 diabetes.
diabetes: American College of Sports Medicine and the American Diabetes Obes Metab. 2012;14(6):575–7.
Diabetes Association: joint position statement. Exercise and type 63. Little JP, Gillen JB, Percival ME, et al. Low-volume high-
2 diabetes. Med Sci Sports Exerc. 2010;42(12):2282–303. intensity interval training reduces hyperglycemia and increases
44. Gautier JF, Berne C, Grimm JJ, et al. Physical activity and dia- muscle mitochondrial capacity in patients with type 2 diabetes.
betes [in French]. Diabetes Metab. 1998;24(3):281–90. J Appl Physiol. 2011;111(6):1554–60.
45. Marwick TH, Hordern MD, Miller T, et al. Exercise training for 64. Bartlett JD, Close GL, MacLaren DP, et al. High-intensity
type 2 diabetes mellitus: impact on cardiovascular risk: a scien- interval running is perceived to be more enjoyable than moderate-
tific statement from the American Heart Association. Circulation. intensity continuous exercise: implications for exercise adher-
2009;119(25):3244–62. ence. J Sports Sci. 2011;29(6):547–53.
46. Sigal RJ, Kenny GP, Wasserman DH, et al. Physical activity/exer- 65. Trost SG, Owen N, Bauman AE, et al. Correlates of adults’
cise and type 2 diabetes: a consensus statement from the American participation in physical activity: review and update. Med Sci
Diabetes Association. Diabetes Care. 2006;29(6):1433–8. Sports Exerc. 2002;34(12):1996–2001.
47. US Department of Health and Human Services, Centers for 66. Wilmore JH. Individual exercise prescription. Am J Cardiol.
Disease Control and Prevention. 2008 Physical Activity Guide- 1974;33(6):757–9.
lines for Americans. Washington DC: US Department of Health 67. Slade SC, Keating JL. Effects of preferred-exercise prescription
and Human Services, 2008. http://www.health.gov/PAguidelines/ compared to usual exercise prescription on outcomes for people with
. Accessed 11 Dec 2011. non-specific low back pain: a randomized controlled trial [ACT-
48. U.S. Department of Health and Human Services. Physical activity RN12608000524392]. BMC Musculoskelet Disord. 2009;10:14.
and health: a report of the Surgeon General Washington DC: US 68. Findorff MJ, Wyman JF, Gross CR. Predictors of long-term
Department of Health and Human Services, 1996. http://www. exercise adherence in a community-based sample of older
cdc.gov/nccdphp/sgr. Accessed 11 Dec 2011. women. J Womens Health (Larchmt). 2009;18(11):1769–76.
49. Perri MG, Anton SD, Durning PE, et al. Adherence to exercise 69. Myers J. Principles of exercise prescription for patients with
prescriptions: effects of prescribing moderate versus higher levels chronic heart failure. Heart Fail Rev. 2008;13(1):61–8.
of intensity and frequency. Health Psychol. 2002;21(5):452–8. 70. Bizzarini E, Saccavini M, Lipanje F, et al. Exercise prescription
50. Lee JY, Jensen BE, Oberman A. Adherence in the training levels in subjects with spinal cord injuries. Arch Phys Med Rehabil.
comparison trial. Med Sci Sports Exerc. 1996;28(1):47–52. 2005;86(6):1170–5.
51. Hansen D, Stevens A, Eijnde BO, et al. Endurance exercise 71. Pescatello LS. Exercise and hypertension: recent advances in
intensity determination in the rehabilitation of coronary artery exercise prescription. Curr Hypertens Rep. 2005;7(4):281–6.
disease patients: a critical re-appraisal of current evidence. Sports 72. Wallman KE, Morton AR, Goodman C, et al. Exercise pre-
Med. 2011;42(1):11–30. scription for individuals with chronic fatigue syndrome. Med J
52. Hansen D, Dendale P, Jonkers RA, et al. Continuous low- to Aust. 2005;183(3):142–3.
moderate-intensity exercise training is as effective as moderate- 73. Jones KD, Clark SR. Individualizing the exercise prescription for
to high-intensity exercise training at lowering blood HbA(1c) in persons with fibromyalgia. Rheum Dis Clin North Am.
obese type 2 diabetes patients. Diabetologia. 2009;52(9): 2002;28(2):419–36, x–xi.
1789–97. 74. Nieuwland W, Berkhuysen MA, Van Veldhuisen DJ, et al.
53. Ghanassia E, Brun JF, Fedou C, et al. Substrate oxidation during Individual assessment of intensity-level for exercise training in
exercise: type 2 diabetes is associated with a decrease in lipid patients with coronary artery disease is necessary. Int J Cardiol.
oxidation and an earlier shift towards carbohydrate utilization. 2002;84(1):15–20.
Diabetes Metab. 2006;32(6):604–10. 75. Brown JC, Huedo-Medina TB, Pescatello LS, et al. Efficacy of
54. Boon H, Blaak EE, Saris WH, et al. Substrate source utilisation in exercise interventions in modulating cancer-related fatigue
long-term diagnosed type 2 diabetes patients at rest, and during among adult cancer survivors: a meta-analysis. Cancer Epidemiol
exercise and subsequent recovery. Diabetologia. 2007;50(1): Biomarkers Prev. 2010;20(1):123–33.
103–12. 76. Klika RJ, Callahan KE, Drum SN. Individualized 12-week
55. Brun JF, Jean E, Ghanassia E, et al. Metabolic training: new exercise training programs enhance aerobic capacity of cancer
paradigms of exercise training for metabolic diseases with exer- survivors. Phys Sportsmed. 2009;37(3):68–77.
cise calorimetry targeting individuals. Ann Readapt Med Phys. 77. Simms K, Myers C, Adams J, et al. Exercise tolerance testing in a
2007;50(6):528–34, 0–7. cardiac rehabilitation setting: an exploratory study of its safety
56. Venables MC, Jeukendrup AE. Endurance training and obesity: and practicality for exercise prescription and outcome data col-
effect on substrate metabolism and insulin sensitivity. Med Sci lection. Proc (Bayl Univ Med Cent). 2007;20(4):344–7.
Sports Exerc. 2008;40(3):495–502. 78. Gossain VV, Carella MJ, Rovner DR. Management of diabetes in
57. van Aggel-Leijssen DP, Saris WH, Wagenmakers AJ. Effect of the elderly: a clinical perspective. J Assoc Acad Minor Phys.
exercise training at different intensities on fat metabolism of 1994;5(1):22–31.
obese men. J Appl Physiol. 2002;92(3):1300–9. 79. Katz MS, Lowenthal DT. Influences of age and exercise on
58. Shulman GI. Cellular mechanisms of insulin resistance. J Clin glucose metabolism: implications for management of older dia-
Invest. 2000;106(2):171–6. betics. South Med J. 1994;87(5):S70–3.
59. Gaesser GA, Angadi SS. High-intensity interval training for 80. Armen J, Smith BW. Exercise considerations in coronary artery
health and fitness: can less be more? J Appl Physiol. disease, peripheral vascular disease, and diabetes mellitus. Clin
2011;111(6):1540–1. Sports Med. 2003;22(1):123–33, viii.
60. Murray AJ. Taking a HIT for the heart: why training intensity 81. Stewart KJ. Exercise training: can it improve cardiovascular
matters. J Appl Physiol. 2011;111(5):1229–30. health in patients with type 2 diabetes? Br J Sports Med.
61. Gibala MJ, Little JP, Macdonald MJ, et al. Physiological adap- 2004;38(3):250–2.
tations to low-volume, high-intensity interval training in health 82. De Feyter HM, Praet SF, van den Broek NM, et al. Exercise
and disease. J Physiol. 2012;590(Pt 5):1077–84. training improves glycemic control in long-standing insulin-
62. Gillen JB, Little JP, Punthakee Z. Acute high-intensity interval treated type 2 diabetic patients. Diabetes Care. 2007;30(10):
exercise reduces the postprandial glucose response and 2511–3.
Prescription of Exercise Training in T2DM 49

83. Praet SF, van Rooij ES, Wijtvliet A, et al. Brisk walking com- 88. Zhang P, Zhang X, Brown J, et al. Global healthcare expenditure
pared with an individualised medical fitness programme for on diabetes for 2010 and 2030. Diabetes Res Clin Pract.
patients with type 2 diabetes: a randomised controlled trial. Di- 2010;87(3):293–301.
abetologia. 2008;51(5):736–46. 89. Volpp KG, Troxel AB, Pauly MV, et al. A randomized, con-
84. Wisse W, Rookhuizen MB, de Kruif MD, et al. Prescription of trolled trial of financial incentives for smoking cessation. N Engl
physical activity is not sufficient to change sedentary behavior J Med. 2009;360(7):699–709.
and improve glycemic control in type 2 diabetes patients. Dia- 90. Volpp KG, John LK, Troxel AB, et al. Financial incentive-based
betes Res Clin Pract. 2010;88(2):e10–3. approaches for weight loss: a randomized trial. JAMA.
85. Ricordeau P, Weill A, Vallier N, et al. The cost of diabetes in 2008;300(22):2631–7.
metropolitan France [in French]. Diabetes Metab. 2000;26(Suppl 91. Wing RR, Jeffery RW, Pronk N, et al. Effects of a personal
6):25–38. trainer and financial incentives on exercise adherence in over-
86. Ricordeau P, Weill A, Vallier N, et al. The prevalence and cost of weight women in a behavioral weight loss program. Obes Res.
diabetes in metropolitan France: what trends between 1998 and 1996;4(5):457–62.
2000? Diabetes Metab. 2003;29(5):497–504. 92. Moller A. Financial motivation undermines maintenance in an
87. Hogan P, Dall T, Nikolov P. Economic costs of diabetes in the intensive diet and activity intervention. J Obesity. 2012;. doi:
US in 2002. Diabetes Care. 2003;26(3):917–32. 10.1155/2012/740519.

S-ar putea să vă placă și