| | Impact of modified glucose target and exercise interventions on vascular risk factorsReceived 16 May 2004; received in revised form 7 September 2005; accepted 12 September 2005. published online 27 October 2005. Abbreviations: BMI, body mass index, EST, exercise stress test, HDL, high-density lipoprotein, IQR, interquartile range, MAP, mean arterial blood pressure, METS, metabolic equivalents, T2D, type 2 diabetes 1. Introduction  Among type 2 diabetes (T2D) patients, those who intentionally lose weight have a 28% lower cardiovascular mortality at 12 years follow-up than those who do not lose weight [1]. However, achieving weight loss is particularly challenging for T2D patients. In a meta-analysis of supervised exercise trials in T2D, dietary counseling ± exercise resulted in net weight loss of less than 4% [2], compared to an 11% weight loss reported in a meta-analysis of weight loss studies among overweight patients without T2D [3]. T2D patients experienced less weight loss than their overweight spouses in a trial assessing an identical weight control program in both groups [4]. Tight glycemic control reduces rates of diabetes-associated complications [5], but is associated with additional weight gain. During the United Kingdom Prospective Diabetes Study (UKPDS), tight control with insulin/secretagogues (preprandial glucose target 6 mmol/l versus 15 mmol/l) was associated with a 3–4 kg additional weight gain. Only metformin-treated patients avoided such a weight increase [5]. T2D patients may limit physical activity because of concerns about exercise-associated risks such as hypoglycemia and ischemia. Exercise initiation in a supervised setting may simultaneously optimize intensity and safety, and significantly improve glycemic control [2]. Less well defined is the impact of supervised exercise on fitness and blood pressure, both important in the development of cardiovascular disease [5], [6], [7], [8], [9]. To facilitate weight loss, improve glycemic control, enhance fitness, and lower blood pressure, we formulated the following three-point intervention: (i) dietary counseling with supervised exercise, (ii) metformin at maximum tolerated doses and (iii) liberalized preprandial glucose threshold for adjustment of other medications to permit reduced use of these medications. This pilot study was conducted to assess the feasibility of such an approach. We report on (i) the impact of a liberalized threshold on hemoglobin A1C levels and (ii) the relationship between changes in fitness to changes in weight and blood pressure. We also provide estimates of the magnitude of change in weight, fitness, and blood pressure levels associated with study interventions. 2. Patients and methods  2.1. Study design This pilot trial (2 × 2 factorial design) was conducted in Montreal, Que., Canada. Following completion of recruitment, participants were randomized to (i) dietary counseling with OR without supervised exercise and (ii) liberalized OR strict preprandial glucose thresholds for adjustment of glucose-lowering medication other than metformin. Procedures were approved by the Institutional Review Board of McGill University. Written informed consent was obtained. 2.2. Participants Eligibility requirements included age 30–70 years, physician T2D diagnosis, body mass index (BMI) ≥28 kg/m2, and ≥5 metabolic equivalents (METS) during a symptom-limited maximal baseline exercise stress test. Exclusion criteria included insulin use, foot ulcers, pregnancy, lactation, untreated diabetic retinopathy, or conditions/medications that could affect weight (e.g. cirrhosis, corticosteroids). Pre-menopausal women were asked to use a reliable method of contraception. Recruitment was conducted between May and September 2003 largely through out-patient clinics (diabetes, internal, family medicine) affiliated with McGill University. 2.3. Interventions Between September 2003 and March 2004, interventions were conducted through the Cardiovascular Health Improvement Program (CHIP), McGill University's cardiac rehabilitation centre. 2.3.1. Dietary counseling A registered dietitian provided individualized dietary counseling based on Canadian Diabetes Association guidelines [10] (six sessions over 24 weeks, 145 min total counseling time). 3. Statistical analyses  3.2. Linear regression analyses Parametric methods were permitted by the larger sample size achieved by combining outcomes from intervention arms. Through linear regression models, we assessed the relationships between 90-day preprandial glucose value and hemoglobin A1C and between change in fitness and changes in each of the following: weight, mean arterial pressure, and hemoglobin A1C. 3.3. Sample size considerations Using a t-test with a 0.025 two-sided significance level, we determined that a sample size of 21 per group for each two-group comparison would have 80% power to detect a difference in weight change of 4.5%, assuming a common standard deviation of 4.5% [17]. 4. Results  4.2. Baseline characteristics There were no significant differences between groups (Table 1, Table 2). None of the participants had a history of diabetic retinopathy or neuropathy. | | |  | | Dietary counseling alone, N = 21 [median (IQRa) or number (%)] | Dietary counseling with supervised exercise, N = 21 [median (IQRa) or number (%)] |  |
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 | Demographic characteristics |  |  | Age (years) | 49 (46, 55) | 54 (47, 58) |  |  | Women | 12 (57) | 9 (43) |  |  | Professional | 8 (38) | 6 (29) |  |  | Technician | 5 (23) | 7 (33) |  |  | Other | 8 (38) | 8 (38) |  |  | |  |  | Body mass and fitness |  |  | BMIb (kg/m2) | 36.6 (31.6, 39.8) | 36.4 (32.8, 41.8) |  |  | Waist circumference (cm) | 114 (104, 121) | 116 (111, 130) |  |  | Stress test duration (min) | 7.3 (6.4, 9.3) | 6.8 (6.3, 8.0) |  |  | |  |  | Glycemic control |  |  | Hemoglobin A1C | 0.071 (0.063, 0.074) | 0.072 (0.061, 0.077) |  |  | Metformin | 16 (76) | 17 (81) |  |  | Sulfonylurea | 10 (48) | 8 (38) |  |  | Thiazolodinedione | 4 (19) | 3 (14) |  |  | Diabetes duration (years) | 3 (1, 5) | 2 (1, 3.5) |  |  | |  |  | Blood pressure |  |  | Mean arterial (mmHg) | 113 (106, 117) | 118 (107, 123) |  |  | Systolic (mmHg) | 130 (120, 130) | 130 (120, 140) |  |  | Diastolic (mmHg) | 80 (74, 90) | 80 (80, 90) |  |  | Number of medications | 1 (0, 1) | 1 (0, 1) |  |  | |  |  | Previous history of cardiovascular disease | 2 (10) | 2 (10) |  |  | |  |  | Habits |  |  | Current smokers | 2 (10) | 0 (0) |  |  | Alcohol use | 11 (52) | 12 (57) |  | | | |
| a Interquartile range. bBody mass index. |
| | |  | | Preprandial capillary plasma glucose threshold |  |
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 | | 7 mmol/l, N = 20 [median (IQRa) or number (%)] | 10 mmol/l, N = 22 [median (IQRa) or number (%)] |  |
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 | Demographic characteristics |  |  | Age (years) | 49 (46, 56.5) | 53.5 (47, 59) |  |  | Women | 11 (55) | 10 (45) |  |  | Professional | 4 (20) | 10 (45) |  |  | Technician | 8 (40) | 4 (18) |  |  | Other | 8 (40) | 8 (36) |  |  | |  |  | Body mass and fitness |  |  | BMIb (kg/m2) | 35.6 (32.4, 41.4) | 37.4 (31.0, 40.8) |  |  | Waist circumference (cm) | 115 (107, 121) | 115 (105, 128) |  |  | Stress test duration (min) | 7.2 (6.4, 9.2) | 7.3 (6.3, 8.5) |  |  | |  |  | Glycemic control |  |  | Hemoglobin A1C | 7.0 (6.3, 7.4) | 6.9 (6.1, 7.6) |  |  | Metformin | 14 (70) | 19 (86) |  |  | Sulfonylurea | 7 (35) | 11 (50) |  |  | Thiazolodinedione | 3 (15) | 4 (18) |  |  | |  |  | Diabetes duration (years) | 2 (1, 4) | 3 (1.8, 5) |  |  | |  |  | Previous history of cardiovascular disease | 1 (5) | 3 (14) |  |  | |  |  | Habits |  |  | Current smokers | 1 (5) | 1 (5) |  |  | Alcohol use | 13 (65) | 10 (45) |  | | | |
| a Interquartile range. bBody mass index. |
4.4. Between-group comparisons 4.4.3. Preprandial glucose thresholds for medication change Median 90-day average preprandial glucose was significantly higher (p = 0.01) in the 10 mmol/l threshold arm (8.4 mmol/l, IQR 6.6–9.4 mmol/l) than the 7 mmol/l arm (6.9 mmol/l, IQR 6.6–7.5 mmol/l). Rates of glycosuria did not differ significantly [0% (IQR 0–14%) versus 6.2% (IQR 0–24%), p = 0.28]. Two participants in each group commenced metformin treatment. In the 10 mmol/l threshold group, two participants discontinued sulfonylurea and three discontinued thiazolodinedione medication. The proportion of participants with a low-recorded glucose value did not differ between groups [45% (10/22) versus 50% (10/20), p = 0.50]. There were no significant between-group differences in terms of changes in weight [−1.2% (IQR −3.7 to 2.0%) versus −0.3% (IQR −2.7 to 7.3%), p = 0.38], hemoglobin A1C [−0.8% (IQR −8.6 to 5.6%) versus 0% (IQR −11.7% to 3.7%), p = 0.37], or waist circumference [−1.3% (IQR −2.5 to 0%) versus −1.4% (IQR −3.1 to 0%), p = 0.62]. 5. Discussion  Overall weight change was small during our 24-week pilot trial (<2%), but similar in magnitude to that experienced by T2D patients in other weight loss interventional studies [2]. The difference in weight change between dietary counseling with and without supervised exercise groups approached statistical significance but was small in magnitude (1.5%) [2]. The small weight change in all patients may have partly been attributable to the fact that the intervention period included the holiday season, a time of weight gain [19]. The weight change difference between differing preprandial threshold arms was smaller (0.9%) and nonsignificant. The low rate of hypoglycemia reported in our patients – and likely the consequent absence of any associated appetite stimulation – may have accounted for the absence of a significant difference in weight change between the two preprandial threshold arms. Most of our patients were receiving metformin only at baseline and would therefore be less likely to experience large excursions in blood glucose levels. Change in hemoglobin A1C did not differ significantly between the dietary counseling with and without supervised exercise arms. This may be attributable to the high level of glycemic control at baseline (Table 1). There was no linear relationship between changes in fitness and hemoglobin A1C. A T2D supervised exercise trial meta-analysis similarly found neither exercise intensity nor volume to be associated with post-intervention hemoglobin A1C, although supervised exercise was associated with improvement in hemoglobin A1C levels [2]. In our study, the 10 mmol/l arm had significantly higher 90-day preprandial glucose levels and some reduction in glucose-lowering medication compared to the 7 mmol/l arm. Nonetheless, these groups did not differ significantly in terms of hemoglobin A1C change. This is consistent with the results of a single previous trial that examined the issue of preprandial glucose thresholds/targets. van der does et al. randomized T2D patients (n = 176) to targets of <6.5 mmol/l versus <8.5 mmol/l [18]. The <6.5 mmol/l group experienced more medication intensification but no greater improvement in hemoglobin A1C levels 1 year later. Preprandial glucose levels of <6 mmol/l are recommended by the International Diabetes Federation and levels of 5–7.2 mmol/l are supported by the American Diabetes Association. Our results suggest that a hemoglobin A1C level of 7% may be achieved with a 90-day preprandial glucose level of 8.1 mmol/l (Fig. 4). Further study examining this issue is warranted. We found consistent attendance of a supervised exercise program to be associated with a statistically and clinically significant fitness improvement. Median improvement was 1.5% in the dietary counseling alone group, 5.4% overall in the dietary counseling with supervised exercise group, and 21.3% among those who participated in ≥75% supervised exercise sessions. Among men with T2D, Church and colleagues demonstrated a steep inverse gradient between fitness and mortality that was independent of BMI, glucose level, blood pressure, total cholesterol level, and history of smoking or cardiovascular disease [9]. In our pilot study, the dietary counseling with supervised exercise arm experienced significantly greater blood pressure improvement compared to the dietary counseling alone arm. This difference was likely driven by the fitness change among those with a high exercise class attendance. Improvements in fitness and blood pressure were linearly related (Fig. 3). One previous trial involving a structured exercise program (treadmills, stationery bicycles, rowing machines) also found exercise to be associated with a significant blood pressure lowering effect among T2D patients [8]. Two other trials did not find walking programs to be associated with a statistically significant blood pressure lowering effect in this population [6], [7]. Exercising at a more intense level than walking may be necessary to lower blood pressure. The occurrence of the holiday period (December/January) during our trial may have attenuated weight change. This period has been associated with weight increases in nondiabetic populations [19]. One previous study that achieved 7% weight loss among T2D patients incorporated cognitive behavioural therapy and incentive-based strategies (e.g. return of a deposit with consistent attendance) [4]. Budgetary constraints precluded use of such approaches during our pilot study. Our ability to identify significant between-group differences was clearly limited by sample size. It is important to note, however, that our study was designed to provide feasibility data. Nonetheless, some significant differences did emerge. Budgetary factors did not permit monitoring of activity/diet. However, self-report of food intake and physical activity is subject to inaccuracies [20]. Weight and fitness measures may be more reliable outcome measures [21]. In conclusion, results from this pilot study suggest that neither supervised exercise programs nor liberalization of preprandial glucose targets offer clinically significant reduction in weight among T2D patients. However, consistent participation in a program of supervised exercise offers clinically and statistically significant improvements in fitness and blood pressure control. Future research should focus on the identification of strategies to maximize exercise class attendance in order to realize these benefits. Our results also suggest that, in conjunction with maximal metformin dosing and dietary counseling, allowing higher capillary blood glucose thresholds may reduce the need for other medications without compromising glycemic control. A larger study is needed to further examine this possibility. Acknowledgements  This research was supported by grants from the Canadian Institute of Health Research-Institute of Nutrition, Metabolism, and Diabetes and from the Research Institute of the McGill University Health Centre. One Touch Ultra glucometers and strips were generously provided by Lifescan®. Funding agencies and suppliers of materials had no role in the design, conduct, analysis, or reporting of this study. Ms. Barbara Greig and Ms. Carmela D’Avella, diabetes educators at the McGill University Health Centre, greatly facilitated recruitment by identifying candidates for our efficient recruitment assistant, Martine Lecomte. 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[21]. [21]Livingstone M, Black A. Markers of the validity of reported energy intake. J. Nutr. 2003;133:895S–920S. McGill University, Montreal, Canada Corresponding author at: Clinical Epidemiology; Montreal General Hospital, 1650 Cedar Avenue, L10-425, Montreal, Que., Canada H3G 1A4. Tel.: +1 514 934 1934x44715; fax: +1 514 934 8293.
PII: S0168-8227(05)00375-X doi:10.1016/j.diabres.2005.09.010 © 2005 Elsevier Ireland Ltd. All rights reserved. | |
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