4.6 Article

High-intensity interval training reduces abdominal fat mass in postmenopausal women with type 2 diabetes

Journal

DIABETES & METABOLISM
Volume 42, Issue 6, Pages 433-441

Publisher

MASSON EDITEUR
DOI: 10.1016/j.diabet.2016.07.031

Keywords

Body composition; Health; Menopause; Physical activity; Type 2 diabetes

Funding

  1. Region Auvergne
  2. Region Auvergne

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Aim. - This study compared the effect of high-intensity interval training (HILT) and moderate-intensity continuous training (MICT) for 16 weeks on whole-body and abdominal fat mass (FM) in postmenopausal women with type 2 diabetes (T2D). Methods. - Seventeen women (69 1 years; BMI: 31 +/- 1 kg.m(-2)) were randomly assigned to either a HIIT [60 x (8 s at 77-85% HRmax, 12 s of active recovery)] or MICT (40 min at 55-60% of their individual HRR) cycling program for 16 weeks, 2 days/week. Dual-energy X-ray absorptiometry was used to measure whole-body and regional FM content, including abdominal adiposity and visceral adipose tissue. Plasma cholesterol, HDL, LDL, triglycerides, glucose and HbA(1c) levels were measured. Levels of nutritional intake and physical activity were evaluated by 7-day self-reports. Results. - Dietary energy (caloric) intake, physical activity level and total body mass did not vary in either group from the beginning to the end of the training intervention. Overall, total FM decreased and total fat-free mass significantly increased over time (by around 2-3%). Total FM reduction at the end of the intervention was not significantly different between groups. However, significant loss of total abdominal (-8.3 +/- 2.2%) and visceral (-24.2 +/- 7.7%) FM was observed only with HIIT. Time effects were noted for HbA(1c) and total cholesterol/HDL ratio. Conclusion. - With no concomitant caloric restriction, an HIIT program in postmenopausal women with T2D (twice a week for 16 weeks) appeared to be more effective for reducing central obesity than MICT, and could be proposed as an alternative exercise training program for this population. (C) 2016 Elsevier Masson SAS. All rights reserved.

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