Participation in a National Lifestyle Change Program is associated with improved diabetes Control outcomes
- PMID: 28673663
- PMCID: PMC5568070
- DOI: 10.1016/j.jdiacomp.2017.06.001
Participation in a National Lifestyle Change Program is associated with improved diabetes Control outcomes
Abstract
Aims: Clinical trials show lifestyle change programs are beneficial, yet large-scale, successful translation of these programs is scarce. We investigated the association between participation in the largest U.S. lifestyle change program, MOVE!, and diabetes control outcomes.
Methods: This longitudinal, retrospective cohort study used Veterans Health Administration databases of patients with diabetes who participated in MOVE! between 2005 and 2012, or met eligibility criteria (BMI ≥25kg/m2) but did not participate. Main outcomes were diabetic eye disease, renal disease, and medication intensification.
Results: There were 400,170 eligible patients with diabetes, including 87,366 (22%) MOVE!
Participants: Included patients were 96% male, 77% white, with mean age 58years and BMI 34kg/m2. Controlling for baseline measurements and age, race, sex, BMI, and antidiabetes medications, MOVE! participants had lower body weight (-0.6kg), random plasma glucose (-2.8mg/dL), and HbA1c (-0.1%) at 12months compared to nonparticipants (each p<0.001). In multivariable Cox models, MOVE! participants had lower incidence of eye disease (hazard ratio 0.80, 95% CI 0.75-0.84) and renal disease (HR 0.89, 95% CI 0.86-0.92) and reduced medication intensification (HR 0.82, 95% CI 0.80-0.84).
Conclusions: If able to overcome participation challenges, lifestyle change programs in U.S. health systems may improve health among the growing patient population with diabetes.
Keywords: Diabetes complications; Diabetes mellitus; Veterans; Weight loss; Weight reduction programs.
Published by Elsevier Inc.
Conflict of interest statement
The authors declare that there is no duality of interest associated with this manuscript. With regard to potential conflicts of interest, within the past several years, Dr. Phillips has served on Scientific Advisory Boards for Boehringer Ingelheim and Janssen, and has or had research support from Merck, Amylin, Eli Lilly, Novo Nordisk, Sanofi, PhaseBio, Roche, Glaxo SmithKline, and the Cystic Fibrosis Foundation. In the past, he was a speaker for Novartis and Merck, but not for the last several years. Qi Long receives support from Cystic Fibrosis Foundation and American Heart Association and was a consultant for Eisai. Sandra Jackson previously received support from Amylin, and Venkat Narayan receives support from Novo Nordisk. These activities involve diabetes, but have nothing to do with this manuscript. Other authors have no potential conflicts of interest to declare.
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