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Randomized Controlled Trial
. 2013 Aug;36(8):2162-8.
doi: 10.2337/dc12-1391. Epub 2013 Feb 14.

Determinants of weight gain in the action to control cardiovascular risk in diabetes trial

Collaborators, Affiliations
Randomized Controlled Trial

Determinants of weight gain in the action to control cardiovascular risk in diabetes trial

Vivian Fonseca et al. Diabetes Care. 2013 Aug.

Abstract

Objective: Identify determinants of weight gain in people with type 2 diabetes mellitus (T2DM) allocated to intensive versus standard glycemic control in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial.

Research design and methods: We studied determinants of weight gain over 2 years in 8,929 participants (4,425 intensive arm and 4,504 standard arm) with T2DM in the ACCORD trial. We used general linear models to examine the association between each baseline characteristic and weight change at the 2-year visit. We fit a linear regression of change in weight and A1C and used general linear models to examine the association between each medication at baseline and weight change at the 2-year visit, stratified by glycemia allocation.

Results: There was significantly more weight gain in the intensive glycemia arm of the trial compared with the standard arm (3.0 ± 7.0 vs. 0.3 ± 6.3 kg). On multivariate analysis, younger age, male sex, Asian race, no smoking history, high A1C, baseline BMI of 25-35, high waist circumference, baseline insulin use, and baseline metformin use were independently associated with weight gain over 2 years. Reduction of A1C from baseline was consistently associated with weight gain only when baseline A1C was elevated. Medication usage accounted for <15% of the variability of weight change, with initiation of thiazolidinedione (TZD) use the most prominent factor. Intensive participants who never took insulin or a TZD had an average weight loss of 2.9 kg during the first 2 years of the trial. In contrast, intensive participants who had never previously used insulin or TZD but began this combination after enrolling in the ACCORD trial had a weight gain of 4.6-5.3 kg at 2 years.

Conclusions: Weight gain in ACCORD was greater with intensive than with standard treatment and generally associated with reduction of A1C from elevated baseline values. Initiation of TZD and/or insulin therapy was the most important medication-related factor associated with weight gain.

Trial registration: ClinicalTrials.gov NCT00000620.

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Figures

Figure 1
Figure 1
Time course of weight gain in the ACCORD trial by treatment allocation.
Figure 2
Figure 2
Plots of change in A1C and change in weight by baseline A1C. Lines represent the estimated equation from the 5th to 95th percentile for each combination of baseline A1C and glycemia arm. Solid lines represent intensive arm, and interrupted lines represent standard treatment. Each treatment group has been divided into tertiles of baseline A1C.

References

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