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Determinants of Weight Gain in the Action to Control Cardiovascular Risk in Diabetes Trial

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 y...

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Autores principales: Fonseca, Vivian, McDuffie, Roberta, Calles, Jorge, Cohen, Robert M., Feeney, Patricia, Feinglos, Mark, Gerstein, Hertzel C., Ismail-Beigi, Faramarz, Morgan, Timothy M., Pop-Busui, Rodica, Riddle, Matthew C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3714487/
https://www.ncbi.nlm.nih.gov/pubmed/23412077
http://dx.doi.org/10.2337/dc12-1391
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author Fonseca, Vivian
McDuffie, Roberta
Calles, Jorge
Cohen, Robert M.
Feeney, Patricia
Feinglos, Mark
Gerstein, Hertzel C.
Ismail-Beigi, Faramarz
Morgan, Timothy M.
Pop-Busui, Rodica
Riddle, Matthew C.
author_facet Fonseca, Vivian
McDuffie, Roberta
Calles, Jorge
Cohen, Robert M.
Feeney, Patricia
Feinglos, Mark
Gerstein, Hertzel C.
Ismail-Beigi, Faramarz
Morgan, Timothy M.
Pop-Busui, Rodica
Riddle, Matthew C.
author_sort Fonseca, Vivian
collection PubMed
description 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.
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spelling pubmed-37144872014-08-01 Determinants of Weight Gain in the Action to Control Cardiovascular Risk in Diabetes Trial Fonseca, Vivian McDuffie, Roberta Calles, Jorge Cohen, Robert M. Feeney, Patricia Feinglos, Mark Gerstein, Hertzel C. Ismail-Beigi, Faramarz Morgan, Timothy M. Pop-Busui, Rodica Riddle, Matthew C. Diabetes Care Original Research 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. American Diabetes Association 2013-08 2013-07-11 /pmc/articles/PMC3714487/ /pubmed/23412077 http://dx.doi.org/10.2337/dc12-1391 Text en © 2013 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Research
Fonseca, Vivian
McDuffie, Roberta
Calles, Jorge
Cohen, Robert M.
Feeney, Patricia
Feinglos, Mark
Gerstein, Hertzel C.
Ismail-Beigi, Faramarz
Morgan, Timothy M.
Pop-Busui, Rodica
Riddle, Matthew C.
Determinants of Weight Gain in the Action to Control Cardiovascular Risk in Diabetes Trial
title Determinants of Weight Gain in the Action to Control Cardiovascular Risk in Diabetes Trial
title_full Determinants of Weight Gain in the Action to Control Cardiovascular Risk in Diabetes Trial
title_fullStr Determinants of Weight Gain in the Action to Control Cardiovascular Risk in Diabetes Trial
title_full_unstemmed Determinants of Weight Gain in the Action to Control Cardiovascular Risk in Diabetes Trial
title_short Determinants of Weight Gain in the Action to Control Cardiovascular Risk in Diabetes Trial
title_sort determinants of weight gain in the action to control cardiovascular risk in diabetes trial
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3714487/
https://www.ncbi.nlm.nih.gov/pubmed/23412077
http://dx.doi.org/10.2337/dc12-1391
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