9
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Relationship between weight change and glycaemic control in patients with type 2 diabetes receiving once‐weekly dulaglutide treatment

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Aim

          To assess the relationship between weight change and glycated haemoglobin ( HbA1c) change in dulaglutide‐treated patients by analysing data from six head‐to‐head phase III AWARD clinical trials.

          Methods

          At 26 weeks, the relationship between weight and HbA1c was analysed in each trial rather than by pooling data because of differences in design and background therapy. The effect of baseline characteristics was also evaluated with regard to weight and HbA1c response.

          Results

          Across the studies, 87–97% and 83–95% of patients treated with dulaglutide 1.5 and 0.75 mg, respectively, had reductions in HbA1c levels, while 57–88% and 43–84% of patients treated with dulaglutide 1.5 and 0.75 mg, respectively, experienced weight loss. The majority (55–83%) of patients receiving dulaglutide 1.5 mg experienced weight loss and HbA1c reductions, while 41–79% of patients in the dulaglutide 0.75 mg arm lost weight and had reductions in HbA1c level. A weak and inconsistent correlation was observed between the changes in weight and HbA1c (range from −0.223 to 0.267) in patients treated with dulaglutide. The baseline characteristics of gender, age, duration of diabetes, HbA1c, body weight and BMI were not related to different combinations of weight and HbA1c responses.

          Conclusions

          Dulaglutide is an effective treatment option across the type 2 diabetes treatment spectrum. Dulaglutide showed dose‐dependent effects on both weight loss and HbA1c reduction. These effects had a weak correlation and appeared to be independent.

          Related collections

          Most cited references7

          • Record: found
          • Abstract: found
          • Article: not found

          Exenatide effects on diabetes, obesity, cardiovascular risk factors and hepatic biomarkers in patients with type 2 diabetes treated for at least 3 years.

          Exenatide, an incretin mimetic for adjunctive treatment of type 2 diabetes (T2DM), reduced hemoglobin A(1c) (A1C) and weight in clinical trials. The objective of this study was to evaluate the effects of > or = 3 years exenatide therapy on glycemic control, body weight, cardiometabolic markers, and safety. Patients from three placebo-controlled trials and their open-label extensions were enrolled into one open-ended, open-label clinical trial. Patients were randomized to twice daily (BID) placebo, 5 mug exenatide, or 10 mug exenatide for 30 weeks, followed by 5 mug exenatide BID for 4 weeks, then 10 mug exenatide BID for > or = 3 years of exenatide exposure. Patients continued metformin and/or sulfonylureas. 217 patients (64% male, age 58 +/- 10 years, weight 99 +/- 18 kg, BMI 34 +/- 5 kg/m(2), A1C 8.2 +/- 1.0% [mean +/- SD]) completed 3 years of exenatide exposure. Reductions in A1C from baseline to week 12 (-1.1 +/- 0.1% [mean +/- SEM]) were sustained to 3 years (-1.0 +/- 0.1%; p or = 3 years in T2DM patients resulted in sustained improvements in glycemic control, cardiovascular risk factors, and hepatic biomarkers, coupled with progressive weight reduction.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Weight management through lifestyle modification for the prevention and management of type 2 diabetes: rationale and strategies: a statement of the American Diabetes Association, the North American Association for the Study of Obesity, and the American Society for Clinical Nutrition.

              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              The prevention and treatment of obesity. Application to type 2 diabetes.

                Bookmark

                Author and article information

                Journal
                Diabetes Obes Metab
                Diabetes Obes Metab
                10.1111/(ISSN)1463-1326
                DOM
                Diabetes, Obesity & Metabolism
                Blackwell Publishing Ltd (Oxford, UK )
                1462-8902
                1463-1326
                13 April 2016
                June 2016
                : 18
                : 6 ( doiID: 10.1111/dom.2016.18.issue-6 )
                : 615-622
                Affiliations
                [ 1 ] Division of EndocrinologyEmory University School of Medicine Atlanta GAUSA
                [ 2 ] Department of EndocrinologyCleveland Clinic Cleveland OHUSA
                [ 3 ]Lilly USA, LLC. Indianapolis INUSA
                [ 4 ]Eli Lilly and Company Indianapolis INUSA
                Author notes
                [*] [* ] Correspondence to: Guillermo E. Umpierrez, Division of Endocrinology, Emory University School of Medicine, 49 Jesse Hill Jr Dr, Atlanta, Georgia, 30303, USA. E‐mail: geumpie@ 123456emory.edu
                Article
                DOM12660
                10.1111/dom.12660
                4934019
                26969812
                c3527d64-da39-403b-9b1c-fd64b818dbf1
                © 2016 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 15 December 2015
                : 15 February 2016
                : 10 January 2016
                Page count
                Pages: 8
                Funding
                Funded by: Eli Lilly and Company
                Funded by: American Diabetes Association
                Award ID: 7‐03‐CR‐35
                Funded by: PHS Grant UL1 RR025008 from the Clinical and Translational Science Award Program
                Award ID: M01 RR‐00039
                Funded by: National Institutes of Health
                Funded by: National Center for Research Resources
                Funded by: Novo Nordisk
                Funded by: Merck
                Funded by: Boehringer Ingelheim
                Funded by: Astra Zeneca
                Funded by: Sanofi
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                dom12660
                June 2016
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.9.4 mode:remove_FC converted:13.09.2016

                Endocrinology & Diabetes
                dulaglutide,glp‐1 analogueincretin therapy,incretin therapy,type 2 diabetes

                Comments

                Comment on this article