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      Glycaemic outcomes of an Individualized treatMent aPproach for oldER vulnerable patIents: A randomized, controlled stUdy in type 2 diabetes Mellitus (IMPERIUM)

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          Abstract

          Aims

          To compare the glycaemic outcomes of 2 glucose‐lowering treatment strategies in vulnerable (moderately ill and/or frail) patients aged ≥65 years with type 2 diabetes whose individual HbA1c targets were not met with diet/exercise and/or oral anti‐hyperglycaemic medications ( OAMs).

          Methods

          The primary endpoint of this study was a composite of achieving/maintaining individualized HbA1c targets without “clinically significant” hypoglycaemia (severe hypoglycaemia or repeated hypoglycaemia causing interruption of patients’ activities or blood glucose <54 mg/dL). Strategy‐ A comprised glucose‐dependent therapies ( n = 99) with a non‐sulphonylurea OAM and a glucagon‐like peptide‐1 receptor agonist as the first injectable. Strategy‐ B comprised non‐glucose‐dependent therapies ( n = 93) with sulphonylurea as the preferred OAM and insulin glargine as the first injectable.

          Results

          There was no significant difference between Strategy‐ A and Strategy‐ B in percentages of patients achieving the primary endpoint (64.5% vs 54.9%; P = .190). Mean incidences ( A vs B) of total (10.2% vs 53.8%), documented symptomatic (5.1% vs 36.6%), and asymptomatic (8.2% vs 32.3%) hypoglycaemia were lower for Strategy‐ A ( P < .001 each). Proportions of patients achieving/maintaining HbA1c target ( A, 63.3% vs B, 55.9%) were similar.

          Conclusion

          Similar proportions of older, vulnerable aged ≥65 years patients with type 2 diabetes achieved/maintained glycaemic treatment goals without clinically significant hypoglycaemia with Strategies A or B. However, Strategy‐A resulted in lower risk of total, documented symptomatic, and asymptomatic hypoglycaemia. These results identify an approach of potential clinical benefit in this age group and will inform future clinical research in older patients with type 2 diabetes.

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          Most cited references25

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          Diabetes in older adults: a consensus report.

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            Incretin therapies: highlighting common features and differences in the modes of action of glucagon‐like peptide‐1 receptor agonists and dipeptidyl peptidase‐4 inhibitors

            M. Nauck (2016)
            Over the last few years, incretin‐based therapies have emerged as important agents in the treatment of type 2 diabetes (T2D). These agents exert their effect via the incretin system, specifically targeting the receptor for the incretin hormone glucagon‐like peptide 1 (GLP‐1), which is partly responsible for augmenting glucose‐dependent insulin secretion in response to nutrient intake (the ‘incretin effect’). In patients with T2D, pharmacological doses/concentrations of GLP‐1 can compensate for the inability of diabetic β cells to respond to the main incretin hormone glucose‐dependent insulinotropic polypeptide, and this is therefore a suitable parent compound for incretin‐based glucose‐lowering medications. Two classes of incretin‐based therapies are available: GLP‐1 receptor agonists (GLP‐1RAs) and dipeptidyl peptidase‐4 (DPP‐4) inhibitors. GLP‐1RAs promote GLP‐1 receptor (GLP‐1R) signalling by providing GLP‐1R stimulation through ‘incretin mimetics’ circulating at pharmacological concentrations, whereas DPP‐4 inhibitors prevent the degradation of endogenously released GLP‐1. Both agents produce reductions in plasma glucose and, as a result of their glucose‐dependent mode of action, this is associated with low rates of hypoglycaemia; however, there are distinct modes of action resulting in differing efficacy and tolerability profiles. Furthermore, as their actions are not restricted to stimulating insulin secretion, these agents have also been associated with additional non‐glycaemic benefits such as weight loss, improvements in β‐cell function and cardiovascular risk markers. These attributes have made incretin therapies attractive treatments for the management of T2D and have presented physicians with an opportunity to tailor treatment plans. This review endeavours to outline the commonalities and differences among incretin‐based therapies and to provide guidance regarding agents most suitable for treating T2D in individual patients.
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              Sulfonylureas and their use in clinical practice

              Many anti-diabetic drugs with different mechanisms of action are now available for treatment of type 2 diabetes mellitus. Sulfonylureas have been extensively used for treatment of type 2 diabetes for nearly 50 years and, even in our times, are widely used for treatment of this devastating chronic illness. Here, we review some of the available data on sulfonylureas, evaluating their mechanism of action and their effects on glycemic control. We can conclude that sulfonylureas are still the most used anti-diabetic agents: maybe this is due to their lower cost, to the possibility of mono-dosing and to the presence of an association with metformin in the same tablet. However, sulfonylureas, especially the older ones, are linked to a greater prevalence of hypoglycemia, and cardiovascular risk; newer prolonged-release preparations of sulfonylureas are undoubtedly safer, mainly due to reducing hypoglycemia, and for this reason should be preferred.
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                Author and article information

                Contributors
                kiljanski_jacek@lilly.com
                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
                08 August 2017
                January 2018
                : 20
                : 1 ( doiID: 10.1111/dom.2018.20.issue-1 )
                : 148-156
                Affiliations
                [ 1 ] University of Sheffield Sheffield UK
                [ 2 ] Florida Hospital and Sanford Burnham Prebys Translational Research Institute Orlando Florida
                [ 3 ] Foundation for Diabetes Research in Older People, Diabetes Frail Limited Droitwich UK
                [ 4 ] Eli Lilly and Company Vienna Austria
                [ 5 ] Eli Lilly and Company Warsaw Poland
                [ 6 ] Lilly USA, LLC Indianapolis Indiana
                [ 7 ] Eli Lilly and Company Indianapolis Indiana
                Author notes
                [*] [* ] Correspondence

                Jacek Kiljański, MD, Eli Lilly and Company, Eli Lilly Polska Sp. z o.o. ul. Żwirki i Wigury 18a, 02‐092 Warsaw, Poland. Email: kiljanski_jacek@ 123456lilly.com

                Author information
                http://orcid.org/0000-0002-2425-9565
                Article
                DOM13051
                10.1111/dom.13051
                5724506
                28671753
                3339681a-4074-440e-8cf2-ab6d5bfc3471
                © 2017 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
                : 01 March 2017
                : 21 June 2017
                : 25 June 2017
                Page count
                Figures: 1, Tables: 4, Pages: 1, Words: 6914
                Funding
                Funded by: Eli Lilly and Company
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                dom13051
                January 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.2.8 mode:remove_FC converted:11.12.2017

                Endocrinology & Diabetes
                glp‐1 analogue , glycaemic control , hypoglycaemia , insulin delivery , sulphonylureas

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