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Review
. 2020 Aug;22(8):1231-1242.
doi: 10.1111/dom.14013. Epub 2020 Mar 11.

Evaluating glucose-lowering treatment in older people with diabetes: Lessons from the IMPERIUM trial

Affiliations
Review

Evaluating glucose-lowering treatment in older people with diabetes: Lessons from the IMPERIUM trial

Alan J Sinclair et al. Diabetes Obes Metab. 2020 Aug.

Abstract

Understanding the benefits and risks of treatments to be used by older individuals (≥65 years old) is critical for informed therapeutic decisions. Glucose-lowering therapy for older patients with diabetes should be tailored to suit their clinical condition, comorbidities and impaired functional status, including varying degrees of frailty. However, despite the rapidly growing population of older adults with diabetes, there are few dedicated clinical trials evaluating glucose-lowering treatment in older people. Conducting clinical trials in the older population poses multiple significant challenges. Despite the general agreement that individualizing treatment goals and avoiding hypoglycaemia is paramount for the therapy of older people with diabetes, there are conflicting perspectives on specific glycaemic targets that should be adopted and on use of specific drugs and treatment strategies. Assessment of functional status, frailty and comorbidities is not routinely performed in diabetes trials, contributing to insufficient characterization of older study participants. Moreover, significant operational barriers and problems make successful enrolment and completion of such studies difficult. In this review paper, we summarize the current guidelines and literature on conducting such trials, as well as the learnings from our own clinical trial (IMPERIUM) that assessed different glucose-lowering strategies in older people with type 2 diabetes. We discuss the importance of strategies to improve study design, enrolment and attrition. Apart from summarizing some practical advice to facilitate the successful conduct of studies, we highlight key gaps and needs that warrant further research.

Keywords: antidiabetic drug; clinical trial; diabetes complications; glycaemic control; hypoglycaemia.

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Conflict of interest statement

S.A.J. has received personal fees from Eli Lilly and Merck. H.S.R. has received fees from Novo Nordisk, Sanofi Aventis, Zealand Pharma, and Eli Lilly for advisory board meetings and consultancy; and personal and speaker fees from Novo Nordisk. R.E.P. reports consulting fees from Boehringer‐Ingelheim, Eisai, Inc., GlaxoSmithKline, Glytec, LLC, Pfizer, Janssen and Mundipharma; grants from Lexicon Pharmaceuticals; speaker and consulting fees from AstraZeneca; grants and consulting fees from Ligand Pharmaceuticals, Inc., Eli Lilly, Sanofi and Merck; grants, speaker fees and consulting fees from Novo Nordisk and Takeda; personal consulting fees from Sanofi US Services, Inc., outside the submitted work. Except for consulting fees in February 2018 and June 2018 from Sanofi US Services, Inc., services by R.E.P. were paid for directly to AdventHealth, a nonprofit organization. A.F. has served on advisory boards for Boehringer Ingelheim, Eli Lilly, Astra Zeneca; as a consultant for Eli Lilly, Sanofi, Boehringer‐Ingelheim, MSD, and on speaker bureaus for Astra Zeneca, Boehringer Ingelheim, Eli Lilly, and Sanofi. R.J.H. and J.K. are employees and stockholders of Eli Lilly and Company, USA, while R.D. is a former employee of Eli Lilly and Company, USA.

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