Insulin resistance:Impact on therapeutic developments in diabetes

Abstract

Insulin resistance has a broad pathogenic impact affecting metabolic, cardio-renal and other disease areas. Extensive studies to dissect the mechanisms of insulin resistance have provided valuable insights to shape current clinical awareness and advance therapeutic practice. However, the development of direct interventions against insulin resistance has been hindered by its complex and highly variable presentations, especially in type 2 diabetes. Among glucose-lowering agents, metformin and thiazolidinediones provide cellular actions that counter some effects of insulin resistance: reduced glucotoxicity and weight-lowering with antidiabetic therapies also improve insulin action, except that endogenously- or exogenously-created hyperinsulinaemia may partially compromise these benefits. Increasing awareness of the pervasiveness and damaging ramifications of insulin resistance heightens the need for more specifically targeted and more effective therapies.

Publication DOI: https://doi.org/10.1177/1479164119827570
Divisions: College of Health & Life Sciences > School of Biosciences
College of Health & Life Sciences > School of Biosciences > Cell & Tissue Biomedical Research
College of Health & Life Sciences
College of Health & Life Sciences > Chronic and Communicable Conditions
Additional Information: © Sage 2019. The final publication is available via Sage at http://dx.doi.org/10.1177/1479164119827570
Uncontrolled Keywords: diabetes therapies,dipeptidyl peptidase-4 inhibitors,glucagon-like peptide-1 receptor agonists,insulin,Insulin resistance,metformin,sulfonylureas,thiazolidinediones,Internal Medicine,Endocrinology, Diabetes and Metabolism,Cardiology and Cardiovascular Medicine
Publication ISSN: 1752-8984
Last Modified: 31 Oct 2024 08:24
Date Deposited: 13 May 2019 11:20
Full Text Link:
Related URLs: http://www.scop ... tnerID=8YFLogxK (Scopus URL)
https://journal ... 479164119827570 (Publisher URL)
PURE Output Type: Review article
Published Date: 2019-04-23
Accepted Date: 2019-03-01
Authors: Bailey, Clifford J. (ORCID Profile 0000-0002-6998-6811)

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