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Targeting inflammation in the treatment of type 2 diabetes: time to start
Targeting inflammation in the treatment of type 2 diabetes: time to start
Journal Article

Targeting inflammation in the treatment of type 2 diabetes: time to start

2014
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Overview
Key Points Inflammation has an important role in the pathogenesis of type 2 diabetes and associated complications. Clinical studies have demonstrated that interleukin-1 (IL-1) antagonists, salsalate and tumour necrosis factor (TNF) antagonists improve glucose metabolism. Anti-inflammatory drugs may have disease-modifying and long-lasting effects. Future genetic and biomarker studies may profile responders to a specific anti-inflammatory treatment. Combining or sequentially using multiple anti-inflammatory drugs may provide a tailored solution for treating patients with type 2 diabetes. Inflammation is now appreciated to have an important role in the pathogenesis of type 2 diabetes and associated complications. Donath describes the underlying mechanisms and discusses the rationale for the use of anti-inflammatory agents — such as those that have been developed for rheumatoid arthritis and other diseases driven by inflammatory processes — in patients with diabetes. The role of inflammation in the pathogenesis of type 2 diabetes and associated complications is now well established. Several conditions that are driven by inflammatory processes are also associated with diabetes, including rheumatoid arthritis, gout, psoriasis and Crohn's disease, and various anti-inflammatory drugs have been approved or are in late stages of development for the treatment of these conditions. This Review discusses the rationale for the use of some of these anti-inflammatory treatments in patients with diabetes and what we could expect from their use. Future immunomodulatory treatments may not target a specific disease, but could instead act on a dysfunctional pathway that causes several conditions associated with the metabolic syndrome.

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