Acute interleukin-1β antagonism decreases systemic inflammation, increases GLP-1 release, and modulates insulin secretion in individuals with prediabetes

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Authors: Justus Fischer, Matthias Hepprich, Marco Cattaneo, Lucia Seeger, Stefanie Dobler, Marc Y. Donath
Cited by: 2
References: 54

Abstract

Acute IL-1 blockade with anakinra markedly reduced CRP and leukocyte counts within 12 h, demonstrating rapid anti-inflammatory efficacy. Anakinra induced a trend toward earlier insulin secretion and significantly increased postprandial IL-6 and GLP-1 levels. The study demonstrates that even short-term IL-1 blockade can modulate both immune and incretin responses in prediabetes. Early IL-1β antagonism may represent a preventive, anti-inflammatory approach to preserve GLP-1 secretion and β-cell function in individuals with prediabetes.

Fields of Study & Subjects

Adipokines Inflammation and Metabolic Diseases Sodium Intake and Health Regulation of Appetite and Obesity

Publication details

Journal / source
American Journal of Physiology-Endocrinology and Metabolism
Publisher
American Physiological Society
Volume
330
Issue
4
Pages
E500–E509
Publication date
4 March 2026
Language
EN