AI Article Synopsis

  • Diacerein may improve glycaemic control in type 2 diabetes patients by reducing inflammation and enhancing insulin sensitivity, as demonstrated in a study involving 25 participants.
  • After 12 weeks, the diacerein group showed a significant decrease in HbA1c levels compared to the placebo group, although fasting plasma glucose levels did not show a significant change.
  • Metabolic profiling indicated a link between threo-isocitric acid levels and HbA1c response, suggesting potential metabolic factors influencing the effectiveness of diacerein in improving glycaemic control.

Article Abstract

Objective: Diacerein inhibits the synthesis and activity of pro-inflammatory cytokines, decreases macrophage infiltration in adipose tissue and thus increases insulin sensitivity and signalling. We conducted this study to determine the efficacy of low-dose diacerein in improving glycaemic control in type 2 diabetes mellitus (T2DM) patients with inadequate glycaemic control and to identify the metabolic determinants for such improvement. We randomised 25 T2DM patients with poor glycaemic control, despite being treated with at least three glucose-lowering agents, to receive diacerein 50 mg once-daily (n = 18) or placebo (n = 17) for 12 weeks. Changes in glycated haemoglobin (HbA1c) were evaluated at the 4th and 12th weeks. Metabolic profiling was performed using liquid chromatography electrospray ionisation quadrupole time-of-flight mass spectrometry.

Results: HbA1c levels were significantly reduced from baseline in the diacerein group at 12 weeks (- 0.6%, p < 0.05), whereas fasting plasma glucose (FPG) levels were not significantly decreased (- 18.9 mg/dl, p = 0.06). Partial least squares-discriminant analysis demonstrated an association between the serum abundance of threo-isocitric acid (ICA) and HbA1c response in the diacerein group. After adjusting for serum high-sensitivity C-reactive protein, ICA was still significantly related to the change in HbA1c. Retrospective trial registration Current Controlled Trials TCTR20200820004, 20 August 2020.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896078PMC
http://dx.doi.org/10.1186/s13104-022-05974-9DOI Listing

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