4.4 Article

Nutraceutical Eriocitrin (Eriomin) Reduces Hyperglycemia by Increasing Glucagon-Like Peptide 1 and Downregulates Systemic Inflammation: A Crossover-Randomized Clinical Trial

Journal

JOURNAL OF MEDICINAL FOOD
Volume 25, Issue 11, Pages 1050-1058

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/jmf.2021.0181

Keywords

citrus flavonoids; eriocitrin; GLP-1; hyperglycemia; nutraceutical; systemic inflammation

Funding

  1. Ingredients by Nature (Montclair, CA, USA) [5045]

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This study found that Eriomin can effectively reduce hyperglycemia and improve diabetes-related biomarkers. Intervention with Eriomin increases GLP-1 levels and decreases systemic inflammation, benefiting individuals with poor blood glucose control in prediabetic and diabetic conditions.
This double-blind, randomized, placebo/controlled, crossover study evaluated the efficacy of Eriomin (R) in reducing hyperglycemia and improving diabetes-related biomarkers in individuals with hyperglycemia above 110 mg/dL (mean 123 +/- 18 mg/dL). Subjects (n = 30), divided into two groups (Eriomin or Placebo), who received a dose of 200 mg/d of the designated supplement for 12 weeks and, after a washout period of 2 weeks, switched to the other supplement in the following 12 weeks. Assessments of biochemical, metabolic, inflammatory, blood pressure, anthropometry, and dietary parameters were performed at the beginning and end of each intervention. Treatment with 200 mg/d of Eriomin significantly decreased blood glucose (-5%), homeostasis model assessment of insulin resistance (-11%), glucagon (-13%), interleukin-6 (-14%), tumor necrosis factor alpha (-20%), and alkaline phosphatase (-13%); but increased glucagon-like peptide 1 (GLP-1) by (17%) (P <= .05). At the end of the placebo period, there was a 13% increase in triglycerides (P <= .05). Other parameters evaluated did not change with Eriomin or placebo. In conclusion, intervention with Eriomin benefited the glycemic control of prediabetic and diabetic patients, with higher blood glucose levels, by increasing GLP-1 and decreasing systemic inflammation.

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