Effects of Ganoderma lucidum Polysaccharide Peptide on Inflammatory and Metabolic Biomarkers in Obese Patients with

Nuril Farid Abshori1, Syanindita Wardhani1, Fatahillah Fatoni1

  • 1Medical Doctor Program, Faculty of Medicine and Health Sciences, Maulana Malik Ibrahim Islamic State University, Malang, Indonesia.

Abstract

Insights

Ganoderma lucidum polysaccharide peptide (GLPP) did not significantly impact inflammatory markers or lipid profiles in obese patients with cardiometabolic syndrome over an 8-week trial. Further research is needed to explore GLPP

Area of Science:

  • Integrative Medicine and Nutritional Science
  • Cardiovascular Disease Research
  • Metabolic Health and Inflammation

Background:

  • Cardiometabolic syndrome (CMS) drives atherosclerosis via chronic inflammation, with residual inflammatory risk often inadequately managed by conventional therapies.
  • Ganoderma lucidum polysaccharide peptide (GLPP) exhibits preclinical anti-inflammatory and antioxidant effects, but clinical data in CMS patients is limited.
  • Obesity exacerbates CMS, increasing cardiovascular event risk and inflammatory burden.

Purpose of the Study:

  • To investigate the anti-inflammatory effects of GLPP supplementation in obese patients diagnosed with cardiometabolic syndrome.
  • To evaluate the impact of GLPP on key metabolic parameters, including lipid profiles and body mass index (BMI), in the target population.
  • To assess changes in specific inflammatory biomarkers (TNF-α, IL-6, hsCRP) and nitric oxide (NO) levels following GLPP intervention.

Main Methods:

  • A randomized, double-blind, placebo-controlled trial involving 60 obese patients with CMS.
  • Participants received either 250 mg of GLPP three times daily or a placebo for 8 weeks.
  • Primary outcomes included changes in inflammatory biomarkers (TNF-α, IL-6, hsCRP); secondary outcomes included nitric oxide, lipid profiles, and BMI, assessed via ELISA and automated analyzers.

Main Results:

  • No statistically significant differences were observed between the GLPP and placebo groups in primary inflammatory markers (IL-6, TNF-α, hsCRP) or nitric oxide levels.
  • Lipid profiles (total cholesterol, triglycerides, HDL, LDL) and BMI showed no significant improvements in the GLPP group compared to placebo.
  • All 60 randomized patients completed the 8-week intervention, with no significant baseline differences between groups.

Conclusions:

  • Eight weeks of GLPP supplementation did not yield significant improvements in inflammatory markers or metabolic parameters in obese patients with CMS.
  • Potential factors influencing these null findings include concomitant medications, unassessed lifestyle factors, short intervention duration, and limited sample size.
  • Future research should explore optimized GLPP formulations (e.g., nanoparticles), longer study durations, larger cohorts, and strategies to enhance bioavailability and gut absorption.

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