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Evidence-Based Supplement Research
Evidence-Based Supplement Research

Study Design

Type
Randomized Controlled Trial (RCT)
Sample size
n = 110
Population
110 participants with dyslipidemia
Methods
randomized, double-blind, placebo-controlled trial, participants randomly assigned to intervention or placebo group
Blinding
Double-blind
Duration
12 weeks
Funding
Unclear
  • Large Human Trial
  • Rigorous Journal
Background: Ganoderma lucidum spore oil (GLSO) is widely recognized for its notable medicinal and nutritional properties. This study aimed to systematically evaluate the efficacy and safety of GLSO extract in individuals with dyslipidemia. Methods: In a randomized, double-blind, placebo-controlled trial, 110 participants were enrolled and randomly assigned to either the intervention group or the placebo group. A chi-square test of baseline characteristics confirmed no significant differences in age or sex distribution between the two groups. Results: After 12 weeks of intervention, the intervention group exhibited significantly lower levels of total cholesterol (CHO), triglycerides (TG), and low-density lipoprotein cholesterol (LDL-C), alongside significantly higher levels of high-density lipoprotein cholesterol (HDL-C), compared to the placebo group, with all differences reaching statistical significance. Furthermore, the relative percentage changes in lipid parameters also demonstrated significant intergroup differences. Safety analyses revealed that the intervention had no notable effects on renal function parameters, whereas hepatic function parameters showed statistically significant improvement in the intervention group. Conclusions: This study demonstrated that GLSO extract effectively improved lipid profiles and liver function, with a favorable safety and tolerability profile. These findings strongly support the potential clinical application of GLSO extract in the management of dyslipidemia.

Research Insights

  • Safety analyses revealed that... hepatic function parameters showed statistically significant improvement in the intervention group

    Effect
    Beneficial
    Effect size
    Small
  • Safety analyses revealed that the intervention had no notable effects on renal function parameters

    Effect
    Neutral
    Effect size
    Small
  • After 12 weeks of intervention, the intervention group exhibited... significantly higher levels of high-density lipoprotein cholesterol (HDL-C), compared to the placebo group

    Effect
    Beneficial
    Effect size
    Small
  • After 12 weeks of intervention, the intervention group exhibited significantly lower levels of total cholesterol (CHO)... compared to the placebo group

    Effect
    Beneficial
    Effect size
    Small
  • After 12 weeks of intervention, the intervention group exhibited significantly lower levels of... low-density lipoprotein cholesterol (LDL-C)... compared to the placebo group

    Effect
    Beneficial
    Effect size
    Small
  • After 12 weeks of intervention, the intervention group exhibited significantly lower levels of... triglycerides (TG)... compared to the placebo group

    Effect
    Beneficial
    Effect size
    Small

Adverse Events Reported

  • Reishirenal function parameters

    Safety analyses revealed that the intervention had no notable effects on renal function parameters

    Finding
    No significant difference
    Significant
    No
  • ReishiOverall tolerability

    favorable safety and tolerability profile

    Finding
    Reported
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