Efficacy and Safety of Tremella fuciformis in Individuals with Subjective Cognitive Impairment: A Randomized Controlled Trial
Authors:
Soonhyun Ban, Suji L. Lee, Hyeonseok S. Jeong, Soo Mee Lim, Shinwon Park, Young Sun Hong, Jieun E. Kim
Journal:
Journal of Medicinal Food
Study Design:
Randomized, double-blind, placebo-controlled clinical trial
Participants:
75 community-dwelling individuals aged 40 to 65 years with subjective cognitive impairment (SCI). Participants were divided into three groups: high-dose Tremella fuciformis (1200 mg/day, n = 30), low-dose Tremella fuciformis (600 mg/day, n = 30), and placebo (n = 15).
Intervention:
- High-dose group: 1200 mg/day of Tremella fuciformis, administered in 6 capsules daily for 8 weeks.
- Low-dose group: 600 mg/day of Tremella fuciformis, administered in 6 capsules daily for 8 weeks.
- Placebo group: 6 placebo capsules daily for 8 weeks.
Outcome Measures:
- Primary Outcome Measure:
- Changes in Subjective Memory Complaints Questionnaire (SMCQ) scores.
- Secondary Outcome Measures:
- Cognitive performance, measured through standardized short-term memory and executive function tests.
- Structural brain changes, assessed via voxel-based morphometry.
- Safety Measures:
- Adverse event frequency, physical exams, and laboratory tests.
Summary:
This clinical trial evaluated the efficacy and safety of Tremella fuciformis supplementation in individuals with SCI. The study found significant improvements in memory complaints (SMCQ scores) in both high-dose (P = .002) and low-dose (P = .007) groups compared to the placebo. High-dose supplementation significantly enhanced executive function (P = .02), while both doses improved short-term memory (P = .001). Imaging results revealed increased gray matter volumes in brain regions, including the dorsolateral prefrontal cortex, which correlated with executive function improvements (P = .02).
No serious adverse events were reported, and the supplementation was well tolerated. This study suggests that Tremella fuciformis is a safe and promising option for improving memory complaints and cognitive performance in middle-aged adults with SCI. Further studies are recommended to optimize dosing and explore broader cognitive benefits
No responses yet