Efficacy of Probiotic Supplements on Brain-Derived Neurotrophic Factor, Inflammatory Biomarkers, Oxidative Stress and Cognitive Function in Patients with Alzheimer's Dementia: A 12-Week Randomized, Double-Blind Active-Controlled Study.
Yu-Chieh HsuYen-Yu HuangShin-Yu TsaiYi-Wei KuoJia-Hung LinHsieh-Hsun HoJui-Fen ChenKo-Chiang HsiaYu SunPublished in: Nutrients (2023)
The role of neurotrophic factors, oxidative stress, and inflammation in the pathogenesis of Alzheimer's disease (AD) has been explored. Animal studies have reported the positive effects of probiotics on these factors. Some clinical studies also support the potential role of probiotics in improving cognitive function via the gut-brain axis in older adults. However, clinical experimental studies evaluating the efficacy of probiotics targeting the neurotrophic factors and inflammatory biomarkers, particularly among AD patients, remain very limited. In this randomized, double-blinded, active-controlled trial, we used multi-strain probiotic supplements, including Bifidobacterium longum subsp. infantis BLI-02, B. breve Bv-889, B. animalis subsp. lactis CP-9, B. bifidum VDD088, and Lactobacillus plantarum PL-02 as the intervention. Participants were divided into an active control group (received probiotic supplements containing 5 × 10 7 colony-forming units per day, CFU/day) and a treatment group (1 × 10 10 CFU/day). Student's t test was applied as the main method of statistical analysis. After 12 weeks of intervention, the treatment group demonstrated a 36% increase in serum brain-derived neurotrophic factor (BDNF) (* p = 0.005), a reduction in IL-1β (* p = 0.041), and an increase in antioxidant superoxide dismutase (SOD) (* p = 0.012). No significant change was found in the active control group. A trend toward less cognitive deterioration was observed, but not statistically significant. In conclusion, this study presents evidence supporting the benefits of multi-strain probiotics in enhancing BDNF, ameliorating inflammation and oxidative stress in AD patients.
Keyphrases
- oxidative stress
- double blind
- placebo controlled
- open label
- newly diagnosed
- randomized controlled trial
- end stage renal disease
- ejection fraction
- dna damage
- diabetic rats
- ischemia reperfusion injury
- clinical trial
- phase ii
- phase iii
- mild cognitive impairment
- stress induced
- risk assessment
- lactic acid
- drug delivery
- anti inflammatory
- climate change
- functional connectivity
- patient reported
- cognitive impairment