The goal of this randomized controlled double-blind parallel-group interventional trial is to evaluate the effects of dietary supplementation with molecular hydrogen and pyrroloquinoline quinone in elderly. The main questions it aims to answer are: (1) whether the supplementation affects biomarkers of mitochondrial function in serum, and (2) whether the supplementation affects cognition and brain metabolism. The participants will be subjected to take the dietary supplement during 6 weeks.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Enrollment
34
Dietary supplement containing molecular hydrogen and pyrroloquinoline quinone
Inert substance
FSPE Applied Bioenergetics Lab
Novi Sad, Vojvodina, Serbia
Fibroblast growth factor 21
Level of fibroblast growth factor 21 in serum
Time frame: Change from baseline serum fibroblast growth factor 21 at 6 weeks
Peroxisome proliferator-activated receptor gamma coactivator 1-alpha
Level of peroxisome proliferator-activated receptor gamma coactivator 1-alpha 21 in serum
Time frame: Change from baseline serum peroxisome proliferator-activated receptor gamma coactivator 1-alpha at 6 weeks
Brain-derived neurotrophic factor
Level of brain-derived neurotrophic factor in serum
Time frame: Change from baseline serum brain-derived neurotrophic factor at 6 weeks
Irisin
Level of irisin in serum
Time frame: Change from baseline serum irisin at 6 weeks
General cognition
Mini-MentalStateExamination (MMSE) score
Time frame: Change from baseline MMSE score at 6 weeks
Brain creatine
MRS spectra for brain creatine
Time frame: Change from baseline brain creatine at 6 weeks
Brain oxygenation
Near-infrared spectroscopy for prefrontal oxygen saturation
Time frame: Change from baseline brain oxygenation at 6 weeks
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