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Evidence suggests Creatine mayincreaseEnergy metabolism.

5 studies (6 claims)

Emerging evidence

Study Claims

7 of 7
InterventionDirectionEndpointTypePopulationDosageTitle
creatine kinase inhibitor (CKi)Increases - increase inglutathione metabolism and ferroptosis protection genes
HumanMolecular
Not specifiedA covalent creatine kinase inhibitor ablates glioblastoma migration and sensitizes tumors to oxidative stress.cited 1×
lactoferrin and creatine combinationIncreases - exert a more significant effectenergy metabolism
Animal
C57BL/6 mice with D-galactose-induced sarcopeniaNot specified in the abstract.The Combination of Lactoferrin and Creatine Ameliorates Muscle Decay in a Sarcopenia Murine Model.cited 2×
Creatine supplementationIncreases - improvesbrain energy metabolism
Human
Not specifiedCreatine Supplementation in Depression: A Review of Mechanisms, Efficacy, Clinical Outcomes, and Future Directions.cited 1×
creatine supplementationIncreases - may lead to improvementsmuscle metabolism
Human
children with JDMNot specified in the abstract.The Effect of Creatine Supplementation on Muscle Function in Childhood Myositis: A Randomized, Double-blind, Placebo-controlled Feasibility Study.cited 10×
creatineIncreases - statistically significant adaptationsmuscle metabolism
Human
patients with juvenile dermatomyositis (JDM)Not specified in the abstract.The Effect of Creatine Supplementation on Muscle Function in Childhood Myositis: A Randomized, Double-blind, Placebo-controlled Feasibility Study.cited 10×
creatine transporter mutation (Slc6a8-/y)No effect - demonstrate marked differences inglucose metabolism in the brains
Animal
wild type and Slc6a8-/y miceNot specified[18F]FDG-PET and [18F]MPPF-PET are brain biomarkers for the creatine transporter Slc6a8 loss of function mutation.
new approaches in treating mutations of the creatine transporter SLC6A8Increases - effectiveness in normalizingbrain metabolism
Animal
Not specified[18F]FDG-PET and [18F]MPPF-PET are brain biomarkers for the creatine transporter Slc6a8 loss of function mutation.