Metabolic Disturbance Clinical Trial
Official title:
Investigation of Sucrose-induced Metabolic Adaptation and Biomarkers of Chronic Sucrose Intake in Humans Using a Multi-omic Approach
With free sugar intake proving to be of a concern within the general public, discovery and validation of a new biomarker will allow for more consistent measurement of sucrose intake. Furthermore, using a multi-omic approach the investigators will identify metabolic perturbations to the metabolome and proteome.
Excessive free sugar intake is of concern within the general public, as intakes have been
associated with weight gain and cardiovascular disease. Average intakes are over double that
of the 5% of total energy intake that is recommended by the Science Advisory Committee on
Nutrition, but intakes are calculated from observational measures that lack sensitivity and
discovery and validation of a new biomarker from biological fluids may allow for more
specific measurement and a better understanding of intake:disease relationships. Furthermore,
understanding the biochemistry of sucrose intake will allow the identification of damage
occurrence and alternative metabolic pathways, as well as novel protein damage that occur
with chronic sucrose exposure.
This study aims to identify a biomarker of chronic sucrose consumption using metabolite
profiling technology. The study will be composed of a randomised controlled intervention
trial, in which participants will be required to consume an amount of sucrose (0-120g/d)
every day for 7 days and provide biofluid samples (urine and blood) before the initiation,
during and following the intervention; that will undergo metabolic analysis. Furthermore,
participants will have their anthropometrics and dietary intake monitored throughout the
study. The biomarker will also be validated against the dietary information and correlated
with indices of health and sucrose-induced damage. The investigators will also monitor the
feasibility and acceptability of chronic sucrose intake during the intervention.
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