The study will enroll 68 overweight male and female subjects with a high (\> 2 3dl-can soda/day) consumption of sweetened beverage per day. After a run-in period of 4 weeks, subjects will be randomized to either a 12-week intervention arm in which sweetened beverages will be replaced by artificially sweetened, calorie-free beverages, or to a control arm. The following measurements will be performed at the end of the run-in period and at the end of the intervention period * intrahepatic fat concentration * visceral fat volume * changes in day-long metabolic profile from baseline(plasma glucose, insulin, and triglyceride concentrations) * changes in food intake and daily energy, carbohydrate and sugars intake from baseline
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
29
subjects will be allowed unlimited consumption of calorie-free, artificially-sweetened sodas, water, tea or coffee
Clinical Research Center, CHUV
Lausanne, Canton of Vaud, Switzerland
changes in intrahepatic fat concentration
intrahepatic fat content measured by 1H-MRS
Time frame: at the end of run-in and after 12 weeks intervention/control
changes in visceral fat volume
Visceral fat volume measured by MRI
Time frame: at the end of run-in and after 12 weeks of intervention/control
changes in day-long metabolic profile
Plasma glucose, insulin, non-esterified fatty acids, and triglycerides will be measured at 2-hourly intervals between 7:00 am and 5:00 pm. Participants will be fed standardized meals and either sweetened or artificially-sweetened beverages according to randomization
Time frame: at the end of run-in and after 12 weeks of intervention/control
changes in food intake from baseline
Total energy intake, total carbohydrate intake, and total sugars intake will be evaluated by 3-day food record
Time frame: at the end of the run-in period and after 6, and 12 weeks of intervention/control
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