The Effect of Hydrolyzed Casein on Energy Expenditure and Subjective Appetite (HerKulES)

University of Copenhagen

Status: Completed

Conditions: Increased Energy Expenditure; Increased Satiety

Treatments: Dietary Supplement: Intact whey protein; Dietary Supplement: Hydrolyzed casein; Dietary Supplement: Intact casein

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT01677273

B299

Details and patient eligibility

About

The primary aim is to examine and compare the effects of hydrolyzed casein (HC), intact casein (IC) and intact whey protein (IWP) on diet-induced thermogenesis (DIT). Furthermore, to study the effects on appetite regulation assessed by subjective appetite sensations, ad libitum energy intake and appetite regulating hormones.

Whey and casein differ in absorption and digestion rate, with whey being a fast protein and casein being a slow protein. When casein undergoes hydrolysis the absorption and digestion rates approaches the rates of whey. In the present study the importance of absorption rate and amino acid composition, in regards to energy expenditure and appetite regulation, will be examined. HC and IC have identical amino acid composition, but differ in absorption rate, whereas HC and IWP have similar absorption rates, but differ in amino acid composition. We hypothesize that consumption of HC will increase DIT and fat oxidation to a greater extend that IC. Moreover, that HC and IWP will increase satiety shortly after protein consumption, whereas IC will be more satiating after several hours.

The study is a controlled, randomized, 3-arm crossover study. It consists of three visits in a respiratory chamber separated by at least two weeks. 26 healthy, overweight and obese (BMI 27-35 kg/m2) young men will be enrolled and randomized to the order of the three protein supplements (HC, IC or IWP). At each visit protein supplements (containing either HC, IC or IWP) will be served as breakfast, lunch and dinner. Respiratory measures will be obtained over 24 hours and appetite will be assessed by visual analogue scales and appetite regulating hormones. Furthermore, ad libitum energy intake will be assessed.

Enrollment: 33 patients

Sex: All

Ages: 18 to 40 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Healthy young men and woman
• Overweight and obese (BMI 27-35 kg/m2)
• 18-40 years
• Women must have a regular menstrual cycle

Exclusion criteria

• Allergic to dairy products or other food components
• Vegetarians
• Weight change >3kg within 2 months prior to start of the study
• Use of alcohol >14 drinks/wk
• Drug abuse
• Smoking
• Physically active >10 hrs/wk
• Use of over-the-counter or prescription medication that influences body weight, appetite or metabolism
• Diabetes Mellitus
• Dyslipidemia
• Diseases, which influence metabolism
• Donation of blood 3 months prior to start of the study
• Subjects with a hemoglobin value < 8 mol/L (measured at screening)
• Subjects with a blood glucose level > 6.1 mmol/l (110 mg/dl) (measured at screening)
• Subjects who are unable to give an informed consent.
• Pregnant and lactating women

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Double Blind

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33 participants in 3 patient groups

Hydrolyzed casein

Active Comparator group

Description:

Hydrolyzed casein

Treatment:

Dietary Supplement: Hydrolyzed casein

Intact casein

Active Comparator group

Description:

Intact casein

Treatment:

Dietary Supplement: Intact casein

Intact whey protein

Active Comparator group

Description:

Intact whey protein

Treatment:

Dietary Supplement: Intact whey protein