Effects of Ketones on Muscle Wasting During Caloric Restriction in Lean Females
Primary Purpose
Muscle Wasting, Protein Intake, Ketosis
Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Ketone supplementation
Increased protein intake
Sponsored by
About this trial
This is an interventional treatment trial for Muscle Wasting focused on measuring resting metabolic rate, β-hydroxybutyrate, caloric restriction, muscle mass, ketone ester
Eligibility Criteria
Inclusion Criteria:
- Females between 18 and 40 years old
- Fat percentage between 16 and 25%
- Regularly involved in physical activity ( > 6 h/week)
- Use of hormonal contraceptives
- Good health status confirmed by a medical screening
- Stable body weight during the last 3 months prior to the study, i.e. no changes > 2 kg
Exclusion Criteria:
- Smoking
- Obsessive pursuit for thinness, evaluated by the Eating Disorder Inventory 3 (EDI-3) 'Pursuit of leanness' (i.e a score higher than 26/32) (see Appendix 5)
- Intake of any medication or nutritional supplement that is proven to affect exercise performance, except oral contraceptives
- Blood donation during the study
- Current participation in another research trial
- Any other argument to believe that the subject is unlikely to successfully complete the full study protocol
Sites / Locations
- KU Leuven
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
No Intervention
Experimental
Experimental
Experimental
Arm Label
Placebo
Ketone
High protein
High protein + ketone
Arm Description
Received 10% protein in nutrition + placebo supplement
Received 10% protein in nutrition + 3x20g B-hydroxybutyrate per day
Received 30% protein in nutrition + placebo supplement
Received 30% protein in nutrition + 3x20g B-hydroxybutyrate per day
Outcomes
Primary Outcome Measures
Muscle mass
The amount of muscle mass loss
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04744142
Brief Title
Effects of Ketones on Muscle Wasting During Caloric Restriction in Lean Females
Official Title
Effects of Ketones on Muscle Wasting During Caloric Restriction in Lean Females
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
December 20, 2018 (Actual)
Study Completion Date
June 1, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
KU Leuven
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Because of these anabolic properties of ketone bodies and the fact that ketone bodies prevent muscle protein breakdown for gluconeogenesis during energetic stress, ketone bodies can be a promising strategy to prevent or treat skeletal muscle wasting. Therefore, our aim is to investigate the effect of 3HHB intake on muscle wasting and its adverse consequences during a period of caloric restriction in lean females. In addition, we compare the effects of 3HHB intake with a high protein diet, which is currently considered as the best strategy to minimize lean loss during hypo-energetic periods. To end, we aim to investigate the synergistic effects of the intake of 3HHB in combination with a high protein diet.
Detailed Description
Thermodynamics state that body mass declines during periods in which energy expenditure exceeds energy intake. This negative energy balance can be obtained either by reducing energy intake, called caloric restriction, by increasing energy expenditure, i.e higher level of physical activity, or the combination of both. The sustained energy deficit results in a net loss of body weight due to losses of both fat and skeletal muscle mass in a ratio of approximately 3:11, depending on the severity of caloric restriction, diet composition and initial body fat percentage. Decreases in muscle mass are due to a combination of downregulated muscle protein synthesis in conjunction with an increased ubiquitin-proteasome-mediated muscle proteolysis, resulting in a negative net protein turnover.
In the context of sports, many athletes try to lose body weight to achieve different goals, such as improving performance by optimizing power-to-weight ratio, competing in a certain body weight category or for aesthetic reasons. However, the loss of body weight is often accompanied by detrimental loss of skeletal muscle mass, which is associated with a myriad of negative consequences including impaired physical performance and increased susceptibility to injury. Hence, athletes undergoing periods of caloric restriction strive for body weight loss via fat loss, while minimizing loss of lean mass. Recent studies have demonstrated that an increased protein intake, higher than the recommended dietary allowance (0.8g/kg/day), attenuates the loss of muscle mass during caloric restriction. Research has shown that the high protein diet has minor effects on muscle proteolysis compared to normal dietary protein but restores muscle protein synthesis, which is probably the primary mechanism by which lean mass is preserved. Specifically, in young healthy athletes, it is shown that a higher protein intake of 1.6-2.4 g per kg body weight per day reduces the loss of muscle mass during short-term caloric restriction periods.
In female athletes, longer periods of low energy availability (with or without an eating disorder) are often interrelated with menstrual dysfunctions and decreased bone mineral density, a syndrome called the 'female athlete triad'. The triad is particularly common in sports that emphasize aesthetics or leanness and can impose lifelong health consequences. However, interventions that minimize loss of lean mass and prevent hormonal and bone metabolism dysregulations in females during periods of caloric restriction, are still missing.
Ketone bodies, i.e. D-β-hydroxybutyrate (βHB), acetoacetate (AcAc) and acetone are naturally occurring chemical compounds synthesized in the liver from circulating fatty acids under conditions of low blood glucose and insulin levels. In normal physiological conditions, the concentration of serum ketone levels remains low (< 0.1 mM). However, during starvation or applying a ketogenic diet, i.e low carbohydrate content, serum concentrations of βHB and AcAc can increase up to 5-8 mM and 1-2 mM, respectively. In these conditions, ketone bodies serve as an alternative and more efficient energy source for various tissues, including the brain, heart and skeletal muscle, thereby 'sparing' the glucose storages. In normal conditions, the brain can only use glucose as an energy fuel to maintain central nervous system functions. Therefore, sparing glucose storages during periods of energetic stress is extremely important for survival. Besides, this sparing of glucose storages prevents the breakdown of muscle proteins which can be used as precursors for gluconeogenesis, providing glucose for the brain and other tissues. Hence, the availability of ketone bodies reduces the breakdown of muscle proteins for gluconeogenesis and, thus, preserves skeletal muscle mass even when energy availability is limited. Therefore, elevating ketone body levels may be an important strategy to prevent skeletal muscle wasting during periods of energetic stress.
Since recently, serum levels of ketone bodies can be increased by the intake of the ketone body ester (R)-3-hydroxybutyl (R)-3-hydroxybutyrate (3HHB). This orally absorbable ketone body ester is proven safe and well-tolerated in both animals and humans and can elevate ketone body levels within 30 min to 5-6 mM, similar to levels after approximately one week of fasting. The availability of this ketone body ester allows for controlled studies on the effect of ketone bodies on muscle homeostasis without the negative side-effects of starvation and a ketogenic diet, i.e high serum triglyceride and cholesterol levels. The effects of 3HHB on endurance performance is still debated. However, a recent study from our lab showed that post-exercise ingestion of 3HHB increases markers of protein synthesis, which was further confirmed by in vitro experiments. C2C12 myoblasts showed increased leucine-mediated muscle protein synthesis by incubation of physiological concentrations of ketone bodies. Most recently, we found that dietary supplementation with 3HHB substantially improved survival and maintenance of functional capacity and muscular integrity in a mouse model of cancer cachexia.
Because of these anabolic properties of ketone bodies and the fact that ketone bodies prevent muscle protein breakdown for gluconeogenesis during energetic stress, ketone bodies can be a promising strategy to prevent or treat skeletal muscle wasting. Therefore, our aim is to investigate the effect of 3HHB intake on muscle wasting and its adverse consequences during a period of caloric restriction in lean females. In addition, we compare the effects of 3HHB intake with a high protein diet, which is currently considered as the best strategy to minimize lean loss during hypo-energetic periods. To end, we aim to investigate the synergistic effects of the intake of 3HHB in combination with a high protein diet.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Muscle Wasting, Protein Intake, Ketosis, Caloric Restriction
Keywords
resting metabolic rate, β-hydroxybutyrate, caloric restriction, muscle mass, ketone ester
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Subjects were pair-matched for body weight, % body fat and energy intake, where after they were randomly allocated to an experimental group
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Subjects were randomized by an external, independent researcher. Supplements were color and taste matched.
Allocation
Randomized
Enrollment
44 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
No Intervention
Arm Description
Received 10% protein in nutrition + placebo supplement
Arm Title
Ketone
Arm Type
Experimental
Arm Description
Received 10% protein in nutrition + 3x20g B-hydroxybutyrate per day
Arm Title
High protein
Arm Type
Experimental
Arm Description
Received 30% protein in nutrition + placebo supplement
Arm Title
High protein + ketone
Arm Type
Experimental
Arm Description
Received 30% protein in nutrition + 3x20g B-hydroxybutyrate per day
Intervention Type
Drug
Intervention Name(s)
Ketone supplementation
Other Intervention Name(s)
Placebo vs ketone supplementation
Intervention Description
Subjects receive either placebo or ketone ester supplementation
Intervention Type
Dietary Supplement
Intervention Name(s)
Increased protein intake
Other Intervention Name(s)
Normal vs increased protein intake
Intervention Description
Subjects receive either normal or increased protein intake
Primary Outcome Measure Information:
Title
Muscle mass
Description
The amount of muscle mass loss
Time Frame
Muscle mass is measured before and after 4 weeks of caloric restriction
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Females
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Females between 18 and 40 years old
Fat percentage between 16 and 25%
Regularly involved in physical activity ( > 6 h/week)
Use of hormonal contraceptives
Good health status confirmed by a medical screening
Stable body weight during the last 3 months prior to the study, i.e. no changes > 2 kg
Exclusion Criteria:
Smoking
Obsessive pursuit for thinness, evaluated by the Eating Disorder Inventory 3 (EDI-3) 'Pursuit of leanness' (i.e a score higher than 26/32) (see Appendix 5)
Intake of any medication or nutritional supplement that is proven to affect exercise performance, except oral contraceptives
Blood donation during the study
Current participation in another research trial
Any other argument to believe that the subject is unlikely to successfully complete the full study protocol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Katrien Koppo, PhD
Organizational Affiliation
KU Leuven
Official's Role
Study Director
Facility Information:
Facility Name
KU Leuven
City
Leuven
State/Province
Vlaams-brabant
ZIP/Postal Code
3000
Country
Belgium
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Results will be published in internationally peer-reviewed journals
Learn more about this trial
Effects of Ketones on Muscle Wasting During Caloric Restriction in Lean Females
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