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Study of Amino Acid Supplementation for Patients With an Excessive Loss of Muscular Body Mass After Obesity Surgery.

Pilot Study of Branched Amino Acid Supplementation for Patients With an Excessive Loss of Muscular Body Mass After Obesity Surgery.

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02716740
Acronym
MUSCAADE
Enrollment
6
Registered
2016-03-23
Start date
2017-02-08
Completion date
2017-07-13
Last updated
2019-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

Post-obesity surgery, Leucine-enriched amino acid supplementation, Anabolic substance, Physical training, Muscular mass, Loss of weight

Brief summary

Despite the demonstrable health and quality of life benefits, there are unknowns within consequences of obesity surgery. Weight loss composition is poorly understood. The objective is to have a significant loss of body fat and a limited loss of muscular weight. A cohort study in the nutrition unit at Toulouse University Hospital shows that 3 months and 1 year after surgery, there are 2 phenotypes of patients. The first one is called 'little loss' and is defined by a contribution of muscular weight lower than 15% of the total weight loss. The other one is called 'big loss' and is defined by a contribution of muscular weight higher than 15% of the total weight loss. Causes of these different phenotypes are unknown for the moment. Some amino acids have an anabolic potential. Leucine induces a muscular protein synthesis in clinical situations like hepatic cirrhosis, and some populations like new born and older people. Assuming that, a leucine-enriched essential amino acid supplementation will have a benefit effect on the muscular mass. That is testing the influence of the quality of protein consumed, more than the quantity. An anabolic substance (amino acid here) can lead to gain of muscle only if it is associated to regular physical training, all patients will follow a physical training.

Detailed description

An excessive loss of lean mass could have negative metabolic consequences. Indeed, lean mass is an essential determinant of weight loss and of the glycaemia regulation. An important loss of muscular mass could expose the person to a reduction of quality of life (because of fatigue), or even a functional loss. Muscles are important for insulin sensibility and glucose metabolism. Muscles are proteolysis target and proteins will be used as sources of amino acid for other cellular functions. Changes in lean mass have been at the centre of several studies, but changes in muscular mass after bariatric surgery have been report only one time. A cohort study in the nutrition unit at Toulouse University Hospital shows that 3 months and 1 year after surgery, there are 2 phenotypes of patients. The first one is called 'little loss' and is defined by a contribution of muscular weight lower than 15% of the total weight loss. The other one is called 'big loss' and is defined by a contribution of muscular weight higher than 15% of the total weight loss. Causes of these different phenotypes are unknown for the moment. Nothing distinguishes them before the surgery. Type of surgery, gender, protein intake (in grams of proteins intake per day) do not appear to have a determining influence about the intensity of muscle mass loss. The only other study published shows changes in muscular mass about 15% at 6 weeks. Relation between glycaemia changes and muscle mass changes suggests that patients with modest changes in muscular mass are patients who have the best improvement of glycaemia after surgery. It is the reason why, it could be interesting to preserve muscular mass. Nowadays, there is no consensual strategy to compensate this loss of muscle mass. It is important to have in the same time an anabolic stimulus (training, hormone…) and a sufficient energy and protein intake. According to a recent study which compares leucine intake with placebo during weight loss driven by a low-calorie diet associated to a muscle strengthening exercises, patients loss the same weight, but leucin group is gaining lean mass, while placebo group is losing it. Accordingly, twe different doses of amino acid will be tested of those used as diet supplement. This study is testing the influence of the quality of protein consumed, more than the quantity. Patients will take leucine-enriched amino acid supplement and follow physical training. Aromatic amino acid supplementation showed an anabolic effect in older people, undernourished children and undernourished patients with chronic obstructive pulmonary disease. There are no known side effects. This amino acid supplementation has not been evaluated in post-obesity surgery context.

Interventions

DIETARY_SUPPLEMENTLeucine-enriched amino acid supplementation and 30 minutes of physical training 3 times per week

After 3 months of obesity-surgery, if patients lost more than 15% of muscular weight, they will take a leucine-enriched amino acid supplementation during 3 months added with a regular physical training (30 minutes, 3 times/week). Arm A will take 2.46g/day of leucine-enriched amino acid supplementation and arm B 4g/day.

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patient older than 18 years of age and younger than 65 years of age, * Patient received an obesity-surgery (gastric bypass or sleeve gastrectomy) * Contribution of muscular weight higher than 15% of the total weight loss after the third month post-surgery. * Patient that be able to increase their physical activity * Patient that give their informed consent before any procedure for the study * Patient affiliated with a health insurance scheme

Exclusion criteria

* Patients allergic to one of the supplement's compound. * Patients with glucocorticoid therapy * Patients with hyperthyroidism * Patients commencing insulin treatment or growth hormone * Protein powder intake (as nutritional complement or as anabolic substance for muscle building practice) * Oral nutritional supplement intake for malnutrition * Bone fracture since the surgery * Infection can cause hypercatabolism (like microbial outbreak or chronic gastric fistula) * Hospitalization for more than 24 hours since the surgery * Known physical handicap * Inability to increase physical activity during 3 months after beginning of the supplementation * Enteral or parenteral nutrition * Patients over 158 kg (DEXA impossible) * Protected adults (guardianship by court order) * Pregnant woman or breastfeeding.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in appendicular muscular mass at 3 monthsBaseline and 3 monthsAppendicular muscular mass measured by dual-energy X-ray absorptiometry (DEXA). It will be measured before and 3 months after supplementation.

Secondary

MeasureTime frameDescription
Change from baseline in muscular function at 3 monthsBaseline and 3 months400 meters walking speed
Change from baseline in fatigue at 3 monthsBaseline and 3 monthsFatigue will be evaluate by the Pichot scale
Change from baseline in general functional assessment at 3 monthsBaseline and 3 monthsGeneral function will be assessed by the Functional Status Questionnaire test.
Change from baseline in protein daily intake at 3 monthsBaseline and 3 monthsPatient will evaluate his/her protein daily intake (in g/day) by the Protein Intake Monitor with a digital tablet
Change from baseline in limbs muscular force at 3 monthsBaseline and 3 monthsThe lower and higher limbs muscular force will be measured with a strain gauge.
Change from baseline in glucose metabolism at 3 monthsBaseline and 3 monthsOral glucose tolerance test will be performed and glucose concentration will be determined into the blood.
Change from baseline in insulin secretion at 3 monthsBaseline and 3 monthsOral glucose tolerance test will be performed and insulin concentration will be determined into the blood.
Change from baseline in leucine complianceBaseline and 3 monthsLeucine concentration and variation between visit before and after 3 months of supplementation will be measured by chromatography to assess the patient's compliance
Change from baseline in physical training adhesion at 3 monthsBaseline and 3 monthsPatients will have an exercise diary to write their organised physical activity. Physical activity will be converted in a multiple of basal metabolic rate.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026