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AV study.

Postprandial muscle perfusion and protein metabolism in healthy young and elderly men.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON22412
Enrollment
48
Registered
2012-09-24
Start date
2011-09-29
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Loss of muscle mass in healthy aging (sarcopenia)

Interventions

The intervention consist of a single test day during which the subjects will receive a drink containing 20 gram intrinsically labeled casein followed by local administration of insulin (0.3 mU/min/100

Sponsors

Maastricht University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy untrained men; 2. Age 70-85 years or age 18-30 years; 3. BMI < 30 kg&#8729;m2, with a stable body weight over the last 3 months.

Exclusion criteria

Exclusion criteria: 1. Cardiac abnormalities; 2. Coagulation disorders; 3. Vascular diseases; 4. Obesity (BMI > 30 kg&#8729;m2); 5. Diabetes mellitus type 1 and type 2; 6. Glucose intolerance; 7. HbA1c > 7.0%; 8. Diagnosed impaired renal or liver function; 9. Smoking; 10. All co-morbidities interacting with mobility and muscle metabolism of the lower limbs (e.g. arthrosis, arthritis, spasticity/rigidity, all neurological disorders and paralysis); 11. Cancer; 12. Hypertension (according to WHO criteria); 13. Acute or chronic pulmonary diseases; 14. Allergy for lidocain or iodine; 15. Use of NSAIDs and acetylsalicylic acid; 16. Patients suffering from PKU (Phenylketonuria); 17. Infectious disease; 18. Participation in any regular exercise program; 19. Unstable body weight over the last 3 months.

Design outcomes

Primary

MeasureTime frame
The main study endpoint is the muscle protein synthesis rate, expressed as fractional synthetic rate (FSR). In order to determine the FSR, the following parameters will be measured in blood and muscle tissue: 1. Plasma and muscle free phenylalanine concentration (expressed as &#956;mol/L); 2. Plasma enrichment of L-[ ring-2H5]phenylalanine (expressed as mole percent excess (MPE)); 3. Muscle protein bound enrichment of L-[ ring-2H5]phenylalanine (expressed as MPE); 4. L-[ ring-2H5]phenylalanine enrichment of the muscle free amino acid pool (expressed as MPE).

Secondary

MeasureTime frame
Secondary endpoints include whole body protein turnover, protein digestion and absorption kinetics and microvascular perfusion. The following parameters will be calculated: 1. Exogenous phenylalanine rate of appearance and plasma availability of phenylalanine; 2. Total rate of phenylalanine appearance and disappearance (= protein turnover); 3. Endogenous phenylalanine rate of appearance (=protein breakdown); 4. Femoral blood flow using Doppler ultrasound expressed as L/min; 5. Leg blood flow using ICG dye dilution expressed as mL/min/100mL leg; 6. Sublingual microvascular perfusion measured using the SDF camera expressed as: Proportion of perfused vessels (PPV; %), perfused vessel density (PVD; n/mm) and Microcirculatory flow index (MFI).

Contacts

Public ContactB. Groen
b.groen@int.umcg.nl+31 (0)6 10475964

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)