Elderly Clinical Trial
Official title:
Effect of Protein High in Leucine on Muscle Protein Balance in Elderly Patients: Acute Study With Protein-tracer-techniques
The aim of this study is to investigate potential protein synthesis effects of whey protein high in leucine compared to whey protein with normal leucin content in elderly patients in a acute crossover setting. We will use the method of a 2 X 3 h tracer infusing protocol with 15Nphenylalanine along with blood samples and muscle biopsies.
Background: Improved muscle function/strength will enhance the quality of life of the more
frail elderly population. Dietary proteins and amino acids act as anabolic substrates in
muscles in elderly people. In particular the amino acid leucine is suggested to have an
impact on muscle protein synthesis. In collaboration with the Danish dairy company Arla
Foods we will use their conventional Whey protein and leucine enriched Whey protein in an
acute study on elderly patients.
Our aim is to examine the acute effects of supplementation with whey protein high in leucine
compared to whey protein with normal leucine content on muscle protein synthesis and protein
balance in elderly patients.
Methods: We include 10 elderly patients, age 60-85 years in a randomized crossover study.
The subjects will be recruited from the Osteoporosis Section at the Department of
Endocrinology at Aarhus University Hospital. The subjects are their own controls in 2 x 1
day interventions A: whey protein high in leucine and B: whey protein with normal leucine
content. Interventions are conducted with a 4 week washout period between them. On the
intervention day postprandial protein synthesis rate will be measured over 2 X 3h using a
tracer infusing protocol with 15Nphenylalanine along with blood samples and muscle biopsies.
For analyzing steps of signaling in muscle protein synthesis initiated by leucine mammalian
target of rapamycin (mTor) and sites downstream from mTor is quantified using western
blotting. Whole body protein kinetics are calculated using the formula Q=i*Ei/Ep-i
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
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