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Clinical Trials/NCT04026607
NCT04026607
Completed
Not Applicable

Efficacy of Higher Versus Lower Quality Protein Supplementation to Support Increased Muscle Protein Synthesis in Older Men

McMaster University1 site in 1 country45 target enrollmentDecember 1, 2019
ConditionsSarcopenia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sarcopenia
Sponsor
McMaster University
Enrollment
45
Locations
1
Primary Endpoint
Integrated Muscle Protein Synthesis
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The age-related decline in muscle mass and strength is collectively referred to as sarcopenia. Canadian recommended daily allowance (RDA) for protein intake (0.8 g/kg/d), however, many expert groups have advocated that older persons should increase their daily intake to ~1.2 g/kg/d to support the preservation of muscle mass. The use of plant-based proteins in food formulation has recently become of interest. This study will examine the impact of consuming higher- versus lower-quality protein supplements on muscle protein synthesis in healthy older men.

Detailed Description

This study will examine the impact of consuming higher- versus lower-quality protein supplements on the integrated rates of muscle protein synthesis in healthy older men. Briefly, participants will consume dietary protein at the RDA for the entire duration of the protocol (2 weeks). Participants will be randomized to consuming collagen (control - CON), whey (WHEY), or pea (PEA) protein supplements twice daily for one week. We will examine the ability of different qualities of protein supplements to stimulate integrated rates of muscle protein synthesis.

Registry
clinicaltrials.gov
Start Date
December 1, 2019
End Date
January 31, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Stuart Phillips

Professor

McMaster University

Eligibility Criteria

Inclusion Criteria

  • Men, between the ages of 65 - 80 years (inclusive)
  • Willing and able to provide informed consent
  • Be in general good health, non-smoking
  • Have a body mass index (BMI) between 20-38 kg/m2 (inclusive)

Exclusion Criteria

  • Use of tobacco or related products.
  • Veganism or vegetarianism
  • Any concurrent medical, orthopedic, or psychiatric condition that, in the opinion of the Investigator, would compromise his/her ability to comply with the study requirements.
  • Use assistive walking devices (e.g., cane or walker)
  • History of cancer within the last 5 years, except basal cell carcinoma, non-squamous skin carcinoma, prostate cancer or carcinoma in situ with no significant progression over the past 2 years.
  • Significant orthopedic, cardiovascular, pulmonary, renal, liver, infectious disease, immune disorder, or metabolic/endocrine disorders or other disease that would preclude oral protein supplement ingestion and/or assessment of safety and study objectives.
  • Any cachexia-related condition (e.g., relating to cancer, tuberculosis or human immunodeficiency virus infection and acquired immune deficiency syndrome) or any genetic muscle diseases or disorders
  • Current illnesses which could interfere with the study (e.g. prolonged severe diarrhea, regurgitation, difficulty swallowing)
  • Hypersensitivity or known allergy to any of the components in the test formulations.
  • Excessive alcohol consumption (\>21 units/week)

Outcomes

Primary Outcomes

Integrated Muscle Protein Synthesis

Time Frame: 7 days x 2

Integrated protein synthesis will be determined during 7 days of consuming the RDA of protein (control phase), and during 7 days of supplementation with a randomised protein supplement (Supplement phase). Integrated rates of muscle protein synthesis (MPS) will be determined using the D2O method. Briefly, 2H enrichment of saliva (precursor) and muscle (product) pools (relative to 1H) will be determined using isotope ratio mass spectrometry and 'myofibrillar fractional synthetic rate' (%/day) determined.

Secondary Outcomes

  • Anabolic Signalling Proteins(1 hour)

Study Sites (1)

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