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Completed

NCT Number: NCT01154400

Hydrolyzed Casein and Whey Protein Supplementation and the Addition of Leucine to Induce Protein Anabolism in Malnourished COPD Patients

The aim of this study is the first aim of a NIH project that consists of 3 aims. The first aim examines the acute effects of two high-quality milk proteins (casein vs. whey) on whole-body and muscle protein metabolism in COPD patients with severe loss of muscle mass and the effects of adding leucine. The principal endpoints will be the extent of stimulation of net whole body protein synthesis as this is the principal mechanism by which either amino acid or protein intake causes muscle anabolism. After determining the optimal nutritional formulation based on the first aim we will continue to work on the second and third aim where fish oil supplementation will be part of the nutritional intervention as well.

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Key information

Age range

45 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Arkansas for Medical Sciences

Little Rock, Arkansas, 72205, United States

About this study

Cachectic COPD patients are characterized by a decreased muscle protein synthesis and an elevated myofibrillar protein breakdown. A substantial number of these patients, characterized by an enhanced systemic inflammatory response, fails to respond to nutritional therapy, which is of clinical relevance as weight gain to nutritional therapy is a significant, independent predictor of mortality in COPD.

In the present study, the acute protein anabolic effect of two high-quality milk protein supplements in COPD will be examined by comparing a hydrolyzed casein and whey protein meal. We make use of hydrolyzed proteins to correct for absorption differences. Furthermore the effects of these milk proteins with or without enrichment of leucine will be investigated.

Variables of interest are: net whole body protein synthesis; whole body protein synthesis and breakdown rate; whole body myofibrillar protein breakdown rate; whole body collagen breakdown; kinetics of insulin; glucose; amino acid levels.

It is the investigators hypothesis that a nutritional supplement containing casein protein and high levels of leucine will target the metabolic alterations of these cachectic COPD patients and will specifically stimulate protein anabolism. The knowledge gained from this study will benefit our insight in terms of promotion of protein anabolism in COPD patients. The long-term goal is to reformulate nutritional composition in accord with the effects of COPD on protein metabolism in order to ameliorate or even prevent progressive muscle wasting in these subjects, and improve their quality of life and survival rates.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of moderate to severe chronic airflow limitation, defined as measured forced expiratory volume in one second (FEV1) ≤ 70% of reference FEV1
  • Shortness of breath on exertion
  • Age 45 years and older
  • Clinically stable condition and not suffering from respiratory tract infection or exacerbation of their disease (defined as a combination of increased cough, sputum purulence, shortness of breath, systemic symptoms such as fever) at least 4 weeks prior to the study
  • Cachexia based on the criteria: Body mass index ≤ 25 kg/m2 and/or FFM-Index: FFM/height2 ≤ 17 (males), 15 (females) kg/m2 and/or recent involuntary weight loss

Exclusion criteria

  • Established diagnosis of malignancy
  • Presence of fever within the last 3 days
  • Established diagnosis of Diabetes Mellitus
  • Untreated metabolic diseases including hepatic or renal disorder
  • Presence of acute illness or metabolically unstable chronic illness
  • Recent myocardial infarction (less than 1 year)
  • Use of long-term oral corticosteroids or short course of oral corticosteroids in the preceding month before enrollment
  • Allergy to cow's milk protein
  • Any other condition according to the PI or study physicians would interfere with proper conduct of the study / safety of the patient
  • Failure to give informed consent

Treatment and study plan

Casein protein hydrolysates

Dietary Supplement

15 g casein protein hydrolysates + 15 g maltodextrin

Other names: Casein

Whey protein hydrolysates

Dietary Supplement

15 g whey protein isolate + 15 g maltodextrin

Other names: Whey

Casein protein hydrolysates + LEU

Dietary Supplement

15 g casein protein hydrolysate + 2.1 g LEU (40% of EAA content) + 15 g maltodextrin

Other names: Casein + LEU

Whey protein hydrolysates + LEU

Dietary Supplement

15 g whey protein isolate + 1.5 g LEU (40% of EAA content) + 15 g maltodextrion

Other names: Whey + LEU

Primary outcomes

  1. Change in net whole body protein balance

    Time frame: 6 hours

    Net whole body protein synthesis before and after protein feeding

Secondary outcomes

  1. Change in whole body protein synthesis rate

    Time frame: 6 hours

    Whole body protein synthesis before and after protein feeding

  2. Change in whole body protein breakdown rate

    Time frame: 6 hours

    Whole body protein breakdown rate before and after protein feeding

  3. Change in whole body collagen breakdown

    Time frame: 6 hours

    Whole body collagen breakdown before and after protein feeding

  4. Change in insulin concentration

    Time frame: 6 hours

    Plasma insulin during protein feeding

  5. Change in glucose concentration

    Time frame: 6 hours

    Plasma glucose concentration during protein feeding

  6. Change in plasma amino acid levels

    Time frame: 6 hours

    Plasma amino acid level during protein feeding

  7. Change in whole body myofibrillar protein breakdown rate

    Time frame: 6 hours

    Whole body myofibrillar protein breakdown before and after protein feeding

Sponsors and collaborators

Lead sponsor

Texas A&M University

Other

Registry information

Official study title

Grant Title: Eicosapentaenoic Acid and Protein Modulation to Induce Anabolism in COPD

Important dates

Study start
2009
Primary completion
2011
Study completion
2011
First posted
Jun 30, 2010
Registry last updated
Oct 15, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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