Chronic Obstructive Pulmonary Disease
Conditions
Keywords
casein protein, whey protein, hydrolysates, leucine, protein metabolism, COPD
Brief summary
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.
Detailed description
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.
Interventions
DIETARY_SUPPLEMENTCasein protein hydrolysates
15 g casein protein hydrolysates + 15 g maltodextrin
DIETARY_SUPPLEMENTWhey protein hydrolysates
15 g whey protein isolate + 15 g maltodextrin
DIETARY_SUPPLEMENTCasein protein hydrolysates + LEU
15 g casein protein hydrolysate + 2.1 g LEU (40% of EAA content) + 15 g maltodextrin
DIETARY_SUPPLEMENTWhey protein hydrolysates + LEU
15 g whey protein isolate + 1.5 g LEU (40% of EAA content) + 15 g maltodextrion
Sponsors
Texas A&M University
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
No
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in net whole body protein balance | 6 hours | Net whole body protein synthesis before and after protein feeding |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in whole body protein breakdown rate | 6 hours | Whole body protein breakdown rate before and after protein feeding |
| Change in whole body collagen breakdown | 6 hours | Whole body collagen breakdown before and after protein feeding |
| Change in insulin concentration | 6 hours | Plasma insulin during protein feeding |
| Change in whole body protein synthesis rate | 6 hours | Whole body protein synthesis before and after protein feeding |
| Change in plasma amino acid levels | 6 hours | Plasma amino acid level during protein feeding |
| Change in whole body myofibrillar protein breakdown rate | 6 hours | Whole body myofibrillar protein breakdown before and after protein feeding |
| Change in glucose concentration | 6 hours | Plasma glucose concentration during protein feeding |
Countries
United States
Outcome results
None listed