Chronic Obstructive Pulmonary Disease Clinical Trial
Official title:
Essential Amino Acid Intake to Optimize Protein Anabolism in Elderly COPD Patients
Verified date | September 2017 |
Source | Texas A&M University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Weight loss commonly occurs in patients with chronic obstructive pulmonary disease (COPD),
negatively influencing their quality of life, treatment response and survival. Loss of muscle
protein is generally a central component of weight loss in COPD patients. Attempts to reverse
muscle loss in COPD by supplying large amounts of protein or calories to these patients have
been unsuccessful. Gains in muscle mass are difficult to achieve in COPD unless specific
metabolic abnormalities are targeted. The investigators recently observed that alterations in
protein metabolism are present in normal weight COPD patients. Elevated levels of protein
synthesis and breakdown rates were found in this COPD group indicating that alterations are
already present before muscle wasting occurs. Furthermore, reduced plasma essential amino
acid (EAA) levels were observed in COPD patients. These reduced EAA plasma levels were
significantly related with the presence of muscle wasting in COPD. Until now, limited
research has been done examining protein metabolism and the response to feeding in patients
with COPD. Previous studies support the concept of essential amino acids (EAA) as an anabolic
stimulus in the young and elderly and in insulin resistant states. Until yet no information
is present on the anabolic effects of EAA in elderly COPD patients.
It is therefore our hypothesis that a high-leucine essential amino acids mixture specifically
designed to stimulate protein anabolism will target the metabolic alterations of COPD
patients. In the present study, the acute effects of an EAA nutritional supplement on whole
body, muscle and liver protein metabolism will be examined in COPD patients and compared to a
supplement consisting of a balanced mixture of total amino acids. The principal endpoints
will be the extent of stimulation of whole body protein synthesis as this is the principal
mechanism by which either amino acid or protein intake causes muscle anabolism, and the
reduction in endogenous protein breakdown. Both endpoints will be assessed by isotope
methodology which is thought to be the reference method.
Status | Active, not recruiting |
Enrollment | 34 |
Est. completion date | June 2018 |
Est. primary completion date | June 2014 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 45 Years and older |
Eligibility |
Inclusion Criteria: - Diagnosis of chronic airflow limitation, defined as measured forced expiratory volume in one second (FEV1) less than 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, and a decrease in FEV1 > 10% compared with values when clinically stable in the preceding year) at least 4 weeks prior to the study - Ability to lie in supine position for 6 hours 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 - 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 |
Country | Name | City | State |
---|---|---|---|
United States | University of Arkansas for Medical Sciences | Little Rock | Arkansas |
Lead Sponsor | Collaborator |
---|---|
Texas A&M University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Net whole body protein synthesis rate | Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement | Up to 2 years | |
Secondary | Whole body collagen breakdown rate | Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement | Up to 3 years | |
Secondary | Urea turnover rate | Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement | Up to 3 years | |
Secondary | Arginine turnover rate | Measured in postabsorptive state | Up to 3 years | |
Secondary | Muscle protein breakdown | Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement | Up to 3 years | |
Secondary | Amino acid kinetics | Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement | Up to 3 years | |
Secondary | Liver protein synthesis rate | Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement | Up to 3 years | |
Secondary | Resting Energy expenditure | Measured in postabsorptive state | Up to 3 years | |
Secondary | Insulin kinetics | Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement | Up to 3 years | |
Secondary | Glucose kinetics | Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement | Up to 3 years | |
Secondary | Fat-free mass | Characterization of subjects | Up to 3 years |
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