MedPath

Fat Metabolism in OSA and COPD

Completed
Conditions
Obstructive Sleep Apnea
Chronic Obstructive Pulmonary Disease
Obesity
Registration Number
NCT02157844
Lead Sponsor
Texas A&M University
Brief Summary

Obstructive sleep apnea (OSA) is the most common type of sleep apnea and is caused by an obstruction of the upper airways. The obstruction results in periods of intermittent hypoxia and re-oxygenation, which lead to increased oxidative stress, increased inflammation, endothelial dysfunction, and insulin resistance. Chronic obstructive pulmonary disease (COPD) is a lung disease that leads to poor airflow. This disease leads to systemic hypoxia, reduced oxidative capacity, and increased inflammation. The direct cause of OSA and COPD is unclear, but OSA and COPD may be linked to other comorbid conditions such as obesity and type II diabetes. Upon onset of OSA and COPD, metabolic disturbances associated with obesity and type II diabetes can be exacerbated.

Obesity is a condition characterized by an increase in visceral fat, elevated plasma levels of free fatty acids, inflammation, and insulin resistance. Although the effects of body fat distribution have not been studied in these patients, an increase in both subcutaneous and abdominal fat mass in non-OSA older women was shown to increase morbidity and mortality. Fat/adipose tissue is an active tissue capable of secreting proinflammatory cytokines such as tumor necrosis factor (TNF)-alpha and interleukin (IL)-6, reactive oxygen species and adipokines. Particularly, abdominal fat is a prominent source of pro-inflammatory cytokines, which contributes to a low grade, chronic inflammatory state in these patients. Additionally, an increased inflammatory state is associated with reduced lean body mass, and together with elevated circulating free fatty acids may increase the occurrence of lipotoxicity and insulin resistance. Thus, increased fat deposition is associated with a poor prognosis in OSA and COPD patients and therefore it is of clinical and scientific importance to understand the changes in fat metabolism and digestion as a result of OSA and COPD.

It is therefore our hypothesis that fat synthesis and insulin resistance is increased and whole body protein synthesis is decreased in OSA and COPD patients, leading to a poor prognosis.

Detailed Description

This research study involves 3 visits for subjects and healthy controls. The first visit is the screening visit and includes review of the informed consent and a DXA scan and the second and third visit for the study days. For the first test day, 3 hours of the subjects time will be for urine and blood sample collection, and to stable isotope administration (deuterated water, isotopically labeled amino acids). Subjects are allowed to go home after and eat normally. On the second study day, subjects will arrive early that morning. For the duration of the study, subjects have to lie in the bed (except for bathroom privileges). They can watch tv or bring and use a book/tablet. The research nurse or study staff will be present in the human subject area to assist the subject if necessary. Subjects are not allowed to eat or drink during the second test day, except for the test drink (meal) and water. One IV catheter will be placed in a vein of the arm/hand for blood draws. The hand will be placed in a hot box during blood collection. Another IV catheter will be placed in the contra-lateral forearm for a primed and continuous infusion of isotopes (isotopically labeled amino acids and glycerol). Each day, a total of 80-100 ml of blood will be obtained. Stable isotopes will be ingested and infused on the first test day and added to the test drinks and infused on the second day. On the second test day, subjects will fill out questionnaires. After completion of the study, we will provide the subject with a meal.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
62
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Adipose tissue triglyceride synthesispre and 4 hours post meal

changes in adipose tissue triglyceride synthesis before and after a meal

Adipose tissue lipolysis - glycerol rate of appearancePre meal ingestion and 15, 30, 45, 60, 75, 90, 105, 120, 150, 180, 210, 240, 270, and 300 min post meal ingestion

changes in adipose tissue lipolysis before and after a meal. plasma enrichment of glycerol.

Rate of appearance of ingested glucosePre meal ingestion and 15, 30, 45, 60, 75, 90, 105, 120, 150, 180, 210, 240, 270, and 300 min post meal ingestion

determine changes in appearance of glucose rate in subjects

Glycine rate of appearancePostabsorptive state during 3 hours

glycine enrichment in plasma

Taurine turnover ratepostabsorptive state during 3 hours

enrichment of taurine in

Endogenous Glucose ProductionPre meal ingestion and 15, 30, 45, 60, 75, 90, 105, 120, 150, 180, 210, 240, 270, and 300 min post meal ingestion

Determine whole body glucose production in subjects

Citrulline Rate of appearancePostabsorptive state during 2 hours

plasma enrichment of citrulline

Adipose tissue de novo lipogenesispre and 4 hours post meal

changes in adipose tissue de novo lipogenesis before and after a meal

Net whole-body protein synthesis0, 15, 30, 45, 60, 75, 90, 105, 120, 150, 180, 210 min post-meal

change in whole-body protein synthesis rate after intake of meal

Hepatic triglyceride synthesisPre meal ingestion and 15, 30, 45, 60, 75, 90, 105, 120, 150, 180, 210, 240, 270, and 300 min post meal ingestion

changes in hepatic triglyceride synthesis before and after a meal

Glucose disposalPre meal ingestion and 15, 30, 45, 60, 75, 90, 105, 120, 150, 180, 210, 240, 270, and 300 min post meal ingestion

Determine whole body glucose uptake in subjects

Hepatic de novo lipogenesisPre meal ingestion and 15, 30, 45, 60, 75, 90, 105, 120, 150, 180, 210, 240, 270, and 300 min post meal ingestion

changes in hepatic de novo lipogenesis before and after a meal

Arginine turnover ratepostabsorptive state during 3 hours

Arginine enrichment in plasma

Tryptophan turnover ratePostabsorptive state during 3 hours

Tryptophan enrichment in plasma

Whole body collagen breakdown ratePostabsorptive state during 3 hours

Hydroxyproline enrichment in plasma

Myofibrillar protein breakdown rate0,15,30,45,60,75,90,105,120,150,180,210 min post-meal

3methylhistidine enrichment in plasma

Secondary Outcome Measures
NameTimeMethod
Insulin response to feedingpre and up to 5 hours post meal

acute changes from postabsorptive state to postprandial state

Fat digestion and absorptionPre meal ingestion and 15, 30, 45, 60, 75, 90, 105, 120, 150, 180, 210, 240, 270, and 300 min post meal ingestion

defining fat digestion and absorption after a meal. Enrichment in palmitic acid and tripalmitin fatty acids in plasma

Protein digestion after feeding0,15,30,45,60,75,90,105,120,150,180,210, min post-meal

Ratio enrichment free phenylalanine vs phenylalanine from protein spirulina

Body composition1 day

body composition will be determined by dual-energy X-ray absorptiometry and by deuterated water dilution technique. Plasma deuterium enrichments will be determined.

Physical activity questionnaire1 day

Outcome of physical activity assessment in breast cancer patients and healthy controls in relation to the fat metabolism

Trial Locations

Locations (1)

Texas A&M University

🇺🇸

College Station, Texas, United States

© Copyright 2025. All Rights Reserved by MedPath