Pulmonary Disease, Chronic Obstructive
Conditions
Keywords
flow-mediated dilation, arterial stiffness, intima-media thickness, pulse wave velocity, dual energy x-ray absorptiometry, inflammatory markers, blood lipids, tetrahydrobiopterin, body mass index, hemoglobin A1c, complete blood count, oxidative stress biomarkers, pulmonary function test, lung, COPD
Brief summary
More patients with chronic obstructive pulmonary disease (COPD) die from cardiovascular disease than direct pulmonary complications. Inflammation and oxidative stress, characteristic in COPD, are likely contributors to the reduction in nitric oxide (NO) bioavailability and vascular endothelial dysfunction in COPD patients; however, this has yet to be determined. Thus, the overall objective of this proposal is to identify the role of NO bioavailability in contributing to vascular endothelial dysfunction in patients with COPD and to provide insight into the molecular mechanisms involved. Our central hypothesis is that inflammation and oxidative stress, both independently, contribute to the reduction in NO bioavailability and vascular endothelial dysfunction in patients with COPD.
Detailed description
Flow-Mediated Dilation (FMD) - Subjects will lie in the supine position for 20 minutes to obtain hemodynamic steady state. A blood pressure cuff (Hokanson) will be placed around the forearm (distal to the Doppler transducer) and rapidly inflated to 250 mmHg for 5 minutes (circulatory arrest). Simultaneous ultrasound images of the vessel (B-mode) and Doppler waveforms will be collected 10 seconds prior to and for 2 minutes following deflation of the cuff. All B-mode images will be analyzed using automated edge detection software (Medical Imaging Applications), while intensity weighted velocity spectra segments will be saved to the GE Logiq 7 hard drive for off-line blood velocity waveform analysis. P.I. has utilized the traditional method of brachial artery flow-mediated dilation (FMD) induced by reactive hyperemia to assess vascular endothelial function in populations ranging from young healthy adults to older adults with pathological conditions. Spygmocor - Pulse Wave Velocity (PWV) - A Spygmocor® device will be used at baseline and following each protocol to assess PWV. PWV analysis provides a non-invasive assessment of arterial stiffness. Increased arterial stiffness is known to be associated with cardiovascular disease. The participant is required to lie in a resting position for approximately 30-45 minutes. The research assistant will place ECG electrode sensors at the carotid, femoral, radial and distal artery locations. A highly sensitive pen-like device, called a tonometer, is then gently applied to record the velocity of the blood flow between each of the points.
Interventions
single dose = 5 mg/kg
1g of vitamin C, 600 IU of vitamin E, and 600 mg of alpha-lipoic acid
Sponsors
Study design
Eligibility
Inclusion criteria
* Patients with COPD (GOLD stages II-IV) and matched healthy controls * Caucasian or African American * Both men and women * Current and former smokers
Exclusion criteria
* GOLD Stage I * Clinical diagnosis of heart disease, hypertension, or metabolic disease * Vasoactive medications (i.e. nitrates, beta-blockers, ACE inhibitors, Viagra, etc.) * Pulmonary hypertension * Hypothyroidism * Hyper-homocysteinemia * Interstitial lung disease * Phenylketonuria * Pregnancy * Sleep apnea * Anemia * Raynod's phenomenon * Gangrene of the digits * History of low platelets or coagulopathies * Aspirin sensitivity or allergy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Flow-Mediated Dilation (FMD) | Post FMD was taken approximately 110 min after baseline | Brachial artery FMD induced by reactive hyperemia will be used to assess vascular endothelial function at baseline and several hours after each experimental intervention. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pulse Wave Velocity | Post PWV was taken approximately 90 min after baseline | A measure of vascular stiffness at baseline and several hours after each experimental intervention. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| All COPD Patients Patients with COPD | 30 |
| All Controls Healthy age- and sex- matched controls | 30 |
| Total | 60 |
Baseline characteristics
| Characteristic | All COPD Patients | All Controls | Total |
|---|---|---|---|
| Age, Customized Age | 66 years STANDARD_DEVIATION 2 | 66 years STANDARD_DEVIATION 2 | 66 years STANDARD_DEVIATION 2 |
| Height | 169 cm STANDARD_DEVIATION 2 | 166 cm STANDARD_DEVIATION 2 | 168 cm STANDARD_DEVIATION 2 |
| Sex: Female, Male Female | 15 Participants | 15 Participants | 30 Participants |
| Sex: Female, Male Male | 15 Participants | 15 Participants | 30 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — |
| other Total, other adverse events | 0 / 30 | 0 / 30 |
| serious Total, serious adverse events | 0 / 30 | 0 / 30 |
Outcome results
Flow-Mediated Dilation (FMD)
Brachial artery FMD induced by reactive hyperemia will be used to assess vascular endothelial function at baseline and several hours after each experimental intervention.
Time frame: Post FMD was taken approximately 110 min after baseline
Population: Participants included patients diagnosed with COPD and healthy age-matched controls.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| All COPD Patients | Flow-Mediated Dilation (FMD) | Placebo | 3.1 percentage of change in FMD | Standard Deviation 0.5 |
| All COPD Patients | Flow-Mediated Dilation (FMD) | AOC Treatment | 4.7 percentage of change in FMD | Standard Deviation 0.6 |
| All Controls | Flow-Mediated Dilation (FMD) | Placebo | 6.7 percentage of change in FMD | Standard Deviation 0.6 |
| All Controls | Flow-Mediated Dilation (FMD) | AOC Treatment | 6.9 percentage of change in FMD | Standard Deviation 0.7 |
Pulse Wave Velocity
A measure of vascular stiffness at baseline and several hours after each experimental intervention.
Time frame: Post PWV was taken approximately 90 min after baseline
Population: Patients diagnosed with COPD compared to healthy age-matched controls.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| All COPD Patients | Pulse Wave Velocity | Placebo | 14 m/sec | Standard Deviation 1 |
| All COPD Patients | Pulse Wave Velocity | AOC Treatment | 11 m/sec | Standard Deviation 1 |
| All Controls | Pulse Wave Velocity | Placebo | 11 m/sec | Standard Deviation 2 |
| All Controls | Pulse Wave Velocity | AOC Treatment | 10 m/sec | Standard Deviation 1 |