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Nitric Oxide Bioavailability in Chronic Obstructive Pulmonary Disease (COPD)

Regulation of Nitric Oxide Bioavailability in Chronic Obstructive Pulmonary Disease: A Mechanistic Approach

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01398943
Enrollment
60
Registered
2011-07-21
Start date
2010-09-30
Completion date
2015-06-30
Last updated
2017-12-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulmonary Disease, Chronic Obstructive

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

DIETARY_SUPPLEMENTAntioxidant Cocktail

1g of vitamin C, 600 IU of vitamin E, and 600 mg of alpha-lipoic acid

Sponsors

American Heart Association
CollaboratorOTHER
Augusta University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

MeasureTime frameDescription
Flow-Mediated Dilation (FMD)Post FMD was taken approximately 110 min after baselineBrachial artery FMD induced by reactive hyperemia will be used to assess vascular endothelial function at baseline and several hours after each experimental intervention.

Secondary

MeasureTime frameDescription
Pulse Wave VelocityPost PWV was taken approximately 90 min after baselineA measure of vascular stiffness at baseline and several hours after each experimental intervention.

Countries

United States

Participant flow

Participants by arm

ArmCount
All COPD Patients
Patients with COPD
30
All Controls
Healthy age- and sex- matched controls
30
Total60

Baseline characteristics

CharacteristicAll COPD PatientsAll ControlsTotal
Age, Customized
Age
66 years
STANDARD_DEVIATION 2
66 years
STANDARD_DEVIATION 2
66 years
STANDARD_DEVIATION 2
Height169 cm
STANDARD_DEVIATION 2
166 cm
STANDARD_DEVIATION 2
168 cm
STANDARD_DEVIATION 2
Sex: Female, Male
Female
15 Participants15 Participants30 Participants
Sex: Female, Male
Male
15 Participants15 Participants30 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 300 / 30
serious
Total, serious adverse events
0 / 300 / 30

Outcome results

Primary

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.

ArmMeasureGroupValue (MEAN)Dispersion
All COPD PatientsFlow-Mediated Dilation (FMD)Placebo3.1 percentage of change in FMDStandard Deviation 0.5
All COPD PatientsFlow-Mediated Dilation (FMD)AOC Treatment4.7 percentage of change in FMDStandard Deviation 0.6
All ControlsFlow-Mediated Dilation (FMD)Placebo6.7 percentage of change in FMDStandard Deviation 0.6
All ControlsFlow-Mediated Dilation (FMD)AOC Treatment6.9 percentage of change in FMDStandard Deviation 0.7
p-value: <0.05ANOVA
p-value: >0.05ANOVA
Secondary

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.

ArmMeasureGroupValue (MEAN)Dispersion
All COPD PatientsPulse Wave VelocityPlacebo14 m/secStandard Deviation 1
All COPD PatientsPulse Wave VelocityAOC Treatment11 m/secStandard Deviation 1
All ControlsPulse Wave VelocityPlacebo11 m/secStandard Deviation 2
All ControlsPulse Wave VelocityAOC Treatment10 m/secStandard Deviation 1
p-value: <0.05ANOVA
p-value: >0.05ANOVA

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026