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Endothelial Dysfunction, Biomarkers, and Lung Function -Ancillary to MESA

Endothelial Dysfunction, Biomarkers, and Lung Function (MESA LUNG) (MESA Lung ClinCoordCtr IRB)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00843271
Acronym
MESA-LUNG
Enrollment
4359
Registered
2009-02-13
Start date
2004-10-01
Completion date
2027-01-01
Last updated
2026-04-23

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

Conditions

Chronic Obstructive Pulmonary Disease (COPD), Emphysema, Endothelial Dysfunction

Keywords

COPD MESA LUNG BIOMARKERS

Brief summary

The purpose of the MESA Lung Study is to assess the role of endothelial dysfunction and genetic susceptibility to subclinical COPD and emphysema.

Detailed description

Chronic obstructive pulmonary disease (COPD) is currently the third leading cause of death in the United States, and morbidity and mortality from COPD continue to rise. Despite the magnitude of the problem, therapeutic options are limited - particularly in comparison to cardiovascular disease. Smoking cessation is essential to the treatment and prevention of COPD. However, although smoking is the principal cause of COPD, only a minority of smokers develops symptomatic COPD and many former smokers develop COPD years to decades after they have stopped smoking. The only other medical intervention proven to reduce mortality from COPD is supplemental oxygen therapy. There is therefore an urgent need for newer understandings of the pathophysiology of COPD and emphysema that might lead to the development of better therapies for COPD. MESA-Lung is ancillary of the ongoing Multi-Ethnic Study of Atherosclerosis (MESA). MESA-lung will utilize the various existing measures of endothelial function that have been already been collected in MESA (flow-mediated dilatation \[FMD\] and related biomarkers and gene polymorphisms) to test the hypotheses that the endothelial dysfunction occurs in the clinical COPD.

Interventions

None listed

Sponsors

Columbia University
Lead SponsorOTHER
National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
45 Years to 84 Years
Healthy volunteers
No

Inclusion criteria

* A random sample of MESA participants active at Exam 3 and/or 4.

Exclusion criteria

* MESA participants without MESA Exam 3 or 4 measurements. * MESA participants without FMD measurements in Exam 1. * MESA participants who have not consented to genetic testing.

Design outcomes

Primary

MeasureTime frame
Lung Function (FEV1 (L), FEV1/FVC (%))Up to 13 years

Secondary

MeasureTime frame
Lung Density/Percent emphysema on CT (%)Up to 13 years

Contacts

PRINCIPAL_INVESTIGATORR. Graham Barr, M.D., Dr.PH.

Columbia University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 24, 2026