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Association of circulating adhesion molecules with lung function. The CARDIA study.
Bharat Thyagarajan1, Lewis J Smith2, R Graham Barr3
1Department of Laboratory Medicine and Pathology, Medical School, Minneapolis, MN.
Systemic inflammation markers, like intercellular adhesion molecule-1 (ICAM-1), are linked to lung function decline. Higher ICAM-1 levels correlate with reduced forced vital capacity (FVC) and forced expiratory volume in one second (FEV1).
Area of Science:
- Pulmonary Medicine
- Immunology
- Cardiovascular Risk Research
Background:
- Systemic inflammation is linked to diminished lung function.
- Adhesion molecules, including intercellular adhesion molecule-1 (ICAM-1) and P-selectin, play a key role in initiating inflammatory responses.
- The Coronary Artery Risk Development in Young Adults (CARDIA) study investigated these associations.
Purpose of the Study:
- To examine the relationship between intercellular adhesion molecule-1 (ICAM-1) and P-selectin concentrations and lung function.
- To determine if adhesion molecule levels predict future lung function.
- To assess if baseline lung function predicts future adhesion molecule levels.
Main Methods:
- Spirometry was performed at study years 5, 10, and 20.
- Intercellular adhesion molecule-1 (ICAM-1) and P-selectin levels were measured at year 15.
- Statistical analyses controlled for multiple covariates including demographics, lifestyle factors, and asthma status.
Main Results:
- Higher baseline intercellular adhesion molecule-1 (ICAM-1) concentrations predicted lower forced vital capacity (FVC) and forced expiratory volume in one second (FEV1) at year 20.
- Lower baseline FVC and FEV1 were associated with higher year-15 ICAM-1 concentrations.
- Increased loss of FVC and FEV1 between years 5 and 10 correlated with higher year-15 ICAM-1 levels.
- P-selectin showed similar, though weaker, associations with lung function.
Conclusions:
- Circulating adhesion molecules like ICAM-1 and P-selectin exhibit a bidirectional relationship with lung function.
- These findings suggest a dynamic interplay between inflammation and lung health over time.
- Adhesion molecules may serve as potential biomarkers for lung function decline.
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