Journal article
Pulmonary hyperinflation due to gas trapping and pulmonary artery size: The MESA COPD Study
PloS one, Vol.12(5), pp.e0176812-e0176812
2017
DOI: 10.1371/journal.pone.0176812
PMCID: PMC5413010
PMID: 28463971
Abstract
Pulmonary hypertension is associated with increased morbidity and mortality in chronic obstructive pulmonary disease (COPD). Since pulmonary artery (PA) size increases in pulmonary hypertension, we measured PA cross-sectional area using magnetic resonance imaging (MRI) to test the hypothesis that pulmonary hyperinflation due to gas trapping is associated with PA cross-sectional area in COPD.
The MESA COPD Study recruited participants with COPD and controls from two population-based cohort studies ages 50-79 years with 10 or more pack-years and free of clinical cardiovascular disease. Body plethysmography was performed according to standard criteria. Cardiac MRI was performed at functional residual capacity to measure the cross-sectional area of the main PA. Percent emphysema was defined as the percentage of lung voxels less than -950 Hounsfield units as assessed via x-ray computed tomography. Analyses were adjusted for age, gender, height, weight, race-ethnicity, the forced expiratory volume in one second, smoking status, pack-years, lung function, oxygen saturation, blood pressure, left ventricular ejection fraction and percent emphysema.
Among 106 participants, mean residual volume was 1.98±0.71 L and the mean PA cross-sectional area was 7.23±1.72 cm2. A one standard deviation increase in residual volume was independently associated with an increase in main PA cross-sectional area of 0.55 cm2 (95% CI 0.18 to 0.92; p = 0.003). In contrast, there was no evidence for an association with percent emphysema or total lung capacity.
Increased residual volume was associated with a larger PA in COPD, suggesting that gas trapping may contribute to pulmonary hypertension in COPD.
Details
- Title: Subtitle
- Pulmonary hyperinflation due to gas trapping and pulmonary artery size: The MESA COPD Study
- Creators
- Hooman D Poor - Department of Medicine, Columbia University Medical Center, New York, New York, United States of AmericaSteven M Kawut - University of PennsylvaniaChia-Ying Liu - Johns Hopkins UniversityBenjamin M Smith - McGill UniversityEric A Hoffman - University of Iowa, RadiologyJoão A Lima - Johns Hopkins MedicineBharath Ambale-Venkatesh - Johns Hopkins MedicineErin D Michos - Johns Hopkins UniversityMartin R Prince - Columbia UniversityR Graham Barr - Columbia University Irving Medical Center
- Resource Type
- Journal article
- Publication Details
- PloS one, Vol.12(5), pp.e0176812-e0176812
- DOI
- 10.1371/journal.pone.0176812
- PMID
- 28463971
- PMCID
- PMC5413010
- NLM abbreviation
- PLoS One
- ISSN
- 1932-6203
- eISSN
- 1932-6203
- Grant note
- P30 ES005605 / NIEHS NIH HHS R01 HL093081 / NHLBI NIH HHS K24 HL103844 / NHLBI NIH HHS R01 HL112986 / NHLBI NIH HHS P30 DK054759 / NIDDK NIH HHS R01 HL077612 / NHLBI NIH HHS
- Language
- English
- Date published
- 2017
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Radiology; Internal Medicine
- Record Identifier
- 9984240438602771
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