Adiposity influences airway wall thickness and the asthma phenotype of HIV-associated obstructive lung disease: A cross-sectional study

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Abstract

Background: Airflow obstruction, which encompasses several phenotypes, is common among HIV-infected individuals. Obesity and adipose-related inflammation are associated with both COPD (fixed airflow obstruction) and asthma (reversible airflow obstruction) in HIV-uninfected persons, but the relationship to airway inflammation and airflow obstruction in HIV-infected persons is unknown. The objective of this study was to determine if adiposity and adipose-associated inflammation are associated with airway obstruction phenotypes in HIV-infected persons. Methods: We performed a cross-sectional analysis of 121 HIV-infected individuals assessed with pulmonary function testing, chest CT scans for measures of airway wall thickness (wall area percent [WA%]) and adipose tissue volumes (mediastinal and subcutaneous), as well as HIV- and adipose-related inflammatory markers. Participants were defined as COPD phenotype (post-bronchodilator FEV1/FVC <0.001) and volume of adipose tissue (subcutaneous, r=0.40; p<0.001; mediastinal, r=0.25; p=0.005). Multivariable regression found the COPD phenotype associated with greater age and pack-years smoking; the asthma phenotype with younger age, female gender, smoking history, and lower adiponectin levels; and greater WA% with greater BMI, younger age, higher soluble CD163, and higher CD4 counts. Conclusions: Adiposity and adipose-related inflammation are associated with an asthma phenotype, but not a COPD phenotype, of obstructive lung disease in HIV-infected persons. Airway wall thickness is associated with adiposity and inflammation. Adipose-related inflammation may play a role in HIV-associated asthma.

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Barton, J. H., Ireland, A., Fitzpatrick, M., Kessinger, C., Camp, D., Weinman, R., … Gingo, M. R. (2016). Adiposity influences airway wall thickness and the asthma phenotype of HIV-associated obstructive lung disease: A cross-sectional study. BMC Pulmonary Medicine, 16(1). https://doi.org/10.1186/s12890-016-0274-5

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