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Analysis of high-resolution computed tomography phenotypes and pulmonary function in chronic obstructive pulmonary disease

OBJECTIVE: To explore the correlation between high-resolution computed tomography (HRCT) phenotype and pulmonary function in patients with chronic obstructive pulmonary disease (COPD). METHODS: Fifty-six patients with COPD were retrospectively evaluated using pulmonary function tests (PFTs) and HRCT...

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Detalles Bibliográficos
Autores principales: He, Shi-Zhen, He, Qian, Su, Yun-Shan, Wang, Peng, Xiang, Shu-Tian, Su, Wei, Mao, Chong-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254595/
https://www.ncbi.nlm.nih.gov/pubmed/31939328
http://dx.doi.org/10.1177/0300060519889459
Descripción
Sumario:OBJECTIVE: To explore the correlation between high-resolution computed tomography (HRCT) phenotype and pulmonary function in patients with chronic obstructive pulmonary disease (COPD). METHODS: Fifty-six patients with COPD were retrospectively evaluated using pulmonary function tests (PFTs) and HRCT, and phenotypic pulmonary function parameters were analyzed. RESULTS: Thirty-one patients were classified as having imaging phenotype A, 11 were phenotype E, and 14 were phenotype M. The total lung capacity (TLC)% of phenotype E was significantly higher than that of phenotypes A and M. The residual volume (RV) to TLC ratio (RV/TLC) in phenotype A was significantly lower than that in phenotypes E and M. The forced expiratory volume in one second percentage (FEV1%) and FEV1/forced vital capacity (FVC) of phenotype A was significantly higher than that of phenotypes E and M. CONCLUSION: FEV1/FVC and FEV1% were higher and RV/TLC was lower, indicating less severe emphysema, in patients with phenotype A compared with patients with phenotypes E and M. TLC% of patients with phenotype E was significantly higher than that of patients with phenotypes A and M. The degree of airflow limitation was most severe in patients with phenotype M.