4.7 Article

Image Phenotyping of Preterm-Born Children Using Hyperpolarized 129Xe Lung Magnetic Resonance Imaging and Multiple-Breath Washout

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AMER THORACIC SOC
DOI: 10.1164/rccm.202203-0606OC

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hyperpolarized Xe-129 MRI; bronchopulmonary dysplasia; lung microstructure; lung function; prematurityassociated lung disease

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This study aimed to investigate the associations between bronchopulmonary dysplasia (BPD) and lung function phenotypes on lung ventilation and microstructure in preterm-born children. The results showed that preterm-born children with POLD had increased ventilation abnormalities, while those with BPD had abnormal lung microstructure.
Rationale: Preterm birth is associated with low lung function in childhood, but little is known about the lung microstructure in childhood. Objectives: We assessed the differential associations between the historical diagnosis of bronchopulmonary dysplasia (BPD) and current lung function phenotypes on lung ventilation and microstructure in preterm-born children using hyperpolarized 129Xe ventilation and diffusion-weighted magnetic resonance imaging (MRI) and multiple-breath washout (MBW). Methods: Data were available from 63 children (aged 9-13 yr), including 44 born preterm (<= 34 weeks' gestation) and 19 term-born control subjects (>= 37 weeks' gestation). Preterm-born children were classified, using spirometry, as prematurity-associated obstructive lung disease (POLD; FEV1, lower limit of normal [LLN] and FEV1/FVC, LLN), prematurity-associated preserved ratio of impaired spirometry (FEV1, LLN and FEV1/FVC >= LLN), preterm-(FEV1 >= LLN) and term-born control subjects, and those with and without BPD. Ventilation heterogeneity metrics were derived from 129Xe ventilation MRI and SF6 MBW. Alveolar microstructural dimensions were derived from Xe-129 diffusion-weighted MRI. Measurements and Main Results: Xe-129 ventilation defect percentage and ventilation heterogeneity index were significantly increased in preterm-born children with POLD. In contrast, mean Xe-129 apparent diffusion coefficient, Xe-129 apparent diffusion coefficient interquartile range, and Xe-129 mean alveolar dimension interquartile range were significantly increased in preterm-born children with BPD, suggesting changes of alveolar dimensions. MBW metrics were all significantly increased in the POLD group compared with preterm- and term-born control subjects. Linear regression confirmed the differential effects of obstructive disease on ventilation defects and BPD on lung microstructure. Conclusion: We show that ventilation abnormalities are associated with POLD, and BPD in infancy is associated with abnormal lung microstructure.

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