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Ancestry and genetic associations with bronchopulmonary dysplasia in preterm infants

16 Aug 2018

Abstract excerpt

Bronchopulmonary dysplasia in premature infants is a common and often severe lung disease with long-term sequelae. A genetic component is suspected but not fully defined. We performed an ancestry and genome-wide association study to identify variants, genes, and pathways associated with survival without bronchopulmonary dysplasia in 387 high-risk infants treated with inhaled nitric oxide in the Trial of Late...

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PMID: 30113228
DOI: 10.1152/ajplung.00073.2018

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