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ABSTRACT: Rationale
Bronchopulmonary dysplasia (BPD) is a major complication of premature birth. Risk factors for BPD are complex and include prenatal infection and O(2) toxicity. BPD pathology is equally complex and characterized by inflammation and dysmorphic airspaces and vasculature. Due to the limited availability of clinical samples, an understanding of the molecular pathogenesis of this disease and its causal mechanisms and associated biomarkers is limited.Objectives
Apply genome-wide expression profiling to define pathways affected in BPD lungs.Methods
Lung tissue was obtained at autopsy from 11 BPD cases and 17 age-matched control subjects without BPD. RNA isolated from these tissue samples was interrogated using microarrays. Standard gene selection and pathway analy
SUBMITTER: Bhattacharya S
PROVIDER: S-EPMC3443810 | biostudies-literature | 2012 Aug
REPOSITORIES: biostudies-literature