| Literature DB >> 26471062 |
Vineet Bhandari1, Jeffrey R Gruen2.
Abstract
Gene-environment interactions likely account for some degree of the variance in response rates that are clinically observed with antenatal corticosteroids, breast milk prophylaxis, surfactant administration, early recognition and treatment of sepsis, utility of non-invasive ventilation, and judicious exposure to supplemental oxygen. While these therapies and practice guidelines have significantly decreased overall neonatal mortality in the NICU, they have not made a marked impact on the frequency and severity of conditions such as bronchopulmonary dysplasia (BPD), necrotizing enterocolitis, and periventricular leukomalacia. One possible explanation is that genetic factors in the neonate modulate response to external intervention or preventative agents, culminating in variable levels of injury and different degrees of resolution and repair. Gene-environment explanations are supported by the observed heritability of BPD in twin studies, but they do not differentiate the interactions between neonate and offending toxin or pathogen, from interactions between neonate and intervention or therapeutic agent. Likely, both kinds of interactions are important in determining outcome.Entities:
Keywords: BPD; IVH; NEC; PDA; RDS; ROP; Twin studies; apnea of prematurity; neonatal sepsis; premature newborn
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Year: 2015 PMID: 26471062 DOI: 10.1053/j.semperi.2015.09.003
Source DB: PubMed Journal: Semin Perinatol ISSN: 0146-0005 Impact factor: 3.300