How lung injury and therapeutic oxygen could alter white matter development.
How lung injury and therapeutic oxygen could alter white matter development.
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DOI:
10.1002/jnr.24816
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发表时间:
2022-12
影响因子:
4.2
通讯作者:
Dizon MLV
中科院分区:
文献类型:
--
作者:
Dettman RW;Dizon MLV
Developmental brain injury describes a spectrum of neurological pathologies resulting from either antenatal or perinatal injury. This includes both cognitive and motor defects that affect patients for their entire lives. Developmental brain injury can be caused by a spectrum of conditions including stroke, perinatal hypoxia-ischemia and intracranial haemorrhage. Additional risk factors have been identified including very low birthweight, mechanical ventilation and oxygen (O2) supplementation. In fact, infants with bronchopulmonary dysplasia, an inflammatory disease associated with disrupted lung development, have been shown to have decreased cerebral white matter and decreased intracranial volumes. Thus, there appears to be a developmental link between the lung, O2 and the brain that leads to proper myelination. Here, we will discuss what is currently known about the link between O2 and myelination and how scientists are exploring mechanisms through which supplemental O2 and/or lung injury can affect brain development. Consideration of a link between the diseased lung and developing brain will allow clinicians to fine tune their approaches in managing preterm lung disease in order to optimize brain health. Here we review the literature to shed light on the possibility that high oxygen levels and/or lung injury, such as bronchopulmonary dysplasia, can lead to neurodevelopmental impairment. The literature is especially convincing that these factors affect the neurodevelopment of extremely preterm or very low birthweight infants.
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