The Effects of Early-Life Iron Deficiency on Brain Energy Metabolism.
Thomas W BastianRaghavendra RaoPhu V TranMichael K GeorgieffPublished in: Neuroscience insights (2020)
Iron deficiency (ID) is one of the most prevalent nutritional deficiencies in the world. Iron deficiency in the late fetal and newborn period causes abnormal cognitive performance and emotional regulation, which can persist into adulthood despite iron repletion. Potential mechanisms contributing to these impairments include deficits in brain energy metabolism, neurotransmission, and myelination. Here, we comprehensively review the existing data that demonstrate diminished brain energetic capacity as a mechanistic driver of impaired neurobehavioral development due to early-life (fetal-neonatal) ID. We further discuss a novel hypothesis that permanent metabolic reprogramming, which occurs during the period of ID, leads to chronically impaired neuronal energetics and mitochondrial capacity in adulthood, thus limiting adult neuroplasticity and neurobehavioral function. We conclude that early-life ID impairs energy metabolism in a brain region- and age-dependent manner, with particularly strong evidence for hippocampal neurons. Additional studies, focusing on other brain regions and cell types, are needed.
Keyphrases
- early life
- iron deficiency
- resting state
- white matter
- cerebral ischemia
- functional connectivity
- traumatic brain injury
- stem cells
- oxidative stress
- brain injury
- multiple sclerosis
- cell therapy
- machine learning
- spinal cord
- blood brain barrier
- subarachnoid hemorrhage
- mesenchymal stem cells
- big data
- electronic health record
- risk assessment
- artificial intelligence
- case control