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Fetal Alcohol Spectrum Disorder and Iron Homeostasis

Prenatal alcohol exposure results in a spectrum of behavioral, cognitive, and morphological abnormalities collectively referred to as fetal alcohol spectrum disorder (FASD). FASD presents with significant phenotypic variability and may be modified by gestational variables such as maternal nutritiona...

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Autores principales: Bradley, Regan, Lakpa, Koffi L., Burd, Michael, Mehta, Sunil, Katusic, Maja Z., Greenmyer, Jacob R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9607572/
https://www.ncbi.nlm.nih.gov/pubmed/36296909
http://dx.doi.org/10.3390/nu14204223
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author Bradley, Regan
Lakpa, Koffi L.
Burd, Michael
Mehta, Sunil
Katusic, Maja Z.
Greenmyer, Jacob R.
author_facet Bradley, Regan
Lakpa, Koffi L.
Burd, Michael
Mehta, Sunil
Katusic, Maja Z.
Greenmyer, Jacob R.
author_sort Bradley, Regan
collection PubMed
description Prenatal alcohol exposure results in a spectrum of behavioral, cognitive, and morphological abnormalities collectively referred to as fetal alcohol spectrum disorder (FASD). FASD presents with significant phenotypic variability and may be modified by gestational variables such as maternal nutritional status. Iron serves a critical function in the development of and processes within central nervous system (CNS) structures. Gestational iron deficiency alters CNS development and may contribute to neurodevelopmental impairment in FASD. This review explores the relationship between iron deficiency and fetal alcohol spectrum disorder as described in small animal and human studies. Consideration is given to the pathophysiologic mechanisms linking iron homeostasis and prenatal alcohol exposure. Existing data suggest that iron deficiency contributes to the severity of FASD and provide a mechanistic explanation linking these two conditions.
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spelling pubmed-96075722022-10-28 Fetal Alcohol Spectrum Disorder and Iron Homeostasis Bradley, Regan Lakpa, Koffi L. Burd, Michael Mehta, Sunil Katusic, Maja Z. Greenmyer, Jacob R. Nutrients Review Prenatal alcohol exposure results in a spectrum of behavioral, cognitive, and morphological abnormalities collectively referred to as fetal alcohol spectrum disorder (FASD). FASD presents with significant phenotypic variability and may be modified by gestational variables such as maternal nutritional status. Iron serves a critical function in the development of and processes within central nervous system (CNS) structures. Gestational iron deficiency alters CNS development and may contribute to neurodevelopmental impairment in FASD. This review explores the relationship between iron deficiency and fetal alcohol spectrum disorder as described in small animal and human studies. Consideration is given to the pathophysiologic mechanisms linking iron homeostasis and prenatal alcohol exposure. Existing data suggest that iron deficiency contributes to the severity of FASD and provide a mechanistic explanation linking these two conditions. MDPI 2022-10-11 /pmc/articles/PMC9607572/ /pubmed/36296909 http://dx.doi.org/10.3390/nu14204223 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Bradley, Regan
Lakpa, Koffi L.
Burd, Michael
Mehta, Sunil
Katusic, Maja Z.
Greenmyer, Jacob R.
Fetal Alcohol Spectrum Disorder and Iron Homeostasis
title Fetal Alcohol Spectrum Disorder and Iron Homeostasis
title_full Fetal Alcohol Spectrum Disorder and Iron Homeostasis
title_fullStr Fetal Alcohol Spectrum Disorder and Iron Homeostasis
title_full_unstemmed Fetal Alcohol Spectrum Disorder and Iron Homeostasis
title_short Fetal Alcohol Spectrum Disorder and Iron Homeostasis
title_sort fetal alcohol spectrum disorder and iron homeostasis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9607572/
https://www.ncbi.nlm.nih.gov/pubmed/36296909
http://dx.doi.org/10.3390/nu14204223
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