The Effects of Maternal Iron Deficiency and Iron Deficiency Anemia on the Developing Fetal and Neonatal Brain

IF 2.3 Q2 OBSTETRICS & GYNECOLOGY
Michael K. Georgieff MD
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Abstract

Iron is an essential micronutrient for fetal and postnatal neurodevelopment because of its role in critical neurologic processes, including myelination, monoamine neurotransmitter metabolism, neuronal adenosine triphosphate generation and structural development, and epigenetic modification of synaptic plasticity genes and networks. All these processes begin in the fetal stage and are at risk when the fetus is iron-deficient. Pregnancy places a tremendous negative strain on maternal iron status because of the expansion of her blood volume, coupled with placental and fetal iron demand. Fetal iron deficiency occurs as a function of multiple common gestational conditions, including maternal iron deficiency, intrauterine growth restriction, premature delivery, and maternal glucose intolerance. Maternal iron deficiency in the first 2 trimesters increases the risk of low birthweight, which, irrespective of fetal iron status, is a risk to neurodevelopment. It also increases the risk of autism and schizophrenia, whereas third trimester iron deficiency is associated with long-term neurocognitive deficits. Fetal iron underloading also increases the risk of postnatal iron deficiency and its attendant short and long-term neurodevelopmental consequences. Current studies are attempting to establish maternal iron status action thresholds early in pregnancy to trigger iron interventions that would better ensure adequate fetal iron status and protect the developing fetal brain. One study demonstrates that a maternal serum ferritin >60 mcg/L is necessary at 15 weeks gestation to ensure adequate fetal loading throughout pregnancy and protect neurodevelopment. In low- and middle-income countries, where moderate to severe iron deficiency is common, early pregnancy iron interventions generally improve maternal status, but it is unclear whether the improvement is sufficient to protect the fetal brain and the child’s neurodevelopment.
母体缺铁和缺铁性贫血对胎儿和新生儿脑发育的影响。
铁元素在髓鞘形成、单胺类神经递质代谢、神经元ATP生成和结构发育以及突触可塑性基因和网络的表观遗传修饰等关键神经过程中发挥重要作用,是胎儿和出生后神经发育所必需的微量营养素。所有这些过程都始于胎儿阶段,当胎儿缺铁时就会有风险。由于孕妇血容量的增加以及胎盘和胎儿对铁的需求,怀孕对孕妇的铁状况造成了巨大的负面影响。胎儿缺铁是多种常见妊娠条件的结果,包括母体缺铁、宫内生长受限、早产和母体葡萄糖耐受不良。母亲在前两个月缺铁会增加低出生体重的风险,这与胎儿的铁状态无关,对神经发育有风险。它还会增加患自闭症和精神分裂症的风险,而妊娠晚期缺铁与长期的神经认知缺陷有关。胎儿铁负荷不足也增加了出生后缺铁及其伴随的短期和长期神经发育后果的风险。目前的研究正试图在妊娠早期建立母体铁状态的作用阈值,以触发铁干预,从而更好地确保胎儿铁状态充足并保护胎儿大脑发育。一项研究表明,在妊娠15周时,母体血清铁蛋白bbb60微克/升是必要的,以确保整个妊娠期间有足够的胎儿负荷和保护神经发育。在低收入和中等收入国家,中度至重度缺铁是常见的,妊娠早期铁干预通常会改善孕产妇状况,但尚不清楚这种改善是否足以保护胎儿大脑和儿童的神经发育。
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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
302
审稿时长
32 days
期刊介绍: Journal of Obstetrics and Gynaecology Canada (JOGC) is Canada"s peer-reviewed journal of obstetrics, gynaecology, and women"s health. Each monthly issue contains original research articles, reviews, case reports, commentaries, and editorials on all aspects of reproductive health. JOGC is the original publication source of evidence-based clinical guidelines, committee opinions, and policy statements that derive from standing or ad hoc committees of the Society of Obstetricians and Gynaecologists of Canada. JOGC is included in the National Library of Medicine"s MEDLINE database, and abstracts from JOGC are accessible on PubMed.
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