Georgieff Michael K
Division of Neonatology, University of Minnesota School of Medicine and University of Minnesota Masonic Children's Hospital, Minneapolis, MN
Am J Clin Nutr. 2017 Dec;106(Suppl 6):1588S-1593S. doi: 10.3945/ajcn.117.155846. Epub 2017 Oct 25.
Iron deficiency (ID) before the age of 3 y can lead to long-term neurological deficits despite prompt diagnosis of ID anemia (IDA) by screening of hemoglobin concentrations followed by iron treatment. Furthermore, pre- or nonanemic ID alters neurobehavioral function and is 3 times more common than IDA in toddlers. Given the global prevalence of ID and the enormous societal cost of developmental disabilities across the life span, better methods are needed to detect the risk of inadequate concentrations of iron for brain development (i.e., brain tissue ID) before dysfunction occurs and to monitor its amelioration after diagnosis and treatment. The current screening and treatment strategy for IDA fails to achieve this goal for 3 reasons. First, anemia is the final state in iron depletion. Thus, the developing brain is already iron deficient when IDA is diagnosed owing to the prioritization of available iron to red blood cells over all other tissues during negative iron balance in development. Second, brain ID, independently of IDA, is responsible for long-term neurological deficits. Thus, starting iron treatment after the onset of IDA is less effective than prevention. Multiple studies in humans and animal models show that post hoc treatment strategies do not reliably prevent ID-induced neurological deficits. Third, most currently used indexes of ID are population statistical cutoffs for either hematologic or iron status but are not bioindicators of brain ID and brain dysfunction in children. Furthermore, their relation to brain iron status is not known. To protect the developing brain, there is a need to generate serum measures that index brain dysfunction in the preanemic stage of ID, assess the ability of standard iron indicators to detect ID-induced brain dysfunction, and evaluate the efficacy of early iron treatment in preventing ID-induced brain dysfunction.
3岁前的缺铁(ID)可导致长期神经功能缺损,尽管通过筛查血红蛋白浓度并随后进行铁剂治疗能及时诊断缺铁性贫血(IDA)。此外,贫血前期或非贫血性缺铁会改变神经行为功能,在幼儿中其发生率是IDA的3倍。鉴于ID在全球的普遍存在以及发育障碍在整个生命周期造成的巨大社会成本,需要更好的方法来在功能障碍发生前检测出脑发育所需铁浓度不足(即脑组织ID)的风险,并在诊断和治疗后监测其改善情况。目前针对IDA的筛查和治疗策略未能实现这一目标,原因有三点。首先,贫血是铁耗竭的最终状态。因此,在发育过程中负铁平衡时,由于红细胞对可用铁的优先级高于所有其他组织,当诊断出IDA时,发育中的大脑已经缺铁。其次,独立于IDA的脑ID是长期神经功能缺损的原因。因此,在IDA发病后开始铁剂治疗不如预防有效。多项针对人类和动物模型的研究表明,事后治疗策略不能可靠地预防ID引起的神经功能缺损。第三,目前大多数用于检测ID的指标是血液学或铁状态的人群统计临界值,而不是儿童脑ID和脑功能障碍的生物指标。此外,它们与脑铁状态的关系尚不清楚。为了保护发育中的大脑,需要生成能够在ID贫血前期阶段指示脑功能障碍的血清指标,评估标准铁指标检测ID引起的脑功能障碍的能力,并评估早期铁剂治疗预防ID引起的脑功能障碍的疗效。