Division of Nutritional Sciences, Cornell University, Ithaca, NY.
Department of Pediatrics Division of Neonatology, The University of Rochester School of Medicine, Rochester, NY.
J Nutr. 2019 Mar 1;149(3):406-415. doi: 10.1093/jn/nxy286.
It has been proposed that the fetus prioritizes iron for hemoglobin production over delivery to tissues. However, few studies have evaluated the interrelations between hemoglobin and multiple iron status biomarkers in umbilical cord blood. A full understanding is needed of how these parameters influence each other within cord blood to fully interpret iron and hematologic status at birth.
We evaluated the determinants of neonatal hemoglobin and assessed the interrelations between hemoglobin, serum iron status indicators, and serum iron regulatory hormones in healthy neonates.
This was an observational study that assessed umbilical cord hemoglobin (Hb), serum ferritin (SF), erythropoietin (EPO), soluble transferrin receptor (sTfR), serum iron, hepcidin, vitamin B-12, folate, IL-6, and CRP measured in 234 neonates born to adolescents or to women carrying multiples. Correlations between these indicators were evaluated and mediation models consistent with the observed significant determinants of cord Hb concentrations were developed.
A highly significant inverse association was found between cord SF and Hb concentrations that was not attributable to neonatal or maternal inflammation (as measured by IL-6 and CRP). The inverse association was present in the combined cohort, as well as in the adolescent and multiples cohorts independently. Mediation analyses found that EPO and hepcidin had significant indirect effects on cord Hb, associations that are explicable by mediation through SF and sTfR.
In contrast to observations made in older infants, a highly significant inverse association between Hb and SF, as well positive associations between Hb and both sTfR and EPO, were observed in umbilical cord blood from neonates born to adolescents or women carrying multiples. These findings, combined with review of the published literature, indicate a need for analysis of the relations between multiple parameters to assess iron and hematologic status at birth. These clinical trials were registered at clinicaltrials.gov as NCT01582802 (https://clinicaltrials.gov/ct2/show/NCT01582802) and NCT01019902 (https://clinicaltrials.gov/ct2/show/NCT01019902).
有人提出,胎儿会优先将铁用于血红蛋白的生成,而不是输送给组织。然而,很少有研究评估脐带血中血红蛋白与多种铁状态生物标志物之间的相互关系。为了充分解释出生时的铁和血液状况,需要全面了解这些参数如何在脐带血中相互影响。
我们评估了新生儿血红蛋白的决定因素,并评估了健康新生儿脐带血中血红蛋白、血清铁状态指标和血清铁调节激素之间的相互关系。
这是一项观察性研究,评估了 234 名青少年或多胎妊娠母亲所生新生儿的脐带血红蛋白(Hb)、血清铁蛋白(SF)、促红细胞生成素(EPO)、可溶性转铁蛋白受体(sTfR)、血清铁、hepcidin、维生素 B-12、叶酸、IL-6 和 CRP。评估了这些指标之间的相关性,并建立了与脐带 Hb 浓度观察到的显著决定因素一致的中介模型。
脐带 SF 与 Hb 浓度之间存在高度显著的负相关,这种负相关与新生儿或母亲的炎症(通过 IL-6 和 CRP 测量)无关。这种负相关在合并队列中以及在青少年和多胎妊娠队列中均存在。中介分析发现,EPO 和 hepcidin 对脐带 Hb 有显著的间接影响,这种关联可以通过 SF 和 sTfR 的中介来解释。
与在年龄较大的婴儿中观察到的结果相反,在青少年或多胎妊娠母亲所生的新生儿脐带血中,Hb 与 SF 之间存在高度显著的负相关,以及 Hb 与 sTfR 和 EPO 之间存在正相关。这些发现,结合对已发表文献的回顾,表明需要分析多个参数之间的关系,以评估出生时的铁和血液状况。这些临床试验在 clinicaltrials.gov 上注册为 NCT01582802(https://clinicaltrials.gov/ct2/show/NCT01582802)和 NCT01019902(https://clinicaltrials.gov/ct2/show/NCT01019902)。