Related Experiment Video
Updated: Oct 4, 2025

Quantitating Iron Transport Across the Mouse Placenta In Vivo Using Nonradioactive Iron Isotopes
Published on: May 10, 2022
Impact and interactions between risk factors on the iron status of at-risk neonates
Christine E Brichta1,2, Jennie Godwin3, Sally Norlin2
1Pediatrics, University of Wisconsin, Madison, WI, USA.
Insights
Congenital iron deficiency (ID) affects 31% of newborns. Preterm birth and small for gestational age significantly increase ID risk, with maternal hypertension being a novel predictor.
Area of Science:
- Perinatal health
- Neonatal nutrition
- Iron metabolism
Background:
- Iron deficiency (ID) is a significant concern in newborns.
- Understanding perinatal risk factors is crucial for early detection and management.
- Congenital and infantile ID require specific diagnostic criteria.
Purpose of the Study:
- To examine the interactions between perinatal risk factors for congenital iron deficiency (ID).
- To analyze iron status in two distinct infant cohorts: cord blood and neonatal intensive care unit (NICU).
- To identify novel predictors of iron deficiency in at-risk infants.
Main Methods:
- Iron status was assessed using ferritin levels in a cord blood cohort (n=767) and a NICU cohort (n=257) of preterm or small for gestational age (SGA) infants.
- Congenital ID was defined by cord ferritin levels < 84 µg/L.
- Infantile ID was defined by serum ferritin levels < 70 µg/L at one month.
Main Results:
- 31% of the cord cohort exhibited congenital ID, with additive risks (p < 0.0015).
- 16% of the NICU cohort had infantile ID; risks were not additive, but 32% had ID if the threshold was 100 µg/L.
- Preterm birth and SGA status significantly impacted cord iron, and maternal hypertension emerged as a novel predictor in both cohorts.
Conclusions:
- Summing risks in term infants and understanding compounding risks in preterm infants can improve screening and management of ID.
- Early identification and intervention for iron deficiency in at-risk newborns are essential.
- Maternal health conditions, like hypertension, play a role in neonatal iron status.
Objective:
Examine interactions between perinatal risk factors for congenital iron deficiency (ID) using two cohorts.
Study Design:
Iron status in a composite 767-member cord blood cohort and a NICU cohort of 257 infants < 33 weeks of gestation or small for gestational age (SGA). Risks for ID were examined. Cord ferritin levels < 84 µg/L defined congenital ID. Serum ferritin < 70 µg/L defined infantile ID at one-month.
Results:
31% of the cord cohort had congenital ID; risks summative (p < 0.0015). 16% of the NICU cohort had infantile ID; risks not summative. However, 32% had ID if the ferritin threshold was 100 µg/L. Being both preterm (p < 0.0001) and SGA (p < 0.05) negatively impacted cord iron status. Maternal hypertension was a novel predictor of iron status (p = 0.023 in preterm cord; p < 0.0025 in NICU).
Conclusion:
Summing risks in term and understanding compounding risks in preterm infants can improve screening and management of ID in at-risk infants.
More Related Videos
04:48Setup of Capillary Electrophoresis-Inductively Coupled Plasma Mass Spectrometry CE-ICP-MS for Quantification of Iron Redox Species FeII, FeIII
Published on: May 4, 2020
19:15Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale
Published on: August 25, 2014
Related Concept Videos
Rh Blood Group
Factors Affecting Erythropoiesis
Several factors influence the erythrocyte production rate, with tissue oxygen level being among the most critical. Intense exercise or high altitudes can cause tissue hypoxia, which triggers the kidneys to release more erythropoietin (EPO) into the bloodstream.
EPO then...
Factors Affecting the Risk of Infection
The integrity and count of the white blood cells help the body resist pathogens and fight infection. When impaired, it reduces the body's resistance to pathogens. The acidic pH levels of the gastrointestinal, genitourinary tracts, and skin...
Pharmacokinetics in Pediatric Patients: Drug Distribution
Teratogenicity
Factors Affecting Drug Response: Overview