2010
DOI: 10.1016/j.jpeds.2009.09.049
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In Utero Iron Status and Auditory Neural Maturation in Premature Infants as Evaluated by Auditory Brainstem Response

Abstract: Objective-To determine if cord ferritin (CF) concentration, an index of in utero iron status, is associated with auditory neural maturation in premature infants.Study design-A prospective cohort study was performed to compare auditory neural maturation between infants with latent iron deficiency (CF 11-75 ng/ml) and infants with normal iron status (CF > 75 ng/ml) at birth. Our inclusion criteria were 27-33 weeks gestational age infants admitted to the Neonatal Intensive Care Unit between July, 2007 and Novembe… Show more

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Cited by 94 publications
(96 citation statements)
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“…We considered fetal-neonatal ID as cord blood SF <75 mg/L or as ZPP/H >118 mmol/mol. The SF cutoff has been used in studies of prenatal ID neurodevelopmental effects (16)(17)(18). The ZPP/H cutoff represents the US 90th percentile (19).…”
Section: Methodsmentioning
confidence: 99%
“…We considered fetal-neonatal ID as cord blood SF <75 mg/L or as ZPP/H >118 mmol/mol. The SF cutoff has been used in studies of prenatal ID neurodevelopmental effects (16)(17)(18). The ZPP/H cutoff represents the US 90th percentile (19).…”
Section: Methodsmentioning
confidence: 99%
“…Ninety-two infants were excluded for inadequate ERPs data (more than 30% data were removed). Because iron deficiency may also affect the hippocampus-based recognition memory (Burden et al, 2007; Congdon et al, 2012; Lukowski et al, 2010), we excluded 53 infants with evidence of prenatal iron deficiency (ferritin concentration lower than 75μg/l (Amin et al, 2010; Tamura et al, 2002) or ZPP higher than 118 μmol/mol (McLimore et al, 2013)). Two infants who did not have cord blood Pb measurements were also excluded.…”
Section: Methodsmentioning
confidence: 99%
“…Outcomes vary depending on the timing of the insult as well as what is developing in specific regions of the developing brain during the time of the insult. For example, ID during the late prenatal period leads to delayed neural processing speed [1] and deficits in recognition memory that can be detected through event-related potentials (ERP) [2]. The recognition memory deficits are consistent with altered development of the hippocampus, which is predominant during the late fetal and early postnatal period.…”
Section: Introductionmentioning
confidence: 99%
“…Oligodendrocyte expression of myelin basic protein and PLP-1 & -2 is compromised by ID and the effects last beyond the period of ID [14]. Physiologically, these changes to the myelin system likely contribute to the reduced speed of processing observed in neonates [1], infants [15] and toddlers [4] with current or previous ID.…”
Section: Introductionmentioning
confidence: 99%