NEUROMATURATION DELAYS IN IRON DEFICIENT ANEMIC INFANTS
Project Number1R01HD033487-01A2
Contact PI/Project LeaderLOZOFF, BETSY
Awardee OrganizationUNIVERSITY OF MICHIGAN AT ANN ARBOR
Description
Abstract Text
The proposed project will 1) test the hypothesis that changes in
neuromaturation observed in iron-deficient anemic infants are due to
hypomyelination and 2) test a model of mechanisms explaining why
iron-deficiency anemia in infancy is associated with poorer
developmental outcome. Given the important role of iron in myelin
formation and maintenance, impaired myelination is a promising
explanation for recent evidence of immature neuromaturation in 6-
month-olds with iron-deficiency anemia (slower Central Conduction
Time, decreased vagal tone). The hypomyelination hypothesis (Aim
1) will be tested directly in a developmental rat model by examining
vagal/optic nerve and regional brain myelination and indirectly in the
child using auditory and visual evoked potentials and vagal tone
measures from sleep studies. Annual neurophysiology evaluations will
be conducted until children are 5 years of age to determine if the
findings to date represent irregular progressions or arrests in
neuromaturation (n=226, half initially anemic or nonanemic). The
proposed model of the effects of early iron-deficiency anemia (Aim 2)
postulates that hypomyelination and impaired dopaminergic function
contribute to altered behavior in anemic infants, which interferes with
their learning from the physical and social environment (functional
isolation~) and makes them more vulnerable to the effects of
environmental stressors, leading to poorer intellectual and motor
development and more internalizing behaviors. Causal modeling
techniques will be used to evaluate this model (n=1000 for testing the
overall model; n=350 for exploring underlying mechanisms related to
neuromaturation, dopaminergic function, and specific behavioral
alterations). The proposed integration of a developmental animal
model, related measures of CNS functioning and behavior in the child,
and an overall model of explanatory mechanisms promises to be a
major advance in understanding poorer developmental and behavioral
outcome in early iron deficiency anemia, which affects 20-25% of the
world~s babies and many poor or minority infants in the U.S.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
child (0-11)child behaviorchild physical developmentclinical researchdevelopmental neurobiologydevelopmental nutritiondisease /disorder modelevoked potentialshearing testshuman subjectinfant human (0-1 year)laboratory ratlongitudinal human studymalnutritionmicrocytic /hypochromic anemiamyelinopathynutrition related tagoptic nervepreschool child (1-5)psychomotor functionsleepvagus nervevisual perception
Eunice Kennedy Shriver National Institute of Child Health and Human Development
CFDA Code
DUNS Number
073133571
UEI
GNJ7BBP73WE9
Project Start Date
05-May-1997
Project End Date
30-April-2001
Budget Start Date
05-May-1997
Budget End Date
30-April-1998
Project Funding Information for 1997
Total Funding
$241,562
Direct Costs
$195,730
Indirect Costs
$45,832
Year
Funding IC
FY Total Cost by IC
1997
Eunice Kennedy Shriver National Institute of Child Health and Human Development
$241,562
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 1R01HD033487-01A2
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Clinical Studies
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