Clinical Trial: Neurodevelopment and Neuroimaging in Parenterally-fed Infants and Young Children

Study Status: Completed
Recruit Status: Completed
Study Type: Observational

Official Title: Neurodevelopment and Neuroimaging in Parenterally-fed Infants and Young Children

Brief Summary: Manganese (Mn) is an essential metal required for normal growth and development. However, exposure to high Mn levels can be toxic to the brain. The objectives of this project are to identify neonatal and young pediatric populations that are at increased risk of excessive brain Mn deposition and altered cognitive and motor development based on their dietary parenteral Mn exposure, and to make sound and evidence-based recommendations for appropriate Mn supplementation and monitoring of infants and young children receiving parenteral nutrition (PN). Our studies are designed to test the hypotheses that, compared with unexposed age-matched controls, infants and young children receiving prolonged Mn-supplemented PN will have increased deposition of Mn in their brains and lower scores on neurodevelopmental, cognitive and psychophysiological assessments.

Detailed Summary:

Specific Aims have been designed to test these hypotheses in three developmentally distinct populations:

  1. preterm infants and
  2. full term infants in the Neonatal Intensive Care Unit (NICU) requiring prolonged PN and
  3. older infants and young children on home PN.

Mn neurotoxicity will be investigated by longitudinal assessments of cognitive (executive functioning battery), neurodevelopmental (Bayley III Scales of Infant Development), and psychophysiological (event-related potential) measures and will be correlated with brain deposition of Mn using the technique of magnetic resonance (MR) relaxometry in a vulnerable population of infants receiving Mn-supplemented PN and age-matched controls. This proposal addresses a clinically relevant and unexplored link between nutritional practices, brain Mn deposition and neurodevelopmental sequelae in an at-risk population of infants and young children utilizing state-of-the-art magnetic resonance imaging (MRI) technology and neurodevelopmental assessment techniques. The potential for increased brain Mn accumulation in infants, and by inference, the potential health risks associated with elevated brain Mn burden, represents crucial, unexplored issues of exposure and susceptibility. The potential contribution of Mn toxicity to the poor outcomes of infants dependent for an extended time on PN has not been fully acknowledged or studied. Improved understanding of the relationships between Mn exposure and developmental outcomes will undoubtedly lead to altered clinical practices and more careful monitoring of Mn intake and blood and/or brain Mn levels in high risk infants. Our studies will also contribute to an improved understanding of the value of non-invasive MR imaging in the monitori
Sponsor: Vanderbilt University

Current Primary Outcome: Brain Mn deposition measured by MR relaxometry [ Time Frame: baseline (at study enrolment) ]

Mn neurotoxicity will be investigated by magnetic resonance (MR) relaxometry in a population of infants receiving Mn-supplemented parenteral nutrition and age-matched controls.


Original Primary Outcome:

Current Secondary Outcome: Neurodevelopmental outcomes [ Time Frame: 2 years ]

Neurodevelopment will be investigated by longitudinal assessments of cognitive (executive functioning battery), neurodevelopmental (Bayley III Scales of Infant Development), and psychophysiological (event-related potential) measures


Original Secondary Outcome:

Information By: Vanderbilt University

Dates:
Date Received: October 25, 2006
Date Started: August 2006
Date Completion:
Last Updated: December 18, 2013
Last Verified: December 2013