4.3 Article

Long-term follow-up of a randomized controlled trial of choline for neurodevelopment in fetal alcohol spectrum disorder: corpus callosum white matter microstructure and neurocognitive outcomes

期刊

出版社

BMC
DOI: 10.1186/s11689-022-09470-w

关键词

Fetal alcohol spectrum disorders; Choline; Cognition; Longitudinal studies; Diffusion MRI; Neurite orientation dispersion and density imaging

资金

  1. National Institutes of Health (NIH)
  2. [R21AA019580]
  3. [R33AA019580]
  4. [R01AA024123]
  5. [P41EB027061]
  6. [P30NS076408]
  7. [1S10OD017974]

向作者/读者索取更多资源

This long-term follow-up study suggests that early choline supplementation in children with FASD can improve lower-order executive function and white matter microstructure organization, providing preliminary evidence for the potential long-term benefits of choline as a neurodevelopmental intervention in this population.
Background: Fetal alcohol spectrum disorder (FASD) is a lifelong condition. Early interventions targeting core neurocognitive deficits have the potential to confer long-term neurodevelopmental benefits. Time-targeted choline supplementation is one such intervention that has been shown to provide neurodevelopmental benefits that emerge with age during childhood. We present a long-term follow-up study evaluating the neurodevelopmental effects of early choline supplementation in children with FASD approximately 7 years on average after an initial efficacy trial. Methods: The initial study was a randomized, double-blind, placebo-controlled trial of choline vs. placebo in 2.5 to 5 year olds with FASD. Participants in this long-term follow-up study include 18 children (9 placebo; 9 choline) seen 7 years on average following initial trial completion. The mean age at follow-up was 11.0 years old. Diagnoses were 28% fetal alcohol syndrome (FAS), 28% partial FAS, and 44% alcohol-related neurodevelopmental disorder. The follow-up included measures of executive functioning and an MRI scan. Results: Children who received choline had better performance on several tasks of lower-order executive function (e.g., processing speed) and showed higher white matter microstructure organization (i.e., greater axon coherence) in the splenium of the corpus callosum compared to the placebo group. Conclusions: These preliminary findings, although exploratory at this stage, highlight potential long-term benefits of choline as a neurodevelopmental intervention for FASD and suggest that choline may affect white matter development, representing a potential target of choline in this population.

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