Four-year follow-up of a randomized controlled trial of choline for neurodevelopment in fetal alcohol spectrum disorder
Autor: | Joshua P. Radke, Jeffrey R. Wozniak, Christopher W. Lindgren, Judith K. Eckerle, Kristin E. Sandness, Neely C. Miller, Michael K. Georgieff, Ann M. Brearley, Christopher J. Boys, Steven H. Zeisel, Birgit A. Fink, Anita J. Fuglestad |
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Rok vydání: | 2019 |
Předmět: |
Male
Pediatrics medicine.medical_specialty Cognitive Neuroscience Intelligence Fetal alcohol syndrome Pathology and Forensic Medicine law.invention lcsh:RC321-571 Choline 03 medical and health sciences 0302 clinical medicine Neurodevelopmental disorder Cognition Randomized controlled trial Double-Blind Method law Pregnancy 030225 pediatrics medicine Attention deficit hyperactivity disorder Humans lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry Nootropic Agents business.industry Working memory Research Longitudinal studies medicine.disease Executive functions 3. Good health Memory Short-Term Fetal Alcohol Spectrum Disorders Child Preschool Prenatal Exposure Delayed Effects Pediatrics Perinatology and Child Health Randomized controlled trials Female Neurology (clinical) Verbal memory business Neurocognitive 030217 neurology & neurosurgery Follow-Up Studies |
Zdroj: | Journal of Neurodevelopmental Disorders Journal of Neurodevelopmental Disorders, Vol 12, Iss 1, Pp 1-13 (2020) |
ISSN: | 1866-1955 |
Popis: | Background Despite the high prevalence of fetal alcohol spectrum disorder (FASD), there are few interventions targeting its core neurocognitive and behavioral deficits. FASD is often conceptualized as static and permanent, but interventions that capitalize on brain plasticity and critical developmental windows are emerging. We present a long-term follow-up study evaluating the neurodevelopmental effects of choline supplementation in children with FASD 4 years after an initial efficacy trial. Methods The initial study was a randomized, double-blind, placebo-controlled trial of choline vs. placebo in 2–5-year-olds with FASD. Participants include 31 children (16 placebo; 15 choline) seen 4 years after trial completion. The mean age at follow-up was 8.6 years. Diagnoses were 12.9% fetal alcohol syndrome (FAS), 41.9% partial FAS, and 45.1% alcohol-related neurodevelopmental disorder. The follow-up included measures of intelligence, memory, executive functioning, and behavior. Results Children who received choline had higher non-verbal intelligence, higher visual-spatial skill, higher working memory ability, better verbal memory, and fewer behavioral symptoms of attention deficit hyperactivity disorder than the placebo group. No differences were seen for verbal intelligence, visual memory, or other executive functions. Conclusions These data support choline as a potential neurodevelopmental intervention for FASD and highlight the need for long-term follow-up to capture treatment effects on neurodevelopmental trajectories. Trial registration ClinicalTrials.Gov #NCT01149538; Registered: June 23, 2010; first enrollment July 2, 2010 |
Databáze: | OpenAIRE |
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