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Neurophysiological correlates of memory change in children with fetal alcohol spectrum disorders treated with choline.
Fuglestad, Anita J; Miller, Neely C; Fink, Birgit A; Boys, Christopher J; Eckerle, Judith K; Georgieff, Michael K; Wozniak, Jeffrey R.
Afiliação
  • Fuglestad AJ; Department of Psychology, University of North Florida, Jacksonville, FL, United States.
  • Miller NC; Masonic Institute for the Developing Brain, University of Minnesota Twin Cities, Minneapolis, MN, United States.
  • Fink BA; Department of Psychiatry & Behavioral Sciences, University of Minnesota Twin Cities, Minneapolis, MN, United States.
  • Boys CJ; Department of Pediatrics, University of Minnesota, Minneapolis, MN, United States.
  • Eckerle JK; Department of Psychiatry & Behavioral Sciences, University of Minnesota Twin Cities, Minneapolis, MN, United States.
  • Georgieff MK; Masonic Institute for the Developing Brain, University of Minnesota Twin Cities, Minneapolis, MN, United States.
  • Wozniak JR; Department of Pediatrics, University of Minnesota, Minneapolis, MN, United States.
Front Psychol ; 13: 936019, 2022.
Article em En | MEDLINE | ID: mdl-36225707
ABSTRACT

Background:

Prenatal and early postnatal choline supplementation reduces cognitive and behavioral deficits in animal models of Fetal Alcohol Spectrum Disorder (FASD). In a previously published 9-month clinical trial of choline supplementation in children with FASD, we reported that postnatal choline was associated with improved performance on a hippocampal-dependent recognition memory task. The current paper describes the neurophysiological correlates of that memory performance for trial completers.

Methods:

Children with FASD (N = 24) who were enrolled in a clinical trial of choline supplementation were followed for 9 months. Delayed recall on a 9-step elicited imitation task (EI) served as the behavioral measure of recognition memory. Neurophysiological correlates of memory were assessed via event-related potentials (ERP).

Results:

Delayed recall on EI was correlated with two ERP components commonly associated with recognition memory in young children middle latency negative component (Nc amplitude; range r = -0.41 to r = -0.44) and positive slow wave (PSW area under the curve; range r = -0.45 to r = -0.63). No significant ERP differences were observed between the choline and placebo groups at the conclusion of the trial.

Conclusion:

Although the small sample size limits the ability to draw clear conclusions about the treatment effect of choline on ERP, the results suggest a relationship between memory performance and underlying neurophysiological status in FASD. This trial was registered.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article