Literature DB >> 19996601

Can prenatal screening for fetal alcohol spectrum disorder be justified? A commentary.

G J Mizejewski1.   

Abstract

Fetal alcohol spectrum disorder (FASD) is the leading cause of non-genetic mental retardation in the USA, possibly exceeding even Down syndrome, which is currently approaching 1 in 500 live births. Alcohol consumption during pregnancy results in brain, craniofacial and heart defects, neurotoxicity, and immune dysfunction. The preferred action taken to prevent alcohol consumption during pregnancy is abstinence. However, the detection, diagnosis, and treatment of FASD remain a major public health need in this country and throughout the world. The biochemical molecules involved in the developmental abnormalities encompass a vast array of signal transduction and synaptic pathways which involve neurotransmitters and neurotrophic peptides. Recent advances in medicine-based therapies for FASD have been reported, and include the use of small molecule agonists, antagonists, and competitive inhibitors. Since biomarkers for FASD have previously been identified in clinical research reports, multicenter screening feasibility studies now seem warranted and could be initiated following adequate funding, protocols, procedures, and institutional review board approvals. Copyright (c) 2009 S. Karger AG, Basel.

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Year:  2009        PMID: 19996601     DOI: 10.1159/000263460

Source DB:  PubMed          Journal:  Gynecol Obstet Invest        ISSN: 0378-7346            Impact factor:   2.031


  5 in total

1.  Modeling Fetal Alcohol Spectrum Disorder: Validating an Ex Vivo Primary Hippocampal Cell Culture System.

Authors:  Elif Tunc-Ozcan; Adriana B Ferreira; Eva E Redei
Journal:  Alcohol Clin Exp Res       Date:  2016-05-10       Impact factor: 3.455

2.  Deletion of TLR-4 attenuates fetal alcohol exposure-induced gene expression and social interaction deficits.

Authors:  Pradeep K Shukla; Avtar S Meena; Rupa Rao; RadhaKrishna Rao
Journal:  Alcohol       Date:  2018-04-18       Impact factor: 2.405

3.  The validity of phosphatidylethanol in dried blood spots of newborns for the identification of prenatal alcohol exposure.

Authors:  Ludmila N Bakhireva; Lawrence Leeman; Renate D Savich; Sandra Cano; Hilda Gutierrez; Daniel D Savage; William F Rayburn
Journal:  Alcohol Clin Exp Res       Date:  2014-02-11       Impact factor: 3.455

4.  Low-dose thyroxine attenuates autism-associated adverse effects of fetal alcohol in male offspring's social behavior and hippocampal gene expression.

Authors:  Elif Tunc-Ozcan; Timothy M Ullmann; Pradeep K Shukla; Eva E Redei
Journal:  Alcohol Clin Exp Res       Date:  2013-06-13       Impact factor: 3.455

5.  A modified Delphi study of screening for fetal alcohol spectrum disorders in Australia.

Authors:  Rochelle E Watkins; Elizabeth J Elliott; Jane Halliday; Colleen M O'Leary; Heather D'Antoine; Elizabeth Russell; Lorian Hayes; Elizabeth Peadon; Amanda Wilkins; Heather M Jones; Anne McKenzie; Sue Miers; Lucinda Burns; Raewyn C Mutch; Janet M Payne; James P Fitzpatrick; Maureen Carter; Jane Latimer; Carol Bower
Journal:  BMC Pediatr       Date:  2013-01-25       Impact factor: 2.125

  5 in total

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