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Brain Metabolic Alterations in Adolescents and Young Adults With Fetal Alcohol Spectrum Disorders
Author(s) -
Fagerlund Åse,
Heikkinen Sami,
AuttiRämö Ilona,
Korkman Marit,
Timonen Marjut,
Kuusi Tuomo,
Riley Edward P.,
Lundbom Nina
Publication year - 2006
Publication title -
alcoholism: clinical and experimental research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.267
H-Index - 153
eISSN - 1530-0277
pISSN - 0145-6008
DOI - 10.1111/j.1530-0277.2006.00257.x
Subject(s) - fetal alcohol syndrome , choline , creatine , corpus callosum , cerebellum , medicine , endocrinology , white matter , cerebrum , alcohol , physiology , psychology , magnetic resonance imaging , central nervous system , pathology , chemistry , biochemistry , radiology
Background: Prenatal alcohol exposure affects brain structure and function. This study examined brain metabolism using magnetic resonance spectroscopy (MRS) and searched for regions of specific vulnerability in adolescents and young adults prenatally exposed to alcohol. Methods: Ten adolescents and young adults with confirmed heavy prenatal alcohol exposure and a diagnosis within the fetal alcohol spectrum disorders (FASD) were included. Three of them had fetal alcohol syndrome (FAS), 3 had partial FAS (PFAS), and 4 had alcohol‐related neurobehavioral disorder (ARND). The control group consisted of 10 adolescents matched for age, sex, head circumference, handedness, and body mass. Exclusionary criteria were learning disorders and prenatal alcohol exposure. Three‐dimensional 1 H magnetic resonance spectroscopic imaging ( 1 H MRSI) was performed in the cerebrum and cerebellum. Metabolite ratios N ‐acetylaspartate/choline (NAA/Cho), NAA/creatine (Cr) and Cho/Cr, and absolute metabolite intensities were calculated for several anatomic regions. Results: In patients with FASD, lower NAA/Cho and/or NAA/Cr compared with controls were found in parietal and frontal cortices, frontal white matter, corpus callosum, thalamus, and cerebellar dentate nucleus. There was an increase in the absolute intensity of the glial markers Cho and Cr but no change in the neuronal marker NAA. Conclusions: Our results suggest that prenatal alcohol exposure alters brain metabolism in a long‐standing or permanent manner in multiple brain areas. These changes are in accordance with previous findings from structural and functional studies. Metabolic alterations represent changes in the glial cell pool rather than in the neurons.