Article

Lower N-acetyl-aspartate levels in prefrontal cortices in pediatric bipolar disorder: a ¹H magnetic resonance spectroscopy study.

University of São Paulo School of Medicine, São Paulo, Brazil.
Journal of the American Academy of Child and Adolescent Psychiatry (impact factor: 4.98). 01/2011; 50(1):85-94. DOI:10.1016/j.jaac.2010.10.007 pp.85-94
Source: PubMed

ABSTRACT The few studies applying single-voxel ¹H spectroscopy in children and adolescents with bipolar disorder (BD) have reported low N-acetyl-aspartate (NAA) levels in the dorsolateral prefrontal cortex (DLPFC), and high myo-inositol / phosphocreatine plus creatine (PCr+Cr) ratios in the anterior cingulate. The aim of this study was to evaluate NAA, glycerophosphocholine plus phosphocholine (GPC+PC) and PCr+Cr in various frontal cortical areas in children and adolescents with BD. We hypothesized that NAA levels within the prefrontal cortex are lower in BD patients than in healthy controls, indicating neurodevelopmental alterations in the former.
We studied 43 pediatric patients with DSM-IV BD (19 female, mean age 13.2 ± 2.9 years) and 38 healthy controls (19 female, mean age 13.9 ± 2.7 years). We conducted multivoxel in vivo ¹H spectroscopy measurements at 1.5 Tesla using a long echo time of 272 ms to obtain bilateral metabolite levels from the medial prefrontal cortex (MPFC), DLPFC (white and gray matter), cingulate (anterior and posterior), and occipital lobes. We used the nonparametric Mann-Whitney U test to compare neurochemical levels between groups.
In pediatric BD patients, NAA and GPC+PC levels in the bilateral MPFC, and PCr+Cr levels in the left MPFC were lower than those seen in the controls. In the left DLPFC white matter, levels of NAA and PCr+Cr were also lower in BD patients than in controls.
Lower NAA and PCr+Cr levels in the PFC of children and adolescents with BD may be indicative of abnormal dendritic arborization and neuropil, suggesting neurodevelopmental abnormalities.

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Keywords

38 healthy controls
 
abnormal dendritic arborization
 
bilateral metabolite levels
 
bilateral MPFC
 
dorsolateral prefrontal cortex
 
DSM-IV BD
 
echo time
 
GPC+PC levels
 
healthy controls
 
left DLPFC white matter
 
left MPFC
 
Lower NAA
 
medial prefrontal cortex
 
NAA levels
 
neurochemical levels
 
nonparametric Mann-Whitney U test
 
PCr+Cr levels
 
pediatric BD patients
 
prefrontal cortex
 
vivo ¹H spectroscopy measurements