Lower N-Acetyl-Aspartate Levels in Prefrontal Cortices in Pediatric Bipolar Disorder: A (1)H Magnetic Resonance Spectroscopy Study


Autoria(s): CAETANO, Sheila C.; OLVERA, Rene L.; HATCH, John P.; SANCHES, Marsal; CHEN, Hua Hsuan; NICOLETTI, Mark; STANLEY, Jeffrey A.; FONSECA, Manoela; HUNTER, Kristina; LAFER, Beny; PLISZKA, Steven R.; SOARES, Jair C.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2011

Resumo

Objective: The few studies applying single-voxel(1)H 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. Method: We studied 43 pediatric patients with DSM-IV BD (19 female, mean age 13.2 +/- 2.9 years) and 38 healthy controls (79 female, mean age 13.9 +/- 2.7 years). We conducted multivoxel in vivo (1)H 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. Results: 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. Conclusions: 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. J. Am. Acad. Child Adolesc. Psychiatry, 2011;50(1):85-94.

University of Texas Health Science Center at San Antonio (UTHSCSA) General Clinical Research Center (GCRC)[M01-RR-01346]

UTHSCSA Krus Endowed Chair in Psychiatry

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) Foundation of Brazil

Fundacao de Amparo a Pesquisa de Sao Paulo, Brazil (FAPESP)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico, Brazil (CNPq)

National Alliance for Research on Schizophrenia and Depression (NARSAD)

American Psychiatric Association/AstraZeneca

Ortho-McNeil Janssen and Shire Inc.

Pfizer

GlaxoSmithKline

Repligen

[MH 01736]

[MH 69774]

[MH 068662]

[RR 020571]

Identificador

JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, v.50, n.1, p.85-94, 2011

0890-8567

http://producao.usp.br/handle/BDPI/22501

10.1016/j.jaac.2010.10.007

http://dx.doi.org/10.1016/j.jaac.2010.10.007

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE BV

Relação

Journal of the American Academy of Child and Adolescent Psychiatry

Direitos

closedAccess

Copyright ELSEVIER SCIENCE BV

Palavras-Chave #magnetic resonance spectroscopy #bipolar disorder #prefrontal cortex #N-acetyl aspartate #ANTERIOR CINGULATE CORTEX #PROTON MR SPECTROSCOPY #FRONTAL-LOBE #LITHIUM TREATMENT #NEURAL CIRCUITRY #RATING-SCALE #HIGH-RISK #BRAIN #CHILDREN #ADOLESCENTS #Psychology, Developmental #Pediatrics #Psychiatry
Tipo

article

original article

publishedVersion