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Thalamic metabolic abnormalities in patients with Huntington's disease measured by magnetic resonance spectroscopy

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Autor(es):
R.F. Casseb [1, 2] ; A. D'Abreu [3, 1] ; H.H. Ruocco [3] ; I. Lopes-Cendes [1, 4] ; F. Cendes [3, 1] ; G. Castellano [1, 2]
Número total de Autores: 6
Afiliação do(s) autor(es):
[1] Cooperacao Interinstituc Apoio Pesquisas Cerebro, Programa CInAPCe, Sao Paulo - Brazil
[2] Univ Estadual Campinas, Inst Fis Gleb Wataghin, Dept Raios Cosmicos & Cronol, BR-13083859 Campinas, SP - Brazil
[3] Univ Estadual Campinas, Fac Ciencias Med, Dept Neurol, Lab Neuroimagem, BR-13083859 Campinas, SP - Brazil
[4] Univ Estadual Campinas, Fac Ciencias Med, Dept Genet Med, BR-13083859 Campinas, SP - Brazil
Número total de Afiliações: 4
Tipo de documento: Artigo Científico
Fonte: Brazilian Journal of Medical and Biological Research; v. 46, n. 8, p. 722-727, 2013-08-13.
Resumo

Huntington's disease (HD) is a neurologic disorder that is not completely understood; its fundamental physiological mechanisms and chemical effects remain somewhat unclear. Among these uncertainties, we can highlight information about the concentrations of brain metabolites, which have been widely discussed. Concentration differences in affected, compared to healthy, individuals could lead to the development of useful tools for evaluating the progression of disease, or to the advance of investigations of different/alternative treatments. The aim of this study was to compare the thalamic concentration of metabolites in HD patients and healthy individuals using magnetic resonance spectroscopy. We used a 2.0-Tesla magnetic field, repetition time of 1500 ms, and echo time of 135 ms. Spectra from 40 adult HD patients and 26 control subjects were compared. Quantitative analysis was performed using the LCModel method. There were statistically significant differences between HD patients and controls in the concentrations ofN-acetylaspartate+N-acetylaspartylglutamate (NAA+NAAG; t-test, P<0.001), and glycerophosphocholine+phosphocholine (GPC+PCh;t-test, P=0.001) relative to creatine+phosphocreatine (Cr+PCr). The NAA+NAAG/Cr+PCr ratio was decreased by 9% and GPC+PCh/Cr+PCr increased by 17% in patients compared with controls. There were no correlations between the concentration ratios and clinical features. Although these results could be caused by T1 and T2 changes, rather than variations in metabolite concentrations given the short repetition time and long echo time values used, our findings point to thalamic dysfunction, corroborating prior evidence. (AU)

Processo FAPESP: 05/56578-4 - Centro multimodal de neuroimagens para estudos em epilepsia
Beneficiário:Fernando Cendes
Modalidade de apoio: Auxílio à Pesquisa - Programa CINAPCE - Temático
Processo FAPESP: 09/02138-4 - Estudo do método LCModel para a quantificação de espectros de RM in vivo de pacientes com doença de Huntington
Beneficiário:Raphael Fernandes Casseb
Modalidade de apoio: Bolsas no Brasil - Iniciação Científica