1H Magnetic prefrontal resonance spectroscopy study of dorsolateral cortex in unipolar mood disorder patients

被引:32
作者
Brambilla, P
Stanley, JA
Nicoletti, MA
Sassi, RB
Mallinger, AG
Frank, E
Kupfer, DJ
Keshavan, MS
Soares, JC
机构
[1] Univ Texas, Hlth Sci Ctr, Div Mood & Anxiety Disorders, Dept Psychiat, San Antonio, TX 78229 USA
[2] Univ Udine, Sch Med, Sect Psychiat, Dept Pathol & Expt & Clin Med, I-33100 Udine, Italy
[3] Univ Genoa, Adv Biotechnol Ctr, Genoa, Italy
[4] Univ Pittsburgh, Sch Med, Dept Psychiat, Western Psychiat Inst & Clin, Pittsburgh, PA USA
[5] Univ Pittsburgh, Sch Med, Dept Pharmacol, Pittsburgh, PA 15261 USA
[6] Univ Sao Paulo, Sch Med, Dept Psychiat, Sao Paulo, Brazil
[7] S Texas Vet Hlth Care Syst, Audie L Murphy Div, San Antonio, TX USA
关键词
neuroimaging; affective disorder; mood disorder; NAA; in vivo proton MRS;
D O I
10.1016/j.pscychresns.2004.12.001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Neuroimaging and postmortem studies have suggested the involvement of the dorsolateral prefrontal cortex (DLPFC) in the pathophysioloy of unipolar disorder. We examined with in vivo H-1 magnetic resonance spectroscopy (MRS) the levels of specific metabolites in the DLPFC of adult unipolar patients and the role of illness chronicity on DLPFC abnormalities. Nineteen unmedicated unipolar mood disorder patients and 19 age- and gender-matched healthy controls underwent a short echo-time H-1 MRS examination localized to an 8-cm(3) single voxel placed in the left DLPFC. There were no significant differences in metabolite levels, including N-acetylaspartate (NAA), phosphocreatine plus creatine (PCr+Cr) and choline-containing-compounds (GPC+PC), between the two groups. However, NAA/PCr+Cr ratios were significantly lower in the chronic than in the less chronically ill patients and healthy controls. The low levels of NAA/PCr+Cr ratios in the left DLPFC of unipolar patients who had been more chronically ill suggest a potential role for illness chronicity in neuronal abnormalities in the DLPFC in unipolar disorder. This could possibly be accounted for by neurodegenerative processes arising with the progression of the illness. Future H-1 MRS investigations should longitudinally examine the role of illness chronicity on DLPFC abnormalities and their relationship with the symptoms of unipolar disorder. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:131 / 139
页数:9
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