Auer D P, Pütz B, Kraft E, Lipinski B, Schill J, Holsboer F
Max Planck Institute of Psychiatry, Munich, Germany.
Biol Psychiatry. 2000 Feb 15;47(4):305-13. doi: 10.1016/s0006-3223(99)00159-6.
Functional imaging studies suggest a specific role of the anterior brain regions in the pathogenesis of major depression. The aim of this study was to evaluate possible neurochemical alterations in the frontomesial cortex in patients with major depressive episode using in vivo proton magnetic resonance spectroscopy ((1)H-MRS).
Single voxel (1)H-MRS was performed in 19 patients with major depressive episodes and 18 age-matched healthy controls within the anterior cingulate cortex and the parietal white matter. Absolute concentrations were estimated for N-acetyl-aspartate, choline-containing compounds, total creatine, myo-inositol, unresolved glutamate and glutamine (Glx) and glutamate alone (Glu). Voxel composition was analyzed by image segmentation into cerebrospinal fluid (CSF), grey and white matter.
MANOVA test for Glx and Glu using age, percent CSF and percent grey matter contribution as covariates yielded a significant group effect within the anterior cingulate due to decrease of Glx in patients (-10.4%, p =.013). Considering only severely depressed patients, both Glx and Glu (-14.3%, p =.03) showed a significant decrease. There was no significant group effect for the neuronal marker NAA, creatine, choline or myo-inositol in either localization.
This study suggests a possible role of altered glutamatergic neurotransmission within the anterior cingulate in the pathogenesis of mood disorders. The otherwise unremarkable findings of major brain metabolites confirms lack of neurodegenerative or membrane metabolic changes in major depression.
功能成像研究表明大脑前部区域在重度抑郁症发病机制中具有特定作用。本研究旨在利用活体质子磁共振波谱((1)H-MRS)评估重度抑郁发作患者额内侧皮质可能存在的神经化学改变。
对19例重度抑郁发作患者和18例年龄匹配的健康对照者在前扣带回皮质和顶叶白质进行单体素质子磁共振波谱分析。估计了N-乙酰天门冬氨酸、含胆碱化合物、总肌酸、肌醇、未分辨的谷氨酸和谷氨酰胺(Glx)以及单独的谷氨酸(Glu)的绝对浓度。通过图像分割为脑脊液(CSF)、灰质和白质来分析体素组成。
以年龄、CSF百分比和灰质贡献百分比作为协变量对Glx和Glu进行多变量方差分析,结果显示在前扣带区内由于患者Glx降低(-10.4%,p = 0.013)而有显著的组间效应。仅考虑重度抑郁患者时,Glx和Glu均显著降低(-14.3%,p = 0.03)。在两个部位,神经元标志物NAA、肌酸、胆碱或肌醇均无显著的组间效应。
本研究提示前扣带区内谷氨酸能神经传递改变在情绪障碍发病机制中可能起作用。主要脑代谢物的其他无明显异常的结果证实重度抑郁症不存在神经退行性变或膜代谢改变。