Bertolino A, Callicott J H, Nawroz S, Mattay V S, Duyn J H, Tedeschi G, Frank J A, Weinberger D R
Clinical Brain Disorders Branch, National Institutes of Health, National Institute of Mental Health, Neurosciences Center at Saint Elizabeths, Washington, DC, USA.
Neuropsychopharmacology. 1998 Jan;18(1):1-9. doi: 10.1016/S0893-133X(97)00090-0.
Using proton magnetic resonance spectroscopic imaging (1H-MRSI) we found in a previous study a specific pattern of neuronal pathology in patients with schizophrenia as determined by relative loss of signal from N-acetyl-containing compounds (NAA). The purpose of the present study was to assess the reproducibility of the results of 1H-MRSI both in patients with schizophrenia and in normal controls. We studied twice 10 patients and 10 controls on 2 days separated by, on average, 3 months. Reproducibility was assessed with several statistical procedures including ANOVA, coefficients of variation (CVs) and intra-class correlation coefficients (ICC). Patients showed significant reductions of NAA/creatine-phosphocreatine (CRE) and NAA/choline-containing compounds (CHO) selectively in the hippocampal region (HIPPO) and in the dorsolateral prefrontal cortex (DLPFC) on both experimental days. A repeated measures ANOVA showed no effect of time on metabolite ratios in all subjects. CVs were fairly low (especially for NAA/CRE and CHO/CRE) and did not differ significantly between patients and controls. The ICCs of the ROIs reached statistical significance only in a few instances. The present multislice 1H-MRSI study shows that: (1) patients with schizophrenia, when compared as a group to normal controls, show a consistent 1H-MRSI pattern of group differences, i.e., bilateral reductions of NAA/CRE and NAA/CHO in HIPPO and DLPFC; (2)1H-MRSI data in both patients and controls do not show significant changes over this 90-day period; however, absolute metabolite ratios in individuals show low predictability over this time interval; (3) 1H-MRSI data show relatively low variability (as measured by the CVs) both in patients and normal controls, especially for NAA/CRE and CHO/CRE.
在之前的一项研究中,我们使用质子磁共振波谱成像(1H-MRSI)发现,精神分裂症患者存在一种特定的神经元病理模式,这是由含N-乙酰化合物(NAA)的信号相对缺失所确定的。本研究的目的是评估1H-MRSI结果在精神分裂症患者和正常对照中的可重复性。我们对10例患者和10例对照进行了两次研究,两次研究间隔平均3个月。通过包括方差分析(ANOVA)、变异系数(CV)和组内相关系数(ICC)在内的多种统计程序评估可重复性。在两个实验日,患者在海马区(HIPPO)和背外侧前额叶皮质(DLPFC)中NAA/磷酸肌酸(CRE)和NAA/含胆碱化合物(CHO)均有选择性显著降低。重复测量方差分析显示,时间对所有受试者的代谢物比率没有影响。CV相当低(尤其是NAA/CRE和CHO/CRE),患者和对照之间没有显著差异。感兴趣区域(ROI)的ICC仅在少数情况下达到统计学显著性。本多层1H-MRSI研究表明:(1)与正常对照相比,精神分裂症患者作为一个群体显示出一致的1H-MRSI组间差异模式,即HIPPO和DLPFC中NAA/CRE和NAA/CHO的双侧降低;(2)患者和对照的1H-MRSI数据在这90天期间均未显示出显著变化;然而,个体的绝对代谢物比率在这个时间间隔内显示出较低的可预测性;(3)1H-MRSI数据在患者和正常对照中均显示出相对较低的变异性(以CV衡量),尤其是NAA/CRE和CHO/CRE。