Meyer E J, Kirov I I, Tal A, Davitz M S, Babb J S, Lazar M, Malaspina D, Gonen O
From the Department of Radiology (E.J.M., I.I.K., M.S.D., J.S.B., M.L., O.G.), Center for Advanced Imaging Innovation and Research, Bernard and Irene Schwartz Center for Biomedical Imaging.
Department of Chemical Physics (A.T.), Weizmann Institute of Science, Rehovot, Israel.
AJNR Am J Neuroradiol. 2016 Dec;37(12):2273-2279. doi: 10.3174/ajnr.A4886. Epub 2016 Jul 21.
Schizophrenia is well-known to be associated with hippocampal structural abnormalities. We used H-MR spectroscopy to test the hypothesis that these abnormalities are accompanied by NAA deficits, reflecting neuronal dysfunction, in patients compared with healthy controls.
Nineteen patients with schizophrenia (11 men; mean age, 40.6 ± 10.1 years; mean disease duration, 19.5 ± 10.5 years) and 11 matched healthy controls (5 men; mean age, 33.7 ± 10.1 years) underwent MR imaging and multivoxel point-resolved spectroscopy (TE/TR, 35/1400 ms) H-MRS at 3T to obtain their hippocampal GM absolute NAA, Cr, Cho, and mIns concentrations. Unequal variance t tests and ANCOVA were used to compare patients with controls. Bilateral volumes from manually outlined hippocampal masks were compared by using unequal variance t tests.
Patients' average hippocampal GM Cr concentrations were 19% higher than that of controls, 8.7 ± 2.2 versus 7.4 ± 1.2 mmol/L (P < .05); showing no differences, concentrations in NAA were 8.8 ± 1.6 versus 8.7 ± 1.2 mmol/L; in Cho, 2.3 ± 0.7 versus 2.1 ± 0.3 mmol/L; and in mIns, 6.1 ± 1.5 versus 5.2 ± 0.9 (all P > .1). There was a positive correlation between mIns and Cr in patients (r = 0.57, P = .05) but not in controls. The mean bilateral hippocampal volume was ∼10% lower in patients: 7.5 ± 0.9 versus 8.4 ± 0.7 cm (P < .05).
These findings suggest that the hippocampal volume deficit in schizophrenia is not due to net loss of neurons, in agreement with histopathology studies but not with prior H-MR spectroscopy reports. Elevated Cr is consistent with hippocampal hypermetabolism, and its correlation with mIns may also suggest an inflammatory process affecting some cases; these findings may suggest treatment targets and markers to monitor them.
众所周知,精神分裂症与海马结构异常有关。我们使用氢磁共振波谱来检验以下假设:与健康对照相比,这些异常伴随着反映神经元功能障碍的N-乙酰天门冬氨酸(NAA)缺乏。
19例精神分裂症患者(11例男性;平均年龄40.6±10.1岁;平均病程19.5±10.5年)和11例匹配的健康对照(5例男性;平均年龄33.7±10.1岁)在3T下接受磁共振成像和多体素质点分辨波谱(TE/TR,35/1400毫秒)氢磁共振波谱检查,以获取其海马灰质NAA、肌酸(Cr)、胆碱(Cho)和肌醇(mIns)的绝对浓度。采用异方差t检验和协方差分析比较患者与对照。使用异方差t检验比较手动勾勒的海马掩码的双侧体积。
患者海马灰质平均Cr浓度比对照高19%,分别为8.7±2.2与7.4±1.2 mmol/L(P<.05);NAA浓度无差异,分别为8.8±1.6与8.7±1.2 mmol/L;Cho浓度分别为2.3±0.7与2.1±0.3 mmol/L;mIns浓度分别为6.1±1.5与5.2±0.9(所有P>.1)。患者中mIns与Cr呈正相关(r = 0.57,P =.05),而对照中无此相关性。患者双侧海马平均体积低约10%:7.5±0.9与8.4±0.7 cm(P<.05)。
这些发现表明,精神分裂症中海马体积减少并非由于神经元净损失,这与组织病理学研究一致,但与先前的氢磁共振波谱报告不同。Cr升高与海马代谢亢进一致,其与mIns的相关性也可能提示影响某些病例的炎症过程;这些发现可能提示治疗靶点及监测它们的标志物。