Brambilla Paolo, Stanley Jeffrey A, Nicoletti Mark A, Sassi Roberto B, Mallinger Alan G, Frank Ellen, Kupfer David, Keshavan Matcheri S, Soares Jair C
Division of Mood and Anxiety Disorders, Department of Psychiatry, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
J Affect Disord. 2005 May;86(1):61-7. doi: 10.1016/j.jad.2004.12.008.
Magnetic resonance spectroscopy studies (MRS) reported abnormally low levels of N-acetylaspartate (NAA, a marker of neuronal integrity) in dorsolateral prefrontal cortex (DLPFC) of adult bipolar patients, suggesting possible neuronal dysfunction. Furthermore, recent MRS reports suggested possible lithium-induced increase in NAA levels in bipolar patients. We examined with in vivo (1)H MRS NAA levels in the DLPFC of adult bipolar patients.
Ten DSM-IV bipolar disorder patients (6 lithium-treated, 4 drug-free) and 32 healthy controls underwent a short echo-time 1H MRS session, which localized an 8 cm3 single-voxel in the left DLPFC using a STEAM sequence.
No significant differences between the two groups were found for NAA, choline-containing molecules (GPC+PC), or phosphocreatine plus creatine (PCr+Cr) (Student t-test, p > 0.05). Nonetheless, NAA/PCr+Cr ratios were significantly increased in lithium-treated bipolar subjects compared to unmedicated patients and healthy controls (Mann-Whitney U-test, p < 0.05).
Relatively small sample size may have reduced the statistical power of our analyses and the utilization of a single-voxel approach did not allow for the examination of other cortical brain areas.
This study did not find abnormally reduced levels of NAA in left DLPFC of adult bipolar patients, in a sample of patients who were mostly on medications. However, elevated NAA/PCr+Cr ratios were shown in lithium-treated bipolar patients. Longitudinal 1H MRS studies should further examine NAA levels in prefrontal cortex regions in untreated bipolar patients before and after mood stabilizing treatment.
磁共振波谱研究(MRS)报告称,成年双相情感障碍患者背外侧前额叶皮质(DLPFC)中的N-乙酰天门冬氨酸(NAA,一种神经元完整性标志物)水平异常低,提示可能存在神经元功能障碍。此外,最近的MRS报告表明,双相情感障碍患者可能因锂治疗导致NAA水平升高。我们使用活体(1)H MRS检测成年双相情感障碍患者DLPFC中的NAA水平。
10名符合《精神疾病诊断与统计手册》第四版(DSM-IV)的双相情感障碍患者(6名接受锂治疗,4名未服药)和32名健康对照者接受了短回波时间的1H MRS检查,使用激励回波采集模式(STEAM)序列在左侧DLPFC定位一个8立方厘米的单体素。
两组在NAA、含胆碱分子(GPC+PC)或磷酸肌酸加肌酸(PCr+Cr)方面未发现显著差异(学生t检验,p>0.05)。然而,与未服药患者和健康对照相比,接受锂治疗的双相情感障碍患者的NAA/PCr+Cr比值显著升高(曼-惠特尼U检验,p<0.05)。
样本量相对较小可能降低了我们分析的统计效力,并且使用单体素方法无法检查其他皮质脑区。
在大多数正在服药的患者样本中,本研究未发现成年双相情感障碍患者左侧DLPFC中NAA水平异常降低。然而,接受锂治疗的双相情感障碍患者的NAA/PCr+Cr比值升高。纵向1H MRS研究应进一步检查未治疗的双相情感障碍患者在情绪稳定治疗前后前额叶皮质区域的NAA水平。