Abdallah Chadi G, Jackowski Andrea, Salas Ramiro, Gupta Swapnil, Sato João R, Mao Xiangling, Coplan Jeremy D, Shungu Dikoma C, Mathew Sanjay J
Clinical Neuroscience Division, National Center for PTSD, VA CT Healthcare System, West Haven, CT, USA.
Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Neuropsychopharmacology. 2017 Jul;42(8):1739-1746. doi: 10.1038/npp.2017.49. Epub 2017 Mar 8.
Animal models of depression repeatedly showed stress-induced nucleus accumbens (NAc) hypertrophy. Recently, ketamine was found to normalize this stress-induced NAc structural growth. Here, we investigated NAc structural abnormalities in major depressive disorder (MDD) in two cohorts. Cohort A included a cross-sectional sample of 34 MDD and 26 healthy control (HC) subjects, with high-resolution magnetic resonance imaging (MRI) to estimate NAc volumes. Proton MR spectroscopy (H MRS) was used to divide MDD subjects into two subgroups: glutamate-based depression (GBD) and non-GBD. A separate longitudinal sample (cohort B) included 16 MDD patients who underwent MRI at baseline then 24 h following intravenous infusion of ketamine (0.5 mg/kg). In cohort A, we found larger left NAc volume in MDD compared to controls (Cohen's d=1.05), but no significant enlargement in the right NAc (d=0.44). Follow-up analyses revealed significant subgrouping effects on the left (d⩾1.48) and right NAc (d⩾0.95) with larger bilateral NAc in non-GBD compared to GBD and HC. NAc volumes were not different between GBD and HC. In cohort B, ketamine treatment reduced left NAc, but increased left hippocampal, volumes in patients achieving remission. The cross-sectional data provided the first evidence of enlarged NAc in patients with MDD. These NAc abnormalities were limited to patients with non-GBD. The pilot longitudinal data revealed a pattern of normalization of left NAc and hippocampal volumes particularly in patients who achieved remission following ketamine treatment, an intriguing preliminary finding that awaits replication.
抑郁症的动物模型反复显示出应激诱导的伏隔核(NAc)肥大。最近,发现氯胺酮可使这种应激诱导的NAc结构生长恢复正常。在此,我们在两个队列中研究了重度抑郁症(MDD)患者的NAc结构异常情况。队列A包括34名MDD患者和26名健康对照(HC)受试者的横断面样本,通过高分辨率磁共振成像(MRI)来估计NAc体积。质子磁共振波谱(H MRS)用于将MDD患者分为两个亚组:基于谷氨酸的抑郁症(GBD)和非GBD。另一个纵向样本(队列B)包括16名MDD患者,他们在基线时接受了MRI检查,然后在静脉注射氯胺酮(0.5mg/kg)后24小时再次接受检查。在队列A中,我们发现MDD患者的左侧NAc体积比对照组更大(Cohen's d=1.05),但右侧NAc没有明显增大(d=0.44)。后续分析显示,在左侧(d⩾1.48)和右侧NAc(d⩾0.95)存在显著的亚组效应,与GBD和HC相比,非GBD患者的双侧NAc更大。GBD患者和HC患者的NAc体积没有差异。在队列B中,氯胺酮治疗使达到缓解的患者左侧NAc体积减小,但左侧海马体积增加。横断面数据首次证明了MDD患者存在NAc增大的情况。这些NAc异常仅限于非GBD患者。初步的纵向数据显示,尤其是在氯胺酮治疗后达到缓解的患者中,左侧NAc和海马体积有恢复正常的趋势,这是一个有趣的初步发现,有待重复验证。