Abdallah Chadi G, Niciu Mark J, Fenton Lisa R, Fasula Madonna K, Jiang Lihong, Black Anne, Rothman Douglas L, Mason Graeme F, Sanacora Gerard
Abraham Ribicoff Research Facilities, Connecticut Mental Health Center (CMHC), Department of Psychiatry, Yale University School of Medicine, New Haven, Conn., USA.
Psychother Psychosom. 2014;83(5):298-307. doi: 10.1159/000361078. Epub 2014 Aug 6.
Previous studies have demonstrated that antidepressant medication and electroconvulsive therapy increase occipital cortical γ-aminobutyric acid (GABA) in major depressive disorder (MDD), but a small pilot study failed to show a similar effect of cognitive-behavioral therapy (CBT) on occipital GABA. In light of these findings we sought to determine if baseline GABA levels predict treatment response and to broaden the analysis to other metabolites and neurotransmitters in this larger study.
A total of 40 MDD outpatients received baseline proton magnetic resonance spectroscopy (1H-MRS), and 30 subjects completed both pre- and post-CBT 1H-MRS; 9 CBT nonresponders completed an open-label medication phase followed by an additional/3rd 1H-MRS. The magnitude of treatment response was correlated with occipital amino acid neurotransmitter levels.
Baseline GABA did not predict treatment outcome. Furthermore, there was no significant effect of CBT on GABA levels. However, we found a significant group × time interaction (F1, 28 = 6.30, p = 0.02), demonstrating reduced glutamate in CBT responders, with no significant glutamate change in CBT nonresponders.
These findings corroborate the lack of effect of successful CBT on occipital cortical GABA levels in a larger sample. A reduction in glutamate levels following treatment, on the other hand, correlated with successful CBT and antidepressant medication response. Based on this finding and other reports, decreased occipital glutamate may be an antidepressant response biomarker. Healthy control comparator and nonintervention groups may shed light on the sensitivity and specificity of these results.
既往研究表明,抗抑郁药物和电休克治疗可增加重度抑郁症(MDD)患者枕叶皮质γ-氨基丁酸(GABA)水平,但一项小型先导研究未能显示认知行为疗法(CBT)对枕叶GABA有类似作用。鉴于这些发现,我们试图确定基线GABA水平是否可预测治疗反应,并在这项更大规模的研究中将分析范围扩大至其他代谢物和神经递质。
共有40名MDD门诊患者接受了基线质子磁共振波谱(1H-MRS)检查,30名受试者完成了CBT前后的1H-MRS检查;9名CBT无反应者完成了开放标签药物治疗阶段,随后进行了第3次1H-MRS检查。治疗反应程度与枕叶氨基酸神经递质水平相关。
基线GABA不能预测治疗结果。此外。CBT对GABA水平无显著影响。然而,我们发现了显著的组×时间交互作用(F1, 28 = 6.30,p = 0.02),表明CBT反应者的谷氨酸水平降低,而CBT无反应者的谷氨酸水平无显著变化。
这些发现证实了在更大样本中成功的CBT对枕叶皮质GABA水平无影响。另一方面,治疗后谷氨酸水平的降低与成功的CBT及抗抑郁药物反应相关。基于这一发现和其他报告,枕叶谷氨酸水平降低可能是一种抗抑郁反应生物标志物。健康对照比较组和非干预组可能有助于阐明这些结果的敏感性和特异性。