Gonzalez Sara, Vasavada Megha, Njau Stephanie, Sahib Ashish K, Espinoza Randall, Narr Katherine L, Leaver Amber M
Ahmanson-Lovelace Brain Mapping Center, Department of Neurology, University of California Los Angeles.
Department of Psychiatry and Biobehavioral Sciences, University of California Los Angeles.
Neurol Psychiatry Brain Res. 2020 Dec;38:5-11. doi: 10.1016/j.npbr.2020.08.006. Epub 2020 Aug 28.
Ketamine provides rapid antidepressant response in those struggling with major depressive disorder (MDD). This study measured acute changes in brain activity over 24 hours after a single infusion of ketamine using arterial spin labeled (ASL) functional magnetic resonance imaging (fMRI) in patients with MDD. ASL is a novel technique that provides quantitative values to measure cerebral blood flow (CBF).
A single sub-anesthetic dose (0.5 mg/kg) of ketamine was delivered intravenously. Treatment-refractory patients (n=11) were assessed at: Baseline (pre-infusion), and approximately 1hr, 6hrs, and 24hrs post-infusion. Linear mixed-effects models detected changes in CBF with respect to treatment outcome, and results were corrected for false discovery rate (FDR).
After ketamine infusion, increased CBF was observed in the thalamus, while decreased CBF was observed in lateral occipital cortex in all patients. Time-by-response interactions were noted in ventral basal ganglia and medial prefrontal cortex, where CBF change differed according to antidepressant response.
Modest sample size is a limitation of this pilot study; strict statistical correction and visualization of single-subject data attempted to ameliorate this issue.
In this pilot study, a sub-anesthetic dose of ketamine was associated with acute neurofunctional changes that may be consistent with altered attention, specifically increased thalamus activity coupled with decreased cortical activity. By contrast, antidepressant response to ketamine was associated with changes in reward-system regions, specifically ventral basal ganglia and medial prefrontal cortex. Further work is needed to determine whether these results generalize to larger samples and/or serial ketamine infusions associated with longer-lasting clinical effects.
氯胺酮能使重度抑郁症(MDD)患者迅速产生抗抑郁反应。本研究采用动脉自旋标记(ASL)功能磁共振成像(fMRI)测量了MDD患者单次输注氯胺酮后24小时内大脑活动的急性变化。ASL是一种可提供测量脑血流量(CBF)定量值的新技术。
静脉注射单次亚麻醉剂量(0.5mg/kg)的氯胺酮。对治疗难治性患者(n = 11)在基线(输注前)以及输注后约1小时、6小时和24小时进行评估。线性混合效应模型检测了与治疗结果相关的CBF变化,并对结果进行了错误发现率(FDR)校正。
输注氯胺酮后,所有患者丘脑的CBF均增加,而枕外侧皮质的CBF减少。在腹侧基底神经节和内侧前额叶皮质观察到时间与反应的相互作用,其中CBF变化因抗抑郁反应而异。
样本量较小是本初步研究的一个局限性;严格的统计校正和单受试者数据可视化试图改善这一问题。
在本初步研究中,亚麻醉剂量的氯胺酮与急性神经功能变化相关,这些变化可能与注意力改变一致,特别是丘脑活动增加和皮质活动减少。相比之下,氯胺酮的抗抑郁反应与奖赏系统区域的变化相关,特别是腹侧基底神经节和内侧前额叶皮质。需要进一步研究以确定这些结果是否适用于更大样本和/或与更持久临床效果相关的氯胺酮系列输注。