Pediatric Brain Research and Intervention Center, Institute for Juvenile Research, Colbeth Clinic, University of Illinois at Chicago, IL 60608, USA.
J Am Acad Child Adolesc Psychiatry. 2012 Feb;51(2):157-170.e5. doi: 10.1016/j.jaac.2011.10.019. Epub 2011 Dec 23.
The current study examined the impact of risperidone and divalproex on affective and working memory circuitry in patients with pediatric bipolar disorder (PBD).
This was a six-week, double-blind, randomized trial of risperidone plus placebo versus divalproex plus placebo for patients with mania (n = 21; 13.6 ± 2.5 years of age). Functional magnetic resonance imaging (fMRI) outcomes were measured using a block design, affective, N-back task with angry, happy, and neutral face stimuli at baseline and at 6-week follow-up. Matched healthy controls (HC; n = 15, 14.5 ± 2.8 years) were also scanned twice.
In post hoc analyses on the significant interaction in a 3×2×2 analysis of variance (ANOVA) that included patient groups and HC, the risperidone group showed greater activation after treatment in response to the angry face condition in the left subgenual anterior cingulate cortex (ACC) and striatum relative to the divalproex group. The divalproex group showed greater activation relative to the risperidone group in the left inferior frontal gyrus and right middle temporal gyrus. Over the treatment course, the risperidone group showed greater change in activation in the left ventral striatum than the divalproex group, and the divalproex group showed greater activation change in left inferior frontal gyrus and right middle temporal gyrus than the risperidone group. Furthermore, each patient group showed increased activation relative to HC in fronto-striato-temporal regions over time. The happy face condition was potentially less emotionally challenging in this study and did not elicit notable findings.
When patients performed a working memory task under emotional duress inherent in the paradigm, divalproex enhanced activation in a fronto-temporal circuit whereas risperidone increased activation in the dopamine (D₂) receptor-rich ventral striatum. Clinical trial registration information-Risperidone and Divalproex Sodium With MRI Assessment in Pediatric Bipolar; http://www.clinicaltrials.gov; NCT00176202.
本研究旨在探讨利培酮和丙戊酸钠对儿科双相障碍(PBD)患者情感和工作记忆回路的影响。
这是一项为期 6 周的双盲、随机试验,比较利培酮联合安慰剂与丙戊酸钠联合安慰剂治疗躁狂症患者(n=21;年龄 13.6±2.5 岁)的效果。使用块设计、情感 N 回任务以及愤怒、快乐和中性面孔刺激,在基线和 6 周随访时测量功能磁共振成像(fMRI)结果。还对 15 名匹配的健康对照者(HC;n=15,14.5±2.8 岁)进行了两次扫描。
在包括患者组和 HC 的 3×2×2 方差分析(ANOVA)的事后分析中,发现利培酮组在治疗后对愤怒面孔的反应中,左侧前扣带回皮质(ACC)和纹状体的激活程度高于丙戊酸钠组。丙戊酸钠组在左额下回和右颞中回的激活程度高于利培酮组。在治疗过程中,利培酮组左侧腹侧纹状体的激活变化大于丙戊酸钠组,而丙戊酸钠组左侧额下回和右颞中回的激活变化大于利培酮组。此外,随着时间的推移,每个患者组在额-纹状体-颞叶区域的激活均高于 HC。在本研究中,快乐面孔条件的情绪挑战性较低,没有发现显著的结果。
当患者在范式固有的情绪压力下执行工作记忆任务时,丙戊酸钠增强了额-颞叶回路的激活,而利培酮增加了富含多巴胺(D₂)受体的腹侧纹状体的激活。临床试验注册信息-利培酮和丙戊酸钠与 MRI 评估儿科双相;http://www.clinicaltrials.gov;NCT00176202。