Department of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Department of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
J Affect Disord. 2023 Jun 15;331:238-244. doi: 10.1016/j.jad.2023.03.025. Epub 2023 Mar 15.
In order to identify biomarkers of prodromal mood disorders, we examined functional brain activation in children and adolescent at familial risk for bipolar disorder.
Offspring of parents with bipolar I disorder (at-risk youth; N = 115, mean ± SD age: 13.6 ± 2.7; 54 % girls) and group-matched offspring of healthy parents (healthy controls; N = 58, mean ± SD age: 14.2 ± 3.0; 53 % girls) underwent functional magnetic resonance imaging while performing a continuous performance task with emotional and neutral distracters. At baseline, at-risk youth had no history of mood episodes or psychotic disorders. Subjects were followed longitudinally until developing their first mood episode or being lost to follow-up. Standard event-related region-of-interest (ROI) analyses were performed to compare brain activation at baseline between groups and in survival analyses.
At baseline, at-risk youth exhibited reduced activation to emotional distracters in the right ventrolateral prefrontal cortex (VLPFC) (p = 0.04). Activation was not significantly altered in additional ROIs, including left VLPFC, bilateral amygdala, caudate, or putamen. In those at-risk youth who developed their first mood episode during follow-up (n = 17), baseline increased activation in right VLPFC, right caudate, and right putamen activation predicted the development of a mood episode.
Sample size of converters, loss to follow-up, and number of statistical comparisons.
We found preliminary evidence that a reduced activation in right VLPFC might be a marker of risk for or resilience to mood disorders in at-risk youth. Conversely, an increased activation in the right VLPFC, caudate, and putamen might indicate an increased risk for the later development of their first mood episode.
为了识别前驱期心境障碍的生物标志物,我们研究了双相障碍家族高危儿童和青少年的大脑功能激活。
双相 I 障碍父母的子女(高危青年;N=115,平均年龄±标准差:13.6±2.7;54%为女孩)和匹配的健康父母的子女(健康对照组;N=58,平均年龄±标准差:14.2±3.0;53%为女孩)在执行带有情绪和中性分心物的连续表现任务时接受了功能磁共振成像。在基线时,高危青年没有心境发作或精神病障碍的病史。这些受试者被进行纵向随访,直到他们首次出现心境发作或失访。对两组的基线脑激活进行标准的基于事件的感兴趣区(ROI)分析,并进行生存分析。
在基线时,高危青年在右侧腹外侧前额叶皮质(VLPFC)对情绪分心物的激活减少(p=0.04)。在其他 ROI 中,包括左侧 VLPFC、双侧杏仁核、尾状核和壳核,激活并没有显著改变。在随访期间首次出现心境发作的高危青年(n=17)中,基线时右侧 VLPFC、右侧尾状核和右侧壳核的激活增加,预测了心境发作的发生。
转化者的样本量、失访和统计比较的数量。
我们发现初步证据表明,右侧 VLPFC 的激活减少可能是高危青年发生心境障碍的风险或对心境障碍的韧性的标志物。相反,右侧 VLPFC、尾状核和壳核的激活增加可能表明首次心境发作的风险增加。