Cecil Kim M, DelBello Melissa P, Sellars Michele C, Strakowski Stephen M
Imaging Research Center, Department of Radiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA.
J Child Adolesc Psychopharmacol. 2003 Winter;13(4):545-55. doi: 10.1089/104454603322724931.
Few studies have examined the neurochemical abnormalities that might be associated with pediatric bipolar disorder. The aim of this study was to use magnetic resonance spectroscopy to evaluate several brain regions implicated in bipolar disorder in children with a mood disorder and a familial risk for bipolar disorder. We hypothesized that these children would exhibit neurochemical differences compared with healthy children of parents without a psychiatric disorder. Specifically, decreased N-acetylaspartate (NAA) and creatine and phosphocreatine (Cr) of the prefrontal cortex and cerebellar vermis would reflect impairments in neuronal function and cellular metabolism, and elevated myo-inositol (mI) would reflect impaired phosphoinositide metabolism, potentially representing early markers of neurophysiologic changes that might underlie the development of bipolar disorder.
Children with a mood disorder and at least one parent with bipolar disorder (n = 9) and healthy children (n = 10) group matched for age (8-12 years), race, sex, education, and Tanner stage were evaluated using the Washington University in St. Louis Kiddie Schedule for Affective Disorders and Schizophrenia. Proton magnetic resonance spectroscopy was acquired using 8-cc volumes within the frontal cortex, frontal white matter, and the cerebellar vermis. Metabolite ratios (NAA/Cr, cholines (Cho)/Cr, mI/Cr, NAA/Cho, NAA/mI, and Cho/mI) and concentrations (NAA, Cr, Cho, and mI) were calculated and compared between groups.
The trend in concentration levels of NAA and Cr was approximately 8% lower for children with a mood disorder than healthy children within the cerebellar vermis. The frontal cortex in children with a mood disorder revealed elevated mI concentration levels, approximately 16% increased, compared with healthy children.
Similar to findings in adults with bipolar disorders, neurochemical abnormalities within the frontal cortex and the cerebellar vermis were present in this preliminary comparison of children with a mood disorder and a familial risk for bipolar disorder. Larger sample sizes are needed to replicate these findings.
很少有研究探讨可能与儿童双相情感障碍相关的神经化学异常。本研究的目的是使用磁共振波谱来评估患有情绪障碍且有双相情感障碍家族风险的儿童中与双相情感障碍相关的几个脑区。我们假设与父母无精神疾病的健康儿童相比,这些儿童会表现出神经化学差异。具体而言,前额叶皮质和小脑蚓部的N-乙酰天门冬氨酸(NAA)、肌酸和磷酸肌酸(Cr)降低将反映神经元功能和细胞代谢受损,而肌醇(mI)升高将反映磷脂酰肌醇代谢受损,这可能代表双相情感障碍发展潜在的神经生理变化的早期标志物。
使用圣路易斯华盛顿大学儿童情感障碍和精神分裂症量表对患有情绪障碍且至少有一位患有双相情感障碍的父母的儿童(n = 9)以及年龄(8 - 12岁)、种族、性别、教育程度和坦纳分期相匹配的健康儿童(n = 10)进行评估。使用8立方厘米的体积在前额叶皮质、额叶白质和小脑蚓部采集质子磁共振波谱。计算并比较两组之间的代谢物比率(NAA/Cr、胆碱(Cho)/Cr、mI/Cr、NAA/Cho、NAA/mI和Cho/mI)和浓度(NAA、Cr、Cho和mI)。
患有情绪障碍的儿童小脑蚓部的NAA和Cr浓度水平趋势比健康儿童低约8%。与健康儿童相比,患有情绪障碍的儿童前额叶皮质的mI浓度水平升高,约升高16%。
与双相情感障碍成人患者的研究结果相似,在对患有情绪障碍且有双相情感障碍家族风险的儿童进行的初步比较中,前额叶皮质和小脑蚓部存在神经化学异常。需要更大的样本量来重复这些发现。