School of Biological Sciences, Nanyang Technological University, Singapore, Singapore.
Neurosci Biobehav Rev. 2013 Mar;37(3):418-35. doi: 10.1016/j.neubiorev.2013.01.003. Epub 2013 Jan 12.
Longitudinal studies of biological domains in bipolar disorder (BD) are crucial in determining if such baseline changes are progressive. We reviewed reported studies of longitudinal brain structural/functional magnetic resonance imaging (MRI) and neuropsychological changes in BD through November 2012. Longitudinal brain structural MRI studies suggest cortical and subcortical abnormalities within networks subserving emotional regulation. There is evidence of neuroprogressive loss of gray matter volume in prefrontal and anterior cingulate cortex and the subgenual region, with less consistent findings in temporal and subcortical regions. Abnormal amygdala neurodevelopment is noted in adolescent onset BD and possible changes in hippocampus require further evaluation. The fewer reported longitudinal functional MRI studies suggest neurobiological changes in activation patterns involving fronto-limbic circuitry which relate to different illness phase and mood states. Early onset pediatric/adolescent BD may signify a more malignant course of illness in which extensive and executive neurocognitive deficits are found early and may persist, with some potential for improvement during remission and perhaps with treatment. Future studies should include larger samples, combine investigational modalities, incorporate genetic profiles, consider standardization of assessments and collaborative ventures across institutions, selection of more homogeneous subgroups and track neurobiological changes longer to clarify trajectories of changes.
双相障碍(BD)中生物学领域的纵向研究对于确定这些基线变化是否具有进展性至关重要。我们回顾了截至 2012 年 11 月有关 BD 的纵向脑结构/功能磁共振成像(MRI)和神经心理学变化的报告研究。纵向脑结构 MRI 研究表明,在情绪调节网络中存在皮质和皮质下异常。有证据表明前额叶和前扣带回皮质以及亚属区域的灰质体积存在神经进行性丧失,而颞叶和皮质下区域的发现则不太一致。在青少年起病的 BD 中注意到杏仁核神经发育异常,而海马体的可能变化需要进一步评估。报告的纵向功能 MRI 研究较少,表明涉及额-边缘回路的激活模式存在神经生物学变化,这与不同的疾病阶段和情绪状态有关。早发性儿科/青少年 BD 可能意味着疾病病程更严重,在缓解期和治疗期间可能会有所改善,早期就会出现广泛的和执行性神经认知缺陷,并可能持续存在。未来的研究应包括更大的样本量,结合研究模式,纳入遗传特征,考虑评估的标准化和机构间的合作,选择更同质的亚组,并更长时间地跟踪神经生物学变化,以阐明变化的轨迹。