Longitudinal Changes in Structural Connectivity in Young People at High Genetic Risk for Bipolar Disorder.

G. Roberts, Alistair Perry, K. Ridgway, V. Leung, Megan Campbell, R. Lenroot, P. Mitchell, M. Breakspear
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引用次数: 6

Abstract

OBJECTIVE Recent studies of patients with bipolar disorder or at high genetic risk reveal structural dysconnections among key brain networks supporting cognitive and affective processes. Understanding the longitudinal trajectories of these networks across the peak age range of bipolar disorder onset could inform mechanisms of illness onset or resilience. METHODS Longitudinal diffusion-weighted MRI and phenotypic data were acquired at baseline and after 2 years in 183 individuals ages 12-30 years in two cohorts: 97 unaffected individuals with a first-degree relative with bipolar disorder (the high-risk group) and 86 individuals with no family history of mental illness (the control group). Whole-brain structural networks were derived using tractography, and longitudinal changes in these networks were studied using network-based statistics and mixed linear models. RESULTS Both groups showed widespread longitudinal changes, comprising both increases and decreases in structural connectivity, consistent with a shared neurodevelopmental process. On top of these shared changes, high-risk participants showed weakening of connectivity in a network encompassing the left inferior and middle frontal areas, left striatal and thalamic structures, the left fusiform, and right parietal and occipital regions. Connections among these regions strengthened in the control group, whereas they weakened in the high-risk group, shifting toward a cohort with established bipolar disorder. There was marginal evidence for even greater network weakening in those who had their first manic or hypomanic episode before follow-up. CONCLUSIONS Neurodevelopment from adolescence into early adulthood is associated with a substantial reorganization of structural brain networks. Differences in these maturational processes occur in a multisystem network in individuals at high genetic risk of bipolar disorder. This may represent a novel candidate to understand resilience and predict conversion to bipolar disorder.
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双相情感障碍高遗传风险年轻人结构连通性的纵向变化。
目的:最近对双相情感障碍患者或高遗传风险患者的研究揭示了支持认知和情感过程的关键脑网络之间的结构异常。了解这些网络在双相情感障碍发病高峰年龄范围内的纵向轨迹可以为疾病发病或恢复机制提供信息。方法:对183名年龄在12-30岁的患者进行纵向弥散加权MRI和2年后的表型数据分析,分为两组:97名未受影响的一级亲属患有双相情感障碍的患者(高危组)和86名无精神疾病家族史的患者(对照组)。全脑结构网络通过神经束成像得到,并使用基于网络的统计和混合线性模型研究这些网络的纵向变化。结果两组均表现出广泛的纵向变化,包括结构连通性的增加和减少,与共同的神经发育过程一致。在这些共同的变化之上,高风险参与者表现出包括左下额区和中额区、左纹状体和丘脑结构、左梭状体、右顶叶和枕叶区域的网络连通性减弱。这些区域之间的联系在对照组中得到加强,而在高风险组中减弱,并向确诊双相情感障碍的队列转移。有边缘证据表明,在随访前首次出现躁狂或轻度躁狂发作的患者中,网络弱化程度更大。结论从青春期到成年早期的神经发育与大脑结构网络的大量重组有关。这些成熟过程的差异发生在双相情感障碍高遗传风险个体的多系统网络中。这可能代表了一个新的候选人来理解弹性和预测转换为双相情感障碍。
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