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

机译:双相情感障碍高遗传风险年轻人结构连通性的纵向变化

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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.
机译:目的:最近对双相情感障碍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大脑网络之间的结构性不连贯。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发病或恢复力的机制提供信息。方法:在基线和 2 年后对 183 名 12-30 岁的个体在两个队列中获取纵向弥散加权 MRI 和表型数据:97 名一级亲属患有双相情感障碍的未受影响的个体(高危组)和 86 名没有精神疾病家族史的个体(对照组)。使用牵引成像推导全脑结构网络,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:两组都表现出广泛的纵向变化,包括结构连接的增加和减少,与共同的神经发育过程一致。除了这些共同的变化之外,高风险参与者在包括左侧额下和中部区域、左侧纹状体和丘脑结构、左侧梭形以及右侧顶骨和枕骨区域在内的网络中表现出连接性减弱。这些区域之间的联系在对照组中加强,而在高危组中减弱,转向已确定双相情感障碍的队列。有边际证据表明,在随访前首次出现躁狂或轻躁狂发作的患者中,网络减弱幅度更大。结论:从青春期到成年早期的神经发育与结构性脑网络的实质性重组有关。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。这可能代表了一种新的候选者,可以理解复原力并预测双相情感障碍的转化。

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