Department of Psychiatry, Psychosomatic Medicine, and Psychotherapy, University Hospital Frankfurt, Goethe University, Frankfurt am Main, Germany.
Max Planck School of Cognition, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.
Schizophr Bull. 2022 May 7;48(3):551-562. doi: 10.1093/schbul/sbab151.
Illuminating neurobiological mechanisms underlying the protective effect of recently discovered common genetic resilience variants for schizophrenia is crucial for more effective prevention efforts. Current models implicate adaptive neuroplastic changes in the visual system and their pro-cognitive effects as a schizophrenia resilience mechanism. We investigated whether common genetic resilience variants might affect brain structure in similar neural circuits.
Using structural magnetic resonance imaging, we measured the impact of an established schizophrenia polygenic resilience score (PRSResilience) on cortical volume, thickness, and surface area in 101 healthy subjects and in a replication sample of 33 224 healthy subjects (UK Biobank).
We observed a significant positive whole-brain correlation between PRSResilience and cortical volume in the right fusiform gyrus (FFG) (r = 0.35; P = .0004). Post-hoc analyses in this cluster revealed an impact of PRSResilience on cortical surface area. The replication sample showed a positive correlation between PRSResilience and global cortical volume and surface area in the left FFG.
Our findings represent the first evidence of a neurobiological correlate of a genetic resilience factor for schizophrenia. They support the view that schizophrenia resilience emerges from strengthening neural circuits in the ventral visual pathway and an increased capacity for the disambiguation of social and nonsocial visual information. This may aid psychosocial functioning, ameliorate the detrimental effects of subtle perceptual and cognitive disturbances in at-risk individuals, and facilitate coping with the cognitive and psychosocial consequences of stressors. Our results thus provide a novel link between visual cognition, the vulnerability-stress concept, and schizophrenia resilience models.
阐明最近发现的精神分裂症常见遗传弹性变异体的保护作用的神经生物学机制对于更有效的预防措施至关重要。目前的模型表明,视觉系统的适应性神经可塑性变化及其促进认知的作用是精神分裂症弹性的一种机制。我们研究了常见的遗传弹性变体是否可能以类似的神经回路影响大脑结构。
我们使用结构磁共振成像,测量了一个已建立的精神分裂症多基因弹性评分(PRSResilience)对 101 名健康受试者和 33224 名健康受试者(英国生物库)的皮质体积、厚度和表面积的影响。
我们观察到 PRSResilience 与右侧梭状回(FFG)皮质体积之间存在显著的全脑正相关(r = 0.35;P =.0004)。在这个聚类中进行的事后分析表明,PRSResilience 对皮质表面积有影响。复制样本显示 PRSResilience 与左侧 FFG 的总皮质体积和表面积之间存在正相关。
我们的发现代表了第一个与精神分裂症遗传弹性因素相关的神经生物学相关性的证据。它们支持这样一种观点,即精神分裂症的弹性来自于加强腹侧视觉通路中的神经回路,并提高对社会和非社会视觉信息的辨别能力。这可能有助于心理社会功能,减轻高危个体中微妙的感知和认知障碍的不利影响,并有助于应对应激源的认知和心理社会后果。因此,我们的研究结果为视觉认知、脆弱性-应激概念和精神分裂症弹性模型之间提供了一个新的联系。