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Cortical Grey Matter and Subcortical White Matter Brain Microstructural Changes in Schizophrenia Are Localised and Age Independent: A Case-Control Diffusion Tensor Imaging Study

机译:精神分裂症的皮层灰色物质和皮层下白色物质大脑微结构变化是局部的且与年龄无关:病例对照扩散张量成像研究

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摘要

It is still unknown whether the structural brain impairments that characterize schizophrenia (SZ) worsen during the lifetime. Here, we aimed to describe age-related microstructural brain changes in cortical grey matter and subcortical white matter of patients affected by SZ. In this diffusion tensor imaging study, we included 69 patients diagnosed with SZ and 69 healthy control (HC) subjects, age and gender matched. We carried out analyses of covariance, with diagnosis as fixed factor and brain diffusion-related parameters as dependent variables, and controlled for the effect of education. White matter fractional anisotropy decreased in the entire age range spanned (18–65 years) in both SZ and HC and was significantly lower in younger patients with SZ, with no interaction (age by diagnosis) effect in fiber tracts including corpus callosum, corona radiata, thalamic radiations and external capsule. Also, grey matter mean diffusivity increased in the entire age range in both SZ and HC and was significantly higher in younger patients, with no age by diagnosis interaction in the left frontal operculum cortex, left insula and left planum polare and in the right temporal pole and right intracalcarine cortex. In individuals with SZ we found that localized brain cortical and white matter subcortical microstructural impairments appear early in life but do not worsen in the 18–65 year age range.
机译:尚不知道精神分裂症(SZ)的结构性脑损伤是否会在其一生中加重。在这里,我们旨在描述受SZ影响的患者的年龄相关的大脑皮层灰质和皮层下白质的微结构大脑变化。在这项扩散张量成像研究中,我们纳入了69位被诊断为SZ的患者和69位年龄和性别相匹配的健康对照(HC)受试者。我们进行了协方差分析,以诊断为固定因素,以脑扩散相关参数为因变量,并控制了教育效果。在SZ和HC的整个年龄段(18-65岁)中,白质分数各向异性均降低,而在年轻的SZ患者中,白质分数各向异性显着降低,并且在包括体,电晕放射线在内的纤维束中无相互作用(根据诊断年龄) ,丘脑辐射和外囊。此外,在SZ和HC的整个年龄范围内,灰质平均扩散率均增加,而在年轻患者中,灰质平均扩散率显着更高,通过额叶皮层,左岛突和左平面极和右颞极的诊断相互作用,没有年龄差异和右calc骨皮质。在SZ患者中,我们发现局部的大脑皮层和白质皮层下微结构损伤在生命的早期出现,但在18-65岁的年龄范围内并没有恶化。

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