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Fronto-striatal gray matter contributions to discrimination learning in Parkinsons disease

机译:额叶纹状体灰质对帕金森病歧视学习的贡献

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摘要

Discrimination learning deficits in Parkinson's disease (PD) have been well-established. Using both behavioral patient studies and computational approaches, these deficits have typically been attributed to dopamine imbalance across the basal ganglia. However, this explanation of impaired learning in PD does not account for the possible contribution of other pathological changes that occur in the disease process, importantly including gray matter loss. To address this gap in the literature, the current study explored the relationship between fronto-striatal gray matter atrophy and learning in PD. We employed a discrimination learning task and computational modeling in order to assess learning rates in non-demented PD patients. Behaviorally, we confirmed that learning rates were reduced in patients relative to controls. Furthermore, voxel-based morphometry imaging analysis demonstrated that this learning impairment was directly related to gray matter loss in discrete fronto-striatal regions (specifically, the ventromedial prefrontal cortex, inferior frontal gyrus and nucleus accumbens). These findings suggest that dopaminergic imbalance may not be the sole determinant of discrimination learning deficits in PD, and highlight the importance of factoring in the broader pathological changes when constructing models of learning in PD.
机译:帕金森氏病(PD)的歧视性学习缺陷已得到充分证实。使用行为患者研究和计算方法,这些缺陷通常归因于整个基底神经节中的多巴胺失衡。但是,这种对PD学习障碍的解释不能解释疾病过程中发生的其他病理变化的可能贡献,重要的是包括灰质损失。为了弥补文献中的这一空白,本研究探索了额叶纹状体灰质萎缩与PD学习之间的关系。为了评估非痴呆型PD患者的学习率,我们采用了歧视性学习任务和计算模型。从行为上,我们证实相对于对照组,患者的学习率降低了。此外,基于体素的形态成像分析表明,这种学习障碍与离散的额叶纹状体区域(特别是腹侧前额叶皮层,额额下回和伏隔核)中的灰质损失直接相关。这些发现表明,多巴胺能失衡可能不是歧视PD学习缺陷的唯一决定因素,并突出了在构建PD学习模型时应考虑更广泛的病理变化的重要性。

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