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Finding the imposter: brain connectivity of lesions causing delusional misidentifications

机译:寻找冒名顶替者:导致错觉误诊的病变的大脑连通性

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>See McKay and Furl (doi:) for a scientific commentary on this article.Focal brain injury can sometimes lead to bizarre symptoms, such as the delusion that a family member has been replaced by an imposter (Capgras syndrome). How a single brain lesion could cause such a complex disorder is unclear, leading many to speculate that concurrent delirium, psychiatric disease, dementia, or a second lesion is required. Here we instead propose that Capgras and other delusional misidentification syndromes arise from single lesions at unique locations within the human brain connectome. This hypothesis is motivated by evidence that symptoms emerge from sites functionally connected to a lesion location, not just the lesion location itself. First, 17 cases of lesion-induced delusional misidentifications were identified and lesion locations were mapped to a common brain atlas. Second, lesion network mapping was used to identify brain regions functionally connected to the lesion locations. Third, regions involved in familiarity perception and belief evaluation, two processes thought to be abnormal in delusional misidentifications, were identified using meta-analyses of previous functional magnetic resonance imaging studies. We found that all 17 lesion locations were functionally connected to the left retrosplenial cortex, the region most activated in functional magnetic resonance imaging studies of familiarity. Similarly, 16 of 17 lesion locations were functionally connected to the right frontal cortex, the region most activated in functional magnetic resonance imaging studies of expectation violation, a component of belief evaluation. This connectivity pattern was highly specific for delusional misidentifications compared to four other lesion-induced neurological syndromes (P < 0.0001). Finally, 15 lesions causing other types of delusions were connected to expectation violation (P < 0.0001) but not familiarity regions, demonstrating specificity for delusion content. Our results provide potential neuroanatomical correlates for impaired familiarity perception and belief evaluation in patients with delusional misidentifications. More generally, we demonstrate a mechanism by which a single lesion can cause a complex neuropsychiatric syndrome based on that lesion’s unique pattern of functional connectivity, without the need for pre-existing or hidden pathology.
机译:>有关本文的科学评论,请参见McKay和Furl(doi:)。局灶性脑损伤有时会导致奇怪的症状,例如妄想家属被冒名顶替者取代(卡普格拉斯综合征) )。目前尚不清楚单个脑部病变如何引起这种复杂的疾病,导致许多人推测需要并发del妄,精神病,痴呆或第二种病变。在这里,我们提出,卡普格拉斯和其他妄想误认综合征是由人脑连接组内唯一位置的单个病变引起的。该假设的依据是,症状从功能上与病变部位相连的部位出现,而不仅仅是病变部位本身。首先,确定了17例由病变引起的妄想误认的病例,并将病变位置映射到普通的大脑图集。其次,病变网络映射用于识别功能连接到病变位置的大脑区域。第三,使用先前的功能磁共振成像研究的荟萃分析,确定了参与熟悉感知和信念评估的区域,这两个过程被认为是妄想错误识别中的异常过程。我们发现,所有17个病变部位均在功能上连接至左侧脾后皮质,这是熟悉的功能性磁共振成像研究中最活跃的区域。同样,在17个病变部位中有16个在功能上与右额叶皮层相连,这是功能磁共振成像研究中对预期违规(信念评估的一部分)最活跃的区域。与其他四个病变引起的神经系统综合症相比,这种连接方式对于错觉误区具有高度特异性(P <0.0001)。最终,导致其他类型妄想的15个病变与预期违规(P <0.0001)相关,但与熟悉区域无关,这说明了妄想含量的特异性。我们的结果提供了潜在的神经解剖学相关性,以减少错觉误诊患者的熟悉感和信念评估。更笼统地说,我们演示了一种机制,该机制可以基于单个病变的功能连接的独特模式来导致复杂的神经精神病综合症,而无需预先存在或隐藏的病理学。

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