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额颞叶痴呆中突发视觉创造力的流行率、时机和网络定位。

Prevalence, Timing, and Network Localization of Emergent Visual Creativity in Frontotemporal Dementia.

机构信息

Department of Neurology, Memory and Aging Center, Weill Institute for Neurosciences, University of California, San Francisco.

Global Brain Health Institute, University of California, San Francisco, and Trinity College Dublin, Dublin, Ireland.

出版信息

JAMA Neurol. 2023 Apr 1;80(4):377-387. doi: 10.1001/jamaneurol.2023.0001.

DOI:10.1001/jamaneurol.2023.0001
PMID:36848111
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9972248/
Abstract

IMPORTANCE

The neurological substrates of visual artistic creativity (VAC) are unknown. VAC is demonstrated here to occur early in frontotemporal dementia (FTD), and multimodal neuroimaging is used to generate a novel mechanistic hypothesis involving dorsomedial occipital cortex enhancement. These findings may illuminate a novel mechanism underlying human visual creativity.

OBJECTIVE

To determine the anatomical and physiological underpinnings of VAC in FTD.

DESIGN, SETTING, AND PARTICIPANTS: This case-control study analyzed records of 689 patients who met research criteria for an FTD spectrum disorder between 2002 and 2019. Individuals with FTD and emergence of visual artistic creativity (VAC-FTD) were matched to 2 control groups based on demographic and clinical parameters: (1) not visually artistic FTD (NVA-FTD) and (2) healthy controls (HC). Analysis took place between September 2019 to December 2021.

MAIN OUTCOMES AND MEASURES

Clinical, neuropsychological, genetic, and neuroimaging data were analyzed to characterize VAC-FTD and compare VAC-FTD with control groups.

RESULTS

Of 689 patients with FTD, 17 (2.5%) met VAC-FTD inclusion criteria (mean [SD] age, 65 [9.7] years; 10 [58.8%] female). NVA-FTD (n = 51; mean [SD] age, 64.8 [7] years; 25 [49.0%] female) and HC (n = 51; mean [SD] age, 64.5 [7.2] years; 25 [49%] female) groups were well matched to VAC-FTD demographically. Emergence of VAC occurred around the time of onset of symptoms and was disproportionately seen in patients with temporal lobe predominant degeneration (8 of 17 [47.1%]). Atrophy network mapping identified a dorsomedial occipital region whose activity inversely correlated, in healthy brains, with activity in regions found within the patient-specific atrophy patterns in VAC-FTD (17 of 17) and NVA-FTD (45 of 51 [88.2%]). Structural covariance analysis revealed that the volume of this dorsal occipital region was strongly correlated in VAC-FTD, but not in NVA-FTD or HC, with a volume in the primary motor cortex corresponding to the right-hand representation.

CONCLUSIONS AND RELEVANCE

This study generated a novel hypothesis about the mechanisms underlying the emergence of VAC in FTD. These findings suggest that early lesion-induced activation of dorsal visual association areas may predispose some patients to the emergence of VAC under certain environmental or genetic conditions. This work sets the stage for further exploration of enhanced capacities arising early in the course of neurodegeneration.

摘要

重要性

视觉艺术创造力(VAC)的神经基础尚不清楚。本研究表明,VAC 发生在额颞叶痴呆(FTD)的早期,并且使用多模态神经影像学生成了一个涉及背内侧枕叶皮层增强的新机制假说。这些发现可能阐明了人类视觉创造力的新机制。

目的

确定 FTD 中 VAC 的解剖学和生理学基础。

设计、设置和参与者:这项病例对照研究分析了 2002 年至 2019 年间符合 FTD 谱系障碍研究标准的 689 名患者的记录。根据人口统计学和临床参数,将具有 FTD 和视觉艺术创造力(VAC-FTD)的个体与 2 个对照组进行匹配:(1)非视觉艺术 FTD(NVA-FTD)和(2)健康对照组(HC)。分析于 2019 年 9 月至 2021 年 12 月进行。

主要结果和测量

分析临床、神经心理学、遗传和神经影像学数据,以描述 VAC-FTD,并将 VAC-FTD 与对照组进行比较。

结果

在 689 名 FTD 患者中,有 17 名(2.5%)符合 VAC-FTD 的纳入标准(平均[标准差]年龄,65[9.7]岁;10[58.8%]为女性)。NVA-FTD(n=51;平均[标准差]年龄,64.8[7]岁;25[49.0%]为女性)和 HC(n=51;平均[标准差]年龄,64.5[7.2]岁;25[49%]为女性)组在人口统计学上与 VAC-FTD 匹配良好。VAC 的出现发生在症状发作的同时,并且在颞叶为主的退化患者中不成比例(17 名中的 8 名[47.1%])。萎缩网络映射确定了一个背内侧枕叶区域,其活动与健康大脑中 VAC-FTD(17 名中的 17 名)和 NVA-FTD(51 名中的 45 名[88.2%])中特定于患者的萎缩模式内发现的区域的活动呈负相关。结构协方差分析表明,在 VAC-FTD 中,该背侧枕叶区域的体积与原发性运动皮层的体积呈强烈相关,而在 NVA-FTD 或 HC 中则没有。

结论和相关性

本研究提出了一个关于 FTD 中 VAC 出现机制的新假设。这些发现表明,早期病变诱导的背侧视觉联合区的激活可能使某些患者在某些环境或遗传条件下出现 VAC。这项工作为进一步探索神经退行性过程早期出现的增强能力奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/656d/9972248/f1d332a8fe6d/jamaneurol-e230001-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/656d/9972248/60528d36ead5/jamaneurol-e230001-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/656d/9972248/62abbc723a43/jamaneurol-e230001-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/656d/9972248/96c680d7390f/jamaneurol-e230001-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/656d/9972248/f1d332a8fe6d/jamaneurol-e230001-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/656d/9972248/60528d36ead5/jamaneurol-e230001-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/656d/9972248/62abbc723a43/jamaneurol-e230001-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/656d/9972248/96c680d7390f/jamaneurol-e230001-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/656d/9972248/f1d332a8fe6d/jamaneurol-e230001-g004.jpg

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