额颞叶痴呆的纹状体多巴胺能模式和临床特征。

IF 4.5 Q1 CLINICAL NEUROLOGY
Brain communications Pub Date : 2025-08-20 eCollection Date: 2025-01-01 DOI:10.1093/braincomms/fcaf284
Daniele Urso, Antonio Anastasia, Valentina Gnoni, Alessia Giugno, Davide Vilella, Alessandra Vitulli, Chiara Zecca, José A Pineda-Pardo, Guglielmo Foffani, José A Obeso, Giancarlo Logroscino
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引用次数: 0

摘要

额颞叶痴呆是一组以行为和语言障碍为主要特征的神经退行性疾病。虽然确切的病理生理学仍然难以捉摸,但新出现的证据指出多巴胺功能障碍的重要作用,特别是在尾状核内。此外,一个理论模型提出,额颞叶痴呆的表现是由目标导向行为的缺陷引起的,这可能与额纹状体回路中多巴胺控制的改变有关。然而,尚无研究利用神经影像学研究纹状体多巴胺转运体水平的梯度及其与临床特征的相关性。本研究使用123i -碘氟烷单光子发射计算机断层成像来测量额颞叶痴呆患者纹状体多巴胺转运体水平及其分布模式,并与帕金森病和健康对照进行比较。此外,我们还探讨了多巴胺转运蛋白摄取与额颞叶痴呆中受影响的两个关键领域:社会认知和语言能力之间的相关性。我们假设额颞叶痴呆将在尾状核中表现出主要的多巴胺能缺陷,并且这将与临床核心特征的严重程度相关。该研究共有139名参与者,其中包括34名散发性和遗传性额颞叶痴呆患者,68名帕金森病患者,以及37名年龄和性别匹配的健康对照。额颞叶痴呆组中22例临床可能为行为变异性额颞叶痴呆,12例为原发性进行性失语。社会认知是通过社会和情绪评估的简化版本来评估的,其中包括心理理论测试和面部情绪识别任务。语言能力评估与筛选失语症在神经退行性变电池。我们发现,与健康对照相比,额颞叶痴呆患者的多巴胺转运蛋白水平降低(P < 0.001),额颞叶痴呆患者的壳核与尾状核比值高于帕金森病患者(P < 0.001),这在已确定致病突变的患者中尤为明显。我们还发现多巴胺转运蛋白水平与帕金森运动特征和额颞叶痴呆患者的一般认知相关。值得注意的是,社会认知——尤其是面部情绪识别——和语言能力都与壳核和尾状核中的多巴胺转运蛋白水平有关。这些发现表明,多巴胺转运体摄取模式可以作为额颞叶痴呆的一个有价值的生物标志物,揭示多巴胺能系统和纹状体在一些基本临床方面的作用。这为进一步研究多巴胺能投射在额颞叶痴呆中的潜在机制和潜在治疗靶点开辟了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Striatal dopaminergic patterns and clinical features in frontotemporal dementia.

Striatal dopaminergic patterns and clinical features in frontotemporal dementia.

Striatal dopaminergic patterns and clinical features in frontotemporal dementia.

Striatal dopaminergic patterns and clinical features in frontotemporal dementia.

Frontotemporal dementia is a group of neurodegenerative disorders mainly characterized by behavioural and language impairments. While the precise pathophysiology remains elusive, emerging evidence points to an important role of dopamine dysfunction, particularly within the caudate nucleus. Moreover, a theoretical model proposes that frontotemporal dementia manifestations result from a deficit in goal-directed behaviour, which may be related to altered dopamine control of the frontostriatal circuitry. However, no study has investigated the gradient of striatal dopamine transporter levels in frontotemporal dementia using neuroimaging and their correlation with clinical features. This study used 123I-Ioflupane Single Photon Emission Computed Tomography imaging to measure striatal dopamine transporter levels and their distribution patterns in frontotemporal dementia, compared to Parkinson's disease and healthy controls. Additionally, we explored the correlation between dopamine transporter uptake and two key domains affected in frontotemporal dementia: social cognition and language abilities. We hypothesized that frontotemporal dementia would show a predominant dopaminergic deficit in the caudate, and that this would correlate with the severity of clinical core features. The study comprised 139 participants, including 34 sporadic and genetic frontotemporal dementia, 68 Parkinson's disease individuals, and 37 age- and sex-matched healthy controls. Among the frontotemporal dementia group, 22 cases had clinically probable behavioural variant frontotemporal dementia, and 12 had primary progressive aphasia. Social cognition was assessed with the abbreviated version of the Social and Emotional Assessment, which includes a Theory of Mind test and a Facial Emotion Recognition Task. Language skills were evaluated with the Screening for Aphasia in NeuroDegeneration battery. We found that dopamine transporter levels were reduced in frontotemporal dementia compared to healthy controls (P < 0.001) and that frontotemporal dementia showed a higher putamen-to-caudate ratio than Parkinson's disease (P < 0.001), particularly notable in patients with identified disease-causing mutation. We also found that dopamine transporter levels were correlated with parkinsonian motor features and general cognition in frontotemporal dementia. Notably, both social cognition-especially facial emotion recognition-and language abilities exhibited associations with dopamine transporter levels in both the putamen and the caudate. These findings suggest that the pattern of dopamine transporter uptake could serve as a valuable biomarker for frontotemporal dementia, shedding light on the role of the dopaminergic system and the striatum in some fundamental clinical aspects. This opens new avenues for further investigating the underlying mechanisms and potential therapeutic targets of the dopaminergic projections in frontotemporal dementia.

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