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蓝斑成像作为神经退行性疾病去甲肾上腺素能功能障碍的生物标志物。

Locus coeruleus imaging as a biomarker for noradrenergic dysfunction in neurodegenerative diseases.

机构信息

German Center for Neurodegenerative Diseases (DZNE), Magdeburg, Germany.

Institute of Cognitive Neurology and Dementia Research, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.

出版信息

Brain. 2019 Sep 1;142(9):2558-2571. doi: 10.1093/brain/awz193.

Abstract

Pathological alterations to the locus coeruleus, the major source of noradrenaline in the brain, are histologically evident in early stages of neurodegenerative diseases. Novel MRI approaches now provide an opportunity to quantify structural features of the locus coeruleus in vivo during disease progression. In combination with neuropathological biomarkers, in vivo locus coeruleus imaging could help to understand the contribution of locus coeruleus neurodegeneration to clinical and pathological manifestations in Alzheimer's disease, atypical neurodegenerative dementias and Parkinson's disease. Moreover, as the functional sensitivity of the noradrenergic system is likely to change with disease progression, in vivo measures of locus coeruleus integrity could provide new pathophysiological insights into cognitive and behavioural symptoms. Locus coeruleus imaging also holds the promise to stratify patients into clinical trials according to noradrenergic dysfunction. In this article, we present a consensus on how non-invasive in vivo assessment of locus coeruleus integrity can be used for clinical research in neurodegenerative diseases. We outline the next steps for in vivo, post-mortem and clinical studies that can lay the groundwork to evaluate the potential of locus coeruleus imaging as a biomarker for neurodegenerative diseases.

摘要

蓝斑是大脑中去甲肾上腺素的主要来源,其结构在神经退行性疾病的早期就会发生病理性改变。目前,新的 MRI 方法为在疾病进展过程中定量分析活体蓝斑的结构特征提供了机会。与神经病理学生物标志物相结合,活体蓝斑成像有助于理解蓝斑神经退行性变对阿尔茨海默病、非典型神经退行性痴呆和帕金森病的临床和病理表现的影响。此外,由于去甲肾上腺素能系统的功能敏感性可能随疾病进展而改变,活体蓝斑完整性的测量可能为认知和行为症状提供新的病理生理学见解。蓝斑成像还有望根据去甲肾上腺素能功能障碍将患者分层到临床试验中。本文就如何将活体蓝斑完整性的非侵入性评估用于神经退行性疾病的临床研究提出了共识。我们概述了活体、死后和临床研究的下一步计划,为评估蓝斑成像作为神经退行性疾病生物标志物的潜力奠定基础。

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