The degeneration of locus coeruleus occurring during Alzheimer’s disease clinical progression: a neuroimaging follow-up investigation

IF 2.7 3区 医学 Q1 ANATOMY & MORPHOLOGY
Alessandro Galgani, Francesco Lombardo, Francesca Frijia, Nicola Martini, Gloria Tognoni, Nicola Pavese, Filippo Sean Giorgi
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Abstract

The noradrenergic nucleus Locus Coeruleus (LC) is precociously involved in Alzheimer’s Disease (AD) pathology, and its degeneration progresses during the course of the disease. Using Magnetic Resonance Imaging (MRI), researchers showed also in vivo in patients the disruption of LC, which can be observed both in Mild Cognitively Impaired individuals and AD demented patients. In this study, we report the results of a follow-up neuroradiological assessment, in which we evaluated the LC degeneration overtime in a group of cognitively impaired patients, submitted to MRI both at baseline and at the end of a 2.5-year follow-up. We found that a progressive LC disruption can be observed also in vivo, involving the entire nucleus and associated with clinical diagnosis. Our findings parallel neuropathological ones, which showed a continuous increase of neuronal death and volumetric atrophy within the LC with the progression of Braak’s stages for neurofibrillary pathology. This supports the reliability of MRI as a tool for exploring the integrity of the central noradrenergic system in neurodegenerative disorders.

Abstract Image

阿尔茨海默病临床进展过程中发生的神经节变性:一项神经影像学跟踪调查
去甲肾上腺素能核(Locus Coeruleus,LC)与阿尔茨海默病(AD)的病理变化密切相关,并且在病程中不断退化。研究人员利用磁共振成像(MRI)在患者体内也显示了 LC 的破坏,这在轻度认知障碍患者和阿兹海默症痴呆患者中都能观察到。在本研究中,我们报告了一项神经放射学随访评估的结果,其中我们评估了一组认知障碍患者的低密度脂蛋白膜退化情况,这些患者在基线和 2.5 年的随访结束时都接受了核磁共振成像检查。我们发现,在体内也能观察到渐进性低密度脂蛋白膜破坏,涉及整个核,并与临床诊断相关。我们的研究结果与神经病理学的研究结果一致,后者显示随着神经纤维病理学布拉克分期的进展,LC 内神经元死亡和体积萎缩持续增加。这证明了核磁共振成像作为一种探索神经退行性疾病中枢去甲肾上腺素能系统完整性的工具的可靠性。
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来源期刊
Brain Structure & Function
Brain Structure & Function 医学-解剖学与形态学
CiteScore
6.00
自引率
6.50%
发文量
168
审稿时长
8 months
期刊介绍: Brain Structure & Function publishes research that provides insight into brain structure−function relationships. Studies published here integrate data spanning from molecular, cellular, developmental, and systems architecture to the neuroanatomy of behavior and cognitive functions. Manuscripts with focus on the spinal cord or the peripheral nervous system are not accepted for publication. Manuscripts with focus on diseases, animal models of diseases, or disease-related mechanisms are only considered for publication, if the findings provide novel insight into the organization and mechanisms of normal brain structure and function.
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