Steiger Tineke K, Weiskopf Nikolaus, Bunzeck Nico
Department of Psychology, University of Lübeck, 23562 Lübeck, Germany, Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany,
Wellcome Trust Centre for Neuroimaging, UCL Institute of Neurology, University College London, WC1N 3BG London, United Kingdom, and Department of Neurophysics, Max Planck Institute for Human Cognitive and Brain Sciences, 04103 Leipzig, Germany.
J Neurosci. 2016 Mar 23;36(12):3552-8. doi: 10.1523/JNEUROSCI.3617-15.2016.
Age-related memory impairments have been associated with structural changes in the dopaminergic system, but the underlying mechanisms remain unclear. Recent work indicates that iron accumulation might be of particular relevance. As iron accumulates, a degeneration of myelin sheaths has been observed in the elderly, but the relationship between both and their impact on memory performance in healthy elderly humans remain important open questions. To address this issue, we combined an established behavioral paradigm to test memory performance [verbal learning memory test (VLMT)] with state of the art quantitative magnetic resonance imaging techniques allowing us to quantify the degree of myelination and iron accumulation via markers of tissue microstructure in a group of young (18-32 years) and healthy elderly humans (55-79 years). As expected, we observed a decrease in gray matter volume and myelin, and an increase of iron in the elderly relative to the young subjects within widespread brain regions, including the basal ganglia. Furthermore, higher levels of iron within the ventral striatum were accompanied by a negative correlation between myelin and iron specific for the elderly participants. Importantly, both markers of iron and myelin (and their ratio) predicted the performance of the elderly in the VLMT. This suggests that ventral striatum iron accumulation is linked to demyelination and impairments in declarative memory. Together, our data provide novel insights into underlying microstructural mechanisms of memory decline in the elderly.
Memory decline in healthy elderly is a common phenomenon, but the underlying neural mechanisms remain unclear. We used a novel approach that allowed us to combine behavior and whole-brain measures of iron, myelin, and gray matter in the participant's individual subspace to analyze structure-structure and structure-behavior interactions. We were able to show, that age-related high levels of iron are accompanied by a negative correlation of iron and myelin in the ventral striatum, which predicted individual memory performance. As such, our findings provide unprecedented insights into the basic mechanisms of memory decline in the elderly.
与年龄相关的记忆障碍与多巴胺能系统的结构变化有关,但其潜在机制仍不清楚。最近的研究表明,铁的积累可能特别重要。随着铁的积累,在老年人中观察到髓鞘变性,但两者之间的关系及其对健康老年人记忆表现的影响仍然是重要的悬而未决的问题。为了解决这个问题,我们将一种既定的行为范式(用于测试记忆表现[言语学习记忆测试(VLMT)])与最先进的定量磁共振成像技术相结合,使我们能够通过一组年轻(18 - 32岁)和健康老年人(55 - 79岁)的组织微观结构标记物来量化髓鞘形成程度和铁的积累。正如预期的那样,我们观察到与年轻受试者相比,老年人在包括基底神经节在内的广泛脑区中灰质体积和髓鞘减少,铁含量增加。此外,腹侧纹状体内较高水平的铁伴随着老年参与者中髓鞘和铁之间的负相关。重要的是,铁和髓鞘的标记物(及其比率)预测了老年人在VLMT中的表现。这表明腹侧纹状体铁积累与脱髓鞘和陈述性记忆障碍有关。总之,我们的数据为老年人记忆衰退的潜在微观结构机制提供了新的见解。
健康老年人的记忆衰退是一种常见现象,但其潜在的神经机制仍不清楚。我们采用了一种新颖的方法,使我们能够在参与者的个体子空间中结合行为以及铁、髓鞘和灰质的全脑测量,以分析结构 - 结构和结构 - 行为相互作用。我们能够表明,与年龄相关的高水平铁伴随着腹侧纹状体中铁和髓鞘的负相关,这预测了个体记忆表现。因此,我们的研究结果为老年人记忆衰退的基本机制提供了前所未有的见解。