Universidad Nacional del Sur (UNS), Bahía Blanca, Argentina, Instituto de Investigaciones en Ingeniería Eléctrica (IIIE) (UNS-CONICET), Bahía Blanca, Buenos Aires, Argentina.
Clínica Privada Bahiense, Bahía Blanca, Buenos Aires, Argentina.
J Alzheimers Dis. 2018;63(1):185-194. doi: 10.3233/JAD-170728.
Patients with Alzheimer's disease (AD) typically present with attentional and oculomotor abnormalities that can have an impact on visual processing and associated cognitive functions. Over the last few years, we have witnessed a shift toward the analyses of eye movement behaviors as a means to further our understanding of the pathophysiology of common disorders such as AD. However, little work has been done to unveil the link between eye moment abnormalities and poor performance on cognitive tasks known to be markers for AD patients, such as the short-term memory-binding task. We analyzed eye movement fixation behaviors of thirteen healthy older adults (Controls) and thirteen patients with probable mild AD while they performed the visual short-term memory binding task. The short-term memory binding task asks participants to detect changes across two consecutive arrays of two bicolored object whose features (i.e., colors) have to be remembered separately (i.e., Unbound Colors), or combined within integrated objects (i.e., Bound Colors). Patients with mild AD showed the well-known pattern of selective memory binding impairments. This was accompanied by significant impairments in their eye movements only when they processed Bound Colors. Patients with mild AD remarkably decreased their mean gaze duration during the encoding of color-color bindings. These findings open new windows of research into the pathophysiological mechanisms of memory deficits in AD patients and the link between its phenotypic expressions (i.e., oculomotor and cognitive disorders). We discuss these findings considering current trends regarding clinical assessment, neural correlates, and potential avenues for robust biomarkers.
阿尔茨海默病(AD)患者通常表现出注意力和眼球运动异常,这些异常可能会影响视觉处理和相关认知功能。在过去的几年中,我们见证了将眼球运动行为分析作为进一步了解 AD 等常见疾病病理生理学的一种手段的转变。然而,很少有工作揭示眼球运动异常与已知认知任务表现不佳之间的联系,这些认知任务是 AD 患者的标志物,例如短期记忆绑定任务。我们分析了 13 名健康老年人(对照组)和 13 名可能患有轻度 AD 的患者在执行视觉短期记忆绑定任务时的眼球运动注视行为。短期记忆绑定任务要求参与者检测两个连续的双色物体数组之间的变化,这些物体的特征(即颜色)必须分别记住(即未绑定颜色),或者组合成一个集成的物体(即绑定颜色)。患有轻度 AD 的患者表现出选择性记忆绑定损伤的典型模式。这伴随着他们在处理绑定颜色时眼球运动显著受损。当患者处理绑定颜色时,他们在编码颜色-颜色绑定时显著减少了平均注视时间。这些发现为 AD 患者记忆缺陷的病理生理学机制及其表型表达(即眼球运动和认知障碍)之间的联系开辟了新的研究窗口。我们考虑了当前关于临床评估、神经相关性和稳健生物标志物的潜在途径的趋势,讨论了这些发现。