Department of Psychiatry, University of California, San Diego, CA, USA; Center for Behavior Genetics of Aging, University of California, San Diego, CA, USA.
Department of Psychiatry, University of California, San Diego, CA, USA; Center for Behavior Genetics of Aging, University of California, San Diego, CA, USA.
Cortex. 2017 Dec;97:60-69. doi: 10.1016/j.cortex.2017.09.025. Epub 2017 Oct 7.
Pupillary responses during cognitive tasks are linked to functioning of the locus coeruleus (LC). The LC is an early site of abnormal tau deposition, which may contribute to key aspects of Alzheimer's disease (AD) pathophysiology. We previously found attenuation of pupillary responses to increases in cognitive load in individuals with mild cognitive impairment (MCI), suggesting pupillary responses may provide a biomarker of early risk for AD associated with LC dysfunction. The LC modulates cortical activity through two modes of operation: tonic and phasic. Early LC damage has been predicted to result in a state of persistent high tonic LC activity that may disrupt task-related phasic activity. To further examine whether pupillary responses are associated with early LC dysfunction, we measured pupil dilation during a digit span task as a measure of phasic activity, and low frequency BOLD variance (LFBV) during resting-state fMRI in key nodes of the ventral attention network (VAN) as a measure of cortical reactivity related to LC tonic activity in 358 middle-aged men. Individuals with greater LFBV in VAN nodes, i.e., higher tonic brain activity at rest, showed a smaller increase in pupil dilation from low to moderate cognitive loads. Thus, higher tonic LFBV activity at rest was related to reduced task-appropriate phasic dilation increases. The results support predictions from prominent models of LC functioning in which early LC dysfunction leads to persistent high tonic rates of activity during rest and lower signal-to-noise of phasic responses during task performance. Taken together with previous findings of early AD pathophysiology in LC and reduced phasic dilation responses to increased cognitive load in individuals with MCI, the present results suggest that pupillary responses may index early LC dysfunction and should receive further study as a potential biomarker of risk for AD.
在认知任务期间瞳孔反应与蓝斑核(LC)的功能有关。LC 是异常 tau 沉积的早期部位,这可能导致阿尔茨海默病(AD)病理生理学的关键方面。我们之前发现,在轻度认知障碍(MCI)个体中,瞳孔对认知负荷增加的反应减弱,这表明瞳孔反应可能为 AD 与 LC 功能障碍相关的早期风险提供生物标志物。LC 通过两种操作模式调节皮质活动:紧张和相位。早期 LC 损伤预计会导致持续的高紧张 LC 活动状态,这可能会破坏与任务相关的相位活动。为了进一步研究瞳孔反应是否与早期 LC 功能障碍有关,我们测量了数字跨度任务期间的瞳孔扩张作为相位活动的指标,以及静息状态 fMRI 中腹侧注意网络(VAN)关键节点中的低频 BOLD 方差(LFBV)作为与 LC 紧张活动相关的皮质反应的指标,在 358 名中年男性中。VAN 节点中 LFBV 较大的个体,即静息时大脑紧张活动较高的个体,从低认知负荷到中等认知负荷时瞳孔扩张的增加较小。因此,静息时较高的紧张 LFBV 活动与任务适当的相位扩张增加减少有关。结果支持 LC 功能的突出模型的预测,即早期 LC 功能障碍导致静息时持续的高紧张活动率,并导致任务表现期间相位反应的信号噪声降低。结合之前在 LC 中发现的早期 AD 病理生理学和 MCI 个体对增加认知负荷的相位扩张反应减少的发现,本研究结果表明,瞳孔反应可能是早期 LC 功能障碍的指标,应作为 AD 风险的潜在生物标志物进一步研究。