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The Effect of Aging in Inhibitory Control of Major Depressive Disorder Revealed by Event-Related Potentials

机译:事件相关电位揭示衰老对主要抑郁症抑制控制的作用

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摘要

Elderly depressed patients manifest pronounced executive dysfunction compared with younger subjects with depressive disorder. Aging-related brain changes may result in executive dysfunction in geriatric depression. We investigated the neural correlates of inhibitory control processing in depressed subjects at different ages using event-related potentials (ERPs). A equiprobable visual Go/Nogo task was used in 19 young (27.4 ± 5.0 years) and 18 elderly (70.8 ± 6.9 years) depressed subjects and their age-matched healthy controls (20 young subjects, 26.2 ± 3.7 years, and 18 elderly subjects, 68.1 ± 4.8 years). The responses were based on two types of equilateral triangular figures of upright (Go) and inverted triangle (Nogo). The elderly subjects exhibited later N2 and P3 latencies, and larger Go-N2 and P3 amplitudes, compared with the younger subjects. Further, the elderly controls displayed smaller P3 in the central and parietal regions, and yielded larger Nogo-P3 amplitude in the frontal region compared with younger controls. While the young depressed patients yielded smaller P3 amplitude than the controls across frontal, central and parietal regions, elderly depressed patients yielded smaller P3 than the elderly controls only in the frontal region. Our results suggest that the inhibitory control subprocesses are differentially affected by depression and aging. The stimulus response speed and the effort intensity of inhibition control are specifically impaired in the elderly depressed patients. And the diminished amplitudes of frontal P3 in the elderly depression imply a frontal dysfunction mechanism.
机译:与年轻的抑郁症患者相比,老年抑郁症患者表现出明显的执行功能障碍。与衰老相关的大脑变化可能会导致老年抑郁症的执行功能障碍。我们调查了使用事件相关电位(ERP)在不同年龄的抑郁症患者中抑制控制过程的神经相关性。在19名年轻(27.4±5.0岁)和18名老年(70.8±6.9岁)抑郁症患者及其年龄匹配的健康对照者(20名年轻受试者,26.2±3.7岁和18名老年患者)中使用了等效的视觉Go / Nogo任务,68.1±4.8年)。响应基于立式(Go)和倒三角形(Nogo)的两种等边三角形图形。与年轻受试者相比,老年受试者表现出更高的N2和P3潜伏期,以及更大的Go-N2和P3振幅。此外,与年轻对照相比,老年对照在中央和顶叶区域显示较小的P3,并且在额叶区域显示较大的Nogo-P3振幅。虽然年轻的抑郁症患者在额,中部和顶叶区域产生的P3振幅要比对照组小,但老年抑郁症患者仅在额叶区域产生的P3振幅要比老年对照组小。我们的结果表明抑制控制子过程受抑郁和衰老的影响不同。老年抑郁症患者的刺激反应速度和抑制控制的努力强度特别受损。老年抑郁症中额叶P3幅度的减少暗示了额叶功能障碍的机制。

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