Thomas Susan J, Gonsalvez Craig J, Johnstone Stuart J
Brain & Behaviour Research Institute and School of Psychology, University of Wollongong, NSW, Australia; Graduate School of Medicine, University of Wollongong, NSW, Australia.
Brain & Behaviour Research Institute and School of Psychology, University of Wollongong, NSW, Australia; Centre for Psychophysics, Psychophysiology & Psychopharmacology, University of Wollongong, NSW, Australia; University of Western Sydney, NSW, Australia.
Clin Neurophysiol. 2016 Jan;127(1):464-478. doi: 10.1016/j.clinph.2015.05.026. Epub 2015 Jun 5.
Repeated experience with stimuli often primes faster, more efficient neuronal and behavioural responses. Exaggerated repetition priming effects have previously been reported in obsessive-compulsive disorder (OCD), however little is known of their underlying neurobiology or disorder-specificity, hence we investigated these factors.
We examined event-related potentials (ERPs) and behaviour while participants with OCD, panic disorder and healthy controls (20 per group) performed a Go/NoGo task which manipulated target repetition sequences.
Both clinical groups showed stronger reaction time (RT) priming than HCs, which in OCD was greater in a checking, than washing, subgroup. Both clinical groups had similar RT deficits and ERP anomalies across several components, which correlated with psychopathology and RT priming. In OCD alone, N1 latency tended to increase to repeated stimuli, correlated with O-C symptoms, whereas it decreased in other groups. OCD-checkers had smaller target P2 amplitude than all other groups.
Enhanced neural priming is not unique to OCD and may contribute to salient sensory-cognitive experiences in anxiety generally. These effects are related to symptom severity and occur to neutral stimuli and in the context of overall RT impairment, suggesting they may be clinically relevant and pervasive. The results indicate overlapping information-processing and neurobiological factors across disorders, with indications of OCD-specific trends and subgroup differences.
This first electrophysiological investigation of OCD priming in OCD to include anxious controls and OCD subgroups allows for differentiation between overlapping and OCD-specific phenomena, to advance neurobiological models of OCD.
对刺激的反复体验通常会引发更快、更高效的神经元和行为反应。先前有报道称,强迫症(OCD)存在夸张的重复启动效应,然而对其潜在的神经生物学机制或疾病特异性知之甚少,因此我们对这些因素进行了研究。
我们在强迫症、惊恐障碍患者及健康对照者(每组20人)执行一个操作目标重复序列的Go/NoGo任务时,检测了事件相关电位(ERP)和行为表现。
两个临床组均表现出比健康对照组更强的反应时(RT)启动效应,在强迫症组中,检查亚型的这种效应比洗涤亚型更明显。两个临床组在几个成分上均有相似的RT缺陷和ERP异常,这些与精神病理学和RT启动效应相关。仅在强迫症组中,对重复刺激的N1潜伏期倾向于增加,与强迫症状相关,而在其他组中则减少。强迫症检查亚型的目标P2波幅比所有其他组都小。
增强的神经启动效应并非强迫症所特有,可能普遍导致焦虑中突出的感觉认知体验。这些效应与症状严重程度相关,发生于中性刺激且在整体RT受损的背景下,表明它们可能具有临床相关性且普遍存在。结果表明不同疾病间存在重叠的信息处理和神经生物学因素,同时显示出强迫症特异性趋势和亚型差异。
这项首次在强迫症中进行的包括焦虑对照组和强迫症亚型的强迫症启动效应的电生理研究,有助于区分重叠现象和强迫症特异性现象,以推进强迫症的神经生物学模型。