Department of Psychosomatic and General Internal Medicine, Centre for Psychosocial Medicine, University Hospital Heidelberg, Thibautstrasse 2, 69115 Heidelberg, Germany.
Psychosom Med. 2012 Feb-Mar;74(2):136-45. doi: 10.1097/PSY.0b013e318242496a. Epub 2012 Jan 30.
To elucidate maladaptive central processing of food cues during recognition tasks in anorexia nervosa (AN), while considering influences of nutritional preload and presentation modality (word versus picture).
Event-related potentials to food-related word and pictorial stimuli were assessed during recognition tasks in 16 patients with AN, 16 control participants with food intake before the study, and 16 control participants with a fasting period before the study.
Patients with AN showed a P3b amplitude reduction especially at the midline parietal site compared with satiated controls (5.7 [standard deviation = 3.3] versus 8.7 [3.1] μV, p < .03). Subtle recognition deficits in patients with AN were indicated by smaller "old/new" effects compared with satiated (p = .049) and fasting controls (p < .003) for pictorial stimuli. Hunger-modulated enhanced old/new effects for food pictures compared with neutral pictorial stimuli could be observed in fasting controls only (2.7 [2.6] versus 0.8 [2.2] μV, p < .01).
The presented data provide evidence for a midline parietal P3b amplitude reduction in patients with AN, which might point to reduced network activation in AN even during satiety. Observed subtle recognition deficits either represent a stable trait characteristic or a "scar" effect of chronic starvation that may play a role in the development and/or persistence of the disorder.
阐明神经性厌食症(AN)患者在识别任务中对食物线索的适应性中枢处理,同时考虑营养预加载和呈现方式(文字与图片)的影响。
在识别任务中,对 16 名 AN 患者、16 名有进食史的对照者和 16 名禁食对照者进行与食物相关的文字和图片刺激的事件相关电位评估。
与饱食对照者相比(5.7 [标准差=3.3] μV 对 8.7 [3.1] μV,p<.03),AN 患者的 P3b 振幅减小,尤其是中线顶区。与饱食(p=.049)和禁食(p<.003)对照者相比,AN 患者的图片刺激识别“旧/新”效应较小,表明存在细微的识别缺陷。仅在禁食对照者中观察到饥饿调节的食物图片与中性图片刺激相比的增强“旧/新”效应(2.7 [2.6] μV 对 0.8 [2.2] μV,p<.01)。
本研究提供了 AN 患者中线顶区 P3b 振幅降低的证据,这可能表明即使在饱腹感时,AN 患者的网络激活减少。观察到的细微识别缺陷要么代表稳定的特质特征,要么是慢性饥饿的“疤痕”效应,这可能在疾病的发展和/或持续中起作用。