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先天性面孔失认症患者对面孔的快速遗忘。

Rapid forgetting of faces in congenital prosopagnosia.

作者信息

Pertzov Yoni, Krill Dana, Weiss Nilly, Lesinger Keren, Avidan Galia

机构信息

The Hebrew University of Jerusalem, Israel.

Ben Gurion University of the Negev, Israel.

出版信息

Cortex. 2020 Aug;129:119-132. doi: 10.1016/j.cortex.2020.04.007. Epub 2020 Apr 28.

DOI:10.1016/j.cortex.2020.04.007
PMID:32450329
Abstract

Congenital prosopagnosia (CP) is a life-long impairment in face recognition that occurs in the absence of any known brain damage. It is still unclear whether this disorder is related to a visual deficit, or to an impairment in encoding, maintaining or retrieving a face from memory. We tested CPs and matched neurotypical controls using a delayed estimation task in which a target face was shown either upright or inverted. Participants were asked to select the target face out of a cyclic space of morphed faces that could either resemble the target face, or not. The inclusion of upright and inverted faces enabled to examine the extent of the face inversion effect, a well-known face specific effect often associated with holistic processing. To enable disentangling visual from mnemonic processing, reports were required either following 1 and 6 sec retention interval, or simultaneously while the target face was still visible. Controls showed slower forgetting of upright compared to inverted faces. In contrast, CPs exhibited rapid forgetting of upright faces that was comparable to their performance and to performance of controls on inverted faces. Such forgetting was evident in random errors in which the selected faces did not resemble the face in memory, implying a time related decrease in the probability to access the correct face in memory. Importantly, CPs exhibited no inversion effect across all retention intervals, including the simultaneous one, suggesting that their abnormal rapid forgetting could be explained by an impairment in holistic visual processing of upright faces.

摘要

先天性面孔失认症(CP)是一种终生存在的面孔识别障碍,在没有任何已知脑损伤的情况下发生。目前仍不清楚这种障碍是与视觉缺陷有关,还是与从记忆中编码、维持或提取面孔的能力受损有关。我们使用延迟估计任务对先天性面孔失认症患者和匹配的神经典型对照组进行了测试,在该任务中,目标面孔以正立或倒立的形式呈现。参与者被要求从一系列变形面孔的循环空间中选出目标面孔,这些变形面孔可能与目标面孔相似,也可能不相似。纳入正立和倒立面孔能够检验面孔倒置效应的程度,这是一种众所周知的、通常与整体加工相关的面孔特异性效应。为了区分视觉加工和记忆加工,要求参与者在1秒和6秒的保持间隔后报告,或者在目标面孔仍然可见时同时报告。与倒立面孔相比,对照组对正立面孔的遗忘速度较慢。相比之下,先天性面孔失认症患者对正立面孔的遗忘速度很快,这与他们对倒立面孔的表现以及对照组的表现相当。这种遗忘在随机错误中很明显,即所选面孔与记忆中的面孔不相似,这意味着随着时间的推移,从记忆中获取正确面孔的概率会降低。重要的是,先天性面孔失认症患者在所有保持间隔,包括同时呈现时,都没有表现出倒置效应,这表明他们异常快速的遗忘可能是由于正立面孔的整体视觉加工受损所致。

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Rapid forgetting of faces in congenital prosopagnosia.先天性面孔失认症患者对面孔的快速遗忘。
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Phasic alertness enhances processing of face and non-face stimuli in congenital prosopagnosia.阶段性警觉性增强先天性面孔失认症患者对面孔和非面孔刺激的加工。
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引用本文的文献

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Prosopagnosia is highly comorbid in individuals with probable developmental coordination disorder.面孔失认症在患有可能的发育性协调障碍的个体中高度共病。
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Holistic and featural processing's link to face recognition varies by individual and task.整体加工和特征加工与人脸识别的联系因个体和任务而异。
Sci Rep. 2023 Oct 6;13(1):16869. doi: 10.1038/s41598-023-44164-w.
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What is the prevalence of developmental prosopagnosia? An empirical assessment of different diagnostic cutoffs.
发展性面孔失认症的患病率是多少?不同诊断界限的实证评估。
Cortex. 2023 Apr;161:51-64. doi: 10.1016/j.cortex.2022.12.014. Epub 2023 Feb 4.
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A new approach to diagnosing and researching developmental prosopagnosia: Excluded cases are impaired too.一种新的发展性面孔失认症诊断和研究方法:排除病例也受到损害。
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