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Cortex; a Journal Devoted To the Study... Aug 2022Developmental prosopagnosia (DP) is a neurodevelopmental disorder associated with difficulties in the perception and recognition of faces. However, the extent to which...
Developmental prosopagnosia (DP) is a neurodevelopmental disorder associated with difficulties in the perception and recognition of faces. However, the extent to which DP affects non-face object is an ongoing debate. In this study, we asked whether pareidolic objects (which give rise to the perception of a face) are also affected in DP. First, we compared performance in DPs (n = 30) and controls (n = 27) on a recognition task with faces, pareidolic objects and non-pareidolic objects (bottles). The pareidolic objects had either similar or dissimilar image statistics to faces. Consistent with our understanding of DP, we found that the pattern of recognition across items between DPs and controls was lowest for faces. Interestingly, there was also a low correlation between DPs and controls for pareidolic-similar objects that was similar to faces. In contrast, there were higher correlations between DPs and controls for pareidolic-dissimilar objects and bottles, which were both significantly different to faces. These findings suggest that the deficit in DP involves processing image properties that are common to faces. Next, using an individual differences approach across a large group of neurotypical adults (n = 94), we found that face recognition covaried with the recognition of pareidolic-similar objects, but not with pareidolic-dissimilar objects or non-pareidolic objects. Together, these findings support the idea that a representation based on image properties plays an important role in the perception and recognition of objects and faces and that the deficit in the perception of some object categories in DP could be explained by their similarity to the image properties found in faces.
Topics: Adult; Facial Recognition; Humans; Individuality; Pattern Recognition, Visual; Prosopagnosia; Recognition, Psychology
PubMed: 35576670
DOI: 10.1016/j.cortex.2022.04.011 -
Acta Neurologica Taiwanica Dec 2022A 56-year-old, right-handed man with no known past medical history presented with sudden onset of inability to recognize familiar individuals in person, including his...
A 56-year-old, right-handed man with no known past medical history presented with sudden onset of inability to recognize familiar individuals in person, including his wife and his mother. He also couldn't recognize himself in the mirror. There was no weakness, numbness, visual disturbances, or speech difficulty. Face recognition test, using Warrington Recognition Memory Test (1), showed the presence of complete prosopagnosia. The rest of the neurological and cranial nerves examinations were normal. Magnetic resonance imaging (MRI) of the brain showed restricted diffusion at the right temporal and occipital lobes (the fusiform gyrus) [Figure 1]. Magnetic resonance angiogram (MRA) of the brain was unremarkable. The 24-hours Holter monitoring showed paroxysmal atrial fibrillation. The transthoracic echocardiogram and carotid doppler ultrasound scan were normal. He was then treated with rivaroxaban 20mg daily for secondary stroke prevention in non-valvular atrial fibrillation. Face recognition skill training was started in the ward, which includes compensatory strategies to achieve person recognition by circumventing the face processing impairment, and remediation to enhance mnemonic function for face recognition. His prosopagnosia resolved completely after one week. Prosopagnosia, also known as face blindness, is an impairment in recognizing faces. The core defects are the loss of familiarity with previously known faces and the inability to recognize new faces. Patients with prosopagnosia may present with poor recognition of familiar individuals in person or in the photograph, confusion with plotlines in movies or plays with numerous characters, and difficulty distinguishing individuals wearing a uniform or similar clothing. Stroke is the most common cause of acquired prosopagnosia (2). Other less common aetiologies include traumatic brain injury, carbon monoxide poisoning, temporal lobectomy, and encephalitis. Literature has shown that areas involved in acquired prosopagnosia are the right fusiform gyrus or anterior temporal cortex, or both (3). The fusiform gyrus is part of the lateral temporal lobe and occipital lobe in 'Brodmann area 37' (4). The fusiform gyrus is considered a key structure for functionally specialized computations of high-level vision such as face perception, object recognition, and reading. Individuals with fusiform lesions are more likely to have apperceptive prosopagnosia, while those with anterior temporal lesions have an amnestic variant (5). In summary, prosopagnosia can be the sole presentation for the right fusiform gyrus stroke. It is important to recognize prosopagnosia for early stroke diagnosis and avoid misdiagnosing it as a psychiatric or ocular disorder. Keywords: prosopagnosia, fusiform gyrus, stroke.
Topics: Humans; Infarction; Magnetic Resonance Imaging; Male; Middle Aged; Occipital Lobe; Prosopagnosia; Stroke; Temporal Lobe
PubMed: 35470413
DOI: No ID Found -
Brain Communications 2022While there have been decades of clinical and theoretical interest in developmental and acquired face recognition difficulties, very little work has examined their...
While there have been decades of clinical and theoretical interest in developmental and acquired face recognition difficulties, very little work has examined their remediation. Here, we report two studies that examined the efficacy of an existing face training programme in improving face-processing skills in adults and children with developmental face recognition impairments. The programme has only been trialled in typical children to date, where 2 weeks of perceptual training (modelled on an adapted version of the popular family game ) resulted in face-specific improvements for memory but not perception after 2 weeks of training. In Study 1, we performed a randomized, parallel groups, placebo-controlled trial of the same programme in 20 adults with a pre-existing diagnosis of developmental prosopagnosia. Assessment tasks were administered immediately before and after training, and 2 weeks later. Face-specific gains in memory (but not perception) were observed in the experimental group and were greatest in those with the poorest face recognition skills at entry. These gains persisted 2 weeks after training ceased. In Study 2, a case-series approach was used to administer the experimental version of the training programme to four children who presented with difficulties in face recognition. Improvements in face memory were observed in three of the participants; while one also improved at face perception, there was mixed evidence for the face specificity of these gains. Together, these findings suggest plasticity in the human face recognition system through to at least mid-adulthood and also pave the way for longer-term implementations of the face training programme that will likely elicit greater gains in both adults and children.
PubMed: 35386218
DOI: 10.1093/braincomms/fcac068 -
Neuropsychologia Jun 2022In right-handed adults, face processing is lateralized to the right hemisphere and visual word processing to the left hemisphere. According to the many-to-many account...
In right-handed adults, face processing is lateralized to the right hemisphere and visual word processing to the left hemisphere. According to the many-to-many account (MTMA) of functional cerebral organization this lateralization pattern is partly dependent on the acquisition of literacy. Hence, the MTMA predicts that: (i) processing of both words and faces should show no or at least less lateralization in individuals with developmental dyslexia compared with controls, and (ii) lateralization in word processing should be normal in individuals with developmental prosopagnosia whereas lateralization in face processing should be absent. To test these hypotheses, 21 right-handed adults with developmental dyslexia and 21 right-handed adults with developmental prosopagnosia performed a divided visual field paradigm with delayed matching of faces, words and cars. Contrary to the predictions, we find that lateralization effects in face processing are within the normal range for both developmental dyslexics and prosopagnosics. Moreover, the group with developmental dyslexia showed right hemisphere lateralization for word processing. We argue that these findings are incompatible with the specific predictions of the MTMA.
Topics: Adult; Dyslexia; Facial Recognition; Functional Laterality; Humans; Pattern Recognition, Visual; Prosopagnosia; Visual Perception
PubMed: 35278463
DOI: 10.1016/j.neuropsychologia.2022.108208 -
Brain Sciences Feb 2022Developmental prosopagnosia (DP)-or 'face blindness'-refers to life-long problems with facial recognition in the absence of brain injury. We know that neurodevelopmental...
Developmental prosopagnosia (DP)-or 'face blindness'-refers to life-long problems with facial recognition in the absence of brain injury. We know that neurodevelopmental disorders tend to co-occur, and this study aims to explore if individuals with self-reported DP also report indications of other neurodevelopmental disorders, deficits, or conditions (developmental comorbidity). In total, 115 individuals with self-reported DP participated in this online cross-sectional survey. Face recognition impairment was measured with a validated self-report instrument. Indications of difficulties with navigation, math, reading, or spelling were measured with a tailored questionnaire using items from published sources. Additional diagnoses were measured with direct questions. We also included open-ended questions about cognitive strengths and difficulties. Results: Overall, 57% reported at minimum one developmental comorbidity of interest, with most reflecting specific cognitive impairment (e.g., in memory or object recognition) rather than diagnostic categories (e.g., ADHD, dyslexia). Interestingly, many participants reported cognitive skills or strengths within the same domains that others reported impairment, indicating a diverse pattern of cognitive strengths and difficulties in this sample. The frequency and diversity of self-reported developmental comorbidity suggests that face recognition could be important to consider in future investigations of neurodevelopmental comorbidity patterns.
PubMed: 35203993
DOI: 10.3390/brainsci12020230 -
Cognitive Research: Principles and... Feb 2022Some research indicates that face masks impair identification and other judgements such as trustworthiness. However, it is unclear whether those effects have abated over...
Some research indicates that face masks impair identification and other judgements such as trustworthiness. However, it is unclear whether those effects have abated over time as individuals adjust to widespread use of masks, or whether performance is related to individual differences in face recognition ability. This study examined the effect of masks and sunglasses on face matching and social judgements (trustworthiness, competence, attractiveness). In Experiment 1, 135 participants across three different time points (June 2020-July 2021) viewed unedited faces and faces with masks, sunglasses, or both. Both masks and sunglasses similarly decreased matching performance. The effect of masks on social judgements varied depending on the judgement and whether the face was depicted with sunglasses. There was no effect of timepoint on any measure, suggesting that the effects of masks have not diminished. In Experiment 2, 12 individuals with developmental prosopagnosia (DP) and 10 super-recognisers (SRs) completed the same tasks. The effect of masks on identity matching was reduced in SRs, whereas the effects of masks and sunglasses for the DP group did not differ from controls. These findings indicate that face masks significantly affect face perception, depending on the availability of other facial information, and are not modified by exposure.
Topics: Eyeglasses; Facial Recognition; Humans; Individuality; Masks; Sociological Factors
PubMed: 35171394
DOI: 10.1186/s41235-022-00371-z -
Cortex; a Journal Devoted To the Study... Feb 2022An 84-year-old man manifested false recognition/misidentification of unfamiliar person after cardiogenic cerebral infarction. He had good visual and hearing acuity, no...
An 84-year-old man manifested false recognition/misidentification of unfamiliar person after cardiogenic cerebral infarction. He had good visual and hearing acuity, no hemianopsia, unilateral spatial neglect and visual object agnosia. However, he was unable to remember faces of his rehabilitation therapists, and repeatedly misidentified other patients' visitors and therapists as his family members and friends, without recognizing his mistakes. General cognitive function was preserved with Hasegawa dementia score-revised (HDS-R) 25/30 (cut-off score 20). In terms of recognition of faces, tasks not requiring recognition of facial identity, such as interpreting facial emotions, and gender and age assessment, were relatively preserved, but recognition of family members and celebrities was severely impaired, and matching unfamiliar faces was slightly impaired. Semantic information of family and friends was retained. Although his symptoms resembled associative prosopagnosia, they differed from general associative prosopagnosia in having phonagnosia. MRI lesions were localized in the frontal and temporal lobes including the right anterior temporal lobe, and not in the right occipital and temporal lobes considered to the lesion site of multimodal people recognition disorders manifesting inability of utilization of visual (face) and auditory (voice) cues for person identification. In addition to the facial cognitive impairment, impaired exploratory (monitoring) function of the frontal lobe on the temporal lobe may also contribute to the false recognition/misidentification of this case.
Topics: Aged, 80 and over; Agnosia; Cerebral Infarction; Cognition; Humans; Male; Prosopagnosia; Temporal Lobe
PubMed: 35051711
DOI: 10.1016/j.cortex.2021.12.005 -
Neuropsychologia Jan 2022In recent years, the number of face identity matching tests in circulation has grown considerably and these are being increasingly utilized to study individual...
In recent years, the number of face identity matching tests in circulation has grown considerably and these are being increasingly utilized to study individual differences in face cognition. Although many of these tests were designed for testing typical observers, recent studies have begun to utilize general-purpose tests for studying specific, atypical populations (e.g., super-recognizers and individuals with prosopagnosia). In this study, we examined the capacity of four tests requiring binary face-matching decisions to study individual differences between healthy observers. Uniquely, we used performance of the patient PS (Rossion, 2018), a well-documented case of acquired prosopagnosia (AP), as a benchmark. Two main findings emerged: (i) PS could exhibit typical rates of accuracy in all tests; (ii) compared to age-matched controls and when considering both accuracy and speed to account for potential trade-offs, only the KFMT - but not the EFCT, PICT or GFMT - was able to detect PS's severe impairment. These findings reflect the importance of considering both accuracy and response times to measure individual differences in face matching, and the need for comparing tests in terms of their sensitivity, when used as a measure of human cognition and brain functioning.
Topics: Face; Humans; Neuropsychological Tests; Pattern Recognition, Visual; Photic Stimulation; Prosopagnosia; Reaction Time
PubMed: 34919897
DOI: 10.1016/j.neuropsychologia.2021.108119 -
Frontiers in Behavioral Neuroscience 2021Face expertise is a pivotal social skill. Developmental prosopagnosia (DP), i.e., the inability to recognize faces without a history of brain damage, affects about 2%...
Face expertise is a pivotal social skill. Developmental prosopagnosia (DP), i.e., the inability to recognize faces without a history of brain damage, affects about 2% of the general population, and is a renowned model system of the face-processing network. Within this network, the right Fusiform Face Area (FFA), is particularly involved in face identity processing and may therefore be a key element in DP. Neural representations within the FFA have been examined with Representational Similarity Analysis (RSA), a data-analytical framework in which multi-unit measures of brain activity are assessed with correlation analysis. Our study intended to scrutinize modifications of FFA-activation during face encoding and maintenance based on RSA. Thirteen participants with DP (23-70 years) and 12 healthy control subjects (19-62 years) participated in a functional MRI study, including morphological MRI, a functional FFA-localizer and a modified Sternberg paradigm probing face memory encoding and maintenance. Memory maintenance of one, two, or four faces represented low, medium, and high memory load. We examined conventional activation differences in response to working memory load and applied RSA to compute individual correlation-matrices on the voxel level. Group correlation-matrices were compared via Donsker's random walk analysis. On the functional level, increased memory load entailed both a higher absolute FFA-activation level and a higher degree of correlation between activated voxels. Both aspects were deficient in DP. Interestingly, control participants showed a homogeneous degree of correlation for successful trials during the experiment. In DP-participants, correlation levels between FFA-voxels were significantly lower and were less sustained during the experiment. In behavioral terms, DP-participants performed poorer and had longer reaction times in relation to DP-severity. Furthermore, correlation levels were negatively correlated with reaction times for the most demanding high load condition. We suggest that participants with DP fail to generate robust and maintained neural representations in the FFA during face encoding and maintenance, in line with poorer task performance and prolonged reaction times. In DP, alterations of neural coding in the FFA might therefore explain curtailing in working memory and contribute to impaired long-term memory and mental imagery.
PubMed: 34867227
DOI: 10.3389/fnbeh.2021.744466 -
Brain Communications 2021Posterior cortical atrophy is a neurodegenerative syndrome with a heterogeneous clinical presentation due to variable involvement of the left, right, dorsal and ventral...
Posterior cortical atrophy is a neurodegenerative syndrome with a heterogeneous clinical presentation due to variable involvement of the left, right, dorsal and ventral parts of the visual system, as well as inconsistent involvement of other cognitive domains and systems. F-fluorodeoxyglucose (FDG)-PET is a sensitive marker for regional brain damage or dysfunction, capable of capturing the pattern of neurodegeneration at the single-participant level. We aimed to leverage these inter-individual differences on FDG-PET imaging to better understand the associations of heterogeneity of posterior cortical atrophy. We identified 91 posterior cortical atrophy participants with FDG-PET data and abstracted demographic, neurologic, neuropsychological and Alzheimer's disease biomarker data. The mean age at reported symptom onset was 59.3 (range: 45-72 years old), with an average disease duration of 4.2 years prior to FDG-PET scan, and a mean education of 15.0 years. Females were more common than males at 1.6:1. After standard preprocessing steps, the FDG-PET scans for the cohort were entered into an unsupervised machine learning algorithm which first creates a high-dimensional space of inter-individual covariance before performing an eigen-decomposition to arrive at a low-dimensional representation. Participant values ('eigenbrains' or latent vectors which represent principle axes of inter-individual variation) were then compared to the clinical and biomarker data. Eight eigenbrains explained over 50% of the inter-individual differences in FDG-PET uptake with left (eigenbrain 1) and right (eigenbrain 2) hemispheric lateralization representing 24% of the variance. Furthermore, eigenbrain-loads mapped onto clinical and neuropsychological data (i.e. aphasia, apraxia and global cognition were associated with the left hemispheric eigenbrain 1 and environmental agnosia and apperceptive prosopagnosia were associated with the right hemispheric eigenbrain 2), suggesting that they captured important axes of normal and abnormal brain function. We used to characterize the eigenbrains through topic-based decoding, which supported the idea that the eigenbrains map onto a diverse set of cognitive functions. These eigenbrains captured important biological and pathophysiologic data (i.e. limbic predominant eigenbrain 4 patterns being associated with older age of onset compared to frontoparietal eigenbrain 7 patterns being associated with younger age of onset), suggesting that approaches that focus on inter-individual differences may be important to better understand the variability observed within a neurodegenerative syndrome like posterior cortical atrophy.
PubMed: 34805993
DOI: 10.1093/braincomms/fcab182