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Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face Area

Rationale: 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 F...

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Autores principales: Haeger, Alexa, Pouzat, Christophe, Luecken, Volker, N’Diaye, Karim, Elger, Christian, Kennerknecht, Ingo, Axmacher, Nikolai, Dinkelacker, Vera
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636799/
https://www.ncbi.nlm.nih.gov/pubmed/34867227
http://dx.doi.org/10.3389/fnbeh.2021.744466
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author Haeger, Alexa
Pouzat, Christophe
Luecken, Volker
N’Diaye, Karim
Elger, Christian
Kennerknecht, Ingo
Axmacher, Nikolai
Dinkelacker, Vera
author_facet Haeger, Alexa
Pouzat, Christophe
Luecken, Volker
N’Diaye, Karim
Elger, Christian
Kennerknecht, Ingo
Axmacher, Nikolai
Dinkelacker, Vera
author_sort Haeger, Alexa
collection PubMed
description Rationale: 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. Objectives: Our study intended to scrutinize modifications of FFA-activation during face encoding and maintenance based on RSA. Methods: 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. Results: 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. Conclusion: 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.
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spelling pubmed-86367992021-12-03 Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face Area Haeger, Alexa Pouzat, Christophe Luecken, Volker N’Diaye, Karim Elger, Christian Kennerknecht, Ingo Axmacher, Nikolai Dinkelacker, Vera Front Behav Neurosci Neuroscience Rationale: 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. Objectives: Our study intended to scrutinize modifications of FFA-activation during face encoding and maintenance based on RSA. Methods: 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. Results: 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. Conclusion: 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. Frontiers Media S.A. 2021-11-18 /pmc/articles/PMC8636799/ /pubmed/34867227 http://dx.doi.org/10.3389/fnbeh.2021.744466 Text en Copyright © 2021 Haeger, Pouzat, Luecken, N’Diaye, Elger, Kennerknecht, Axmacher and Dinkelacker. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Haeger, Alexa
Pouzat, Christophe
Luecken, Volker
N’Diaye, Karim
Elger, Christian
Kennerknecht, Ingo
Axmacher, Nikolai
Dinkelacker, Vera
Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face Area
title Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face Area
title_full Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face Area
title_fullStr Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face Area
title_full_unstemmed Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face Area
title_short Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face Area
title_sort face processing in developmental prosopagnosia: altered neural representations in the fusiform face area
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636799/
https://www.ncbi.nlm.nih.gov/pubmed/34867227
http://dx.doi.org/10.3389/fnbeh.2021.744466
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