TY - JOUR
T1 - Functional MRI Reveals Compromised Neural Integrity of the Face Processing Network in Congenital Prosopagnosia
AU - Avidan, Galia
AU - Behrmann, Marlene
N1 - Funding Information:
We thank Grace Lee Leonard for her substantial help with stimulus preparation and testing, and Michal Tanzer for help with data analysis. We also thank Cibu Thomas, Mayu Nishimura, and Suzy Scherf for valuable comments on this manuscript and Cibu Thomas for his help in testing participants K.E. and W.S. This work was supported by a NIMH 54246 grant to M.B. This paper is dedicated to the memory of B.E., who participated enthusiastically in many of our studies.
PY - 2009/7/14
Y1 - 2009/7/14
N2 - The summed activity of multiple nodes of a distributed cortical network supports face recognition in humans, including "core" ventral occipitotemporal cortex (VOTC) regions [1-3], and "extended" regions outside VOTC [4, 5]. Many individuals with congenital prosopagnosia-an impairment in face processing [6-9]-exhibit normal blood oxygenation level-dependent (BOLD) activation in the core VOTC regions [10, 11]. These individuals evince a reduction in the structural integrity of the white matter tracts connecting VOTC to anterior temporal and frontal cortices [12], part of the "extended" face network. The impairment in congenital prosopagnosia may arise, therefore, not from a dysfunction of the core VOTC areas but from a failure to propagate signals between the intact VOTC and the extended nodes of the network. Using the fMR adaptation paradigm with famous and unknown faces, we show that individuals with congenital prosopagnosia evince normal adaptation effects in VOTC, indicating sensitivity to facial identity, but show no differential activation for familiar versus unknown faces outside VOTC, particularly in the precuneus/posterior cingulate cortex and the anterior paracingulate cortex. Normal BOLD activation in VOTC is thus insufficient to subserve intact face recognition, and disrupted information propagation between VOTC and the extended face processing network may explain the functional impairment in congenital prosopagnosia.
AB - The summed activity of multiple nodes of a distributed cortical network supports face recognition in humans, including "core" ventral occipitotemporal cortex (VOTC) regions [1-3], and "extended" regions outside VOTC [4, 5]. Many individuals with congenital prosopagnosia-an impairment in face processing [6-9]-exhibit normal blood oxygenation level-dependent (BOLD) activation in the core VOTC regions [10, 11]. These individuals evince a reduction in the structural integrity of the white matter tracts connecting VOTC to anterior temporal and frontal cortices [12], part of the "extended" face network. The impairment in congenital prosopagnosia may arise, therefore, not from a dysfunction of the core VOTC areas but from a failure to propagate signals between the intact VOTC and the extended nodes of the network. Using the fMR adaptation paradigm with famous and unknown faces, we show that individuals with congenital prosopagnosia evince normal adaptation effects in VOTC, indicating sensitivity to facial identity, but show no differential activation for familiar versus unknown faces outside VOTC, particularly in the precuneus/posterior cingulate cortex and the anterior paracingulate cortex. Normal BOLD activation in VOTC is thus insufficient to subserve intact face recognition, and disrupted information propagation between VOTC and the extended face processing network may explain the functional impairment in congenital prosopagnosia.
KW - SYSNEURO
UR - http://www.scopus.com/inward/record.url?scp=67649848119&partnerID=8YFLogxK
U2 - 10.1016/j.cub.2009.04.060
DO - 10.1016/j.cub.2009.04.060
M3 - Article
C2 - 19481456
AN - SCOPUS:67649848119
SN - 0960-9822
VL - 19
SP - 1146
EP - 1150
JO - Current Biology
JF - Current Biology
IS - 13
ER -