TY - JOUR
T1 - Altered reward processing in the nucleus accumbens and mesial prefrontal cortex of patients with posttraumatic stress disorder
AU - Sailer, Uta
AU - Robinson, Simon
AU - Fischmeister, Florian Ph S
AU - König, Dorothea
AU - Oppenauer, Claudia
AU - Lueger-Schuster, Brigitte
AU - Moser, Ewald
AU - Kryspin-Exner, Ilse
AU - Bauer, Herbert
N1 - Funding Information:
This study was funded by a fellowship of the Deutsche Forschungsgemeinschaft (DFG) to U.S. and grant no. 11437 from the Austrian National Bank (OENB). We thank the Schuhfried GmbH for providing the test material and S. Nieuwenhuis for making available the instruction of his experiment.
PY - 2008/9
Y1 - 2008/9
N2 - Posttraumatic stress disorder (PTSD) is known to be associated with altered medial prefrontal activation in response to threatening stimuli and with behavioural deficits in prefrontal functions such as working memory and attention. Given the importance of these areas and processes for decision-making, this functional magnetic resonance imaging study investigated whether decision-making is altered in patients with PTSD. In particular, the neural response to gain and loss feedback was evaluated in a decision-making task in which subjects could maximise their number of points total by learning a particular response pattern. Behaviourally, controls learned the correct response pattern faster than patients. Functionally, patients and controls differed in their neural response to gains, but not in their response to losses. During the processing of gains in the late phase of learning, PTSD patients as compared to controls showed lower activation in the nucleus accumbens and the mesial PFC, critical structures in the reward pathway. This reduced activation was not due to different rates of learning, since it was similarly present in patients with unimpaired learning performance. These findings suggest that positive outcome information lost its salience for patients with PTSD. This may reflect decreasing motivation as the task progressed.
AB - Posttraumatic stress disorder (PTSD) is known to be associated with altered medial prefrontal activation in response to threatening stimuli and with behavioural deficits in prefrontal functions such as working memory and attention. Given the importance of these areas and processes for decision-making, this functional magnetic resonance imaging study investigated whether decision-making is altered in patients with PTSD. In particular, the neural response to gain and loss feedback was evaluated in a decision-making task in which subjects could maximise their number of points total by learning a particular response pattern. Behaviourally, controls learned the correct response pattern faster than patients. Functionally, patients and controls differed in their neural response to gains, but not in their response to losses. During the processing of gains in the late phase of learning, PTSD patients as compared to controls showed lower activation in the nucleus accumbens and the mesial PFC, critical structures in the reward pathway. This reduced activation was not due to different rates of learning, since it was similarly present in patients with unimpaired learning performance. These findings suggest that positive outcome information lost its salience for patients with PTSD. This may reflect decreasing motivation as the task progressed.
KW - Adult
KW - Case-Control Studies
KW - Decision Making/physiology
KW - Feedback
KW - Female
KW - Humans
KW - Image Processing, Computer-Assisted/methods
KW - Magnetic Resonance Imaging/methods
KW - Male
KW - Mental Processes/physiology
KW - Neuropsychological Tests
KW - Nucleus Accumbens/blood supply
KW - Oxygen/blood
KW - Prefrontal Cortex/blood supply
KW - Psychomotor Performance/physiology
KW - Reward
KW - Statistics, Nonparametric
KW - Stress Disorders, Post-Traumatic/pathology
UR - http://www.scopus.com/inward/record.url?scp=47349107423&partnerID=8YFLogxK
U2 - 10.1016/j.neuropsychologia.2008.05.022
DO - 10.1016/j.neuropsychologia.2008.05.022
M3 - Journal article
C2 - 18597797
SN - 0028-3932
VL - 46
SP - 2836
EP - 2844
JO - Neuropsychologia
JF - Neuropsychologia
IS - 11
ER -