Clinical response to treatment with a partial dopamine agonist is related to changes in reward processing
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Clinical response to treatment with a partial dopamine agonist is related to changes in reward processing. / Tangmose, Karen; Rostrup, Egill; Bojesen, Kirsten Borup; Sigvard, Anne; Glenthøj, Birte Y.; Nielsen, Mette Ødegaard.
I: Psychiatry Research, Bind 326, 115308, 2023.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Clinical response to treatment with a partial dopamine agonist is related to changes in reward processing
AU - Tangmose, Karen
AU - Rostrup, Egill
AU - Bojesen, Kirsten Borup
AU - Sigvard, Anne
AU - Glenthøj, Birte Y.
AU - Nielsen, Mette Ødegaard
N1 - Publisher Copyright: © 2023
PY - 2023
Y1 - 2023
N2 - Aberrant neuronal coding of reward processing has been linked to psychosis. It remains unresolved how treatment with a partial dopamine agonist affects reward processing, and whether treatment affects reward processing differently in patients responding and not responding to treatment. Here, 33 antipsychotic-naïve psychosis patients and 33 matched healthy controls underwent functional magnetic resonance imaging before and after patients received aripiprazole monotherapy for six weeks. Processing of motivational salient events and negative outcome evaluation (NOE) was examined using a monetary incentive delay task. Psychopathology was assessed with the Positive and Negative Syndrome Scale, and responders were identified by having ≥30% reduction in positive symptoms (N=21). At baseline, patients displayed an increased NOE signal in the caudate and dorsolateral prefrontal cortex compared to healthy controls. In the caudate, the NOE signal was normalized at follow-up, and normalization was driven by responders. In responders only, there was a significant improvement in the motivational salience signal in the caudate at follow-up. Motivational salience and NOE signals in the caudate may be associated with a dopaminergic mechanism in patients characterized as responders which may not be the case in non-responders. Likewise, non-dopaminergic mechanism may underly abnormal NOE processing in dorsolateral prefrontal cortex.
AB - Aberrant neuronal coding of reward processing has been linked to psychosis. It remains unresolved how treatment with a partial dopamine agonist affects reward processing, and whether treatment affects reward processing differently in patients responding and not responding to treatment. Here, 33 antipsychotic-naïve psychosis patients and 33 matched healthy controls underwent functional magnetic resonance imaging before and after patients received aripiprazole monotherapy for six weeks. Processing of motivational salient events and negative outcome evaluation (NOE) was examined using a monetary incentive delay task. Psychopathology was assessed with the Positive and Negative Syndrome Scale, and responders were identified by having ≥30% reduction in positive symptoms (N=21). At baseline, patients displayed an increased NOE signal in the caudate and dorsolateral prefrontal cortex compared to healthy controls. In the caudate, the NOE signal was normalized at follow-up, and normalization was driven by responders. In responders only, there was a significant improvement in the motivational salience signal in the caudate at follow-up. Motivational salience and NOE signals in the caudate may be associated with a dopaminergic mechanism in patients characterized as responders which may not be the case in non-responders. Likewise, non-dopaminergic mechanism may underly abnormal NOE processing in dorsolateral prefrontal cortex.
KW - Antipsychotic-naive
KW - First episode psychoses
KW - Longitudinal study
KW - Motivational salience
KW - Outcome evaluation
KW - Treatment response
U2 - 10.1016/j.psychres.2023.115308
DO - 10.1016/j.psychres.2023.115308
M3 - Journal article
C2 - 37399765
AN - SCOPUS:85163454227
VL - 326
JO - Psychiatry Research
JF - Psychiatry Research
SN - 0165-1781
M1 - 115308
ER -
ID: 363360739