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Original Article |

Improvement of Brain Reward Abnormalities by Antipsychotic Monotherapy in Schizophrenia

Mette Odegaard Nielsen, MD, PhD; Egill Rostrup, MD, DMSc; Sanne Wulff, MD; Nikolaj Bak, PhD, MSc; Brian Villumsen Broberg, PhD, MSc; Henrik Lublin, MD, DMSc; Shitij Kapur, MD, PhD; Birte Glenthoj, MD, DMSc
Arch Gen Psychiatry. 2012;69(12):1195-1204. doi:10.1001/archgenpsychiatry.2012.847.
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Context  Schizophrenic symptoms are linked to a dysfunction of dopamine neurotransmission and the brain reward system. However, it remains unclear whether antipsychotic treatment, which blocks dopamine transmission, improves, alters, or even worsens the reward-related abnormalities.

Objective  To investigate changes in reward-related brain activations in schizophrenia before and after antipsychotic monotherapy with a dopamine D2/D3 antagonist.

Design  Longitudinal cohort study.

Setting  Psychiatric inpatients and outpatients in the Capital Region of Denmark.

Participants  Twenty-three antipsychotic-naive patients with first-episode schizophrenia and 24 healthy controls initially matched on age, sex, and parental socioeconomic status were examined with functional magnetic resonance imaging while playing a variant of the monetary incentive delay task.

Interventions  Patients were treated for 6 weeks with the antipsychotic compound amisulpride. Controls were followed up without treatment.

Main Outcome Measures  Task-related blood oxygen level–dependent activations as measured by functional magnetic resonance imaging before and after antipsychotic treatment.

Results  At baseline, patients, as compared with controls, demonstrated an attenuation of brain activation during reward anticipation in the ventral striatum, bilaterally. After 6 weeks of treatment, patients showed an increase in the anticipation-related functional magnetic resonance imaging signal and were no longer statistically distinguishable from healthy controls. Among the patients, there was a correlation between the improvement of positive symptoms and normalization of reward-related activation. Those who showed the greatest clinical improvement in positive symptoms also showed the greatest increase in reward-related activation after treatment.

Conclusions  To our knowledge, this is the first controlled, longitudinal study of reward disturbances in schizophrenic patients before and after their first antipsychotic treatment. Our results demonstrate that alterations in reward processing are fundamental to the illness and are seen prior to any treatment. Antipsychotic treatment tends to normalize the response of the reward system; this was especially seen in the patients with the most pronounced treatment effect on the positive symptoms.

Trial Registration  clinicaltrials.gov Identifier: NCT01154829.

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Figures

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Figure 1. The modified monetary incentive delay task. A cue indicating the trial condition initiates each trial (1). After a short delay (2), a target appears briefly on the screen (3). For each condition, the goal is to press a button while the target is on the screen. After another delay (4), subjects receive feedback (5) on whether they lost or won money and how much money they have won so far. One of the 6 cues is presented in each trial. The color indicates if it is a certain (blue) or uncertain (green) condition; the direction of the arrow indicates if it is a gain (up), loss (down), or neutral (both) trial.

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Figure 2. Behavioral data (see “Behavioral Data” subsection in the “Results” section for description). Error bars indicate standard error. cg Indicates certain gain; cl, certain loss; cn, certain neutral; ug, uncertain gain; ul, uncertain loss; and un, uncertain neutral.

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Figure 3. Activation map for the salience contrast at baseline and follow-up. A-C, Group differences in the voxelwise comparison at baseline (A) and activation map for the patients (B) and controls (C) at baseline. D-F, Group differences in the voxelwise comparison at follow-up (D) and activation map for the patients (E) and controls (F) at follow-up. The threshold is P < .001 uncorrected, except in the healthy controls, where the threshold is lowered to P < .000001 for illustrative purposes. A indicates anterior; COR, coronal; L, left; P, posterior; R, right; SAG, sagittal; and TRA, transverse.

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Figure 4. Interaction in the right ventral striatum region of interest. There was an overall signal increase in the patients, whereas a signal decrease was found in healthy controls.

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Figure 5. Improvement in Positive and Negative Syndrome Scale (PANSS) positive symptoms in patients correlated with the signal increase in the salience contrast. The most pronounced change in positive symptoms was in the patients with the largest signal increase. VS indicates ventral striatum.

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