This is a competitive renewal of an R01 project titled """"""""Schizophrenia, Prefrontal Cortex, and Emotion Regulation."""""""" In our current funding cycle, we tested the hypothesis that at least a subset of emotional disturbances in schizophrenia reflect deficits in the ability to use goals and context information maintained in dorsolateral prefrontal cortex (DLPFC) to and modulate emotional processing. Consistent with this hypothesis, the work conducted under the current funding cycle demonstrated that individuals with schizophrenia show: 1) relatively intact self-reports of valence and arousal in response to a range of affect producing stimuli;2) relatively intact activity in frontal and limbic regions in response to emotionally evocative stimuli when emotional regulation is not required;and 3) altered DLPFC and anterior cingulate activity when required to use goals and/or context information to modulate the influence of affective stimuli on cognitive processing. Importantly, our data also suggest that individuals with schizophrenia have deficits in the ability to use affective information to regulate or facilitate goal directed behavior. Specifically, individuals with schizophrenia seem to have difficulties using internal representations of emotional experiences, previous rewards, and motivational goals to drive current and future behavior that should allow them to obtain desired outcomes. Such deficits have major implications for understanding functional outcome in schizophrenia, as many individuals with this illness seem unable to engage in goal directed behavior (e.g., social, occupational, and educational pursuits) that would bring them into contact with potentially enjoyable experiences and positive outcomes, despite an apparently intact ability to enjoy those experiences once achieved. Clinically, such disturbances manifest as abnormalities in motivation, social engagement, and even anhedonia, or the self-reported inability to experience pleasure (or at least to anticipate experiencing pleasure). We hypothesize that individuals with schizophrenia have impairments in the ability to use reward information to guide behavior because they cannot translate such information into action plans, due to deficits in DLPFC function. However, we need to determine whether such a deficit in reward translation is primary, or simply secondary to deficits in other parts of the system that identify, maintain, and update information about rewards. For example, there is mixed evidence as to whether individuals with schizophrenia can learn cues that predict reward, or compute and update value/utility representations that drive action plans. The goal of the current study is to use state-of-the art functional neuroimaging and behavioral paradigms derived from the affective science literature to examine the integrity of the components of the neural systems linking rewards and actions. We feel it is critical to examine the function of the different components of the system in the same study in the same individuals so that we can address issues related to heterogeneity in symptom expression that may be leading to conflicting results across different studies in the literature. For each of the Specific Aims, we ask: 1) do individuals with schizophrenia differ from either community controls;and 2) do the non-psychotic siblings of individuals with schizophrenia also show deficits compared to controls (as a way to study processes associated with liability for schizophrenia unconfounded by medication status).
This project has high relevance for public health by providing critical information about the behavioral and brain mechanisms that may contribute to problems with motivation, social function, and occupational function among individuals with schizophrenia. We will examine changes in different aspects of the ability to understand and use reward and loss information to make decisions (as well as the neural systems that support these aspects of thinking) among individuals who have schizophrenia, their first-degree relatives, and among individuals with no psychiatric disorder. This information can help us to design interventions that may help to improve social and occupational function and quality of life among individuals with schizophrenia.
|Eisenstein, Sarah A; Bogdan, Ryan; Chen, Ling et al. (2017) Preliminary evidence that negative symptom severity relates to multilocus genetic profile for dopamine signaling capacity and D2 receptor binding in healthy controls and in schizophrenia. J Psychiatr Res 86:9-17|
|Moran, Erin K; Culbreth, Adam J; Barch, Deanna M (2017) Ecological momentary assessment of negative symptoms in schizophrenia: Relationships to effort-based decision making and reinforcement learning. J Abnorm Psychol 126:96-105|
|Culbreth, Adam J; Westbrook, Andrew; Daw, Nathaniel D et al. (2016) Reduced model-based decision-making in schizophrenia. J Abnorm Psychol 125:777-787|
|Luby, Joan L; Belden, Andy C; Jackson, Joshua J et al. (2016) Early Childhood Depression and Alterations in the Trajectory of Gray Matter Maturation in Middle Childhood and Early Adolescence. JAMA Psychiatry 73:31-8|
|Culbreth, Adam; Westbrook, Andrew; Barch, Deanna (2016) Negative symptoms are associated with an increased subjective cost of cognitive effort. J Abnorm Psychol 125:528-536|
|Lerman-Sinkoff, Dov B; Barch, Deanna M (2016) Network community structure alterations in adult schizophrenia: identification and localization of alterations. Neuroimage Clin 10:96-106|
|Sheffield, Julia M; Barch, Deanna M (2016) Cognition and resting-state functional connectivity in schizophrenia. Neurosci Biobehav Rev 61:108-20|
|Eisenstein, Sarah A; Bogdan, Ryan; Love-Gregory, Latisha et al. (2016) Prediction of striatal D2 receptor binding by DRD2/ANKK1 TaqIA allele status. Synapse 70:418-31|
|Chung, Yu Sun; Barch, Deanna M (2016) Frontal-striatum dysfunction during reward processing: Relationships to amotivation in schizophrenia. J Abnorm Psychol 125:453-69|
|Dowd, Erin C; Frank, Michael J; Collins, Anne et al. (2016) Probabilistic Reinforcement Learning in Patients With Schizophrenia: Relationships to Anhedonia and Avolition. Biol Psychiatry Cogn Neurosci Neuroimaging 1:460-473|
Showing the most recent 10 out of 55 publications