Psychosis is a construct that has classically been treated as the ?hallmark feature? of schizophrenia, but is nonetheless present in other disorders including schizoaffective disorder and bipolar disorder. Persons with psychosis experience profound and disabling dysfunction in multiple domains of function, including motor system, cognitive control, and social function. This exacts a tremendous toll on afflicted persons, their communities, and society at large. Due to definitional issues, any two persons with psychosis may have vastly different psychotic features. This leads to significant within-diagnosis heterogeneity, which may contribute to the lack of disease specific diagnostic findings. In addition, there is significant comorbidity across diagnoses, which potentially results in under-sampling of the full range of disease expression when only one diagnostic group is included in a given study. To address these issues, the NIMH developed the Research Domain Criteria (RDoC) project to link behavioral endpoints with their underlying neural mechanisms. In line with the RDoC goals, the proposed project focuses upon determining dimensional neural predictors of three recognized domains of dysfunction in psychosis using a transdiagnostic subject population comprised of persons with schizophrenia, schizoaffective disorder, and bipolar disorder. To accomplish this, multiset canonical correlation analysis + joint independent components analysis (mCCA+jICA) will be employed to analyze a multimodal neuroimaging dataset comprised of gray-matter, white matter, and functional connectivity measures using a meta-analytic approach to selecting areas empirically identified as related to three psychosis domains of interest. Methodologies will be prototyped using data from the Human Connectome Project (HCP) and then extended to a dataset comprised of persons with psychosis. For each specific aim, analyses will: 1) select meta-analytically determined areas; 2) extract gray-matter, white-matter, and functional connectivity measures; 3) perform mCCA+jICA to identify the significant orthogonal sources of variance; and, 4) use a regression approach to link domain-specific behavioral and self-report measures to the sources identified by mCCA+jICA.
In Aim 1, motor system dysfunction will be examined and linked to mCCA+jICA results using two measures of the motor system.
In Aim 2, cognitive control dysfunction will be examined and linked to mCCA+jICA results using a composite measure of cognitive control and then followed-up with four individual measures. And, in Aim 3, social dysfunction will be examined and linked to mCCA+jICA results using a composite measure of social function and then followed-up with four individual measures. The proposed research may lead to findings that better support dimensional models of dysfunction within domains of psychosis and better modeling of psychopathology. Further, it may allow future research efforts to study more homogenous subject populations enabling more targeted diagnosis and treatment of specific dysfunction in psychosis.

Public Health Relevance

This project aims to identify the underlying brain systems that are responsible for abnormalities seen in the motor system, control of thought and speech processes (cognitive control), and social function in persons with psychosis including diagnoses of schizophrenia, schizoaffective disorder, and bipolar disorder. There is strong evidence for abnormalities in all three of these behavioral domains across all three diseases, and we propose to use innovative methods that allow us to combine and simultaneously analyze multiple different measures of brain function and structure in order to identify how changes in the brain are linked to our three targeted domains of behavioral abnormality in psychosis. The results of this work will help researchers define better models for mental illness, select more precise groups of persons for research studies, and will enable to clinicians to better identify and treat specific aspects of mental illness.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Individual Predoctoral NRSA for M.D./Ph.D. Fellowships (ADAMHA) (F30)
Project #
5F30MH109294-04
Application #
9716655
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Chavez, Mark
Project Start
2016-07-01
Project End
2020-06-30
Budget Start
2019-07-01
Budget End
2020-06-30
Support Year
4
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Washington University
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Lerman-Sinkoff, Dov B; Sui, Jing; Rachakonda, Srinivas et al. (2017) Multimodal neural correlates of cognitive control in the Human Connectome Project. Neuroimage 163:41-54