The study """"""""Vulnerability Markers in Prodromal Schizophrenia"""""""" will identify, assess and follow individuals at high risk for schizophrenia (at-risk group) who will be compared to normal subjects using 1) clinical assessment 2) psychophysiological and 3) neuropsychological measures of information processing.
The specific aims of the study are to better understand pre-psychotic symptomatology and the predictive profile of prodromal signs and symptoms of schizophrenia through longitudinal clinical assessment and to determine whether at-risk subjects have information processing deficits consistent with those observed in other schizophrenic spectrum populations. Increased knowledge regarding the onset of psychosis may help to better identify individuals who are at-risk for psychosis and provide insight into the neurodevelopmental processes that occur in this stage. The first hypothesis of the proposed study is that the at-risk group will have abnormalities of information processing when compared to normals. In this context, it is predicted that the at-risk group will have decreased prepulse inhibition and habituation of the startle response; impaired visual backward masking; reduced P50 event related potential gating; and neuropsychological deficits. The second hypothesis states that information processing performance will be reliable across repeated test sessions that will occur over a 2 year period, suggesting that the information processing measures are stable measures of trait-related deficits. The third hypothesis states that the clinical and information processing measures will be differentially correlated with each other and one or more factors will predict which individuals will make the transition to psychosis. If neurobiological markers can be identified that are predictive of later psychosis, these markers could be used in conjunction with clinical assessment in determining which subjects would benefit from early treatment. Appropriate intervention at this early stage could possible thwart the development of a psychotic illness along with associated difficulties and deterioration. Delaying the emergence of psychosis may in itself be beneficial because a more mature individual may be better able to deal with the onset of a psychotic illness. The disruption of social networks, education and occupational activity as well as the high incidence of suicide and crime that often accompany psychosis might be reduced or averted.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH060720-05
Application #
6757863
Study Section
Special Emphasis Panel (ZRG1-BBBP-5 (01))
Program Officer
Meinecke, Douglas L
Project Start
2000-07-05
Project End
2006-04-30
Budget Start
2004-07-01
Budget End
2006-04-30
Support Year
5
Fiscal Year
2004
Total Cost
$331,491
Indirect Cost
Name
University of California San Diego
Department
Psychiatry
Type
Schools of Medicine
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Velthorst, Eva; Meyer, Eric C; Giuliano, Anthony J et al. (2018) Neurocognitive profiles in the prodrome to psychosis in NAPLS-1. Schizophr Res :
Velthorst, Eva; Zinberg, Jamie; Addington, Jean et al. (2018) Potentially important periods of change in the development of social and role functioning in youth at clinical high risk for psychosis. Dev Psychopathol 30:39-47
Hampton, Joya N; Trotman, Hanan D; Addington, Jean et al. (2018) The relation of atypical antipsychotic use and stress with weight in individuals at clinical high risk for psychosis. Stress Health 34:591-600
Kline, Emily R; Seidman, Larry J; Cornblatt, Barbara A et al. (2018) Depression and clinical high-risk states: Baseline presentation of depressed vs. non-depressed participants in the NAPLS-2 cohort. Schizophr Res 192:357-363
Lu, Yun; Marshall, Catherine; Cadenhead, Kristin S et al. (2017) Perceptual abnormalities in clinical high risk youth and the role of trauma, cannabis use and anxiety. Psychiatry Res 258:462-468
Addington, Jean; Piskulic, Danijela; Liu, Lu et al. (2017) Comorbid diagnoses for youth at clinical high risk of psychosis. Schizophr Res 190:90-95
Obermeit, Lisa C; Beltran, Jessica; Casaletto, Kaitlin B et al. (2017) Evaluating the accuracy of self-report for the diagnosis of HIV-associated neurocognitive disorder (HAND): defining ""symptomatic"" versus ""asymptomatic"" HAND. J Neurovirol 23:67-78
McAusland, Laina; Buchy, Lisa; Cadenhead, Kristin S et al. (2017) Anxiety in youth at clinical high risk for psychosis. Early Interv Psychiatry 11:480-487
Marshall, Catherine; Lu, Yun; Lyngberg, Kristina et al. (2017) Changes in symptom content from a clinical high-risk state to conversion to psychosis. Early Interv Psychiatry :
Deighton, Stephanie; Buchy, Lisa; Cadenhead, Kristin S et al. (2016) Traumatic brain injury in individuals at clinical high risk for psychosis. Schizophr Res 174:77-81

Showing the most recent 10 out of 68 publications