The NGERC seeks to advance research on the antecedents of neurodevelopmental schizophrenia, i.e., on the origins and early manifestations of neurodevelopmental disturbance in this disorder. We will use data from life course cohorts that have been followed from early life and are now either in the age of risk for schizophrenia. Drawing on the resources and infrastructure of the MHCRC, we propose to extend the uses of the data for each of three types of life course cohorts: population- based birth cohorts, genetic high-risk cohorts, and epigenetic high-risk cohorts. Population-based birth cohorts are unselected for any specific etiology, whereas a genetic high-risk cohort is selected so as to be enriched for genetic etiology, and an epigenetic high-risk cohort is selected so as to be enriched for an environmental factor which can impact on genetically programmed neurodevelopment (e.g., prenatal brain insult).
The specific aims are to investigate antecedents of neurodevelopmental schizophrenia in: 1. a collaborative study that combines data across four birth cohorts. This study includes the large Oakland Child Health and Development Study birth cohort together with three cohorts derived from the multi-site National Collaborative Perinatal Project. Each cohort was based on births during 1959-1966, was followed from the prenatal period into childhood or later, and is currently being followed up for schizophrenia by Co- investigators in this proposal. Taken alone each cohort has limited statistical power, especially for rare exposures. By contrast, the combined sample of approximately 30,000 live births provide adequate power for a comprehensive investigation. Using the infrastructure of the MHCRC, we will be able to create a combined database, conduct collaborative research, and make this database a resource for other schizophrenia researchers. 2. a cohort enriched for genetic etiology. In the New York High-Risk Project, of L. Erlenhmeyer-Kimling of the NGERC, 324 offspring of schizophrenic, affectively ill, and normal parents have been followed into mid-adulthood. The present study undertakes to extend the data analysis to focus on early manifestations of neurodevelopmental disturbance in schizophrenia. 3. a cohort enriched for epigenetic etiology. in the Rubella Birth Defects Evaluation Project, 70 individuals exposed to rubella during gestation have been followed into adulthood and have been shown to have a greatly increased risk of schizophrenia. The present study will extend the collection and uses of family history and brain imaging data. While the other Cores of the MCHRC are essential to all three aims, this Core in turn is designed to contribute to each of the other Cores, not only by providing unique data, but also by fostering interdisciplinary research that is jointly conceived and conducted.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Center Core Grants (P30)
Project #
5P30MH059342-02
Application #
6336704
Study Section
Clinical Centers and Special Projects Review Committee (CCSP)
Project Start
2000-09-01
Project End
2001-08-31
Budget Start
Budget End
Support Year
2
Fiscal Year
2000
Total Cost
$143,423
Indirect Cost
Name
New York State Psychiatric Institute
Department
Type
DUNS #
167204994
City
New York
State
NY
Country
United States
Zip Code
10032
Goetz, Raymond R; Corcoran, Cheryl; Yale, Scott et al. (2007) Validity of a 'proxy'for the deficit syndrome derived from the Positive And Negative Syndrome Scale (PANSS). Schizophr Res 93:169-77
Kimhy, David; Yale, Scott; Goetz, Raymond R et al. (2006) The factorial structure of the schedule for the deficit syndrome in schizophrenia. Schizophr Bull 32:274-8
Kayser, Jurgen; Tenke, Craig E (2006) Principal components analysis of Laplacian waveforms as a generic method for identifying ERP generator patterns: I. Evaluation with auditory oddball tasks. Clin Neurophysiol 117:348-68
Kayser, Jurgen; Tenke, Craig E (2006) Principal components analysis of Laplacian waveforms as a generic method for identifying ERP generator patterns: II. Adequacy of low-density estimates. Clin Neurophysiol 117:369-80
van Berckel, Bart N M; Kegeles, Lawrence S; Waterhouse, Rikki et al. (2006) Modulation of amphetamine-induced dopamine release by group II metabotropic glutamate receptor agonist LY354740 in non-human primates studied with positron emission tomography. Neuropsychopharmacology 31:967-77
Slifstein, Mark; Narendran, Raj; Hwang, Dah-Ren et al. (2004) Effect of amphetamine on [(18)F]fallypride in vivo binding to D(2) receptors in striatal and extrastriatal regions of the primate brain: Single bolus and bolus plus constant infusion studies. Synapse 54:46-63
Slifstein, Mark; Hwang, Dah-Ren; Huang, Yiyun et al. (2004) In vivo affinity of [18F]fallypride for striatal and extrastriatal dopamine D2 receptors in nonhuman primates. Psychopharmacology (Berl) 175:274-86
Waterhouse, Rikki N; Slifstein, Mark; Dumont, Filip et al. (2004) In vivo evaluation of [11C]N-(2-chloro-5-thiomethylphenyl)-N'-(3-methoxy-phenyl)-N'-methylguanidine ([11C]GMOM) as a potential PET radiotracer for the PCP/NMDA receptor. Nucl Med Biol 31:939-48
Huang, Yiyun; Hwang, Dah-Ren; Bae, Sung-A et al. (2004) A new positron emission tomography imaging agent for the serotonin transporter: synthesis, pharmacological characterization, and kinetic analysis of [11C]2-[2-(dimethylaminomethyl)phenylthio]-5-fluoromethylphenylamine ([11C]AFM). Nucl Med Biol 31:543-56
Harkavy-Friedman, Jill M; Nelson, Elizabeth A; Venarde, David F et al. (2004) Suicidal behavior in schizophrenia and schizoaffective disorder: examining the role of depression. Suicide Life Threat Behav 34:66-76

Showing the most recent 10 out of 30 publications