Ignite Creation Date:
2024-05-05 @ 7:23 PM
Last Modification Date:
2024-10-26 @ 9:48 AM
Study NCT ID:
NCT00666432
Status:
COMPLETED
Last Update Posted:
2021-05-03
First Post:
2008-04-21
Brief Title:
Bipolar and Schizophrenia Consortium for Parsing Intermediate Phenotypes
Sponsor:
University of Maryland Baltimore
Organization:
University of Maryland Baltimore
Study Overview
Official Title:
Bipolar and Schizophrenia Consortium for Parsing Intermediate Phenotypes
Status:
COMPLETED
Status Verified Date:
2021-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Briefly this multisite study is designed to identify endophenotypes ie heritable biomarkers associated with either schizophrenia or bipolar disorder alone or both together The subsequent genetic analyses will search genomic loci and candidate genes associated with each of the independent endophenotypes This is a five site study that is slotted for NIMH funding
Detailed Description:
We propose to recruit 100 case probands with a diagnosis of SZ 100 case probands with a diagnosis of BP Disorder I with history of psychosis BPI-P and 400 1st degree case relatives All 1st degree family members who are willing to participate will provide clinical information and blood sample only a proportion will be eligible for endophenotypic studies Individuals with psychotic disorder not otherwise specified are also eligible for testing Their data will be incorporated with the schizophrenia or bipolar data upon confirmation of diagnosis Family members of individuals with psychotic disorder not otherwise specified will not be tested unless the individual has a later confirmed diagnosis of schizophrenia or bipolar disorder Probands will not be tested during the acute phase of the illness as judged clinically eg significant increase in core symptoms from their stable baseline that requires a change in treatment such increased dose of medication drug change or hospitalization As part of another existing protocol we have collected most of the endophynotypic information in schizophrenia probands and 1st degree relatives other than brain imaging and few other tests We will attempt to recruit these subjects to complete the imaging studies and the data will be used in the current study
We will recruit 100 healthy comparison subjects from the community in order to describe the distribution of normal values for our endophenotype procedures in a demographically matched sample The SZ and BPI-P probands and 50 healthy control subjects will be frequency matched on age sex ratio and head of the households socio-economic status SES Another group of 50 healthy control subjects will be similarly matched to the relative groups recruited
Participants will undergo a number of clinical electrophysiological structural brain imaging perceptual and cognitive assessments These data will be used to identify phenotypes likely to be associated with genetic risk for schizophrenia andor bipolar disorder and to determine how these phenotypes aggregate in families Some of the analyses will focus on examining associations between candidate genes and these alternative phenotypes Thus if we are not able to recruit relatives we may still collect these phenotypic data in probands and their genetic sample for future genotypephenotype association studies Family members may elect to participate only in the clinical and blood draw portions of the study Testing procedures require a 12 -15 hour time commitment and testing will be completed over 2 or more days Participants will be asked to give a blood or saliva if difficult to obtain blood sample for instance because of fear of blood draws which will be stored for future genetic analyses Data from the previous family study will be combined with the data collected in this protocol for some of the analyses
We will recruit 100 healthy comparison subjects from the community in order to describe the distribution of normal values for our endophenotype procedures in a demographically matched sample The SZ and BPI-P probands and 50 healthy control subjects will be frequency matched on age sex ratio and head of the households socio-economic status SES Another group of 50 healthy control subjects will be similarly matched to the relative groups recruited
Participants will undergo a number of clinical electrophysiological structural brain imaging perceptual and cognitive assessments These data will be used to identify phenotypes likely to be associated with genetic risk for schizophrenia andor bipolar disorder and to determine how these phenotypes aggregate in families Some of the analyses will focus on examining associations between candidate genes and these alternative phenotypes Thus if we are not able to recruit relatives we may still collect these phenotypic data in probands and their genetic sample for future genotypephenotype association studies Family members may elect to participate only in the clinical and blood draw portions of the study Testing procedures require a 12 -15 hour time commitment and testing will be completed over 2 or more days Participants will be asked to give a blood or saliva if difficult to obtain blood sample for instance because of fear of blood draws which will be stored for future genetic analyses Data from the previous family study will be combined with the data collected in this protocol for some of the analyses
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| R01MH077852 | NIH | None | httpsreporternihgovquickSearchR01MH077852 |