The Role of Dysmyelination in Cognitive Impairment of Psychotic Spectrum Disorders

Sponsor
NYU Langone Health (Other)
Overall Status
Recruiting
CT.gov ID
NCT03166098
Collaborator
(none)
210
1
67.8
3.1

Study Details

Study Description

Brief Summary

This is a single center study that uses both between-group comparisons and correlational analyses to establish biomarkers of dysmyelination and cognitive impairment in Psychotic Spectrum Disorders using imaging and neuropsychological assays.The study will provide non-invasive biomarkers of cognitive dysfunction in Psychotic Spectrum Disorder.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Cognitive Function Assessments

Study Design

Study Type:
Observational
Anticipated Enrollment :
210 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
The Role of Dysmyelination in Cognitive Impairment of Psychotic Spectrum Disorders
Actual Study Start Date :
Jul 5, 2016
Anticipated Primary Completion Date :
Mar 1, 2022
Anticipated Study Completion Date :
Mar 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Diagnosis of Schizophrenia

Diagnostic Test: Cognitive Function Assessments
The NIMH-Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) is a consensus battery that is considered state-of-the art in the evaluation of cognitive skills for schizophrenia research.(Burton et al., 2013, Harvey, 2014) The complete cognitive battery takes about one hour to administer, and is comprised of 10 subtests measuring seven essential domains of function, with very good reliability and validity.(Nuechterlein 2008, August et al., 2012) The MATRICS subtests have been incorporated into the cognitive battery described below, with supplementary subtests included where indicated within each domain.

Diagnosis of Bipolar Disorder

Diagnostic Test: Cognitive Function Assessments
The NIMH-Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) is a consensus battery that is considered state-of-the art in the evaluation of cognitive skills for schizophrenia research.(Burton et al., 2013, Harvey, 2014) The complete cognitive battery takes about one hour to administer, and is comprised of 10 subtests measuring seven essential domains of function, with very good reliability and validity.(Nuechterlein 2008, August et al., 2012) The MATRICS subtests have been incorporated into the cognitive battery described below, with supplementary subtests included where indicated within each domain.

Unaffected siblings of the SZ groups

Diagnostic Test: Cognitive Function Assessments
The NIMH-Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) is a consensus battery that is considered state-of-the art in the evaluation of cognitive skills for schizophrenia research.(Burton et al., 2013, Harvey, 2014) The complete cognitive battery takes about one hour to administer, and is comprised of 10 subtests measuring seven essential domains of function, with very good reliability and validity.(Nuechterlein 2008, August et al., 2012) The MATRICS subtests have been incorporated into the cognitive battery described below, with supplementary subtests included where indicated within each domain.

Unaffected siblings of the BP group

Diagnostic Test: Cognitive Function Assessments
The NIMH-Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) is a consensus battery that is considered state-of-the art in the evaluation of cognitive skills for schizophrenia research.(Burton et al., 2013, Harvey, 2014) The complete cognitive battery takes about one hour to administer, and is comprised of 10 subtests measuring seven essential domains of function, with very good reliability and validity.(Nuechterlein 2008, August et al., 2012) The MATRICS subtests have been incorporated into the cognitive battery described below, with supplementary subtests included where indicated within each domain.

Healthy control (HC) comparison group

Diagnostic Test: Cognitive Function Assessments
The NIMH-Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) is a consensus battery that is considered state-of-the art in the evaluation of cognitive skills for schizophrenia research.(Burton et al., 2013, Harvey, 2014) The complete cognitive battery takes about one hour to administer, and is comprised of 10 subtests measuring seven essential domains of function, with very good reliability and validity.(Nuechterlein 2008, August et al., 2012) The MATRICS subtests have been incorporated into the cognitive battery described below, with supplementary subtests included where indicated within each domain.

Outcome Measures

Primary Outcome Measures

  1. DKI(metrics RDextra, faxon, and ADextra) Metrics [6 Years]

    To compare DKI metrics (faxon, RDextra, and ADextra) in patients with SZ or BP, their unaffected siblings (SIB), and healthy comparison control (HC) subjects

  2. Magnetic Resonance Spectroscopy will be employed to obtain quantitative metrics of choline (Cho) [1 Hour]

    Choline Concentration (1H-MRS)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 30 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
Patients:
  • current DSM-5-defined diagnosis of a schizophrenia or bipolar disorder. A best estimate diagnostic approach will be utilized in which information from the Diagnostic Interview for Genetic Studies (DIGS) is supplemented by information from family informants, psychiatrists, and medical records to generate a diagnosis as needed

  • no alcohol or substance abuse during the last 6 month

  • no current substance-induced psychotic disorder or a psychotic disorder due to a general medical condition determined by DSM-5 criteria

  • ages 18 to 30 years old;

  • any race

  • competent and willing to sign informed consent

  • within 5 years from the disease onset.

Siblings:
  • have the same biological parents as their PSD sibling

  • any race

  • no current or past history of psychotropic medication usage

  • no alcohol or substance abuse during the last 6 months

  • competent and willing to sign informed consent;

  • ages 18 to 30 years old.

Healthy controls:
  • matched for age to PSD patients

  • no current or past history of psychotropic medication usage

  • no prodromal symptoms and no family history of PSD

  • no alcohol or substance abuse during the last 6 months

  • competent and willing to sign informed consent.

  • all attempts will be made to recruit controls with similar parental SES as patients. However, given that PSD are both a neurodevelopmental and familial disorder, exact matching for educational level or IQ may neither be possible nor desirable.

have the same biological parents as their PSD sibling

  • any race

  • no current or past history of psychotropic medication usage

  • no alcohol or substance abuse during the last 6 months

  • competent and willing to sign informed consent;

  • ages 18 to 30 years old.

Exclusion Criteria:
  • a serious neurological or endocrine disorder or any medical condition or treatment known to affect the brain, 2) organic brain disorder, mental retardation, or significant medical illness;

  • significant risk of suicidal or homicidal behavior;

  • must not have met DSM-5 criteria for current alcohol or drug dependence in the last 6 months;

  • contraindications to MRI scanning (i.e., metal implants, pacemakers, pregnancy, etc.);

  • documented loss of consciousness (LOC) for longer than 30 minutes or LOC with any neurological sequelae.

Contacts and Locations

Locations

Site City State Country Postal Code
1 New York University School of Medicine New York New York United States 10016

Sponsors and Collaborators

  • NYU Langone Health

Investigators

  • Principal Investigator: Mariana Lazar, MD, NYU Langone Health

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
NYU Langone Health
ClinicalTrials.gov Identifier:
NCT03166098
Other Study ID Numbers:
  • 15-00754
First Posted:
May 24, 2017
Last Update Posted:
Feb 14, 2022
Last Verified:
Feb 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by NYU Langone Health
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 14, 2022