Childhood Trauma in Schizophrenia: Exploration of Links Between Gene Expression, Cerebral Morphology and Symptomatology (SCHIZO'TRAUMA)

Childhood Trauma in Schizophrenia: Exploration of Links Between Gene Expression, Cerebral Morphology and Symptomatology. SCHIZO' TRAUMA

Childhood trauma is known as a vulnerability factor in schizophrenia. In healthy volunteers, these adversities are linked to a decrease of grey matter of the brain, similar to those observed in schizophrenia.

In a previous study based on Voxel-Based Morphometry (VBM), including 21 schizophrenic patients and 30 healthy volunteers, the investigators shown a negative correlation between emotional neglect (important dimension in childhood trauma) and grey matter decrease. This strong correlation was significantly higher in schizophrenic patients than in healthy volunteers, suggesting a higher genetic predisposition to environmental factors in schizophrenic people.

Currently, interaction between genetic predisposition and environmental stress factors is the major model for understanding in schizophrenia. In order to analyze both effects on human body, particularly on brain, several studies currently focus on the product of genetic expression, the ribonucleic acid (ARN).

The purpose of this study is to provide an explanatory model of links between childhood trauma, candidate gene for schizophrenia expression, cerebral morphology and schizophrenic symptomatology. Using conceptual framework of stress vulnerability, structural equation modeling (SEM) will allow testing causal link between these different variables.

Study Overview

Study Type

Observational

Enrollment (Actual)

78

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Saint-Étienne, France, 42055
        • CHU de Saint Étienne

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 50 years (Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Schizophrenic patients, related volunteers (first degree relative of patient) and healthy volunteers

Description

Inclusion Criteria of patients :

  • For women with reproductively active age period: suitable contraceptive method and negative pregnancy test
  • Schizophrenia diagnosis (according to DSM 5)
  • Regular follow-up care at hospital
  • No change in antipsychotic medication (medication AND dosage) within at least six weeks
  • Patient into remission : constant dosage, out-patient and meeting Andreassen criteria
  • Who have given their informed consent before participating in the study.
  • Physical examination without significant clinical physical anomaly
  • No serious somatic pathology
  • Affiliates or entitled to a social security scheme

Exclusion Criteria of patients :

  • For women with reproductively active age period: no suitable contraceptive method (oral, hormonal, intramuscular, intrauterine device, or surgical)
  • Pregnancy or breastfeeding
  • Not meeting schizophrenic criteria according to DSM 5 or presenting resistant schizophrenic criteria according Kane criteria
  • Presenting a serious somatic disorder or neurological (particularly Parkinson disease, epilepsy, tardive dyskinesia)
  • Cardiovascular, hepatic or serious renal diseases
  • Contraindication to MRI examination, particularly ocular or intracranial metallic foreign object,pacemaker, artificial heart valve, surgical clip
  • Claustrophobia, significant tatoo in the high part of the body, IUD incompatible with MRI 3Tesla
  • Alcohol or drug addiction, within the last year
  • Recruited in other clinical trial or exclusion period from previous trial.
  • Susceptibility to self-harm behaviour according to investigator

Inclusion Criteria of Related volunteers :

  • Age, gender and socio-educational level similar to recruited patients
  • Who have given their informed consent before participating in the study.
  • First degree relative of schizophrenic patient diagnosed according DSM IV criteria
  • No schizophrenia diagnosis according DSM IV criteria
  • No psychiatric history and free of psychotropic drugs/treatment
  • Physical examination without significant clinical anomaly
  • Affiliates or entitled to a social security scheme

Exclusion Criteria of Related volunteers :

  • For women with reproductively active age period: no suitable contraceptive method (oral, hormonal, intramuscular, intrauterine device, or surgical)
  • Pregnancy or breastfeeding
  • Presenting somatic, neurological or psychiatric disorder
  • Alcohol or drug addiction, within the last year
  • Recruited in other clinical trial or exclusion period from previous trial.
  • Contraindication to MRI examination, particularly ocular or intracranial metallic foreign object, pacemaker, artificial heart valve, surgical clip
  • Claustrophobia, significant tatoo in the high part of the body, IUD incompatible with MRI 3Tesla

Inclusion Criteria of Healthy volunteers :

  • Age, gender and socio-educational level similar to recruited patients
  • Who have given their informed consent before participating in the study.
  • No schizophrenia diagnosis according DSM IV criteria
  • No personal or family history of psychiatric disorders
  • Free of psychotropic drugs/treatment
  • Physical examination without significant clinical anomaly
  • Affiliates or entitled to a social security scheme

Exclusion Criteria of Healthy volunteers :

Beside the absence of schizophrenia diagnosis, healthy volunteers should meet the same exclusion criteria as patients

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Schizophrenic patients
Patients will have clinical psychiatric evaluation, brain imaging and blood sample
brain imaging : structural anatomy, emotional congruence, anatomic connectivity, functional connectivity
27,5 ml of blood sample : genetic analysis and biobank
Global Assessment Scale(GAS),Mini International Neuropsychiatric Interview(MINI),Positive and Negative Symptoms Scale(PANSS),Family Interview for Genetic Studies(FIGS),Calgary Depression Scale for Schizophrenia(CDSS),extrapyramidal side effects evaluation or Simpson-Angus scale evaluation(ESRS),Apathy Evaluation Scale(AES-C),State-Trait Anxiety Inventory(STAI),Beck Depression Inventory(BDI-13),Eysenck Personality Questionnaire-Revised(EPQ-R),Assessment of Schizotypal Personality(SPQ),Emotion Regulation Questionnaire(ERQ),Emotional Reactivity Scale(ERS),Toronto Alexithymia Scale(TAS-20),social anhedonia scale(SAS),Childhood Trauma Questionnaire(CTQ),Clinical-administered Post Traumatic Stress Disorder Scale(CAPS),Wechsler Adult Intelligence Scale(WAIS-III),Trail Making Test(TMT),Pen and paper visuospatial working memory(DOT-test),impulsivity test(GoStop),Stroop test,National Adult Reading Test(NART),Wechsler Adult Intelligence Scale(WAIS-III),Facial Emotion Recognition task(FER)
Related volunteers (first degree relative of patient)
Related volunteers will have clinical psychiatric evaluation, brain imaging and blood sample
brain imaging : structural anatomy, emotional congruence, anatomic connectivity, functional connectivity
27,5 ml of blood sample : genetic analysis and biobank
Global Assessment Scale(GAS),Mini International Neuropsychiatric Interview(MINI),Positive and Negative Symptoms Scale(PANSS),Family Interview for Genetic Studies(FIGS),Calgary Depression Scale for Schizophrenia(CDSS),extrapyramidal side effects evaluation or Simpson-Angus scale evaluation(ESRS),Apathy Evaluation Scale(AES-C),State-Trait Anxiety Inventory(STAI),Beck Depression Inventory(BDI-13),Eysenck Personality Questionnaire-Revised(EPQ-R),Assessment of Schizotypal Personality(SPQ),Emotion Regulation Questionnaire(ERQ),Emotional Reactivity Scale(ERS),Toronto Alexithymia Scale(TAS-20),social anhedonia scale(SAS),Childhood Trauma Questionnaire(CTQ),Clinical-administered Post Traumatic Stress Disorder Scale(CAPS),Wechsler Adult Intelligence Scale(WAIS-III),Trail Making Test(TMT),Pen and paper visuospatial working memory(DOT-test),impulsivity test(GoStop),Stroop test,National Adult Reading Test(NART),Wechsler Adult Intelligence Scale(WAIS-III),Facial Emotion Recognition task(FER)
Healthy volunteers
Healthy volunteers will have clinical psychiatric evaluation, brain imaging and blood sample
brain imaging : structural anatomy, emotional congruence, anatomic connectivity, functional connectivity
27,5 ml of blood sample : genetic analysis and biobank
Global Assessment Scale(GAS),Mini International Neuropsychiatric Interview(MINI),Positive and Negative Symptoms Scale(PANSS),Family Interview for Genetic Studies(FIGS),Calgary Depression Scale for Schizophrenia(CDSS),extrapyramidal side effects evaluation or Simpson-Angus scale evaluation(ESRS),Apathy Evaluation Scale(AES-C),State-Trait Anxiety Inventory(STAI),Beck Depression Inventory(BDI-13),Eysenck Personality Questionnaire-Revised(EPQ-R),Assessment of Schizotypal Personality(SPQ),Emotion Regulation Questionnaire(ERQ),Emotional Reactivity Scale(ERS),Toronto Alexithymia Scale(TAS-20),social anhedonia scale(SAS),Childhood Trauma Questionnaire(CTQ),Clinical-administered Post Traumatic Stress Disorder Scale(CAPS),Wechsler Adult Intelligence Scale(WAIS-III),Trail Making Test(TMT),Pen and paper visuospatial working memory(DOT-test),impulsivity test(GoStop),Stroop test,National Adult Reading Test(NART),Wechsler Adult Intelligence Scale(WAIS-III),Facial Emotion Recognition task(FER)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Childhood Trauma Questionnaire (CTQ) for childhood trauma.
Time Frame: 5 days

development of an etiopathogenic model characteristic of schizophrenia

Childhood Trauma Questionnaire : to assess five types of childhood trauma :

  1. Emotional neglect
  2. physical abuse
  3. emotional abuse
  4. physical neglect
  5. sexual abuse

Each item being rated in 5 answer choice from 1 to 5 (never, rarely, sometimes, often or very often)

5 days
Quantitative measurement of RNAs
Time Frame: 5 days
development of an etiopathogenic model characteristic of schizophrenia
5 days
Voxel-based morphometry (VBM) for total gray matter
Time Frame: 5 days
development of an etiopathogenic model characteristic of schizophrenia
5 days
Voxel-based morphometry (VBM) for regional gray matter density.
Time Frame: 5 days
development of an etiopathogenic model characteristic of schizophrenia
5 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Connectivity in the cortico-limbic circuit
Time Frame: 5 days
5 days
Volumetry of the brain
Time Frame: 5 days
5 days
Correlation of BOLD activity in the cortico-limbic circuit in patients with patients with symptomatic variables
Time Frame: 5 days
symptomatic variables : PANSS scale
5 days
Correlation of BOLD activity in the cortico-limbic circuit with emotional variables
Time Frame: 5 days
emotional variables : ERS scale, ERQ scale, TAS-20 scale, SAS scale, AES-C scale
5 days
Correlation of BOLD activity in the cortico-limbic circuit with personality characteristics
Time Frame: 5 days
personality characteristics : EPQ-R scale, SPQ scale
5 days
Correlation of BOLD activity in the cortico-limbic circuit with history of trauma in childhood
Time Frame: 5 days
history of trauma in childhood : CTQ scale
5 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 14, 2018

Primary Completion (Actual)

November 30, 2023

Study Completion (Actual)

November 30, 2023

Study Registration Dates

First Submitted

November 10, 2017

First Submitted That Met QC Criteria

November 22, 2017

First Posted (Actual)

November 28, 2017

Study Record Updates

Last Update Posted (Actual)

January 17, 2024

Last Update Submitted That Met QC Criteria

January 16, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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