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Emotion Endophenotypes in Schizophrenia

Not Applicable
Conditions
Schizophrenia
Interventions
Other: MRI (Magnetic resonance imaging)
Genetic: Polymorphism (SNP in DNA)
Genetic: quantitative measures of mRNA
Other: Neuropsychological assessment
Registration Number
NCT02834208
Lead Sponsor
Assistance Publique Hopitaux De Marseille
Brief Summary

Schizophrenia is an invalidating psychiatric illness with a strong genetic component characterized by abnormal processing of emotional information. This alteration in emotion processing has been described in acute as well as in remission phases of the illness. It has also been found in healthy relatives of patients with schizophrenia and in subjects at high risk of psychosis. Thus, alterations in emotional information processing are not only linked to the prognosis but can also be considered as a marker of vulnerability of schizophrenia. In addition, schizophrenia patients differ from healthy controls in neural activity in brain regions implicated in emotions processing. However, interpretation of findings in patients is limited by confounding factors, such as antipsychotic treatments or alterations due to the course of illness. Also, there is no data concerning genetic factors (polymorphisms or gene expression) underlying these patterns of cerebral activation in emotion information processing.

So, the main objective of this study is to compare the cerebral activity of schizophrenia patients to that of healthy siblings and healthy controls in an emotional processing task.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
105
Inclusion Criteria
  • Male or female participant, right-handed, aged from 18 to 45 years old
  • Haven given their written consent
  • DSM-5 (Diagnostic and Statistical Manual of Mental Disorders version 5) diagnosis of schizophrenia
  • Remitted phase (criteria of Andreasen)
  • Stable doses of antipsychotics during the last 6 weeks
  • No severe somatic illness
  • Normal clinical exam
  • Inscription to the social security
Exclusion Criteria
  • Women in genitally active period without contraception
  • Women pregnant or breast feeding
  • Participants presenting a severe somatic /neurologic condition
  • Present/history in the last year of alcohol or drug abuse
  • Participating in another clinical study or still in period of exclusion of a previous clinical trial
  • Contraindication to an MRI test (metallic foreign body, pacemaker, heart valve, chirurgical clip, claustrophobia...)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Schizophrenia subjectsPolymorphism (SNP in DNA)35 patients suffering from schizophrenia
Schizophrenia subjectsNeuropsychological assessment35 patients suffering from schizophrenia
Healthy siblingsPolymorphism (SNP in DNA)35 healthy siblings of the patients suffering from schizophrenia
Schizophrenia subjectsquantitative measures of mRNA35 patients suffering from schizophrenia
Schizophrenia subjectsMRI (Magnetic resonance imaging)35 patients suffering from schizophrenia
Healthy siblingsMRI (Magnetic resonance imaging)35 healthy siblings of the patients suffering from schizophrenia
Healthy controlsNeuropsychological assessment35 healthy "controls "patients
Healthy controlsquantitative measures of mRNA35 healthy "controls "patients
Healthy siblingsquantitative measures of mRNA35 healthy siblings of the patients suffering from schizophrenia
Healthy controlsMRI (Magnetic resonance imaging)35 healthy "controls "patients
Healthy siblingsNeuropsychological assessment35 healthy siblings of the patients suffering from schizophrenia
Healthy controlsPolymorphism (SNP in DNA)35 healthy "controls "patients
Primary Outcome Measures
NameTimeMethod
Blood Oxygen Level dependent (BOLD) signal activity in Anterior Cingulate Cortex (ACC) measured by functional MRI4 hours
Secondary Outcome Measures
NameTimeMethod
Assessment of the functional connectivity in cortico-limbic circuit which underlie the emotional information using functional MRI4 hours
Description of whole brain neuro-anatomy based using Voxel Brain Morphometry (VBM)4 hours
Quantitative expression of messenger Ribo Nucleic Acid (mRNA) in Peripheral Blood Mononuclear Cells (PBMC)4 hours
Polymorphism (single-nucleotide polymorphism SNP) of DNA (DeoxyriboNucleic Acid)4 hours

Trial Locations

Locations (1)

Pôle Psychiatrie Centre CHU Conception, Marseille, APHM

🇫🇷

Marseille, France

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