Definitive Selection of Neuroimaging Biomarkers for the Diagnosis and Treatment to Common Mental Disorders

Sponsor
Central South University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04218981
Collaborator
(none)
200
1
4
46.5
4.3

Study Details

Study Description

Brief Summary

To explore the whole-brain anatomical and functional abnormalities in drug-naive patients with schizophrenia ,drug-naive patients with BD, drug-naive patients with MDD and healthy controls by using a combination of cross-sectional and longitudinal study designs, including a longitudinal study with 8 weeks of drugs treatment. And explore whether there are shared imaging biomarkers between these three common mental disorders.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

Previous studies suggest that there are brain anatomical and functional abnormalities in patients with schizophrenia, bipolar disorder(BD), major depressive disorder(MDD), and the pathogenesis of these three mental disorders may exist overlaps. However, it remains unclear whether these abnormalities can be used for the diagnosis and prediction of treatment effects in mental disorders. It is also unclear whether there are shared imaging biomarkers between these three common mental disorders. In a word, there still lacks reliable neuroimaging biomarkers in mental disorders. Based on the previous studies, this study aims to examine the whole-brain anatomical and functional abnormalities in drug-naive patients with schizophrenia ,drug-naive patients with BD, drug-naive patients with MDD and healthy controls by using a combination of cross-sectional and longitudinal study designs, including a longitudinal study with 8 weeks of drugs treatment( schizophrenia patients are treated with one antipsychotic drug(olanzapine, risperidone; amisulpride); patients with bipolar disorder are treated with one mood stabilizer(lithium;valproate);patients with major depressive disorder are treated with paroxetine). First, neuroimaging biomarkers are definitively selected in patients with different mental disorders for the purpose of diagnosis by using a cross-sectional design. After that, a longitudinal study is conducted in patients after 8 weeks of drugs treatment to validate that the selected neuroimaging biomarkers can be used to predict treatment response of medication. The definitively selected neuroimaging biomarkers are expected to be useful for the diagnosis and prediction of treatment effects in these three mental disorders; and therefore to be helpful for understanding the pathophysiology of mental disorders.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Diagnostic
Official Title:
Definitive Selection of Neuroimaging Biomarkers for the Diagnosis and Treatment to Common Mental Disorders
Actual Study Start Date :
Jan 15, 2020
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Schizophrenia group

Schizophrenia was diagnosed using the Structural Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V). MRI scan and evaluation of clinical symptoms at baseline and 8 weeks Choose one of the antipsychotics drugs treatment( olanzapine, risperidone, aminosulpiride) according to the patient's condition

Drug: Antipsychotic drugs
Choose one of these antipsychotics (olanzapine, risperidone; amisulpride) for schizophrenia group
Other Names:
  • MRI scan
  • Experimental: Bipolar disorder group

    Bipolar disorder was diagnosed using the Structural Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V). MRI scan and evaluation of clinical symptoms at baseline and 8 weeks Choose one of the mood stabilizer drugs treatment( lithium, valproate) according to the patient's condition

    Drug: Mood stabilizer
    Choose lithium or valproate for bipolar disorder group
    Other Names:
  • MRI scan
  • Experimental: Major depressive disorder group

    Major depressive disorder was diagnosed using the Structural Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V). MRI scan and evaluation of clinical symptoms at baseline and 8 weeks Choose paroxetine treatment

    Drug: Paroxetine
    Patients with major depressive disorder are treated with paroxetine
    Other Names:
  • MRI scan
  • No Intervention: Healthy controls

    MRI scan at baseline and no drugs treatment

    Outcome Measures

    Primary Outcome Measures

    1. Resting-state functional magnetic resonance imaging (fMRI) data acquisition for all participants [8 week]

      A 3.0 T Siemens scanner (Germany) was applied to obtain the MRI images in the Second Xiangya Hospital of Central South University.The MRI data will be obtained before and after treatment at different follow up point.All participants were told to lie on the scanner with their eyes closed. They wore soundproof headphones and asked to remain still. The parameters were as follows: repetition time of 2710 ms, echo time of 3.78 ms, flip angle of 7°, inversion time of 1000 ms, slice thickness of 1 mm, field of view of 256 mm × 256 mm, matrix of 256 × 256, no gap, and 188 slices.

    2. Positive and Negative Syndrome Scale (PANSS) [8 week]

      The PANSS total scores ,subscale scores were used to evaluate the severity of psychotic symptoms at baseline and eight weeks for schizophrenia.The total score of the PANSS was more than 60.The higher scores mean a worse outcome.

    3. Hamilton Depression Scale-17 (HAMD-17) [8 week]

      HAMD-17 total scores were used to evaluate the severity of depressive symptoms at baseline and eight weeks for major depressive disorder. The total score of the HAMD-17 was more than 17.The higher scores mean a worse outcome.

    4. Young Mania Rating Scale (YMRS) [8 week]

      YMRS total scores were used to evaluate the severity of manic symptoms for bipolar disorder before and after treatment at different follow up point.The higher scores mean a worse outcome.

    5. Brief Cognitive Assessment Tool for schizophrenia(B-CATS) [8 week]

      The investigators will use the B-CATS scale to assess cognitive function before and after treatment at different follow up point.The higher scores mean a better outcome.

    Secondary Outcome Measures

    1. Social Disability Screening Schedule(SDSS) [8 week]

      The investigators will use the SDSS scale to assess social function before and after treatment at different follow up point.The higher scores mean a worse outcome.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 50 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Diagnostic criteria for schizophrenia,bipolar disorder, major depressive disorder according to the Structural Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV)

    • Never received any treatment before.

    • For healthy controls: their first-degree relative had no history of psychiatric disorders.

    Exclusion Criteria:
    • The exclusion criteria for all subjects were as follows: any physical illnesses, such as liver, kidney, and cardiovascular diseases; any current or past neuropsychiatric disorders; any traumatic brain injury; seizures; serious impulsive behavior; drug or alcohol addiction; contraindications for MRI; and pregnancy.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The Second Xiangya Hospital of Central South University Changsha China

    Sponsors and Collaborators

    • Central South University

    Investigators

    • Study Director: Wenbin Guo, The Second Xiangya Hospital, Central South University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Guo Wenbin, professor, Central South University
    ClinicalTrials.gov Identifier:
    NCT04218981
    Other Study ID Numbers:
    • 81771447
    First Posted:
    Jan 6, 2020
    Last Update Posted:
    Aug 12, 2020
    Last Verified:
    Dec 1, 2019
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Guo Wenbin, professor, Central South University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 12, 2020