Schizophrenia Clinical Trial
Official title:
The Validity of Intra-cortical Inhibition as a Biomarker of Cognitive Deficits in Schizophrenia and in Predicting the Efficacy of TMS Treatment
Cognitive deficit is a core symptom of schizophrenia (SZ), but its pathological mechanism is poorly understood and the treatment effect is poor. The excitatory-inhibitory microcircuit (E-I) function imbalance formed by inhibitory interneurons and excitatory pyramidal cells in the cerebral cortex is a new mechanism of cognitive deficits in SZ discovered in recent years. Cortical E-I is expected to be a new target for the treatment of cognitive deficits in SZ. Paired transcranial magnetic stimulation (ppTMS)-induced intracortical inhibition (ICI) is dependent on cortical E-I functional integrity. We found that ICI deficiency is stable in SZ and is closely related to cognitive function. Therefore, ICI is likely to be a system-level biomarker for cognitive deficits caused by E-I imbalance. However, no study has yet explored the genetic basis of ICI and its impact on the occurrence, development and treatment response of cognitive deficits in SZ. Based on this, we intend to verify the value of ppTMS-induced ICI as a biomarker of E-I imbalance in SZ patients and normal controls at different stages: 1. To explore the correlation of ICI with multidimensional cognitive deficits and E-I pathway genes; 2. To explore ICI Combining candidate genes and serum inflammatory factors can predict whether TMS can improve the efficacy of cognitive deficits, and can be used for precise treatment of SZ cognitive deficits at the level of pathological mechanisms.
Status | Recruiting |
Enrollment | 200 |
Est. completion date | February 2024 |
Est. primary completion date | December 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Healthy Volunteers or Schizophrenia patients: To be diagnosed as "schizophrenia" by the research doctor using the DSM-IV-TR Axis I Disorder Clinical Examination Guidelines Research Edition (SCID-I/P) ; - Right-handed; - Education level of junior high school or above; - The patient is a permanent resident of Shanghai, and there is no plan to move to another place in the next 3 months, and can cooperate with follow-ups; - Has signed an informed Consent; - The patient should meet one of the following two conditions: A. First-time onset of schizophrenia, never taking antipsychotics, and PANSS score = 70 points; B. Schizophrenia with less than 3 episodes Symptomatic patients, whose symptoms were relieved within the past 3 months (PANSS score <60 points). Exclusion Criteria: - Those who have local or diffuse brain injury or severe brain trauma, and those who have intracranial hypertension; - Those who have a history of epileptic seizures or a family history of idiopathic epilepsy; - Those who have paramagnetic or non-paramagnetic metals in the head and neck Implants (such as cochlear implants, titanium clips, etc.); - Those who have Alcohol dependence and other drug abusers; - Those who have Severe heart disease, pacemaker or stent implantation; - Have taken benzodiazepines or received TMS or electroconvulsive therapy within 3 months; - Patients with moderate or higher depression (HAMD=17) and anxiety (HAMA=14) mood; - Those who are considered unsuitable for enrollment by the researchers. |
Country | Name | City | State |
---|---|---|---|
China | Shanghai Pudong New Area Mental Health Center | Shanghai | Shanghai |
Lead Sponsor | Collaborator |
---|---|
Tongji University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Percent Change from Baseline Speed of Information Processing score at 2 weeks and 4 weeks assessed by MATRICS toolkit. | Measured by summation of Trail Making Test, BACS Symbol coding and Verbal Fluency scores in MATRICS (Measurement and Treatment Research to Improve Cognition in Schizophrenia) | Baseline, 2 weeks, 4 weeks | |
Primary | Percent Change from Attention/Vigilance score at 2 weeks and 4 weeks assessed by MATRICS toolkit. | Measured by Continuous Performence Test scores in MATRICS | Baseline, 2 weeks, 4 weeks | |
Primary | Percent Change from Working Memory score at 2 weeks and 4 weeks assessed by MATRICS toolkit. | Measured by WMS-III SS scores in MATRICS | Baseline, 2 weeks, 4 weeks | |
Primary | Percent Change from Verbal Learning score at 2 weeks and 4 weeks assessed by MATRICS toolkit. | Measured by HVLT-R scores in MATRICS | Baseline, 2 weeks, 4 weeks | |
Primary | Percent Change from Visual Learning score at 2 weeks and 4 weeks assessed by MATRICS toolkit. | Measured by BVMT-R scores in MATRICS | Baseline, 2 weeks, 4 weeks | |
Primary | Percent Change from Reasoning and Problem Solving score at 2 weeks and 4 weeks assessed by MATRICS toolkit. | Measured by NAB Mazes scores in MATRICS | Baseline, 2 weeks, 4 weeks | |
Primary | Percent Change from Social Cognition score at 2 weeks and 4 weeks assessed by MATRICS toolkit. | Measured by MSCEIT Branch 4 scores in MATRICS | Baseline, 2 weeks, 4 weeks | |
Secondary | Change from baseline Intracortical inhibition | Intracortical inhibition is the Percent Inhibition of Movement Evokded Potentials of the test TMS stimulus by a conditinal TMS stimulus | Baseline, 2 weeks, 4 weeks |
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