Psychosis Clinical Trial
Official title:
THE ROLE OF BBB BREAKDOWN IN THE PATHOGENESIS OF PSYCHIATRIC DISORDERS
NCT number | NCT01396850 |
Other study ID # | sor497310ctil |
Secondary ID | |
Status | Not yet recruiting |
Phase | N/A |
First received | July 17, 2011 |
Last updated | July 18, 2011 |
Verified date | July 2011 |
Source | Soroka University Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | Israel: Clalit Health Services |
Study type | Observational |
BBB dysfunction has been indicated in some groups of schizophrenia patients by measuring
increased albumin and immunoglobulin (IgG) cerebrospinal fluid (CSF) levels. Most of the
authors described a raised protein level in 5-20% of the schizophrenic patients (Muller &
Ackenheil, 1995). Increased S100B levels were demonstrated in the serum of patients
suffering from schizophrenia as well as depression, and this may reflect increased BBB
permeability. Furthermore, this increase remains in those patients who develop a residual
state with relevant negative symptoms, whereas S100B levels normalize in recovering patients
(Shalev, Serlin & Friedman, 2009). CSF albumin and CSF IgG values correlate significantly
with some of the SANS (Scale for the Assessment of Negative Symptoms) subscales and the SANS
total score, this shows the correlation between BBB permeability and behavioral changes. It
is important to say that although negative symptoms are often signs of chronicity of the
disease, the abnormal CSF findings in Muller's experiment (1995) are not related to the
duration of the disease, because the patients were quite young and the duration of the
disease was less than 3 years.
The investigators hypothesize that a primary vascular pathology, which leads to BBB
breakdown, will result a leakage of serum-derived vascular components in to the brain tissue
and may cause brain dysfunction such as disturbed thinking processes, mood and behavior, as
we can see in psychiatric patients.
Status | Not yet recruiting |
Enrollment | 120 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 16 Years to 65 Years |
Eligibility |
Inclusion Criteria: Psychotic, affective disorders or anxiety disorders patients admitted
to Soroka Medical Center from the psychiatric hospital or self admissions to the
Psychiatric department. Patients were evaluated by study psychiatrist. Signed informed consent by the patient or his legal custodian. Subjects Age 16-65 years. Exclusion Criteria:1. Patients with neurological disease, including epilepsy, ischemic stroke, multiple sclerosis, Parkinson's disease, etc. 2. Drug or alcohol abuse. 3. Patients that will need anesthesia in order to perform the MR study (not including patients who are already ventilated). 4. Patients with metal foreign body, or other contraindication to MR (according to the MR regulations). 5. Tourists or foreign residents that long terms follow up is not feasible for them. 6. Patients with renal failure / any other kind of kidney problems. 7. Pregnant women. 8. Patient with brain-injury. 9. Suicidal patients/patients with high risk for suicide/violent patients or patients that their condition might deteriorate due to participation in this study. |
Observational Model: Case Control, Time Perspective: Prospective
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Soroka University Medical Center |
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