PET Imaging Study of Amish and Mennonite Patients With CNTNAP2 Mutations

This is an interventional basic science trial for Schizophrenia Read More

Inclusion Criteria:

Patients:

• Meets DSM-5 diagnostic criteria for psychotic disorder, including schizophrenia, schizoaffective disorder or psychotic disorder not elsewhere classified
• Aged 18-59 years
• Genetic confirmation that patient carries CNTNAP2 mutation
• All patients will be of Amish and/or Mennonite descent
• Has a relative willing to be part of the study and this relative will travel with the participant to Columbia University Medical Center in New York City and back to Lancaster, PA
• In the judgment of the participant's treating physician as well as the evaluating consenter, the patient is stable enough to travel and participate in the study

Control subjects:

• Aged 18-59 years
• Genetic confirmation that subject does not carry CNTNAP2 mutation
• First-degree or second-degree relative of subject of Amish/Mennonite descent with CNTNAP2 mutation

Exclusion Criteria (for patients and controls):

• Positive urine toxicology for drugs of abuse, including cannabinoids, amphetamine, benzodiazepines, barbiturates, cocaine, methadone, opiates, and phencyclidine
• Positive history of severe neurological illness or history of brain trauma
• Positive history of severe medical illness that would increase risk due to PET scan procedure, or interfere with interpretation of research findings
• Low hemoglobin (Hb < 11 g/dL in males, Hb <10 g/dL in females)

• Lifetime exposure to radiation in the workplace, or lifetime history of participation in nuclear medicine procedures, including research protocols. However, in case of previous exposure to radioactivity due to research studies, subjects will be eligible if all conditions listed below are fulfilled:

  • research studies in question have been performed in the context of a protocol from the Division of Translational Imaging (Anissa Abi-Dargham, M.D., Director) or as part of a research study within another division at Columbia University/NYSPI and the injected dose and dosimetry of the radiotracer are known
  • Except for research studies, the patient has had no lifetime exposure to radiation in the workplace or in nuclear medicine procedures
  • Adding the previous exposure to the exposure due to this study will result in a yearly cumulative exposure lower than the limit defined by the FDA for research subjects
• Blood donation within 8 weeks of study
• Presence of clinically significant brain abnormalities
• For female patients of child-bearing age who are not surgically sterilized and between menarche and 1 year postmenopausal: Must test negative for pregnancy at the time of enrollment and prior to PET scan based on a serum pregnancy test. Women who are breast-feeding are also excluded.
• Metal implants, pacemaker, other metal (e.g., shrapnel or surgical prostheses) or paramagnetic objects contained within the body which may present a risk to the subject or interfere with the MR scan, as determined in consultation with a neuroradiologist and according to the guidelines set forth in the following reference book commonly used by neuroradiologist: "Guide to MR procedures and metallic objects", F.G. Shellock, Lippincott Williams and Wilkins NY 2001.
• Medicinal patch, unless removed prior to the MR scan.
• Patients: Current treatment with clozapine and/or medications other than antipsychotics/PRN anxiolytics
• Use of the medications that would interfere with mGluR5 binding, including lamotrigine, gabapentin, topiramate, phenobarbital, pregabalin, zonisamide, N-acetylcysteine, D-cycloserine
• Control subjects: Lifetime history of antipsychotic or antidepressant use