The purpose of this study is to learn more about the medical problems and the genetic factors involved in a recently defined form of inherited dementia called "familial dementia with neuroserpin inclusion bodies (FDNIB)." Abnormal substances in nerve cells of patients with this disease affect brain and nervous system function, causing confusion, memory decline and impaired cognition (thinking ability). Patients also develop movement disorders and, possibly, seizures. Symptoms begin in midlife, between 45 and 55 years of age.

Patients with FDNIB and family members 18 years of age or older at risk for the disease may be eligible for this 3-year study.

Participants will have a medical and family history and review of medical records; interview with a medical geneticist (specialist in genetics); physical, neurological and psychiatric examinations; and the following tests and procedures:

1. Blood tests to assess general health

2. Chest and skull X-rays

3. Electrocardiogram (EKG)-record of the electrical activity of the heart using electrodes placed on the chest

4. Electroencephalogram (EEG)-record of the electrical activity of the brain using electrodes placed on the head

5. Ultrasound of the abdomen-imaging of abdominal organs using sound waves

6. Brain magnetic resonance imaging (MRI)-imaging of the brain using a strong magnetic field and radio waves

7. Hearing evaluation

8. Assessment of performance of daily living activities

9. Single photon emission computed tomography (SPECT)-imaging of brain metabolism and blood flow using a radioactive substance injected into a vein

The evaluation will be done over a 3- to 4-day period. At their completion, participants will meet with a physician and a genetics counselor to discuss the clinically significant findings. Participants may be asked to return for follow-up evaluations every 6 months to a year (depending on the individual's condition) for 3 years.

Condition
Familial Dementia with Neuroserpin Inclusion Bodies Nervous System Heredodegenerative Disorder

Further Study Details: 

Expected Total Enrollment:  100

This project involves the study of a novel familial neurodegenerative disorder, familial encephalopathy with neuroserpin inclusion bodies (FENIB). This disorder, which has a characteristic clinical course of progressive dementia and neurologic involvement, was defined in one extended family. Neuroserpin is a strong candidate gene for this disorder and a mutation is present in this large kindred. This protocol will characterize the clinical phenotype, delineate the natural history of the disorder and explore genotype/phenotype correlations in the index family. Families with immunohistopathologically-neuroserpin positive neuronal inclusions on autopsy/biopsy in an affected member(s) or with familial presenile dementia with neurologic features consistent with the original FENIB family will be enrolled.

Genders Eligible for Study:  Both

Criteria

INCLUSION CRITERIA:
Patients with a family history of early-onset progressive dementia or decline in cognition and neuronal inclusion bodies which are immunohistopathologically consistent with neuroserpin inclusion bodies.
Children with progressive dementia and myoclonic epilepsy which is consistent with the reported clinical course in pediatric patients or children with the clinical phenotype and on autopsy neuronal inclusion boidies which are immunohistopathologically consistent with neuroserpin inclusion bodies.
Family members at risk, of at least 18 years of age, including first degree relatives of affected patients and the children of these first degree relatives.
In rare instances probands and their at risk family members with known presenile dementia and a neurologic course typical of that seen in FENIB will be enrolled.
Individuals who have any of the above findings but are too medically fragile to travel to the Clinical Center and for whom a durable power of attorney (DPA) is available. The physical examination and laboratory research studies will be performed by the Investigator(s). All clinical studies will be done in a local accredited hospital according to similar procedures.
Family members either not at risk or unwilling to travel and unaffected spouses who enroll primarily for genetic linkage information. These individuals will contribute a blood sample for molecular analysis only. No clinical studies will be performed on individuals from this category.
EXCLUSION CRITERIA:
Individuals will be excluded if:
Another diagnosis of presenile demential is made by a physician including but not limited to: 1) Huntington Disease, 2) Parkinson Disease/Diffuse Lewy Body Disease, 3) Familial Alzheimer Disease with known mutations in presenilin 1, presenilin 2 or beta-amyloid precursor protein, 4) Lafora Body Disease, 5) Pick's Disease, and 6) fronto-temporal dementia.
A Durable Power of Attorney is not available in a human subject that is not medically competent to give consent.

Maryland
      National Human Genome Research Institute (NHGRI), 9000 Rockville Pike,  Bethesda,  Maryland,  20892,  United States; Recruiting

Study ID Numbers:  000191; 00-HG-0191
Record last reviewed:  July 21, 2004
Last Updated:  November 23, 2004
Record first received:  August 12, 2000
ClinicalTrials.gov Identifier:  NCT00006176
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08