Clinical Trial: Clinical Studies of Progeria
Study Status: Completed
Recruit Status: Completed
Study Type: Observational
Official Title: Clinical Investigations Into Hutchison-Gilford Progeria Syndrome
Brief Summary:
This study will examine children with Hutchinson-Gilford Progeria syndrome, a genetic disease that causes many changes to the body over time, including heart disease, bone changes, hair loss, and joint and skin changes. Often called a "premature aging" disease, progeria does not mimic aging completely. This study will examine which body systems are affected in progeria and how each system is affected over time in order to try to develop new treatments.
Patients with progeria who are between 6 months and 70 years of age and who are able to travel to the NIH in Bethesda, Md., may be eligible for this 5- to 10-year study.
Participants come to the NIH Clinical Center for evaluation every 2 years. Each 4-5 day visit includes the following tests and procedures:
- Medical history and physical examination
- Blood tests to analyze cardiovascular risk factors, blood counts, blood chemistries, and for research
- Urine tests for sugar and proteins
- Photographs to study growth problems
- X-ray studies to determine bone density and body composition, such as body fat and muscle
- Electrocardiogram (EKG) and echocardiogram (heart ultrasound) to study the heart and blood vessels
- Lung function tests to measure energy consumption and lung capacity
- Skin biopsy (surgical removal of a small skin sample) to examine cellular changes
- Hearing tests
- Eye examination to evaluate eyesight, eye pressure and structures of the eye
- P
Detailed Summary: Hutchison-Gilford Progeria Syndrome (HGPS) is a rare "premature aging" disease in which children die of severe atherosclerosis at an average age of thirteen years (range 8-20 years). Children with HGPS appear healthy at birth, but within months display signs of growth failure, lipodystrophy, hair loss, and aged skin. Within just a few years they exhibit boney abnormalities including osteoporosis and resorption, coax valga and hip dislocation. The final height approximates 3 feet. Mortality is caused by generalized artherosclerosis leading to strokes and heart attacks. The gene defect causing HGPS has recently been identified as a single base mutation in the gene LMNA, coding for the nuclear protein Lamin A. The spectrum of effects of this gene defect on cellular function, and how these effects culminate in the HGPS disease phenotype, remain to be elucidated. Furthermore, no in-patient multisubject clinical evaluation of children with HGPS has ever been performed, and no therapy exists for any of the complications of HGPS. Hence, baseline studies are critical to determine the extent of organ involvement in HGPS, evaluate disease progression, and design clinical trials of potential treatments. The purpose of this study is to longitudinally investigate the disease characteristics of HGPS using state-of the-art measures of cardiovascular function, comprehensive laboratory testing, in vitro cell culture studies, and extensive medical consultations. HGPS patients will be admitted to the NIH Clinical center as inpatients for approximately 5 days every two years. The information emanating from the proposed studies will assist in assuring appropriate care for children with HGPS, provide a better understanding of the variations in phenotype of HGPS, and stimulate new research into HGPS and the aging diseases associated with HGPS, such as atherosclerosis. These studies will also allow us to evaluate new clinical outcome parameters and to design appropriate therapeuti
Sponsor: National Human Genome Research Institute (NHGRI)
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Information By: National Institutes of Health Clinical Center (CC)
Dates:
Date Received: October 16, 2004
Date Started: October 12, 2004
Date Completion:
Last Updated: April 21, 2017
Last Verified: April 13, 2017
