BBD Longitudinal Study of Osteogenesis Imperfecta
Start Date
6/1/2015
Completion Date
12/31/2031
Summary
Osteogenesis Imperfecta (OI) is a rare disorder of increased bone fragility characterized by fractures with minimal or absent trauma, dentinogenesis imperfecta (DI), and, in adult years, hearing loss. It is seen in both genders and all races. The clinical features of OI represent a continuum varying from perinatal lethality to individuals with severe skeletal deformities, mobility impairments, and very short stature to nearly asymptomatic individuals with a mild predisposition to fractures, normal stature, and normal lifespan. Fractures can occur in any bone, but are most common in the extremities. These disorders can be devastating and progressive and result in deformity, chronic pain, impaired function and loss of quality of life. The overall goal of this study is to answer specific question about the natural history of brittle bone diseases as defined by molecular etiology and to develop the foundation for prospective clinical studies.
Detailed Description
The purpose of this natural history study is to perform a long-term follow-up of a large group of people with osteogenesis imperfecta (OI). The research aims are: 1. To collect natural history data on all individuals enrolled in this longitudinal study. The cause of the brittle bone disease will be compared with things like severity, various features and response to treatments. 2. To determine how often people with type I OI have vertebral compression fractures of the spine. 3. To determine how often people with OI develop scoliosis (curvature of the spine). 4. To determine how often people with OI have problems with teeth alignment and how dental health impacts a person's quality of life. 5. To determine the effect of pregnancy in women with OI. There will be a total of 1000 people with OI in this study. Participants will be asked to come in every year if 17Y and younger or every other year if 18Y and older for a total of five years. The following information will be collected at the study visits: Birth History and past surgical history, Current medical history, Scoliosis evaluation, Walking ability Questionnaire, Dental Quality of Life Questionnaire, Scoliosis and fractures Quality of Life Questionnaires, Physical development evaluation, Medications Use The following tests will be performed: Physical exam, dental exam, lung function test, hearing test, mobility test. The following X-rays will be taken: DEXA scan, X-ray of the spine, X-ray of the jaw. Biospecimen (urine and blood) samples will be collected.
Eligibility Criteria
Age Range: No minimum to No maximum
Conditions
Locations
Phoenix Children's Hospital
Phoenix, Arizona 85016
United States
University of California Los Angeles
Los Angeles, California 90095
United States
AI Dupont Hospital for Children
Wilmington, Delaware 19803
United States
Children's National Medical Center
Washington D.C., District of Columbia 21205
United States
University of South Florida
Tampa, Florida 33620
United States
Kennedy Krieger Institute / Hugo W. Moser Research Institute
Baltimore, Maryland 21205
United States
University of Nebraska Medical Center
Omaha, Nebraska 68198
United States
Hospital for Special Surgery
New York, New York 10021
United States
Oregon Health and Science University
Portland, Oregon 97239
United States
Baylor College of Medicine
Houston, Texas 77030
United States
Shriners Hospital for Children, Chicago / Marquette University
Milwaukee, Wisconsin 53201
United States
Shriners Hospital for Children
Montreal, Quebec H3G 1A6
Canada