Primary Sclerosing Cholangitis in Children
Start Date
12/30/2021
Completion Date
5/31/2029
Summary
Primary sclerosing cholangitis (PSC) is a rare liver disease that damages the liver's bile ducts. Bile ducts are tiny tubes that carry bile from the liver to the small intestine. Bile is a liquid produced by the liver that helps us absorb and use the nutrients in the food we eat. In people with PSC, the bile backs up into the liver and will damage it, causing scarring of the liver. The purposes of this study are to: * Collect medical and other data to learn more about PSC, how it progresses, and identify factors that may cause the disease to progress more quickly. * Ask questions about how PSC symptoms affect your child's life to learn more about its impact on your child's daily functioning * Children with PSC who are seen at one of the participating clinical sites in the Childhood Liver Disease Research Network (ChiLDReN) will be asked to contribute information, DNA, and other specimens. The information and specimens will be available to investigators to carry out approved research aimed at learning more about the possible causes and long-term effects of PSC.
Detailed Description
Pediatric primary sclerosing cholangitis (PSC) is a rare autoimmune biliary fibrosing disease that leads to significant morbidity, the need for liver transplantation in \~50% of patients, and an increased risk for biliary and colorectal cancers in adulthood. The progression of the biliary disease in children is variable and risk factors associated with a more rapid progression of disease have not been adequately studied. Importantly, pediatric hepatologists have never previously collaborated with inflammatory bowel disease (IBD) specialists to rigorously explore interactions between colonic inflammation and liver disease. New non-invasive imaging modalities to measure fibrosis have not been explored in pediatric PSC. Furthermore, the impact that PSC has on the global functioning of children is not well understood, and likely underappreciated. The natural history of pediatric PSC is poorly understood. This study aims to determine risk factors, including activity of co-existent IBD, associated with more rapid progression of disease, characterize the impact of PSC on global functioning, define the spectrum and prognostic value of biliary tract disease and liver fibrosis based on novel imaging techniques, and establish a biobank of specimens for future mechanistic studies aimed at discovering biomarkers pertaining to etiology and severity of PSC and novel mechanisms of immunopathogenesis of disease. This comprehensive observational and longitudinal study will delineate unique aspects of the natural history and severity of pediatric PSC and of associated IBD and provide necessary data for future therapeutic trials. It aims to provide a platform to discover and validate circulating and imaging biomarkers, which may serve as surrogate endpoints in future interventional studies.
Eligibility Criteria
Age Range: 2 years to 25 years
Conditions
Locations
Children's Hospital of Los Angeles
Los Angeles, California 90027
United States
Children's Hospital Colorado
Aurora, Colorado 80045
United States
Children's Healthcare of Atlanta
Atlanta, Georgia 30322
United States
Ann & Robert H Lurie Children's Hospital
Chicago, Illinois 60611
United States
Riley Hospital for Children
Indianapolis, Indiana 46202
United States
Cincinnati Children's Hospital Medical
Cincinnati, Ohio 45229
United States
The Children's Hospital of Philadelphia
Philadelphia, Pennsylvania 19104
United States
UPMC Children's Hospital of Pittsburgh
Pittsburgh, Pennsylvania 15224
United States
Texas Children's Hospital (Baylor College of Medicine)
Houston, Texas 77030
United States
The University of Utah
Salt Lake City, Utah 84113
United States
Seattle Children's Hospital
Seattle, Washington 98105
United States
The Hospital for Sick Children
Toronto, Ontario M5G 1X8
Canada