We have extended the clinical arm of this project to acquire longitudinal data on the pattern of disease progression and identify potential biomarkers. The first Wolfram Syndrome Research Clinic was held August 6-7, 2010, supported by contributions from the Department of Medicine, Mallinckrodt Institute of Radiology and St. Louis Children’s Hospital. The Clinic was held primarily in the Pediatric Clinical Research Unit located on the 11th floor at St. Louis Children’s Hospital and has six components. This clinic represents a joint research and clinical activity in collaboration with the Divisions of Adult and Pediatric Endocrinology, Ophthalmology, Pediatric Neurology, Radiology, Psychiatry, and Pediatric Otorhinolaryngology. Monitoring disease progression will serve as the basis for clinical intervention when therapeutic agents become available. The second clinic was held in 2011 and largely supported by the Snow Foundation.
Since 2010, we have hosted a research clinic annually for five consecutive years. These multidisciplinary clinics have also provided the opportunities to assemble a team of physician scientists with first-hand knowledge of this rare disease who can provide a valuable resource for patients and their families now and in the future. Together with the Snow Foundation, we are currently planning interventional studies as well as patient centered Wolfram syndrome subspecialty clinic.
Funding: National Institute of Child Health and Development (HD070855); 2012-2023
“Tracking Neurodegeneration in Early Wolfram Syndrome (TRACK)”
Link to Study at Clinical Trials
ClinicalTrials.gov Identifier: NCT03951298
Clinical Trials # (https://clinicaltrials.gov/)
Principal Investigator and Scientific Director: Tamara Hershey, PhD
Medical Director: Bess Marshall, MD
Hershey Lab at Washington University School of Medicine