First DNA from National Psoriasis Victor Henschel BioBank released for study
The first-ever release of National Psoriasis Victor Henschel BioBank DNA samples brings millions of Americans struggling with psoriasis and psoriatic arthritis one step closer to a cure. Scientists will use the samples for research that hopes to uncover the unknowns about the genetics of psoriatic disease and its causes.
James T. Elder, M.D., Ph.D., professor of molecular genetic dermatology in the Department of Dermatology at the University of Michigan Health System, and his research team received the first 1,250 BioBank DNA samples on Sept. 1, 2010. They will use them to identify new genes that increase a person's risk for developing psoriasis and also examine the connection between psoriasis and other autoimmune diseases, such as Crohn's disease.
The National Psoriasis BioBank, started by the National Psoriasis Foundation in 2006, is a collection of DNA samples and clinical information used by scientists to advance the field of psoriasis genetics. Once it meets its completion goals, the BioBank will be the largest single collection of psoriasis DNA samples in the world.
"The BioBank is a critical resource for bringing us one step closer to a cure for psoriasis, and we are honored to partner with Dr. Elder and his team on this landmark project," said Rick Seiden, chair of the National Psoriasis Foundation Board of Trustees. "This endeavor would not be possible without the hundreds of people with and without psoriatic disease who donated DNA over the past four years. We thank all of them for their vital contribution to psoriasis research."
The BioBank honors Victor Henschel, a highly respected member of the psoriasis community who lived with psoriasis and psoriatic arthritis for 35 years. The Henschel family, many of whom also live with psoriatic disease, donated money to the Foundation to start the BioBank.
About the National Psoriasis Foundation
Over the last 50 years, the National Psoriasis Foundation (NPF) has become the world’s leading nonprofit patient advocacy organization fighting for individuals with psoriasis and psoriatic arthritis. NPF leads this fight by driving efforts for a cure and improving the lives of the more than 8 million Americans affected by this chronic disease. To date, NPF has funded more than $15 million in research grants and fellowships, and to commemorate 50 years, NPF plans to raise an additional $2 million for early scientific career research programs in 2017 alone. Each year, NPF strives to support, educate and advocate on behalf of more individuals living with or caring for someone with the disease than ever before. As part of that effort, NPF established the Patient Navigation Center to offer personalized assistance to everyone with psoriasis or psoriatic arthritis. Join our community today and help drive discovery and create community for all living with psoriatic disease.