Ichthyosis and 12R-Eicosanoid Metabolism in Sjögren-Larsson Syndrome (2006)

William B. Rizzo, MD,
University of Nebraska Medical Center, Omaha, NE
Dr. William Rizzo
Looks at a defective lipid (fat) metabolic pathway that is seen in Sjögren-Larsson syndrome (SLS) and several other genetic forms of ichthyosis.  This project is relevant to the mission of the Foundation and the interests of our members because: “Therapy of the ichthyosis in SLS is non-specific.  Our research may lead to new approaches for cutaneous therapy for selectively bypassing the metabolic block in lipid metabolism and providing the metabolites that cannot be made by SLS patients.”

UPDATE:  SEPTEMBER 2007
Sjögren-Larsson syndrome (SLS) is a form of ichthyosis that is associated with neurologic symptoms of spasticity and mental retardation.  The ichthyosis is present at birth and has a disturbing itchy characteristic.  Like most other types of ichthyosis, no specific treatment is available.  SLS is caused by mutations in a gene that normally makes an enzyme called fatty aldehyde dehydrogenase, which is necessary for lipid (fat) metabolism.  This enzyme acts on several related lipids.  We hypothesize that defective metabolism of one of these lipids is responsible for causing the ichthyosis, but it is not yet known which one.  Recently, the research team headed by Dr. Judith Fischer in Paris has found that genetic defects in metabolism of a group of lipids called 12R-eicosanoids cause certain forms of ichthyosis.  There is reason to suspect that fatty aldehyde dehydrogenase is also necessary for metabolizing 12-eicosanoid lipids.  The research grant from FIRST has given us the resources to begin investigating whether defective metabolism of 12R-eicosanoids is responsible for the ichthyosis in SLS.  Using a variety of biochemical and molecular techniques, our lab is studying the 12R-eicosanoid pathway in cultured skin cells (keratinocytes) from SLS patients.  If metabolism of this lipid is found to be defective, our research would point to new therpeutic approaches for treating SLS and other forms of ichthyosis caused by abnormalities in the 12R-eicosanoid pathway.
 

Dr. William Rizzo is a Professor of Pediatrics at the University of Nebraska Medical Center, Omaha, Nebraska.  Dr. Rizzo received his education at Northwestern University, Evanston, Illinois, the University of Illinois at Chicago, and Johns Hopkins University, Baltimore, Maryland.  A pediatrician by training, Dr. Rizzo has a strong interest in medical genetics and in Sjogren-Larsson (SLS) syndrome in particular.  His into the genetic and metabolic pathways for SLS spans almost twenty years.

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