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New Treatment Directions: 2012 Rosacea Research Grants

The National Rosacea Society (NRS) has awarded funding for five new studies as part of its research grants program to increase knowledge and understanding of the potential causes and other key aspects of rosacea.

Enzymes Causing Inflammation

Dr. Anna Di Nardo, associate professor of medicine at the University of California-San Diego, was awarded $25,000 to study the role of mast cells as a possible link between an overabundance of the antimicrobial peptides called cathelicidins in individuals with rosacea and the inflammation that appears on rosacea skin.

Dr. Di Nardo will endeavor to identify inflammation-causing enzymes that are produced by mast cells as well as the influence of neuropeptides on the formation of these key enzymes.

Kallikrein Enzymes

Drs. Ulf Meyer-Hoffert and Thomas Schwartz of the Department of Dermatology, University Clinic Schleswig-Holstein, were awarded $20,000 to study whether and how kallikreins, enzymes that contribute to inflammation in rosacea, can activate cytokines, which might contribute to the disease activity. The investigators will also research inhibitors of this substance that could have the potential to treat the disease.

Genetics

Drs. Meg Gerstenblith and Daniel Popkin, assistant professors of dermatology at Case Western Reserve University, were awarded $10,000 to study the incidence of rosacea in fraternal and identical twins, recruited at the annual Twins Day festival in Ohio.

The study aims to document potential genetic factors by determining if there is a statistically significant difference in the correlation of rosacea between identical and fraternal twins.

Also see the earlier Study Suggests Hereditary Rosacea Link.

Microbes Specific to Rosacea Skin

Dr. Barbara Summerer, postdoctoral research fellow in dermatology at Johns Hopkins University School of Medicine, was awarded $25,000 to use sophisticated analytical technology to evaluate specific microbes in rosacea patients.

She will further use epifluorescence microscopy to identify possible biofilms — communities of bacteria that adhere to surfaces — that may exist in rosacea patients, as well as the differences in types of bacteria present in subtype 1 (erythematotelangiectatic) rosacea and subtype 2 (papulopustular) rosacea, so that therapy can target these bacteria.

Enhancing Beta-Defensin 2 Production

Dr. Yoshikazu Uchida, associate research dermatologist, and Dr. Peter Elias, professor of dermatology, at the University of California-San Francisco, were awarded $20,000 to study whether and how enhancing the production of human beta-defensin 2 and conversely suppressing the production of cathelicidin antimicrobial peptide, part of the body's innate immune system, may help suppress the excess of inflammation-causing peptides found in rosacea skin.

The NRS is also continuing to fund studies by Dr. Richard Granstein at Cornell University on the potential role of Th17 cells in rosacea and Dr. Edward Wladis at Albany Medical College on identifying cytokines involved in ocular rosacea.

Related Emerging Research and Treatment Topics

Updates on the Pathophysiology and Managment of Rosacea.

Angiogenesis and Mast Cells in Rosacea.

Moisturizers Containing Niacinamide Benefit Rosacea.

Information About Rosacea Is Not Rosacea Treatment Knowledge.

Paraben Preservatives and Sun Damage.

Excess Iron Exacerbates Rosacea

During the past half century, excessive/misplaced iron has been observed to be a risk factor for an increasing number and diversity of disease conditions.

An extensive list of conditions and of the types of iron association were published in early 2008.

Within the subsequent year, four additional disorders have been recognized to be enhanced by iron: aging muscle atrophy, viral replication, rosacea and pulmonary alveolar proteinosis.

This paper adds new data and emphasis on these disorders as entities associated with increased iron load and toxicity.


Author: Peter Wilson.

Reviewed: Friday, 20 May 2005.



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