Two international teams of researchers have made significant gains in understanding the genetic basis of psoriasis, a chronic skin condition that can be debilitating in some patients. Their research, involving thousands of patients, is reported in two studies published in the advance online Nature Genetics.
“Taken together, the studies help us get closer to realizing the promise of personalized medicine,” said a senior author of both papers, Anne Bowcock, Ph.D., professor of genetics. “Eventually, we hope to be able to target treatments for psoriasis patients based on the genetic alterations that have contributed to their disease.”
The researchers found new genetic variants that affect an individual’s risk of psoriasis. Their discoveries point to different biological pathways that underlie the disease and may eventually lead to targeted drugs and treatments, Bowcock said.
An estimated 7 million Americans have psoriasis, an auto-immune disease that occurs when the body’s immune cells mistakenly attack the skin. The condition is usually characterized by red, scaly skin patches that can be itchy, painful or both. Some 10 percent to 30 percent of patients with psoriasis develop psoriatic arthritis, which occurs when inflammation attacks the joints, causing pain and disability.
Both studies looked for common variants in the genomes of psoriasis patients to uncover associations with the disease.
The first study, conducted in collaboration with the University of Michigan, the University of Utah and colleagues in Canada and Europe, focused on sites within the genome where a single unit of DNA is changed, called a single nucleotide polymorphism (SNP). The researchers scanned nearly 450,000 SNPs in each of the genomes of 1,409 psoriasis patients and compared the DNA variations with those in 1,436 healthy controls.
They initially discovered 21 suspect variants associated with psoriasis and then tested the validity of these variants in another group of psoriasis patients and controls. This revealed seven confirmed variants, all of which appear to increase the risk of the disease. Five of the variants cluster in two distinct pathways.
A second study of 2,831 patients with psoriasis looked for links between the disease and copy number variations, in which a gene is produced in multiple copies. Bowcock and her colleagues in Barcelona, Spain, and elsewhere found that the absence of two skin genes — LCE3B and LCE3C — increases the risk of psoriasis.
Both genes normally are activated after an injury to the skin. The researchers suspect the absence of the genes could lead to an inappropriate immune response, which may cause the inflammation that is a hallmark of the disease.
“Until now, all of the genes linked to psoriasis have been involved in the immune system,” Bowcock said. “But psoriasis is a disease of the immune system and the skin, and it makes sense that we would eventually find genes in the skin that are involved in the disease.”