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Scientists Identify Genomic Cause & Potential Treatment for Disabling Pansclerotic Morphea

ReachMD Healthcare Image
06/02/2023
practicaldermatology.com

Researchers have identified genomic variants that cause disabling pansclerotic morphea and have found a potential treatment.

People with the disorder have an overactive version of a protein called STAT4, which regulates inflammation and wound healing. The work also identified a drug that targets an important feedback loop controlled by the STAT4 protein and significantly improves symptoms in these patients. 

The results were published in the New England Journal of Medicine

Only a handful of patients have been diagnosed with disabling pansclerotic morphea, a disorder first described in the medical literature around 100 years ago. The disorder causes severe skin lesions and poor wound healing, leading to deep scarring of all layers of the skin and muscles. The muscles eventually harden and break down while the joints stiffen, leading to reduced mobility. Because the disorder is so rare, its genetic cause had not been identified until now.  

“Researchers previously thought that this disorder was caused by the immune system attacking the skin,” saus study author Sarah Blackstone, a predoctoral fellow within the National Human Genome Research Institute’s (NHGRI) Inflammatory Disease Section and a medical student at the University of South Dakota. “However, we found that this is an oversimplification, and that both skin and the immune system play an active role in disabling pansclerotic morphea.”  

The researchers used genome sequencing to study four individuals with disabling pansclerotic morphea and found that all four have genomic variants in the STAT4 gene. The STAT4 gene encodes a type of protein that helps turn genes on and off, known as a transcription factor. The STAT4 protein not only plays a role in fighting infections but also controls important aspects of wound-healing in the skin.  

The scientists found that the STAT4 genomic variants result in an overactive STAT4 protein in these four patients, creating a positive feedback loop of inflammation and impaired wound-healing that worsens over time. To stop this harmful feedback loop, they targeted another protein in the inflammatory pathway that interacts with the STAT4 molecule and is called Janus kinase, also known as JAK. When the researchers treated the patients with ruxolitinib, the patients’ rashes and ulcers dramatically improved.   

“So far, there has not been a standard treatment for this disorder because it’s so rare and not well-understood. However, our study gives an important new treatment option for these patients,” says Blackstone.    

Existing treatments for disabling pansclerotic morphea are designed to halt the progression of the disorder, but previous therapies have been mostly ineffective, often with severe side effects. People with the disorder typically don’t live more than 10 years after their diagnosis.  

The study suggests that ruxolitinib could be an effective treatment for patients with this disorder. 

“The findings of this study open doors for JAK inhibitors to be a potential treatment for other inflammatory skin disorders or disorders related to tissue scarring, whether it is scarring of the lungs, liver or bone marrow,” says Dan Kastner, M.D., Ph.D., an National Institute of Health distinguished investigator, head of NHGRI’s Inflammatory Disease Section and a senior author of the paper.   

“We hope to continue studying other molecules in this pathway and how they are altered in patients with disabling pansclerotic morphea and related conditions to find clues to understanding a broader array of more common diseases,” adds Lori Broderick, M.D., Ph.D., a senior author of the paper and an associate professor at UC San Diego.   

PHOTO CAPTION:

Fibroblasts, shown in green, are cells that connect tissues and organs in the body and play an important role in healing wounds. Genomic variation in the STAT4 gene causes disorganized fibroblasts that fail to heal wounds properly. The nuclei of the fibroblasts are shown in blue.

PHOTO CREDIT:

Ernesto Del Aguila III, NHGRI

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Schedule25 Jun 2024