Crohn’s disease appears to have at least two distinct genetic subtypes, which could explain why the condition is so hard to treat, a new study suggests.
“The one-treatment-fits-all approach doesn’t seem to be working for Crohn’s patients,” said study co-senior author Dr. Shehzad Sheikh. He’s an assistant professor in the departments of medicine and genetics at the University of North Carolina School of Medicine.
“It’s plausible that this is because only a subset of patients has the type of disease that responds to standard therapy, whereas, for the rest of the patients, we’re really not hitting the right targets,” Sheikh said in a university news release.
Crohn’s is a chronic inflammatory disorder of the intestinal tract. The most common symptoms are diarrhea, stomach cramps and weight loss. The course and severity of the disease vary widely from patient to patient, which is one reason it’s difficult to treat, the researchers noted.
For the study, Sheikh and his team analyzed colon tissue samples from 21 Crohn’s patients and discovered at least two separate genetic subtypes of the disease. Each had its own pattern of gene expression and mix of clinical characteristics, the researchers reported Oct. 12 in the journal Gut.
These differences existed independently of patients’ ages or treatment histories, Sheikh said.
The researchers said they believe the finding could lead to more effective treatments for Crohn’s, which affects nearly 1 million people in the United States.
“We hope one day to be able to test Crohn’s patients for the subtype of the disease they have, and thus determine which treatment should work best,” Sheikh said.
The U.S. National Institute of Diabetes and Digestive and Kidney Diseases has more on Crohn’s disease.
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