Crohn’s vs. Celiac: How They Differ

Staff
By Staff
4 Min Read

Crohn’s disease and celiac disease are both lifelong conditions related to the immune system.

Symptoms of the two conditions that overlap:
  • Digestive issues like abdominal pain, diarrhea, and weight loss
  • Periods of flare-ups followed by remission
  • Complications like malnutrition, vitamin deficiencies, and anemia 

One key difference in the conditions is the parts of the body they affect.

“In celiac disease, the primary location that’s affected is the duodenum (though it can affect anywhere in the small bowel), which is the first part of the small intestine,” says Jansson-Knodell. Crohn’s can affect anywhere along the gastrointestinal tract — from the mouth to the rectum.”

The disease processes are different as well. Crohn’s is an autoimmune condition in which the immune system may attack normal and harmless bacteria in the gut, irritating the small and large intestines.

In a person with celiac disease, eating gluten triggers an immune response in the small intestine. The immune system reacts, sending inflammatory cells and antibodies to destroy the gluten molecules, which causes symptoms.

“There is ongoing research to identify similarities and differences between Crohn’s disease and celiac disease, particularly in the areas of genetics, immune factors, microbiome interactions, and environmental triggers,” says Ekta Gupta, MBBS, chief of gastroenterology at the UMMC-Midtown Medical Center at the University of Maryland Medical Center in Baltimore.

Crohn’s disease has a complex genetic-environmental interaction, says Dr. Gupta.

People with parents or siblings with Crohn’s have an increased risk of also having the condition. Researchers believe that environmental factors can interact with a person’s microbiome and immune system, increasing their risk of Crohn’s. For example, evidence suggests that smoking may double a person’s chances of developing Crohn’s.
Celiac disease has a stronger genetic predisposition, says Gupta. People with a first-degree relative (such as a parent or child) with celiac have about a 1 in 10 chance of developing the disease.

“But only 2 to 5 percent of people with celiac disease genes [actually] develop the disease, suggesting possible underlying environmental triggers as well,” she says.

Even with the overlap in symptoms, it’s not difficult to differentiate between the two diagnoses by checking serologies (lab work) on patients to screen them for celiac disease, says Melissa Teitelman, MD, a gastroenterologist at Duke Health and professor of medicine at Duke University School of Medicine in Durham, North Carolina.

Celiac disease is diagnosed using blood tests that detect specific antibodies and usually confirmed by performing a biopsy of the small intestine to assess damage to the villi, the tiny hairlike structures responsible for nutrient absorption.
Crohn’s disease is typically confirmed through a combination of medical history, blood tests (including inflammatory markers), endoscopy and/or colonoscopy with biopsies, and imaging studies (such as CT or MRI scans) to look for evidence of chronic inflammation.

Read the full article here

Share This Article
Leave a comment

Leave a Reply

Your email address will not be published. Required fields are marked *