Celiac Disease (CD)
Not yet clinically reviewed
This protocol was migrated from the earlier Pharmapedia and Ward Guide apps for educational use. Follow your hospital's own policies and consult seniors when in doubt.
Celiac disease is a genetic autoimmune condition disease that mainly affects the gastrointestinal tract when gluten is ingested. Gluten is a protein found in wheat, barley, and rye. When someone with CD eats gluten, the lining of the small intestine becomes damaged and is unable to absorb nutrients properly.
Symptoms of Celiac Disease
There are over 200 symptoms of CD and they vary so widely that there is no such thing as a typical case. Many people do not experience any of the gastric symptoms that were previously thought to typify the condition. These individuals often face a delay in diagnosis.
Physical Symptoms May Include
Abdominal cramping
Amenorrhea (absence of menstruation)
Anemia
Bloating/distention
Brain fog/inability to concentrate
Canker sores
Constipation
Dental abnormalities
Diarrhea
Edema/swelling
Electrolyte imbalance
Elevated liver enzymes
Fatigue
Headaches
Infertility/miscarriage
Osteopenia/ osteoporosis
Pain in bones and joints
Peripheral neuropathy
Rash (see dermatitis herpetiformis)
Stool abnormalities
Vitamin and mineral deficiencies
Vomiting
Weight loss or gain
Emotional Symptoms May Include
Anxiety
Depression
Irritability
Mood changes
Common Symptoms in Children
Children with CD may exhibit any of the previously listed symptoms as well as:
Failure to thrive
Delayed puberty
ADHD-like symptoms
Diagnosis
The steps leading to a diagnosis of celiac disease are:
- A thorough physical examination with complete medical history.
- Blood work that includes a celiac panel. A celiac panel will measure the number of particular antibodies in the blood. The most common tests include: TG (tissue transglutaminase antibody) and total serum IgA. Other available tests include an EMA (endomysial antibody), DGP (deaminated gliadin peptide), IgA, and IgG.
- An upper endoscopy with several biopsies of the small intestine including the duodenum.
It is important to continue to consume gluten throughout the testing process. Failure to do so can lead to a false negative or an inconclusive result.
It’s important to go through the testing process to get an accurate diagnosis since other serious medical conditions can present in a similar way to CD and need to be ruled out. Additionally, keeping to a lifelong, strict GF diet can be burdensome and is more difficult to maintain without a proven medical need. Once you are diagnosed with CD and a GF diet has started, your antibody levels will start to drop and your villi will heal.
Treatment of Celiac Disease
Currently the only treatment for CD is the lifelong adherence to a strict gluten-free (GF) diet.
All food that either contains gluten or might have had contact with gluten (known as cross-contact) must be avoided. Even levels of cross-contact that do not produce a noticeable reaction may cause damage to the intestine and should be avoided.
People with CD must watch for cross-contact and/or items that have been used with gluten containing food and cannot be sufficiently cleaned. For example:
toasters, toaster ovens, air fryers
food preparation surfaces
condiments and spreads
shared utensils
colanders/strainers
deep fryers
It takes time to heal, but for most people, keeping to a strict GF diet can result in an improvement in symptoms.
Do not start a GF diet without first confirming the diagnosis of CD, NCGS, or DH with your doctor. The diagnosis of CD is based upon blood tests and a biopsy of the small intestine. If testing is done after a GF diet is started, blood tests can normalize, the small intestine may heal, and your doctor will be unable to make an accurate diagnosis.
