CELIAC DISEASE
Celiac disease is a digestive disease that damages the small intestine and interferes with absorption of nutrients from food. People who have celiac disease cannot tolerate a protein called gluten, which is found in wheat, rye, barley, and possibly oats. When people with celiac disease eat foods containing gluten, their immune system responds by damaging the small intestine. Specifically, tiny fingerlike protrusions, called villi, on
the lining of the small intestine are lost. Nutrients from food are absorbed into the bloodstream through these villi. Without villi, a person becomes malnourished--regardless of the quantity of food eaten.
Because the body's own immune system causes the damage, celiac
disease is considered an autoimmune disorder. However, it is also
classified as a disease of malabsorption because nutrients are not absorbed. Celiac disease is also known as celiac sprue, nontropical sprue, and gluten-sensitive enteropathy.
Celiac disease is a genetic disease, meaning that it runs in families. Sometimes the disease is triggered--or becomes active for the firsttime--after surgery, pregnancy, childbirth, viral infection, or severe emotional stress.
WHAT ARE THE SYMPTOMS?
Celiac disease affects people differently. Some people develop symptoms as children, others as adults. One factor thought to play a role in when and how celiac appears is whether and how long a person was breastfed--the longer one was breastfed,the later symptoms of celiac disease appear, and the more atypical the symptoms. Other factors include the age at which one began eating foods containing gluten and how much gluten is eaten.
Symptoms may or may not occur in the digestive system. For example, one person might have diarrhea and abdominal pain, while another person has irritability or depression. In fact, irritability is one of the most common symptoms in children.
Symptoms of celiac disease may include one or more of the following:
- Recurring abdominal bloating and pain.
- Chronic diarrhea.
- Weight loss.
- Pale, foul-smelling stool.
- Unexplained anemia (low count of red blood cells).
- Gas.
- Bone pain.
- Behavior changes.
- Muscle cramps.
- Fatigue.
- Delayed growth.
- Failure to thrive in infants.
- Pain in the joints.
- Seizures.
- Tingling numbness in the legs (from nerve damage).
- Pale sores inside the mouth, called aphthus ulcers.
- Painful skin rash, called dermatitis herpetiformis.
- Tooth discoloration or loss of enamel.
- Missed menstrual periods (often because of excessive weight
loss).
Anemia, delayed growth, and weight loss are signs of malnutrition--not getting enough nutrients. Malnutrition is a serious problem for anyone,but particularly for children because they need adequate nutrition to develop properly. Some people with celiac disease may not have symptoms. The undamaged part of their small intestine is able to absorb enough nutrients to prevent symptoms. However, people without symptoms are
still at risk for the complications of celiac disease.
HOW IS CELIAC DISEASE DIAGNOSED??
Diagnosing celiac disease can be difficult because some of its symptoms are similar to those of other diseases, including irritable bowel syndrome, Crohn's disease, ulcerative colitis, diverticulosis, intestinal infections, chronic fatigue syndrome, and depression.
Recently, researchers discovered that people with celiac disease have higher than normal levels of certain antibodies in their blood. Antibodies are produced by the immune system in response to substances that the body perceives to be threatening. To diagnose celiac disease,physicians test blood to measure levels of antibodies to gluten. These antibodies are antigliadin, anti-endomysium, and antireticulin.
If the tests and symptoms suggest celiac disease, the physician may remove a tiny piece of tissue from the small intestine to check for damage to the villi. This is done in a procedure called a biopsy: the physician eases a long, thin tube called an endoscope through the mouth and stomach into the small intestine, and then takes a sample of tissue using instruments passed through the endoscope. Biopsy of the small intestine is the best way to diagnose celiac disease.
SCREENING
Screening for celiac disease involves testing asymptomatic people for the antibodies to gluten. Americans are not routinely screened for celiac disease. However, because celiac disease is hereditary, family members--particularly first-degree relatives--of people who have been diagnosed may need to be tested for the disease. About 10 percent of an affected person's first-degree relatives (parents, siblings, or children)will also have the disease. The longer a person goes undiagnosed and
untreated, the greater the chance of developing malnutrition and other complications.
In Italy, where celiac disease is common, all children are screened by age 6 so that even asymptomatic disease is caught early. In addition, Italians of any age are tested for the disease as soon as they show symptoms. As a result of this vigilance, the time between when symptoms begin and the disease is diagnosed is usually only 2 to 3 weeks. In the United States, the time between the first symptoms and diagnosis averages about 10 years.
WHAT IS THE TREATMENT??
The only treatment for celiac disease is to follow a gluten-free diet--that is, to avoid all foods that contain gluten. For most people, following this
diet will stop symptoms, heal existing intestinal damage, and prevent further damage. Improvements begin within days of starting the diet,and the small intestine is usually completely healed--meaning the villi are ntact and working--in 3 to 6 months. (It may take up to 2 years for older adults.)
The gluten-free diet is a lifetime requirement. Eating any gluten, no matter how small an amount, can damage the intestine. This is true for anyone with the disease, including people who do not have noticeable symptoms. Depending on a person's age at diagnosis, some problems, such as delayed growth and tooth discoloration, may not improve. A small percentage of people with celiac disease do not improve on the gluten-free diet. These people often have severely damaged intestine that cannot heal even after they eliminate gluten from their diets. Because their intestines are not absorbing enough nutrients, they may
need to receive intravenous nutrition supplements. Drug treatments are being evaluated for unresponsive celiac disease. These patients may need to be evaluated for complications of the disease. If a person responds to the gluten-free diet, the physician will know for certain that the diagnosis of celiac disease is correct.
POINTS TO REMEMBER!!
People with celiac disease cannot tolerate gluten, a protein in
wheat, rye, barley, and possibly oats.Celiac disease damages the small intestine and interferes with nutrient absorption. Treatment is important because people with celiac disease could
develop complications like cancer, osteoporosis, anemia, and
seizures. A person with celiac disease may or may not have symptoms. Diagnosis involves blood tests and biopsy. Because celiac disease is hereditary, family members of a person with celiac disease may need to be tested. Celiac disease is treated by eliminating all gluten from the diet. The gluten-free diet is a lifetime requirement.
BACK