CELIAC DISEASE
Celiac disease occurs when the immune system attacks the small
intestine after exposure to gluten (a protein found in wheat, rye and
barley). This causes inflammation and damage to the small intestine, which
can prevent the absorption of water and nutrients into the body. Celiac disease
is also known as coeliac disease, celiac sprue, non-tropical sprue, and gluten
sensitive enteropathy. Celiac disease is hereditary, meaning that it runs in
families. About 1 in 10 people with a first-degree relative with celiac
disease (parent, child and/or sibling) will develop celiac disease.
Celiac disease is estimated to affect 1 in 100 people in the
United States and its incidence appears to be rising. In addition, 2.5 million
Americans are undiagnosed and may be at risk for long-term health
complications. Celiac disease can develop at any age, affecting both children
and adults. Left untreated, celiac disease can lead to additional serious
health problems. These include nutritional deficiencies, anemia, increased risk
of infections, osteoporosis, dermatitis herpetiformis (an itchy skin rash),
infertility or miscarriage, neurological conditions including seizures and
migraines, and intestinal cancers.
Currently, the only treatment for celiac disease is lifelong
adherence to a strict gluten-free diet. People living gluten-free must avoid
wheat, rye and barley, found in many foods including bread, pasta and beer.
Gluten is also used commonly as a filler in many processed foods. With the
increased marketing and development of gluten-free foods, a gluten-free diet
has become easier to follow. However, many people with celiac disease still
find the diet restrictive and difficult to follow, especially when eating
outside their home. In addition, the majority of people with celiac disease
continue to demonstrate evidence of ongoing intestinal damage even while
attempting to adhere to a strict gluten-free diet. Thus, there is a clear need
for adjunctive therapies in the treatment of celiac disease.
There are additionally some people who may have “gluten
intolerance” without having celiac disease. These people may experience
symptoms of abdominal pain, bloating, diarrhea or fatigue when they eat a diet
containing gluten. While these are common symptoms of celiac disease, these
individuals do not have the characteristic small intestinal damage or tissue transglutaminase
(tTG) antibodies found in celiac disease. It is not yet clearly understood what
causes non-celiac gluten intolerance. Some experts have suggested that many
symptoms attributed to gluten intolerance may be caused by FODMAP (fructose,
olygosaccharides, disaccharides, monosaccharides and polyols)-containing foods
that are largely eliminated in gluten-free diets.
Celiac disease is restricted to people with certain HLA class II
genes. About 40 percent of people have these genes but only one percent gets
the disease. This suggests that there are other important genetic or
environmental factors that play into the immune reaction in celiac disease.
SYMPTOMS OF CELIAC DISEASE
Celiac disease can be difficult to diagnose because it may
affect many organ systems outside the intestines. Some people with celiac
disease have no symptoms. However, all people with celiac disease are
at risk for long-term complications, whether or not they display any
symptoms.
Does
My Child Have Celiac Disease?
Digestive symptoms are more common in infants and children. Here
are the most common symptoms found in children:
- abdominal
bloating and pain
- chronic
diarrhea
- vomiting
- constipation
- pale,
foul-smelling, or fatty stool
- weight
loss
- fatigue
- irritability
and behavioral issues
- dental
enamel defects of the permanent teeth
- delayed growth
and puberty
- short
stature
- failure
to thrive
- Attention Deficit Hyperactivity Disorder (ADHD)