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OPTIMIZE YOUR HEALTH
Living With Celiac Disease
What Does Celiac Disease Have to Do With
Me? The Importance of Identifying Subclinical Celiac Disease
By Sue Kim-Saechao, RN, MSN, CRNP, and Jannet Huang,
MD, FRCPC, FACE, ABHM
Celiac disease is more common than many people realize. Even individuals
without gastrointestinal complaints can be affected by celiac disease.
Establishing the diagnosis of subclinical celiac disease is of
potential importance for four reasons: the danger of malignancy,
the presence of unsuspected nutritional deficiencies, the association
with low-birth weight infants in affected mothers, and the occurrence
of autoimmune disorders.
Celiac disease, also known as gluten intolerance, is an inherited
autoimmune disorder affecting 1 in 133 Americans. It is an inflammatory
condition in which our immune system attacks the small intestine
when gluten is consumed. Unfortunately, gluten is used in many
food products so treatment can be challenging (for more info, please
read Nutrition News). Most people have no signs or symptoms for
years and the disease is suddenly “activated” for an
unknown reason, whereas for others, symptoms can start as young
as age 2. Symptoms can range from bloating, irritable bowel symptoms,
constipation, diarrhea, weight loss, and malnutrition, to no gastrointestinal
symptoms at all. Whether gastrointestinal symptoms are present
or not, all affected by celiac disease can manifest the nutritional
consequences of malabsorption, such as iron/folate/Vitamin D deficiency,
chronic fatigue, chronic pain, and unexplained fractures.
The risk
of malignancy, specifically non-Hodgkin’s lymphoma
and other gastrointestinal tract malignancies is modestly increased
in patients with celiac disease. Interestingly, risk of cancers
of the breast and possibly lung appears to be reduced.
No single
test can confidently establish the diagnosis of celiac disease
in every individual. All testing should be performed while
patients are on a gluten-containing diet. As a general rule,
testing should begin with screening blood tests such as endomysial
antibodies, tissue transglutaminase antibodies and anti-gliadin
antibodies. Patients with a positive IgA endomysial or transglutaminase
antibody tests should undergo a small bowel biopsy. Exceptions
are those who have biopsy-proven dermatitis herpetiformis in whom
the diagnosis can be established without a small bowel biopsy.
HLA typing for DQ2 and DQ8 may be useful in individuals with equivocal
small bowel biopsy findings since celiac disease is unlikely if
neither is present. The diagnosis of celiac disease is confirmed
when symptoms resolve subsequently on a gluten-free diet.
Who Should Be Tested
Testing for celiac disease should be considered in the following
groups of patients:
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Those with gastrointestinal symptoms including chronic
diarrhea, malabsorption, weight loss, and abdominal distension.
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Individuals without other explanations for signs and symptoms
such as persistent elevation in liver enzymes, short stature,
delayed puberty, iron-deficiency anemia, recurrent fetal
loss, and infertility.
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Symptomatic individuals at high risk for celiac disease
including patients with type 1 diabetes mellitus or other
autoimmune endocrine disorders (such as Hashimoto’s
thyroiditis and adrenal insufficiency), first- and second-degree
relatives of individuals with celiac disease, patients with
Turner, Down, or Williams syndromes.
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There are other conditions in which testing may also be
considered such as patients with irritable bowel syndrome,
persistent apthous stomatitis, autoimmune diseases (lupus,
rheumatoid arthritis), primary biliary cirrhosis, peripheral
neuropathy, cerebellar ataxia, Sjogren's syndrome, recurrent
migraine, and dental enamel hypoplasia.
Fortunately, in celiac disease, removal of gluten from the diet
brings about quick relief of symptoms, intestinal healing, and
resolution of symptoms, usually within weeks to months.
Our goal
at The Center for Optimal Health is to provide a holistic, comprehensive
approach so we can accurately diagnosis, treat, and prevent illnesses
for the best quality of life possible.
Resources:
—October 2007
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Wellness e-Letter
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