Crohn's Disease- Pathophysiology and Conventional and Alternative Treatment Options
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Crohn's Disease- Pathophysiology and Conventional and Alternative Treatment Options
Kathleen A. Head, ND- Technical Advisor, Thorne Research
Julie S. Jurenka, MT (ASCP)- Research Assistant
Alternative Medicine Review . Volume 9, Number 4 . 2004
Crohn’s disease, a subcategory of
inflammatory bowel disease, contributes to
significant morbidity, particularly in
industrialized nations. It can affect people of
any age, but is more commonly diagnosed in
adolescence and young adulthood.
Inflammation and ulceration occur primarily in
the terminal ileum and colon, although any
portion of the intestinal tract can be affected.
No etiology has been identified for Crohn’s
disease, although a number of factors
contribute to its etiopathogenesis, including
genetic, microbial, inflammatory, immune, and
permeability abnormalities. Conventional
medications are not curative but can contribute
to resolution of acute flare-ups and help
maintain remission. Because significant side
effects are associated with many of these
medications, more natural interventions to help
maintain remission should be considered.
Associated nutrient deficiencies, dietary
interventions, and nutrient and botanical
supplementation are discussed.
Crohn’s disease (CD) is one of two main
forms of inflammatory bowel disease (IBD), the
other being ulcerative colitis (UC). Crohn's Disease
is a chronic, relapsing, transmural (affecting all
layers of the intestine) inflammation of uncertain
etiology that can affect any portion of the digestive
tract from mouth to anus, but is predominantly
seen in the terminal ileum and/or colon. Intestinal
inflammation and ulceration in Crohn's Disease is asymmetrical
and occurs in "patches" with areas of healthy
tissue interspersed, and extends deeply into the
intestinal wall, forming granulomatous lesions.
The disease is named after Dr. Burrill B. Crohn
who, with his colleagues Ginzburg and
Oppenheimer, published a landmark paper in 1932
describing the features of what is known today as
Crohn’s disease. Several categories of Crohn's Disease have
been described, defined by the portion of the digestive
tract involved and the presenting symptomatology (Table 1).
Current statistics indicate 1-2 million
Americans suffer from IBD, with approximately
half of those cases diagnosed as Crohn’s disease.
Crohn's Disease affects men and women equally, with a majority
of cases diagnosed in adolescents and young
adults ages 15-35 years. The disease, however, can
affect people at any age and approximately 10
percent of cases are under age 18. Crohn’s disease
predominantly affects Caucasians; with a
prevalence rate of 149 per 100,000, although there
has been a steady increase in reported cases of Crohn's Disease and Ulcerative Colitis among African Americans. IBD is
largely a disease of the industrialized world, especially
the United States and Europe, and is more
common in urban areas and northern climates. Crohn's Disease
has a known genetic component, with 25 percent
of Crohn’s patients having a family member with
some form of IBD. Statistics also indicate those
with a sibling with IBD are 30 times more likely
than the general population to develop IBD.1
Signs and symptoms of Crohn's Disease are similar to
Ulcerative Colitis, making diagnosis difficult. For a complete
comparison of Crohn’s and UC signs and symptoms,
see Table 2. Patients diagnosed with Crohn's Disease
present with some or all of the following symptoms:
frequent diarrhea, abdominal pain in the
lower right quadrant appearing soon after meals,
fatigue, loss of appetite, weight loss, fever, stomatitis,
and perianal fistula or fissures. Some patients
also present with rectal bleeding, arthritis,
and erythema nodosum lesions on the extremities.1
In pediatric cases of Crohn's Disease, growth failure is observed
in 75 percent of patients.2
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