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Celiac sprue

Coeliac disease (also called celiac disease, non-tropical sprue, c(o)eliac sprue, gluten enteropathy and gluten intolerance) is a digestive disorder. It is characterised by damage or flattening to all or part of the villi lining the small intestine, causing scar tissue that cannot absorb nutrients. This damage is caused by exposure to gluten and related proteins found in wheat, rye, malt, barley and oats. more...

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Signs and symptoms

Damage to the villi reduces the ability of the intestines to absorb nutrients, and it is believed that the resulting nutritional deficiencies likely cause the wide spectrum of symptoms associated with the disorder. Coeliac disease may lead to digestive problems, such as indigestion, heartburn and irritable bowel syndrome, unexplained weight loss or other signs of nutritional deficiency due to malabsorption, and a wide range of other problems in different bodily systems, including the nervous system, the heart, and the teeth and bones.

Other symptoms can include dermatitis (an itchy rash), diarrhea, excessive tiredness or fatigue, aching in joints and a general feeling of being unwell.

Coeliacs (people with coeliac disease) may also be symptom-free, but they are still doing damage to their small intestines. Regardless of the presence or absence of symptoms, the disorder is associated with an increased risk of osteoporosis and MALT lymphoma, a form of intestinal cancer.

Strict adherence to a gluten-free diet typically resolves all symptoms and conditions caused by coeliac disease. In coeliacs who are not on a gluten-free diet, the disease may present through one or more of the following symptoms. The presence of these symptoms does not mean the individual is coeliac. These symptoms are also associated with other diseases, some of which are life-threatening; therefore, patients with these symptoms should promptly consult a doctor for differential diagnosis.

Dietary deficiencies, which may manifest as symptoms in particular body systems (e.g., digestive or nervous system) or may be noticed on routine blood tests, are common in coeliacs. Up to 50% of coeliac disease patients have malabsorption-related diarrhea (with bulky, pale, offensive-smelling stools which may float in the toilet bowl). This symptom is known as steatorrhea. However, some coeliacs suffer from constipation. Excess flatulence is common, and some coeliacs also experience infrequent, minor rectal bleeding. Unexplained weight loss (or even obesity occasioned by overeating due to cravings for nutrients), indigestion, acid reflux, excessive tiredness (coeliacs have reported falling asleep while driving) and an itchy rash (dermatitis) may also be a sign of the disorder. Delayed puberty (or short stature prior to adolescence) might also be a symptom. Rarely, coeliacs may experience symtoms similar to those of sinus infections and/or the formation of thick, choking plugs or ropes of mucus that require considerable effort to expel. A low-grade, persistent pain may be present, possibly lessened by eating, which may all too easily be taken for the presence of ulcers.

In young children, the most common symptoms are steatorrhoea, weight loss, abdominal distension, and slow growth/failure to thrive, but irritability, vomiting and tiredness are common. It has been suggested that some cases of autism may be caused by coeliac disease.

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Better Diagnostic Testing for Celiac Sprue: A Review - Brief Article
From American Family Physician, 6/15/02 by Bill Zepf

Heretofore regarded as an uncommon disease, celiac sprue is increasingly being recognized as an underdiagnosed condition affecting an estimated one of every 120 to 300 persons in Europe and North America. Farrell and Kelly reviewed the essentials of diagnosis and management of patients with celiac sprue, highlighting serologic tests now available for investigating suspected cases of the disease.

Classically, celiac sprue has been diagnosed in a young infant who fails to thrive and has chronic diarrhea, but it is now apparent that the condition affects persons of all ages, with about 20 percent of cases occurring in persons older than 60 years. In about one half of adults with celiac sprue, presenting symptoms include diarrhea, flatulence, and weight loss. The other 50 percent, however, have more subtle manifestations such as anemia (either iron-deficiency anemia from intestinal blood loss or macrocytic anemia from folate malabsorption), a coagulopathy caused by vitamin K deficiency, or hypocalcemia and osteoporosis from malabsorption of vitamin D.

Celiac sprue is an autoimmune disease of the small intestine resulting from ingestion of gluten (found in wheat, barley, and rye grains) in sensitive persons. An abnormal T-cell response leads to production of antibodies against various intestinal targets. Serologic testing is now integral to establishing the diagnosis of celiac sprue. IgA anti-endomysial and anti-gliadin antibodies, as well as antibodies against tissue transglutaminase, have reasonable sensitivity and specificity for diagnosing celiac sprue. Endoscopic biopsy of the distal duodenum is still the gold standard for diagnosis, showing marked changes in the intestinal mucosa with loss of villi and crypt hyperplasia.

When celiac sprue is apparent by serologic and histologic findings, a trial gluten-free diet is indicated (see the accompanying table). The majority of patients improve rapidly in the first few weeks of the diet, although complete reversion to a normal intestinal mucosa on repeat biopsy is usually seen only in children.

Failure to improve while on a gluten-free diet should increase suspicion for other causes of small bowel enteropathy or may indicate noncompliance with the strict diet, which for most patients is difficult to follow. Patients with severe, refractory celiac sprue are at increased risk of developing intestinal T-cell lymphoma. Steroids and other immunosuppressants may be used when symptoms remain severe despite a gluten-free diet.

2002;346:180-8.

COPYRIGHT 2002 American Academy of Family Physicians
COPYRIGHT 2002 Gale Group

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