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Celiac Disease

Definition

Celiac disease is a disease of the digestive system that damages the small intestine and interferes with the absorption of nutrients from food.

Description

Celiac disease occurs when the body reacts abnormally to gluten, a protein found in wheat, rye, barley, and possibly oats. When someone with celiac disease eats foods containing gluten, that person's immune system causes an inflammatory response in the small intestine, which damages the tissues and results in impaired ability to absorb nutrients from foods. The inflammation and malabsorption create wide-ranging problems in many systems of the body. Since the body's own immune system causes the damage, celiac disease is classified as an "autoimmune" disorder. Celiac disease may also be called sprue, nontropical sprue, gluten sensitive enteropathy, celiac sprue, and adult celiac disease.

Celiac disease may be discovered at any age, from infancy through adulthood. The disorder is more commonly found among white Europeans or in people of European descent. It is very unusual to find celiac disease in African or Asian people. The exact incidence of the disease is uncertain. Estimates vary from one in 5000, to as many as one in every 300 individuals with this background. The prevalence of celiac disease seems to be different from one European country to another, and between Europe and the United States. This may be due to differences in diet and/or unrecognized disease. A recent study of random blood samples tested for celiac disease in the US showed one in 250 testing positive. It is clearly underdiagnosed, probably due to the symptoms being attributed to another problem, or lack of knowledge about celiac disease by physicians and laboratories. Because of the known genetic component, relatives of patients with celiac disease are considered at higher risk for the disorder.

Because celiac disease has a hereditary influence, close relatives (especially first degree relatives, such as children, siblings, and parents) have a higher risk of being affected with the condition. The chance that a first degree relative of someone with celiac disease will have the disease is about 10%.

As more is learned about celiac disease, it becomes evident that it has many variations which may not produce typical symptoms. It may even be clinically "silent," where no obvious problems related to the disease are apparent.

— Amy Vance, MS, CGC



 
 
Dictionary: celiac disease

n.

A chronic nutritional disturbance, usually of young children, caused by the inability to metabolize gluten, which results in malnutrition, a distended abdomen, muscle wasting, and the passage of stools having a high fat content. The disorder can be controlled by a special diet that emphasizes the elimination of all foods containing gluten.


 
Food and Nutrition: coeliac disease

celiac disease

Intolerance of the proteins of wheat, rye, and barley; specifically, the gliadin fraction of the protein gluten. The villi of the small intestine are severely affected and absorption of food is poor. Stools are bulky and fermenting from unabsorbed carbohydrate, and contain a large amount of unabsorbed fat (steatorrhoea). As a result of malabsorption, affected people are malnourished and children suffer from growth retardation. Treatment is by exclusion of wheat, rye, and barley proteins (the starches are tolerated); rice, oats, and maize are generally tolerated. Manufactured foods that are free from gluten, and hence suitable for consumption by people with coeliac disease are usually labelled as ‘gluten-free’. Also known as gluten-induced enteropathy, and sometimes as non-tropical sprue.

 
Food and Fitness: coeliac disease

gluten intolerance; sprue

A digestive disorder caused by hypersensitivity to gluten, a mixture of two proteins found in wheat, barley, oats, and rye. The name ‘coeliac’ is derived from the Greek for ‘suffering in the bowels’. The condition is characterized by swelling of the intestinal wall and disappearance of the microvilli (the very fragile, highly folded membrane of some intestinal cells) in the presence of gluten. This results in impaired absorption of all nutrients (general malabsorption). Coeliac disease can be controlled by eating a strict and lifelong, gluten-free diet (i.e. a diet excluding wheat, barley, and rye products). The structure and function of the intestine returns to normal if gluten is removed from the diet.

 

Definition

Celiac disease occurs when the body reacts abnormally to gluten, a protein found in wheat, rye, barley, and oats. Gluten causes an inflammatory response in the small intestine, which damages the tissues and results in impaired ability to absorb nutrients from foods.

Description

Celiac disease—also called sprue, nontropical sprue, gluten sensitive enteropathy, celiac sprue, and adult celiac disease—may be discovered at any age. Researchers believe that a combination of genetic and environmental factors trigger the disease. Environmental events that may provoke celiac disease in those with a genetic predisposition to the disorder include surgery or a viral infection.

The disorder is more commonly found among white Europeans or those of European descent. The exact incidence of the disease is uncertain. Estimates vary from one in 5,000 to as many as one in every 300 individuals with this background. In 2002, new research in Italy followed patients with type 1 diabetes. Celiac disease is 20 times more common among these patients than in the general population, yet often goes undetected in these children. The study authors recommended celiac disease screening programs for children recently diagnosed with type 1 diabetes.

Causes & Symptoms

Celiac disease is caused by an inflammatory response of the small intestine. The exact mechanism of the disorder is not clearly understood, but it is known that both heredity and the immune system play a part. When food containing gluten reaches the small intestine, the immune system begins to attack a substance called gliadin, which is found in the gluten. The resulting inflammation causes damage to the delicate finger-like structures in the intestine, called villi, where food absorption actually takes place.

The most commonly recognized symptoms of celiac disease relate to the improper absorption of food in the gastrointestinal system. The patient will have diarrhea and fatty, greasy, unusually foul-smelling stools. The patient may complain of excessive gas (flatulence), distended abdomen, weight loss, and generalized weakness.

Not all patients have these problems. Unrecognized celiac disease may cause or contribute to a variety of other conditions. The decreased ability to digest, absorb, and utilize food properly (malabsorption) may cause anemia from iron deficiency or easy bruising from a lack of vitamin K. Poor mineral absorption may result in osteoporosis, which may lead to bone fractures. Vitamin D levels may be insufficient and bring about a "softening" of bones (osteomalacia), which produces pain and bony deformities. Defects in the tooth enamel, characteristic of celiac disease, may also occur. Celiac disease may be discovered during medical tests performed to investigate failure to thrive in infants, or lack of proper growth in children and adolescents. People with celiac disease may also experience lactose intolerance because they do not produce enough of the enzyme lactase, which breaks down the sugar in milk into a form the body can absorb.

A distinctive skin rash, called dermatitis herpetiformis, may be the first sign of celiac disease. Approximately 10% of patients with celiac disease have this rash, but it is estimated that 85% or more of patients with the rash have the disease.

Because of the variety of ways celiac disease can manifest itself, it is often not discovered promptly. The condition may persist without diagnosis for so long that the patient accepts a general feeling of illness as normal. This leads to further delay in identifying and treating the disorder.

Diagnosis

If celiac disease is suspected, a blood test that looks for the antibodies that the immune system produces in celiac disease is ordered. Some experts advocate not just evaluating patients with symptoms, but using these blood studies as a screening test for high-risk individuals, such as those with relatives known to have the disorder. An abnormal result points towards celiac disease, but further tests are needed to confirm the diagnosis. Other tests may be ordered to look for nutritional deficiencies. For example, doctors may order a test of iron levels in the blood because low levels of iron (anemia) may accompany celiac disease. Doctors may also order a test for fat in the stool, since celiac disease prevents the body from absorbing fat from food.

The next step is a biopsy of the small intestine. This is usually done by a gastroenterologist, a physician who specializes in diagnosing and treating bowel disorders. It is generally performed in the office, or in an outpatient department in a hospital. The patient remains awake, but is sedated. A narrow tube is passed through the mouth, down through the stomach, and into the small intestine. A small sample of tissue is taken and sent to the laboratory for analysis. If it shows a pattern of tissue damage characteristic of celiac disease, the diagnosis is established.

Treatment

The treatment for celiac disease is a gluten-free diet (GFD). This may be easy for the doctor to prescribe, but difficult for the patient to follow. Gluten is present in any product that contains wheat, rye, barley, or oats. It helps make bread rise, and gives many foods a smooth, pleasing texture.

In addition to the many obvious places gluten can be found in a normal diet, such as breads, cereals, and pasta, there are many hidden sources of gluten. These include ingredients added to foods to improve texture or enhance flavor and products used in food packaging. Gluten may even be present on surfaces used for food preparation or cooking.

Fresh foods that have not been artificially processed, such as fruits, vegetables, and meats, are permitted as part of a GFD. Gluten-free foods can be found in health food stores, mail-order companies, and in some super-markets. Help in dietary planning is available from support groups for individuals with celiac disease. There are many cookbooks on the market specifically for those on a GFD.

Treating celiac disease with a GFD is almost always completely effective in alleviating symptoms. Secondary complications, such as anemia and osteoporosis, resolve in almost all patients. People who have experienced lactose intolerance related to their celiac disease usually see those symptoms subside as well.

Allopathic Treatment

Both complementary and allopathic healthcare practitioners generally agree that a gluten-free diet is the best treatment for celiac disease.

There are a small number of patients who develop a refractory type of celiac disease, where the GFD no longer seems effective. Once the diet has been thoroughly assessed to ensure no hidden sources of gluten are causing the problem, medications may be prescribed. Steroids or immunosuppressant drugs are often used to try to control the disease.

Expected Results

The physician will periodically recheck the level of antibody in the patient's blood after a diagnosis of celiac disease has been made. After several months on a GFD, the small intestine of the patient is biopsied again. If the diagnosis of celiac disease was correct, healing of the intestine will be apparent. Most experts agree that it is necessary to follow these steps in order to be sure of an accurate diagnosis.

Patients with celiac disease must keep a strict GFD as long as they live. Although the disease may have symptom-free periods, silent damage will continue to occur if the diet is not followed. Patients who do not follow their diets run higher risks of serious complications like gastrointestinal cancers, iron–deficiency anemia, and decreased bone mineral density. Celiac disease cannot be "outgrown" or cured, according to medical authorities.

Once the diet has been followed for several years, individuals with celiac disease have similar mortality rates to the general population. However, about 10% of people with celiac disease develop a cancer involving the lymphatic system (lymphoma).

Prevention

There is no way to completely prevent celiac disease. However, the key to decreasing its impact on over-all health is early diagnosis and strict adherence to the prescribed diet. Interestingly, a 2002 study of Swedish children found that the gradual introduction of glutencontaining foods into infant's diets while they are still being breast–fed can reduce the risk of celiac disease, at least in early childhood.

Resources

Books

Lowell, Jax Peters. Against the Grain: The Slightly Eccentric Guide to Living Well without Wheat or Gluten. New York: Henry Holt, 1996.

Periodicals

"Celiac Disease Develops Early in Type 1 Diabetes Course." Diabetes Week. (June 17, 2002): 3.

Ivarsson, Aneeli, et al. "Breast–feeding Protects Against Celiac Disease." American Journal of Clinical Nutrition. (May 2002): 914–918.

Jancin, Bruce. "Lifelong, Gluten%ndash;free Diet Boosts Celiac Disease Outcomes. (Avoids Anemia, Increased GI Cancers)." Internal Medicine News. (May 15, 2002): 14.

Pruessner, H. "Detecting Celiac Disease in Your Patients." American Family Physician. 57 (March 1998): 1023-1034.

Organizations

Celiac Disease Foundation. 13251 Ventura Blvd., Suite 1, Studio City, CA 91604-1838. (818) 990-2354. http://www.cdf@celiac.org.

Celiac Sprue Association/United States of America (CSA/USA). PO Box 31700, Omaha, NE 68131-0700. (402) 558-0600.

Gluten Intolerance Group. PO Box 23053, Seattle, WA 98102-0353. (206) 325-6980.

[Article by: Paula Ford-Martin; Teresa G. Odle]

 

Definition

Celiac disease is a disease of the digestive system in which the inside lining of the small intestine (mucosa) is damaged after eating wheat, rye, oats, or barley, resulting in interference with the absorption of nutrients from food.

Description

Celiac disease occurs when the body reacts abnormally to gluten, a protein found in grains, including wheat, rye, barley, and possibly oats. When someone with celiac disease eats foods containing gluten, that person's immune system causes an inflammatory response in the small intestine, which damages the tissues and results in impaired ability to absorb nutrients from foods (malabsorption). The inflammation and malabsorption create wide-ranging problems in many systems of the body. Since the body's own immune system causes the damage, celiac disease is classified as an autoimmune disorder.

Each person with celiac disease is affected differently. When food containing gluten reaches the small intestine, the immune system begins to attack a substance called gliadin, which is found in the gluten. The resulting inflammation causes damage to the delicate finger-like structures in the intestine, called villi, where food absorption actually takes place. This damage is referred to as villus atrophy. The patient may experience a number of symptoms related to the inflammation and the chemicals it releases, and/or the lack of ability to absorb nutrients from food, which can cause malnutrition.

Celiac disease is also called sprue, nontropical sprue, gluten sensitive enteropathy, and celiac sprue.

Demographics

Celiac disease may be discovered at any age, from infancy through adulthood. The disorder is more commonly found among white Europeans and in people of European descent. It is very unusual to find celiac disease in African or Asian people. The exact incidence of the disease is uncertain. Estimates vary from one in 5,000, to as many as one in every 300 individuals with this background. The prevalence of celiac disease seems to be different from one European country to another and between Europe and the United States. This discrepancy may be due to differences in diet and/or the possibility that the disease goes unrecognized in some areas. One study of random blood samples tested for celiac disease in the United States showed one in 250 testing positive. It is clearly underdiagnosed, probably because the symptoms are attributed to another problem, and physicians and laboratory technicians lack knowledge about celiac disease.

Because celiac disease has a hereditary influence or genetic component, close relatives (especially first-degree relatives, such as children, siblings, and parents) have a higher risk of being affected with the condition. The chance that a first-degree relative of someone with celiac disease has the disease is about 10 percent.

Causes and Symptoms

The pattern of inheritance is complicated regarding this disease. The type of inheritance pattern that celiac disease follows is called multifactorial (caused by many factors, both genetic and environmental). Researchers think that several factors must exist in order for the disease to occur. The patient must have a genetic predisposition to develop the disorder. Then something in their environment acts as a stimulus, or trigger, to their immune system, causing the disease to become active for the first time. For conditions with multifactorial inheritance, people without the genetic predisposition are less likely to develop the condition with exposure to the same triggers, or they may require more exposure to the stimulus before developing the disease than someone with a genetic predisposition. Stimuli that may provoke a reaction include surgery, especially gastrointestinal surgery; a change to a low fat diet, which includes an increased number of wheat-based foods; severe emotional stress; or a viral infection. The combination of genetic susceptibility and an outside agent leads to celiac disease.

The most commonly recognized symptoms of celiac disease relate to the improper absorption of food in the gastrointestinal system. Many patients with gastrointestinal symptoms will have diarrhea and fatty, greasy, unusually foul-smelling stools. The patient may complain of excessive gas (flatulence), distended abdomen, weight loss, and generalized weakness. Not all people have digestive system complications; some people only have irritability or depression. Irritability is one of the most common symptoms in children with celiac disease.

Not all individuals with celiac disease exhibit typical symptoms. As more is learned about celiac disease, it has become evident that the disease has many variations that may not produce typical symptoms. Unrecognized and therefore untreated celiac disease may cause or contribute to a variety of other conditions. The decreased ability to digest, absorb, and utilize food properly (malabsorption) may cause anemia (low red blood count from iron deficiency) or easy bruising from a lack of vitamin K. Poor mineral absorption may result in osteoporosis, or brittle bones, which may lead to bone fractures. Vitamin D levels may be insufficient and bring about a softening of bones (osteomalacia), which produces pain and bony deformities, such as flattening or bending. Defects in the tooth enamel, characteristic of celiac disease, may be recognized by dentists. Celiac disease may be discovered during medical tests performed to investigate failure to thrive in infants or lack of proper growth in children and adolescents. People with celiac disease may also experience lactose intolerance because they do not produce enough of the enzyme lactase, which breaks down the sugar in milk into a form the body can absorb. Other symptoms can include muscle cramps, fatigue, delayed growth, tingling or numbness in the legs (from nerve damage), pale sores in the mouth (called aphthus ulcers), tooth discoloration, or missed menstrual periods (due to severe weight loss).

A distinctive, painful skin rash, called dermatitis herpetiformis, may be the first sign of celiac disease in adults but rarely occurs in children with celiac disease.

Many disorders are associated with celiac disease, although the nature of the connection is unclear. One type of epilepsy is linked to celiac disease. Once their celiac disease is successfully treated, a significant number of these patients have fewer or no seizures. Patients with alopecia areata, a condition in which hair loss occurs in sharply defined areas, have been shown to have a higher risk of celiac disease than the general population. There appears to be a higher percentage of celiac disease among people with Down syndrome, but the link between the conditions was unknown as of 2004.

Several conditions attributed to a disorder of the immune system have been associated with celiac disease. People with insulin-dependent diabetes (type I) have a much higher incidence of celiac disease. One source estimates that as many as one in 20 insulin-dependent diabetics may have celiac disease. Patients with other conditions in which celiac disease may be more commonly found include those with juvenile chronic arthritis, some thyroid diseases, and IgA deficiency.

There is an increased risk of intestinal lymphoma, a type of cancer, in individuals with celiac disease. Successful treatment of the celiac disease seems to decrease the chance of developing lymphoma.

When to Call the Doctor

A doctor should be consulted when a child exhibits symptoms characteristic of this disease.

Diagnosis

Because of the variety of ways celiac disease can manifest itself, it is often not discovered promptly. Its symptoms are similar to many other conditions including irritable bowel syndrome, Crohn's disease, ulcerative colitis, diverticulosis, intestinal infections, chronic fatigue syndrome, and depression. The condition may persist without diagnosis for so long that the patient accepts a general feeling of illness as normal. This acceptance leads to further delay in identifying and treating the disorder. It is not unusual for the disease to be identified in the course of medical investigations for seemingly unrelated problems.

If celiac disease is suspected, based on symptoms, physical appearance, or delayed growth, a blood test should be ordered. This test looks for the antibodies to gluten (called antigliadin, anti-endomysium, and antireticulin) that the immune system produces in celiac disease. Antibodies are chemicals produced by the immune system in response to substances such as germs and other potentially harmful substances. Some experts advocate not just evaluating patients with symptoms, but using these blood studies as a screening test for high-risk individuals, such as those with relatives (especially first-degree relatives) known to have the disorder. An abnormal result points toward celiac disease, but further tests are needed to confirm the diagnosis. Because celiac disease affects the ability of the body to absorb nutrients from food, several tests may be ordered to look for nutritional deficiencies. For example, doctors may order a test of iron levels in the blood because low levels of iron (anemia) may accompany celiac disease. Doctors may also order a test for fat in the stool, since celiac disease prevents the body from absorbing fat from food.

If these tests are suspicious for celiac disease, the next step is a biopsy (surgical removal of a tiny piece of tissue) of the small intestine. This is usually done by a gastroenterologist, a physician who specializes in diagnosing and treating bowel disorders. It is generally performed in the office or in a hospital's outpatient department. The patient remains awake but is sedated. A narrow tube, called an endoscope, is passed through the mouth, down through the stomach, and into the small intestine. A small sample of tissue is taken and sent to the laboratory for analysis. If it shows a pattern of tissue damage characteristic of celiac disease, the diagnosis is established.

Treatment

The only treatment for celiac disease is a gluten-free diet (GFD). This diet is easy for the doctor to prescribe but may be difficult for a child to follow. For most people, adhering to this diet stops symptoms and prevents damage to the intestines. Damaged villi can be functional again in three to six months. This diet must be followed permanently, however. The fact that people had symptoms that were cured by the GFD is further evidence that the diagnosis was correct.

The physician will periodically recheck the level of antibody in the child's blood. After several months, the small intestine is biopsied again. If the diagnosis of celiac disease was correct (and the child followed the rigorous diet), healing of the intestine will be apparent. Most experts agree that it is necessary to follow these steps in order to be sure of an accurate diagnosis. Disorders other than celiac disease can cause a similar type of villus atrophy, especially in children under two years of age, so rechecking the intestine is especially important for very young children. If healing is evident, then gluten is reintroduced to the diet and a third biopsy is performed weeks to months later to see if the reintroduction of gluten results in villus atropy again. If the atrophy returns, the child has celiac disease, and a gluten-free diet should be continued for life.

A child with undiagnosed celiac disease may become very ill with severe diarrhea and malnutrition. Corticosteroids such as prednisone and intravenous (IV) fluids may be temporarily given while the child begins a GFD. Because celiac disease is diagnosed more quickly than in the past, corticosteroids are seldom required.

Nutritional Concerns

Although there is no risk and much potential benefit to the use of GFD for treatment of celiac disease, the widespread use of gluten-containing grains in Western cultures makes adapting to a gluten-free diet challenging. Gluten is present in any product that contains wheat, rye, barley, or oats. It helps make bread rise and gives many foods a smooth, pleasing texture. In addition to the many obvious places gluten can be found in a normal diet, such as breads, cereals, and pasta, there are many hidden sources of gluten. Thickening agents, emulsifiers, fillers, flavor enhancers, and food stabilizers as well as products used in food packaging may contain gluten. Gluten may even be present on surfaces used for food preparation or cooking.

Fresh foods that have not been artificially processed, such as fruits, vegetables, and meats, are permitted as part of a GFD. Gluten-free foods can be found in health food stores and in some supermarkets. Mail-order food companies often have a selection of gluten-free products. Help in dietary planning is available from dieticians (healthcare professionals specializing in food and nutrition) or from support groups for individuals with celiac disease. There are many cookbooks on the market specifically for those on a GFD.

Prognosis

Treating celiac disease with a strict GFD is almost always completely effective. Gastrointestinal complaints and other symptoms are alleviated. Secondary complications, such as anemia and osteoporosis, resolve in almost all patients. People who have experienced lactose intolerance related to their celiac disease usually see those symptoms subside as well.

Once the diet has been followed for several years, individuals with celiac disease have similar mortality rates as the general population. However, about 10 percent of people with celiac disease develop a cancer involving the gastrointestinal tract (both carcinoma and lymphoma).

A few patients develop a refractory type of celiac disease, in which the GFD no longer seems effective. Once the diet has been thoroughly assessed to ensure no hidden sources of gluten are causing the problem, medications may be prescribed. Steroids or immunosuppressant drugs are often used to try to control the disease. It is unclear whether these efforts meet with much success.

Experts emphasize the need for lifelong adherence to the GFD to avoid the long-term complications of this disorder. They point out that although the disease may have symptom-free periods if the diet is not followed, silent damage continues to occur. Celiac disease cannot be outgrown or cured, according to medical authorities.

Prevention

There is no way to prevent celiac disease. However, the key to decreasing its impact on overall health is early diagnosis and strict adherence to the prescribed GFD.

Parental Concerns

For parents used to preparing gluten-containing meals, searching for and cooking with gluten-free products may be difficult at first. Changing cooking habits will be easier if initially gluten-free recipes and food products are used. When they use any commercial food products, they must read carefully the list of ingredients. Although ingredients are listed in order of decreasing content, any product containing the smallest of amount of gluten must be avoided. Many food manufacturers are willing to provide additional information about their products. Most food labels contain addresses of the manufacturers and many include a toll-free telephone number. Some restaurants have ingredient lists for their products posted in the restaurant or available on request.

When a child with celiac disease eats at a friend's house, the friend's parent should be aware of the child's dietary limitations. The child may have to take lunch from home to eat at school, unless the school has a dietician who can ensure that gluten-free food is provided for the child.

Family support is important in ensuring acceptance of the diet. The child must not be made to feel that he/she is abnormal and a nuisance to the family. After the GFD is begun, the benefits to the child with celiac disease will initially be obvious and enthusiastically accepted. However, as the child gets older, the period of ill health may be forgotten, and the child may be reject the diet, especially during adolescence, when there is a desire for conformity. Unfortunately, in older children, the symptoms may not reappear immediately although intestinal damage is occurring. The child may interpret the delay in the return of symptoms as evidence that the child has recovered from celiac disease, but they have not, as celiac disease cannot be cured.

Resources

Books

Icon Health Publications. The Official Patient's Sourcebook on Celiac Disease. San Diego, CA: Icon Health Publications, 2002.

Korn, Danna. Kids with Celiac Disease. Bethesda, MD: Woodbine House, 2001.

Kruszka, Bonnie J., and Richard S. Cihlar. Eating Gluten-Free with Emily. Bethesda, MD: Woodbine House, 2004.

Sanderson, Sheri L. Incredible Edible Gluten-Free Food for Kids. Bethesda, MD: Woodbine House, 2002.

Organizations

American Celiac Society. 58 Musano Court, West Orange, NJ 07052. Telephone: 201/325–8837.

Celiac Disease Foundation. 13251 Ventura Blvd., Suite 1, Studio City, CA 91604–1838. Web site: .

Celiac Sprue Association/United State of America (CSA/USA). PO Box 31700, Omaha, NE 68131–0700. Web site: www.csaceliacs.org.

Gluten Intolerance Group of North America. PO Box 23053, Seattle, WA, 98102–0353. Web site: www.gluten.net.

National Center for Nutrition and Dietetics, American Dietetic Association. 216 West Jackson Boulevard, Suite 800, Chicago, IL 60606–6995. Telephone: 800/366–1655. Web site: www.unl.edu2020/alpha/National_Center_for_Nutrition_and_Dietetics.html.

ROCK: Raising Our Celiac Children. 216 West Jackson Boulevard, Suite 800, Chicago, IL 60606–6995. Telephone: 800/366–1655. Web site: www.celiac.com/cgi-bin/webc.cgi/st_main.html?p_catid=8.

Web Sites

"Celiac Disease." National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 2004. Available online at (accessed October 25, 2004).

Celiac Disease and Diet Support Center. Available online at www.celiac.com/ (accessed October 25, 2004).

Other

Gluten-Free Living, a bimonthly newsletter. PO Box 105, Hastings-on-Hudson, NY 10706. Available online at www.glutenfreeliving.com/ (accessed October 25, 2004).

[Article by: Judith Sims, MS Amy Vance, MS, CGC]



 

Digestive disorder in which people cannot tolerate gluten, a protein constituent of wheat, barley, malt, and rye flours. In celiac disease, gluten generates an immune response that damages the mucous lining of the small intestine; it is believed that a deficiency of gluten-digesting enzymes may underlie the disease. Poor nutrient absorption causes foul, bulky, fatty stools; malnutrition; stunting of growth; and anemia similar to pernicious anemia. It can run in families. Children begin having intermittent intestinal upset, diarrhea, and wasting at 6 – 21 months. In adults it usually begins after 30, with appetite loss, depression, irritability, and diarrhea. Symptoms in advanced cases stem from nutritional deficiencies and may require supportive measures. A high-protein diet low in glutens and saturated fats usually relieves symptoms.

For more information on celiac disease, visit Britannica.com.

 
Wikipedia: coeliac disease
Coeliac disease
Classification & external resources
Coeliac_path.jpg
Biopsy of small bowel showing coeliac disease manifested by blunting of villi, crypt hyperplasia, and lymphocyte infiltration of crypts.
ICD-10 K90.0
ICD-9 579.0
OMIM 212750
DiseasesDB 2922
MedlinePlus 000233
eMedicine med/308  ped/2146 radio/652
MeSH D002446

Coeliac disease, also spelled celiac disease, is an autoimmune disorder of the small bowel that occurs in genetically predisposed people of all ages from middle infancy. Symptoms include chronic diarrhoea, failure to thrive (in children) and fatigue, but these may be absent and symptoms in all other organ systems have been described. It is estimated to affect about 1% of Indo-European populations, although significantly underdiagnosed. A growing portion of diagnoses are being made in asymptomatic persons as a result of increasing screening.[1]

Coeliac disease is caused by a reaction to gliadin, a gluten protein found in wheat (and similar proteins of the tribe Triticeae which includes other cultivars such as barley and rye). Upon exposure to gliadin, the enzyme tissue transglutaminase modifies the protein, and the immune system cross-reacts with the bowel tissue, causing an inflammatory reaction. That leads to flattening of the lining of the small intestine, which interferes with the absorption of nutrients. The only effective treatment is a lifelong gluten-free diet.

This condition has several other names, including: cœliac disease (with "œ" ligature), c(o)eliac sprue, non-tropical sprue, endemic sprue, gluten enteropathy or gluten-sensitive enteropathy, and gluten intolerance. The term coeliac derives from the Greek κοιλιακος (koiliakos, abdominal), and was introduced in the 19th century in a translation of what is generally regarded as an ancient Greek description of the disease by Aretaeus of Cappadocia.[2]

Signs and symptoms

Classic symptoms of coeliac disease include diarrhoea, weight loss (or stunted growth in children), and fatigue, but while coeliac disease is primarily a bowel disease, bowel symptoms may also be limited or even absent. Some patients are diagnosed with symptoms related to the decreased absorption of nutrients or with various symptoms which, although statistically linked, have no clear relationship with the malfunctioning bowel. Given this wide range of possible symptoms, the classic triad is no longer a requirement for diagnosis.

Children between 9 and 24 months tend to present with bowel symptoms and growth problems shortly after first exposure to gluten-containing products. Older children may have more malabsorption-related problems and psychosocial problems, while adults generally have malabsorptive problems.[3] Many adults with subtle disease only have fatigue or anaemia.[1]

Gastrointestinal

The diarrhoea characteristic of coeliac disease is pale, voluminous and malodorous. Abdominal pain and cramping, bloatedness with abdominal distention (thought to be due to fermentative production of bowel gas) and mouth ulcers[4] may be present. As the bowel becomes more damaged, a degree of lactose intolerance may develop. However, the variety of gastrointestinal symptoms that may be present in patients with coeliac disease is great, and some may have a normal bowel habit or even tend towards constipation. Frequently the symptoms are ascribed to irritable bowel syndrome (IBS), only later to be recognised as coeliac disease; a small proportion of patients with symptoms of IBS have underlying coeliac disease, and screening may be justified.[5]

Coeliac disease leads to an increased risk of both adenocarcinoma and lymphoma of the small bowel, which returns to baseline with diet. Longstanding disease may lead to other complications, such as ulcerative jejunitis (ulcer formation of the small bowel) and stricturing (narrowing as a result of scarring).[6]

Malabsorption-related

The changes in the bowel make it less able to absorb nutrients, minerals and the fat-soluble vitamins A, D, E, and K.[3]

Miscellaneous

Coeliac disease has been linked with a number of conditions. In many cases it is unclear whether the gluten-induced bowel disease is a causative factor or whether these conditions share a common predisposition.

Role of other grains

Wheat varieties or subspecies containing gluten such as spelt and Kamut®, and the rye/wheat hybrid triticale, also trigger symptoms.[17]

Barley and rye also induce symptoms of coeliac disease.[17] A small minority of coeliac patients also react to oats.[18][19] Most probably oats produce symptoms due to cross contamination with other grains in the fields or in the distribution channels.[3] There is at least one oat vendor, Gluten Free Oats®, that offers oats that can be considered SAFE for people who are gluten intolerant because they are tested to be below 10 parts per million (ppm) by the University of Nebraska FARRP Laboratory [20]. Another vendor (McCann's) which, while not claiming to be gluten-free, points out that the risk of contamination from their Oats product is low due to the processes they use.[21] Other cereals, such as maize (corn), quinoa, millet, sorghum, rice are safe for a patient to consume. Other carbohydrate-rich foods such as potatoes and bananas do not contain gluten and do not trigger symptoms.

Diagnosis

There are several tests that can be used to assist in diagnosis. The level of symptoms may determine the order of the tests, but all tests lose their usefulness if the patient is already taking a gluten-free diet. Intestinal damage begins to heal within weeks of gluten being removed from the diet, and antibody levels decline over months. For those who have already started on a gluten-free diet, it may be necessary to perform a re-challenge with 10 g of gluten (four slices of bread) per day over 2–6 weeks before repeating the investigations. Those who experience severe symptoms (e.g. diarrhoea) earlier can be regarded as sufficiently challenged and can be tested earlier.[3]

Combining findings into a prediction rule to guide use of endoscopy reported a sensitivity of 100% (it would identify all the cases) and specificity of 61% (it would be incorrectly positive in 39%). The prediction rule recommends that patients with high risk symptoms or positive serology should undergo endoscopy. The study defined high risk symptoms as weight loss, anaemia (haemoglobin less than 120 g/l in females and less than 130 g/l in males), or diarrhoea (more than three loose stools per day).[22]

Blood tests

Antibody testing

Serology by blood test is useful both in diagnosing coeliac disease (high sensitivity of about 98%, i.e. it misses 2 in 100 cases) and in excluding it (high specificity of over 95%, i.e. a positive test is most likely confirmative of coeliac disease rather than another condition). Because of the major implications of a diagnosis of coeliac disease, professional guidelines recommend that a positive blood test is still followed by an endoscopy. A negative test may still prompt a biopsy if the suspicion remains very high; this would pick up the remaining 2% undiagnosed cases, as well as offering alternative explanations for the symptoms. As such, endoscopy with biopsy is still considered the gold standard in the diagnosis of coeliac disease.[3][6]

Blood antibody tests for coeliac disease[23]
Test sensitivity specificity
AGA IgA 50% 98%
AGA IgA 25% 98%
Anti-EMA 81% 99%
ATA (Anti-TTG) 81% 99%

Four serological blood tests exist for coeliac disease. The most widely used ones detect an antibody of the IgA type against particular antigens in the small bowel. Older tests detected antibodies against reticulin (ARA) or gliadin (AGA), but recent evidence supports the use of the more modern tests, namely those detecting IgA antibodies against endomysium (EMA) or tissue transglutaminase (TTG). Generally, serology may be unreliable in young children, with anti-gliadin performing somewhat better than other tests in children under five.[24] Serology tests are based on indirect immunofluorescence (reticulin, gliadin and endomysium) or ELISA (gliadin or tissue transglutaminase).[25]

Guidelines recommend that a total serum IgA level is checked in parallel, as coeliac patients with IgA deficiency may be unable to produce the antibodies on which these tests depend ("false negative"). In those patients, IgG antibodies against transglutaminase (IgG-TTG) may be diagnostic.[26]

Blood HLA tests for coeliac disease[23]
Test sensitivity specificity
HLA-DQ2 94% 73%
HLA-DQ8 12% 81%

HLA genetic typing

Antibody testing and HLA testing have similar accuracies.[23]



Endoscopy

Endoscopic still of duodenum of patient with coeliac disease showing scalloping of folds.
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Endoscopic still of duodenum of patient with coeliac disease showing scalloping of folds.
Schematic of the Marsh classification of upper jejunal pathology in coeliac disease
Enlarge
Schematic of the Marsh classification of upper jejunal pathology in coeliac disease

An upper endoscopy with biopsy of the duodenum (beyond the duodenal bulb) or jejunum is performed. It is important for the physician to obtain multiple samples (four to eight) from the duodenum. Not all areas may be equally affected; if biopsies are taken from healthy bowel, it would result in false negative results.[6]

Most patients with coeliac disease have a small bowel that appears normal on endoscopy; however, five endoscopic findings have been associated with a high specificity for coeliac disease when all are found: scalloping of the small bowel folds (pictured), paucity in the folds, a mosaic pattern to the mucosa (described as a cracked-mud appearance), prominence of the submucosal blood vessels and a nodular pattern to the mucosa.[27]

Until the 1970s, biopsies were obtained using metal capsules attached to a suction device. The capsule was swallowed and allowed to pass into the small intestine. After X-ray verification of its position, suction was applied to collect part of the intestinal wall inside the capsule. One much utilized capsule system is the Watson capsule. This method has now been largely replaced by fiberoptic endoscopy, which carries a higher sensitivity rate and a lower error frequency.[28]

Pathology

The classic pathology changes of coeliac disease in the small bowel are categorized by the "Marsh classification":[29]

The changes classically improve or reverse after gluten is removed from the diet, so many official guidelines recommend a repeat biopsy several (4–6) months after commencement of gluten exclusion.[3]

In some cases a deliberate gluten challenge, followed by biopsy, may be conducted to confirm or refute the diagnosis. A normal biopsy and normal serology after challenge indicates the diagnosis may have been incorrect.[3] Patients are warned that one does not "outgrow" coeliac disease in the same way as childhood food intolerances.

Other diagnostic tests

Other tests that may assist in the diagnosis are blood tests for a full blood count, electrolytes, calcium, renal function, liver enzymes, vitamin B12 and folic acid levels. Coagulation testing (prothrombin time and partial thromboplastin time) may be useful to identify deficiency of vitamin K, which predisposes patients to hemorrhage. These tests should be repeated on follow-up, as well as anti-tTG titres.[3]

Some professional guidelines[3] recommend screening of all patients for osteoporosis by DXA/DEXA scanning.

Pathophysiology

Coeliac disease appears to be polyfactorial, both in that more than one abnormal factor can cause the disease and also more than one factor is necessary for the disease to manifest in a patient.

Most all coeliac patients have abnormal HLA DQ2 allele.[1] However, about 20–30% of people without coeliac disease have inherited an abnormal HLA-DQ2 allele.[23] This suggests additional factors are needed for coeliac disease to develop. Furthermore, about 5% of those people who do develop coeliac disease do not have the DQ2 gene.[1]

The HLA-DQ2 allele shows incomplete penetrance, as the gene alleles associated with the disease appear in most patients, but are neither present in all cases nor sufficient by themselves cause the disease.

Genetics

The vast majority of coeliac patients have one of two types of HLA DQ.[23] This gene is part of the MHC class II antigen-presenting receptor (also called the human leukocyte antigen) system and distinguishes cells between self and non-self for the purposes of the immune system. There are 7 HLA DQ variants (DQ2 and DQ4 through 9). Two of these variants—DQ2 and DQ8—are associated with coeliac disease. The gene is located on the short arm of the sixth chromosome, and as a result of the linkage this locus has been labeled CELIAC1.

Over 95% of coeliac patients have an isoform of DQ2 (encoded by DQA1*05 and DQB1*02 genes) and DQ8 (encoded by the haplotype DQA1*03:DQB1*0302), which is inherited in families. The reason these genes produce an increase in risk of coeliac disease is that the receptors formed by these genes bind to gliadin peptides more tightly than other forms of the antigen-presenting receptor. Therefore, these forms of the receptor are is more likely to activate T lymphocytes and initiate the autoimmune process.[1]

DQ α5-β2 -binding cleft with a deamidated gliadin peptide (yellow), modified from PDB 1S9V[30]
DQ α52 -binding cleft with a deamidated gliadin peptide (yellow), modified from PDB 1S9V[30]

Most coeliac patients bear a two-gene HLA-DQ haplotype referred to as DQ2.5 haplotype. This haplotype is composed of 2 adjacent gene alleles, DQA1*0501 and DQB1*0201, which encode the two subunits, DQ α5 and DQ β2. In most individuals, this DQ2.5 isoform is encoded by one of two chromosomes 6 inherited from parents. Most coeliacs inherit only one copy of this DQ2.5 haplotype, while some inherit it from both parents; the latter are especially at risk for coeliac disease, as well as being more susceptible to severe complications.[31] Some individuals inherit DQ2.5 from one parent and portions of the haplotype (DQB1*02 or DQA1*05) from the other parent, increasing risk. Less commonly, some individuals inherit the DQA1*05 allele from one parent and the DQB1*02 from the other parent, called a trans-haplotype association, and these individuals are at similar risk for coeliac disease as those with a single DQ2.5 bearing chromosome 6, but in this instance disease tends not to be familial. Among the 6% of European celiacs that do not have DQ2.5(cis or trans) or DQ8, 4% are DQ2 and 2% DQA1*05, 0.4% cannot be linked to DQ8, DQA1*05, or DQB1*02.[32]

The frequency of these genes varies geographically. DQ2.5 has high frequency in peoples of North and Western Europe (Basque Country, Ireland,[33] with highest frequencies), portions of Africa, and is associated disease in India,[34] but is not found along portions of the West Pacific rim. DQ8, spread more globally than DQ2.5, is more prevalent from South and Central America (up to 90% phenotype frequency).[35]

In addition to the CELIAC1 locus, CELIAC2 (5q31-q33 - IBD5 locus), CELIAC3 (2q33 -CTLA4 locus), CELIAC4 (19q13.1 - MYOIXB locus), have been linked to coeliac disease. The CTLA4 and myosin IXB and gene have been found to be linked to coeliac disease and other autoimmune diseases.[36][37] Two additional loci on chromosome 4, 4q27 (IL2 or IL21 locus) and 4q14, have been found to be linked to coeliac disease.[38][39]

Prolamins

The proteins in food responsible for the immune reaction in coeliac disease are the prolamins. These are storage proteins rich in proline (prol-) and glutamine- (-amin) that dissolve in alcohols and are resistant to pepsin and chymotrypsin, the two main digestive proteases in the gut. Gliadin in wheat is the best-understood member of this family, but other prolamins exist and hordein (from barley), and secalin (from rye) m