The only accepted treatment of coeliac disease is a strict lifelong gluten-free diet.
The diet should not be started until definitive diagnosis has been made by small intestinal histology. After diagnosis the patient should be referred to a dietician with specific training in coeliac disease and the gluten-free diet. Dietary counselling is important because the gluten-free diet has been associated with lower intake of fibre, as well as vitamin and micronutrient deficiencies, and a higher intake of calories, simple carbohydrates, and saturated fats. Coeliac disease patients are at risk of becoming overweight/obese.
Quality of life for coeliac patients has been shown to improve with adherence to a gluten-free diet. However, gluten-free diet adherence is difficult, with dietary lapses in the majority of patients. The importance of the diet should be stressed, and social support evaluated and encouraged within the family and by membership in coeliac disease advocacy groups.
After diagnosis patients should be checked for common deficiencies including iron and vitamin D. All patients with coeliac disease should be recommended to take calcium and vitamin D supplements. Iron should only be given to individuals with iron deficiency. Bone mineral density should be evaluated after approximately 1 year on a gluten-free diet to assess for osteopenia or osteoporosis.
For individuals who do not respond to a gluten-free diet, the most common problem is continued gluten exposure. The initial step in the evaluation should be repeating immunoglobulin A-tissue transglutaminase titre and referral to a dietician with expertise in coeliac disease. If there is no evidence of continuing gluten intake, referral to a gastroenterologist with experience in the evaluation of non-responsive coeliac disease is recommended. Although gluten exposure is the most common cause of non-responsive coeliac disease, many other conditions could explain the symptoms, such as irritable bowel syndrome, other food intolerances, microscopic colitis, or small intestinal bacterial overgrowth.
Refractory coeliac disease is defined as the persistence of villous atrophy despite strict gluten withdrawal and no evidence of another abnormality including overt lymphoma. It is present in <1% of patients with coeliac disease and is felt to be a spectrum determined by T-cell clonality and loss of normal intra-epithelial cell markers. Common associations with refractory coeliac disease include ulcerative jejunitis and enteropathy-associated T-cell lymphoma. The outlook for patients is generally poor. They should be cared for at a centre experienced in coeliac disease.
Coeliac crisis is rare and presents with hypovolaemia, severe watery diarrhoea, acidosis, hypocalcaemia, and hypoalbuminaemia. Patients are often emaciated and have nutritional deficiencies caused by long-standing, untreated coeliac disease. In addition to rehydration and correction of electrolyte abnormalities, these few patients may benefit from a short course of systemic glucocorticoid therapy until the gluten-free diet takes effect.
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