Learn more about symptoms and testing for celiac disease.
Understanding Coeliac Disease >
Learn more about symptoms and testing for celiac disease.
Understanding Coeliac Disease >
Coeliac disease is a prevalent, under-recognised autoimmune disease caused by the ingestion of gluten, and can develop at any age.1,2
Its prevalence has historically been underestimated, but it is now recognised as one of the most common genetic disorders in the Western world, with a prevalence of 1 percent in the general population.1 However, about 75 percent of patients with coeliac disease remain undiagnosed.1,2
A patient who presents with any symptoms of coeliac disease is more likely to have the condition than someone who is asymptomatic.3 However, coeliac disease can be clinically 'silent', with no obvious symptomology. Silent disease often results in severe intestinal villous atrophy and detrimental health-effects in the long-term, which makes the identification and treatment of asymptomatic patients important.1,4
Coeliac disease arises in people with predisposing genetic factors, involving both HLA and non-HLA genetic variants. This has been indicated by several genetic studies, and the presence of high disease concordance in monozygotic twins.1
There are a number of medical conditions that may predispose to, or be a sign of, coeliac disease.1
Other autoimmune conditions are more common in patients with coeliac disease than in the general population.1 The prevalence of coeliac disease is:
Certain genetic syndromes are associated with a higher prevalence of coeliac disease than that of the general population, including:8-10
Unexplained iron, vitamin B12, or folate deficiency can be a sign of coeliac disease.11
Elevated serum aminotransferase levels can be a sign of coeliac disease.4
People with a diagnosis of irritable bowel syndrome (IBS) are more likely to have coeliac disease than the general population.13
Subfertility or recurrent miscarriages can be a sign of coeliac disease.15
Screening for coeliac disease is recommended in these patient populations and may help identify the large proportion of undiagnosed cases, facilitating the implementation of the appropriate management.4
Tissue transglutaminase (tTG) IgA is the recommended first-line test for coeliac disease, together with total IgA to check for IgA deficiency.4
HLA: human leukocyte antigen; IgA: immunoglobulin A
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2. West J, Fleming K M et al. Incidence and prevalence of celiac disease and dermatitis herpetiformis in the UK over two decades: population-based study. Am J Gastroenterol 2014;109(5):757-768
3. Fasano A, Berti I et al. Prevalence of celiac disease in at-risk and not-at-risk groups in the United States: a large multicenter study. Arch Intern Med 2003;163(3):286-292
4. Al-Toma A, Volta U et al. European Society for the Study of Coeliac Disease (ESsCD) guideline for coeliac disease and other gluten-related disorders. United European Gastroenterol J 2019;7(5):583-613
5. Singh P, Arora S et al. Risk of celiac disease in the first- and second-degree relatives of patients with celiac disease: a systematic review and meta-analysis. Am J Gastroenterol 2015;110(11):1539-1548
6. Ch'ng C L, Jones M K, Kingham J G. Celiac disease and autoimmune thyroid disease. Clin Med Res 2007;5(3):184-192
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10. Giannotti A, Tiberio G et al. Coeliac disease in Williams syndrome. J Med Genet 2001;38(11):767-768
11. Halfdanarson T R, Litzow M R, Murray J A. Hematologic manifestations of celiac disease. Blood 2007;109(2):412-421
12. Sainsbury A, Sanders D S, Ford A C. Meta-analysis: coeliac disease and hypertransaminasaemia. Aliment Pharmacol Ther 2011;34(1):33-40
13. El-Salhy M, Hatlebakk J G et al. The relation between celiac disease, nonceliac gluten sensitivity and irritable bowel syndrome. Nutr J 2015;14:92
14. Card T R, Siffledeen J et al. An excess of prior irritable bowel syndrome diagnoses or treatments in celiac disease: evidence of diagnostic delay. Scand J Gastroenterol 2013;48(7):801-807
15. Shah S, Leffler D. Celiac disease: an underappreciated issue in women's health. Womens Health (Lond) 2010;6(5):753-766