Coeliac disease: Difference between revisions

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Coeliac disease, also called coeliac sprue or gluten-sensitive enteropathy, is a chronic immune-mediated systemic disorder triggered by consumption of gluten.
'''Coeliac disease''', also called '''coeliac sprue''' or '''gluten-sensitive enteropathy''', is a chronic immune-mediated systemic disorder triggered by consumption of gluten.


It’s a relatively common condition, affecting 1 per 100 in Western Europe, but it’s also common in the Middle East. The prevalence has increased significantly in the recent 50 years. It’s likely underdiagnosed due to its heterogenous clinical presentation.
It’s a relatively common condition, affecting 1 per 100 in Western Europe, but it’s also common in the Middle East. The prevalence has increased significantly in the recent 50 years. It’s likely underdiagnosed due to its heterogenous clinical presentation.
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== Diagnosis and evaluation ==
== Diagnosis and evaluation ==
For diagnosis of coeliac disease, the patient must be on a gluten-containing diet for some time, to allow the pathological signs to appear. Presence of anti-tTG, anti-EMA, and anti-DGP antibodies is characteristic but unfortunately not diagnostic alone for coeliac disease, except in children. In adults, upper endoscopy with biopsy is required for the diagnosis.
For diagnosis of coeliac disease, the patient must be on a gluten-containing diet for some time, to allow the pathological signs to appear. Presence of anti-tTG, anti-EMA, and anti-DGP antibodies is characteristic but unfortunately not diagnostic alone for coeliac disease, except in children. In adults, [[upper endoscopy]] with biopsy is required for the diagnosis.


Histological severity is classified according to the Marsh classification from Marsh 1 to 3c.
Histological severity is classified according to the Marsh classification from Marsh 1 to 3c.

Revision as of 12:31, 27 October 2023

Coeliac disease, also called coeliac sprue or gluten-sensitive enteropathy, is a chronic immune-mediated systemic disorder triggered by consumption of gluten.

It’s a relatively common condition, affecting 1 per 100 in Western Europe, but it’s also common in the Middle East. The prevalence has increased significantly in the recent 50 years. It’s likely underdiagnosed due to its heterogenous clinical presentation.

Etiology

Coeliac disease is highly related to genetic susceptibility, namely the HLA DQ2 (95%) and DQ8 (5%) variants. The disease can develop in the absence of these factors, but it’s extremely rare. Presence of other autoimmune disorders is also a risk factor.

Pathomechanism

When gluten is digested, it will be degraded in the intestines. The gliadin molecule is unable to be digested by our bodies and will only become deaminated. The deaminated gliadin then interacts with the HLA-molecules on antigen-presenting cells. In individuals with the HLA-DQ2/HLA-DQ8 allele, gliadin will be recognized as a pathogen by the CD4+ and initiate an immune response. Cytokines by CD4+ cells will cause damage of the mucosa, and CD8+ cells not specific for gliadin accumulate as well and cause damage. B-cells response follows and results in formation of anti-deaminated gliadin antibodies.

Clinical features

Typical symptoms include diarrhoea, abdominal pain, bloating, and weight loss. In severe cases, nutrient deficiencies and extraintestinal manifestations (dermatitis herpetiformis, arthritis, +++) may develop. However, many have different presentations.

Diagnosis and evaluation

For diagnosis of coeliac disease, the patient must be on a gluten-containing diet for some time, to allow the pathological signs to appear. Presence of anti-tTG, anti-EMA, and anti-DGP antibodies is characteristic but unfortunately not diagnostic alone for coeliac disease, except in children. In adults, upper endoscopy with biopsy is required for the diagnosis.

Histological severity is classified according to the Marsh classification from Marsh 1 to 3c.

Treatment

The treatment is a strict gluten-free diet for life.