Diagnosing coeliac disease

Routine screening for coeliac disease is not recommended unless you have symptoms or are at an increased risk of developing them.

In 2009, the National Institute for Health and Clinical Excellence (NICE) issued guidance about when testing for coeliac disease should be carried out. The guidance recommended testing for adults or children with the following signs or symptoms:

  • long-term (chronic) diarrhoea or repeated and regular episodes of diarrhoea
  • persistent or unexplained gastrointestinal symptoms (such as feeling sick and being sick)
  • fatigue (feeling tired all the time)
  • recurring abdominal pain
  • cramping or bloating
  • sudden or unexplained weight loss
  • unexplained anaemia  
  • failure to thrive in infants/toddlers

Testing is also recommended if you have the following conditions:

In some circumstances, testing may also be recommended if you have any of the following conditions:

Screening for coeliac disease involves a two stage process:

  • blood tests – to help identify people who may have coeliac disease
  • biopsy – to confirm the diagnosis

These procedures are described in more detail below.

Blood test

Your GP will take a blood sample and test it for antibodies usually present in the bloodstream of people with coeliac disease. You should not be avoiding gluten in your diet when the blood test is done as this could lead to an inaccurate result.

If coeliac disease antibodies are found in your blood, your GP will refer you for a biopsy of your gut.

However, it is sometimes possible to have coeliac disease and not have these antibodies in your blood. So if you continue to have coeliac disease-like symptoms, despite having a negative blood test, your GP may still recommend you have a biopsy.

Biopsy

A biopsy is carried out in hospital, usually by a gastroenterologist (a specialist in treating conditions of the stomach and intestines). A biopsy can help confirm a diagnosis of coeliac disease.

If you need to have a biopsy, an endoscope (a thin, flexible tube with a light) will be inserted into your mouth and gently passed down to your small intestine.

Before the procedure, you will be given a local anaesthetic to numb your throat or a sedative to help you relax.

 

The gastroenterologist will pass a tiny biopsy tool through the endoscope to take samples of the lining of your small intestine. The sample will then be examined under a microscope for signs of coeliac disease. 

Tests after diagnosis

If you are diagnosed with coeliac disease, you may also have other tests to assess how the condition has affected you so far.

You may have further blood tests to check levels of iron and other vitamins and minerals in your blood. This will help determine whether coeliac disease has led to you developing anaemia (a lack of iron in your blood) due to poor digestion.

If you appear to have dermatitis herpetiformis (an itchy rash that is also caused by gluten intolerance), you may have a skin biopsy to confirm it. 

This is carried out under local anaesthetic where a small skin sample is taken from the area so it can be examined under a microscopic.

In some cases of coeliac disease, a DEXA scan may also be recommended. A DEXA scan is a type of X-ray that measures bone density. It may be necessary if your GP thinks that your condition may have started to thin your bones. In coeliac disease, a lack of nutrients caused by poor digestion, can make bones weak and brittle (osteoporosis). This is not a test for arthritis and only looks at bone density to see if you are at risk of bone fractures as you get older.

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