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Coeliac Disease Diagnosis & Management in Christchurch

Coeliac disease is a common immune-mediated condition affecting approximately 1 in 100 New Zealanders. In people with coeliac disease, the immune system reacts abnormally to gluten (a protein found in wheat, barley, and rye), causing damage to the lining of the small bowel.

If left undiagnosed, it can lead to long-term health issues, including nutritional deficiencies, osteoporosis, and chronic fatigue. At Canterbury Endoscopy, we provide expert diagnostic pathways for patients in Christchurch and the wider Canterbury region.

The Important "Golden Rule" for Diagnosis

Important: If you suspect you have coeliac disease, it is vital that you do not start a gluten-free diet before your diagnostic tests are complete.

To accurately diagnose the condition, gluten must be present in your system so that any related intestinal damage can be identified.

What are the common symptoms of Coeliac Disease?

The common symptoms of Coeliac Disease are:

  • Persistent bloating and abdominal pain.

  • Unexplained iron-deficiency anaemia or B12 deficiency.

  • Chronic fatigue or "brain fog."

  • Unintended weight loss.

  • Changes in bowel habits, such as chronic diarrhoea or constipation.

How is Coeliac Disease diagnosed?

While blood tests (serology) are an important first step, in adults, Gastroscopy is generally required to confirm the diagnosis.

1. Gastroscopy and Biopsy

During a gastroscopy performed at our Christchurch facility, Dr Mehul Lamba will take small tissue samples (biopsies) from the lining of the small bowel (duodenum). This is a quick, routine procedure typically performed under sedation for your comfort.

2. Pathological Review

The biopsy samples are examined under a microscope by a specialist pathologist. They look for two hallmark features of coeliac disease: villous atrophy (flattening of the tiny finger-like projections that line the small bowel and absorb nutrients) and lymphocytic infiltration (an increase in inflammatory cells within the gut lining). Together, these microscopic changes confirm the diagnosis. 

My blood test was negative, but I still have symptoms. Could I still have coeliac disease?

The blood tests are generally very reliable, and with negative serology, the likelihood of Coeliac disease is very low. However, if symptoms persist, Gastroscopy may still be indicated to assess for coeliac disease, but more importantly, exclude other conditions mimicking coeliac disease.

How long do I need to eat gluten before my gastroscopy?

To ensure the biopsy results are accurate, you must be consuming 10 grams of gluten daily (equivalent to 2 to 4 slices of bread) for at least 4-6  weeks leading up to your procedure. If you have already started a gluten-free diet, please contact our Christchurch clinic for specific advice on a "gluten challenge."

What happens after I am diagnosed?

A diagnosis is the first step toward recovery. Once coeliac disease is confirmed, we will provide you with a detailed report for your GP and can refer you to a specialist registered dietitian in Christchurch who specializes in gluten-free transitions. We also recommend baseline blood tests to check for nutritional deficiencies (like Iron, Vitamin D, and B12) and, in some cases, a bone density (DEXA) scan.

What if my tests are negative, but I still feel better on a gluten-free diet?

It is possible to have Non-Coeliac Gluten Sensitivity (NCGS). This is a condition where individuals experience symptoms similar to coeliac disease—such as bloating, abdominal pain, and fatigue—that improve when gluten is removed, even though their blood tests and bowel biopsies are normal.

Because there is currently no specific "test" for NCGS, the diagnosis is made by first definitively ruling out coeliac disease and wheat allergies. At our Christchurch clinic, we focus on ensuring you have a clear diagnostic answer before you commit to long-term dietary restrictions, as the management for sensitivity differs from the strict medical requirements of coeliac disease.

Should my family members be tested for Coeliac Disease?

Coeliac disease has a strong genetic component. First-degree relatives (parents, siblings, and children) have approximately a 1-in-10 lifetime risk of developing the condition. We recommend that if family members develop any suggestive symptoms, they are encouraged undergo a specific blood test to assess for coeliac disease. It is important they remain on a gluten-containing diet until the testing is complete.

Disclaimer: The information provided on this website is for educational purposes only and is intended to support, not replace, the relationship between a patient and their healthcare professional.

This information should not be used to diagnose or treat a health problem or disease. Always seek the advice of a healthcare professional regarding any medical condition or symptoms.