Coeliac Disease

Overview

Coeliac disease is a systemic autoimmune disease triggered (T-lymphocytes) by dietary gluten peptides found in wheat, rye, barley, and related grains. Immune activation in the small intestine leads to villous atrophy, hypertrophy of the intestinal crypts, and increased numbers of lymphocytes in the epithelium and lamina propria. Locally these changes lead to gastrointestinal symptoms and malabsorption. The disease is common (1/~1000) and is more common in the Irish.

Anatomy and Physiology

The small intestine is divided into three sections: Duodenum, Jejunum and Ileum.

The three sections of the small intestine

• Duodenum is a secretory and digestive organ. Four parts (The second part is where the common bile and pancreatic ducts enters duodenum). The duodenum is where most of absorption takes place.
• Jejunum is a secretory and digestive organ.
• Ileum is predominantly an absorptive organ. Important in absorbing fats, vitamin B12 and IgA. The ileum is also where peyer’s patches are located which are immunological gastrointestinal sites for antigen sampling and immune cell activation.

Blood Supply (branches of the celiac trunk)

• Superior pacreaticoduodenal artery
• Posterior pacreaticoduodenal artery

Blood supply (3/5 branches of the superior mesenteric artery)

• Inferior pancreaticoduodenal artery –
• Intestinal artery
• Ileiocaecal artery (gives rise to appendiceal artery)

Physiology

Pathophysiology

Pathology

Macroscopic

• Atrophy and scalloping of mucosal folds
• Nodular and mosaic pattern of mucosa

Microscopic

• Villous atrophy
• Hypertrophy of the intestinal crypts
• Increased numbers of lymphocytes in the epithelium and lamina propria.

Aetiology and Risk Factors

Risk Factors

• Family history
• IgA deficiency
• Type 1 diabetes
• Autoimmune diseases – autoimmune thyroid, Sjogren’s syndrome, Addison’s disease
• Inflammatory Bowel disease
• Genetic disorder – Down’s syndrome, Turners syndrome

Clinical Manifestation

Clinical Presentation

• Asymptomatic (1/3)
• Stinking stools/steatorrhoea
• Diarrhoea
• Bloating
• Abdominal pain and discomfort
• Anemia
• Weight loss
• Failure to thrive (children)

Clinical Examination – Usually normal, signs are seen in severe cases

• Anorexia
• Delayed puberty
• Atrophic glossitis
• Dermatitis herpitaformis
• Apthanous ulcers
• Osteopenia/osteoporosis

Differential Diagnosis

Childhood other food-sensitive enteropathies (milk sensitivity)

Adults

• Lymphoma
• Whipple’s disease
• Crohn’s Disease
• Giardiasis
• Irritable Bowel Syndrome

Investigations

• Serology
  • Immunoglobin A-tissue transglutaminase (IgA-tTG)
  • Endomysial antibody
  • α-Gliadin antibody
  • FBC – Low blood count
  • Blood smear – Microcytic anemia due to folate deficiency
• Small bowel histology
• HLA testing (HLADQ2 & HLADQ8)
• Endoscopy
• Gluten Challenge – patients consume gluten diet and serological tests and small bowel histology is obtained 2-8 weeks after.

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Diagnosis Small Bowel Histological changes including:

• Villous atrophy
• Hypertrophy of the intestinal crypts
• Increased numbers of lymphocytes in the epithelium and lamina propria

Treatment

General

• Gluten free diet
• Calcium supplement
• Vitamin Supplement
• Iron supplement

Coeliac crisis management – Medical Emergency

• Rehydration
• Electrolytes
• Corticosteroids

Complications and Prognosis

Complications

• Anaemia
• 2° lactose-intolerance
• GIT-cell lymphoma
• Malignancy (gastric, oesophageal, bladder, breast, brain)
• Myopathies
• Neuropathies
• Hyposplenism
• Osteoporosis
• Dermatitis herpetiformis

Dermatitis Herpetiformis: Very itchy/“burning” blisters on elbows, scalp, shoulders, ankles

Prognosis

• Gluten-free diet can have a normal life expectancy
• Adults with coeliac disease have an increased incidence of carcinoma in a number of sites. The risk reduces after gluten withdrawal. J

References

A Colour Handbook of Gastroenterology
Oxford Clinical Handbook of Clinical Medicine
Sleisenger and Fordtran’s Gastrointestinal and Liver Disease 10th Ed.