Coeliac disease Flashcards
Define coeliac disease
Immune Disorder, genetically susceptible people, gluten (wheat, barley, rye +oats)
Gluten - names
Prolamin -antigenic factor, gliadin, hordein, secalinin, avenin
Genetically susceptible people? Aetiology
Interaction between gluten, environment (weaning, infections) and genetics, Altered HLA genes especially HLA-DQA2/B1 ->2 (>90%) and 8 (5%)
Pathogenesis
Gluten-> goes through gut (small peptide chain, immune to protease enzymes)-> gets deanimated by tTG -> forms complexes with altered DQ -> presented to T-cell-> immune response and circle begins
Pathophysiology
Immuneresponse leads to increased inflammation -> gut permeability increases -> antibodies created against tTG -> tTGA and EmA endomysium -> mucosal distruction/ villous atrophy-> malabsoprtion
Refactory? Classic vs non-classic?
Persistent/recurrent symptoms and villous atrophy even though gluten free diet 6-12 months. Classis has intestinal symptoms
Symptoms of coeliac disease?
Intestinal symptoms: Stomach pain, cramps, bloating, distention, diarrhoea, weight loss, nausea. Non -intestinal: Skin, eye, joint reactions, chronic fatigue, depression, mouth ulcers. Lactose intolerance
Complications?
Anaemia, osteoporosis, vitamin deficiencies, some cancers, infertility other autoimmune disorders
Prevalence?
1-2% UK, increased risk with 1st degree relatives
Presentation?
Kids vs adults 1:9, peak onset 40-60 yrs
Diagnosis
Blood tests and then intestinal biopsy. Check for IgA tTGA/EmA-> test for IgA deficiency-> IgG tTGA/EmA
Intestinal biopsy?
Check for villous atrophy and increased amounts of lymphocytes
Problem with testing?
Only accurate if consuming gluten. At least for 6 weeks, on one meal
Treatment?
Completely gluten free diet: advice, counselling, follow-up. Manage symptoms/complications:deficiencies, lacto-int. Increase calcium due to increased risk of osteoporosis (20-50%)/ fracture. Assess current bone condition and vitamin D
Treatment for refactory?
Immunosuppressants, parental nutrition