Coeliac disease Flashcards

1
Q

Define coeliac disease

A

Immune Disorder, genetically susceptible people, gluten (wheat, barley, rye +oats)

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2
Q

Gluten - names

A

Prolamin -antigenic factor, gliadin, hordein, secalinin, avenin

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3
Q

Genetically susceptible people? Aetiology

A

Interaction between gluten, environment (weaning, infections) and genetics, Altered HLA genes especially HLA-DQA2/B1 ->2 (>90%) and 8 (5%)

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4
Q

Pathogenesis

A

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

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5
Q

Pathophysiology

A

Immuneresponse leads to increased inflammation -> gut permeability increases -> antibodies created against tTG -> tTGA and EmA endomysium -> mucosal distruction/ villous atrophy-> malabsoprtion

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6
Q

Refactory? Classic vs non-classic?

A

Persistent/recurrent symptoms and villous atrophy even though gluten free diet 6-12 months. Classis has intestinal symptoms

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7
Q

Symptoms of coeliac disease?

A

Intestinal symptoms: Stomach pain, cramps, bloating, distention, diarrhoea, weight loss, nausea. Non -intestinal: Skin, eye, joint reactions, chronic fatigue, depression, mouth ulcers. Lactose intolerance

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8
Q

Complications?

A

Anaemia, osteoporosis, vitamin deficiencies, some cancers, infertility other autoimmune disorders

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9
Q

Prevalence?

A

1-2% UK, increased risk with 1st degree relatives

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10
Q

Presentation?

A

Kids vs adults 1:9, peak onset 40-60 yrs

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11
Q

Diagnosis

A

Blood tests and then intestinal biopsy. Check for IgA tTGA/EmA-> test for IgA deficiency-> IgG tTGA/EmA

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12
Q

Intestinal biopsy?

A

Check for villous atrophy and increased amounts of lymphocytes

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13
Q

Problem with testing?

A

Only accurate if consuming gluten. At least for 6 weeks, on one meal

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14
Q

Treatment?

A

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

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15
Q

Treatment for refactory?

A

Immunosuppressants, parental nutrition

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16
Q

Dermatitis hepetiformis? Other immune disorders?

A
Type 1 (1%), Sjogren’s Syndrome (secretary glands)   (4.5-15%)               	
Addison’s disease