coeliac disease Flashcards

1
Q

what is it

A

condition in which there is inflammation of the mucosa of the upper small bowel

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2
Q

when does mucosa improve

A

when gluten is withdrawn

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3
Q

what is gluten present in

A
  • cereals
  • wheats
  • barley
  • rye
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4
Q

what is the damaging factor of gluten

A

prolamins

  • gliadin from gluten
  • hordeins from barley
  • secalins from rye
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5
Q

what are prolamins resistant to

A

digestion by pepsin and chymotrypsin because of their high glutamate and proline content

so they remain in intestinal lumen triggering immune response

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6
Q

what is gliadin demented by

A

tissue transglutaminase

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7
Q

what does gliagin peptide bind to

A

antigen-presenting cells which interact with CD4 in the lamina propria

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8
Q

how does gliadin interact with CD4

A

via HLA class II

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9
Q

what else does CD4 interact with

A

B cells to produce endomysial and tissue transglutaminase

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10
Q

what else can gliadin cause release of

A

IL-5

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11
Q

what does the inflammatory cascade release

A

metalloproteins

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12
Q

what does metalloproteinases contribute to

A

villous atrophy and crypt hyperplasia

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13
Q

is it genetic inherited

A

unsure

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14
Q

what virus in infancy increases risk

A

rotavirus

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15
Q

what can be seen in blood test to diagnose

A
  • raised MCV

- iron deficiency in pregnancy

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16
Q

symptoms

A
  • tiredness
  • malaise
  • anaemia
  • IBS
  • diarrhoea
  • steatorrhoea
  • abdominal pain
  • weight loss
  • mouth ulcers
  • infertility
  • anxiety
  • depression
17
Q

complications

A
  • tetany
  • osteomalacia
  • gross malnutrition
  • peripheral oedema
  • parasthesia
  • ataxia
  • muscle weakness
  • polyneuropathy
18
Q

gold standard for diagnosis

A

small bowel biopsy

19
Q

what are the endoscopic signs

A
  • absence of mucosal folds
  • mosaic pattern of surface
  • scalloping of mucosal folds
20
Q

what is most common cause of villous atrophy

A

coeliac disease

21
Q

what does histological examination show

A
  • crypt hyperplasia
  • chronic inflammatory cells in lamina propria
  • villous atrophy
22
Q

what happens to the enterocytes

A

they become cuboidal with an increase in number of intraepithelial lymphocytes

23
Q

when would you test someone

A
  • persistent diarrhoea
  • folate or iron deficiency
  • unexplained abnormal liver biochemistry
  • family history of coeliac disease
24
Q

what is useful for risk assessment

A

HLA typing

25
Q

treatment

A
  • replace minerals and vitamins e.g. iron, folic acid, calcium, vitamin D
  • gluten free diet
26
Q

what should patients have every 5 years

A

pneumococcal vaccinations

27
Q

complications

A
  • IBD
  • small bacterial overgrowth
  • lactase deficiency
  • T cell lymphoma
  • small bowel adenocarcinoma
  • ulcerative jejunitis
28
Q

what does ulcerative jejunitis present with

A
  • fever
  • abdominal pain
  • perforation
  • bleeding
29
Q

what is diagnosis of the complications done

A

MRI or barium studies

30
Q

what is treatment of ulcerative jejunitis

A
  • steroids

- immunosuppressive agents such as azathioprine

31
Q

what is dermatitis herpetiforms

A

blistering, subepidermal eruption of the skin

32
Q

what is dermatitis herpetiformis associated with

A

gluten-sensitive enteropathy