237 - Malabsorption Flashcards

1
Q

what are the gastric causes of malabsorption?

A
  • atrophic gastritis - inflammation of glandular tissue caused by chronic H.pylori infection and inflammation or autoimmune against parietal cells (intrinsic factor and acid)
  • gastrectomy - reduction in acid and intrinsic factor - leads to bacteria in SI (no acid) and reduced vit b12 absorption >macrocytic anaemia
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2
Q

what are the bile system causes of malabsorption?

A
  • obstructed bile duct (bile salts turn lipids into micelles for absorp)
  • liver failure - clotting factors (vit K for 2,7,9,10) - test prothrombin and albumin
  • defective bile salt reuptake from terminal ileum (cant be reused and liver cant replace quickly)
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3
Q

what are the pancreatic causes of malabsorption?

A
  • pancreatic failure, pancreatitis, Cystic fibrosis
  • reduced enzyme secretion so chyme cannot be broken down
  • also zollinger ellison syndrome causes excess gastrin production causing peptic ulcers, inflammation and sometimes malabsorption
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4
Q

what is absorbed in the ileum?

A
  • proximal - fat soluble vits (ADEK), water and soluble vits

* distal - bilesalts, intrinsic factor/vit B12 comlez

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5
Q

what is absorbed in the jejenum?

A

ADEK, folate, proteins, Ca

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6
Q

what does the caecum do to the SI?

A

*prevents bacterial contamination and regulates flow of chyme from it

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7
Q

what is absorbed in the colon?

A

water, electrolytes (minimal), SCFA from microbial fermentation

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8
Q

what are the two types of glucose transporters?

A
  • SGLT - Sodium coupled glucose-galactose transporter

* GLUT - Glucose transporter

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9
Q

what are starch, maltose, lactose and sucrose broken down to?

A
  • starch and maltose > glucose
  • lactose > glucose and galactose
  • sucrose > glucose and fructose
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10
Q

name a brush border enzyme deficiency?

A
  • lactose intolerance congential (rare - more common after 5yo) or arise post infection/inflammation
  • brush border lactase breaks down lactose to glucose and galactase. if defective lactose passes down bowel causing diarrhoea (osmotic), flatus and bloating (gut bacteria ferment and make acidic)
  • investigate with lactose breath test -incr H2 exhale
  • treat with low lactose diet, Ca in yogurt and lactase in milk
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11
Q

what are defective transport causes of malabsorption?

A

*abetalipoproteinaemia - deficiency of two beta-lipoproteins > inability to make chylomicrons > impaired lipd and fat soluble vit absorption > steatorrhoea, acanthocytosis (star shaped RBC)

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12
Q

what does a reduction in the absorption of fat soluble vitamins cause?

A

A - compromised mucosa and night blindness
D - rickets/osteomalacia
E - oxidant stress (CVD), haemolysis, neuropathy
K - Coagulopathy - prolonged PT

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13
Q

what is lymphangiectasia?

A

dilation of superficial lymphatic vessels due to congenital malformation or obstruction due to crohns, TB, malinancy, infection
*cause malabsorption of fat and fat soluble vitamins and protein loss

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14
Q

where does cholecystokinin act/ is produced?

A

produced - duodenum, jejenum, ileum, colon

acts on - pancreas (inc secretion) and gall bladder (contraction)

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15
Q

where does gastrin act/ is produced?

A
  • produced in G cells of gastric antrum

* acts on parietal cells in gastric body (H+ secretion)

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16
Q

where does gastrin RH act/ is produced?

A
  • produced in vagal nerves

* acts on g cells in gastric antrum (gastrin release)

17
Q

where does glucagon act/ is produced?

A
  • produced in islets of langerhan (pancreas)

* acts on liver (incr glucose production and gylcogen breakdown)

18
Q

where does guanylin act/ is produced?

A
  • produced - ileum, colon

* acts - SI and LI (fluid absorption)

19
Q

where does somatostatin act/ is produced?

A
  • produced - D cells in stomach and duodenum and delta cells in pancreatic islets
  • acts - stomach (decr gastrin), intestine (incr fluid absorb/decr secretion), pancrease (decr endo/exocrine secretion), liver (decr bile flow)
20
Q

where does vasoactive intestinal peptide act/ is produced?

A
  • produced - enteric nervous system

* acts - SI and pancreas (inc secretions) and relaxes SI smooth muscle

21
Q

what is coeliac disease?

A

autoimmune inflammatory reaction to gliadin (contained in gluten) producing vilous atrophy and malabsorption

22
Q

who is at risk of coeliacs?

A
  • genetic factors alleles DQ2 and * for human leukocyte antigen on Thcells - FHx 10% chance if 1st degree relative
  • other autoimmune diseases
23
Q

how does gliadin cause a reaction in coeliacs?

A

modified by Tissue TransGlutaminase in enterocytes breaking it down and releasing highly immunogenic antigens. Th cell response and IgA and IgG produced against TTG and gliadin. Macrophages produce IFN-gamma causing villous atrophy esp in duodenum and SI

24
Q

what are the signs of coeliacs?

A
  • diarrhoea and abdo pain and steatorrhoea
  • abdo distension and flatus
  • mouth ulcers
  • lactose intolerance with incr damage
  • failure to thrive, weight loss, fatigue/malaise
  • anaemia (Fe and folate)
  • osteopaenia/porosis due to Ca and vit D malabsorption
  • neuro symptoms
  • abnormal liver function - vit K deficiency
  • dermatitis herpetiformis
25
Q

investigations for coeliacs?

A
  • serology Ig A decr and Ig G anti TTG
  • barium swallow - dilated SI
  • endoscopy and biopsy - villous atrophy, hyperblastic crypts, hypercellular lamina propria