Inflammatory Disease: Lower GI tract Paul L. Crotty Department of Pathology

1. Inflammatory Disease: Lower GI tract Paul L. Crotty Department of Pathology Trinity Medical Student Lecture October 2007

2. Outline of Lecture Mechanism of diarrhoea Chronic Inflammatory Bowel Disease Crohn’s disease Ulcerative colitis Infective enterocolitis Vascular disease

3. Fluid dynamics Food intake: ~2 litres/d Saliva: ~1 litre/d Gastric secretions: ~2 litres/d Bile: ~1 litre/d Pancreas: ~2-3 litres/d Small intestinal secretions: ~1 litre/d Total 9-10 litres/d

4. Fluid dynamics Re-absorption: Small intestine: ~6 litres/d Large intestine: normally ~2-3 litres/d but with capacity to increase up to ~6 litres/d Average stool weight 200-250g/d of which 65-85% is water

5. Mechanisms of Diarrhoea Secretory: increased secretions: persists after fasting. Examples: cholera, some viral infections Osmotic: some solute present: osmotic retention of fluid in stool, resolves on fasting. Examples: disaccharidase deficiency; some viral infections Exudative: pus present: ulceration in bowel. Examples: invasive bacterial infection: CIBD Dysmotility-associated: Examples: Irritable bowel syndrome, hyperthyroidism Malabsorption: Steatorrhoea

6. Chronic Inflammatory Bowel Disease Most (but not all) can be separated into 1 of 2 patterns: (1) Crohn’s disease (2) Ulcerative colitis based on clinical, endoscopic and pathological features important to first exclude infective and ischaemic colitis

7. Features of both Crohn’s disease and ulcerative colitis Idiopathic chronic inflammatory diseases Both have acute exacerbations and remissions Typically onset 15-40 y: (small second peak ~ 65-70y) - Active inflammation during acute exacerbation - Neutrophils in crypts (cryptitis, crypt abscesses) - Over time: destruction of mucosal architecture

8. Crohn’s disease - Granulomatous inflammation - May involve any part of bowel - Typically small intestine and/or colon (one third each) - Discontinuous: ‘skip lesions’ typically with rectal sparing - Aphthous ulcers early: linear ulcers later - Transmural inflammation - Wall thickening/strictures with luminal narrowing - Deep fissures/fistulas - Extra-intestinal disease - Probable small increased risk of colorectal carcinoma

9. Ulcerative colitis - NOT granulomatous - Colon only involved (no small bowel involvement) - Extends variable distance in continuity from rectum - Rectum always involved - Has well-defined proximal limit - No skip lesions - Broad-based ulcers with pseudo-polyps - Mucosal-based inflammation: NOT transmural - No wall thickening, no strictures, - No fissures , no fistulas - Extra-intestinal disease: also P.S.C. - Significant risk of dysplasia and carcinoma

10. Normal colonic mucosa

11. Crypt abscesses

12. Transmural inflammation, serosal granulomas Crohn’s colitis

13. Granulomas in Crohn’s disease

14. Fissure in Crohn’s disease

15. Normal

16. Crohn’s disease

17. Crohn’s disease Crohn: 1932 [Morgagni: 1761: “ileal passion”] initially termed terminal/regional ileitis - later identified could also have colonic involvement - later still recognised colonic-only pattern of disease “Idiopathic”: but what do we know about its causes? Important new information since 2001

18. Crohn’s disease Genetic predisposition: Sibling risk: 15-40x risk of general population MZ twin concordance: 40-50% DZ twin concordance: 3-7% Linkage to loci on 16 (IBD1) also chromosome 3, 12

19. Crohn’s disease linkage to locus on chromosome 16: high LOD score ~ 5.8 2001: NOD2 (nucleotide-binding oligomerisation domain) - normal function as signalling protein in macrophages - activates NFkB in response to bacterial LPS - 40% of Crohn’s disease patients: NOD2 polymorphism - but polymorphism also in ~15% of general population - heterozygous 2-4x risk/ homozygous 40x risk

20. Crohn’s disease Smoking: 2-3X increased risk of Crohn’s disease counterbalanced by decrease in risk of ulcerative colitis Urban > Rural “Good” hygiene > Poor ? Theory: Delayed exposure to antigens/bacteria

21. Crohn’s disease Is there an infectious agent? Animal models do not develop disease if kept in a strict germ-free environment Candidates ??Atypical mycobacteria ??Measles virus

22. Crohn’s disease Is there immune dys-regulation? Is there a defect in the normal mechanisms of suppression of the inflammatory response to normal gut flora? New NOD2 data supportive of this theory

23. Crohn’s disease Present with pain, variable diarrhoea, fever Diagnosis: Clinical, endoscopy, mucosal biopsies, barium Complications: Strictures: obstruction Fissures: abscesses Fistulas: bladder, vagina, skin, entero-enteric Peri-anal disease Malabsorption (terminal ileal disease, blind loops) Slight increased risk of cancer

24. Ulcerative colitis

26. Pseudopolyps in ulcerative colitis

27. Mucosal-based inflammation and ulceration Ulcerative colitis

28. Dysplasia in ulcerative colitis

29. Ulcerative colitis

30. Ulcerative colitis Wilks: 1859 claim on first distinction from dysentery 1888: RSM in London debate on aetiology of the disease ? Diet ? Infection ? Psychosocial Genetic: MZ concordance HLA association ? Infection ? Allergy ? Immune dys-regulation

31. Ulcerative colitis Mucosal inflammation leading to ulceration Chronicity leads to mucosal destruction, regeneration 40% rectum/ recto-sigmoid only 40% extends from rectum to point x 20% pan-colonic Presents with diarrhoea, pain, weight loss Diagnosis: Clinical, endoscopy, biopsy

32. Ulcerative colitis Complications: Fulminant colitis: Toxic megacolon Extra-intestinal manifestations Including primary sclerosing cholangitis Significant risk of dysplasia and malignancy especially with pan-colitis, long duration

34. Infective organisms causing diarrhoea World-wide: mortality 5 million /year, most children Mechanisms by which infectious agents cause diarrhoea: (1) Pre-formed toxin in food no live organisms ingested e.g. C botulinum, some S. aureus (2) Live organisms: Non-invasive: (a) organisms colonise gut and produces toxin e.g. V. cholerae, C. difficile, some E. coli (b) organisms bind to brush border e.g. Cryptosporidium Invasive: (a) mucosal e.g. Shigella, most Salmonella, some E. coli (b) deeper layers e.g. S. typhi, Yersinia

35. Viral enterocolitis Rotavirus infects enterocytes lining villi in small intestine near-normal/minimal shortening of villi main effect is absence of lactase => osmotic diarrhoea Norwalk virus Adenovirus Astrovirus

36. Winter vomiting bug SRSVs (small round structured viruses) Non-cultivatable gastro-enteritis viruses related to Norwalk virus 1968: Norwalk, Ohio nausea, vomiting, diarrhoea x 24h volunteers: stool filtrates ‘Norwalk agent’ <36nm, ether-resistant, heat stable 1972: 27nm virus on EM: specific antibody present

37. Winter vomiting bug ssRNA: classified as calicivirus (HuCV) first member of calicivirus group was Norwalk virus Error-prone replication: 1 mutation per replication Consensus PCR identifies >90% of strains (in UK) Different epidemics are slightly different in sequence Infects enterocytes (short incubation) In animal models: causes enterocyte apoptosis

39. Vibrio cholerae Toxin production includes binding units, catalytic unit => binds to glycolipid on surface of enterocyte => catalytic unit taken up into enterocyte => activated intracellularly => stimulates G-protein => increases intracellular cAMP => actively stimulates secretion of Na, Cl, water

40. Shigella => stimulates its own endocytosis => proliferates within cell => rapid cell death, lysis => infects adjacent cells

41. Pseudo-membranous colitis Broad spectrum antibiotic => normal gut flora includes Clostridium difficile => other bacteria eradicated by antibiotics => Clostridium difficile proliferates => selection of toxin producing forms enterotoxin (A) and cytotoxin (B) => disrupt cytoskeleton, toxin A also pro-inflammatory

42. Vascular disease of the intestines • SMA, IMA -> mesenteric arcades • collateral supply • watershed areas: splenic flexure • venous drainage • acute, subacute, chronic

43. Vascular disease of the intestines • arterial thrombosis • atherosclerosis, dissection, hypercoagulation • arterial embolism • atherosclerosis, arrhythmias, SBE • venous thrombosis • hypercoagulation • generalised hypoperfusion • hypotensive shock, CCF

44. Vascular disease of the intestines • Transmural infarction • acute occlusion (arterial or venous, thrombotic or embolic) -> acute abdomen • perforation/gangrene if untreated • Mucosal/submucosal infarction • acute/subacute hypoperfusion • can mimic acute colitis • Fibrosis and mucosal atrophy • chronic, strictures: can mimic Crohn’s

48. Crohn’s disease - Granulomatous inflammation - May involve any part of bowel - Typically small intestine and/or colon (one third each) - Discontinuous: ‘skip lesions’ typically with rectal sparing - Aphthous ulcers early: linear ulcers later - Transmural inflammation - Wall thickening/strictures with luminal narrowing - Deep fissures/fistulas - Extra-intestinal disease - Probable small increased risk of colorectal carcinoma

49. Ulcerative colitis - Not granulomatous - Colon only involved (no small bowel except backwash) - Extends variable distance in continuity from rectum - Rectum always involved - Has well-defined proximal limit - No skip lesions - Broad-based ulcers with pseudo-polyps - Mucosal-based inflammation: not transmural - No wall thickening, no strictures, - No fissures , no fistulas - Extra-intestinal disease: also P.S.C. - Significant risk of dysplasia and carcinoma

50. Summary Mechanism of diarrhoea Chronic Inflammatory Bowel Disease Crohn’s disease Ulcerative colitis Infective enterocolitis Vascular disease