Download Free Medical Pathogenesis of IBS PowerPoint Presentation

Pathogenesis of IBS PowerPoint Presentation

DOWNLOAD MEDICAL POWERPOINT PRESENTATION

About This Presentation

Description : Check out this medical presentation on Irritable Bowel Syndrome, which is titled "Pathogenesis of IBS", to know about functional bowel disorders.

Tags : Irritable Bowel Syndrome, functional bowel disorders, digestive system

Published on : Jul 10, 2021 | Views : 1912 | Downloads : 4

Shareable Url :

Embed Code :

Comment

Transcript

Slide 1-

Elizabeth Mentzer, PA-S Robert D. Hadley, Advisor
Slide 2-

IBS is a diagnosis of exclusion with a female predominance Affects at least 20% of the American population Classic Symptoms: Chronic abdominal pain or discomfort associated with chaotic bowel motility Heightened visceral sensitivity Constipation dominant IBS, diarrhea dominant IBS or mixed
Slide 3-

At least 12 weeks or more, with onset of at least 6 months previously of recurrent abdominal pain or discomfort associated with two or more of the following: Improvement with defecation; and/or Onset associated with a change in frequency of stool; and/or Onset associated with a change in form (appearance) of stool
Slide 4-

Common Treatments Fiber Supplements Antispasmodics Ex. dicyclomine, hyoscyamine Anti-diarrheals Tricyclic Antidepressants Amitryptaline for d-IBS Probiotics Lactobacillus plantarum or the combo. L. plantarum + L. acidophilus or Bifidobacterium Antibiotics New Possibilities Mesalamine derivative (ATB-429) Budesonide
Slide 5-

Post - Infectious IBS Interstitial Cells of Cajal Serotonin Pathway
Slide 6-

How do GI –Infections Lead to IBS? Genetics Polymorphisms of gene coding for cytokine production of Interleukin 10 (IL-10) Increased Production of Tumor Necrosis Factor –α (TNF-α) Mast Cell Activation Mast cell release of inflammatory mediators could alter gastrointestinal motility Relationship to IBS and Pain Spacial relationships between mast cells and gastrointestinal nerves
Slide 7-

Pacemakers of the Gastrointestinal System Play roles in intestinal motor activity, balanced control of gut motility and a functional role in neuronal motor activity Located within close proximity to enteric nerve endings Damaged ICCs (ex., immune reactions or endometriosis) could lead to disruption of musculature electrical activity leading to IBS symptoms
Slide 8-

Defects in 5-HT signaling could lead to colonic aberrations and sensations typical of IBS and Ulcerative Colitis (UC). A 2004 study by Coates et al., found that: IBS and UC patients all had significant reductions in expression of the SERT transcript when compared to control subjects as well as a reduction in the rate limiting enzyme TpH, which is essential for the biosynthesis of 5-HT Is there a connection between IBS and UC?
Slide 9-

5-HT and the relationship to ICCs 5-HT may indirectly regulate proliferation of ICCs Impaired and/or decreased numbers of ICCs have been associated with bowel dysfunction A study by Gershon (2005), showed that decreased expression of SERT (required for the termination of 5-HT) could have negative downstream effects on 5-HT As a result, constipation and diarrhea type symptoms were seen due to 5-HT desensitization or 5-HT amplification Decreased SERT expression was also found in biopsies of UC patients -> Possible connection?
Slide 10-

ppt slide no 10 content not found
Slide 11-

It may even be a mild form of UC So far there have been strong arguments for IBS being an inflammatory response There is no single definitive answer for the pathogenesis of IBS yet.
Slide 12-

IBS is real It is not a psychological problem Stay up-to-date on drug therapies Realize that patients with IBS need a tailored treatment plan. Exclude other possibilities like celiac disease and endometriosis. Treat based on a patient’s history For example: presence or history of enteric infection, do other family members have it etc. Be sympathetic and understanding as IBS can be life-altering
Slide 13-

Andresen V, Camilleri M. Irritable Bowel Syndrome: Recent and Novel Therapeutic Approaches. Drugs 2006; 66(8): 1073-1088. Bercik P, Verdu EF, Collins SM. Is Irritable Bowel Syndrome a Low-Grade Inflammatory Bowel Disease? Gastroenterol Clin N Am 2005; 34: 235-245. Bijkerk CJ, de Wit NJ, Stalman WA, Knottnerus JA, Hoes AW, Muris JW. Irritable Bowel Syndrome in Primary Care: The Patients’ and Doctors’ Views On Symptoms, Etiology and Management. Can J Gastroenterol 2003: 17(6): 363-368. Coates MD, Mahoney CR, Linden DR, Sampson JE, Chen J, Blaszyk H, et.al. Molecular Defects in Mucosal Serotonin Content and Decreased Serotonin Reuptake Transporter in Ulcerative Colitis and Irritable Bowel Syndrome. Gastroenterol 2004; 126(7): 1657-1664. Crentsil V. Will corticosteroids and Other Anti-inflammatory Agents Be Effective For Diarrhea Predominant Irritable Bowel Syndrome? Medical Hypotheses 2005; 65: 97-102. Der T, Bercik P, Donnelly G, Jackson T, Berezin I, Collins SM, Huizinga JD. Interstitial Cells of Cajal and Inflammation-Induced Motor Dysfunction in the Mouse Small Intestine. Gastroenterol 2000; 119: 1590-1599. Dhaliwal SK, Hunt RH. Doctor-Patient Interaction for Irritable Bwoel Syndrome in Primary Care: A Systematic Perspective. European Journal of Gastroenterol and Hepatology 2004; 16: 1161-1166. Distrutti E, Sediari L, Mencarelli A, Renga B, Orlandi S, Russo G, et.al. 5-Amino-2-hydroxybenzoic Acid 4-(5-Thioxo-5H-{1,2}dithiol-3yl)-phenyl Ester (ATB-429), a Hydrogen Sulfide-Releasing Derivative of Mesalamine, Exerts Antinociceptive Effects in a Model of Postinflammatory Hypersensitivity. JPET 2006; 319:447-458.
Slide 14-

Gershon, MD. Nerves, Reflexes, and the Enteric Nervous System; Pathogenesis of the Irritable Bowel Syndrome. J Clin Gastroenterol 2005; 39: S184-S193. Giovania B, Vincenzo S, Roberto G, Cesare C, Graeme SC, Donatella S, et.al. Activated MastCells in Proximity to Colonic Nerves Correlate With Abdominal Pain in Irritable Bowel Syndrome. Gastroenterology 2004; 126: 693-702. Gonsalkorale WM, Perrey C, Pravica V, Whorwell PJ, Hutchinson IV. Interleukin 10 Genotypes in Irritable Bowel Syndrome: Evidence for an inflammatorycomponent? Gut 2003; 52: 91-93. Komuro T. Comparative Morphology of Interstitial Cells of Cajal: Ultrastructural Characterization. Microscopy Research and Technique 1999; 47: 267-285. Longstreth GF. Definition and Classification of Irritable Bowel Syndrome: Current Consensus and Controversies. Gastroenterol Clin N Am 2005: 34: 173-187. Marshall JK, Thabane M, Garg AX, Clark WF, Salvadori M, Collins SM. Incidence and Epidemiology of Irritable Bowel Syndrome After a Large Waterborne Outbreak of Bacterial Dysentery. Gastroenterology 2006; 131: 445-450. McKay M, Bienenstock J. The Interaction Between Mast Cells and Nerves in the Gastrointestinal Tract. Immunology Today 1994; 15(11): 533-538. O’Sullivan M. Inflammatory Mediators in Irritable Bowel Syndrome. Adelaide & Meath Hospital, Trinity College, Dublin Ireland. [cited 2007 Dec 10] Available From: www.med.unc.edu/ibs. Remorgida V, Ragni N, Ferrero S, Anserini P, Torelli P, Fulcheri E. The Involvement of The Interstitial Cajal Cells and the Enteric Nervous system in Bowel Endometriosis. Hum Reprod 2005; 20(1): 264-271.
Slide 15-

Simonetta M, Pellegrini F. Relationships Between Neurokinin Receptor-Expressing Interstitial Cells of Cajal and Tachykininergic Nerves in the Gut. J Cell Mol Med 2006; 1: 20-32. Spiller RC. Irritable Bowel Syndrome. British Medical Bulletin 2005; 72(1): 15-29. Thaben M, Kottachchi DT, Marshall JK. Systematic Review and Meta-Analysis: The Incidence and Prognosis of Post-Infectious Irritable Bowel Syndrome. Aliment Pharmacol Ther 2007; 26: 535-544. Tornblom H, Bethan L, Clover L, Knowles C, Vincent A, Lindberg G. Autoantibodies in Patients With Gut Motility Disorders and Enteric Neuropathy. Scand J Gastroenterol 2007; 42: 1289-1293. Van der Veck Patrick PJ, Van den Berg M, de Kroon YE, Verspaget HW, Masclee AM. Role of Tumor Necrosis Factor-α and Interleukin-10 Gene Polymorphisms in Irritable Bowel Syndrome. Am J Gastroenterol 2005; 100: 2510-2516. Wald A. Overview of Irritable Bowel Syndrome. Up To Date 2007. Gut 1999 [cited 2007 Nov 11] Available From: www.fda.gov/ohrms/dockets/ac/00/slides/3627s1_2_wald/tsl Wouters MM, Gibbons SJ, Roeder JL, Distad M, Ou Y, Strege PR, et.al. Exogenous Serotonin Regulates Proliferation of Interstitial Cells of Cajal in Mouse Jejunum Through 5-HT2B Receptors. Gastroenterology 2007; 133: 897-906.