Irritable bowel syndrome pathophysiology: Difference between revisions
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{{ | {{familytree |boxstyle=text-align: left; | | | | | | B01 | | | |B01= '''Environmental factors''': <br>•Diet <br>•[[Infections]]}} | ||
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*[[Diet (nutrition)|Diet]] | *[[Diet (nutrition)|Diet]] | ||
**Fermentable [[Oligosaccharide|oligosaccharides]], [[Monosaccharide|monosaccharides]], [[Disaccharide|disaccharides]], and [[Polyol|polyols]] (FODMAPs) are present in stone fruits, artificial sweeteners, lactose-containing foods, and [[Legume|legumes]]. Changes in diet such as increased amounts (FODMAPs) can alter [[Gut flora|gut microflora]].<ref name="pmid23935555">{{cite journal |vauthors=Muir JG, Gibson PR |title=The Low FODMAP Diet for Treatment of Irritable Bowel Syndrome and Other Gastrointestinal Disorders |journal=Gastroenterol Hepatol (N Y) |volume=9 |issue=7 |pages=450–2 |year=2013 |pmid=23935555 |pmc=3736783 |doi= |url=}}</ref> | **Fermentable [[Oligosaccharide|oligosaccharides]], [[Monosaccharide|monosaccharides]], [[Disaccharide|disaccharides]], and [[Polyol|polyols]] (FODMAPs) are present in stone fruits, artificial sweeteners, lactose-containing foods, and [[Legume|legumes]]. Changes in diet such as increased amounts (FODMAPs) can alter [[Gut flora|gut microflora]].<ref name="pmid23935555">{{cite journal |vauthors=Muir JG, Gibson PR |title=The Low FODMAP Diet for Treatment of Irritable Bowel Syndrome and Other Gastrointestinal Disorders |journal=Gastroenterol Hepatol (N Y) |volume=9 |issue=7 |pages=450–2 |year=2013 |pmid=23935555 |pmc=3736783 |doi= |url=}}</ref> | ||
**[[Fermentation (biochemistry)|Fermentation]] and [[Osmosis|osmotic]] effects of FODMAPs produce [[Abdominal pain|abdominal discomfort]] and [[diarrhea]] in IBS. | ***[[Fermentation (biochemistry)|Fermentation]] and [[Osmosis|osmotic]] effects of FODMAPs produce [[Abdominal pain|abdominal discomfort]] and [[diarrhea]] in IBS. | ||
**FODMAPs yield carbon dioxide, methane, and hydrogen that are responsible for bloating. | ***FODMAPs yield carbon dioxide, methane, and hydrogen that are responsible for bloating. | ||
**[[Osmosis|Osmotically]] active carbohydrate by products lead to [[diarrhea]] by enhancing [[Intestine|intestinal]] contractions and precipitating fluid secretion.<ref name="pmid23644955">{{cite journal |vauthors=Böhn L, Störsrud S, Törnblom H, Bengtsson U, Simrén M |title=Self-reported food-related gastrointestinal symptoms in IBS are common and associated with more severe symptoms and reduced quality of life |journal=Am. J. Gastroenterol. |volume=108 |issue=5 |pages=634–41 |year=2013 |pmid=23644955 |doi=10.1038/ajg.2013.105 |url=}}</ref><ref name="pmid7910231">{{cite journal |vauthors=Young E, Stoneham MD, Petruckevitch A, Barton J, Rona R |title=A population study of food intolerance |journal=Lancet |volume=343 |issue=8906 |pages=1127–30 |year=1994 |pmid=7910231 |doi= |url=}}</ref><ref name="pmid24336217">{{cite journal |vauthors=David LA, Maurice CF, Carmody RN, Gootenberg DB, Button JE, Wolfe BE, Ling AV, Devlin AS, Varma Y, Fischbach MA, Biddinger SB, Dutton RJ, Turnbaugh PJ |title=Diet rapidly and reproducibly alters the human gut microbiome |journal=Nature |volume=505 |issue=7484 |pages=559–63 |year=2014 |pmid=24336217 |pmc=3957428 |doi=10.1038/nature12820 | **[[Osmosis|Osmotically]] active carbohydrate by products lead to [[diarrhea]] by enhancing [[Intestine|intestinal]] contractions and precipitating fluid secretion.<ref name="pmid23644955">{{cite journal |vauthors=Böhn L, Störsrud S, Törnblom H, Bengtsson U, Simrén M |title=Self-reported food-related gastrointestinal symptoms in IBS are common and associated with more severe symptoms and reduced quality of life |journal=Am. J. Gastroenterol. |volume=108 |issue=5 |pages=634–41 |year=2013 |pmid=23644955 |doi=10.1038/ajg.2013.105 |url=}}</ref><ref name="pmid7910231">{{cite journal |vauthors=Young E, Stoneham MD, Petruckevitch A, Barton J, Rona R |title=A population study of food intolerance |journal=Lancet |volume=343 |issue=8906 |pages=1127–30 |year=1994 |pmid=7910231 |doi= |url=}}</ref><ref name="pmid24336217">{{cite journal |vauthors=David LA, Maurice CF, Carmody RN, Gootenberg DB, Button JE, Wolfe BE, Ling AV, Devlin AS, Varma Y, Fischbach MA, Biddinger SB, Dutton RJ, Turnbaugh PJ |title=Diet rapidly and reproducibly alters the human gut microbiome |journal=Nature |volume=505 |issue=7484 |pages=559–63 |year=2014 |pmid=24336217 |pmc=3957428 |doi=10.1038/nature12820 |url=}}</ref><ref name="pmid26867199">{{cite journal |vauthors=Elli L, Tomba C, Branchi F, Roncoroni L, Lombardo V, Bardella MT, Ferretti F, Conte D, Valiante F, Fini L, Forti E, Cannizzaro R, Maiero S, Londoni C, Lauri A, Fornaciari G, Lenoci N, Spagnuolo R, Basilisco G, Somalvico F, Borgatta B, Leandro G, Segato S, Barisani D, Morreale G, Buscarini E |title=Evidence for the Presence of Non-Celiac Gluten Sensitivity in Patients with Functional Gastrointestinal Symptoms: Results from a Multicenter Randomized Double-Blind Placebo-Controlled Gluten Challenge |journal=Nutrients |volume=8 |issue=2 |pages=84 |year=2016 |pmid=26867199 |pmc=4772047 |doi=10.3390/nu8020084 |url=}}</ref><ref name="pmid26522233">{{cite journal |vauthors=Coletta M, Gates FK, Marciani L, Shiwani H, Major G, Hoad CL, Chaddock G, Gowland PA, Spiller RC |title=Effect of bread gluten content on gastrointestinal function: a crossover MRI study on healthy humans |journal=Br. J. Nutr. |volume=115 |issue=1 |pages=55–61 |year=2016 |pmid=26522233 |doi=10.1017/S0007114515004183 |url=}}</ref><ref name="pmid24308871">{{cite journal |vauthors=Yang J, Fox M, Cong Y, Chu H, Zheng X, Long Y, Fried M, Dai N |title=Lactose intolerance in irritable bowel syndrome patients with diarrhoea: the roles of anxiety, activation of the innate mucosal immune system and visceral sensitivity |journal=Aliment. Pharmacol. Ther. |volume=39 |issue=3 |pages=302–11 |year=2014 |pmid=24308871 |doi=10.1111/apt.12582 |url=}}</ref><ref name="pmid24445613">{{cite journal |vauthors=Staudacher HM, Irving PM, Lomer MC, Whelan K |title=Mechanisms and efficacy of dietary FODMAP restriction in IBS |journal=Nat Rev Gastroenterol Hepatol |volume=11 |issue=4 |pages=256–66 |year=2014 |pmid=24445613 |doi=10.1038/nrgastro.2013.259 |url=}}</ref> | ||
* | * [[Infection]] | ||
**[[Infection|Infectious]] [[gastroenteritis]] triggers micro [[inflammation]] | **[[Infection|Infectious]] [[gastroenteritis]] triggers micro [[inflammation]] and up to one third of [[irritable bowel syndrome]] cases follow [[Gastroenteritis|acute gastroenteritis.]] | ||
**Micro [[inflammation]] of the [[Gastrointestinal tract|gut]] causes activation of the [[Lymphocyte|lymphocytes]], [[Mast cell|mast cells]] and pro inflammatory [[Cytokine|cytokines]] that stimulate the [[enteric nervous system]] and lead to abnormal [[Viscus|visceral]] and [[Motor skill|motor]] responses within the [[Gastrointestinal tract|gastrointestinal]] tract. | **Micro [[inflammation]] of the [[Gastrointestinal tract|gut]] causes activation of the [[Lymphocyte|lymphocytes]], [[Mast cell|mast cells]] and pro inflammatory [[Cytokine|cytokines]] that stimulate the [[enteric nervous system]] and lead to abnormal [[Viscus|visceral]] and [[Motor skill|motor]] responses within the [[Gastrointestinal tract|gastrointestinal]] tract. | ||
**[[Immunity (medical)|Immune]] activation due to GI [[infection]] also increases [[Enteroendocrine cells|enteroendocrine]] cells, calprotectin-positive [[Macrophage|macrophages]], [[Intraepithelial lymphocyte|intraepithelial]] [[Lymphocyte|lymphocytes]], and l[[Lamina propria|amina propria]] [[T cell|T cells]] which contribute directly to [[abdominal pain]] perception. | **[[Immunity (medical)|Immune]] activation due to GI [[infection]] also increases [[Enteroendocrine cells|enteroendocrine]] cells, calprotectin-positive [[Macrophage|macrophages]], [[Intraepithelial lymphocyte|intraepithelial]] [[Lymphocyte|lymphocytes]], and l[[Lamina propria|amina propria]] [[T cell|T cells]] which contribute directly to [[abdominal pain]] perception. <ref name="pmid20101257">{{cite journal |vauthors=Ohman L, Simrén M |title=Pathogenesis of IBS: role of inflammation, immunity and neuroimmune interactions |journal=Nat Rev Gastroenterol Hepatol |volume=7 |issue=3 |pages=163–73 |year=2010 |pmid=20101257 |doi=10.1038/nrgastro.2010.4 |url=}}</ref><ref name="pmid22730468">{{cite journal |vauthors=Simrén M, Barbara G, Flint HJ, Spiegel BM, Spiller RC, Vanner S, Verdu EF, Whorwell PJ, Zoetendal EG |title=Intestinal microbiota in functional bowel disorders: a Rome foundation report |journal=Gut |volume=62 |issue=1 |pages=159–76 |year=2013 |pmid=22730468 |pmc=3551212 |doi=10.1136/gutjnl-2012-302167 |url=}}</ref><ref name="pmid23580243">{{cite journal |vauthors=Ohman L, Simrén M |title=Intestinal microbiota and its role in irritable bowel syndrome (IBS) |journal=Curr Gastroenterol Rep |volume=15 |issue=5 |pages=323 |year=2013 |pmid=23580243 |doi=10.1007/s11894-013-0323-7 |url=}}</ref><ref name="pmid17148502">{{cite journal |vauthors=Posserud I, Stotzer PO, Björnsson ES, Abrahamsson H, Simrén M |title=Small intestinal bacterial overgrowth in patients with irritable bowel syndrome |journal=Gut |volume=56 |issue=6 |pages=802–8 |year=2007 |pmid=17148502 |pmc=1954873 |doi=10.1136/gut.2006.108712 |url=}}</ref><ref name="pmid22180058">{{cite journal |vauthors=Jeffery IB, O'Toole PW, Öhman L, Claesson MJ, Deane J, Quigley EM, Simrén M |title=An irritable bowel syndrome subtype defined by species-specific alterations in faecal microbiota |journal=Gut |volume=61 |issue=7 |pages=997–1006 |year=2012 |pmid=22180058 |doi=10.1136/gutjnl-2011-301501 |url=}}</ref><ref name="pmid19457422">{{cite journal |vauthors=Spiller R, Garsed K |title=Postinfectious irritable bowel syndrome |journal=Gastroenterology |volume=136 |issue=6 |pages=1979–88 |year=2009 |pmid=19457422 |doi=10.1053/j.gastro.2009.02.074 |url=}}</ref><ref name="pmid25611066">{{cite journal |vauthors=Joo YE |title=Alteration of fecal microbiota in patients with postinfectious irritable bowel syndrome |journal=J Neurogastroenterol Motil |volume=21 |issue=1 |pages=135–7 |year=2015 |pmid=25611066 |pmc=4288086 |doi=10.5056/jnm14133 |url=}}</ref><ref name="pmid10026328">{{cite journal |vauthors=Gwee KA, Leong YL, Graham C, McKendrick MW, Collins SM, Walters SJ, Underwood JE, Read NW |title=The role of psychological and biological factors in postinfective gut dysfunction |journal=Gut |volume=44 |issue=3 |pages=400–6 |year=1999 |pmid=10026328 |pmc=1727402 |doi= |url=}}</ref><ref name="pmid24646319">{{cite journal |vauthors=Nielsen HL, Engberg J, Ejlertsen T, Nielsen H |title=Psychometric scores and persistence of irritable bowel after Campylobacter concisus infection |journal=Scand. J. Gastroenterol. |volume=49 |issue=5 |pages=545–51 |year=2014 |pmid=24646319 |doi=10.3109/00365521.2014.886718 |url=}}</ref> | ||
** The role of [[small intestinal bacterial overgrowth syndrome]] is strongest when testing with glucose breath tests (relative risk = 4.2) or jejunal aspirates (relative risk = 3.0) are compared among patients with IBS and controls<ref name="pmid31750966">{{cite journal| author=Ghoshal UC, Nehra A, Mathur A, Rai S| title=A meta-analysis on small intestinal bacterial overgrowth in patients with different subtypes of irritable bowel syndrome. | journal=J Gastroenterol Hepatol | year= 2020 | volume= 35 | issue= 6 | pages= 922-931 | pmid=31750966 | doi=10.1111/jgh.14938 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=31750966 }} </ref>. | |||
==='''Intrinsic gastrointestinal factors'''=== | ==='''Intrinsic gastrointestinal factors'''=== | ||
*'''Motor abnormalities:''' | *'''Motor abnormalities:''' | ||
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*****Secondary to activation of [[Neurotransmitter|neurotransmitters]] such as: | *****Secondary to activation of [[Neurotransmitter|neurotransmitters]] such as: | ||
*****[[NMDA receptor|N-methyl D aspartate (NMDA) receptor]] | *****[[NMDA receptor|N-methyl D aspartate (NMDA) receptor]] | ||
*****[[ | *****[[Nitric oxide]] | ||
****'''Activation of specific [[Gastrointestinal tract|gastrointestinal]] mediators''' that lead to [[Afferent nerve|afferent]] [[nerve]] fiber sensitization: | ****'''Activation of specific [[Gastrointestinal tract|gastrointestinal]] mediators''' that lead to [[Afferent nerve|afferent]] [[nerve]] fiber sensitization: | ||
*****[[ | *****[[Kinins]] | ||
*****[[ | *****[[Serotonin]] | ||
****'''Central ([[Brain stem|brainstem]] and [[Cerebral cortex|cortical]]) modulation''' with increased activation of anterior [[cingulate cortex]], [[thalamus]] and [[Insular cortex|insula]]. | ****'''Central ([[Brain stem|brainstem]] and [[Cerebral cortex|cortical]]) modulation''' with increased activation of anterior [[cingulate cortex]], [[thalamus]] and [[Insular cortex|insula]]. | ||
*****These structures are involved in processing of pain. | *****These structures are involved in processing of pain. | ||
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*****Semi permanent changes(seen on functional [[magnetic resonance imaging]] and [[positron emission tomography]]) in the [[Nervous system|neural]] response to [[Viscus|visceral]] stimulation contribute to [[Viscus|visceral]] [[hypersensitivity]].''<ref name="pmid21537962" /><ref name="pmid10784583">{{cite journal |vauthors=Mertz H, Morgan V, Tanner G, Pickens D, Price R, Shyr Y, Kessler R |title=Regional cerebral activation in irritable bowel syndrome and control subjects with painful and nonpainful rectal distention |journal=Gastroenterology |volume=118 |issue=5 |pages=842–8 |year=2000 |pmid=10784583 |doi= |url=}}</ref> '' | *****Semi permanent changes(seen on functional [[magnetic resonance imaging]] and [[positron emission tomography]]) in the [[Nervous system|neural]] response to [[Viscus|visceral]] stimulation contribute to [[Viscus|visceral]] [[hypersensitivity]].''<ref name="pmid21537962" /><ref name="pmid10784583">{{cite journal |vauthors=Mertz H, Morgan V, Tanner G, Pickens D, Price R, Shyr Y, Kessler R |title=Regional cerebral activation in irritable bowel syndrome and control subjects with painful and nonpainful rectal distention |journal=Gastroenterology |volume=118 |issue=5 |pages=842–8 |year=2000 |pmid=10784583 |doi= |url=}}</ref> '' | ||
****'''Recruitment of peripheral silent [[Nociceptor|nociceptors]]''' cause increased end [[Organ (anatomy)|organ]] sensitivity due to | ****'''Recruitment of peripheral silent [[Nociceptor|nociceptors]]''' cause increased end [[Organ (anatomy)|organ]] sensitivity due to | ||
*****[[Hormone| | *****[[Hormone|Hormonal]] activation ( increased [[serotonin]] affects [[Gastrointestinal tract|gastrointestinal]] [[motility]] and [[Viscus|visceral]] [[pain]] perception) | ||
*****[[Immunity (medical)| | *****[[Immunity (medical)|Immune]] activation(recruitment of [[Inflammation|inflammatory]] mediators)<ref name="pmid21537962" /> | ||
{{familytree/start |summary=PE diagnosis Algorithm.}} | {{familytree/start |summary=PE diagnosis Algorithm.}} | ||
{{familytree | | | | | | | | | |,|-| A01 |-| A02 | | | |A01=[[Spinal cord|Spinal]] hyperexcitability |A02= Activation of <br>• [[NMDA receptor|N-methyl D aspartate (NMDA) receptor]] <br>• [[nitric oxide]] }} | {{familytree | | | | | | | | | |,|-| A01 |-| A02 | | | |A01=[[Spinal cord|Spinal]] hyperexcitability |A02= Activation of <br>• [[NMDA receptor|N-methyl D aspartate (NMDA) receptor]] <br>• [[nitric oxide]] }} | ||
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* IBS patients have higher [[Mucous membrane|mucosal]] counts of ''[[Lymphocyte|lymphocytes]]'' (T cells, B cells), ''[[Mast cell|mast]] cells'' and immune ''mediators'' such as prostanoids, [[Protease|proteases]], [[Cytokine|cytokines]] and [[Histamine|histamines]].<ref name="pmid17383420" /><ref name="pmid20427395">{{cite journal |vauthors=Marshall JK, Thabane M, Garg AX, Clark WF, Moayyedi P, Collins SM |title=Eight year prognosis of postinfectious irritable bowel syndrome following waterborne bacterial dysentery |journal=Gut |volume=59 |issue=5 |pages=605–11 |year=2010 |pmid=20427395 |doi=10.1136/gut.2009.202234 |url=}}</ref><ref name="pmid21911849">{{cite journal |vauthors=Wensaas KA, Langeland N, Hanevik K, Mørch K, Eide GE, Rortveit G |title=Irritable bowel syndrome and chronic fatigue 3 years after acute giardiasis: historic cohort study |journal=Gut |volume=61 |issue=2 |pages=214–9 |year=2012 |pmid=21911849 |doi=10.1136/gutjnl-2011-300220 |url=}}</ref><ref name="pmid19711225">{{cite journal |vauthors=Mearin F, Perelló A, Balboa A, Perona M, Sans M, Salas A, Angulo S, Lloreta J, Benasayag R, García-Gonzalez MA, Pérez-Oliveras M, Coderch J |title=Pathogenic mechanisms of postinfectious functional gastrointestinal disorders: results 3 years after gastroenteritis |journal=Scand. J. Gastroenterol. |volume=44 |issue=10 |pages=1173–85 |year=2009 |pmid=19711225 |doi=10.1080/00365520903171276 |url=}}</ref><ref name="pmid12631663">{{cite journal |vauthors=Gwee KA, Collins SM, Read NW, Rajnakova A, Deng Y, Graham JC, McKendrick MW, Moochhala SM |title=Increased rectal mucosal expression of interleukin 1beta in recently acquired post-infectious irritable bowel syndrome |journal=Gut |volume=52 |issue=4 |pages=523–6 |year=2003 |pmid=12631663 |pmc=1773606 |doi= |url=}}</ref> | * IBS patients have higher [[Mucous membrane|mucosal]] counts of ''[[Lymphocyte|lymphocytes]]'' (T cells, B cells), ''[[Mast cell|mast]] cells'' and immune ''mediators'' such as prostanoids, [[Protease|proteases]], [[Cytokine|cytokines]] and [[Histamine|histamines]].<ref name="pmid17383420" /><ref name="pmid20427395">{{cite journal |vauthors=Marshall JK, Thabane M, Garg AX, Clark WF, Moayyedi P, Collins SM |title=Eight year prognosis of postinfectious irritable bowel syndrome following waterborne bacterial dysentery |journal=Gut |volume=59 |issue=5 |pages=605–11 |year=2010 |pmid=20427395 |doi=10.1136/gut.2009.202234 |url=}}</ref><ref name="pmid21911849">{{cite journal |vauthors=Wensaas KA, Langeland N, Hanevik K, Mørch K, Eide GE, Rortveit G |title=Irritable bowel syndrome and chronic fatigue 3 years after acute giardiasis: historic cohort study |journal=Gut |volume=61 |issue=2 |pages=214–9 |year=2012 |pmid=21911849 |doi=10.1136/gutjnl-2011-300220 |url=}}</ref><ref name="pmid19711225">{{cite journal |vauthors=Mearin F, Perelló A, Balboa A, Perona M, Sans M, Salas A, Angulo S, Lloreta J, Benasayag R, García-Gonzalez MA, Pérez-Oliveras M, Coderch J |title=Pathogenic mechanisms of postinfectious functional gastrointestinal disorders: results 3 years after gastroenteritis |journal=Scand. J. Gastroenterol. |volume=44 |issue=10 |pages=1173–85 |year=2009 |pmid=19711225 |doi=10.1080/00365520903171276 |url=}}</ref><ref name="pmid12631663">{{cite journal |vauthors=Gwee KA, Collins SM, Read NW, Rajnakova A, Deng Y, Graham JC, McKendrick MW, Moochhala SM |title=Increased rectal mucosal expression of interleukin 1beta in recently acquired post-infectious irritable bowel syndrome |journal=Gut |volume=52 |issue=4 |pages=523–6 |year=2003 |pmid=12631663 |pmc=1773606 |doi= |url=}}</ref> | ||
** '''Lymphocytes:''' | ** '''Lymphocytes:''' | ||
**Activation of [[humoral immunity]] in [[Irritable bowel syndrome|IBS]] is specific for the [[gastrointestinal tract]]. Increased number of [[Lymphocyte|lymphocytes]] have been found in the [[small intestine]] and [[Colon (anatomy)|colon]] of [[Irritable bowel syndrome|IBS]] patients.<ref name="pmid12055584" /><ref name="pmid12454854" /><ref name="pmid19222763">{{cite journal |vauthors=Ohman L, Lindmark AC, Isaksson S, Posserud I, Strid H, Sjövall H, Simrén M |title=B-cell activation in patients with irritable bowel syndrome (IBS) |journal=Neurogastroenterol. Motil. |volume=21 |issue=6 |pages=644–50, e27 |year=2009 |pmid=19222763 |doi=10.1111/j.1365-2982.2009.01272.x |url=}}</ref><ref name="pmid25209656">{{cite journal |vauthors=Vicario M, González-Castro AM, Martínez C, Lobo B, Pigrau M, Guilarte M, de Torres I, Mosquera JL, Fortea M, Sevillano-Aguilera C, Salvo-Romero E, Alonso C, Rodiño-Janeiro BK, Söderholm JD, Azpiroz F, Santos J |title=Increased humoral immunity in the jejunum of diarrhoea-predominant irritable bowel syndrome associated with clinical manifestations |journal=Gut |volume=64 |issue=9 |pages=1379–88 |year=2015 |pmid=25209656 |doi=10.1136/gutjnl-2013-306236 |url=}}</ref> | ***Activation of [[humoral immunity]] in [[Irritable bowel syndrome|IBS]] is specific for the [[gastrointestinal tract]]. Increased number of [[Lymphocyte|lymphocytes]] have been found in the [[small intestine]] and [[Colon (anatomy)|colon]] of [[Irritable bowel syndrome|IBS]] patients.<ref name="pmid12055584" /><ref name="pmid12454854" /><ref name="pmid19222763">{{cite journal |vauthors=Ohman L, Lindmark AC, Isaksson S, Posserud I, Strid H, Sjövall H, Simrén M |title=B-cell activation in patients with irritable bowel syndrome (IBS) |journal=Neurogastroenterol. Motil. |volume=21 |issue=6 |pages=644–50, e27 |year=2009 |pmid=19222763 |doi=10.1111/j.1365-2982.2009.01272.x |url=}}</ref><ref name="pmid25209656">{{cite journal |vauthors=Vicario M, González-Castro AM, Martínez C, Lobo B, Pigrau M, Guilarte M, de Torres I, Mosquera JL, Fortea M, Sevillano-Aguilera C, Salvo-Romero E, Alonso C, Rodiño-Janeiro BK, Söderholm JD, Azpiroz F, Santos J |title=Increased humoral immunity in the jejunum of diarrhoea-predominant irritable bowel syndrome associated with clinical manifestations |journal=Gut |volume=64 |issue=9 |pages=1379–88 |year=2015 |pmid=25209656 |doi=10.1136/gutjnl-2013-306236 |url=}}</ref> | ||
**[[Irritable bowel syndrome|IBS]] patients with [[diarrhea]] have enhanced [[Mucous membrane|mucosal]] [[Humoral immunity|humoral]] activity, associated with activation and [[Cell growth|proliferation]] of [[B cell|B cells]] and [[Antibody|immunoglobulin]] production, identified by microarray profiling.<ref name="pmid25209656" /> | ***[[Irritable bowel syndrome|IBS]] patients with [[diarrhea]] have enhanced [[Mucous membrane|mucosal]] [[Humoral immunity|humoral]] activity, associated with activation and [[Cell growth|proliferation]] of [[B cell|B cells]] and [[Antibody|immunoglobulin]] production, identified by microarray profiling.<ref name="pmid25209656" /> | ||
**[[Irritable bowel syndrome|IBS]] patients with severe disease have an increase in [[lymphocyte]] [[Infiltration (medical)|infiltration]] in the myentric plexus.<ref name="pmid12454854" /> | ***[[Irritable bowel syndrome|IBS]] patients with severe disease have an increase in [[lymphocyte]] [[Infiltration (medical)|infiltration]] in the myentric plexus.<ref name="pmid12454854" /> | ||
**Mediators released by [[Lymphocyte|lymphocytes]] include [[histamine]], [[Protease|proteases]] and [[nitric oxide]]. The stimulation of the [[enteric nervous system]] by these mediators leads to abnormal [[Viscus|visceral]] and [[Muscle|motor]] responses within the [[gastrointestinal tract]].<ref name="pmid12055584" /> | ***Mediators released by [[Lymphocyte|lymphocytes]] include [[histamine]], [[Protease|proteases]] and [[nitric oxide]]. The stimulation of the [[enteric nervous system]] by these mediators leads to abnormal [[Viscus|visceral]] and [[Muscle|motor]] responses within the [[gastrointestinal tract]].<ref name="pmid12055584" /> | ||
**Stool in patients with [[diarrhea]] prominent [[Irritable bowel syndrome|IBS]] demonstrates high levels of [[serine]] [[protease]] activity, which is produced by [[Lymphocyte|lymphocytes]].<ref name="pmid18924448">{{cite journal |vauthors=Bueno L |title=Protease activated receptor 2: a new target for IBS treatment |journal=Eur Rev Med Pharmacol Sci |volume=12 Suppl 1 |issue= |pages=95–102 |year=2008 |pmid=18924448 |doi= |url=}}</ref><ref name="pmid18194983">{{cite journal |vauthors=Gecse K, Róka R, Ferrier L, Leveque M, Eutamene H, Cartier C, Ait-Belgnaoui A, Rosztóczy A, Izbéki F, Fioramonti J, Wittmann T, Bueno L |title=Increased faecal serine protease activity in diarrhoeic IBS patients: a colonic lumenal factor impairing colonic permeability and sensitivity |journal=Gut |volume=57 |issue=5 |pages=591–9 |year=2008 |pmid=18194983 |doi=10.1136/gut.2007.140210 |url=}}</ref> | ***Stool in patients with [[diarrhea]] prominent [[Irritable bowel syndrome|IBS]] demonstrates high levels of [[serine]] [[protease]] activity, which is produced by [[Lymphocyte|lymphocytes]].<ref name="pmid18924448">{{cite journal |vauthors=Bueno L |title=Protease activated receptor 2: a new target for IBS treatment |journal=Eur Rev Med Pharmacol Sci |volume=12 Suppl 1 |issue= |pages=95–102 |year=2008 |pmid=18924448 |doi= |url=}}</ref><ref name="pmid18194983">{{cite journal |vauthors=Gecse K, Róka R, Ferrier L, Leveque M, Eutamene H, Cartier C, Ait-Belgnaoui A, Rosztóczy A, Izbéki F, Fioramonti J, Wittmann T, Bueno L |title=Increased faecal serine protease activity in diarrhoeic IBS patients: a colonic lumenal factor impairing colonic permeability and sensitivity |journal=Gut |volume=57 |issue=5 |pages=591–9 |year=2008 |pmid=18194983 |doi=10.1136/gut.2007.140210 |url=}}</ref> | ||
**In response to high levels of [[serine protease]], there is increased [[Viscus|visceral]] pain and [[Colon (anatomy)|colonic]] cellular permeability. <ref name="pmid18924448" /> | ***In response to high levels of [[serine protease]], there is increased [[Viscus|visceral]] pain and [[Colon (anatomy)|colonic]] cellular permeability. <ref name="pmid18924448" /> | ||
**[[Serine protease]] inhibitors prevent effects mediated by high levels of [[serine protease]] in [[Irritable bowel syndrome|IBS]] patients.<ref name="pmid18194983" /><ref name="pmid18924448" /> | ***[[Serine protease]] inhibitors prevent effects mediated by high levels of [[serine protease]] in [[Irritable bowel syndrome|IBS]] patients.<ref name="pmid18194983" /><ref name="pmid18924448" /> | ||
**'''Mast cells:''' | **'''Mast cells:''' | ||
** [[Irritable bowel syndrome|IBS]] leads to an increased number of [[Mast cell|mast cells]] in [[Irritable bowel syndrome|IBS]] patients in the [[jejunum]], [[terminal ileum]] and [[Colon (anatomy)|colon]].<ref name="pmid14988823" /> | *** [[Irritable bowel syndrome|IBS]] leads to an increased number of [[Mast cell|mast cells]] in [[Irritable bowel syndrome|IBS]] patients in the [[jejunum]], [[terminal ileum]] and [[Colon (anatomy)|colon]].<ref name="pmid14988823" /> | ||
** Higher numbers of activated [[Mast cell|mast cells]] are found in proximity to [[Colon (anatomy)|colonic]] nerve fibres in the mucosa of the [[Gastrointestinal tract|gastrointestinal]] [[tract]] of [[Irritable bowel syndrome|IBS]] patients. <ref name="pmid14988823" /><ref name="pmid17005763" /> | *** Higher numbers of activated [[Mast cell|mast cells]] are found in proximity to [[Colon (anatomy)|colonic]] nerve fibres in the mucosa of the [[Gastrointestinal tract|gastrointestinal]] [[tract]] of [[Irritable bowel syndrome|IBS]] patients. <ref name="pmid14988823" /><ref name="pmid17005763" /> | ||
** '''Proinflammatory cytokines:''' | ** '''Proinflammatory cytokines:''' | ||
** [[Cytokine|Cytokines]] are protein mediators of the [[Immunity (medical)|immune]] response. | *** [[Cytokine|Cytokines]] are protein mediators of the [[Immunity (medical)|immune]] response. Increased levels of [[Cytokine|cytokines]] have been found in [[Irritable bowel syndrome|IBS]] patients.<ref name="pmid19711225" /><ref name="pmid12631663" /> | ||
** Higher amounts of [[Tumour necrosis factor|tumor necrosis factor]] are produced by the peripheral blood [[Monocyte|mononuclear]] cells of [[Irritable bowel syndrome|IBS]] patients.<ref name="pmid16472586">{{cite journal |vauthors=Dinan TG, Quigley EM, Ahmed SM, Scully P, O'Brien S, O'Mahony L, O'Mahony S, Shanahan F, Keeling PW |title=Hypothalamic-pituitary-gut axis dysregulation in irritable bowel syndrome: plasma cytokines as a potential biomarker? |journal=Gastroenterology |volume=130 |issue=2 |pages=304–11 |year=2006 |pmid=16472586 |doi=10.1053/j.gastro.2005.11.033 |url=}}</ref | *** Higher amounts of [[Tumour necrosis factor|tumor necrosis factor]] are produced by the peripheral blood [[Monocyte|mononuclear]] cells of [[Irritable bowel syndrome|IBS]] patients.<ref name="pmid17383420" /><ref name="pmid16472586">{{cite journal |vauthors=Dinan TG, Quigley EM, Ahmed SM, Scully P, O'Brien S, O'Mahony L, O'Mahony S, Shanahan F, Keeling PW |title=Hypothalamic-pituitary-gut axis dysregulation in irritable bowel syndrome: plasma cytokines as a potential biomarker? |journal=Gastroenterology |volume=130 |issue=2 |pages=304–11 |year=2006 |pmid=16472586 |doi=10.1053/j.gastro.2005.11.033 |url=}}</ref> | ||
** Other [[Cytokine|cytokines]] such as [[Interleukin|interleukin 1β]], [[interleukin]] 6, [[Interleukin 10|interleukin10]], and [[Tumor necrosis factor-alpha|TNFα]] are raised in [[Irritable bowel syndrome|IBS]] patients. | *** Other [[Cytokine|cytokines]] such as [[Interleukin|interleukin 1β]], [[interleukin]] 6, [[Interleukin 10|interleukin10]], and [[Tumor necrosis factor-alpha|TNFα]] are raised in [[Irritable bowel syndrome|IBS]] patients. | ||
** Increased concentration of [[Cytokine|cytokines]] is directly proportional to the severity and frequency of pain.<ref name="pmid17383420" /><ref name=" | *** Increased concentration of [[Cytokine|cytokines]] is directly proportional to the severity and frequency of pain.<ref name="pmid17383420" /><ref name="pmid16472586" /><ref name="pmid25063707" /> | ||
** The [[Tumor necrosis factors|TNF]] [[antagonist]] [[infliximab]] counteracts pain in [[Irritable bowel syndrome|IBS]] patients, proving [[Tumor necrosis factors|TNF]] involvement in mechanical [[hypersensitivity]] of the [[Colon (anatomy)|colonic]] [[afferent nerve]] endings . <ref name="pmid25063707">{{cite journal |vauthors=Hughes PA, Moretta M, Lim A, Grasby DJ, Bird D, Brierley SM, Liebregts T, Adam B, Blackshaw LA, Holtmann G, Bampton P, Hoffmann P, Andrews JM, Zola H, Krumbiegel D |title=Immune derived opioidergic inhibition of viscerosensory afferents is decreased in Irritable Bowel Syndrome patients |journal=Brain Behav. Immun. |volume=42 |issue= |pages=191–203 |year=2014 |pmid=25063707 |doi=10.1016/j.bbi.2014.07.001 |url=}}</ref> | *** The [[Tumor necrosis factors|TNF]] [[antagonist]] [[infliximab]] counteracts pain in [[Irritable bowel syndrome|IBS]] patients, proving [[Tumor necrosis factors|TNF]] involvement in mechanical [[hypersensitivity]] of the [[Colon (anatomy)|colonic]] [[afferent nerve]] endings.<ref name="pmid25063707">{{cite journal |vauthors=Hughes PA, Moretta M, Lim A, Grasby DJ, Bird D, Brierley SM, Liebregts T, Adam B, Blackshaw LA, Holtmann G, Bampton P, Hoffmann P, Andrews JM, Zola H, Krumbiegel D |title=Immune derived opioidergic inhibition of viscerosensory afferents is decreased in Irritable Bowel Syndrome patients |journal=Brain Behav. Immun. |volume=42 |issue= |pages=191–203 |year=2014 |pmid=25063707 |doi=10.1016/j.bbi.2014.07.001 |url=}}</ref> | ||
* '''Altered gut microbiota''' | * '''Altered gut microbiota''' | ||
** [[Gut flora|Fecal microflora]] in [[Irritable bowel syndrome|IBS]] patients differ from healthy individuals. Some IBS patients have [[Colon (anatomy)|colonic]] [[Spirochaete|spirochaetosis]], with a unique pathology of increased [[Lymphatic system|lymphoid]] follicles and [[Eosinophil granulocyte|eosinophils]] on [[histology]].<ref name="pmid20427395" /><ref name="pmid25540866">{{cite journal |vauthors=Walker MM, Talley NJ, Inganäs L, Engstrand L, Jones MP, Nyhlin H, Agréus L, Kjellstrom L, Öst Å, Andreasson A |title=Colonic spirochetosis is associated with colonic eosinophilia and irritable bowel syndrome in a general population in Sweden |journal=Hum. Pathol. |volume=46 |issue=2 |pages=277–83 |year=2015 |pmid=25540866 |doi=10.1016/j.humpath.2014.10.026 |url=}}</ref><ref name="pmid17631127">{{cite journal |vauthors=Kassinen A, Krogius-Kurikka L, Mäkivuokko H, Rinttilä T, Paulin L, Corander J, Malinen E, Apajalahti J, Palva A |title=The fecal microbiota of irritable bowel syndrome patients differs significantly from that of healthy subjects |journal=Gastroenterology |volume=133 |issue=1 |pages=24–33 |year=2007 |pmid=17631127 |doi=10.1053/j.gastro.2007.04.005 |url=}}</ref><ref name="pmid15667495">{{cite journal |vauthors=Malinen E, Rinttilä T, Kajander K, Mättö J, Kassinen A, Krogius L, Saarela M, Korpela R, Palva A |title=Analysis of the fecal microbiota of irritable bowel syndrome patients and healthy controls with real-time PCR |journal=Am. J. Gastroenterol. |volume=100 |issue=2 |pages=373–82 |year=2005 |pmid=15667495 |doi=10.1111/j.1572-0241.2005.40312.x |url=}}</ref><ref name="pmid21820992">{{cite journal |vauthors=Rajilić-Stojanović M, Biagi E, Heilig HG, Kajander K, Kekkonen RA, Tims S, de Vos WM |title=Global and deep molecular analysis of microbiota signatures in fecal samples from patients with irritable bowel syndrome |journal=Gastroenterology |volume=141 |issue=5 |pages=1792–801 |year=2011 |pmid=21820992 |doi=10.1053/j.gastro.2011.07.043 |url=}}</ref><ref name="pmid21741921">{{cite journal |vauthors=Saulnier DM, Riehle K, Mistretta TA, Diaz MA, Mandal D, Raza S, Weidler EM, Qin X, Coarfa C, Milosavljevic A, Petrosino JF, Highlander S, Gibbs R, Lynch SV, Shulman RJ, Versalovic J |title=Gastrointestinal microbiome signatures of pediatric patients with irritable bowel syndrome |journal=Gastroenterology |volume=141 |issue=5 |pages=1782–91 |year=2011 |pmid=21741921 |pmc=3417828 |doi=10.1053/j.gastro.2011.06.072 |url=}}</ref><ref name="pmid22180058">{{cite journal |vauthors=Jeffery IB, O'Toole PW, Öhman L, Claesson MJ, Deane J, Quigley EM, Simrén M |title=An irritable bowel syndrome subtype defined by species-specific alterations in faecal microbiota |journal=Gut |volume=61 |issue=7 |pages=997–1006 |year=2012 |pmid=22180058 |doi=10.1136/gutjnl-2011-301501 |url=}}</ref><ref name="pmid20117111">{{cite journal |vauthors=Ford AC, Thabane M, Collins SM, Moayyedi P, Garg AX, Clark WF, Marshall JK |title=Prevalence of uninvestigated dyspepsia 8 years after a large waterborne outbreak of bacterial dysentery: a cohort study |journal=Gastroenterology |volume=138 |issue=5 |pages=1727–36; quiz e12 |year=2010 |pmid=20117111 |doi=10.1053/j.gastro.2010.01.043 |url=}}</ref> | ** [[Gut flora|Fecal microflora]] in [[Irritable bowel syndrome|IBS]] patients differ from healthy individuals. Some IBS patients have [[Colon (anatomy)|colonic]] [[Spirochaete|spirochaetosis]], with a unique pathology of increased [[Lymphatic system|lymphoid]] follicles and [[Eosinophil granulocyte|eosinophils]] on [[histology]].<ref name="pmid20427395" /><ref name="pmid25540866">{{cite journal |vauthors=Walker MM, Talley NJ, Inganäs L, Engstrand L, Jones MP, Nyhlin H, Agréus L, Kjellstrom L, Öst Å, Andreasson A |title=Colonic spirochetosis is associated with colonic eosinophilia and irritable bowel syndrome in a general population in Sweden |journal=Hum. Pathol. |volume=46 |issue=2 |pages=277–83 |year=2015 |pmid=25540866 |doi=10.1016/j.humpath.2014.10.026 |url=}}</ref><ref name="pmid17631127">{{cite journal |vauthors=Kassinen A, Krogius-Kurikka L, Mäkivuokko H, Rinttilä T, Paulin L, Corander J, Malinen E, Apajalahti J, Palva A |title=The fecal microbiota of irritable bowel syndrome patients differs significantly from that of healthy subjects |journal=Gastroenterology |volume=133 |issue=1 |pages=24–33 |year=2007 |pmid=17631127 |doi=10.1053/j.gastro.2007.04.005 |url=}}</ref><ref name="pmid15667495">{{cite journal |vauthors=Malinen E, Rinttilä T, Kajander K, Mättö J, Kassinen A, Krogius L, Saarela M, Korpela R, Palva A |title=Analysis of the fecal microbiota of irritable bowel syndrome patients and healthy controls with real-time PCR |journal=Am. J. Gastroenterol. |volume=100 |issue=2 |pages=373–82 |year=2005 |pmid=15667495 |doi=10.1111/j.1572-0241.2005.40312.x |url=}}</ref><ref name="pmid21820992">{{cite journal |vauthors=Rajilić-Stojanović M, Biagi E, Heilig HG, Kajander K, Kekkonen RA, Tims S, de Vos WM |title=Global and deep molecular analysis of microbiota signatures in fecal samples from patients with irritable bowel syndrome |journal=Gastroenterology |volume=141 |issue=5 |pages=1792–801 |year=2011 |pmid=21820992 |doi=10.1053/j.gastro.2011.07.043 |url=}}</ref><ref name="pmid21741921">{{cite journal |vauthors=Saulnier DM, Riehle K, Mistretta TA, Diaz MA, Mandal D, Raza S, Weidler EM, Qin X, Coarfa C, Milosavljevic A, Petrosino JF, Highlander S, Gibbs R, Lynch SV, Shulman RJ, Versalovic J |title=Gastrointestinal microbiome signatures of pediatric patients with irritable bowel syndrome |journal=Gastroenterology |volume=141 |issue=5 |pages=1782–91 |year=2011 |pmid=21741921 |pmc=3417828 |doi=10.1053/j.gastro.2011.06.072 |url=}}</ref><ref name="pmid22180058">{{cite journal |vauthors=Jeffery IB, O'Toole PW, Öhman L, Claesson MJ, Deane J, Quigley EM, Simrén M |title=An irritable bowel syndrome subtype defined by species-specific alterations in faecal microbiota |journal=Gut |volume=61 |issue=7 |pages=997–1006 |year=2012 |pmid=22180058 |doi=10.1136/gutjnl-2011-301501 |url=}}</ref><ref name="pmid20117111">{{cite journal |vauthors=Ford AC, Thabane M, Collins SM, Moayyedi P, Garg AX, Clark WF, Marshall JK |title=Prevalence of uninvestigated dyspepsia 8 years after a large waterborne outbreak of bacterial dysentery: a cohort study |journal=Gastroenterology |volume=138 |issue=5 |pages=1727–36; quiz e12 |year=2010 |pmid=20117111 |doi=10.1053/j.gastro.2010.01.043 |url=}}</ref> | ||
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** There is an established relationship between [[Irritable bowel syndrome|IBS]] and [[polymorphisms]] in the gene for [[serotonin]] transport causing alteration in [[Intestine|intestinal]] [[peristalsis]] due to change in the [[serotonin]] reuptake efficacy.<ref name="pmid24060757">{{cite journal |vauthors=Grasberger H, Chang L, Shih W, Presson AP, Sayuk GS, Newberry RD, Karagiannides I, Pothoulakis C, Mayer E, Merchant JL |title=Identification of a functional TPH1 polymorphism associated with irritable bowel syndrome bowel habit subtypes |journal=Am. J. Gastroenterol. |volume=108 |issue=11 |pages=1766–74 |year=2013 |pmid=24060757 |pmc=4067697 |doi=10.1038/ajg.2013.304 |url=}}</ref><ref name="pmid21073637">{{cite journal |vauthors=Jun S, Kohen R, Cain KC, Jarrett ME, Heitkemper MM |title=Associations of tryptophan hydroxylase gene polymorphisms with irritable bowel syndrome |journal=Neurogastroenterol. Motil. |volume=23 |issue=3 |pages=233–9, e116 |year=2011 |pmid=21073637 |pmc=3057463 |doi=10.1111/j.1365-2982.2010.01623.x |url=}}</ref><ref name="pmid15138209">{{cite journal |vauthors=Kim HJ, Camilleri M, Carlson PJ, Cremonini F, Ferber I, Stephens D, McKinzie S, Zinsmeister AR, Urrutia R |title=Association of distinct alpha(2) adrenoceptor and serotonin transporter polymorphisms with constipation and somatic symptoms in functional gastrointestinal disorders |journal=Gut |volume=53 |issue=6 |pages=829–37 |year=2004 |pmid=15138209 |pmc=1774073 |doi= |url=}}</ref><ref name="pmid15361494">{{cite journal |vauthors=Yeo A, Boyd P, Lumsden S, Saunders T, Handley A, Stubbins M, Knaggs A, Asquith S, Taylor I, Bahari B, Crocker N, Rallan R, Varsani S, Montgomery D, Alpers DH, Dukes GE, Purvis I, Hicks GA |title=Association between a functional polymorphism in the serotonin transporter gene and diarrhoea predominant irritable bowel syndrome in women |journal=Gut |volume=53 |issue=10 |pages=1452–8 |year=2004 |pmid=15361494 |pmc=1774243 |doi=10.1136/gut.2003.035451 |url=}}</ref> | ** There is an established relationship between [[Irritable bowel syndrome|IBS]] and [[polymorphisms]] in the gene for [[serotonin]] transport causing alteration in [[Intestine|intestinal]] [[peristalsis]] due to change in the [[serotonin]] reuptake efficacy.<ref name="pmid24060757">{{cite journal |vauthors=Grasberger H, Chang L, Shih W, Presson AP, Sayuk GS, Newberry RD, Karagiannides I, Pothoulakis C, Mayer E, Merchant JL |title=Identification of a functional TPH1 polymorphism associated with irritable bowel syndrome bowel habit subtypes |journal=Am. J. Gastroenterol. |volume=108 |issue=11 |pages=1766–74 |year=2013 |pmid=24060757 |pmc=4067697 |doi=10.1038/ajg.2013.304 |url=}}</ref><ref name="pmid21073637">{{cite journal |vauthors=Jun S, Kohen R, Cain KC, Jarrett ME, Heitkemper MM |title=Associations of tryptophan hydroxylase gene polymorphisms with irritable bowel syndrome |journal=Neurogastroenterol. Motil. |volume=23 |issue=3 |pages=233–9, e116 |year=2011 |pmid=21073637 |pmc=3057463 |doi=10.1111/j.1365-2982.2010.01623.x |url=}}</ref><ref name="pmid15138209">{{cite journal |vauthors=Kim HJ, Camilleri M, Carlson PJ, Cremonini F, Ferber I, Stephens D, McKinzie S, Zinsmeister AR, Urrutia R |title=Association of distinct alpha(2) adrenoceptor and serotonin transporter polymorphisms with constipation and somatic symptoms in functional gastrointestinal disorders |journal=Gut |volume=53 |issue=6 |pages=829–37 |year=2004 |pmid=15138209 |pmc=1774073 |doi= |url=}}</ref><ref name="pmid15361494">{{cite journal |vauthors=Yeo A, Boyd P, Lumsden S, Saunders T, Handley A, Stubbins M, Knaggs A, Asquith S, Taylor I, Bahari B, Crocker N, Rallan R, Varsani S, Montgomery D, Alpers DH, Dukes GE, Purvis I, Hicks GA |title=Association between a functional polymorphism in the serotonin transporter gene and diarrhoea predominant irritable bowel syndrome in women |journal=Gut |volume=53 |issue=10 |pages=1452–8 |year=2004 |pmid=15361494 |pmc=1774243 |doi=10.1136/gut.2003.035451 |url=}}</ref> | ||
** Increased [[serotonin]] production contributes to [[postprandial]] symptoms in [[Irritable bowel syndrome|IBS]] patients, hence providing the rationale for the therapeutic efficacy of 5-HT 3 receptor [[Receptor antagonist|antagonists]] and 5-HT 4 receptor [[Agonist|agonists]] on symptoms in [[Irritable bowel syndrome|IBS]] patients.<ref name="pmid17241888">{{cite journal |vauthors=Gershon MD, Tack J |title=The serotonin signaling system: from basic understanding to drug development for functional GI disorders |journal=Gastroenterology |volume=132 |issue=1 |pages=397–414 |year=2007 |pmid=17241888 |doi=10.1053/j.gastro.2006.11.002 |url=}}</ref><ref name="pmid22071696">{{cite journal |vauthors=Camilleri M |title=Pharmacology of the new treatments for lower gastrointestinal motility disorders and irritable bowel syndrome |journal=Clin. Pharmacol. Ther. |volume=91 |issue=1 |pages=44–59 |year=2012 |pmid=22071696 |doi=10.1038/clpt.2011.261 |url=}}</ref> | ** Increased [[serotonin]] production contributes to [[postprandial]] symptoms in [[Irritable bowel syndrome|IBS]] patients, hence providing the rationale for the therapeutic efficacy of 5-HT 3 receptor [[Receptor antagonist|antagonists]] and 5-HT 4 receptor [[Agonist|agonists]] on symptoms in [[Irritable bowel syndrome|IBS]] patients.<ref name="pmid17241888">{{cite journal |vauthors=Gershon MD, Tack J |title=The serotonin signaling system: from basic understanding to drug development for functional GI disorders |journal=Gastroenterology |volume=132 |issue=1 |pages=397–414 |year=2007 |pmid=17241888 |doi=10.1053/j.gastro.2006.11.002 |url=}}</ref><ref name="pmid22071696">{{cite journal |vauthors=Camilleri M |title=Pharmacology of the new treatments for lower gastrointestinal motility disorders and irritable bowel syndrome |journal=Clin. Pharmacol. Ther. |volume=91 |issue=1 |pages=44–59 |year=2012 |pmid=22071696 |doi=10.1038/clpt.2011.261 |url=}}</ref> | ||
===''' | |||
==='''Psychosocial factors and CNS dysregulation'''=== | |||
* [[Symptom]] exacerbation occurs in [[Irritable bowel syndrome|IBS]] patients with emotional disturbances,[[Stress (medicine)|stress]], [[anxiety]] or [[depression]]. Traumatic experiences before 18 years of age directly shape adult connectivity in the executive control network consisting of structures such as the [[Insular cortex|insula]], anterior [[cingulate cortex]] and the [[thalamus]]. | * [[Symptom]] exacerbation occurs in [[Irritable bowel syndrome|IBS]] patients with emotional disturbances,[[Stress (medicine)|stress]], [[anxiety]] or [[depression]]. Traumatic experiences before 18 years of age directly shape adult connectivity in the executive control network consisting of structures such as the [[Insular cortex|insula]], anterior [[cingulate cortex]] and the [[thalamus]]. | ||
* Semipermanent/permanent changes in complex [[Nervous system|neural]] circuits lead to central pain amplification and contribute to [[abdominal pain]] in IBS patients.<ref name="pmid27061107">{{cite journal |vauthors=Park SH, Videlock EJ, Shih W, Presson AP, Mayer EA, Chang L |title=Adverse childhood experiences are associated with irritable bowel syndrome and gastrointestinal symptom severity |journal=Neurogastroenterol. Motil. |volume=28 |issue=8 |pages=1252–60 |year=2016 |pmid=27061107 |pmc=4956522 |doi=10.1111/nmo.12826 |url=}}</ref><ref name="pmid25003944">{{cite journal |vauthors=Gupta A, Kilpatrick L, Labus J, Tillisch K, Braun A, Hong JY, Ashe-McNalley C, Naliboff B, Mayer EA |title=Early adverse life events and resting state neural networks in patients with chronic abdominal pain: evidence for sex differences |journal=Psychosom Med |volume=76 |issue=6 |pages=404–12 |year=2014 |pmid=25003944 |pmc=4113723 |doi=10.1097/PSY.0000000000000089 |url=}}</ref> | * Semipermanent/permanent changes in complex [[Nervous system|neural]] circuits lead to central pain amplification and contribute to [[abdominal pain]] in IBS patients.<ref name="pmid27061107">{{cite journal |vauthors=Park SH, Videlock EJ, Shih W, Presson AP, Mayer EA, Chang L |title=Adverse childhood experiences are associated with irritable bowel syndrome and gastrointestinal symptom severity |journal=Neurogastroenterol. Motil. |volume=28 |issue=8 |pages=1252–60 |year=2016 |pmid=27061107 |pmc=4956522 |doi=10.1111/nmo.12826 |url=}}</ref><ref name="pmid25003944">{{cite journal |vauthors=Gupta A, Kilpatrick L, Labus J, Tillisch K, Braun A, Hong JY, Ashe-McNalley C, Naliboff B, Mayer EA |title=Early adverse life events and resting state neural networks in patients with chronic abdominal pain: evidence for sex differences |journal=Psychosom Med |volume=76 |issue=6 |pages=404–12 |year=2014 |pmid=25003944 |pmc=4113723 |doi=10.1097/PSY.0000000000000089 |url=}}</ref> | ||
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===Headache, Fibromyalgia, and Depression=== | ===Headache, Fibromyalgia, and Depression=== | ||
[[Irritable bowel syndrome|IBS]] patients may be identified with comorbidities such as [[headache]], [[fibromyalgia]] and [[depression]].<ref>{{cite journal |author=Cole JA, Rothman KJ, Cabral HJ, Zhang Y, Farraye FA |title=Migraine,[[fibromyalgia]], and depression among people with IBS: a prevalence study |journal=BMC gastroenterology |volume=6 |issue=|pages=26 |year=2006 |pmid=17007634 |doi=10.1186/1471-230X-6-26}}</ref><ref name="pmid16614951">{{cite journal |author=Kurland JE, Coyle WJ, Winkler A, Zable E |title=Prevalence of irritable bowel syndrome and depression in [[fibromyalgia]] |journal=Dig. Dis. Sci. |volume=51 |issue=3 |pages=454-60 |year=2006|pmid=16614951 |doi=10.1007/s10620-006-3154-7}}</ref><ref name="pmid16042909">{{cite journal |author=Frissora CL, Koch KL|title=Symptom overlap and comorbidity of irritable bowel syndrome with other conditions |journal=Current gastroenterology reports|volume=7 |issue=4 |pages=264-71 |year=2005 |pmid=16042909 |doi=}}</ref> | [[Irritable bowel syndrome|IBS]] patients may be identified with comorbidities such as [[headache]], [[fibromyalgia]] and [[depression]].<ref>{{cite journal |author=Cole JA, Rothman KJ, Cabral HJ, Zhang Y, Farraye FA |title=Migraine,[[fibromyalgia]], and depression among people with IBS: a prevalence study |journal=BMC gastroenterology |volume=6 |issue=|pages=26 |year=2006 |pmid=17007634 |doi=10.1186/1471-230X-6-26}}</ref><ref name="pmid16614951">{{cite journal |author=Kurland JE, Coyle WJ, Winkler A, Zable E |title=Prevalence of irritable bowel syndrome and depression in [[fibromyalgia]] |journal=Dig. Dis. Sci. |volume=51 |issue=3 |pages=454-60 |year=2006|pmid=16614951 |doi=10.1007/s10620-006-3154-7}}</ref><ref name="pmid16042909">{{cite journal |author=Frissora CL, Koch KL|title=Symptom overlap and comorbidity of irritable bowel syndrome with other conditions |journal=Current gastroenterology reports|volume=7 |issue=4 |pages=264-71 |year=2005 |pmid=16042909 |doi=}}</ref> | ||
===Inflammatory Bowel Disease=== | |||
* [[Irritable bowel syndrome|IBS]] and [[Inflammatory bowel disease|IBD]] are interrelated diseases, as patients with [[Inflammatory bowel disease|IBD]] experience [[Irritable bowel syndrome|IBS]]-like symptoms when their [[Inflammatory bowel disease|IBD]] is in remission.<ref name="SIMREN_2002">{{cite journal |author=Simrén M, Axelsson J, Gillberg R, Abrahamsson H, Svedlund J, Björnsson ES|title=Quality of life in inflammatory bowel disease in remission: the impact of IBS-like symptoms and associated psychological factors |journal=Am. J. Gastroenterol. |volume=97 |issue=2 |pages=389-96 |year=2002 |pmid=11866278 |doi=}}</ref><ref name="MINDERHOUD_2004">{{cite journal |author=Minderhoud IM, Oldenburg B, Wismeijer JA, van Berge Henegouwen GP, Smout AJ|title=IBS-like symptoms in patients with inflammatory bowel disease in remission; relationships with quality of life and coping behavior |journal=Dig. Dis. Sci. |volume=49 |issue=3 |pages=469-74 |year=2004 |pmid=15139501 |doi=}}</ref><ref name="QUIGLEY_2005">{{cite journal |author=Quigley EM |title=Irritable bowel syndrome and inflammatory bowel disease: interrelated diseases? |journal=Chinese journal of digestive diseases |volume=6 |issue=3 |pages=122-32 |year=2005 |pmid=16045602|doi=10.1111/j.1443-9573.2005.00202.x}}</ref> | |||
* [[Irritable bowel syndrome|IBS]] is believed to be a type of low-grade [[inflammatory bowel disease]] as serum markers associated with [[inflammation]] have also been found in patients with [[Irritable bowel syndrome|IBS]].<ref name="BERCIK_2005">{{cite journal |author=Bercik P, Verdu EF, Collins SM |title=Is irritable bowel syndrome a low-grade inflammatory bowel disease? |journal=Gastroenterol. Clin. North Am. |volume=34 |issue=2 |pages=235-45, vi-vii |year=2005|pmid=15862932 |doi=10.1016/j.gtc.2005.02.007}}</ref> | |||
* [[Irritable bowel syndrome|IBS]] patients are16.3 times more likely to develop [[Inflammatory bowel disease|IBD]].<ref name="GARCIA_2000">{{cite journal |author=García Rodríguez LA, Ruigómez A, Wallander MA, Johansson S, Olbe L |title=Detection of colorectal tumor and inflammatory bowel disease during follow-up of patients with initial diagnosis of irritable bowel syndrome |journal=Scand. J. Gastroenterol. |volume=35 |issue=3 |pages=306-11 |year=2000 |pmid=10766326 |doi=}}</ref> | |||
===Abdominal Surgery=== | |||
* [[Irritable bowel syndrome|IBS]] patients are 87% more likely to undergo [[Abdomen|abdominal]] and [[Pelvis|pelvic]] [[surgery]], and three times more likely to undergo [[gallbladder]] [[surgery]].<ref name="pmid16416174">{{cite journal |author=Cole JA, Yeaw JM, Cutone JA, ''et al'' |title=The incidence of abdominal and pelvic surgery among patients with irritable bowel syndrome |journal=Dig. Dis. Sci. |volume=50 |issue=12 |pages=2268–75 |year=2005 |pmid=16416174|doi=10.1007/s10620-005-3047-1}}</ref> | |||
* [[Irritable bowel syndrome|IBS]] patients were twice as likely to undergo [[hysterectomy]].<ref name="pmid15188159">{{cite journal |author=Longstreth GF, Yao JF|title=Irritable bowel syndrome and surgery: a multivariable analysis |journal=Gastroenterology |volume=126 |issue=7 |pages=1665–73|year=2004 |pmid=15188159 |doi=}}</ref> | |||
===Endometriosis=== | |||
There is a statistically significant link between [[Migraine|migraine headaches]], [[Irritable bowel syndrome|IBS]], and [[endometriosis]].<ref name="pmid17635599">{{cite journal |author=Tietjen GE, Bushnell CD, Herial NA, Utley C, White L, Hafeez F|title=Endometriosis is associated with prevalence of comorbid conditions in migraine |journal=Headache |volume=47 |issue=7|pages=1069-78 |year=2007 |pmid=17635599 |doi=10.1111/j.1526-4610.2007.00784.x}}</ref> | |||
==Medical conditions that accompany IBS== | |||
Several medical [[comorbidities]] appear with greater frequency in [[Irritable bowel syndrome|IBS]] patients. | |||
===Headache, Fibromyalgia, and Depression=== | |||
[[Irritable bowel syndrome|IBS]] patients may be identified with comorbidities such as [[headache]], [[fibromyalgia]] and [[depression]].<ref name="pmid16614951">{{cite journal |author=Kurland JE, Coyle WJ, Winkler A, Zable E |title=Prevalence of irritable bowel syndrome and depression in [[fibromyalgia]] |journal=Dig. Dis. Sci. |volume=51 |issue=3 |pages=454-60 |year=2006|pmid=16614951 |doi=10.1007/s10620-006-3154-7}}</ref><ref name="pmid16042909">{{cite journal |author=Frissora CL, Koch KL|title=Symptom overlap and comorbidity of irritable bowel syndrome with other conditions |journal=Current gastroenterology reports|volume=7 |issue=4 |pages=264-71 |year=2005 |pmid=16042909 |doi=}}</ref><ref>{{cite journal |author=Cole JA, Rothman KJ, Cabral HJ, Zhang Y, Farraye FA |title=Migraine,[[fibromyalgia]], and depression among people with IBS: a prevalence study |journal=BMC gastroenterology |volume=6 |issue=|pages=26 |year=2006 |pmid=17007634 |doi=10.1186/1471-230X-6-26}}</ref> | |||
===Inflammatory Bowel Disease=== | ===Inflammatory Bowel Disease=== | ||
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==Microscopic Pathology== | ==Microscopic Pathology== | ||
[[Microscopic]] changes that may be found in [[Irritable bowel syndrome|IBS]] patients are as follows: | [[Microscopic]] changes that may be found in [[Irritable bowel syndrome|IBS]] patients are as follows:<ref name="pmid12454854" /><ref name="pmid14988823" /><ref name="pmid14724817">{{cite journal |vauthors=Dunlop SP, Jenkins D, Neal KR, Spiller RC |title=Relative importance of enterochromaffin cell hyperplasia, anxiety, and depression in postinfectious IBS |journal=Gastroenterology |volume=125 |issue=6 |pages=1651–9 |year=2003 |pmid=14724817 |doi= |url=}}</ref><ref name="pmid11076879">{{cite journal |vauthors=Spiller RC, Jenkins D, Thornley JP, Hebden JM, Wright T, Skinner M, Neal KR |title=Increased rectal mucosal enteroendocrine cells, T lymphocytes, and increased gut permeability following acute Campylobacter enteritis and in post-dysenteric irritable bowel syndrome |journal=Gut |volume=47 |issue=6 |pages=804–11 |year=2000 |pmid=11076879 |pmc=1728147 |doi= |url=}}</ref><ref name="pmid10026328">{{cite journal |vauthors=Gwee KA, Leong YL, Graham C, McKendrick MW, Collins SM, Walters SJ, Underwood JE, Read NW |title=The role of psychological and biological factors in postinfective gut dysfunction |journal=Gut |volume=44 |issue=3 |pages=400–6 |year=1999 |pmid=10026328 |pmc=1727402 |doi= |url=}}</ref><ref name="pmid12873581">{{cite journal |vauthors=Dunlop SP, Jenkins D, Spiller RC |title=Distinctive clinical, psychological, and histological features of postinfective irritable bowel syndrome |journal=Am. J. Gastroenterol. |volume=98 |issue=7 |pages=1578–83 |year=2003 |pmid=12873581 |doi=10.1111/j.1572-0241.2003.07542.x |url=}}</ref><ref name="pmid8359068">{{cite journal |vauthors=Weston AP, Biddle WL, Bhatia PS, Miner PB |title=Terminal ileal mucosal mast cells in irritable bowel syndrome |journal=Dig. Dis. Sci. |volume=38 |issue=9 |pages=1590–5 |year=1993 |pmid=8359068 |doi= |url=}}</ref><ref name="pmid11012945">{{cite journal |vauthors=O'Sullivan M, Clayton N, Breslin NP, Harman I, Bountra C, McLaren A, O'Morain CA |title=Increased mast cells in the irritable bowel syndrome |journal=Neurogastroenterol. Motil. |volume=12 |issue=5 |pages=449–57 |year=2000 |pmid=11012945 |doi= |url=}}</ref><ref name="pmid12692417">{{cite journal |vauthors=Park CH, Joo YE, Choi SK, Rew JS, Kim SJ, Lee MC |title=Activated mast cells infiltrate in close proximity to enteric nerves in diarrhea-predominant irritable bowel syndrome |journal=J. Korean Med. Sci. |volume=18 |issue=2 |pages=204–10 |year=2003 |pmid=12692417 |pmc=3055014 |doi=10.3346/jkms.2003.18.2.204 |url=}}</ref><ref name="pmid15247174">{{cite journal |vauthors=Wang LH, Fang XC, Pan GZ |title=Bacillary dysentery as a causative factor of irritable bowel syndrome and its pathogenesis |journal=Gut |volume=53 |issue=8 |pages=1096–101 |year=2004 |pmid=15247174 |pmc=1774156 |doi=10.1136/gut.2003.021154 |url=}}</ref><ref name="pmid2733385">{{cite journal |vauthors=Salzmann JL, Peltier-Koch F, Bloch F, Petite JP, Camilleri JP |title=Morphometric study of colonic biopsies: a new method of estimating inflammatory diseases |journal=Lab. Invest. |volume=60 |issue=6 |pages=847–51 |year=1989 |pmid=2733385 |doi= |url=}}</ref><ref name="pmid13907162">{{cite journal |vauthors=HIATT RB, KATZ L |title=Mast cells in inflammatory conditions of the gastrointestinal tract |journal=Am. J. Gastroenterol. |volume=37 |issue= |pages=541–5 |year=1962 |pmid=13907162 |doi= |url=}}</ref> | ||
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Latest revision as of 19:15, 28 August 2021
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Irritable bowel syndrome Microchapters |
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Differentiating Irritable bowel syndrome from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Irritable bowel syndrome pathophysiology On the Web |
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American Roentgen Ray Society Images of Irritable bowel syndrome pathophysiology |
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Risk calculators and risk factors for Irritable bowel syndrome pathophysiology |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sudarshana Datta, MD [2]
Overview
Irritable Bowel Syndrome is caused by a complex interaction of various factors such as intrinsic gastrointestinal factors, CNS dysregulation and psychosocial factors, genetic, and environmental factors. Intrinsic gastrointestinal factors include motor abnormalities, visceral hypersensitivity, immune activation, mucosal inflammation, altered gut microbiota, and abnormal serotonin pathways. Visceral hypersensitivity refers to a decreased threshold for the perception of visceral stimuli that affects spinal excitability, brain stem and cortical modulation, activation of specific gastrointestinal mediators, and recruitment of peripheral silent nociceptors. Immune activation and mucosal inflammation involves an interaction of lymphocytes, mast cells, and proinflammatory cytokines. Environmental factors encompass dietary changes and infections. Psychosocial factors such as stress, anxiety, and depression directly shape adult connectivity in the executive control network consisting of structures such as the insula, anterior cingulate cortex, and the thalamus. Semipermanent or permanent changes in complex neural circuits lead to central pain amplification contributing to abdominal pain in IBS patients. The dorsolateral prefrontal cortex activity (responsible for vigilance and alertness of the human brain) and the mid-cingulate cortex (engaged in attention pathways and responses) is reduced in IBS patients. This reduction may lead to alterations in the subjective sensations of pain. Genetic factors also play a role in IBS. IBS has a high twin concordance and familial aggregation. IBS is associated with single nucleotide polymorphisms (SNPs) in genes involved in immune activation, neuropeptide hormone function, oxidative stress, nociception, permeability of the GI tract, host-microbiota interaction, inflammation, and TNF activity.
Pathophysiology
Pathogenesis
IBS occurs as a result of an interplay between four main factors:
| CNS dysregulation and psychosocial factors | |||||||||||||||||||||||||||||
| Intrinsic gastrointestinal factors: • Motor abnormalities • Visceral hypersensitivity • Immune activation and mucosal inflammation • Altered gut microbiota • Abnormal serotonin pathways | IRRITABLE BOWEL SYNDROME | Genetic factors: • Twin concordance • Familial aggregation • Single nucleotide polymorphisms(SNPs) • TNF polymorphism | |||||||||||||||||||||||||||
| Environmental factors: •Diet •Infections | |||||||||||||||||||||||||||||
Environmental factors
- Diet
- Fermentable oligosaccharides, monosaccharides, disaccharides, and polyols (FODMAPs) are present in stone fruits, artificial sweeteners, lactose-containing foods, and legumes. Changes in diet such as increased amounts (FODMAPs) can alter gut microflora.[1]
- Fermentation and osmotic effects of FODMAPs produce abdominal discomfort and diarrhea in IBS.
- FODMAPs yield carbon dioxide, methane, and hydrogen that are responsible for bloating.
- Osmotically active carbohydrate by products lead to diarrhea by enhancing intestinal contractions and precipitating fluid secretion.[2][3][4][5][6][7][8]
- Fermentable oligosaccharides, monosaccharides, disaccharides, and polyols (FODMAPs) are present in stone fruits, artificial sweeteners, lactose-containing foods, and legumes. Changes in diet such as increased amounts (FODMAPs) can alter gut microflora.[1]
- Infection
- Infectious gastroenteritis triggers micro inflammation and up to one third of irritable bowel syndrome cases follow acute gastroenteritis.
- Micro inflammation of the gut causes activation of the lymphocytes, mast cells and pro inflammatory cytokines that stimulate the enteric nervous system and lead to abnormal visceral and motor responses within the gastrointestinal tract.
- Immune activation due to GI infection also increases enteroendocrine cells, calprotectin-positive macrophages, intraepithelial lymphocytes, and lamina propria T cells which contribute directly to abdominal pain perception. [9][10][11][12][13][14][15][16][17]
- The role of small intestinal bacterial overgrowth syndrome is strongest when testing with glucose breath tests (relative risk = 4.2) or jejunal aspirates (relative risk = 3.0) are compared among patients with IBS and controls[18].
Intrinsic gastrointestinal factors
- Motor abnormalities:
- IBS is referred to as ‘spastic colon’ due to changes in colonic motor function.
- Manometry recordings from the transverse, descending and sigmoid colon have shown that IBS leads to altered colonic and small intestinal motor function, such as increased frequency and irregularity of luminal contractions.
- Motor changes lead to symptoms of diarrhea and constipation.[19][20][21]
- Diarrhea-prone IBS patients have increased responses to ingestion, CRH (corticotropin releasing hormone), CCK (cholecystokinin), which increase the peak amplitude of high-amplitude propagating contractions (HAPCs) and lead to abdominal discomfort with accelerated transit through the colon. [22][23][24][25][26]
- Constipation-prone IBS patients show fewer high-amplitude propagating contractions (HAPCs) as compared to diarrhea prone IBS patients, delayed transit through the colon and decreased motility.
- Changes in the motor function of the colon are responsible for producing the gastrointestinal symptoms of IBS such as altered bowel habits and abdominal pain.[25]
- Visceral hypersensitivity:
- IBS is associated with a decreased threshold for perception of visceral stimuli (i.e. visceral hypersensitivity)[25][27][28]
- Rectal distension produces painful and non-painful sensations at lower volumes in IBS patients as compared to healthy controls, suggesting the presence of afferent pathway disturbances in visceral innervation[29][30][31][32].
- Visceral hypersensitivity contributes to IBS by involving the following:
- Spinal hyperexcitability
- Secondary to activation of neurotransmitters such as:
- N-methyl D aspartate (NMDA) receptor
- Nitric oxide
- Activation of specific gastrointestinal mediators that lead to afferent nerve fiber sensitization:
- Central (brainstem and cortical) modulation with increased activation of anterior cingulate cortex, thalamus and insula.
- These structures are involved in processing of pain.
- Cortical and brain stem modulation translate into long term hypersensitivity due to neuroplasticity.
- Semi permanent changes(seen on functional magnetic resonance imaging and positron emission tomography) in the neural response to visceral stimulation contribute to visceral hypersensitivity.[27][33]
- Recruitment of peripheral silent nociceptors cause increased end organ sensitivity due to
- Hormonal activation ( increased serotonin affects gastrointestinal motility and visceral pain perception)
- Immune activation(recruitment of inflammatory mediators)[27]
- Spinal hyperexcitability
| Spinal hyperexcitability | Activation of • N-methyl D aspartate (NMDA) receptor • nitric oxide | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Central (brainstem and cortical) modulation | Increased activation of: • Anterior cingulate cortex • Thalamus • insula | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Visceral hypersensitivity | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Activation of specific gastrointestinal mediators | Kinins and serotonin activation lead to afferent nerve fiber sensitization | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Recruitment of peripheral silent nociceptors | Increased end organ sensitivity due to hormonal or immune activation | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
- Immune activation and mucosal inflammation
Mast cells IMMUNE ACTIVATION AND MUCOSAL INFLAMMATION Lymphocytes Proinflammatory cytokines - IBS in patients with history of inflammatory bowel disease, celiac disease or microscopic colitis points towards the fact that immune activation and local GI mucosal inflammation play an important role in its pathogenesis.[34][35][36][37][38][39][36]
- IBS patients have higher mucosal counts of lymphocytes (T cells, B cells), mast cells and immune mediators such as prostanoids, proteases, cytokines and histamines.[36][40][41][42][43]
- Lymphocytes:
- Activation of humoral immunity in IBS is specific for the gastrointestinal tract. Increased number of lymphocytes have been found in the small intestine and colon of IBS patients.[35][37][44][45]
- IBS patients with diarrhea have enhanced mucosal humoral activity, associated with activation and proliferation of B cells and immunoglobulin production, identified by microarray profiling.[45]
- IBS patients with severe disease have an increase in lymphocyte infiltration in the myentric plexus.[37]
- Mediators released by lymphocytes include histamine, proteases and nitric oxide. The stimulation of the enteric nervous system by these mediators leads to abnormal visceral and motor responses within the gastrointestinal tract.[35]
- Stool in patients with diarrhea prominent IBS demonstrates high levels of serine protease activity, which is produced by lymphocytes.[46][47]
- In response to high levels of serine protease, there is increased visceral pain and colonic cellular permeability. [46]
- Serine protease inhibitors prevent effects mediated by high levels of serine protease in IBS patients.[47][46]
- Mast cells:
- IBS leads to an increased number of mast cells in IBS patients in the jejunum, terminal ileum and colon.[39]
- Higher numbers of activated mast cells are found in proximity to colonic nerve fibres in the mucosa of the gastrointestinal tract of IBS patients. [39][38]
- Proinflammatory cytokines:
- Cytokines are protein mediators of the immune response. Increased levels of cytokines have been found in IBS patients.[42][43]
- Higher amounts of tumor necrosis factor are produced by the peripheral blood mononuclear cells of IBS patients.[36][48]
- Other cytokines such as interleukin 1β, interleukin 6, interleukin10, and TNFα are raised in IBS patients.
- Increased concentration of cytokines is directly proportional to the severity and frequency of pain.[36][48][49]
- The TNF antagonist infliximab counteracts pain in IBS patients, proving TNF involvement in mechanical hypersensitivity of the colonic afferent nerve endings.[49]
- Lymphocytes:
- Altered gut microbiota
- Fecal microflora in IBS patients differ from healthy individuals. Some IBS patients have colonic spirochaetosis, with a unique pathology of increased lymphoid follicles and eosinophils on histology.[40][50][51][52][53][54][13][55]
- Acute GI infection alters gut microflora switches on a T-helper-2 immune-cell response with increased numbers of CD8 and CD4RA-positive intraepithelial lymphocytes, causing increased susceptibility to the development of IBS. [56][57][58]
- Altered gut microbiota causes increased colonic hypersensitivity. [59]
- Abnormal serotonin pathways
- Serotonin(5-HT) is an important neurotransmitter produced by the enterochromaffin cells in the colon, in response to chemical stimuli (short chain fatty acids produced by gastrointestinal microflora ) and mechanical stimuli ( food) and is increased in IBS patients.[60][61][62][63][64][65][66]
- Serotonin affects gastrointestinal motility and visceral pain perception. Spontaneous release of 5-HT correlates with abdominal pain severity.[67]
- There is an established relationship between IBS and polymorphisms in the gene for serotonin transport causing alteration in intestinal peristalsis due to change in the serotonin reuptake efficacy.[68][69][70][71]
- Increased serotonin production contributes to postprandial symptoms in IBS patients, hence providing the rationale for the therapeutic efficacy of 5-HT 3 receptor antagonists and 5-HT 4 receptor agonists on symptoms in IBS patients.[72][73]
Psychosocial factors and CNS dysregulation
- Symptom exacerbation occurs in IBS patients with emotional disturbances,stress, anxiety or depression. Traumatic experiences before 18 years of age directly shape adult connectivity in the executive control network consisting of structures such as the insula, anterior cingulate cortex and the thalamus.
- Semipermanent/permanent changes in complex neural circuits lead to central pain amplification and contribute to abdominal pain in IBS patients.[74][75]
- The dorsolateral prefrontal cortex activity (responsible for vigilance and alertness of the human brain) and the mid-cingulate cortex (engaged in attention pathways and responses) is reduced in IBS patients, seen on advanced brain imaging techniques as irregularities in the mid- cingulate cortex and prefrontal cortex on diffusion tensor imaging. [76]
- prefrontal cortex modulation may lead to increased perception of visceral pain.
- Modulation of the mid-cingulate cortex is associated with alterations in the subjective sensations of pain.[77][78]
- Patients with IBS have aberrant processing of central information, with decreased feedback on the emotional arousal network that controls the autonomic activity of the gastrointestinal tract and changes gut motility.[79][80]
- IBS is a brain gut disorder as rectal distension in patients causes increased engagement of regions of the brain associated with attentional and behavioral responses.[77][81][82]
- Psychological stress also impacts the release of gut proinflammatory cytokines, contributing to pain in IBS patients.[34]
Genetic factors
- IBS has high twin concordance and familial aggregation:[83][84][85][86][87][88]
- IBS has higher concordance in monozygotic as compared to dizygotic twins.[83][84][85][89]
- Individuals with a biologic relative with IBS have two times a higher risk of developing IBS. [90]
- Single nucleotide polymorphisms (SNPs) in genes:
- IBS has SNPs in genes playing an important role in host-microbiota interaction (TLR9, IL-6 and CDH1), immune activation and epithelial barriers.
- SNPs cause inflammation and increased permeability of the GI tract, leading to abdominal discomfort and increased motility.[91][92]
- Mutation of type V (alpha subunit) of SCN5A-encoded voltage gated sodium channel causes IBS.[93][94]
- Genome wide DNA methylation profiling is impaired in IBS and this involves genes linked to neuropeptide hormone function and oxidative stress.[95]
- IBS causes mutation in the neuropeptide S receptor gene (NPSR1) involved in nociception, inflammation and anxiety with abdominal pain.[96]
- Genes involved in the regulation of hepatic bile acid synthesis such as a functional Klothoβ gene are mutated in IBS.[97][98]
- TNF polymorphisms:
- SNPs in tumour necrosis factor alpha (TNFα) and genes coding for superfamily member 15 (TNFSF15) have proven associations with IBS.[92][99][100]
- TNF polymorphisms are also associated with post infectious IBS such as rs4263839 in TNFSF15 and IBS, particularly IBS associated with constipation.[99][100]
Associated conditions
Several medical comorbidities appear with greater frequency in IBS patients.
Headache, Fibromyalgia, and Depression
IBS patients may be identified with comorbidities such as headache, fibromyalgia and depression.[101][102][103]
Inflammatory Bowel Disease
- IBS and IBD are interrelated diseases, as patients with IBD experience IBS-like symptoms when their IBD is in remission.[104][105][106]
- IBS is believed to be a type of low-grade inflammatory bowel disease as serum markers associated with inflammation have also been found in patients with IBS.[107]
- IBS patients are16.3 times more likely to develop IBD.[108]
Abdominal Surgery
- IBS patients are 87% more likely to undergo abdominal and pelvic surgery, and three times more likely to undergo gallbladder surgery.[109]
- IBS patients were twice as likely to undergo hysterectomy.[110]
Endometriosis
There is a statistically significant link between migraine headaches, IBS, and endometriosis.[111]
Medical conditions that accompany IBS
Several medical comorbidities appear with greater frequency in IBS patients.
Headache, Fibromyalgia, and Depression
IBS patients may be identified with comorbidities such as headache, fibromyalgia and depression.[102][103][112]
Inflammatory Bowel Disease
- IBS and IBD are interrelated diseases, as patients with IBD experience IBS-like symptoms when their IBD is in remission.[104][105][106]
- IBS is believed to be a type of low-grade inflammatory bowel disease as serum markers associated with inflammation have also been found in patients with IBS .[107]
- IBS patients are16.3 times more likely to develop IBD.[108]
Abdominal Surgery
- IBS patients are 87% more likely to undergo abdominal and pelvic surgery, and three times more likely to undergo gallbladder surgery.[109]
- IBS patients were twice as likely to undergo hysterectomy.[110]
Endometriosis
There is a statistically significant link between migraine headaches, IBS, and endometriosis.[111]
Gross Pathology
Microscopic Pathology
Microscopic changes that may be found in IBS patients are as follows:[37][39][60][113][16][114][115][116][117][118][119][120]
LOCATION LAYER OF INTESTINE INVOLVED MAST CELLS T LYMPHOCYTES ENTEROCHROMAFFIN CELLS Rectum Mucosa +++/- +/- +/- Terminal ileum Mucosa - ++ - Cecum Mucosa ++ - - Colon Muscularis externa +/- - - Jejunum Myentric plexus ++ - - References
- ↑ Muir JG, Gibson PR (2013). "The Low FODMAP Diet for Treatment of Irritable Bowel Syndrome and Other Gastrointestinal Disorders". Gastroenterol Hepatol (N Y). 9 (7): 450–2. PMC 3736783. PMID 23935555.
- ↑ Böhn L, Störsrud S, Törnblom H, Bengtsson U, Simrén M (2013). "Self-reported food-related gastrointestinal symptoms in IBS are common and associated with more severe symptoms and reduced quality of life". Am. J. Gastroenterol. 108 (5): 634–41. doi:10.1038/ajg.2013.105. PMID 23644955.
- ↑ Young E, Stoneham MD, Petruckevitch A, Barton J, Rona R (1994). "A population study of food intolerance". Lancet. 343 (8906): 1127–30. PMID 7910231.
- ↑ David LA, Maurice CF, Carmody RN, Gootenberg DB, Button JE, Wolfe BE, Ling AV, Devlin AS, Varma Y, Fischbach MA, Biddinger SB, Dutton RJ, Turnbaugh PJ (2014). "Diet rapidly and reproducibly alters the human gut microbiome". Nature. 505 (7484): 559–63. doi:10.1038/nature12820. PMC 3957428. PMID 24336217.
- ↑ Elli L, Tomba C, Branchi F, Roncoroni L, Lombardo V, Bardella MT, Ferretti F, Conte D, Valiante F, Fini L, Forti E, Cannizzaro R, Maiero S, Londoni C, Lauri A, Fornaciari G, Lenoci N, Spagnuolo R, Basilisco G, Somalvico F, Borgatta B, Leandro G, Segato S, Barisani D, Morreale G, Buscarini E (2016). "Evidence for the Presence of Non-Celiac Gluten Sensitivity in Patients with Functional Gastrointestinal Symptoms: Results from a Multicenter Randomized Double-Blind Placebo-Controlled Gluten Challenge". Nutrients. 8 (2): 84. doi:10.3390/nu8020084. PMC 4772047. PMID 26867199.
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