General Information of Disease (ID: DIS27206)

Disease Name Irritable bowel syndrome
Synonyms psychogenic IBS; irritable bowel syndrome; irritable colon; IBS; mucus colitis; spastic colon; IBD
Disease Class DD91: Irritable bowel syndrome
Definition
Irritable bowel syndrome (IBS) is a chronic functional condition of the lower gastrointestinal (GI) tract characterized by abdominal pain or discomfort and disordered bowel habit (diarrhea, constipation, or fluctuation between the two).
Disease Hierarchy
DIS6SVEE: Syndromic disease
DISGPMUQ: Intestinal disorder
DIS27206: Irritable bowel syndrome
ICD Code
ICD-11
ICD-11: DD91.0
ICD-10
ICD-10: K55-K64, K58
ICD-9
ICD-9: 564.1, 787.91
Expand ICD-11
'DD91.0
Expand ICD-10
'K55-K64; 'K58
Expand ICD-9
564.1,787.91
Disease Identifiers
MONDO ID
MONDO_0005052
MESH ID
D043183
UMLS CUI
C0022104
MedGen ID
5897
SNOMED CT ID
10743008

Drug-Interaction Atlas (DIA) of This Disease

Drug-Interaction Atlas (DIA)
This Disease is Treated as An Indication in 23 Approved Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
Alosetron DML2A03 Approved Small molecular drug [1]
AST-120 DM718MD Approved Small molecular drug [2]
Calcium polycarbophil DMU381I Approved NA [2]
Chlordiazepoxide DMTN5XI Approved Small molecular drug [3]
Clidinium DMUMQZ0 Approved Small molecular drug [4]
Dicyclomine DMZSDGX Approved Small molecular drug [5]
Drotaverine DM96FA1 Approved Small molecular drug [2]
Homatropine Methylbromide DMGBPSH Approved Small molecular drug [6]
Ispaghula DMWCRN1 Approved NA [7]
Linaclotide DM4EGV0 Approved Small molecular drug [8]
MD-1100 DM4IAKR Approved Small molecular drug [7]
Mebeverine DMNOBFQ Approved Small molecular drug [7]
Methantheline DM8X4A1 Approved Small molecular drug [2]
Milnacipran DMBFE74 Approved Small molecular drug [9]
Plecanatide DMKEX7O Approved Small molecular drug [10]
Prifinium DMMZB0K Approved Small molecular drug [2]
R0-93877 DMM4U9G Approved Small molecular drug [11]
Ramosetron DMH7GN8 Approved Small molecular drug [12]
Scopolamine DMOM8AL Approved Small molecular drug [13]
Sulfasalazine DMICA9H Approved Small molecular drug [2]
Tegaserod DM3XYD1 Approved Small molecular drug [2]
Tenapanor DMCOZJY Approved Small molecular drug [14]
Trimebutine DMPYQ7B Approved Small molecular drug [2]
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⏷ Show the Full List of 23 Drug(s)
This Disease is Treated as An Indication in 23 Clinical Trial Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
Cilansetron DMP0NGX Phase 3 Small molecular drug [15]
Ibodutant DMT67EH Phase 3 Small molecular drug [16]
M-17 E. Coli DMJ0864 Phase 3 NA [17]
Pinaverium bromide DM7OSHC Phase 3 Small molecular drug [7]
Renzapride DM7HQNX Phase 3 Small molecular drug [18]
Arverapamil DML27AE Phase 2 Small molecular drug [7]
ASP-7147 DMGDF2X Phase 2 NA [19]
Blautix DMCP3YO Phase 2 Live biotherapeutic [20]
DDP-225 DM9REBL Phase 2 Small molecular drug [7]
Dextofisopam DM9L15R Phase 2 Small molecular drug [7]
GTP-010 DMN6IDO Phase 2 NA [7]
LX-1031 DMZ2XAP Phase 2 Small molecular drug [21]
LX-1033 DM5PK9S Phase 2 NA [22]
ONO-2952 DMOGYQ0 Phase 2 NA [23]
ORP-101 DMSH20P Phase 2 Small molecule [24]
Pumosetrag DMBUSNL Phase 2 Small molecular drug [7]
SB-207266A DM27KFY Phase 2 Small molecular drug [25]
Talnetant DMQKZDT Phase 2 Small molecular drug [26]
TC-6499-12 DMWPI2U Phase 2 NA [27]
Tofisopam DMTGNWU Phase 2 Small molecular drug [28]
CIN-103 DMTB925 Phase 1 Small molecule [29]
DA-6886 DMKPAOD Phase 1 NA [30]
RWJ-68023 DM4O07Q Phase 1 NA [31]
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⏷ Show the Full List of 23 Drug(s)
This Disease is Treated as An Indication in 6 Discontinued Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
DNK-333 DM4ZO01 Discontinued in Phase 2 Small molecular drug [32]
Ezlopitant DMTUPZ2 Discontinued in Phase 2 Small molecular drug [33]
Fabesetron DMMSFK0 Discontinued in Phase 2 Small molecular drug [34]
GW876008 DMAXRBI Discontinued in Phase 2 Small molecular drug [35]
SLV-323 DMHRYX6 Discontinued in Phase 1 NA [36]
SR-58878 DMS9EJ5 Terminated NA [37]
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⏷ Show the Full List of 6 Drug(s)
This Disease is Treated as An Indication in 2 Preclinical Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
ATI-17000 DMZJVR5 Preclinical Small molecular drug [7]
SLV-332 DMY9DA3 Preclinical Small molecular drug [7]
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This Disease is Treated as An Indication in 6 Investigative Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
ALB-137391(a) DMYKI8T Investigative NA [38]
ATB-284 DMA7N9G Investigative NA [38]
LPG-1030S DM8AHQE Investigative NA [38]
MLR-1045 DMYEO1V Investigative NA [38]
R-1 DMK0YP7 Investigative Small molecular drug [39]
RQ-00310941 DMYK6OU Investigative NA [39]
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⏷ Show the Full List of 6 Drug(s)

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 69 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
CNR1 TT6OEDT Limited Biomarker [40]
COMT TTKWFB8 Limited Genetic Variation [41]
F2RL1 TTQR74A Limited Biomarker [42]
GLP1R TTVIMDE Limited Biomarker [43]
GUCY2C TTLDPRG Limited Biomarker [44]
IL23R TT6H4QR Limited Genetic Variation [45]
PYY TTVFJLX Limited Biomarker [46]
SCN5A TTZOVE0 Limited Genetic Variation [47]
TRPV1 TTMI6F5 Disputed Biomarker [48]
CRHR1 TT7EFHR moderate Biomarker [49]
ADCY1 TTV1ZSQ Strong Biomarker [50]
ADORA2B TTNE7KG Strong Altered Expression [51]
ADRA2A TTWG9A4 Strong Genetic Variation [52]
ANK1 TTKFPMH Strong Biomarker [53]
CCR9 TTIPS8B Strong Altered Expression [54]
CFP TTLA0VS Strong Genetic Variation [55]
CHRNA5 TTH2QRX Strong Biomarker [56]
CNR2 TTMSFAW Strong Biomarker [57]
CRHR2 TTIY658 Strong Altered Expression [58]
CSF2RA TT6MP2Z Strong Biomarker [59]
FAP TTGPQ0F Strong Biomarker [60]
FDXR TT3W4IX Strong Genetic Variation [61]
FGF19 TTGCH11 Strong Biomarker [62]
FGFR4 TT1KX2S Strong Biomarker [63]
GCG TT6Y4PN Strong Biomarker [43]
GFRA3 TT63XRS Strong Biomarker [64]
GHSR TTWDC17 Strong Genetic Variation [65]
GNRH1 TT0ID4A Strong Biomarker [66]
GPBAR1 TTSDVTR Strong Biomarker [67]
GRIA1 TTVPQTF Strong Biomarker [68]
GRM7 TT0I76D Strong Biomarker [69]
HTR1B TTK8CXU Strong Biomarker [70]
HTR2A TTJQOD7 Strong Genetic Variation [71]
HTR2B TT0K1SC Strong Biomarker [72]
HTR3A TTPC4TU Strong Biomarker [73]
HTR4 TT07C3Y Strong Biomarker [74]
HTR7 TTO9X1H Strong Biomarker [75]
IL10 TTT0Q1F Strong Genetic Variation [76]
KCNQ4 TT8HGRW Strong Altered Expression [77]
KCNQ5 TTWVL5Q Strong Genetic Variation [77]
KLB TTARBVH Strong Genetic Variation [78]
LANCL2 TTMK3EX Strong Altered Expression [79]
LCT TTA0OSE Strong Genetic Variation [80]
MAGEC2 TTKGUEB Strong Biomarker [81]
MCM6 TTQGKSD Strong Genetic Variation [82]
MRGPRX2 TT3YV20 Strong Genetic Variation [83]
MYLK2 TTHLGB2 Strong Biomarker [84]
NLRX1 TTKT026 Strong Biomarker [85]
NOD2 TTYPUHA Strong Biomarker [86]
NPR3 TTWVLS6 Strong Biomarker [87]
OPRK1 TTQW87Y Strong Biomarker [88]
PEPD TTLZXI0 Strong Biomarker [89]
PLK2 TT976FS Strong Biomarker [81]
PRKCD TT7A1BO Strong Genetic Variation [90]
PRSS1 TT2WR1T Strong Biomarker [91]
PTPN2 TTY8PUS Strong Genetic Variation [92]
RPSA TTLUW5B Strong Biomarker [93]
SCG3 TTY5R9H Strong Biomarker [94]
SIRPA TTBRJS9 Strong Altered Expression [95]
SLC5A7 TTRV7W3 Strong Biomarker [96]
SSX2IP TTZXB07 Strong Altered Expression [97]
TESK1 TTWKT3Y Strong Posttranslational Modification [98]
TLR5 TTCXP8J Strong Altered Expression [99]
TNFRSF17 TTZ3P4W Strong Genetic Variation [100]
TNFRSF25 TTDV6BQ Strong Altered Expression [101]
TPH2 TT3KLDP Strong Genetic Variation [41]
TPSAB1 TTM1TDX Strong Biomarker [102]
TST TT51OTS Strong Biomarker [103]
XDH TT7RJY8 Strong Altered Expression [104]
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⏷ Show the Full List of 69 DTT(s)
This Disease Is Related to 1 DTP Molecule(s)
Gene Name DTP ID Evidence Level Mode of Inheritance REF
SLC26A2 DTFSLX5 Strong Genetic Variation [105]
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This Disease Is Related to 3 DME Molecule(s)
Gene Name DME ID Evidence Level Mode of Inheritance REF
FAAH DEUM1EX Limited Biomarker [40]
SI DE5EO4Y Limited Genetic Variation [106]
TPMT DEFQ8VO Limited Genetic Variation [107]
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This Disease Is Related to 67 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
ACAD8 OT3JI5GB Limited Altered Expression [108]
ATG16L1 OTEOYC5D Limited Genetic Variation [109]
C1QL1 OTNQ0G3E Limited Biomarker [110]
ITGAX OTOGIMHE Limited Altered Expression [111]
NLRP6 OTEREN4W Limited Biomarker [110]
OR2AG1 OTEITRP4 Limited Altered Expression [112]
PRSS3 OTN3S5YB Limited Altered Expression [113]
ACSBG1 OTM040MW Strong Biomarker [114]
APOL2 OT303Q7B Strong Biomarker [115]
AQP6 OTXS6UYY Strong Genetic Variation [116]
AQP8 OT99JKME Strong Altered Expression [117]
BCLAF1 OT7T8H6A Strong Altered Expression [118]
CCL16 OTOOQI1F Strong Altered Expression [119]
CDAN1 OTCVZRG6 Strong Biomarker [120]
CELA3A OT9JAL80 Strong Biomarker [121]
CLCN5 OT9YXZSO Strong Altered Expression [122]
CLDN1 OT27KV99 Strong Altered Expression [123]
CLDN2 OTRF3D6Y Strong Altered Expression [124]
COPE OTBKHBT7 Strong Biomarker [125]
CT83 OTQEGHAB Strong Genetic Variation [80]
ENDOU OTB7OF7Y Strong Altered Expression [126]
ETFA OTXX61VZ Strong Biomarker [127]
EXOSC6 OTAC10N6 Strong Altered Expression [126]
FATE1 OTPYXV64 Strong Genetic Variation [80]
FCRL3 OTIFXFWL Strong Biomarker [128]
FLVCR1 OT9XCFOC Strong Biomarker [129]
GSDMB OTWA7P10 Strong Genetic Variation [130]
HGD OTTKLQOO Strong Biomarker [131]
HTR3E OTIWF1R5 Strong Biomarker [132]
IKBKG OTNWJWSD Strong Therapeutic [133]
IRGM OTKD3O5Z Strong Biomarker [134]
ITM2B OTMXEPXB Strong Biomarker [135]
KALRN OT8WRCBH Strong Biomarker [136]
KIR2DL5A OT09FZE1 Strong Biomarker [137]
KIR2DL5B OTSV0JL9 Strong Biomarker [137]
KIR2DS5 OTXLEN11 Strong Genetic Variation [137]
KIR3DS1 OTJWIO4T Strong Genetic Variation [137]
LTO1 OTQ17ZDT Strong Biomarker [138]
MAGI2 OTXDDKZS Strong Biomarker [139]
MAST3 OT6VVQ84 Strong Biomarker [140]
MLXIPL OTR9MLLW Strong Biomarker [141]
MOS OTNMQPFJ Strong Genetic Variation [142]
MYLK3 OTC58V2Q Strong Biomarker [84]
NAPSA OT6F8IAL Strong Genetic Variation [108]
NCF2 OTAUW7L2 Strong Genetic Variation [143]
NEUROG3 OT6DIPWC Strong Biomarker [144]
NKX2-3 OTF4IL5J Strong Genetic Variation [145]
NMS OTFYS4LO Strong Biomarker [146]
NUDT15 OTX8SZOT Strong Genetic Variation [147]
NXPH1 OTGKX860 Strong Genetic Variation [105]
OXT OT48M72Z Strong Genetic Variation [148]
PACC1 OTKBS8CC Strong Biomarker [149]
PDIA3 OTHPQ0Q3 Strong ModifyingMutation [150]
PELI1 OTMLBCLC Strong Genetic Variation [151]
PIEZO2 OTQ7AT38 Strong Biomarker [152]
PRDM6 OTKY12D9 Strong Genetic Variation [151]
PROK2 OT70IFEZ Strong Biomarker [153]
RAN OT2TER5M Strong Biomarker [154]
RARRES2 OT1BJE8K Strong Biomarker [155]
REM1 OTUXL0HC Strong Biomarker [156]
RNF183 OTWPNZF9 Strong Altered Expression [157]
S100A10 OTI71243 Strong Altered Expression [70]
STH OTK8ULTH Strong Altered Expression [108]
SUMF2 OT37I8JL Strong Genetic Variation [158]
SYNM OTOI8TRJ Strong Biomarker [159]
TRAF3IP2 OTLLZERL Strong Genetic Variation [160]
AGA OTNWT1WB Definitive Biomarker [127]
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⏷ Show the Full List of 67 DOT(s)

References

1 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 2296).
2 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services. 2015
3 Chlordiazepoxide FDA Label
4 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 366).
5 Dicyclomine FDA Label
6 Homatropine Methylbromide FDA Label
7 Emerging drugs for irritable bowel syndrome. Expert Opin Emerg Drugs. 2006 May;11(2):293-313.
8 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 5017).
9 Levomilnacipran FDA Label
10 2017 FDA drug approvals.Nat Rev Drug Discov. 2018 Feb;17(2):81-85.
11 2018 FDA drug approvals.Nat Rev Drug Discov. 2019 Feb;18(2):85-89.
12 ClinicalTrials.gov (NCT01225237) A Study to Evaluate Efficacy of Ramosetron on Diarrhea-predominant Irritable Bowel Syndrome (IBS) in Male Patients. U.S. National Institutes of Health.
13 Scopolamine FDA Label
14 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2019
15 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 2297).
16 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 2117).
17 ClinicalTrials.gov (NCT00324532) to Assess the Efficacy and Safety of the Probiotic E. Coli Strain M17 on Patients With GERD. U.S. National Institutes of Health.
18 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 244).
19 ClinicalTrials.gov (NCT01896583) A Phase 2 Pilot Study to Assess ASP7147 in Patients With Diarrhea Predominant Irritable Bowel Syndrome (IBS-D). U.S. National Institutes of Health.
20 ClinicalTrials.gov (NCT03721107) A Phase II Randomized, Double Blind, Placebo-controlled, Parallel Group, Multicenter Study to Evaluate the Safety and Efficacy of Repeated Oral Doses of Blautix in Adult Subjects With Irritable Bowel Syndrome (IBS) Subtypes IBS-C and IBS-D. U.S.National Institutes of Health.
21 ClinicalTrials.gov (NCT00813098) Study of LX1031 in Subjects With Non-Constipating Irritable Bowel Syndrome. U.S. National Institutes of Health.
22 ClinicalTrials.gov (NCT01494233) A Multi-Center Trial to Determine the Safety and Efficacy of LX1033 in Subjects With Diarrhea-Predominant Irritable Bowel Syndrome. U.S. National Institutes of Health.
23 ClinicalTrials.gov (NCT01887002) Study to Evaluate the Effects of ONO-2952 on Pain Perception Produced by Rectal Distention in Female Subjects With Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D). U.S. National Institutes of Health.
24 ClinicalTrials.gov (NCT04129619) A Double-Blind, Placebo-Controlled, Phase 2, Responsive Adaptive Randomization Study of ORP-101 in Patients With Irritable Bowel Syndrome With Diarrhea (IBS-D). U.S.National Institutes of Health.
25 Clinical pipeline report, company report or official report of Department of Pharmacology University of Wisconsin School of Medicine.
26 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 2132).
27 ClinicalTrials.gov (NCT01149200) Proof-of-Principle Study of TC-6499 in the Treatment of Constipation Predominant Irritable Bowel Syndrome (IBS). U.S. National Institutes of Health.
28 ClinicalTrials.gov (NCT00486876) A Study of 3 Doses of Dextofisopam in Females With Irritable Bowel Syndrome. U.S. National Institutes of Health.
29 Clinical pipeline report, company report or official report of Cinphloro
30 ClinicalTrials.gov (NCT01633723) Phase I Clinical Trial of DA-6886 in Healthy Male Subjects. U.S. National Institutes of Health.
31 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800021456)
32 Emerging drugs for the treatment of chronic obstructive pulmonary disease. Expert Opin Emerg Drugs. 2006 May;11(2):275-91.
33 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 5751).
34 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800001434)
35 Novel drugs and therapeutic targets for severe mood disorders. Neuropsychopharmacology. 2008 Aug;33(9):2080-92.
36 Emerging drugs for chemotherapy-induced emesis. Expert Opin Emerg Drugs. 2006 Mar;11(1):137-51.
37 Clinical pipeline report, company report or official report of Sanofi-Synthelabo.
38 The ChEMBL database in 2017. Nucleic Acids Res. 2017 Jan 4;45(D1):D945-D954.
39 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 7).
40 Association of cannabinoid type 1 receptor and fatty acid amide hydrolase genetic polymorphisms in Chinese patients with irritable bowel syndrome.J Gastroenterol Hepatol. 2014 Jun;29(6):1186-91. doi: 10.1111/jgh.12513.
41 Association of Fatigue With TPH2 Genetic Polymorphisms in Women With Irritable Bowel Syndrome.Biol Res Nurs. 2019 Jan;21(1):72-79. doi: 10.1177/1099800418806055. Epub 2018 Oct 11.
42 Protease Activated Receptor-2 Induces Immune Activation and Visceral Hypersensitivity in Post-infectious Irritable Bowel Syndrome Mice.Dig Dis Sci. 2019 Mar;64(3):729-739. doi: 10.1007/s10620-018-5367-y. Epub 2018 Nov 16.
43 The Glucagon-like peptide-1 receptor agonist, exendin-4, ameliorated gastrointestinal dysfunction in the Wistar Kyoto rat model of Irritable Bowel Syndrome.Neurogastroenterol Motil. 2020 Feb;32(2):e13738. doi: 10.1111/nmo.13738. Epub 2019 Oct 11.
44 Guanylate cyclase-C as a therapeutic target in gastrointestinal disorders.Gut. 2018 Aug;67(8):1543-1552. doi: 10.1136/gutjnl-2018-316029. Epub 2018 Mar 21.
45 Candidate single nucleotide polymorphisms of irritable bowel syndrome: a systemic review and meta-analysis.BMC Gastroenterol. 2019 Oct 15;19(1):165. doi: 10.1186/s12876-019-1084-z.
46 Possible role of peptide YY (PYY) in the pathophysiology of irritable bowel syndrome (IBS).Neuropeptides. 2020 Feb;79:101973. doi: 10.1016/j.npep.2019.101973. Epub 2019 Oct 24.
47 Irritable bowel syndrome patients have SCN5A channelopathies that lead to decreased Na(V)1.5 current and mechanosensitivity.Am J Physiol Gastrointest Liver Physiol. 2018 Apr 1;314(4):G494-G503. doi: 10.1152/ajpgi.00016.2017. Epub 2017 Nov 22.
48 Bile acids induce visceral hypersensitivity via mucosal mast cell-to-nociceptor signaling that involves the farnesoid X receptor/nerve growth factor/transient receptor potential vanilloid 1 axis.FASEB J. 2019 Feb;33(2):2435-2450. doi: 10.1096/fj.201800935RR. Epub 2018 Sep 27.
49 Brain and Gut CRF Signaling: Biological Actions and Role in the Gastrointestinal Tract.Curr Mol Pharmacol. 2018;11(1):51-71. doi: 10.2174/1874467210666170224095741.
50 Cyclic AMP-dependent positive feedback signaling pathways in the cortex contributes to visceral pain.J Neurochem. 2020 Apr;153(2):252-263. doi: 10.1111/jnc.14903. Epub 2020 Feb 9.
51 The role of mechanical forces and adenosine in the regulation of intestinal enterochromaffin cell serotonin secretion.Am J Physiol Gastrointest Liver Physiol. 2012 Feb 1;302(3):G397-405. doi: 10.1152/ajpgi.00087.2011. Epub 2011 Oct 28.
52 Association of alpha 2A adrenergic receptor gene (ADRAlpha2A) polymorphism with irritable bowel syndrome, microscopic and ulcerative colitis.Clin Chim Acta. 2010 Jan;411(1-2):59-63. doi: 10.1016/j.cca.2009.10.003. Epub 2009 Oct 13.
53 Histamine-mediated potentiation of transient receptor potential (TRP) ankyrin 1 and TRP vanilloid 4 signaling in submucosal neurons in patients with irritable bowel syndrome.Am J Physiol Gastrointest Liver Physiol. 2019 Mar 1;316(3):G338-G349. doi: 10.1152/ajpgi.00116.2018. Epub 2019 Jan 10.
54 Immunohistochemical staining with chemokine panel of non-specific colitis predicts future IBD diagnosis.Cytokine. 2020 Mar;127:154935. doi: 10.1016/j.cyto.2019.154935. Epub 2019 Nov 27.
55 Altered Brain Structure and Functional Connectivity and Its Relation to Pain Perception in Girls With Irritable Bowel Syndrome.Psychosom Med. 2019 Feb/Mar;81(2):146-154. doi: 10.1097/PSY.0000000000000655.
56 Smoking Interacts With CHRNA5, a Nicotinic Acetylcholine Receptor Subunit Gene, to Influence the Risk of IBD-Related Surgery.Inflamm Bowel Dis. 2018 Apr 23;24(5):1057-1064. doi: 10.1093/ibd/izx094.
57 Activation of cannabinoid 2 receptor relieves colonic hypermotility in a rat model of irritable bowel syndrome.Neurogastroenterol Motil. 2019 Jun;31(6):e13555. doi: 10.1111/nmo.13555. Epub 2019 Feb 21.
58 The comprehensive pathophysiological changes in a novel rat model of postinflammatory visceral hypersensitivity.FASEB J. 2019 Dec;33(12):13560-13571. doi: 10.1096/fj.201901489R. Epub 2019 Sep 28.
59 Defective leukocyte GM-CSF receptor (CD116) expression and function in inflammatory bowel disease.Gastroenterology. 2011 Jul;141(1):208-16. doi: 10.1053/j.gastro.2011.03.060. Epub 2011 Apr 7.
60 Increased Gut Permeability in First-degree Relatives of Children with Irritable Bowel Syndrome or Functional Abdominal Pain.Clin Gastroenterol Hepatol. 2020 Feb;18(2):375-384.e1. doi: 10.1016/j.cgh.2019.05.011. Epub 2019 May 14.
61 Candidate genes and sensory functions in health and irritable bowel syndrome.Am J Physiol Gastrointest Liver Physiol. 2008 Aug;295(2):G219-25. doi: 10.1152/ajpgi.90202.2008. Epub 2008 May 29.
62 Bile and fat excretion are biomarkers of clinically significant diarrhoea and constipation in irritable bowel syndrome.Aliment Pharmacol Ther. 2019 Mar;49(6):744-758. doi: 10.1111/apt.15106. Epub 2019 Feb 10.
63 Irritable bowel syndrome-diarrhea: characterization of genotype by exome sequencing, and phenotypes of bile acid synthesis and colonic transit.Am J Physiol Gastrointest Liver Physiol. 2014 Jan 1;306(1):G13-26. doi: 10.1152/ajpgi.00294.2013. Epub 2013 Nov 7.
64 Effect of moxibustion on the expression of GDNF and its receptor GFR3 in the colon and spinal cord of rats with irritable bowel syndrome.Acupunct Med. 2019 Aug;37(4):244-251. doi: 10.1136/acupmed-2017-011455. Epub 2019 Jun 12.
65 GHSR-1 agonist sensitizes rat colonic intrinsic and extrinsic neurons to exendin-4: A role in the manifestation of postprandial gastrointestinal symptoms in irritable bowel syndrome?.Neurogastroenterol Motil. 2019 Oct;31(10):e13684. doi: 10.1111/nmo.13684. Epub 2019 Jul 16.
66 Gonadotropin-Releasing Hormone and Its Role in the Enteric Nervous System.Front Endocrinol (Lausanne). 2017 Jun 7;8:110. doi: 10.3389/fendo.2017.00110. eCollection 2017.
67 Genetic variation in GPBAR1 predisposes to quantitative changes in colonic transit and bile acid excretion.Am J Physiol Gastrointest Liver Physiol. 2014 Sep 1;307(5):G508-16. doi: 10.1152/ajpgi.00178.2014. Epub 2014 Jul 10.
68 Hippocampal AMPARs involve the central sensitization of rats with irritable bowel syndrome.Brain Behav. 2017 Feb 22;7(3):e00650. doi: 10.1002/brb3.650. eCollection 2017 Mar.
69 Activating metabotropic glutamate receptor? attenuates visceral hypersensitivity in neonatal maternally separated rats.Int J Mol Med. 2019 Feb;43(2):761-770. doi: 10.3892/ijmm.2018.4022. Epub 2018 Dec 11.
70 S100A expression and interleukin-10 polymorphisms are associated with ulcerative colitis and diarrhea predominant irritable bowel syndrome.Dig Dis Sci. 2013 Aug;58(8):2314-23. doi: 10.1007/s10620-013-2677-y. Epub 2013 Apr 18.
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99 Expression of Toll-like Receptors, Pro-, and Anti-inflammatory Cytokines in Relation to Gut Microbiota in Irritable Bowel Syndrome: The Evidence for Its Micro-organic Basis.J Neurogastroenterol Motil. 2018 Oct 1;24(4):628-642. doi: 10.5056/jnm18130.
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154 Gastrointestinal Adverse Events of Cannabinoid 1 Receptor Inverse Agonists suggest their Potential Use in Irritable Bowel Syndrome with Constipation: A Systematic Review and Meta-Analysis.J Gastrointestin Liver Dis. 2019 Dec 9;28(4):473-481. doi: 10.15403/jgld-265.
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