Altered profiles of fecal metabolites correlate with visceral hypersensitivity and may contribute to symptom severity of diarrhea-predominant irritable bowel syndrome
Open accessAbstract
BACKGROUND: Fecal metabolites are associated with gut visceral sensitivity, mucosal immune function and intestinal barrier function, all of which have critical roles in the pathogenesis of irritable bowel syndrome (IBS). However, the metabolic profile and pathophysiology of IBS are still unclear. We hypothesized that altered profiles of fecal metabolites might be involved in the pathogenesis of IBS with predominant diarrhea (IBS-D). AIM: To investigate the fecal metabolite composition and the role of metabolites in IBS-D pathophysiology. METHODS: Thirty IBS-D patients and 15 age- and sex-matched healthy controls (HCs) underwent clinical and psychological assessments, including the IBS Symptom Severity System (IBS-SSS), an Italian modified version of the Bowel Disease Questionnaire, the Bristol Stool Form Scale (BSFS), the Hospital Anxiety and Depression Scale, and the Visceral Sensitivity Index. Visceral sensitivity to rectal distension was tested using high-resolution manometry system by the same investigator. Fecal metabolites, including amino acids and organic acids, were measured by targeted metabolomics approaches. Correlation analyses between these parameters were performed. RESULTS: < 0.001). In this regression model, the levels of Tyr, Val, hexanoate, fumarate, and pyruvate were significantly associated with the symptom severity of IBS-D. Furthermore, visceral sensation, including abdominal pain and visceral hypersensitivity, was correlated with isovalerate, valerate and isohexanoate. CONCLUSION: increasing visceral sensitivity.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In patients with irritable bowel syndrome, concentrations of isovalerate and valerate were positively associated with abdominal pain and hypersensitivity.
“In patients with irritable bowel syndrome, concentrations of isovalerate and valerate were positively associated with abdominal pain and hypersensitivity (385).”
From Diet and the Microbiota–Gut–Brain Axis: Sowing the Seeds of Good Mental Health (2021) · cites this paper as [385]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The Hospital Anxiety and Depression Scale
Zigmond, A. S., & Snaith, R. P. (1983) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.1983.tb09716.x · Cited by 47,139 · see citing works
Depression and quality of life in older persons: A review
Sivertsen, H., Bjørkløf, G. H., Engedal, K., Selbæk, G., & Helvik, A.-S. (2015) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000437299 · Cited by 14,152 · see citing works
The validity of the Hospital Anxiety and Depression Scale
Bjelland, I., Dahl, A. A., Haug, T. T., & Neckelmann, D. (2002) · Journal of Psychosomatic Research · doi:10.1016/s0022-3999(01)00296-3 · Cited by 9,779 · see citing works
Changes of Intestinal Functions in Liver Cirrhosis
Fukui, H., & Wiest, R. (2016) · Inflammatory Intestinal Diseases · doi:10.1159/000444436 · Cited by 6,820 · see citing works
Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells
Furusawa, Y., Obata, Y., Fukuda, S., Endo, T. A., Nakato, G., Takahashi, D., Nakanishi, Y., Uetake, C., Kato, K., Kato, T., et al. (2013) · Nature · doi:10.1038/nature12721 · Cited by 5,549 · see citing works
Longstreth, G. F., Thompson, W. G., Chey, W. D., Houghton, L. A., Mearin, F., & Spiller, R. C. (2006) · Gastroenterology · doi:10.1053/j.gastro.2005.11.061 · Cited by 4,856 · see citing works
Amino acids: Metabolism, functions, and nutrition
Wu, G. (2009) · Amino Acids · doi:10.1007/s00726-009-0269-0 · Cited by 3,004 · see citing works
Lacy, B. E., Mearin, F., Chang, L., Chey, W. D., Lembo, A. J., Simren, M., & Spiller, R. (2016) · Gastroenterology · doi:10.1053/j.gastro.2016.02.031 · Cited by 2,866 · see citing works
The role of short chain fatty acids in health and disease
Tan, J., McKenzie, C., Potamitis, M., Thorburn, A. N., Mackay, C. R., & Macia, L. (2014) · Advances in immunology · doi:10.1016/b978-0-12-800100-4.00003-9 · Cited by 2,425 · see citing works
Regulation of inflammation by short chain fatty acids
Vinolo, M. A. R., Rodrigues, H. G., Nachbar, R. T., & Curi, R. (2011) · Nutrients · doi:10.3390/nu3100858 · Cited by 1,724 · see citing works
FRANCIS, C. Y., MORRIS, J., & WHORWELL, P. J. (1997) · Alimentary Pharmacology & Therapeutics · doi:10.1046/j.1365-2036.1997.142318000.x · Cited by 1,708 · see citing works
De Filippis, F., Pellegrini, N., Vannini, L., Jeffery, I. B., La Storia, A., Laghi, L., Serrazanetti, D. I., Di Cagno, R., Ferrocino, I., Lazzi, C., et al. (2016) · Gut · doi:10.1136/gutjnl-2015-309957 · Cited by 1,638 · see citing works
Epithelial-cell recognition of commensal bacteria and maintenance of immune homeostasis in the gut
Artis, D. (2008) · Nature reviews. Immunology · doi:10.1038/nri2316 · Cited by 1,136 · see citing works
Immunity, Inflammation, and Allergy in the Gut
MacDonald, T. T., & Monteleone, G. (2005) · Science · doi:10.1126/science.1106442 · Cited by 1,035 · see citing works
Enterochromaffin cells are gut chemosensors that couple to sensory neural pathways
Bellono, N. W., Bayrer, J. R., Leitch, D. B., Castro, J., Zhang, C., O’Donnell, T. A., Brierley, S. M., Ingraham, H. A., & Julius, D. (2017) · Cell · doi:10.1016/j.cell.2017.05.034 · Cited by 910 · see citing works
Hungin, A. P. S., Whorwell, P. J., Tack, J. F., & Mearin, F. (2003) · Alimentary Pharmacology & Therapeutics · doi:10.1046/j.1365-2036.2003.01456.x · Cited by 774 · see citing works
Homeostasis of the gut barrier and potential biomarkers
Wells, J. M., Brummer, R. J., Derrien, M., MacDonald, T. T., Troost, F. J., Cani, P. D., Théodorou, V., Dekker, J. P., Méheust, A., de Vos, W. M., et al. (2016) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00048.2015 · Cited by 616 · see citing works
Furness, J. B., Rivera, L. R., Cho, H., Bravo, D. M., & Callaghan, B. P. (2013) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2013.180 · Cited by 549 · see citing works
De Palma, G., Lynch, M. D. J., Lu, J., Dang, V. T., Deng, Y., Jury, J., Umeh, G., Miranda, P. M., Pigrau Pastor, M., Sidani, S., et al. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aaf6397 · Cited by 505 · see citing works
Neuroepithelial circuit formed by innervation of sensory enteroendocrine cells
Bohórquez, D. V., Shahid, R. A., Erdmann, A., Kreger, A. M., Wang, Y., Calakos, N., Wang, F., & Liddle, R. A. (2015) · Journal of Clinical Investigation · doi:10.1172/jci78361 · Cited by 484 · see citing works
Labus, J. S., Bolus, R., Chang, L., Wiklund, I., Naesdal, J., Mayer, E. A., & Naliboff, B. D. (2004) · Alimentary Pharmacology & Therapeutics · doi:10.1111/j.1365-2036.2004.02007.x · Cited by 475 · see citing works
tana, C., umesaki, Y., imaoka, A., handa, T., kanazawa, M., & fukudo, S. (2009) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2009.01427.x · Cited by 474 · see citing works
A Patient Questionnaire to Identify Bowel Disease
Talley, N. J., Phillips, S. F., Melton, L. J., Wiltgen, C., & Zinsmeister, A. R. (1989) · Annals of Internal Medicine · doi:10.7326/0003-4819-111-8-671 · Cited by 444 · see citing works
Staudacher, H. M., Lomer, M. C. E., Farquharson, F. M., Louis, P., Fava, F., Franciosi, E., Scholz, M., Tuohy, K. M., Lindsay, J. O., Irving, P. M., et al. (2017) · Gastroenterology · doi:10.1053/j.gastro.2017.06.010 · Cited by 430 · see citing works
Chang, L., Toner, B. B., Fukudo, S., Guthrie, E., Locke, G. R., Norton, N. J., & Sperber, A. D. (2006) · Gastroenterology · doi:10.1053/j.gastro.2005.09.071 · Cited by 374 · see citing works
'Gut health': a new objective in medicine?
Bischoff, S. C. (2011) · BMC Medicine · doi:10.1186/1741-7015-9-24 · Cited by 338 · see citing works
The amino acid sensor GCN2 controls gut inflammation by inhibiting inflammasome activation
Ravindran, R., Loebbermann, J., Nakaya, H. I., Khan, N., Ma, H., Gama, L., Machiah, D. K., Lawson, B., Hakimpour, P., Wang, Y.-C., et al. (2016) · Nature · doi:10.1038/nature17186 · Cited by 312 · see citing works
Peripheral Mechanisms in Irritable Bowel Syndrome
Kassam, Z., Collins, S. M., & Moayyedi, P. (2013) · New England Journal of Medicine · doi:10.1056/nejmc1214185 · Cited by 285 · see citing works
Claudin-2 as a mediator of leaky gut barrier during intestinal inflammation
Luettig, J., Rosenthal, R., Barmeyer, C., & Jd, S. (2015) · Tissue Barriers · doi:10.4161/21688370.2014.977176 · Cited by 281 · see citing works
Microbial community and metabolomic comparison of irritable bowel syndrome faeces
Ponnusamy, K., Choi, J. N., Kim, J., Lee, S., & Lee, C. H. (2011) · Journal of Medical Microbiology · doi:10.1099/jmm.0.028126-0 · Cited by 249 · see citing works
A targeted metabolomic protocol for short-chain fatty acids and branched-chain amino acids
Zheng, X., Qiu, Y., Zhong, W., Baxter, S. A., Su, M., Li, Q., Xie, G., Ore, B. M., Qiao, S., Spencer, M., et al. (2013) · Metabolomics · doi:10.1007/s11306-013-0500-6 · Cited by 241 · see citing works
Meta‐analysis: factors affecting placebo response rate in the irritable bowel syndrome
Ford, A. C., & Moayyedi, P. (2010) · Alimentary Pharmacology & Therapeutics · doi:10.1111/j.1365-2036.2010.04328.x · Cited by 226 · see citing works
Functions and Signaling Pathways of Amino Acids in Intestinal Inflammation
He, F., Wu, C., Li, P., Li, N., Zhang, D., Zhu, Q., Ren, W., & Peng, Y. (2018) · BioMed Research International · doi:10.1155/2018/9171905 · Cited by 209 · see citing works
Food Components and Irritable Bowel Syndrome
Gibson, P. R., Varney, J. E., Malakar, S., & Muir, J. G. (2015) · Gastroenterology · doi:10.1053/j.gastro.2015.02.005 · Cited by 194 · see citing works
Sensitivity to wheat, gluten and FODMAPs in IBS: facts or fiction?
GIORGIO, R. D., Volta, U., & Gibson, P. R. (2015) · Gut · doi:10.1136/gutjnl-2015-309757 · Cited by 190 · see citing works
Wei, R., Wang, J., Jia, E., Chen, T., Ni, Y., & Jia, W. P. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005973 · Cited by 175 · see citing works
DuPont, H. L. (2014) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.12728 · Cited by 171 · see citing works
From microbe to man: the role of microbial short chain fatty acid metabolites in host cell biology
Natarajan, N., & Pluznick, J. L. (2014) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00228.2014 · Cited by 163 · see citing works
Boogers, I., Plugge, W., Stokkermans, Y. Q., & Duchateau, A. L. L. (2007) · Journal of Chromatography A · doi:10.1016/j.chroma.2007.11.052 · Cited by 160 · see citing works
Treem, W. R., Ahsan, N., Kastoff, G., & Hyams, J. S. (1996) · Journal of Pediatric Gastroenterology &amp Nutrition · doi:10.1097/00005176-199610000-00013 · Cited by 146 · see citing works
Gut Microbiota as Potential Orchestrators of Irritable Bowel Syndrome
Bennet, S., Öhman, L., & Simrén, M. (2015) · Gut and Liver · doi:10.5009/gnl14344 · Cited by 143 · see citing works
Long-term irritable bowel syndrome symptom control with reintroduction of selected FODMAPs
Harvie, R. M., Chisholm, A. W., Bisanz, J. E., Burton, J. P., Herbison, P., Schultz, K., & Schultz, M. (2017) · World Journal of Gastroenterology · doi:10.3748/wjg.v23.i25.4632 · Cited by 143 · see citing works
Wang, H., Ji, Y. S., Wu, G., Sun, K., Sun, Y., Li, W., Wang, B., He, B., Zhang, Q., Dai, Z., et al. (2015) · Journal of Nutrition · doi:10.3945/jn.114.209817 · Cited by 127 · see citing works
Brain-Gut Response to Stress and Cholinergic Stimulation in Irritable Bowel Syndrome
Fukudo, S., Nomura, T., Muranaka, M., & Taguchi, F. (1993) · Journal of Clinical Gastroenterology · doi:10.1097/00004836-199309000-00009 · Cited by 124 · see citing works
Comparison of the Rome IV and Rome III criteria for IBS diagnosis: A cross‐sectional survey
Bai, T., Xia, J., Jiang, Y., Cao, H., Zhao, Y., Zhang, L., Wang, H., Song, J., & Hou, X. (2016) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.13642 · Cited by 118 · see citing works
L-Glutamate Enhances Barrier and Antioxidative Functions in Intestinal Porcine Epithelial Cells,
Jiao, N., Wu, Z., Ji, Y. S., Wang, B., Dai, Z., & Wu, G. (2015) · Journal of Nutrition · doi:10.3945/jn.115.217661 · Cited by 114 · see citing works
Impact of irritable bowel syndrome (IBS) on health-related quality of life (HRQOL)
Amouretti, M., Le Pen, C., Gaudin, A.-F., Bommelaer, G., Frexinos, J., Ruszniewski, P., Poynard, T., Maurel, F., Priol, G., & El Hasnaoui, A. (2006) · Gastroentérologie Clinique et Biologique · doi:10.1016/s0399-8320(06)73160-8 · Cited by 110 · see citing works
Demehri, F. R., Barrett, M., Ralls, M. W., Miyasaka, E. A., Feng, Y., & Teitelbaum, D. H. (2013) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2013.00105 · Cited by 102 · see citing works
Song, Z. H., Tong, G., Xiao, K., Jiao, L. F., Ke, Y. L., & Hu, C. H. (2016) · Innate Immunity · doi:10.1177/1753425916632303 · Cited by 97 · see citing works
Short-Chain Fatty Acids and the Irritable Bowel Syndrome: The Effect of Wheat Bran
Mortensen, P. B., Andersen, J. R., Arffmann, S., & KRAG, E. (1987) · Scandinavian Journal of Gastroenterology · doi:10.3109/00365528708991878 · Cited by 88 · see citing works
Shankar, V., Homer, D., Rigsbee, L., Khamis, H. J., Michail, S. K., Raymer, M. L., Reo, N. V., & Paliy, O. (2015) · The ISME Journal · doi:10.1038/ismej.2014.258 · Cited by 77 · see citing works
Subtyping the irritable bowel syndrome by predominant bowel habit: Rome II versus Rome III
Ersryd, A. L., Posserud, I., Abrahamsson, H., & Simrén, M. (2007) · Alimentary Pharmacology & Therapeutics · doi:10.1111/j.1365-2036.2007.03422.x · Cited by 71 · see citing works
Functional Bowel Disorders: A Roadmap to Guide the Next Generation of Research
Chang, L., Lorenzo, C. D., Farrugia, G., Hamilton, F. A., Mawe, G. M., Pasricha, P. J., & Wiley, J. W. (2017) · Gastroenterology · doi:10.1053/j.gastro.2017.12.010 · Cited by 62 · see citing works
Wils-Plotz, E. L., Jenkins, M. C., & Dilger, R. N. (2013) · Poultry Science · doi:10.3382/ps.2012-02755 · Cited by 59 · see citing works
Mine, Y., & Zhang, H. (2015) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5b03749 · Cited by 55 · see citing works
Yang, Y., Li, W., Sun, Y., Han, F. X., Hu, C. A., & Wu, Z. (2014) · Amino Acids · doi:10.1007/s00726-014-1844-6 · Cited by 52 · see citing works
Ren, W., Zou, L., Li, N., Wang, Y., Liu, G., Peng, Y., Ding, J., Cai, L., Yin, Y., & Wu, G. (2012) · British Journal Of Nutrition · doi:10.1017/s0007114512002681 · Cited by 50 · see citing works
Saigo, T., Tayama, J., Hamaguchi, T., Nakaya, N., Tomiie, T., Bernick, P. J., Kanazawa, M., Labus, J. S., Naliboff, B. D., Shirabe, S., et al. (2014) · BioPsychoSocial Medicine · doi:10.1186/1751-0759-8-10 · Cited by 50 · see citing works
Dietary Tryptophan Enhanced the Expression of Tight Junction Protein ZO‐1 in Intestine
Liu, W., Mi, S., Ruan, Z., Li, J., Shu, X., Kang, Y., Jiang, M., & Deng, Z. (2017) · Journal of Food Science · doi:10.1111/1750-3841.13603 · Cited by 48 · see citing works
A novel biomarker panel for irritable bowel syndrome and the application in the general population
Mujagic, Z., Tigchelaar, E. F., Zhernakova, A., Ludwig, T. G., Ramiro‐Garcia, J., Baranska, A., Swertz, M. A., Masclee, A., Wijmenga, C., van Schooten, F., et al. (2016) · Scientific Reports · doi:10.1038/srep26420 · Cited by 46 · see citing works
Nagarjun, S., Dhadde, S. B., Veerapur, V. P., Thippeswamy, B. S., & Chandakavathe, B. N. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2017.02.042 · Cited by 44 · see citing works
Xu, D., Wu, X., Grabauskas, G., & Owyang, C. (2012) · Gut · doi:10.1136/gutjnl-2012-302260 · Cited by 43 · see citing works
Liu, H., Tan, B., Huang, B., Li, J., Wang, J., Liao, P., Guan, G., Ji, P., & Yin, Y. (2018) · British Journal Of Nutrition · doi:10.1017/s0007114518002891 · Cited by 42 · see citing works
Zhang, Y., Qin, G., De-rong, L., Wang, Y., & Yao, S. (2019) · World Journal of Gastroenterology · doi:10.3748/wjg.v25.i2.269 · Cited by 40 · see citing works
Aerssens, J., Hillsley, K., Peeters, P. J., Hoogt, R. D., STANISZ, A. M., Lin, J., den Wyngaert, I. V., Göhlmann, H. W. H., Grundy, D., Stead, R. H., et al. (2007) · Gastroenterology · doi:10.1053/j.gastro.2007.02.019 · Cited by 39 · see citing works
Cellular and mitochondrial determination of low molecular mass organic acids by LC–MS/MS
Fiori, J., Amadesi, E., Fanelli, F., Tropeano, C. V., Rugolo, M., & Gotti, R. (2017) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2017.11.071 · Cited by 37 · see citing works
Shankar, V., Reo, N. V., & Paliy, O. (2015) · Microbiome · doi:10.1186/s40168-015-0139-9 · Cited by 26 · see citing works
Robles, H. V., Castro-Ochoa, K. F., Nava, P., Silva-Olivares, A., Shibayama, M., & Michael Schnoor, A. (2017) · Journal of Visualized Experiments · doi:10.3791/55095 · Cited by 18 · see citing works
Starving Intestinal Inflammation with the Amino Acid Sensor GCN2
Revelo, X. S., Winer, S., & Winer, D. A. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.04.020 · Cited by 16 · see citing works
[An analysis of amino acid metabolic profile and its clinical significance in ulcerative colitis].
Xin, L., Li, N., Zhu, W., Wu, K., Zhang, L., Zhai, J., Wang, Y., Zhu, J., Wang, X., Shi, Y., et al. (2015) · PubMed · Cited by 7 · see citing works
Tan, B., Huang, B., Wang, J., Guang, G. P., Yang, C. B., & Yin, Y. (2017) · Journal of Animal Science · doi:10.2527/asasann.2017.408 · Cited by 7 · see citing works
Flagged first, then by citations
1 of the 72 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Diet and the Microbiota–Gut–Brain Axis: Sowing the Seeds of Good Mental Health
Berding, K., Vlckova, K., Marx, W., Schellekens, H., Stanton, C., Clarke, G., Jacka, F., Dinan, T. G., & Cryan, J. F. (2021) · Advances in Nutrition · doi:10.1093/advances/nmaa181 · Cited by 451 · see citing works
Microbiota–neuroepithelial signalling across the gut–brain axis
Ohara, T. E., & Hsiao, E. Y. (2025) · Nature Reviews Microbiology · doi:10.1038/s41579-024-01136-9 · Cited by 147 · see citing works
Depommier, C., Everard, A., Druart, C., Maiter, D. M., Thissen, J., Loumaye, A., Hermans, M. P., Delzenne, N. M., de Vos, W. M., & Cani, P. D. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1994270 · Cited by 57 · see citing works
Liu, T., Gu, X., Li, L., Li, M., Li, B., Cui, X., & Zuo, X. (2020) · BMC Microbiology · doi:10.1186/s12866-020-01841-4 · Cited by 55 · see citing works
Ahluwalia, B., Iribarren, C., Magnusson, M. K., Sundin, J., Clevers, E., Savolainen, O. I., Ross, A. B., Törnblom, H., Simrén, M., & Öhman, L. (2021) · Cells · doi:10.3390/cells10061459 · Cited by 43 · see citing works
Review article: current and future treatment approaches for pain in IBS
Paine, P. (2021) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.16550 · Cited by 39 · see citing works
Ju, X., Jiang, Z., Ma, J., & Yang, D. J. (2024) · Nutrients · doi:10.3390/nu16111727 · Cited by 37 · see citing works
Changes in signalling from faecal neuroactive metabolites following dietary modulation of IBS pain
Tuck, C. J., Omar, A. A., Palma, G. D., Osman, S., Jiménez-Vargas, N. N., Yu, Y., Bennet, S., López-López, C., Jaramillo-Polanco, J., Baker, C. C., et al. (2022) · Gut · doi:10.1136/gutjnl-2022-327260 · Cited by 31 · see citing works
Yang, N., Ma, T., Xie, Y., Li, Q., Li, Y., Zheng, L., Li, Y., Xiao, Q., Sun, Z., Zuo, K., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-51094-2 · Cited by 29 · see citing works
The role of the gut microbiome in disorders of gut–brain interaction
Gawey, B. J., Mars, R. A. T., & Kashyap, P. (2024) · FEBS Journal · doi:10.1111/febs.17200 · Cited by 28 · see citing works
Ethnic differences in genetic polymorphism associated with irritable bowel syndrome
Xiao, Q.-Y., Fang, X., Li, X., & Fei, G. (2020) · World Journal of Gastroenterology · doi:10.3748/wjg.v26.i17.2049 · Cited by 21 · see citing works
Nikolaki, M. D., Kasti, A. N., Katsas, K., Petsis, K., Lambrinou, S., Patsalidou, V., Stamatopoulou, S., Karlatira, K., Kapolos, J., Papadimitriou, K., et al. (2023) · Microorganisms · doi:10.3390/microorganisms11102387 · Cited by 21 · see citing works
Gargari, G., Mantegazza, G., Taverniti, V., Gardana, C., Valenza, A., Rossignoli, F., Barbaro, M. R., Marasco, G., Cremon, C., Barbara, G., et al. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2274128 · Cited by 21 · see citing works
Regulation of Pain Perception by Microbiota in Parkinson Disease
Manjarres, Z., Calvo, M., & Pacheco, R. (2023) · Pharmacological Reviews · doi:10.1124/pharmrev.122.000674 · Cited by 15 · see citing works
Stenlund, H. C., Nilholm, C., Chorell, E., Roth, B., D’Amato, M., & Ohlsson, B. (2021) · Metabolites · doi:10.3390/metabo11070440 · Cited by 16 · see citing works
Iribarren, C., Nordlander, S., Sundin, J., Isaksson, S., Savolainen, O. I., Törnblom, H., Magnusson, M. K., Simrén, M., & Öhman, L. (2022) · Neurogastroenterology & Motility · doi:10.1111/nmo.14390 · Cited by 13 · see citing works
Kulecka, M., Żeber‐Lubecka, N., Bałabas, A., Czarnowski, P., Bagińska, K., Głowienka, M., Kluska, A., Piątkowska, M., Dąbrowska, M., Waker, E., et al. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1190910 · Cited by 13 · see citing works
A host-centric view of the microbiota metabolome
Yamada, T., & Palm, N. W. (2025) · Immunity · doi:10.1016/j.immuni.2025.11.006 · Cited by 12 · see citing works
Iribarren, C., Maasfeh, L., Öhman, L., & Simrén, M. (2022) · Gut Microbiome · doi:10.1017/gmb.2022.6 · Cited by 8 · see citing works
Fraser, K., James, S. C., Young, W., Gearry, R. B., Heenan, P. E., Keenan, J. I., Talley, N. J., McNabb, W. C., & Roy, N. C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252413465 · Cited by 7 · see citing works
Kosińska–Kaczyńska, K., Krawczyk, D., Bednorz, M., Chaberek, K., Czapska, A. H., Zgliczyńska, M., Goryca, K., Piątkowska, M., Bałabas, A., Czarnowski, P., et al. (2025) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2025.1596588 · Cited by 6 · see citing works
Berens, S., Dong, Y., Fritz, N., Walstab, J., D’Amato, M., Zheng, T., Wahl, V., Boekstegers, F., Bermejo, J. L., Martínez, C., et al. (2022) · World Journal of Gastroenterology · doi:10.3748/wjg.v28.i21.2334 · Cited by 6 · see citing works
Cheng, B., Sun, Q., Li, X., Xiao, M., Wei, X., & Wang, S. (2023) · Behavioural Brain Research · doi:10.1016/j.bbr.2023.114520 · Cited by 5 · see citing works
Serological and faecal markers of irritable bowel syndrome: a systematic review and meta-analysis
Burns, G. L., Roberts, F., Wark, J. A., Fowler, S., Jones, M. P., Duncanson, K., Talley, N. J., & Keely, S. (2026) · EBioMedicine · doi:10.1016/j.ebiom.2026.106198 · Cited by 5 · see citing works
Aatsinki, A., Kråkström, M., Salonen, K., Isokääntä, H., Paul, A., Bastiaanssen, T. F. S., Lahti, L., Lukkarinen, M. M., Munukka, E., Paunio, T., et al. (2026) · Gut Microbiology · doi:10.1016/j.gutmic.2026.100013 · Cited by 4 · see citing works
Multi-Omics Analysis to Generate Hypotheses for Mild Health Problems in Monkeys
Hamano, F., Tokuoka, S. M., Ishibashi, M., Yokoi, Y., Tourlousse, D. M., Kita, Y., Sekiguchi, Y., Yasui, H., Shimizu, T., & Oda, Y. (2021) · Metabolites · doi:10.3390/metabo11100701 · Cited by 2 · see citing works
Intelligent information retrieval and web mining architecture using soa
Chang, P. H., & El-Bathy, N. (2010) · ProQuest LLC eBooks
Yu, L.-M., Weng, M.-N., Chen, H., Ye, W., & Fan, Y. (2021) · World Chinese Journal of Digestology · doi:10.11569/wcjd.v29.i24.1421
Fedorin, M. M., Livzan, M. A., Gaus, O. V., & Pashkova, E. (2024) · Meditsinskiy sovet = Medical Council · doi:10.21518/ms2024-168
Fu, M., Chen, Y., Gong, L., Wang, Z., Fang, X., Duan, Y., & Li, X. (2026) · Frontiers in Medicine · doi:10.3389/fmed.2026.1810265
Ichikawa, S., Shimura, A., Kikuchi, A., Sanda, R., Sasayama, K., Nonoue, K., Tamura, H., Kano, T., & Shimada, Y. (2026) · Scientific Reports · doi:10.1038/s41598-026-59018-4
Gorini, F., Tonacci, A., Gabriele, M., & Borghini, A. (2026) · Nutrients · doi:10.3390/nu18213535
- Authors
- Zhang, W.-X., Zhang, Y., Qin, G., Li, K.-M., Wei, W., Li, S.-Y., & Yao, S.-K.
- Affiliations
- Qingdao University (CN)
- Venue
- World Journal of Gastroenterology
- Publisher
- Baishideng Publishing Group Inc.
- Published
- 2019-11-21
- Volume
- 25
- Issue
- 43
- Pages
- 6416-6429
- ISSN
- 1007-9327 (ISSN-L)
- PMC
- PMC6881512
- OpenAlex
- W2989970781
- Cited by
- 32
- References
- 72
- Citations by year
- 2026: 5 · 2025: 3 · 2024: 5 · 2023: 5 · 2022: 4 · 2021: 6 · 2020: 3
- FWCI
- 2.96
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by-nc
- Locations
- World Journal of Gastroenterology (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Inflammatory Bowel Disease
- Keywords
- diarrhea-predominant irritable bowel syndrome, fecal metabolites, visceral hypersensitivity, visceral sensitivity, symptom severity, amino acids, organic acids, isovalerate, valerate, tyrosine, valine, fumarate, pyruvate, hexanoate, rectal distension, abdominal pain, gut-brain axis
- MeSH terms
- Adult, Carboxylic Acids, Feces, Female, Humans, Male, Severity of Illness Index, Abdominal Pain, Case-Control Studies, Irritable Bowel Syndrome
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review