Diet promotes dysbiosis and colitis in susceptible hosts

Linking long-term dietary patterns with gut microbial enterotypes

Wu, G. D., Chen, J., Hoffmann, C., Bittinger, K., Chen, Y.-Y., Keilbaugh, S. A., Bewtra, M., Knights, D., Walters, W. A., Knight, R., et al. (2011) · Science · doi:10.1126/science.1208344 · Cited by 6,513 · see citing works

Increasing Incidence and Prevalence of the Inflammatory Bowel Diseases With Time, Based on Systematic Review

Molodecky, N. A., Soon, I. S., Rabi, D. M., Ghali, W. A., Ferris, M., Chernoff, G., Benchimol, E. I., Panaccione, R., Ghosh, S., Barkema, H. W., et al. (2012) · Gastroenterology · doi:10.1053/j.gastro.2011.10.001 · Cited by 4,833 · see citing works

Microbial Influences in Inflammatory Bowel Diseases

Sartor, R. B. (2008) · Gastroenterology · doi:10.1053/j.gastro.2007.11.059 · Cited by 1,927 · see citing works

Dietary-fat-induced taurocholic acid promotes pathobiont expansion and colitis in Il10-/- mice

Devkota, S., Wang, Y., Musch, M. W., Leone, V., Fehlner-Peach, H., Nadimpalli, A., Antonopoulos, D. A., Jabri, B., & Chang, E. B. (2012) · Nature · doi:10.1038/nature11225 · Cited by 1,904 · see citing works

Glycan foraging in vivo by an intestine-adapted bacterial symbiont

Sonnenburg, J. L., Xu, J., Leip, D. D., Chen, C.-H., Westover, B. P., Weatherford, J., Buhler, J. D., & Gordon, J. I. (2005) · Science · doi:10.1126/science.1109051 · Cited by 1,184 · see citing works

Contributions of the microbial hydrogen economy to colonic homeostasis

Carbonero, F. G., Benefiel, A. C., & Gaskins, H. R. (2012) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2012.85 · Cited by 291 · see citing works

Dietary Beliefs and Behavior Among Inflammatory Bowel Disease Patients

Zallot, C., Quilliot, D., Chevaux, J., Peyrin-Biroulet, C., Guéant‐Rodriguez, R., Fréling, E., Collet-Fenêtrier, B., Williet, N., Ziegler, O., Bigard, M., et al. (2012) · Inflammatory Bowel Diseases · doi:10.1002/ibd.22965 · Cited by 242 · see citing works

Existing dietary guidelines for Crohn’s disease and ulcerative colitis

Brown, A. C., Rampertab, S. D., & Mullin, G. E. (2011) · Expert Review of Gastroenterology & Hepatology · doi:10.1586/egh.11.29 · Cited by 115 · see citing works

Challenges associated with identifying the environmental determinants of the inflammatory bowel diseases

Molodecky, N. A., Panaccione, R., Ghosh, S., Barkema, H. W., & Kaplan, G. G. (2011) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21511 · Cited by 109 · see citing works

Food and the gut microbiota in inflammatory bowel diseases

Albenberg, L. G., Lewis, J. D., & Wu, G. D. (2012) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e328354586f · Cited by 99 · see citing works

Diet and the Intestinal Microbiome: Associations, Functions, and Implications for Health and Disease

Albenberg, L. G., & Wu, G. D. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.01.058 · Cited by 606 · see citing works

Diet in the Pathogenesis and Treatment of Inflammatory Bowel Diseases

Lee, D. Y., Albenberg, L. G., Compher, C. W., Baldassano, R. N., Piccoli, D. A., Lewis, J. D., & Wu, G. D. (2015) · Gastroenterology · doi:10.1053/j.gastro.2015.01.007 · Cited by 377 · see citing works

Regulation of intestinal homeostasis and immunity with probiotic lactobacilli

van Baarlen, P., Wells, J. M., & Kleerebezem, M. (2013) · Trends in Immunology · doi:10.1016/j.it.2013.01.005 · Cited by 369 · see citing works

Alteration of intestinal dysbiosis by fecal microbiota transplantation does not induce remission in patients with chronic active ulcerative colitis

Kump, P. K., Gröchenig, H.-P., Lackner, S., Trajanoski, S., Reicht, G., Hoffmann, K. M., Deutschmann, A., Wenzl, H. H., Petritsch, W., Krejs, G. J., et al. (2013) · Inflammatory Bowel Diseases · doi:10.1097/mib.0b013e31829ea325 · Cited by 235 · see citing works

Mycobiota in gastrointestinal diseases

Mukherjee, P. K., Sendid, B., Hoarau, G., Colombel, J., Poulain, D., & Ghannoum, M. A. (2014) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2014.188 · Cited by 211 · see citing works

Diet and Inflammatory Bowel Disease: Review of Patient-Targeted Recommendations

Hou, J. K., Lee, D. Y., & Lewis, J. D. (2013) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2013.09.063 · Cited by 204 · see citing works

The Gordian Knot of dysbiosis, obesity and NAFLD

Mehal, W. Z. (2013) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2013.146 · Cited by 150 · see citing works

Mucosal Immunology of Food Allergy

Berin, M. C., & Sampson, H. A. (2013) · Current Biology · doi:10.1016/j.cub.2013.02.043 · Cited by 144 · see citing works

The interaction between gut microbiota and age-related changes in immune function and inflammation

Magrone, T., & Jirillo, E. (2013) · Immunity & Ageing · doi:10.1186/1742-4933-10-31 · Cited by 124 · see citing works

Rational identification of diet-derived postbiotics for improving intestinal microbiota function

Klemashevich, C. L., Wu, C., Howsmon, D. P., Alaniz, R. C., Lee, K., & Jayaraman, A. (2013) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2013.10.006 · Cited by 101 · see citing works

Oral iron exacerbates colitis and influences the intestinal microbiome

Mahalhal, A., Williams, J. M., Johnson, S., Ellaby, N., Duckworth, C. A., Burkitt, M. D., Liu, X., Hold, G. L., Campbell, B. J., Pritchard, D. M., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0202460 · Cited by 98 · see citing works

Influence of Stressor-Induced Nervous System Activation on the Intestinal Microbiota and the Importance for Immunomodulation

Bailey, M. T. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-1-4939-0897-4_12 · Cited by 88 · see citing works

Upper gastrointestinal microbiota and digestive diseases

Wang, Z.-K. (2013) · World Journal of Gastroenterology · doi:10.3748/wjg.v19.i10.1541 · Cited by 88 · see citing works

Gut microbiota in pathophysiology, diagnosis, and therapeutics of inflammatory bowel disease

Pandey, H., Jain, D., Tang, D. W. T., Wong, S. H., & Lal, D. (2023) · Intestinal Research · doi:10.5217/ir.2023.00080 · Cited by 89 · see citing works

Can control of gut microbiota be a future therapeutic option for inflammatory bowel disease?

Nishida, A., Nishino, K., Sakai, K., Owaki, Y., Noda, Y., & Imaeda, H. (2021) · World Journal of Gastroenterology · doi:10.3748/wjg.v27.i23.3317 · Cited by 52 · see citing works

Metabolomics in the Clinical Diagnosis of Inflammatory Bowel Disease

Preter, V. D. (2015) · Digestive Diseases · doi:10.1159/000437033 · Cited by 50 · see citing works

Postbiotics, Metabolic Signaling, and Cancer

Vrzáčková, N., Ruml, T., & Zelenka, J. (2021) · Molecules · doi:10.3390/molecules26061528 · Cited by 41 · see citing works

Microbiome, gut dysbiosis and inflammatory bowel disease: That moment when the function is more important than taxonomy

Sitkin, S. I., Vakhitov, T., & Demyanova, E. V. (2018) · Almanac of Clinical Medicine · doi:10.18786/2072-0505-2018-46-5-396-425 · Cited by 38 · see citing works

Distinctive Gut Microbiota Is Associated with Diarrheagenic Escherichia coli Infections in Chilean Children

Gallardo, P., Izquierdo, M., Vidal, R. M., Chamorro-Veloso, N., Rossello-Mora, R. A., O’Ryan, M., & Farfán, M. J. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00424 · Cited by 39 · see citing works

The Mycobiome: Impact on Health and Disease States

El‐Jurdi, N., & Ghannoum, M. A. (2017) · Microbiology Spectrum · doi:10.1128/microbiolspec.funk-0045-2016 · Cited by 27 · see citing works

Gut microbiota: an Indicator to Gastrointestinal Tract Diseases

Patel, T., Bhattacharya, P., & Das, S. (2016) · Journal of Gastrointestinal Cancer · doi:10.1007/s12029-016-9820-x · Cited by 24 · see citing works

Ascl2 facilitates IL-10 production in Th17 cells to restrain their pathogenicity in inflammatory bowel disease

Qian, Y., Wang, J., Song, Y., Guo, Z., Lei, S., Yang, X., Li, L., Gao, C., & Zhou, Z. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.01.123 · Cited by 20 · see citing works

Oral Ferric Maltol Does Not Adversely Affect the Intestinal Microbiome of Patients or Mice, but Ferrous Sulphate Does

Mahalhal, A., Frau, A., Burkitt, M. D., Ijaz, U. Z., Lamb, C. A., Mansfield, J. C., Lewis, S. J., Pritchard, D. M., & Probert, C. S. (2021) · Nutrients · doi:10.3390/nu13072269 · Cited by 18 · see citing works

A Review of the Epidemiology of Inflammatory Bowel Disease with a Focus on Diet, Infections and Antibiotic Exposure

Lewis, J. D. (2014) · Nestlé Nutrition Institute Workshop series · doi:10.1159/000360664 · Cited by 14 · see citing works

Immunobiology of hepatocarcinogenesis: Ways to go or almost there?

Patel, P., Schutzer, S. E., & Pyrsopoulos, N. (2016) · World Journal of Gastrointestinal Pathophysiology · doi:10.4291/wjgp.v7.i3.242 · Cited by 14 · see citing works

Gut Microbiota and Liver Injury (II): Chronic Liver Injury

Baker, S. S., & Baker, R. D. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-2385-4_4 · Cited by 10 · see citing works

Integrated Analysis of Gut Microbiome and Adipose Transcriptome Reveals Beneficial Effects of Resistant Dextrin from Wheat Starch on Insulin Resistance in Kunming Mice

Chen, X., Hou, Y., Liao, A., Pan, L., Yang, S., Liu, Y., Wang, J. J., Xue, Y., Zhang, M., Zhu, Z., et al. (2024) · Biomolecules · doi:10.3390/biom14020186 · Cited by 8 · see citing works

The Mycobiome: Impact on Health and Disease States

El‐Jurdi, N., & Ghannoum, M. A. (2017) · ASM Press eBooks · doi:10.1128/9781555819583.ch40 · Cited by 5 · see citing works

Nutrition and gastrointestinal disorders

Newberry, C. A., Parks, E. P., & Maqbool, A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818460-8.00023-x · Cited by 4 · see citing works

Nutritional Supports in Patients with Inflammatory Bowel Disease

Kye, B. (2016) · Journal of Clinical Nutrition · doi:10.15747/jcn.2016.8.1.11 · Cited by 3 · see citing works

Dietary Therapies for Inflammatory Bowel Disease

Stein, R. E., & Baldassano, R. N. (2017) · Springer eBooks · doi:10.1007/978-3-319-49215-5_38 · Cited by 3 · see citing works

Postbiotics: Potential as functional ingredients—A review

Sarkar, S. (2024) · Food Nutrition Chemistry · doi:10.18686/fnc241 · Cited by 2 · see citing works

Absorption, Transport, and Retention

Kohlmeier, M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-387784-0.00003-1 · Cited by 1 · see citing works

Flora bakteryjna jelit i jej potencjalny związek z otyłością

Marlicz, W. M., Ostrowska, L., & Łoniewski, I. (2013) · Endokrynologia, Otyłość i Zaburzenia Przemiany Materii · Cited by 2 · see citing works

Verdauungsoptimierung – wie sich Ernährung und Mikrobiom gegenseitig beeinflussen

Bischoff, S. C. (2019) · DMW - Deutsche Medizinische Wochenschrift · doi:10.1055/a-0826-1977 · Cited by 2 · see citing works

Classification and Antitumor Activities of Postbiotics from the Biotic Family

Aşit, M., & Saka, M. (2023) · Ankara sağlık bilimleri dergisi · doi:10.46971/ausbid.1249911 · Cited by 1 · see citing works

Elimination Diets for Inflammatory Bowel Disease

Hou, J. K. (2014) · Springer eBooks · doi:10.1007/978-3-319-26890-3_7 · Cited by 1 · see citing works

Verdauungsoptimierung – wie sich Ernährung und Mikrobiom gegenseitig beeinflussen

Bischoff, S. C. (2020) · Aktuelle Ernährungsmedizin · doi:10.1055/a-1295-6604 · Cited by 1 · see citing works

Influence of Iron Supplementation on Gut Microbiota and the Natural History of Inflammatory Bowel Disease

Mahalhal, A. (2017) · University of Liverpool · doi:10.17638/03009111 · Cited by 1 · see citing works

Colon: Structure, function, and disorders

Maqbool, A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821848-8.00059-7

Dietary Therapies for Inflammatory Bowel Disease

Stoner, N. L., & Stein, R. E. (2023) · Springer eBooks · doi:10.1007/978-3-031-14744-9_37

Harnessing Gut Bacteria: Short- Chain Fatty Acids Against Diarrheagenic E. coli?

Molina, P. G. (2024) · doi:10.33612/diss.1158582819

Rôle de Vanin-1 dans l'intéraction hôte-microbiote et la physiopathologie des maladies inflammatoires chroniques de l'intestin (MICI)

Maltese, M. (2016) · doi:10.70675/1608506az6698z4d19z9b71z1b286cd6102c

Dietary-fat-induced taurocholic acid promotes pathobiont expansion and colitis in Il10-/- mice

Devkota, S., Wang, Y., Musch, M. W., Leone, V., Fehlner-Peach, H., Nadimpalli, A., Antonopoulos, D. A., Jabri, B., & Chang, E. B. (2012) · Nature · doi:10.1038/nature11225 · Cited by 1,904 · see citing works

Dietary fat‐induced taurocholic acid production promotes pathobiont and colitis in IL‐10−/− mice

Devkota, S., Wang, Y., Leone, V., Musch, M. W., Nadimpalli, A., Antonopoulos, D., Jabrì, B., & Chang, E. B. (2012) · The FASEB Journal · doi:10.1096/fasebj.26.1_supplement.1155.2 · Cited by 25 · see citing works

Skewing the microbiome

Dempsey, L. A. (2012) · Nature Immunology · doi:10.1038/ni.2383

Fat, bile and gut microbes

Turnbaugh, P. J. (2012) · Nature · doi:10.1038/487047a · Cited by 41 · see citing works

Bile Acids as Modulators of Gut Microbiota Linking Dietary Habits and Inflammatory Bowel Disease: A Potentially Dangerous Liaison

Trauner, M. A., Fickert, P., & Tilg, H. (2013) · Gastroenterology · doi:10.1053/j.gastro.2013.02.029 · Cited by 16 · see citing works