Mechanisms and consequences of intestinal dysbiosis

The “Golden Age” of Probiotics: A Systematic Review and Meta-Analysis of Randomized and Observational Studies in Preterm Infants

Dermyshi, E., Wang, Y., Yan, C., Hong, W., Qiu, G., Gong, X., & Zhang, T. (2017) · Neonatology · doi:10.1159/000454668 · Cited by 24,586

An obesity-associated gut microbiome with increased capacity for energy harvest

Turnbaugh, P. J., Ley, R. E., Mahowald, M. A., Magrini, V., Mardis, E. R., & Gordon, J. I. (2006) · Nature · doi:10.1038/nature05414 · Cited by 12,444

Human gut microbes associated with obesity

Ley, R. E., Turnbaugh, P. J., Klein, S., & Gordon, J. I. (2006) · Nature · doi:10.1038/4441022a · Cited by 8,785

Enterotypes of the human gut microbiome

MetaHIT Consortium (additional members), Arumugam, M., Raes, J., Pelletier, E., Le Paslier, D., Yamada, T., Mende, D. R., Fernandes, G. R., Tap, J., Bruls, T., et al. (2011) · Nature · doi:10.1038/nature09944 · Cited by 7,548

Changes of Intestinal Functions in Liver Cirrhosis

Fukui, H., & Wiest, R. (2016) · Inflammatory Intestinal Diseases · doi:10.1159/000444436 · Cited by 6,820

Metabolic Endotoxemia Initiates Obesity and Insulin Resistance

Cani, P. D., Amar, J., Iglesias, M. A., Poggi, M., Knauf, C., Bastelica, D., Neyrinck, A. M., Fava, F., Tuohy, K. M., Chabo, C., et al. (2007) · Diabetes · doi:10.2337/db06-1491 · Cited by 6,638

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

The gut microbiota as an environmental factor that regulates fat storage

Bäckhed, F., Ding, H., Wang, T., Hooper, L. V., Koh, G. Y., Nagy, A., Semenkovich, C. F., & Gordon, J. I. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407076101 · Cited by 6,245

Effects of chronic stress and intestinal inflammation on commercial poultry health and performance: A review

Téllez‐Isaías, G., Eisenreich, W., Petrone-García, V. M., Hernández-Velasco, X., Castellanos-Huerta, C.-H., Téllez‐Isaías, G., Latorre, J. D., Bottje, W. G., Señas-Cuesta, R., Coles, M. E., et al. (2023) · German Journal of Veterinary Research · doi:10.51585/gjvr.2023.1.0051 · Cited by 28

Asiaticoside ameliorates DSS ‐induced colitis in mice by inhibiting inflammatory response, protecting intestinal barrier and regulating intestinal microecology

Liu, K., Yin, Y., Shi, C., Yan, C., Zhang, Y., Qiu, L., He, S., & Li, G. (2024) · Phytotherapy Research · doi:10.1002/ptr.8129 · Cited by 27

Modulation of Gut Microbiota in Korean Navy Trainees following a Healthy Lifestyle Change

Jung, Y., Tagele, S. B., Son, H., Ibal, J. C., Kerfahi, D., Yun, H., Lee, B., Park, C. Y., Kim, E. S., Kim, S.-J., et al. (2020) · Microorganisms · doi:10.3390/microorganisms8091265 · Cited by 24

Antimicrobial Resistance Profile by Metagenomic and Metatranscriptomic Approach in Clinical Practice: Opportunity and Challenge

Waskito, L. A., Rezkitha, Y. A. A., Vilaichone, R., Wibawa, I. D. N., Mustika, S., Sugihartono, T., & Miftahussurur, M. (2022) · Antibiotics · doi:10.3390/antibiotics11050654 · Cited by 29

Role of the Gut Microbiota in Children with Kidney Disease

Tain, Y., & Hsu, C. (2023) · Children · doi:10.3390/children10020269 · Cited by 24

Microbiome-liver crosstalk: A multihit therapeutic target for liver disease

Kirundi, J., Moghadamrad, S., & Urbaniak, C. (2023) · World Journal of Gastroenterology · doi:10.3748/wjg.v29.i11.1651 · Cited by 24

Beyond the Hayflick limit: How microbes influence cellular aging

Abavisani, M., Faraji, S., Ebadpour, N., Karav, S., & Sahebkar, A. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102657 · Cited by 24

Gut dysbiosis in cancer immunotherapy: microbiota-mediated resistance and emerging treatments

Eiman, L., Moazzam, K., Anjum, S., Kausar, H., Sharif, E. A. M., & Ibrahim, W. N. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1575452 · Cited by 28

Microbiota-Dependent Fiber Responses: A Proof-of-Concept Study on Short-Chain Fatty Acid Production in Prevotella- and Bacteroides-Dominated Healthy Individuals

Bartsch, M., Vital, M., Woltemate, S., Bouwman, F. G., Berkemeyer, S., Hahn, A., & Müller, M. (2025) · Journal of Nutrition · doi:10.1016/j.tjnut.2025.08.034 · Cited by 25

Intestinal Population in Host with Metabolic Syndrome during Administration of Chitosan and Its Derivatives

Yan, C., Zhang, C., Cao, X., Feng, B., & Li, X. (2020) · Molecules · doi:10.3390/molecules25245857 · Cited by 24

Fecal Microbiota Analysis in Cats with Intestinal Dysbiosis of Varying Severity

Bugrov, N. S., Rudenko, P. A., Lutsay, V., Gurina, R., Жаров, А. А., Khairova, N., Molchanova, M., Krotova, E. A., Shopinskaya, M. I., Bolshakova, M., et al. (2022) · Pathogens · doi:10.3390/pathogens11020234 · Cited by 29

Predictable Changes in Eelgrass Microbiomes with Increasing Wasting Disease Prevalence across 23° Latitude in the Northeastern Pacific

Beatty, D. S., Aoki, L. R., Rappazzo, B., Bergman, C., Domke, L. K., Duffy, J. E., DuBois, K., Eckert, G. L., Gomes, C. P., Graham, O., et al. (2022) · mSystems · doi:10.1128/msystems.00224-22 · Cited by 21

Gut-Brain Axis Deregulation and Its Possible Contribution to Neurodegenerative Disorders

Villavicencio-Tejo, F., Olesen, M. A., Navarro, L., Calisto, N., Iribarren, C., GARCÍA, K. P., Corsini, G., & Quintanilla, R. A. (2023) · Neurotoxicity Research · doi:10.1007/s12640-023-00681-0 · Cited by 24

MDPbiome: microbiome engineering through prescriptive perturbations

García-Jiménez, B., de la Rosa, T., & Wilkinson, M. D. (2018) · Bioinformatics · doi:10.1093/bioinformatics/bty562 · Cited by 23

Oxalobacter formigenes: A new hope as a live biotherapeutic agent in the management of calcium oxalate renal stones

Hiremath, S. S., & Viswanathan, P. (2022) · Anaerobe · doi:10.1016/j.anaerobe.2022.102572 · Cited by 23

The gut microbiome: an important role in neurodegenerative diseases and their therapeutic advances

Li, S., Zhao, L., Xiao, J., Guo, Y., Fu, R., Zhang, Y., & Xu, S. (2023) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-023-04853-6 · Cited by 23

Dose-dependent S-allyl cysteine ameliorates multiple sclerosis disease-related pathology by reducing oxidative stress and biomarkers of dysbiosis in experimental autoimmune encephalomyelitis

Escribano, B. M., Luque, E., Aguilar-Luque, M., Feijóo, M., Caballero‐Villarraso, J., Torres, L. A., Ramirez, V., García-Maceira, F. I., Agüera, E., Santamarı́a, A., et al. (2017) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2017.09.025 · Cited by 22

The Promising Role of Microbiome Therapy on Biomarkers of Inflammation and Oxidative Stress in Type 2 Diabetes: A Systematic and Narrative Review

Paul, P., Kaul, R., Abdellatif, B., Arabi, M., Upadhyay, R., Saliba, R., Sebah, M., & Châari, A. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.906243 · Cited by 22

Parenteral Nutrition, Inflammatory Bowel Disease, and Gut Barrier: An Intricate Plot

Covello, C., Becherucci, G., Di Vincenzo, F., Del Gaudio, A., Pizzoferrato, M., Cammarota, G., Gasbarrini, A., Scaldaferri, F., & Mentella, M. C. (2024) · Nutrients · doi:10.3390/nu16142288 · Cited by 21

Poultry gut health: industry drivers, management determinants, and emerging research directions

Aminullah, N., Aminullah, N., Alam, S., & Danish, F. (2026) · Veterinary and Animal Science · doi:10.1016/j.vas.2026.100566 · Cited by 21

Relationship between Nutrient Intake and Human Gut Microbiota in Monozygotic Twins

Matsumoto, N., Park, J., Tomizawa, R., Kawashima, H., Hosomi, K., Mizuguchi, K., Honda, C., Ozaki, R., Iwatani, Y., Watanabe, M., et al. (2021) · Medicina · doi:10.3390/medicina57030275 · Cited by 20

A Class IIb Bacteriocin Plantaricin NC8 Modulates Gut Microbiota of Different Enterotypes in vitro

Pu, J., Hang, S., Liu, M., Chen, Z., Xiong, J., Li, Y., Wu, H., Zhao, X., Liu, S., Gu, Q., et al. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.877948 · Cited by 21

Small Intestinal Bacterial Overgrowth in Patients with Roux-en-Y Gastric Bypass and One-Anastomosis Gastric Bypass

Novljan, U., & Pintar, T. (2022) · Obesity Surgery · doi:10.1007/s11695-022-06299-z · Cited by 21

The human microbiome: A promising target for lung cancer treatment

Sun, Y. H., Wen, M., Liu, Y., Wang, Y., Jing, P., Gu, Z., Jiang, T., & Wang, W. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1091165 · Cited by 24

Pharmacomicrobiomics of Antidepressants in Depression: A Systematic Review

Brown, L. C., Bobo, W. V., Gall, C. A., Müller, D. J., & Bousman, C. (2023) · Journal of Personalized Medicine · doi:10.3390/jpm13071086 · Cited by 26

Determinants of microbial colonization in the premature gut

Chen, X., & Shi, Y. (2023) · Molecular Medicine · doi:10.1186/s10020-023-00689-4 · Cited by 27

Viral metagenomics of the gut virome of diarrheal children with Rotavirus A infection

Bao, S., Wang, H., Li, W., Wu, H., Lu, C., Liang, Y., Zhang, Q., Lü, X., Zhao, M., Lü, J., et al. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2234653 · Cited by 21

Clinical and Preclinical Evidence for Gut Microbiome Mechanisms in Substance Use Disorders

Hofford, R. S., & Kiraly, D. D. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.08.004 · Cited by 20

The Intestinal Microbiota in the Development of Chronic Liver Disease: Current Status

Stojić, J., Kukla, M., & Grgurević, I. (2023) · Diagnostics · doi:10.3390/diagnostics13182960 · Cited by 21

The potential role of gut microbiota outer membrane vesicles in colorectal cancer

Meng, R., Zeng, M., Ji, Y., Huang, X., & Xu, M. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1270158 · Cited by 21

Neuroimmunomodulation of tissue injury and disease: an expanding view of the inflammatory reflex pathway

Tanaka, S., HAMMOND, B. F., Rosin, D. L., & Okusa, M. D. (2019) · Bioelectronic Medicine · doi:10.1186/s42234-019-0029-8 · Cited by 22

Role of chemokines in aging and age-related diseases

Chaudhary, J. K., Danga, A. K., Kumari, A., Bhardwaj, A., & Rath, P. C. (2024) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2024.112009 · Cited by 24

Betaine regulates the gut-liver axis: a therapeutic approach for chronic liver diseases

Perumal, S. K., Arumugam, M. K., Osna, N. A., Rasineni, K., & Kharbanda, K. K. (2025) · Frontiers in Nutrition · doi:10.3389/fnut.2025.1478542 · Cited by 22

Immune cells: the key mediator between the gut microbiota and osteoporosis

Ma, T., Zhang, T., Peng, C., Liu, K., Xiong, Y., Chen, K., Peng, N., Wei, Z., Kuang, J., & Ou, L. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1680021 · Cited by 22

The Effect of Voluntary Exercise on Gut Microbiota in Partially Hydrolyzed Guar Gum Intake Mice under High-Fat Diet Feeding

Aoki, T., Oyanagi, E., Watanabe, C., Kobiki, N., Miura, S., Yokogawa, Y., Kitamura, H., Teramoto, F., Kremenik, M. J., & Yano, H. (2020) · Nutrients · doi:10.3390/nu12092508 · Cited by 21

FATORES ASSOCIADOS À OBESIDADE: UMA BREVE REVISÃO NARRATIVA

do Nascimento, O. V., do Nascimento, W. M., Melo, C. D. S., & Lima, É. S. (2022) · RECISATEC - REVISTA CIENTÍFICA SAÚDE E TECNOLOGIA · doi:10.53612/recisatec.v2i5.108 · Cited by 24

Microbiome and osteoarthritis: New insights from animal and human studies

Tan, T. C., Chong, T. K. Y., Low, A. H. L., & Leung, Y. Y. (2021) · International Journal of Rheumatic Diseases · doi:10.1111/1756-185x.14123 · Cited by 19

Short-term changes in the serum metabolome after laparoscopic sleeve gastrectomy and Roux-en-Y gastric bypass

Lee, G., Park, Y. S., Cho, C., Lee, H., Park, J.-Y., Park, D. J., Lee, J. H., Lee, H., Ha, T. K., Kim, Y.-J., et al. (2021) · Metabolomics · doi:10.1007/s11306-021-01826-y · Cited by 19

Clinical Manifestations of Neonatal Hyperbilirubinemia Are Related to Alterations in the Gut Microbiota

Zhang, X., Zeng, S., Cheng, G., He, L., Chen, M., Wang, M., Zhou, W., Qiu, H., & Wang, Z. (2022) · Children · doi:10.3390/children9050764 · Cited by 22

Gastrointestinal Changes and Alzheimer's Disease

Sohrabi, M., Sahu, B., Kaur, H., Hasler, W. A., Prakash, A. K., & Combs, C. K. (2022) · Current Alzheimer Research · doi:10.2174/1567205019666220617121255 · Cited by 18

The Activity of Prebiotics and Probiotics in Hepatogastrointestinal Disorders and Diseases Associated with Metabolic Syndrome

Rodríguez-Pastén, A., Pérez‐Hernández, N., Añorve‐Morga, J., Jiménez-Alvarado, R., Cariño‐Cortés, R., Sosa-Lozada, T., & Fernández‐Martínez, E. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23137229 · Cited by 20

Causal inference on microbiome-metabolome relations in observational host-microbiome data via in silico in vivo association pattern analyses

Hertel, J., Heinken, A., Fässler, D., & Thiele, I. (2023) · Cell Reports Methods · doi:10.1016/j.crmeth.2023.100615 · Cited by 21

Microbiota Composition and Probiotics Supplementations on Sleep Quality—A Systematic Review and Meta-Analysis

Santi, D., Debbi, V., Costantino, F., Spaggiari, G., Simoni, M., Greco, C., & Casarini, L. (2023) · Clocks & Sleep · doi:10.3390/clockssleep5040050 · Cited by 20

Mechanisms of intestinal dysbiosis: new insights into tuft cell functions

Coutry, N., Gasmi, I., Herbert, F., & Jay, P. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2379624 · Cited by 20

Impact of dietary compounds on cancer-related gut microbiota and microRNA

Rajoka, M. S. R., Jin, M., Zhao, H., Li, Q., Shao, D., Huang, Q., & Shi, J. (2018) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-018-8935-3 · Cited by 19

Brussels Chicory Stabilizes Unstable Atherosclerotic Plaques and Reshapes the Gut Microbiota in Apoe−/− Mice

Li, Q., Zhang, X., Du, Y., Liu, X., Chen, G., Xiang, P., Wu, H., Liu, C., & Wang, D. (2022) · Journal of Nutrition · doi:10.1093/jn/nxac103 · Cited by 19

The Use of Gut Microbial Modulation Strategies as Interventional Strategies for Ageing

Siddiqui, R., Mungroo, M. R., Alharbi, A. M., Alfahemi, H. H., & Khan, N. A. (2022) · Microorganisms · doi:10.3390/microorganisms10091869 · Cited by 19

Extract of Gardenia jasminoides Ellis Attenuates High-Fat Diet-Induced Glycolipid Metabolism Disorder in Rats by Targeting Gut Microbiota and TLR4/Myd88/NF-κB Pathway

Lv, C., Liu, X., Chen, S., Yi, Y., Wen, X., Li, T., & Qin, S. (2024) · Antioxidants · doi:10.3390/antiox13030293 · Cited by 21

Leaky Gut Biomarkers as Predictors of Depression and Suicidal Risk: A Systematic Review and Meta-Analysis

Morena, D., Lippi, M., Scopetti, M., Turillazzi, E., & Fineschi, V. (2025) · Diagnostics · doi:10.3390/diagnostics15131683 · Cited by 24

In the Age of Viral Pandemic, Can Ingredients Inspired by Human Milk and Infant Nutrition Be Repurposed to Support the Immune System?

Brink, L., Chichlowski, M., Pastor, N., Athmaram, T. N., & Shah, N. (2021) · Nutrients · doi:10.3390/nu13030870 · Cited by 18

Exploring the Effects of Six Weeks of Resistance Training on the Fecal Microbiome of Older Adult Males: Secondary Analysis of a Peanut Protein Supplemented Randomized Controlled Trial

Moore, J. H., Smith, K. S., Chen, D., Lamb, D. A., Smith, M. A., Osburn, S. C., Ruple, B. A., Morrow, C. D., Huggins, K. W., McDonald, J. R., et al. (2022) · Sports · doi:10.3390/sports10050065 · Cited by 20

Chronic Critical Illness: Current Aspects of the Problem (Review)

Parfenov, A., Razzhivin, V. P., & Petrova, M. V. (2022) · Современные технологии в медицине · doi:10.17691/stm2022.14.3.08 · Cited by 21

Metabolome, microbiome, and gene expression alterations in the colon of newborn piglets with intrauterine growth restriction

Tang, W., Zhang, W., Azad, M. A. K., Ma, C., Zhu, Q., & Kong, X. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.989060 · Cited by 18

The Role of Probiotics as an Adjunctive Therapy in Psoriasis

Gilli, I. O., SILVA, G. C. D., Mendes, V. M. D., Duarte, M. G., & Tanaka, A. A. (2022) · Journal of Psoriasis and Psoriatic Arthritis · doi:10.1177/24755303221142296 · Cited by 18

The gut microbiome meets nanomaterials: exposure and interplay with graphene nanoparticles

Wojciechowska, O., Costabile, A., & Kujawska, M. (2023) · Nanoscale Advances · doi:10.1039/d3na00696d · Cited by 22

Advancing gut microbiome insights: Graphene quantum dot nanobiosensors for microbial metabolite detection

Sadr, S., Nazemian, S., Dianaty, S., Hajjafari, A., Fazel, B., Rezaei, A., Rahdar, A., Fathi‐karkan, S., Bayat, M., Pandey, S., et al. (2025) · Chemical Engineering Journal · doi:10.1016/j.cej.2025.162954 · Cited by 19

Imbalance in the force: the dark side of the microbiota on stroke risk and progression

Kumar, K. P., & Wong, C. H. Y. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.10.002 · Cited by 18

Treating the Metabolic Syndrome by Fecal Transplantation—Current Status

Malnick, S. D. H., Fisher, D. L., Somin, M., & Neuman, M. G. (2021) · Biology · doi:10.3390/biology10050447 · Cited by 18

Impact of the gut microbiota on the immune system

Kogut, M. H. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-818708-1.00017-8 · Cited by 19

Probiotic activity traits in vitro and production of antimicrobial peptides by Lactobacillaceae isolates from pulque using Lactobacillus acidophilus NCFM as control

Ruiz-Ramírez, Y., Guadarrama-Mendoza, P. C., Escalante, A., Gilés-Gómez, M., & Valadez-Blanco, R. (2022) · Brazilian Journal of Microbiology · doi:10.1007/s42770-022-00684-7 · Cited by 18

Sirtuins and Gut Microbiota: Dynamics in Health and a Journey from Metabolic Dysfunction to Hepatocellular Carcinoma

Zhra, M., Elahi, M. A., Tariq, A., Abu‐Zaid, A., & Yaqinuddin, A. (2025) · Cells · doi:10.3390/cells14060466 · Cited by 18

Akkermansia muciniphila ameliorates chronic stress-induced colorectal tumor growth by releasing outer membrane vesicles

Jin, S., Lu, Y., Zuo, Y., Xu, Q., Hao, Y., Zuo, H., Cui, Z., Zhang, X., Wang, M., Li, H., et al. (2025) · Gut Microbes · doi:10.1080/19490976.2025.2555618 · Cited by 19

Crosstalk Among Gut Microbiota, Microbial Metabolites, and Inflammatory Cytokines: Current Understanding and Future Directions

Wu, G., Wang, R., Wang, Y., Sun, S., Chen, J., & Zhang, Q. (2025) · Foods · doi:10.3390/foods14223836 · Cited by 17

Changes in the Oxidative Stress Status of Dogs Affected by Acute Enteropathies

Candellone, A., Girolami, F., Badino, P., Jarriyawattanachaikul, W., & Odore, R. (2022) · Veterinary Sciences · doi:10.3390/vetsci9060276 · Cited by 17

Review of the relationship and underlying mechanisms between the Qinghai–Tibet plateau and host intestinal flora

Lv, J., Qi, P., Bai, L.-H., Yan, X.-D., & Zhang, L. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1055632 · Cited by 17

How the interplay among the tumor microenvironment and the gut microbiota influences the stemness of colorectal cancer cells

Díaz, M. B. N., Carriere, P., & Gentili, C. (2023) · World Journal of Stem Cells · doi:10.4252/wjsc.v15.i5.281 · Cited by 20

The impact of Astragaloside IV on the inflammatory response and gut microbiota in cases of acute lung injury is examined through the utilization of the PI3K/AKT/mTOR pathway

Luo, C., Ye, Y., Lv, A., Zuo, W., Yang, Y., Jiang, C., & Ke, J. (2024) · PLoS ONE · doi:10.1371/journal.pone.0305058 · Cited by 17

Bifidobacterium breve IPLA20005 affects in vitro the expression of hly and luxS genes, related to the virulence of Listeria monocytogenes Lm23

Ríos-Covián, D., Nogacka, A. M., Salazar, N., Hernández‐Barranco, A. M., Cuesta, I., Gueimonde, M., & Reyes‐Gavilán, C. G. D. L. (2018) · Canadian Journal of Microbiology · doi:10.1139/cjm-2017-0625 · Cited by 17

Aronia melanocarpa (Michx.) Elliott. attenuates dextran sulfate sodium-induced Inflammatory Bowel Disease via regulation of inflammation-related signaling pathways and modulation of the gut microbiota

Li, Y., Tsopmejio, I. S. N., Diao, Z., Xiao, H., Wang, X., Jin, Z., & Song, H. (2022) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2022.115190 · Cited by 17

Crosstalk Between the Spleen and Other Organs/Systems: Downstream Signaling Events

Tarantino, G., & Citro, V. (2024) · Immuno · doi:10.3390/immuno4040030 · Cited by 18

The Gut-Brain Axis in Alzheimer’s Disease: Exploring Microbial Influences and Therapeutic Strategies

Mustafa, M. A., Vadia, N., Varma, P., Al‐Shaker, H., Mohanty, B., Dhyani, A., Kaur, I., Chauhan, A. S., & Garg, G. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-05474-4 · Cited by 18

Involvement of the Intestinal Microbiota in the Appearance of Multiple Sclerosis: Aloe vera and Citrus bergamia as Potential Candidates for Intestinal Health

Maiuolo, J., Musolino, V., Gliozzi, M., Carresi, C., Scarano, F., Nucera, S., Scicchitano, M., Oppedisano, F., Bosco, F., Macrì, R., et al. (2022) · Nutrients · doi:10.3390/nu14132711 · Cited by 16

Polycystic Ovary Syndrome and Endometrial Cancer: A Scoping Review of the Literature on Gut Microbiota

Prakash, A., Nourianpour, M., Senok, A. C., & Atiomo, W. (2022) · Cells · doi:10.3390/cells11193038 · Cited by 16

Passion fruit peel and its zymolyte enhance gut function in Sanhuang broilers by improving antioxidation and short-chain fatty acids and decreasing inflammatory cytokines

Ju, Y., Huang, L., Luo, H. L., Huang, Y. C., Huang, X., Chen, G., Gui, J., Liu, Z. L., Yang, L., & Liu, X. Z. (2023) · Poultry Science · doi:10.1016/j.psj.2023.102672 · Cited by 17

Obesity, the Adipose Organ and Cancer in Humans: Association or Causation?

Trevellin, E., Bettini, S., Pilatone, A., Vettor, R., & Milan, G. (2023) · Biomedicines · doi:10.3390/biomedicines11051319 · Cited by 17

Hybrid nutraceutical of 2-ketoglutaric acid in improving inflammatory bowel disease: Role of prebiotics and TAK1 inhibitor

Kim, S., Jang, S., Kim, M. J., Lee, J. J., Kim, K., Kim, Y. H., Lee, J.-H., & Jung, S. K. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116126 · Cited by 16

The Interplay of Microbiome Dysbiosis and Cardiovascular Disease

Zaher, A., ElSaygh, J., Peterson, S. J., Weisberg, I. S., Parikh, M. A., & Frishman, W. H. (2024) · Cardiology in Review · doi:10.1097/crd.0000000000000701 · Cited by 17

Modulating effects of heat-killed and live Limosilactobacillus reuteri PSC102 on the immune response and gut microbiota of cyclophosphamide-treated rats

Ali, M. S., Lee, E., Quah, Y., Sayem, S. A. J., Abbas, M. A., Suk, K., Lee, S., & Park, S. (2024) · Veterinary Quarterly · doi:10.1080/01652176.2024.2344765 · Cited by 17

The role of Shigella spp. in propagating bacillary dysentery in humans and the prominence of nanotechnology in disease prevention

Hmar, E. B. L., Paul, S., & Sharma, H. K. (2024) · Future Journal of Pharmaceutical Sciences · doi:10.1186/s43094-024-00676-4 · Cited by 17

Curcumin Mitigates Gut Dysbiosis and Enhances Gut Barrier Function to Alleviate Metabolic Dysfunction in Obese, Aged Mice

Lamichhane, G., Olawale, F., Liu, J., Lee, D., Lee, S., Chaffin, N., Alake, S. E., Lucas, E. A., Zhang, G., Egan, J. M., et al. (2024) · Biology · doi:10.3390/biology13120955 · Cited by 17

Back to Roots: Dysbiosis, Obesity, Metabolic Syndrome, Type 2 Diabetes Mellitus, and Obstructive Sleep Apnea—Is There an Objective Connection? A Narrative Review

Timofticiuc, D. C. P., Bădescu, D., Moța, M., Ștefan, A. G., Mitrea, A., Clenciu, D., Efrem, I. C., Roșu, M. M., Vladu, B. E., Gheonea, T. C., et al. (2024) · Nutrients · doi:10.3390/nu16234057 · Cited by 20

The human microbiome: redefining cancer pathogenesis and therapy

Adlakha, Y. K., & Chhabra, R. (2025) · Cancer Cell International · doi:10.1186/s12935-025-03787-x · Cited by 20

Intestinal inflammation alters mucosal carbohydrate foraging and monosaccharide incorporation into microbial glycans

Weiss, G. A., Grabinger, T., Garzon, J. F. G., Hasler, T., Greppi, A., Lacroix, C., Khanzhin, N., & Hennet, T. (2020) · Cellular Microbiology · doi:10.1111/cmi.13269 · Cited by 17

Micro(nano)plastics in the total environment – A holistic review

Jaszczyszyn, K., Kiedrzyńska, E., Matuszewska, D., Xue, J., & Kiedrzyński, M. (2025) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2025.179806 · Cited by 17

Interaction between dietary omega‐3 polyunsaturated fatty acids, obesity and gut microbiota in preclinical models: A systematic review of randomized controlled trials

Cao, B., Sun, Y., Lam, C., Chen, Y., Dri, C. E., & McIntyre, R. S. (2025) · Diabetes Obesity and Metabolism · doi:10.1111/dom.16535 · Cited by 17

Effects of Microencapsulated Sodium Butyrate, Probiotics and Short Chain Fructooligosaccharides in Patients with Irritable Bowel Syndrome: A Study Protocol of a Randomized Double-Blind Placebo-Controlled Trial

Gąsiorowska, A., Romanowski, M., Walecka‐Kapica, E., Kaczka, A., Chojnacki, C. J., Padysz, M., Siedlecka, M., Bierła, J. B., Steinert, R. E., & Cukrowská, B. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11216587 · Cited by 18

Garlic supplementation improves intestinal transit time, lipid accumulation product and cardiometabolic indices in subjects with metabolic syndrome: A randomized controlled trial

Sangouni, A. A., Alizadeh, M., Jamalzehi, A., Hosseinzadeh, M., & Parastouei, K. (2023) · Phytotherapy Research · doi:10.1002/ptr.7741 · Cited by 15

Microbiome Alterations and Alzheimer’s Disease: Modeling Strategies with Transgenic Mice

López-Villodres, J. A., Escamilla, A., Mercado-Sáenz, S., Alba-Tercedor, C., Rodríguez‐Pérez, L., Arranz‐Salas, I., Sanchez-Varo, R. M., & Bermúdez, D. (2023) · Biomedicines · doi:10.3390/biomedicines11071846 · Cited by 16

Intestinal microbiota: A bridge between intermittent fasting and tumors

Liu, J., Shao, N., Qiu, H., Zhao, J., Chen, C., Wan, J., He, Z., Zhao, X., & Xu, L. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115484 · Cited by 15

Antidepressant-like Effects of Representative Types of Food and Their Possible Mechanisms

Piao, J., Wang, Y., Zhang, T., Zhao, J., Lv, Q., Ruan, M., Yu, Q., & Li, B. (2023) · Molecules · doi:10.3390/molecules28196992 · Cited by 16

Artemether Attenuates Gut Barrier Dysfunction and Intestinal Flora Imbalance in High-Fat and High-Fructose Diet-Fed Mice

Ren, X., Xu, J., Xu, Y., Wang, Q., Huang, K., & He, X. (2023) · Nutrients · doi:10.3390/nu15234860 · Cited by 15

Gut-immune axis and cardiovascular risk in chronic kidney disease

Behrens, F., Bartolomaeus, H., Wilck, N., & Holle, J. B. (2023) · Clinical Kidney Journal · doi:10.1093/ckj/sfad303 · Cited by 17

The Significance of Plant Nutrition in the Creation of the Intestinal Microbiota—Prevention of Chronic Diseases: A Narrative Review

Jovandarić, M. Z., Jovanović, K., Raus, M., Babić, S., Igic, T., Kotlica, B., & Milićević, S. (2024) · Medicina · doi:10.3390/medicina60121969 · Cited by 18

The Complex Role of Gut Microbiota in Systemic Lupus Erythematosus and Lupus Nephritis: From Pathogenetic Factor to Therapeutic Target

Parodi, E. L., Novi, M., Bottino, P., Porta, E. L., Merlotti, G., Castello, L. M., Gotta, F., Rocchetti, A., & Quaglia, M. (2025) · Microorganisms · doi:10.3390/microorganisms13020445 · Cited by 16

Gut Microbiota–Brain Axis as a Potential Modulator of Psychological Stress after Spinal Cord Injury

Musleh-Vega, S., Ojeda, J., & Vidal, P. M. (2022) · Biomedicines · doi:10.3390/biomedicines10040847 · Cited by 15

Supplementation with yeast culture improves the integrity of intestinal tight junction proteins via NOD1/NF‐κB P65 pathway in weaned piglets and H2O2-challenged IPEC-J2 cells

Wang, S., Zhu, S., Zhang, J., Li, H., Yang, D., Huang, S., Wei, Z., Liang, X., & Wang, Z. (2020) · Journal of Functional Foods · doi:10.1016/j.jff.2020.104058 · Cited by 15

Gut microbiota and bronchopulmonary dysplasia

Yang, K., He, S., & Dong, W. (2021) · Pediatric Pulmonology · doi:10.1002/ppul.25508 · Cited by 14

How Perturbated Metabolites in Diabetes Mellitus Affect the Pathogenesis of Hypertension?

Ning, Z., Song, Z., Wang, C., Peng, S., Wan, X., Liu, Z., & Lü, A. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.705588 · Cited by 15

Clostridioides difficile Infection in Patients after Organ Transplantation—A Narrative Overview

Dudzicz, S., Więcek, A., & Adamczak, M. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11154365 · Cited by 14

A Systematic Review of Mixed Studies Exploring the Effects of Probiotics on Gut-Microbiome to Modulate Therapy in Children With Autism Spectrum Disorder

Patel, M., Atluri, L. M., Gonzalez, N. A., Sakhamuri, N., Athiyaman, S., Randhi, B., Gutlapalli, S. D., Pu, J., Zaidi, M. F., & Khan, S. (2022) · Cureus · doi:10.7759/cureus.32313 · Cited by 18

Pathogenic role of the gut microbiota in gastrointestinal diseases

Nagao‐Kitamoto, H., Kitamoto, S., Kuffa, P., & Kamada, N. (2016) · Intestinal Research · doi:10.5217/ir.2016.14.2.127 · Cited by 178

Relationship between intestinal microbiota, diet and biological systems: an integrated view

Ferreira, R. D. S., Mendonça, L. A. B. M., Ribeiro, C. F. A., Calças, N. C., Guimarães, R. D. C. A., do Nascimento, V. A., Freitas, K. D. C., Carvalho, C. M. E., de Castro, A. P., & Franco, O. L. (2020) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2020.1836605 · Cited by 46

Gut dysbacteriosis and intestinal disease: mechanism and treatment

Meng, X., ZHANG, G., Cao, H., Yu, D., Fang, X., de Vos, W. M., & Wu, H. (2020) · Journal of Applied Microbiology · doi:10.1111/jam.14661 · Cited by 130

Disbiosis en la microbiota intestinal

Moreno, X. (2024) · Revista GEN · doi:10.61155/gen.v76i1.602

The intestinal microbiota: its role in health and disease

Biedermann, L., & Rogler, G. (2015) · European Journal of Pediatrics · doi:10.1007/s00431-014-2476-2 · Cited by 227