Gut microbiota and metabolic syndrome

International Diabetes Federation 2017

Carracher, A. M., Marathe, P. H., & Close, K. L. (2018) · Journal of Diabetes · doi:10.1111/1753-0407.12644 · Cited by 13,379

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

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Diet rapidly and reproducibly alters the human gut microbiome

David, L. A., Maurice, C. F., Carmody, R. N., Gootenberg, D. B., Button, J. E., Wolfe, B. E., Ling, A. V., Devlin, A. S., Varma, Y., Fischbach, M. A., et al. (2014) · Nature · doi:10.1038/nature12820 · Cited by 10,100

Human gut microbes associated with obesity

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A core gut microbiome in obese and lean twins

Turnbaugh, P. J., Hamady, M., Yatsunenko, T., Cantarel, B. L., Duncan, A., Ley, R. E., Sogin, M. L., Jones, W. J., Roe, B. A., Affourtit, J. P., et al. (2009) · Nature · doi:10.1038/nature07540 · Cited by 7,823

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

A metagenome-wide association study of gut microbiota in type 2 diabetes

Qin, J., Li, Y., Cai, Z., Li, S., Zhu, J., Zhang, F., Liang, S., Zhang, W., Guan, Y., Shen, D., et al. (2012) · Nature · doi:10.1038/nature11450 · Cited by 6,762

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

Impact of Saskatoon berry powder on insulin resistance and relationship with intestinal microbiota in high fat–high sucrose diet-induced obese mice

Zhao, R., Khafipour, E., Sepehri, S., Huang, F., Trust Beta, & Shen, G. X. (2019) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2019.03.023 · Cited by 33

Oxidative Stress and Gut Microbiota * *Conflict of interest: None.

Marciano, F., & Vajro, P. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805377-5.00008-4 · Cited by 34

Pathophysiological Commonality Between Irritable Bowel Syndrome and Metabolic Syndrome: Role of Corticotropin-releasing Factor-Toll-like Receptor 4-Proinflammatory Cytokine Signaling

Nozu, T., & Okumura, T. (2022) · Journal of Neurogastroenterology and Motility · doi:10.5056/jnm21002 · Cited by 31

Long-term high-fructose high-fat diet feeding elicits insulin resistance, exacerbates dyslipidemia and induces gut microbiota dysbiosis in WHHL rabbits

Moughaizel, M., Dagher, E., Jablaoui, A., Thorin, C., Rhimi, M., Desfontis, J., & Mallem, Y. (2022) · PLoS ONE · doi:10.1371/journal.pone.0264215 · Cited by 34

Algal polysaccharides and derivatives as potential therapeutics for obesity and related metabolic diseases

Yang, Z., Wang, H., Liu, N., Zhao, K., Sheng, Y., Pang, H., Shao, K., Zhang, M., Li, S., & He, N. (2022) · Food & Function · doi:10.1039/d2fo02185d · Cited by 31

Eubacterium siraeum suppresses fat deposition via decreasing the tyrosine-mediated PI3K/AKT signaling pathway in high-fat diet-induced obesity

Lai, X., Liu, S., Miao, J., Shen, R., Wang, Z., Zhang, Z., Gong, H., Li, M., Pan, Y., & Wang, Q. (2024) · Microbiome · doi:10.1186/s40168-024-01944-4 · Cited by 34

Key Insights into Gut Alterations in Metabolic Syndrome

Boicean, A., Ichim, C., Sasu, S.-M., & Todor, S. B. (2025) · Journal of Clinical Medicine · doi:10.3390/jcm14082678 · Cited by 32

Key Considerations and Methods in the Study of Gene–Environment Interactions

Simon, P. H. G., Sylvestre, M., Tremblay, J., & Hamet, P. (2016) · American Journal of Hypertension · doi:10.1093/ajh/hpw021 · Cited by 32

The Effect of Synbiotic Supplementation on Body Composition and Lipid Profile in Patients with NAFLD: A Randomized, Double Blind, Placebo-Controlled Clinical Trial Study

Asgharian, A., Mohammadi, V., Gholi, Z., Esmaillzade, A., Feizi, A., & Askari, G. (2017) · Iranian Red Crescent Medical Journal · doi:10.5812/ircmj.42902 · Cited by 30

Endotoxin and Other Microbial Translocation Markers in the Blood: A Clue to Understand Leaky Gut Syndrome

Fukui, H. (2016) · Cellular & Molecular Medicine Open access · doi:10.21767/2573-5365.100023 · Cited by 30

Whole Grains, Dietary Fibers and the Human Gut Microbiota: A Systematic Review of Existing Literature

Tangestani, H., Emamat, H., Ghalandari, H., & Shab‐Bidar, S. (2020) · Recent Patents on Food Nutrition & Agriculture · doi:10.2174/2212798411666200316152252 · Cited by 30

Hop bitter acids: resources, biosynthesis, and applications

Zhang, G., Zhang, N., Yang, A., Huang, J., Ren, X., Xian, M., & Zou, H. (2021) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-021-11329-4 · Cited by 29

Impact of the Mediterranean Diet on the Gut Microbiome of a Well-Defined Cohort of Healthy Individuals

Vázquez‐Cuesta, S., Lozano-García, N., Fernández, S. R., Fernández, A. I., Bermejo, J., Fernández‐Avilés, F., Muñóz, P., Bouza, E., & Reigadas, E. (2024) · Nutrients · doi:10.3390/nu16060793 · Cited by 29

Insights into the unique roles of extracellular vesicles for gut health modulation: Mechanisms, challenges, and perspectives

Wu, Q., Kan, J., Fu, C., Liu, X., Cui, Z., Wang, S., Le, Y., Li, Z., Liu, Q., Zhang, Y., et al. (2024) · Current Research in Microbial Sciences · doi:10.1016/j.crmicr.2024.100301 · Cited by 29

Effect of a Fiber D-Limonene-Enriched Food Supplement on Intestinal Microbiota and Metabolic Parameters of Mice on a High-Fat Diet

Valerii, M. C., Turroni, S., Ferreri, C., Zaro, M., Sansone, A., Dalpiaz, A., Botti, G., Ferraro, L., Spigarelli, R., Bellocchio, I., et al. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13111753 · Cited by 28

Fermented brown rice beverage distinctively modulates the gut microbiota in Okinawans with metabolic syndrome: A randomized controlled trial

赤嶺ゆかり, Millman, J. F., Uema, T., Okamoto, S., Yonamine, M., Uehara, M., Kozuka, C., Kaname, T., Shimabukuro, M., Kinjo, K., et al. (2022) · Nutrition Research · doi:10.1016/j.nutres.2022.03.013 · Cited by 32

The Metabolic Syndrome Puzzles; Possible Pathogenesis and Management

Marzoog, B. A. (2022) · Current Diabetes Reviews · doi:10.2174/1573399818666220429100411 · Cited by 30

Proanthocyanidins: Impact on Gut Microbiota and Intestinal Action Mechanisms in the Prevention and Treatment of Metabolic Syndrome

Redondo‐Castillejo, R., Garcimartín, A., Hernández-Martín, M., López‐Oliva, M. E., Bocanegra, A., Macho‐González, A., Bastida, S., Benedı́, J., & Sánchez-Muniz, F. J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065369 · Cited by 31

Small intestinal bacterial overgrowth and non‐alcoholic fatty liver disease diagnosed by transient elastography and liver biopsy

Mikolašević, I., Delija, B., Mijić, A., Stevanović, T., Skenderević, N., Šoša, I., Zrnić, I. K., Abram, M., Krznarić, Ž., Domislović, V., et al. (2021) · International Journal of Clinical Practice · doi:10.1111/ijcp.13947 · Cited by 28

A Scoping Review of the Relationship between Intermittent Fasting and the Human Gut Microbiota: Current Knowledge and Future Directions

Popa, A. D., Niță, O., Gherasim, A., Enache, A. I., Caba, L., Mihalache, L., & Arhire, L. I. (2023) · Nutrients · doi:10.3390/nu15092095 · Cited by 31

Characterization of gut microbiota in mouse models of aging and sarcopenia

Lee, S. Y., Kim, J. H., Lee, D. Y., & Hur, S. J. (2023) · Microbiological Research · doi:10.1016/j.micres.2023.127462 · Cited by 29

Effect of chrysin on changes in intestinal environment and microbiome induced by fructose-feeding in rats

Andrade, N., Marques, C., Andrade, S., Silva, C., Rodrigues, I., Guardão, L., Guimarães, J. T., Keating, E., Calhau, C., & Martel, F. (2019) · Food & Function · doi:10.1039/c9fo01142k · Cited by 29

Cranberry polyphenols‐gut microbiota interactions and potential health benefits: An updated review

PRASAIN, J. K., & Barnes, S. (2020) · Food Frontiers · doi:10.1002/fft2.56 · Cited by 27

Green and Oolong Tea Extracts With Different Phytochemical Compositions Prevent Hypertension and Modulate the Intestinal Flora in a High-Salt Diet Fed Wistar Rats

Ye, X., Tang, X., Li, F., Zhu, J., Wu, M., Wei, X., & Wang, Y. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.892801 · Cited by 27

Evaluation of the prebiotic potential of arabinoxylans extracted from wheat distillers’ dried grains with solubles (DDGS) and in-process samples

Monteagudo-Mera, A., Chatzifragkou, A., Kosík, O., Gibson, G. R., Lovegrove, A., Shewry, P. R., & Charalampopoulos, D. (2018) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-018-9171-6 · Cited by 28

There is No Distinctive Gut Microbiota Signature in the Metabolic Syndrome: Contribution of Cardiovascular Disease Risk Factors and Associated Medication

Cortés‐Martín, A., Iglesias‐Aguirre, C. E., Meoro, A., Selma, M. V., & Espín, J. C. (2020) · Microorganisms · doi:10.3390/microorganisms8030416 · Cited by 27

Erratum: (1) Pediatric Obesity and Cardiometabolic Disorders: Risk Factors and Biomarkers.

Levy, E. H., Saenger, A. K., Steffes, M. W., & DELVIN, E. E. (2017) · Europe PMC (PubMed Central) · Cited by 26

Gut Microbial Profiles in Nereis succinea and Their Contribution to the Degradation of Organic Pollutants

Wang, D., Ren, J., Tan, Z., & You, J. (2020) · Environmental Science & Technology · doi:10.1021/acs.est.9b07854 · Cited by 26

Gallstone Disease and Bacterial Metabolic Performance of Gut Microbiota in Middle-Aged and Older Patients

Georgescu, D., Ioniță, I., Lascu, A., Huţ, E. F., Dragan, S. R., Ancusa, O., Ionita, M., Călămar-Popovici, D., Georgescu, L.-A., & Lighezan, D.-F. (2022) · International Journal of General Medicine · doi:10.2147/ijgm.s350104 · Cited by 26

Towards early detection of neurodegenerative diseases: A gut feeling

Makdissi, S., Parsons, B., & Cara, F. D. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1087091 · Cited by 28

Gut microbiome influences incidence and outcomes of breast cancer by regulating levels and activity of steroid hormones in women

Chapadgaonkar, S. S., Bajpai, S., & Godbole, M. S. (2023) · Cancer Reports · doi:10.1002/cnr2.1847 · Cited by 28

Diets link metabolic syndrome and colorectal cancer development

Saetang, J., & Sangkhathat, S. (2017) · Oncology Reports · doi:10.3892/or.2017.5385 · Cited by 26

New insights into the interplay between autophagy, gut microbiota and insulin resistance in metabolic syndrome

Zhao, J., Duan, L., Li, J., Yao, C., Wang, G., Mi, J., Yu, Y., Ding, L., Zhao, Y., Yan, G., et al. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116807 · Cited by 26

Glycomacropeptide: A Bioactive Milk Derivative to Alleviate Metabolic Syndrome Outcomes

Sauvé, M. F., Spahis, S., DELVIN, E. E., & Levy, E. H. (2020) · Antioxidants and Redox Signaling · doi:10.1089/ars.2019.7994 · Cited by 25

The role of microbiome: a novel insight into urolithiasis

Hong, S., Xia, Q., Yang, Y., Li, C., Zhang, J., Xu, J., Qin, B., Xun, Y., & Wang, S. (2022) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2022.2045899 · Cited by 27

Recent advances in molecular biology of metabolic syndrome pathophysiology: endothelial dysfunction as a potential therapeutic target

Marzoog, B. A. (2022) · Journal of Diabetes & Metabolic Disorders · doi:10.1007/s40200-022-01088-y · Cited by 25

Genistein protects against hyperglycemia and fatty liver disease in diet-induced prediabetes mice via activating hepatic insulin signaling pathway

Zhang, N., Zhang, W., Guo, X., Liu, J., Li, S., Zhang, H., & Fan, B. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1072044 · Cited by 25

Dietary phytic acid prevents fatty liver by reducing expression of hepatic lipogenic enzymes and modulates gut microflora in rats fed a high-sucrose diet

Sekita, A., Okazaki, Y., & Katayama, T. (2016) · Nutrition · doi:10.1016/j.nut.2016.01.003 · Cited by 25

Gut Microbiota, Obesity and Bariatric Surgery: Current Knowledge and Future Perspectives

Cătoi, A. F., Vodnar, D. C., Corina, A., Nikolić, D., Citarrella, R., Pérez‐Martínez, P., & Rizzo, M. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666190708190437 · Cited by 26

Resveratrol treatment improves the altered metabolism and related dysbiosis of gut programed by prenatal high-fat diet and postnatal high-fat diet exposure

Huang, Y., Huang, L., Sheen, J., Hou, C., Yeh, Y., Chiang, C.-P., Lin, I.-C., Tiao, M., Tsai, C., Lin, Y., et al. (2019) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2019.108260 · Cited by 24

Nutritionally Attenuating the Human Gut Microbiome To Prevent and Manage Metabolic Syndrome

Louis-Jean, S. F., & Martirosyan, D. M. (2019) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.9b04879 · Cited by 24

Mendelian Randomization Analysis Reveals Causal Effects of the Human Gut Microbiota on Abdominal Obesity

Xu, Q., Zhang, S., Wang, R., Weng, Y.-J., Cui, X., Wei, X., Ni, J., Ren, H., Zhang, L., & Pei, Y. (2021) · Journal of Nutrition · doi:10.1093/jn/nxab025 · Cited by 24

Gut Microbiota Interactions With Obesity

Falalyeyeva, T. M., Chornenka, N., Cherkasova, L., Tsyryuk, O., Molchek, N., Kovalchuk, O. I., Kyriachenko, Y., Остапченко, Л. І., & Kobyliak, N. M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819265-8.00030-9 · Cited by 24

Profiling gut microbiota and bile acid metabolism in critically ill children

Kean, I. R. L., Wagner, J., Wijeyesekera, A., de Goffau, M. C., Thurston, S., Clark, J. A., White, D. K., Ridout, J. A., Agrawal, S., Kayani, R., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-13640-0 · Cited by 25

Nonrestorative sleep is a risk factor for metabolic syndrome in the general Japanese population

Otsuka, Y., Kaneita, Y., Tanaka, K., Itani, O., Kaneko, Y., Suzuki, M., Matsumoto, Y., & Kuriyama, K. (2023) · Diabetology & Metabolic Syndrome · doi:10.1186/s13098-023-00999-x · Cited by 24

Alterations in the Gut Microbiota in Pregnant Women with Pregestational Type 2 Diabetes Mellitus

Ren, Y., Hao, L., Liu, J., Wang, P., Ding, Q., Chen, C., & Song, Y. (2023) · mSystems · doi:10.1128/msystems.01146-22 · Cited by 28

Comorbid brain disorders associated with diabetes: therapeutic potentials of prebiotics, probiotics and herbal drugs

Thakur, A. K., Tyagi, S., & Shekhar, N. (2019) · Translational Medicine Communications · doi:10.1186/s41231-019-0043-6 · Cited by 25

Akkermansia muciniphila and host interaction within the intestinal tract

Karamzin, A. M., Ropot, A. V., Sergeyev, O. V., & Халтурина, Е. О. (2021) · Anaerobe · doi:10.1016/j.anaerobe.2021.102472 · Cited by 24

Gut Microbiome in the Progression of NAFLD, NASH and Cirrhosis, and Its Connection with Biotics: A Bibliometric Study Using Dimensions Scientific Research Database

Pezzino, S., Sofia, M., Mazzone, C., Castorina, S., Puleo, S., Barchitta, M., Agodi, A., Gallo, L., Greca, G. L., & Latteri, S. (2023) · Biology · doi:10.3390/biology12050662 · Cited by 27

Gut‐on‐a‐chip platforms: Bridging in vitro and in vivo models for advanced gastrointestinal research

Ofori‐Kwafo, A., Sigdel, I., Mamun, E. A., Zubcevic, J. A., & Tang, Y. (2025) · Physiological Reports · doi:10.14814/phy2.70356 · Cited by 23

Dietary Influence on the Dynamics of the Human Gut Microbiome: Prospective Implications in Interventional Therapies

Adithya, K. K., Rajeev, R., Selvin, J., & Kiran, G. S. (2021) · ACS Food Science & Technology · doi:10.1021/acsfoodscitech.0c00075 · Cited by 23

Manipulation of cadmium and diethylhexyl phthalate on Rana chensinensis tadpoles affects the intestinal microbiota and fatty acid metabolism

Shen, Y., Jiang, Z., Zhong, X., Wang, H., Liu, Y., & Li, X. (2022) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2022.153455 · Cited by 22

Gut bacteria-derived peptidoglycan induces a metabolic syndrome-like phenotype via NF-κB-dependent insulin/PI3K signaling reduction in Drosophila renal system

Zugasti, O., Raphael, T., & Royet, J. (2020) · Scientific Reports · doi:10.1038/s41598-020-70455-7 · Cited by 21

Characterization of gut microbiota composition in HIV-infected patients with metabolic syndrome

Villanueva-Millán, M. J., Pérez‐Matute, P., Recio‐Fernández, E., Rosales, J. M. L., & Oteo, J. A. (2019) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-019-00673-9 · Cited by 21

Gypenosides counteract hepatic steatosis and intestinal barrier injury in rats with metabolic associated fatty liver disease by modulating the adenosine monophosphate activated protein kinase and Toll-like receptor 4/nuclear factor kappa B pathways

Shen, S., Wang, K., Zhi, Y., & Dong, Y. (2022) · Pharmaceutical Biology · doi:10.1080/13880209.2022.2126503 · Cited by 21

Biomolecular Actions by Intestinal Endotoxemia in Metabolic Syndrome

Charitos, I. A., Aliani, M., Tondo, P., Venneri, M. G., Castellana, G., Scioscia, G., Castellaneta, F., Lacedonia, D., & Carone, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25052841 · Cited by 26

Efficacy of the Synbiotic Supplementation on the Metabolic Factors in Patients with Metabolic Syndrome: A Randomized, Triple‐Blind, Placebo‐Controlled Trial

Rahimi, F. C., Pasdar, Y., Kaviani, M., Abbasi, S., Fry, H. L., Hekmatdoost, A., Nikpayam, O., Sohrab, G., Rezaei, M., Nachvak, S. M., et al. (2022) · International Journal of Clinical Practice · doi:10.1155/2022/2967977 · Cited by 21

The Role of 4-Phenylbutyric Acid in Gut Microbial Dysbiosis in a Mouse Model of Simulated Microgravity

Shama, S., Qaisar, R., Khan, N. A., Tauseef, I., & Siddiqui, R. (2022) · Life · doi:10.3390/life12091301 · Cited by 20

Obesity, diabetes mellitus, and pancreatic carcinogenesis: Correlations, prevention, and diagnostic implications

Ruze, R., Chen, Y., Xu, R., Song, J., Yin, X., Wang, C., & Xu, Q. (2022) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2022.188844 · Cited by 19

Dietary 5-demethylnobiletin prevents antibiotic-associated dysbiosis of gut microbiota and damage to the colonic barrier

Zhan, M., Liang, X., Chen, J., Yang, X., Han, Y., Zhao, C., Xiao, J., Cao, Y., Xiao, H., & Song, M. (2023) · Food & Function · doi:10.1039/d3fo00516j · Cited by 21

The effects of curcumin and Lactobacillus acidophilus on certain hormones and insulin resistance in rats with metabolic syndrome

Kapar, F. S., & Çiftçi, G. (2020) · Journal of Diabetes & Metabolic Disorders · doi:10.1007/s40200-020-00578-1 · Cited by 20

Changes to trimethylamine-N-oxide and its precursors in nascent metabolic syndrome

Lent-Schochet, D., Silva, R., McLaughlin, M. J., Huet, B., & Jialal, I. (2018) · Hormone Molecular Biology and Clinical Investigation · doi:10.1515/hmbci-2018-0015 · Cited by 22

Probiotic Lactobacillus fermentum TSF331, Lactobacillus reuteri TSR332, and Lactobacillus plantarum TSP05 improved liver function and uric acid management-A pilot study

Lin, J., Lin, C.-H., Kuo, Y., Liao, C., Chen, J., Tsai, S., Li, C.-M., Hsu, Y.-C., Huang, Y.-Y., Hsia, K.-C., et al. (2024) · PLoS ONE · doi:10.1371/journal.pone.0307181 · Cited by 21

Probiotics and obesity associated disease: an extended view beyond traditional strains

Falalyeyeva, T. M., MAMULA, Y., Scarpellini, E., Leshchenko, I. V., HUMENIUK, A., Pankiv, І. V., & Kobyliak, N. M. (2022) · Minerva Gastroenterology · doi:10.23736/s2724-5985.21.02909-0 · Cited by 19

Structures and functions of the gut microbial lipidome

Morozumi, S., Ueda, M., Okahashi, N., & Arita, M. (2022) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2021.159110 · Cited by 20

Deciphering Intertwined Molecular Pathways Underlying Metabolic Syndrome Leading to Parkinson’s Disease

Soni, R., & Shah, J. (2022) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.2c00165 · Cited by 19

Analysis of the gut microbiome in obese native Tibetan children living at different altitudes: A case–control study

Du, W., Liu, L., Ma, Y., Zhu, Q., Jia, R., Han, Y., Wu, Z., Yan, X., Ailizire, A., & Zhang, W. (2022) · Frontiers in Public Health · doi:10.3389/fpubh.2022.963202 · Cited by 21

Effect of sucroferric oxyhydroxide on gastrointestinal microbiome and uremic toxins in patients with chronic kidney disease undergoing hemodialysis

Iguchi, A., Yamamoto, S., Oda, A., Tanaka, K., Kazama, J. J., Saeki, T., Yamazaki, H., Ishioka, K., Suzutani, T., & Narita, I. (2020) · Clinical and Experimental Nephrology · doi:10.1007/s10157-020-01892-x · Cited by 19

Gut microbiota of obese and diabetic Thai subjects and interplay with dietary habits and blood profiles

Gruneck, L., Kullawong, N., Kespechara, K., & Popluechai, S. (2020) · PeerJ · doi:10.7717/peerj.9622 · Cited by 19

Branched chain amino acids: Passive biomarkers or the key to the pathogenesis of cardiometabolic diseases?

Siomkajło, M., & Daroszewski, J. (2019) · Advances in Clinical and Experimental Medicine · doi:10.17219/acem/104542 · Cited by 19

Consistent gut bacterial and short-chain fatty acid signatures in hypoabsorptive bariatric surgeries correlate with metabolic benefits in rats

Mukorako, P., Lemoine, N., Biertho, L. D., Lebel, S., Roy, M.-C., Plamondon, J., Tchernof, A., Varin, T. V., Anhê, F. F., St-Pierre, D. H., et al. (2021) · International Journal of Obesity · doi:10.1038/s41366-021-00973-5 · Cited by 19

Metformin Influence on the Intestinal Microbiota and Organism of Rats with Metabolic Syndrome

Ермоленко, Е. И., Симаненкова, А. В., Alferova, L. S., Lavrenova, N. S., Kotyleva, M., Минасян, С. М., Chernikova, A. T., Тимкина, Н. В., Сергеевич, Г. Н., Dmitriev, A., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23126837 · Cited by 17

Nutritional Elements in Sleep

Pattnaik, H., Mir, M., Boike, S., Kashyap, R., Khan, S. A., & Surani, S. (2022) · Cureus · doi:10.7759/cureus.32803 · Cited by 21

Metal transporter SLC39A14/ZIP14 modulates regulation between the gut microbiome and host metabolism

Mitchell, S. B., Thorn, T. L., Lee, M.-T., Kim, Y., Comrie, J. M. C., Bai, Z. S., Johnson, E. L., & Aydemir, T. B. (2023) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00091.2023 · Cited by 18

From Microbes to Myocardium: A Comprehensive Review of the Impact of the Gut-Brain Axis on Cardiovascular Disease

Singh, A. K., Kishore, P. S., & Khan, S. (2024) · Cureus · doi:10.7759/cureus.70877 · Cited by 21

Mediators of insulin resistance & cardiometabolic risk

Bodhini, D., & Mohan, V. (2018) · The Indian Journal of Medical Research · doi:10.4103/ijmr.ijmr_969_18 · Cited by 18

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

Composition, polyphenol bioavailability, and health benefits of aronia berry: a review

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Role of gut microbiota in the pathogenesis of metabolic syndrome: an updated comprehensive review from mechanisms to clinical implications

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