The DOI matches its Crossref record; 201 of the 201 references it cites were found in a registry or an index.
Gut microbiome and aging: Physiological and mechanistic insights
Open accessAbstract
) and is exposed to innumerable microorganisms from the mother as well as the surrounding environment. Concurrently, the host responses to these microbes during early life manifest during the development of an otherwise hitherto immature immune system. The human gut microbiome, which comprises an extremely diverse and complex community of microorganisms inhabiting the intestinal tract, keeps on fluctuating during different stages of life. While these deviations are largely natural, inevitable and benign, recent studies show that unsolicited perturbations in gut microbiota configuration could have strong impact on several features of host health and disease. Our microbiota undergoes the most prominent deviations during infancy and old age and, interestingly, our immune health is also in its weakest and most unstable state during these two critical stages of life, indicating that our microbiota and health develop and age hand-in-hand. However, the mechanisms underlying these interactions are only now beginning to be revealed. The present review summarizes the evidences related to the age-associated changes in intestinal microbiota and vice-versa, mechanisms involved in this bi-directional relationship, and the prospective for development of microbiota-based interventions such as probiotics for healthy aging.
Overview
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
Verification
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 the citing paper
“Although continued development of the microbiota in adolescence has been indicated in some studies, a core, albeit individualized, microbial profile develops in adulthood that is relatively stable and resilient in the absence of extreme external stressors (e.g., dietary changes or antibiotic treatment) (233-235).”
From Diet and the Microbiota–Gut–Brain Axis: Sowing the Seeds of Good Mental Health (2021) · cites this paper as [235]
In the citing paper
“In general, microbial diversity decreases and numbers of beneficial bacteria (bifidobacteria, lactobacilli, Clostridium cluster XIVa, F. prausnitzii) reduce, whereas facultative anaerobes and opportunists or even proinflammatory pathogenic bacteria (Escherichia spp., Enterobacteriaceae spp., Bacteroides spp., C. difficile, etc.) increase when compared with younger individuals (235, 295, 296).”
From Diet and the Microbiota–Gut–Brain Axis: Sowing the Seeds of Good Mental Health (2021) · cites this paper as [235]
In the citing paper
“The gut microbiome can modulate many of the host physiological processes including metabolism, cognitive function, innate immunity as well as cellular senescence, thereby potentially contributing to frailty, dysfunction, and disease (44,47).”
From Senolytic Combination of Dasatinib and Quercetin Alleviates Intestinal Senescence and Inflammation and Modulates the Gut Microbiome in Aged Mice (2021) · cites this paper as [44]
In the citing paper
“Emerging evidence suggests that the gut microbiota imbalance (dysbiosis) is associated with the development of age-associated disorders and reduced survival (44).”
From Senolytic Combination of Dasatinib and Quercetin Alleviates Intestinal Senescence and Inflammation and Modulates the Gut Microbiome in Aged Mice (2021) · cites this paper as [44]
In the citing paper
“The microbiota change drastically over the course of host’s lifetime, and aging is correlated with a reduction in microbial diversity and alterations in microbiota composition (24,44).”
From Senolytic Combination of Dasatinib and Quercetin Alleviates Intestinal Senescence and Inflammation and Modulates the Gut Microbiome in Aged Mice (2021) · cites this paper as [44]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2013) · Cell · doi:10.1016/j.cell.2013.05.039 · Cited by 14,982
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
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
Hill (2014) · doi:10.1038/nrgastro.2014.66 · Cited by 9,592
Dietary Modulation of the Human Colonic Microbiota: Introducing the Concept of Prebiotics
Gibson, G. R., & Roberfroid, M. B. (1995) · Journal of Nutrition · doi:10.1093/jn/125.6.1401 · Cited by 7,659
De Filippo, C., Cavalieri, D., Di Paola, M., Ramazzotti, M., Poullet, J. B., Massart, S., Collini, S., Pieraccini, G., & Lionetti, P. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005963107 · Cited by 5,579
Role of the microbiota in immunity and inflammation.
Belkaid, Y., & Hand, T. W. (2014) · Cell · doi:10.1016/j.cell.2014.03.011 · Cited by 5,385
Inflamm‐aging: An Evolutionary Perspective on Immunosenescence
FRANCESCHI, C., BONAFÈ, M., VALENSIN, S., OLIVIERI, F., DE LUCA, M., OTTAVIANI, E., & DE BENEDICTIS, G. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06651.x · Cited by 5,358
Cani, P. D., Bibiloni, R., Knauf, C., Waget, A., Neyrinck, A. M., Delzenne, N. M., & Burcelin, R. (2008) · Diabetes · doi:10.2337/db07-1403 · Cited by 4,819
Dominguez-Bello, M. G., Costello, E. K., Contreras, M., Magris, M., Hidalgo, G., Fierer, N., & Knight, R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002601107 · Cited by 4,774
Host-gut microbiota metabolic interactions
Nicholson, J. K., Holmes, E., Kinross, J., Burcelin, R., Gibson, G., Jia, W., & Pettersson, S. (2012) · Science · doi:10.1126/science.1223813 · Cited by 4,760
Recognition of Commensal Microflora by Toll-Like Receptors Is Required for Intestinal Homeostasis
Rakoff-Nahoum, S., Paglino, J., Eslami-Varzaneh, F., Edberg, S., & Medzhitov, R. (2004) · Cell · doi:10.1016/j.cell.2004.07.002 · Cited by 4,251
Dissemination and growth of cancer cells in metastatic sites
Chambers, A. F., Groom, A. C., & MacDonald, I. C. (2002) · Nature reviews. Cancer · doi:10.1038/nrc865 · Cited by 4,018
Dynamics and Stabilization of the Human Gut Microbiome during the First Year of Life
Bäckhed, F., Roswall, J., Peng, Y., Feng, Q., Jia, H., Kovatcheva-Datchary, P., Li, Y., Xia, Y., Xie, H., Zhong, H., et al. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.04.004 · Cited by 3,315
Gut microbiota composition correlates with diet and health in the elderly
Claesson, M. J., Jeffery, I. B., Conde, S., Power, S. E., O’Connor, E. M., Cusack, S., Harris, H. M. B., Coakley, M., Lakshminarayanan, B., O’Sullivan, O., et al. (2012) · Nature · doi:10.1038/nature11319 · Cited by 3,314
Regulation of inflammatory responses by gut microbiota and chemoattractant receptor GPR43
Maslowski, K. M., Vieira, A. T., Ng, A., Kranich, J., Sierro, F., Yu, D., Schilter, H. C., Rolph, M. S., Mackay, F., Artis, D., et al. (2009) · Nature · doi:10.1038/nature08530 · Cited by 3,241
An Immunomodulatory Molecule of Symbiotic Bacteria Directs Maturation of the Host Immune System
Mazmanian, S. K., Liu, C. H., Tzianabos, A. O., & Kasper, D. L. (2005) · Cell · doi:10.1016/j.cell.2005.05.007 · Cited by 2,910
Development of the Human Infant Intestinal Microbiota
Palmer, C., Bik, E. M., DiGiulio, D. B., Relman, D. A., & Brown, P. O. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050177 · Cited by 2,877
Kenyon, C. J. (2010) · Nature · doi:10.1038/nature08980 · Cited by 2,739
Review article: the role of butyrate on colonic function
HAMER, H. M., JONKERS, D., VENEMA, K., VANHOUTVIN, S., TROOST, F. J., & BRUMMER, R. ‐. (2008) · Alimentary Pharmacology & Therapeutics · doi:10.1111/j.1365-2036.2007.03562.x · Cited by 2,721
Metabolomics analysis reveals large effects of gut microflora on mammalian blood metabolites
Wikoff, W. R., Anfora, A. T., Liu, J., Schultz, P. G., Lesley, S. A., Peters, E. C., & Siuzdak, G. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812874106 · Cited by 2,677
Human nutrition, the gut microbiome and the immune system
Kau, A. L., Ahern, P. P., Griffin, N. W., Goodman, A. L., & Gordon, J. I. (2011) · Nature · doi:10.1038/nature10213 · Cited by 2,588
The Placenta Harbors a Unique Microbiome
Aagaard, K., Ma, J., Antony, K. M., Ganu, R., Petrosino, J., & Versalovic, J. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3008599 · Cited by 2,494
Intestinal Short Chain Fatty Acids and their Link with Diet and Human Health
Ríos-Covián, D., Ruas‐Madiedo, P., Margollés, A., Gueimonde, M., Reyes‐Gavilán, C. G. D. L., & Salazar, N. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00185 · Cited by 2,300
Factors influencing the composition of the intestinal microbiota in early infancy
Penders, J., Thijs, C., Vink, C., Stelma, F. F., Snijders, B., Kummeling, I., van den Brandt, P. A., & Stobberingh, E. E. (2006) · PEDIATRICS · doi:10.1542/peds.2005-2824 · Cited by 2,232
Butyrate improves insulin sensitivity and increases energy expenditure in mice
Gao, Z., Yin, J., Zhang, J., Ward, R. E., Martin, R. J., Lefevre, M., Cefalu, W. T., & Ye, J. (2009) · Diabetes · doi:10.2337/db08-1637 · Cited by 2,204
Microbiota-Generated Metabolites Promote Metabolic Benefits via Gut-Brain Neural Circuits
De Vadder, F., Kovatcheva-Datchary, P., Goncalves, D., Vinera, J., Zitoun, C., Duchampt, A., Bäckhed, F., & Mithieux, G. (2014) · Cell · doi:10.1016/j.cell.2013.12.016 · Cited by 2,200
The microbiome and butyrate regulate energy metabolism and autophagy in the mammalian colon
Donohoe, D. R., Garge, N., Zhang, X., Sun, W., O'Connell, T. M., Bunger, M. K., & Bultman, S. J. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.02.018 · Cited by 2,003 · cited 2×
“[148] Donohoe DR, Garge N, Zhang X, Sun W, O’Connell TM, Bunger MK, Bultman SJ.”
BackgroundIvanov, I. I., Frutos, R. D. L., Manel, N., Yoshinaga, K., Rifkin, D. B., Sartor, R. B., Finlay, B. B., & Littman, D. R. (2008) · Cell Host & Microbe · doi:10.1016/j.chom.2008.09.009 · Cited by 1,770
Composition, variability, and temporal stability of the intestinal microbiota of the elderly
Claesson, M. J., Cusack, S., O'Sullivan, O., Greene-Diniz, R., de Weerd, H., Flannery, E., Marchesi, J. R., Falush, D., Dinan, T., Fitzgerald, G., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000097107 · Cited by 1,754
Interactions between commensal intestinal bacteria and the immune system
Macpherson, A. J., & Harris, N. L. (2004) · Nature reviews. Immunology · doi:10.1038/nri1373 · Cited by 1,683
The enteric nervous system and neurogastroenterology
Furness, J. B. (2012) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2012.32 · Cited by 1,619
The interplay between the intestinal microbiota and the brain
Collins, S. M., Surette, M., & Bercik, P. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2876 · Cited by 1,611 · cited 2×
“thereby instigating an abnormal (hyper) inflammatory responses eventually affecting (disturbing) the gut-brain communication [84, 90, 93, 103, 104, 109, 112, 124, 158].”
BackgroundOdamaki, T., Kato, K., Sugahara, H., Hashikura, N., Takahashi, S., Xiao, J.-Z., Abe, F., & Osawa, R. (2016) · BMC Microbiology · doi:10.1186/s12866-016-0708-5 · Cited by 1,521
Through Ageing, and Beyond: Gut Microbiota and Inflammatory Status in Seniors and Centenarians
Biagi, E., Nylund, L., Candela, M., Ostan, R., Bucci, L., Pini, E., Nikkïla, J., Monti, D., Satokari, R., Franceschi, C., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010667 · Cited by 1,483
Antibiotics, birth mode, and diet shape microbiome maturation during early life
Bokulich, N. A., Chung, J., Battaglia, T., Henderson, N., Jay, M., Li, H., D. Lieber, A., Wu, F., Perez-Perez, G. I., Chen, Y., et al. (2016) · Science Translational Medicine · doi:10.1126/scitranslmed.aad7121 · Cited by 1,469
Metformin improves healthspan and lifespan in mice
Martin-Montalvo, A., Mercken, E. M., Mitchell, S. J., Palacios, H. H., Mote, P. L., Scheibye-Knudsen, M., Gomes, A. P., Ward, T. M., Minor, R. K., Blouin, M.-J., et al. (2013) · Nature Communications · doi:10.1038/ncomms3192 · Cited by 1,445
Thevaranjan, N., Puchta, A., Schulz, C., Naidoo, A., Szamosi, J. C., Verschoor, C. P., Loukov, D., Schenck, L. P., Jury, J., Foley, K. P., et al. (2017) · Cell Host & Microbe · doi:10.1016/j.chom.2017.03.002 · Cited by 1,322
Kelly, C. P., Pothoulakis, C., & LaMont, J. T. (1994) · New England Journal of Medicine · doi:10.1056/nejm199401273300406 · Cited by 1,320
Low counts of Faecalibacterium prausnitzii in colitis microbiota
Sokol, H., Seksik, P., Furet, J. P., Firmesse, O., Nion-Larmurier, I., Beaugerie, L., Cosnes, J., Corthier, G., Marteau, P., & Doré, J. (2009) · Inflammatory Bowel Diseases · doi:10.1002/ibd.20903 · Cited by 1,275
Diet, gut microbiota and immune responses
Maslowski, K. M., & Mackay, C. R. (2011) · Nature Immunology · doi:10.1038/ni0111-5 · Cited by 1,261
O’Toole, P. W., & Jeffery, I. B. (2015) · Science · doi:10.1126/science.aac8469 · Cited by 1,202
Lymphoid tissue genesis induced by commensals through NOD1 regulates intestinal homeostasis
Bouskra, D., Brézillon, C., Bérard, M., Werts, C., Varona, R., Boneca, I. G., & Eberl, G. (2008) · Nature · doi:10.1038/nature07450 · Cited by 1,107
Collado, M. C., Rautava, S., Aakko, J., Isolauri, E., & Salminen, S. (2016) · Scientific Reports · doi:10.1038/srep23129 · Cited by 1,098
Mueller, S., Saunier, K., Hanisch, C., Norin, E., Alm, L., Midtvedt, T., Cresci, A., Silvi, S., Orpianesi, C., Verdenelli, M. C., et al. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.72.2.1027-1033.2006 · Cited by 1,006
Commensal bacteria calibrate the activation threshold of innate antiviral immunity
Abt, M. C., Osborne, L. C., Monticelli, L. A., Doering, T. A., Alenghat, T., Sonnenberg, G. F., Paley, M. A., Antenus, M., Williams, K. L., Erikson, J., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.04.011 · Cited by 993
Interactions Between the Intestinal Microbiome and Liver Diseases
Schnabl, B., & Brenner, D. A. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.01.020 · Cited by 971
Metformin retards aging in C. elegans by altering microbial folate and methionine metabolism
Cabreiro, F., Au, C., Leung, K.-Y., Vergara-Irigaray, N., Cochemé, H. M., Noori, T., Weinkove, D., Schuster, E., Greene, N. D. E., & Gems, D. (2013) · Cell · doi:10.1016/j.cell.2013.02.035 · Cited by 967
Intestinal barrier function in health and gastrointestinal disease
Camilleri, M., Madsen, K., Spiller, R., Van Meerveld, B. G., & Verne, G. N. (2012) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2012.01921.x · Cited by 908
Christensen, H. R., Frøkiær, H., & Pestka, J. J. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.1.171 · Cited by 905
Grölund, M., Lehtonen, O. ‐., Eerola, E., & Kero, P. O. (1999) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/00005176-199901000-00007 · Cited by 873
Molecular Monitoring of Succession of Bacterial Communities in Human Neonates
Favier, C. F., Vaughan, E. E., de Vos, W. M., & Akkermans, A. D. L. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.1.219-226.2002 · Cited by 859
Gut instincts: microbiota as a key regulator of brain development, ageing and neurodegeneration
Dinan, T. G., & Cryan, J. F. (2017) · The Journal of Physiology · doi:10.1113/jp273106 · Cited by 813
Bartosch, S., Fite, A., Macfarlane, G. T., & McMurdo, M. E. T. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.6.3575-3581.2004 · Cited by 762 · cited 4×
“between gut microbiota and host chronological aging 276 are still limited [8, 36, 73], but a reduced gut 277 microbiota diversity has been speculated to be asso278 ciated with increased old-age frailty [23, 31, 74, 75].”
BackgroundInfluentialDynamics and stabilization of the human gut microbiome during the first year of life
Bäckhed, F., Roswall, J., Peng, Y., Feng, Q., Jia, H., Kovatcheva-Datchary, P., Li, Y., Xia, Y., Xie, H., Zhong, H., et al. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.05.012 · Cited by 738
Therapeutic Potential of Fecal Microbiota Transplantation
Smits, L. P., Bouter, K. E. C., de Vos, W. M., Borody, T. J., & Nieuwdorp, M. (2013) · Gastroenterology · doi:10.1053/j.gastro.2013.08.058 · Cited by 717
Jiménez, E., Fernández, L., Marín, M. L., Martı́n, R., Odriozola, J. M., Nueno‐Palop, C., Narbad, A., Olivares, M. M., Xaus, J., & Rodríguez, J. M. (2005) · Current Microbiology · doi:10.1007/s00284-005-0020-3 · Cited by 681
Leaky Gut As a Danger Signal for Autoimmune Diseases
Mu, Q., Kirby, J. L., Reilly, C. M., & Luo, X. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00598 · Cited by 634
IL-1β Causes an Increase in Intestinal Epithelial Tight Junction Permeability
Al-Sadi, R. M., & Ma, T. Y. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.7.4641 · Cited by 601
Hickson, M., D'Souza, A. L., Muthu, N., Rogers, T. R., Want, S., Rajkumar, C., & Bulpitt, C. J. (2007) · BMJ · doi:10.1136/bmj.39231.599815.55 · Cited by 599
Kleessen, B., Sykura, B., Zunft, H. ‐., & Blaut, M. (1997) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/65.5.1397 · Cited by 573
Microbiome, probiotics and neurodegenerative diseases: deciphering the gut brain axis
Westfall, S., Lomis, N., Kahouli, I., Dia, S. Y., Singh, S. P., & Prakash, S. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2550-9 · Cited by 570
Probiotics, their health benefits and applications for developing healthier foods: a review
Nagpal, R., Kumar, A., Kumar, M., Behare, P. V., Jain, S., & Yadav, H. (2012) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2012.02593.x · Cited by 517
Self-citationStevens, B. R., Goel, R., Seungbum, K., Richards, E. M., Holbert, R. C., Pepine, C. J., & Raizada, M. K. (2018) · Gut · doi:10.1136/gutjnl-2017-314759 · Cited by 508
Gill, H. S., Rutherfurd, K. J., Cross, M. L., & Gopal, P. K. (2001) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/74.6.833 · Cited by 485 · cited 1×
“[175] Gill HS, Rutherfurd KJ, Cross ML, Gopal PK.”
BackgroundHopkins, M. J., & Macfarlane, G. T. (2002) · Journal of Medical Microbiology · doi:10.1099/0022-1317-51-5-448 · Cited by 485
The Enteric Network: Interactions between the Immune and Nervous Systems of the Gut
Yoo, B. B., & Mazmanian, S. K. (2017) · Immunity · doi:10.1016/j.immuni.2017.05.011 · Cited by 485
Neyrinck, A. M., Possemiers, S., Druart, C., Van de Wiele, T., De Backer, F., Cani, P. D., Larondelle, Y., & Delzenne, N. M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020944 · Cited by 465
Gut microbiota: A player in aging and a target for anti-aging intervention
Vaiserman, A. M., Koliada, A. K., & Marotta, F. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2017.01.001 · Cited by 465
Self-citationVulevic, J., Drakoularakou, A., Yaqoob, P., Tzortzis, G., & Gibson, G. R. (2008) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.2008.26242 · Cited by 451
Finch, C. E., & Ruvkun, G. (2001) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.2.1.435 · Cited by 446
Sato, J., Kanazawa, A., Ikeda, F., Yoshihara, T., Goto, H., Abe, H., Komiya, K., Kawaguchi, M., Shimizu, T., Ogihara, T., et al. (2014) · Diabetes Care · doi:10.2337/dc13-2817 · Cited by 441
Signatures of early frailty in the gut microbiota
Jackson, M. A., Jeffery, I. B., Beaumont, M., Bell, J. T., Clark, A. G., Ley, R. E., O’Toole, P. W., Spector, T. D., & Steves, C. J. (2016) · Genome Medicine · doi:10.1186/s13073-016-0262-7 · Cited by 436
Composition and temporal stability of the gut microbiota in older persons
Jeffery, I. B., Lynch, D. B., & O’Toole, P. W. (2016) · The ISME Journal · doi:10.1038/ismej.2015.88 · Cited by 421
(Dis)Trust your gut: the gut microbiome in age-related inflammation, health, and disease
Buford, T. W. (2017) · Microbiome · doi:10.1186/s40168-017-0296-0 · Cited by 409
Development of the human gastrointestinal microbiota and insights from high-throughput sequencing
Dominguez-Bello, M. G., Blaser, M. J., Ley, R. E., & Knight, R. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.02.011 · Cited by 405
The role of DNA damage and repair in aging through the prism of Koch-like criteria
Moskalev, A. A., Shaposhnikov, M. V., Plyusnina, E. N., Zhavoronkov, A., Budovsky, A., Yanai, H., & Fraifeld, V. E. (2013) · Ageing Research Reviews · doi:10.1016/j.arr.2012.02.001 · Cited by 387
Compartmentalized and systemic control of tissue immunity by commensals
Belkaid, Y., & Naik, S. (2013) · Nature Immunology · doi:10.1038/ni.2604 · Cited by 382
Ageing of the human metaorganism: the microbial counterpart
Biagi, E., Candela, M., Fairweather‐Tait, S. J., Franceschi, C., & Brigidi, P. (2011) · AGE · doi:10.1007/s11357-011-9217-5 · Cited by 375
Frailty in older adults: insights and interventions.
Espinoza, S. E., & Walston, J. D. (2005) · Cleveland Clinic Journal of Medicine · doi:10.3949/ccjm.72.12.1105 · Cited by 365
The Intestinal Metabolome: An Intersection Between Microbiota and Host
Ursell, L. K., Haiser, H. J., Treuren, W. V., Garg, N., Reddivari, L., Vanamala, J., Dorrestein, P. C., Turnbaugh, P. J., & Knight, R. D. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.03.001 · Cited by 365
Functional metagenomic profiling of intestinal microbiome in extreme ageing
Rampelli, S., Candela, M., Turroni, S., Biagi, E., Collino, S., Franceschi, C., O'Toole, P. W., & Brigidi, P. (2013) · Aging · doi:10.18632/aging.100623 · Cited by 359
Microbiota controls the homeostasis of glial cells in the gut lamina propria
Kabouridis, P. S., Lasrado, R., McCallum, S., Chng, S. H., Snippert, H. J., Clevers, H., Pettersson, S., & Pachnis, V. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.037 · Cited by 358
Human intestinal microbiota and healthy ageing
Tiihonen, K., Ouwehand, A. C., & Rautonen, N. (2009) · Ageing Research Reviews · doi:10.1016/j.arr.2009.10.004 · Cited by 357
Microbial Genetic Composition Tunes Host Longevity
Han, B., Sivaramakrishnan, P., Lin, C.-C., Neve, I. A. A., He, J., Tay, L. W. R., Sowa, J. N., Sizovs, A., Du, G., Wang, J., et al. (2017) · Cell · doi:10.1016/j.cell.2017.05.036 · Cited by 355
Vulevic, J., Juric, A., Tzortzis, G., & Gibson, G. R. (2013) · The Journal of Nutrition · doi:10.3945/jn.112.166132 · Cited by 349
Haenen, D., Zhang, J., Souza da Silva, C., Bosch, G., van der Meer, I. M., van Arkel, J., van den Borne, J. J. G. C., Pérez Gutiérrez, O., Smidt, H., Kemp, B., et al. (2013) · The Journal of Nutrition · doi:10.3945/jn.112.169672 · Cited by 341
Mechanisms of Molecular Mimicry Involving the Microbiota in Neurodegeneration
Friedland, R. P. (2015) · Journal of Alzheimer's Disease · doi:10.3233/jad-142841 · Cited by 338
Org, E., Blum, Y., Kasela, S., Mehrabian, M., Kuusisto, J., Kangas, A. J., Soininen, P., Wang, Z., Ala‐Korpela, M., Hazen, S. L., et al. (2017) · Genome biology · doi:10.1186/s13059-017-1194-2 · Cited by 337
Davis, L. M. G., Martínez, I., Walter, J., Goin, C., & Hutkins, R. W. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025200 · Cited by 329
Luna, R. A., & Foster, J. A. (2015) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2014.10.007 · Cited by 325
Intestinal microbiota influence the early postnatal development of the enteric nervous system
Collins, J., Borojevic, R., Verdu, E. F., Huizinga, J. D., & Ratcliffe, E. M. (2014) · Neurogastroenterology & Motility · doi:10.1111/nmo.12236 · Cited by 318
Schwab, L., Goroncy, L., Palaniyandi, S., Gautam, S., Triantafyllopoulou, A., Mócsai, A., Reichardt, W., Karlsson, F. J., Radhakrishnan, S. V., Hanke, K., et al. (2014) · Nature Medicine · doi:10.1038/nm.3517 · Cited by 302
McVey Neufeld, K. A., Mao, Y. K., Bienenstock, J., Foster, J. A., & Kunze, W. A. (2013) · Neurogastroenterology & Motility · doi:10.1111/nmo.12049 · Cited by 299
Recycling Metchnikoff: Probiotics, the Intestinal Microbiome and the Quest for Long Life
Mackowiak, P. A. (2013) · Frontiers in Public Health · doi:10.3389/fpubh.2013.00052 · Cited by 294
Obata, Y., & Pachnis, V. (2016) · Gastroenterology · doi:10.1053/j.gastro.2016.07.044 · Cited by 286
Chang, J., Leong, R. W., Wasinger, V. C., Ip, M., Yang, M., & Phan, T. G. (2017) · Gastroenterology · doi:10.1053/j.gastro.2017.05.056 · Cited by 286
Grasset, E., Puel, A., Charpentier, J., Collet, X., Christensen, J. E., Tercé, F., & Burcelin, R. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.04.013 · Cited by 284
Innervation of the gastrointestinal tract: Patterns of aging
Phillips, R. J., & Powley, T. L. (2007) · Autonomic Neuroscience · doi:10.1016/j.autneu.2007.04.005 · Cited by 282
The Microbiota and Microbiome in Aging: Potential Implications in Health and Age‐Related Diseases
Zapata, H. J., & Quagliarello, V. J. (2015) · Journal of the American Geriatrics Society · doi:10.1111/jgs.13310 · Cited by 279
Ageing and gut microbes: Perspectives for health maintenance and longevity
Biagi, E., Candela, M., Turroni, S., Garagnani, P., Franceschi, C., & Brigidi, P. (2013) · Pharmacological Research · doi:10.1016/j.phrs.2012.10.005 · Cited by 276 · cited 2×
“717 Since prebiotics are ‘favorite’ foods for probiotics, 718 combining them as “synbiotics” for preventive as 719 well as therapeutic health effects could be envis720 aged for better gut and overall health [46, 163].”
BackgroundHooda, S., Boler, B. M. V., Serao, M. C. R., Brulc, J. M., Staeger, M. A., Boileau, T. W., Dowd, S. E., Fahey, G. C., & Swanson, K. S. (2012) · The Journal of Nutrition · doi:10.3945/jn.112.158766 · Cited by 272
Collino, S., Montoliu, I., Martin, F.-P. J., Scherer, M., Mari, D., Salvioli, S., Bucci, L., Ostan, R., Monti, D., Biagi, E., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056564 · Cited by 270
Gut microbiota and diabetes: from pathogenesis to therapeutic perspective
Burcelin, R., Sérino, M., Chabo, C., Blasco‐Baqué, V., & Amar, J. (2011) · Acta Diabetologica · doi:10.1007/s00592-011-0333-6 · Cited by 270
Commensal bacteria modulate cullin‐dependent signaling via generation of reactive oxygen species
Kumar, A., Wu, H., Collier-Hyams, L. S., Hansen, J. M., Li, T., Yamoah, K., Pan, Z., Jones, D. P., & Neish, A. S. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601867 · Cited by 268
Is butyrate the link between diet, intestinal microbiota and obesity-related metabolic diseases?
Brahe, L. K., Astrup, A., & Larsen, L. H. (2013) · Obesity Reviews · doi:10.1111/obr.12068 · Cited by 264
Romero, R., Erez, O., Hüttemann, M., Maymon, E., Panaitescu, B., Conde-Agudelo, A., Pacora, P., Yoon, B. H., & Grossman, L. I. (2017) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2017.06.003 · Cited by 253
Guillemard, E., Tondu, F., Lacoin, F., & Schrezenmeir, J. (2009) · British Journal of Nutrition · doi:10.1017/s0007114509991395 · Cited by 249
Piazzon, M. C., Calduch-Giner, J. À., Fouz, B., Estensoro, I., Simó‐Mirabet, P., Puyalto, M., Karalazos, V., Palenzuela, O. R., Sitjà‐Bobadilla, A., & Pérez‐Sánchez, J. (2017) · Microbiome · doi:10.1186/s40168-017-0390-3 · Cited by 245
Mäkivuokko, H., Tiihonen, K., Tynkkynen, S., Paulin, L. G., & Rautonen, N. (2009) · British Journal Of Nutrition · doi:10.1017/s0007114509991553 · Cited by 243
Gut permeability and mucosal inflammation: bad, good or context dependent
Ahmad, R., Sorrell, M. F., Batra, S. K., Dhawan, P., & Singh, A. B. (2017) · Mucosal Immunology · doi:10.1038/mi.2016.128 · Cited by 243
Köhler, C. A., Maes, M. H. J., Slyepchenko, A., Berk, M., Solmi, M., Lanctôt, K. L., & Carvalho, A. D. S. (2016) · Current Pharmaceutical Design · doi:10.2174/1381612822666160907093807 · Cited by 234
Bacterial Translocation from the Gut to the Distant Organs: An Overview
Nagpal, R., & Yadav, H. (2017) · Annals of Nutrition and Metabolism · doi:10.1159/000479918 · Cited by 234
Self-citationRea, M. C., O’Sullivan, Ó., Shanahan, F., O’Toole, P. W., Stanton, C., Ross, R. P., & Hill, C. (2011) · Journal of Clinical Microbiology · doi:10.1128/jcm.05176-11 · Cited by 224
Biological aging and the human gut microbiota
Maffei, V. J., Kim, S., Blanchard, E., Luo, M., Jazwinski, S. M., Taylor, C. M., & Welsh, D. A. (2017) · The Journals of Gerontology Series A · doi:10.1093/gerona/glx042 · Cited by 219
Comalada, M., Bailón, E., de Haro, O., Lara‐Villoslada, F., Xaus, J., Zarzuelo, A., & Gálvez, J. (2006) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-006-0092-x · Cited by 207
Microbe-host interactions: influence of the gut microbiota on the enteric nervous system
Hyland, N. P., & Cryan, J. F. (2016) · Developmental Biology · doi:10.1016/j.ydbio.2016.06.027 · Cited by 207
To be or not to be a pathogen: that is the mucosally relevant question
Sansonetti, P. J. (2010) · Mucosal Immunology · doi:10.1038/mi.2010.77 · Cited by 205
Zwielehner, J., Liszt, K. I., Handschur, M., Laßl, C., Lapin, A., & Haslberger, A. G. (2009) · Experimental Gerontology · doi:10.1016/j.exger.2009.04.002 · Cited by 201
Comparison of fecal microflora of elderly persons in rural and urban areas of Japan
Benno, Y., Endo, K., Mizutani, T., Namba, Y., Komori, T., & MITSUOKA, T. (1989) · Applied and Environmental Microbiology · doi:10.1128/aem.55.5.1100-1105.1989 · Cited by 195
Molecular Analysis of Fecal Microbiota in Elderly Individuals Using 16S rDNA Library and T‐RFLP
Hayashi, H., Sakamoto, M., Kitahara, M., & Benno, Y. (2003) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2003.tb03418.x · Cited by 189
Probiotics and prebiotics and health in ageing populations
Duncan, S. H., & Flint, H. J. (2013) · Maturitas · doi:10.1016/j.maturitas.2013.02.004 · Cited by 189
Probiotics, prebiotics and synbiotics: A role in chemoprevention for colorectal cancer?
Geier, M. S., Butler, R. N., & Howarth, G. S. (2006) · Cancer Biology & Therapy · doi:10.4161/cbt.5.10.3296 · Cited by 186
Aging of the myenteric plexus: neuronal loss is specific to cholinergic neurons
Phillips, R. J., Kieffer, E. J., & Powley, T. L. (2003) · Autonomic Neuroscience · doi:10.1016/s1566-0702(03)00072-9 · Cited by 181
Walton, G., van den Heuvel, E. G. H. M., Kosters, M. H. W., Rastall, R. A., Tuohy, K. M., & Gibson, G. R. (2011) · British Journal Of Nutrition · doi:10.1017/s0007114511004697 · Cited by 174
Immune responses to commensal and environmental microbes
Pamer, E. G. (2007) · Nature Immunology · doi:10.1038/ni1526 · Cited by 173
Manipulation of the Microbiota for Treatment of IBS and IBD—Challenges and Controversies
Shanahan, F., & Quigley, E. M. M. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.01.050 · Cited by 172
Cevenini, E., Caruso, C., Candore, G., Capri, M., Nuzzo, D., Duro, G., Rizzo, C., Colonna‐Romano, G., Lio, D., Carlo, D., et al. (2010) · Current Pharmaceutical Design · doi:10.2174/138161210790883840 · Cited by 168
Intestinal Permeability Biomarker Zonulin is Elevated in Healthy Aging
Qi, Y., Goel, R., Kim, S., Richards, E. M., Carter, C. S., Pepine, C. J., Raizada, M. K., & Buford, T. W. (2017) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2017.05.018 · Cited by 165
Nagpal, R., Tsuji, H., Takahashi, T., Nomoto, K., Kawashima, K., Nagata, S., & Yamashiro, Y. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01388 · Cited by 165
Self-citationOh, K. J., Lee, S. E., Jung, H., Kim, G., Romero, R. J., & Yoon, B. H. (2010) · Journal of Perinatal Medicine · doi:10.1515/jpm.2010.040 · Cited by 162
In Vitro and In Vivo Antioxidant Activity of Bifidobacterium animalis 01 Isolated from Centenarians
Shen, Q., Shang, N., & Li, P. (2010) · Current Microbiology · doi:10.1007/s00284-010-9827-7 · Cited by 157
Kelsall, B. L., & Leon, F. (2005) · Immunological Reviews · doi:10.1111/j.0105-2896.2005.00292.x · Cited by 154
(2015) · PubMed · Cited by 152
The enteric nervous system promotes intestinal health by constraining microbiota composition
Rolig, A. S., Mittge, E. K., Ganz, J., Troll, J. V., Melancon, E., Wiles, T. J., Alligood, K., Stephens, W. Z., Eisen, J. S., & Guillemin, K. (2017) · PLOS Biology · doi:10.1371/journal.pbio.2000689 · Cited by 152
He, F., Ouwehand, A. C., Isolauri, E., Hosoda, M., Benno, Y., & Salminen, S. (2001) · Current Microbiology · doi:10.1007/s002840010315 · Cited by 150
Bifidobacterium microbiota and parameters of immune function in elderly subjects
Ouwehand, A. C., Bergsma, N., Parhiala, R., Lahtinen, S., Gueimonde, M., Finne-Soveri, H., Strandberg, T., Pitkälä, K., & Salminen, S. (2008) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2008.00392.x · Cited by 148 · cited 1×
“For example, increased levels 300 of TNF, IL-6 and IL-8 in old-age may be associated 301 with changes in gut microbiota [34, 82, 83].”
BackgroundNagpal, R., Tsuji, H., Takahashi, T., Kawashima, K., Nagata, S., Nomoto, K., & Yamashiro, Y. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01997 · Cited by 148
Self-citationRestricted diet rescues rat enteric motor neurones from age related cell death
Cowen, T., Johnson, R. J. R., Soubeyre, V., & Santer, R. M. (2000) · Gut · doi:10.1136/gut.47.5.653 · Cited by 147
Aging of the mammalian gastrointestinal tract: a complex organ system
Saffrey, M. J. (2013) · AGE · doi:10.1007/s11357-013-9603-2 · Cited by 141
Nagata, S., Asahara, T., Ohta, T., Yamada, T., Kondo, S., Bian, L., Wang, C., Yamashiro, Y., & Nomoto, K. (2011) · British Journal Of Nutrition · doi:10.1017/s000711451100064x · Cited by 136
Thrasivoulou, C., Soubeyre, V., Ridha, H., Giuliani, D., Giaroni, C., Michael, G. J., Saffrey, M. J., & Cowen, T. (2006) · Aging Cell · doi:10.1111/j.1474-9726.2006.00214.x · Cited by 134
Bouhnik, Y., Achour, L., Paineau, D., Riottot, M., Attar, A., & Bornet, F. R. J. (2007) · Nutrition Journal · doi:10.1186/1475-2891-6-42 · Cited by 134
Cellular changes in the enteric nervous system during ageing
Saffrey, M. J. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.03.015 · Cited by 124
Excessive folate synthesis limits lifespan in the C. elegans: E. coliaging model
Virk, B., Correia, G. D. S., Dixon, D. P., Feyst, I., Jia, J., Oberleitner, N., Briggs, Z., Hodge, E., Edwards, R., Ward, J. M., et al. (2012) · BMC Biology · doi:10.1186/1741-7007-10-67 · Cited by 123
The human superorganism – Of microbes and men
Sleator, R. D. (2009) · Medical Hypotheses · doi:10.1016/j.mehy.2009.08.047 · Cited by 118
The impact of ageing on the intestinal epithelial barrier and immune system
Man, A., Gicheva, N., & Nicoletti, C. (2014) · Cellular Immunology · doi:10.1016/j.cellimm.2014.04.001 · Cited by 118
O'Mahony, D., O'Leary, P., & Quigley, E. (2002) · Drugs & Aging · doi:10.2165/00002512-200219070-00005 · Cited by 117
Moro‐García, M. A., Alonso‐Arias, R., BALTADJIEVA, M., Benítez, C. F., Barrial, M. A. F., Ruisánchez, E. D., Santos, R. A., Sánchez, M. Á., Miján, J. S., & López‐Larrea, C. (2012) · AGE · doi:10.1007/s11357-012-9434-6 · Cited by 117
Britton, E., & McLaughlin, J. T. (2012) · Proceedings of The Nutrition Society · doi:10.1017/s0029665112002807 · Cited by 111
Enteric neurodegeneration in ageing
Camilleri, M., Cowen, T., & Koch, T. R. (2008) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2007.01072.x · Cited by 109
Reduced intestinal motility, mucosal barrier function, and inflammation in aged monkeys
Mitchell, E. L., Davis, A., Brass, K., Dendinger, M. D., Barner, R., Gharaibeh, R. Z., Fodor, A. A., & Kavanagh, K. (2016) · The journal of nutrition health & aging · doi:10.1007/s12603-016-0725-y · Cited by 109
Self-citationNagpal, R., Kurakawa, T., Tsuji, H., Takahashi, T., Kawashima, K., Nagata, S., Nomoto, K., & Yamashiro, Y. (2017) · Scientific Reports · doi:10.1038/s41598-017-10711-5 · Cited by 108
Self-citationEvidence For Early Aging in the Mucosal Immune System
Koga, T., McGhee, J. R., Kato, H., Kato, R., Kiyono, H., & Fujihashi, K. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.165.9.5352 · Cited by 105
Age-related changes in the morphology of the myenteric plexus of the human colon
Menachem Hanani, A., Fellig, Y., Udassin, R., & Freund, H. R. (2004) · Autonomic Neuroscience · doi:10.1016/j.autneu.2004.05.007 · Cited by 104
Loss of glia and neurons in the myenteric plexus of the aged Fischer�344 rat
Phillips, R. J., Kieffer, E. J., & Powley, T. L. (2004) · Anatomy and Embryology · doi:10.1007/s00429-004-0426-x · Cited by 103
Slyepchenko, A., Maes, M. H. J., Machado‐Vieira, R., Anderson, G., Solmi, M., Sanz, Y., Berk, M., Köhler, C. A., & Carvalho, A. F. (2016) · Current Pharmaceutical Design · doi:10.2174/1381612822666160922165706 · Cited by 103
Lahtinen, S. J., Forssten, S. D., Aakko, J., Granlund, L., Rautonen, N., Salminen, S., Viitanen, M. H., & Ouwehand, A. C. (2011) · AGE · doi:10.1007/s11357-011-9208-6 · Cited by 101
Hall, K. E., Proctor, D. D., Fisher, L. J., & Rose, S. (2005) · Gastroenterology · doi:10.1053/j.gastro.2005.06.013 · Cited by 99
Gavini, F., Cayuela, C., Antoine, J., Lecoq, C., Lefebvre, B., Membré, J., & Neut, C. (2001) · Microbial Ecology in Health and Disease · doi:10.3402/mehd.v13i1.7998 · Cited by 98
Gut microbiota in health and disease: an overview focused on metabolic inflammation
Nagpal, R., Kumar, M., Yadav, A. K., Hemalatha, R., Yadav, H., Marotta, F., & Yamashiro, Y. (2016) · Beneficial Microbes · doi:10.3920/bm2015.0062 · Cited by 97
Self-citationProbiotics modulate the Bifidobacterium microbiota of elderly nursing home residents
Lahtinen, S. J., Tammela, L. I., Korpela, J., Parhiala, R., Ahokoski, H., Mykkänen, H. M., & Salminen, S. (2008) · AGE · doi:10.1007/s11357-008-9081-0 · Cited by 96
Compositional dynamics of the human intestinal microbiota with aging: Implications for health
Lakshminarayanan, B., Stanton, C., O’Toole, P. W., & Ross, R. P. (2014) · The journal of nutrition health & aging · doi:10.1007/s12603-014-0549-6 · Cited by 93
Foong, J. P. P., Nguyen, T. V., Furness, J. B., Bornstein, J. C., & Young, H. M. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2011.225938 · Cited by 91
Broad segmental progeroid changes in short-lived Ercc1 −/Δ7 mice
Dollé, M. E. T., Kuiper, R. V., Roodbergen, M., Robinson, J., de Vlugt, S., Wijnhoven, S. W. P., Beems, R. B., de la Fonteyne, L., de With, P., van der Pluijm, I., et al. (2011) · Pathobiology of Aging & Age-related Diseases · doi:10.3402/pba.v1i0.7219 · Cited by 91
(2007) · PubMed · Cited by 90
Gavini, F., Cayuela, C., Antoine, J.-M., Lecoq, C., Lefebvre, B., Membré, J., & Neut, C. (2001) · Microbial Ecology in Health and Disease · doi:10.1080/089106001750071690 · Cited by 90
Intestinal aganglionosis is associated with early and sustained disruption of the colonic microbiome
Ward, N. L., Pieretti, A. C., Dowd, S. E., Cox, S. B., & Goldstein, A. M. (2012) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2012.01937.x · Cited by 88
Molecular monitoring of the development of intestinal microbiota in Japanese infants
Tsuji, H., Oozeer, R., Matsuda, K., Matsuki, T., Ohta, T., Nomoto, K., Tanaka, R., Kawashima, M., Kawashima, K., Nagata, S., et al. (2012) · Beneficial Microbes · doi:10.3920/bm2011.0038 · Cited by 88
Effect of prebiotics on the human gut microbiota of elderly persons
Toward, R. E., Montandon, S., Walton, G., & Gibson, G. R. (2012) · Gut Microbes · doi:10.4161/gmic.19411 · Cited by 86
Annaert, P., Brouwers, J., Bijnens, A., Lammert, F., Tack, J. F., & Augustijns, P. (2009) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2009.10.005 · Cited by 85
Clostridium difficile Infection in the Elderly
Keller, J. M., & Surawicz, C. M. (2013) · Clinics in Geriatric Medicine · doi:10.1016/j.cger.2013.10.008 · Cited by 82
Fecal Microbiota Transplantation for the Management of Clostridium difficile Infection
Rao, K. K., & Young, V. B. (2015) · Infectious Disease Clinics of North America · doi:10.1016/j.idc.2014.11.009 · Cited by 79
Nier, A., Engstler, A. J., Maier, I. B., & Bergheim, I. (2017) · PLoS ONE · doi:10.1371/journal.pone.0183282 · Cited by 76
Intestinal dysbiosis and bacterial enteroinvasion in a murine model of Hirschsprung’s disease
Pierre, J. F., Barlow, A. J., Erickson, C. S., Heneghan, A. F., LEVERSON, G. E., Dowd, S. E., Epstein, M. L., Kudsk, K. A., & Gosain, A. (2014) · Journal of Pediatric Surgery · doi:10.1016/j.jpedsurg.2014.01.060 · Cited by 73
Small intestinal permeability in older adults
Valentini, L., Ramminger, S., Haas, V., Postrach, E., Werich, M., Fischer, A., Koller, M., Swidsinski, A., Bereswill, S., Lochs, H., et al. (2014) · Physiological Reports · doi:10.1002/phy2.281 · Cited by 73
Yang, H., Liu, S., Ibrahim, S. A., Zhao, L., Jiang, J., Sun, W.-F., & Ren, F. (2009) · Nutrition Research · doi:10.1016/j.nutres.2009.03.010 · Cited by 71
Small intestinal permeability in older adults
Valentini, L., Ramminger, S., Haas, V., Postrach, E., Werich, M., Fischer, A., Koller, M., Swidsinski, A., Bereswill, S., Lochs, H., et al. (2014) · Physiological Reports · doi:10.14814/phy2.281 · Cited by 68
Role of the Gut Microbiota in Age-Related Chronic Inflammation
Rehman, T. (2012) · Endocrine, Metabolic & Immune Disorders-Drug Targets · doi:10.2174/187153012803832620 · Cited by 67
Vries, P. D., Soret, R., Suply, E., Héloury, Y., & Neunlist, M. (2010) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00092.2010 · Cited by 67
Paun, A., & Danska, J. S. (2016) · Pediatric Diabetes · doi:10.1111/pedi.12424 · Cited by 67
Alpha-synuclein immunopositive aggregates in the myenteric plexus of the aging Fischer 344 rat
Phillips, R. J., Walter, G. C., Ringer, B. E., Higgs, K. M., & Powley, T. L. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.07.025 · Cited by 66
Sanduzzi‐Zamparelli, M., Compare, D., Coccoli, P., Rocco, A., Nardone, O. M., Marrone, G., Gasbarrini, A., Grieco, A., Nardone, G., & Miele, L. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17081225 · Cited by 64
Newton, J. L., Jordan, N., Pearson, J. P., Williams, G., Allen, A., & James, O. (2000) · Gerontology · doi:10.1159/000022151 · Cited by 60
Matsumoto, M., & Benno, Y. (2006) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.50464 · Cited by 56
Immunosenescence and Anti-Immunosenescence Therapies: The Case of Probiotics
Candore, G., Balistreri, C. R., Colonna‐Romano, G., Grimaldi, M. P., Lio, D., Listı̀, F., Scola, L., Vasto, S., & Caruso, C. (2008) · Rejuvenation Research · doi:10.1089/rej.2008.0662 · Cited by 55
Age- and Diet-Related Increase in Transepithelial Colon Permeability of Fischer 344 Rats
Mullin, J. M., Valenzano, M. C., Verrecchio, J. J., & Kothari, R. (2002) · Digestive Diseases and Sciences · doi:10.1023/a:1020191412285 · Cited by 54
Nagpal, R., Tsuji, H., Takahashi, T., Nomoto, K., Kawashima, K., Nagata, S., & Yamashiro, Y. (2017) · Beneficial Microbes · doi:10.3920/bm2016.0216 · Cited by 53
Self-citationThe Intestinal Epithelial Barrier: Does It Become Impaired with Age?
Meier, J., & Sturm, A. (2009) · Digestive Diseases · doi:10.1159/000228556 · Cited by 50
Myenteric neuron numbers are maintained in aging mouse distal colon
Gamage, P. P. K. M., Ranson, R. N., Patel, B. A., Yeoman, M. S., & Saffrey, M. J. (2013) · Neurogastroenterology & Motility · doi:10.1111/nmo.12114 · Cited by 47
Ileal myenteric plexus in aged guinea‐pigs: loss of structure and calretinin‐immunoreactive neurones
Abalo, R., rivera, A. J., Vera, G., & Martin, M. (2005) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2004.00612.x · Cited by 45
An, H. M., Baek, E. H., Jang, S., Lee, D. K., Kim, M. J., Kim, J. R., Lee, K. O., Park, J. G., & Ha, N. J. (2010) · Nutrition Journal · doi:10.1186/1475-2891-9-5 · Cited by 44
Morphological changes in the enteric nervous system of aging and APP23 transgenic mice
Ginneken, C. J. V., Schäfer, K., Dam, D. V., Huygelen, V., & Deyn, P. P. D. (2011) · Brain Research · doi:10.1016/j.brainres.2011.01.030 · Cited by 42
Kim, Y.-R., Volpert, G., Shin, K., Kim, S., Shin, S., Lee, Y., Sung, S. H., Lee, Y., Ahn, J., Pewzner‐Jung, Y., et al. (2017) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.13267 · Cited by 42
Myers, J. S. (2008) · Rehabilitation Nursing · doi:10.1002/j.2048-7940.2008.tb00215.x · Cited by 38
Yamada, M., Arai, H., Yoshimura, K., Kajiwara, Y., Sonoda, T., Nishiguchi, S., & Aoyama, T. (2012) · The Journal of frailty & aging · doi:10.14283/jfa.2012.12 · Cited by 35
Faecal microbiota transplantation for the treatment of recurrent Clostridium difficile infection
Koenigsknecht, M. J., & Young, V. B. (2013) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e328365d326 · Cited by 30
Age-related gene expression analysis in enteric ganglia of human colon after laser microdissection
Hetz, S., Acikgoez, A., Moll, C., Jahnke, H., Robitzki, A. A., Metzger, R., & eMetzger, R. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00276 · Cited by 26
Abalo, R., Vera, G., Rivera, A. J., & Martín, M. I. (2007) · Life Sciences · doi:10.1016/j.lfs.2007.04.004 · Cited by 26
Early-Life Gut Microbial Composition
Yamashiro, Y., & Nagpal, R. (2015) · Journal of Pediatric Biochemistry · doi:10.1055/s-0035-1564573 · Cited by 11
Self-citation
Flagged first, then by citations
Research works printed but not linked: 13
- Kenyon CJ, 2010, Nature, 464
- Buford TW, 2017, Microbiome, 5, 1
- Collado MC, 2016, Sci Re, 6, 23129
- Gavini F, 2001, Microb Ecol Health Dis, 13, 40
- Yamada M, 2012, J Frailty Aging, 1, 64
- Paun A, 2016, Diabetes, 17, 469
- Stevens BR, 2017, Gut
- Valentini L, 2014, Physiol Ree, 2, 00281
- Lahtinen SJ, 2009, Age(Dordr), 31, 59
- Pitkala KH, 2007, J Nutr Health Aging, 11, 305
- An HM, 2010, J Nutr, 9
- Bouhnik Y, 2007, Nutr J, 6
- Konturek PC, 2015, J Physiol pharmacol, 66, 483
Cited by
Sorted by citations
Malnutrition in Older Adults—Recent Advances and Remaining Challenges
Norman, K., Haß, U., & Pirlich, M. (2021) · Nutrients · doi:10.3390/nu13082764 · Cited by 905
The Gut Microbiota and Inflammation: An Overview
Bander, Z. A., Nitert, M. D., Mousa, A., & Naderpoor, N. (2020) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph17207618 · Cited by 804
The Gut Virome Database Reveals Age-Dependent Patterns of Virome Diversity in the Human Gut
Gregory, A., Zablocki, O., Zayed, A. A., Howell, A., Bolduc, B., & Sullivan, M. B. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.08.003 · Cited by 656
Nagpal, R., Neth, B. J., Wang, S., Craft, S., & Yadav, H. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2019.08.032 · Cited by 653
Self-citationAntimicrobial Stewardship: Fighting Antimicrobial Resistance and Protecting Global Public Health
Majumder, M. A. A., Rahman, S., Cohall, D., Bharatha, A., Singh, K., Haque, M., & Hilaire, M. G.-S. (2020) · Infection and Drug Resistance · doi:10.2147/idr.s290835 · Cited by 694
Metadata
- Authors
- Nagpal, R., Mainali, R., Ahmadi, S., Wang, S., Singh, R., Kavanagh, K., Kitzman, D. W., Kushugulova, A., Marotta, F., & Yadav, H.
- Affiliations
- Atrium Health Wake Forest Baptist (US)
- Wake Forest University Health Sciences (US)
- Nazarbayev University (KZ)
- ReGenera Research and Development for Aging Interventions, and San Babila Clinic, Corso Matteotti 1/A, Milano, Italy
- Corresponding author
- Yadav, Hariom
- ORCID
- Venue
- Nutrition and Healthy Aging
- Publisher
- SAGE Publications
- Published
- 2017-11-06
- Volume
- 4
- Issue
- 4
- Pages
- 267-285
- ISSN
- 2451-9480 (ISSN-L)
- 2451-9502
- PMC
- PMC6004897
- OpenAlex
- W2767624273
- Cited by
- 670
- References
- 200
- Citations by year
- 2026: 44 · 2025: 69 · 2024: 93 · 2023: 73 · 2022: 103 · 2021: 118 · 2020: 116 · 2019: 48 · 2018: 6
- FWCI
- 4.35
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Nutrition and Healthy Aging (publishedVersion, cc-by-nc)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Nazarbayev University Repository (Nazarbayev University) (submittedVersion)
- Funders
- National Institutes of Health (P30AG12232, R01AG18915)
- Wake Forest School of Medicine
- National Institute on Aging (R01AG018915, R37AG018915, P30AG021332)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
- Health Sciences › Dentistry › Periodontics › Oral microbiology and periodontitis research
- Keywords
- gut microbiota, aging, microbiota-immune interactions, immune system development, infancy, probiotics, microbiota-targeted interventions, healthy aging
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