Gut microbiota in common elderly diseases affecting activities of daily living
Open accessAbstract
Gut microbiota are involved in the development or prevention of various diseases such as type 2 diabetes, fatty liver, and malignancy such as colorectal cancer, breast cancer and hepatocellular carcinoma. Alzheimer's disease, osteoporosis, sarcopenia, atherosclerotic stroke and cardiovascular disease are major diseases associated with decreased activities of daily living (ADL), especially in elderly people. Recent analyses have revealed the importance of gut microbiota in the control of these diseases. The composition or diversity of these microbiota is different between patients with these conditions and healthy controls, and administration of probiotics or prebiotics has been shown effective in the treatment of these diseases. Gut microbiota may affect distant organs through mechanisms that include regulating the absorption of nutrients and/or the production of microbial metabolites, regulating and interacting with the systemic immune system, and translocating bacteria/bacterial products through disrupted mucosal barriers. Thus, the gut microbiota may be important regulators in the development of diseases that affect ADL. Although adequate exercise and proper diet are important for preventing these diseases, their combination with interventions that manipulate the composition and/or diversity of gut microbiota could be a promising strategy for maintaining health condition and preserving ADL. This review thus summarizes current understanding of the role of gut microbiota in the development or prevention of diseases closely associated with the maintenance of ADL.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The observed landmarks of sarcopenia and physical frailty in the fecal microbiota may simply represent the consequence of reduced physical activity, an epiphenomenon of pathophysiological processes driven by environmental factors.
“From this perspective, the observed landmarks of sarcopenia and physical frailty in the fecal microbiota may simply represent the consequence of reduced physical activity [133], just an epiphenomenon of pathophysiological processes driven by environmental factors [134].”
From Gut Microbiota, Muscle Mass and Function in Aging: A Focus on Physical Frailty and Sarcopenia (2019) · cites this paper as [133]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The 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 · see citing works
Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease
Wang, Z., Klipfell, E., Bennett, B. J., Koeth, R., Levison, B. S., DuGar, B., Feldstein, A. E., Britt, E. B., Fu, X., Chung, Y.-M., et al. (2011) · Nature · doi:10.1038/nature09922 · Cited by 5,597 · see citing works
den Besten, G., van Eunen, K., Groen, A. K., Venema, K., Reijngoud, D.-J., & Bakker, B. M. (2013) · Journal of Lipid Research · doi:10.1194/jlr.r036012 · Cited by 5,048 · see citing works
Intestinal microbial metabolism of phosphatidylcholine and cardiovascular risk
Tang, W. H. W., Wang, Z., Levison, B. S., Koeth, R. A., Britt, E. B., Fu, X., Wu, Y., & Hazen, S. L. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1109400 · Cited by 3,402 · see citing works
Normal gut microbiota modulates brain development and behavior
Heijtz, R. D., Wang, S., Anuar, F., Qian, Y., Björkholm, B., Samuelsson, A., Hibberd, M. L., Forssberg, H., & Pettersson, S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010529108 · Cited by 3,228 · see citing works
Gut microbiome alterations in Alzheimer’s disease
Vogt, N. M., Kerby, R. L., Dill-McFarland, K. A., Harding, S. J., Merluzzi, A. P., Johnson, S. C., Carlsson, C. M., Asthana, S., Zetterberg, H., Blennow, K., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-13601-y · Cited by 2,137 · see citing works
Interactions between the microbiota, immune and nervous systems in health and disease
Fung, T. C., Olson, C. A., & Hsiao, E. Y. (2017) · Nature Neuroscience · doi:10.1038/nn.4476 · Cited by 1,900 · see citing works
Gut microbiota in cardiovascular health and disease
Tang, W. H. W., Kitai, T., & Hazen, S. L. (2017) · Circulation Research · doi:10.1161/circresaha.117.309715 · Cited by 1,670 · see citing works
The gut microbiome in atherosclerotic cardiovascular disease
Jie, Z., Xia, H., Zhong, S.-L., Feng, Q., Li, S., Liang, S., Zhong, H., Liu, Z., Gao, Y., Zhao, H., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00900-1 · Cited by 1,638 · see citing works
Bacteria as vitamin suppliers to their host: A gut microbiota perspective
LeBlanc, J. G., Milani, C., de Giori, G. S., Sesma, F., van Sinderen, D., & Ventura, M. (2013) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2012.08.005 · Cited by 1,613 · see citing works
Symptomatic atherosclerosis is associated with an altered gut metagenome
Karlsson, F. H., Fåk, F., Nookaew, I., Tremaroli, V., Fagerberg, B., Petranovic, D., Bäckhed, F., & Nielsen, J. (2012) · Nature Communications · doi:10.1038/ncomms2266 · Cited by 1,371 · see citing works
Dong, Y., & Benveniste, E. N. (2001) · Glia · doi:10.1002/glia.1107 · Cited by 1,286 · see citing works
Ryu, D., Mouchiroud, L., Andreux, P. A., Katsyuba, E., Moullan, N., Nicolet-dit-Félix, A. A., Williams, E. G., Jha, P., Lo Sasso, G., Huzard, D., et al. (2016) · Nature Medicine · doi:10.1038/nm.4132 · Cited by 1,105 · see citing works
Bacterial infection causes stress-induced memory dysfunction in mice
Gareau, M. G., Wine, E., Rodrigues, D. M., Cho, J. H., Whary, M. T., Philpott, D. J., MacQueen, G., & Sherman, P. M. (2011) · Gut · doi:10.1136/gut.2009.202515 · Cited by 909 · see citing works
Reduction of Abeta amyloid pathology in APPPS1 transgenic mice in the absence of gut microbiota
Harach, T., Marungruang, N., Duthilleul, N., Cheatham, V., Mc Coy, K. D., Frisoni, G., Neher, J. J., Fåk, F., Jucker, M., Lasser, T., et al. (2017) · Scientific Reports · doi:10.1038/srep41802 · Cited by 901 · see citing works
The gut microbiota regulates bone mass in mice
Sjögren, K., Engdahl, C., Henning, P., Lerner, U. H., Tremaroli, V., Lagerquist, M. K., Bäckhed, F., & Ohlsson, C. (2012) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.1588 · Cited by 822 · see citing works
Gut microbiota induce IGF-1 and promote bone formation and growth
Yan, J., Herzog, J. W., Tsang, K., Brennan, C. A., Bower, M. A., Garrett, W. S., Sartor, B. R., Aliprantis, A. O., & Charles, J. F. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1607235113 · Cited by 750 · see citing works
Yin, J., Liao, S., He, Y., Wang, S., Xia, G., Liu, F., Zhu, J., You, C., Chen, Q., Zhou, L., et al. (2015) · Journal of the American Heart Association · doi:10.1161/jaha.115.002699 · Cited by 669 · see citing works
Butyrate, neuroepigenetics and the gut microbiome: Can a high fiber diet improve brain health?
Bourassa, M. W., Alim, I., Bultman, S. J., & Ratan, R. R. (2016) · Neuroscience Letters · doi:10.1016/j.neulet.2016.02.009 · Cited by 636 · see citing works
Gut-derived short-chain fatty acids are vividly assimilated into host carbohydrates and lipids
den Besten, G., Lange, K., Havinga, R., van Dijk, T. H., Gerding, A., van Eunen, K., Müller, M. M., Groen, A. K., Hooiveld, G. J. E. J., Bakker, B. M., et al. (2013) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00265.2013 · Cited by 606 · see citing works
Sochocka, M., Donskow-Łysoniewska, K., Diniz, B. S., Kurpas, D., Brzozowska, E., & Leszek, J. (2019) · Molecular Neurobiology · doi:10.1007/s12035-018-1188-4 · Cited by 584 · see citing works
Messaoudi, M., Violle, N., Bisson, J.-F., Desor, D., Javelot, H., & Rougeot, C. (2011) · Gut Microbes · doi:10.4161/gmic.2.4.16108 · Cited by 574 · see citing works
Probiotic <i>L. reuteri</i> Treatment Prevents Bone Loss in a Menopausal Ovariectomized Mouse Model
Britton, R. A., Irwin, R., Quach, D., Schaefer, L., Zhang, J., Lee, T., Parameswaran, N., & McCabe, L. R. (2014) · Journal of Cellular Physiology · doi:10.1002/jcp.24636 · Cited by 499 · see citing works
Transmission of Atherosclerosis Susceptibility with Gut Microbial Transplantation
Gregory, J. C., Buffa, J. A., Org, E., Wang, Z., Levison, B. S., Zhu, W., Wagner, M. A., Bennett, B. J., Li, L., DiDonato, J. A., et al. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.618249 · Cited by 486 · see citing works
Age‐related changes in the gut microbiota influence systemic inflammation and stroke outcome
Spychala, M. S., Venna, V. R., Jandzinski, M., Doran, S. J., Durgan, D. J., Ganesh, B. P., Ajami, N. J., Putluri, N., Graf, J., Bryan, R. M., et al. (2018) · Annals of Neurology · doi:10.1002/ana.25250 · Cited by 437 · see citing works
Gut Microbiota: An Integral Moderator in Health and Disease
Feng, Q., Chen, W.-D., & Wang, Y.-D. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00151 · Cited by 407 · see citing works
Kobayashi, Y., Sugahara, H., Shimada, K., Mitsuyama, E., Kuhara, T., Yasuoka, A., Kondo, T., Abe, K., & Xiao, J. (2017) · Scientific Reports · doi:10.1038/s41598-017-13368-2 · Cited by 406 · see citing works
Govindarajan, N., Agis-Balboa, R. C., Walter, J., Sananbenesi, F., & Fischer, A. (2011) · Journal of Alzheimer's Disease · doi:10.3233/jad-2011-110080 · Cited by 405 · see citing works
Ticinesi, A., Lauretani, F., Milani, C., Nouvenne, A., Tana, C., Del Rio, D., Maggio, M., Ventura, M., & Meschi, T. (2017) · Nutrients · doi:10.3390/nu9121303 · Cited by 401 · see citing works
Gómez-Arango, L. F., Barrett, H. L., McIntyre, D. H., Callaway, L. K., Morrison, M., & Nitert, M. D. (2016) · Hypertension · doi:10.1161/hypertensionaha.116.07910 · Cited by 384 · see citing works
Alzheimer’s disease and gut microbiota
Hu, X., Wang, T., & Jin, F. (2016) · Science China Life Sciences · doi:10.1007/s11427-016-5083-9 · Cited by 371 · see citing works
A review of the relationship between the gut microbiota and amino acid metabolism
Lin, R., Liu, W., Piao, M., & Hong, Z. (2017) · Amino Acids · doi:10.1007/s00726-017-2493-3 · Cited by 348 · see citing works
Probiotics Protect Mice from Ovariectomy-Induced Cortical Bone Loss
Ohlsson, C., Engdahl, C., Fåk, F., Andersson, A., Windahl, S. H., Farman, H. H., Movérare-Skrtic, S., Islander, U., & Sjögren, K. (2014) · PLoS ONE · doi:10.1371/journal.pone.0092368 · Cited by 339 · see citing works
Intestinal microbiota determine severity of myocardial infarction in rats
Lam, V., Su, J., Koprowski, S. L., Hsu, A., Tweddell, J. S., Rafiee, P., Gross, G. J., Salzman, N. H., & Baker, J. E. (2012) · The FASEB Journal · doi:10.1096/fj.11-197921 · Cited by 338 · see citing works
Walsh, M. E., Bhattacharya, A., Sataranatarajan, K., Qaisar, R., Sloane, L., Rahman, M. M., Kinter, M., & Van Remmen, H. (2015) · Aging Cell · doi:10.1111/acel.12387 · Cited by 334 · see citing works
Gan, X. T., Ettinger, G., Huang, C. X., Burton, J. P., Haist, J. V., Rajapurohitam, V., Sidaway, J. E., Martin, G., Gloor, G. B., Swann, J. R., et al. (2014) · Circulation: Heart Failure · doi:10.1161/circheartfailure.113.000978 · Cited by 329 · see citing works
Microbial Short-Chain Fatty Acids and Blood Pressure Regulation
Pluznick, J. L. (2017) · Current Hypertension Reports · doi:10.1007/s11906-017-0722-5 · Cited by 301 · see citing works
Bindels, L. B., Beck, R., Schakman, O., Martin, J. C., De Backer, F., Sohet, F. M., Dewulf, E. M., Pachikian, B. D., Neyrinck, A. M., Thissen, J.-P., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037971 · Cited by 278 · see citing works
McCabe, L. R., Irwin, R., Schaefer, L., & Britton, R. A. (2013) · Journal of Cellular Physiology · doi:10.1002/jcp.24340 · Cited by 274 · see citing works
Targeting neuroinflammation in Alzheimer’s disease
Bronzuoli, M. R., Iacomino, A., Steardo, L., & Scuderi, C. (2016) · Journal of Inflammation Research · doi:10.2147/jir.s86958 · Cited by 255 · see citing works
Diet, Gut Microbiome, and Bone Health
Weaver, C. M. (2015) · Current Osteoporosis Reports · doi:10.1007/s11914-015-0257-0 · Cited by 246 · see citing works
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 · see citing works
Parvaneh, K., Ebrahimi, M. M., Sabran, M. R., Karimi, G., Ng, M. H., Abdul-Majeed, S., Ahmad, Z., Ibrahim, Z., & Jamaluddin, R. (2015) · BioMed Research International · doi:10.1155/2015/897639 · Cited by 227 · see citing works
Effect of a Prebiotic Formulation on Frailty Syndrome: A Randomized, Double-Blind Clinical Trial
Buigues, C., Fernández-Garrido, J., Pruimboom, L., Hoogland, A., Navarro-Martínez, R., Martínez-Martínez, M., Verdejo, Y., Mascarós, M., Peris, C., & Cauli, O. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17060932 · Cited by 222 · see citing works
Links between the microbiome and bone
Hernandez, C. J., Guss, J. D., Luna, M., & Goldring, S. R. (2016) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2887 · Cited by 200 · see citing works
Wastney, M. E., Zafar, T. A., Weaver, C. M., Zhao, Y., & Martin, B. R. (2004) · Journal of Nutrition · doi:10.1093/jn/134.2.399 · Cited by 178 · see citing works
Gut microbiota and liver diseases
Minemura, M. (2015) · World Journal of Gastroenterology · doi:10.3748/wjg.v21.i6.1691 · Cited by 175 · see citing works
Towards understanding brain-gut-microbiome connections in Alzheimer’s disease
Xu, R., & Wang, Q. (2016) · BMC Systems Biology · doi:10.1186/s12918-016-0307-y · Cited by 175 · see citing works
Weaver, C. M., Martin, B. R., Nakatsu, C. H., Armstrong, A. P., Clavijo, A. P., McCabe, L. D., McCabe, G. P., Duignan, S., Schoterman, M. H. C., & van den Heuvel, E. G. H. M. (2011) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf2009777 · Cited by 173 · see citing works
St‐Jean‐Pelletier, F., Pion, C. H., Leduc‐Gaudet, J., Sgarioto, N., Zovilé, I., Barbat‐Artigas, S., Reynaud, O., Alkaterji, F., Lemieux, F. C., Grenon, A., et al. (2017) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12139 · Cited by 156 · see citing works
Intestinal Microbial Metabolites Are Linked to Severity of Myocardial Infarction in Rats
Lam, V., Su, J., Hsu, A., Gross, G. J., Salzman, N. H., & Baker, J. E. (2016) · PLoS ONE · doi:10.1371/journal.pone.0160840 · Cited by 139 · see citing works
Yacon Flour and <i>Bifidobacterium longum</i> Modulate Bone Health in Rats
Rodrigues, F. C., Castro, A. S. B., Rodrigues, V. C., Fernandes, S. A., Fontes, E. A. F., de Oliveira, T. T., Martino, H. S. D., & de Luces Fortes Ferreira, C. L. (2012) · Journal of Medicinal Food · doi:10.1089/jmf.2011.0296 · Cited by 131 · see citing works
Dietary Chicory Inulin Increases Whole-Body Bone Mineral Density in Growing Male Rats
Roberfroid, M. B., Cumps, J., & Devogelaer, J. (2002) · Journal of Nutrition · doi:10.1093/jn/132.12.3599 · Cited by 130 · see citing works
Chiang, S.-S., & Pan, T.-M. (2011) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf2013716 · Cited by 128 · see citing works
den Besten, G., Gerding, A., van Dijk, T. H., Čiapaitė, J., Bleeker, A., van Eunen, K., Havinga, R., Groen, A. K., Reijngoud, D., & Bakker, B. M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0136364 · Cited by 126 · see citing works
Steves, C. J., Bird, S., Williams, F. M. K., & Spector, T. D. (2015) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2765 · Cited by 119 · see citing works
Dukes, A., Davis, C., Refaey, M. E., Upadhyay, S. K., Mork, S., Arounleut, P., Johnson, M. H., Hill, W., Isales, C. M., & Hamrick, M. W. (2015) · Nutrition · doi:10.1016/j.nut.2015.02.011 · Cited by 106 · see citing works
Effect of Galactooligosaccharides on Calcium Absorption in Rats.
Chonan, O., & Watanuki, M. (1995) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.41.95 · Cited by 88 · see citing works
Effects of three strains of bifidobacteria on cholesterol
Tahri, K., Crociani, J., Ballongue, J., & Schneider, F. (1995) · Letters in Applied Microbiology · doi:10.1111/j.1472-765x.1995.tb01028.x · Cited by 83 · see citing works
Slevin, M. M., Allsopp, P. J., Magee, P. J., Bonham, M. P., Naughton, V. R., Strain, J., Duffy, M. E., Wallace, J. M. W., & McSorley, E. M. (2014) · Journal of Nutrition · doi:10.3945/jn.113.188144 · Cited by 82 · see citing works
Kuo, H.-K., Liao, K., Leveille, S. G., Bean, J. F., Yen, C., Chen, J.-H., Yu, Y., & Tai, T. Y. (2007) · The Journals of Gerontology Series A · doi:10.1093/gerona/62.4.434 · Cited by 81 · see citing works
Qi, Y., Aranda, J. M., Rodriguez, V., Raizada, M. K., & Pepine, C. J. (2015) · International Journal of Cardiology · doi:10.1016/j.ijcard.2015.07.078 · Cited by 79 · see citing works
Ohta, A. (1998) · Scandinavian Journal of Gastroenterology · doi:10.1080/003655298750026769 · Cited by 65 · see citing works
Mathey, J., Puel, C., Kati-Coulibaly, S., Bennetau‐Pelissero, C., Davicco, M. J., Lebecque, P., Horcajada, M.-N., & Coxam, V. (2004) · Calcified Tissue International · doi:10.1007/s00223-004-0128-7 · Cited by 57 · see citing works
Hygiene and the world distribution of Alzheimer’s disease
Fox, M. M., Knapp, L. A., Andrews, P. W., & Fincher, C. L. (2013) · Evolution Medicine and Public Health · doi:10.1093/emph/eot015 · Cited by 50 · see citing works
Influence of Altered Gut Microbiota Composition on Aging and Aging-Related Diseases
Choi, J., Hur, T., & Hong, Y. (2018) · Journal of Lifestyle Medicine · doi:10.15280/jlm.2018.8.1.1 · Cited by 40 · see citing works
Cultivable butyrate-producing bacteria of elderly Japanese diagnosed with Alzheimer’s disease
Nguyen, T. T. T., Fujimura, Y., Mimura, I., Fujii, Y., Nguyen, N. L., Arakawa, K., & Morita, H. (2018) · The Journal of Microbiology · doi:10.1007/s12275-018-8297-7 · Cited by 32 · see citing works
Shiga, K., Nishimukai, M., Tomita, F., & Hara, H. (2006) · Scandinavian Journal of Gastroenterology · doi:10.1080/00365520600575753 · Cited by 15 · see citing works
Causes of decreased activity of daily life in elderly patients who need daily living care
Yoshino, H., Sakurai, T., Hasegawa, K., & Yokono, K. (2011) · Geriatrics and gerontology international/Geriatrics & gerontology international · doi:10.1111/j.1447-0594.2010.00683.x · Cited by 13 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Gut Microbiota, Muscle Mass and Function in Aging: A Focus on Physical Frailty and Sarcopenia
Ticinesi, A., Nouvenne, A., Cerundolo, N., Catania, P., Prati, B., Tana, C., & Meschi, T. (2019) · Nutrients · doi:10.3390/nu11071633 · Cited by 418 · see citing works
Wang, S., Ahmadi, S., Nagpal, R., Jain, S., Mishra, S. P., Kavanagh, K., Zhu, X., Wang, Z., McClain, D. A., Kritchevsky, S. B., et al. (2019) · GeroScience · doi:10.1007/s11357-019-00137-4 · Cited by 228 · see citing works
Xia, G., You, C., Gao, X., Zeng, X., Zhu, J., Xu, K., Tan, C., Xu, R., Wu, Q., Zhou, H., et al. (2019) · Frontiers in Neurology · doi:10.3389/fneur.2019.00397 · Cited by 220 · see citing works
Diets intervene osteoporosis via gut-bone axis
Zhang, Y., Song, P., Wang, S., Liu, H., Shi, Z., & Su, J. (2024) · Gut Microbes · doi:10.1080/19490976.2023.2295432 · Cited by 180 · see citing works
Sarcopenia and Diabetes: A Detrimental Liaison of Advancing Age
Lisco, G., Disoteo, O., Tullio, A. D., Geronimo, V. D., Giagulli, V. A., Monzani, F., Jirillo, E., Cozzi, R. C., Guastamacchia, E., Pergola, G. D., et al. (2023) · Nutrients · doi:10.3390/nu16010063 · Cited by 109 · see citing works
Flexibility of Gut Microbiota in Ageing Individuals during Dietary Fiber Long‐Chain Inulin Intake
Kiewiet, M. B. G., Elderman, M. E., Aidy, S. E., Burgerhof, J. G. M., Visser, H., Vaughan, E. E., Faas, M. M., & de Vos, P. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202000390 · Cited by 92 · see citing works
Holmes, A., Finger, C. E., Morales‐Scheihing, D., Lee, J., & McCullough, L. D. (2020) · Translational research · doi:10.1016/j.trsl.2020.07.012 · Cited by 87 · see citing works
Effects of exercise frequency on the gut microbiota in elderly individuals
Zhu, Q., Jiang, S., & Du, G. (2020) · MicrobiologyOpen · doi:10.1002/mbo3.1053 · Cited by 79 · see citing works
Koszewicz, M. A., Jaroch, J., Brzecka, A., Ejma, M., Budrewicz, S. P., Михалева, Л. М., Muresanu, C., Schield, P., Somasundaram, S. G., Kirkland, C. E., et al. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.105277 · Cited by 77 · see citing works
Szilagyi, A. (2019) · Clinical Journal of Gastroenterology · doi:10.1007/s12328-019-01037-y · Cited by 54 · see citing works
Liver Cirrhosis and Sarcopenia from the Viewpoint of Dysbiosis
Nishikawa, H., Enomoto, H., Nishiguchi, S., & Iijima, H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155254 · Cited by 48 · see citing works
Tao, P., Ji, J., Wang, Q., Cui, M., Cao, M., & Xu, Y. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1080456 · Cited by 45 · see citing works
Zhang, Y., Cao, M., Li, Y., Chen, X.-X., Yu, Q., & Rui, Y. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03700-4 · Cited by 36 · see citing works
Chen, N., Chan, C. K., Khan, F. U., Makhijani, P., Valentino, T. R., Winer, S., Luk, C. T., & Winer, D. A. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103036 · Cited by 35 · see citing works
Gemikonakli, G., Mach, J., Zhang, F., Bullock, M., Tran, T., El-Omar, E. M., & Hilmer, S. N. (2022) · The Journals of Gerontology Series A · doi:10.1093/gerona/glac195 · Cited by 37 · see citing works
Thomaz, F. S., Altemani, F. H., Panchal, S. K., Worrall, S., & Nitert, M. D. (2020) · Journal of Human Hypertension · doi:10.1038/s41371-020-0359-8 · Cited by 31 · see citing works
Potential neuroprotective effects of fermented foods and beverages in old age: a systematic review
Porras‐García, E., Calderón, I. F.-E., González, J. G., & Fernández‐García, J. C. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1170841 · Cited by 33 · see citing works
The role ofBacillus acidophilusin osteoporosis and its roles in proliferation and differentiation
Chen, C., Dong, B., Wang, Y., Zhang, Q., Wang, B., Feng, S., & Zhu, Y. T. (2020) · Journal of Clinical Laboratory Analysis · doi:10.1002/jcla.23471 · Cited by 29 · see citing works
Elsheikh, M., Sabagh, A. E., Mohamed, I. B., Bhongade, M., Hassan, M. M., & Jalal, P. K. (2023) · World Journal of Gastroenterology · doi:10.3748/wjg.v29.i46.6028 · Cited by 26 · see citing works
Novel Mechanisms and Therapeutic Targets for Ischemic Stroke: A Focus on Gut Microbiota
Bao, Z., Zhang, Z., Zhou, G., Zhang, A., Shao, A., & Zhou, F. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.871720 · Cited by 22 · see citing works
The Role of the Gut Microbiota and the Immune System in the Development of Autism
Lungba, R. M., Khan, S. Z. A., Ajibawo-Aganbi, U., Bastidas, M. V. P., Veliginti, S., Saleem, S., & Cancarevic, I. (2020) · Cureus · doi:10.7759/cureus.11226 · Cited by 13 · see citing works
Polyamines and microbiota in bicuspid and tricuspid aortic valve aortopathy
Forte, A., Balistreri, C. R., FEO, M. D., Corte, A. D., Hellstrand, P., Persson, L., & Nilsson, B. (2019) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2019.02.014 · Cited by 13 · see citing works
Ruiz‐Limón, P., Muralidharan, J., Gómez‐Pérez, A. M., Murri, M., Vioqué, J., Corella, D., Fitó, M., Vidal, J., Salas‐Salvadó, J., Collado, L. T., et al. (2023) · Biology of Sport · doi:10.5114/biolsport.2024.133005 · Cited by 12 · see citing works
Winardi, K., Mach, J., McKay, M. J., Molloy, M. P., Mitchell, S. J., MacArthur, M. R., McKenzie, C. A., Couteur, D. G. L., & Hilmer, S. N. (2024) · Aging Cell · doi:10.1111/acel.14357 · Cited by 11 · see citing works
Analysis of intestinal flora in elderly Uygur patients with sarcopenia
Shan, Z., Cheng, N., Zhu, J., Chen, F., Ji, J., & Meilibana (2024) · Immunity Inflammation and Disease · doi:10.1002/iid3.1097 · Cited by 10 · see citing works
Guo, J., Schupf, N., Cruz, E., Stern, Y., Mayeux, R. P., & Gu, Y. (2022) · The Journals of Gerontology Series A · doi:10.1093/gerona/glac011 · Cited by 10 · see citing works
Lee, K. J., Kim, H., & Wang, J. (2025) · Bone · doi:10.1016/j.bone.2025.117644 · Cited by 9 · see citing works
Men, J., Li, H., Cui, C., Ma, X., Liu, P., Yu, Z., Gong, X., Yao, Y., Ren, J., Zhao, C., et al. (2025) · PLoS ONE · doi:10.1371/journal.pone.0314698 · Cited by 7 · see citing works
Perturbations in gut microbiota composition in osteoporosis: a systematic review and meta-analysis
Cao, Y., Gao, Y., & Huang, J. (2024) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-024-01517-3 · Cited by 6 · see citing works
Jampílek, J., Kráľová, K., & Bella, V. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823733-5.00009-x · Cited by 7 · see citing works
Zhang, W., Yu, X., Wei, M., Zhou, J., Zhou, Y., Zhou, X., Zhao, K., & Zhu, X. (2024) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2024.111115 · Cited by 5 · see citing works
Food, nutrition and microbiota: what about the elderly?
Troncoso-Pantoja, C. (2021) · Anales de la Facultad de Ciencias Médicas (Asunción) · doi:10.18004/anales/2021.054.01.125 · Cited by 4 · see citing works
Repercussions of gastrointestinal microbiota in postmenopausal osteoporosis
Shah, F. I., Akram, F., & Shehzadi, S. (2025) · Women s Health · doi:10.1177/17455057251363684 · Cited by 3 · see citing works
Фролова, Ю. В., Dymova, O. V., Petrenko, К. N., Tsatsurova, S. A., & Bedzhanyan, A. L. (2024) · MD-Onco · doi:10.17650/2782-3202-2024-4-2-87-92 · Cited by 2 · see citing works
Gut Microbiota and Aging: A Broad Perspective
Pitchumoni, C. S., Mishra, S. P., & Yadav, H. (2020) · Springer eBooks · doi:10.1007/978-3-319-90761-1_59-1 · Cited by 2 · see citing works
The gut microbiota in the elderly
Novak, K. Š., & Pražnikar, Z. J. (2021) · Založba Univerze na Primorskem / University of Primorska Press eBooks · doi:10.26493/978-961-293-129-2.191-197 · Cited by 1 · see citing works
Zdravje starostnikov / Health of the Elderly
(2021) · Založba Univerze na Primorskem / University of Primorska Press eBooks · doi:10.26493/978-961-293-129-2 · Cited by 1 · see citing works
Gut Microbiota and Aging: A Broad Perspective
Pitchumoni, C. S., Mishra, S. P., & Yadav, H. (2021) · Springer eBooks · doi:10.1007/978-3-030-30192-7_59 · Cited by 1 · see citing works
Amarta, P. R., & Dewi, N. S. R. (2023) · Health & Medical Sciences · doi:10.47134/phms.v1i4.58
Huang, A., Chen, S., Lin, B., & Hou, L. (2026) · The journal of nutrition health & aging · doi:10.1016/j.jnha.2026.100861
- Authors
- Shimizu, Y.
- Affiliations
- Nanto Municipal Hospital (JP)
- Corresponding author
- Shimizu, Yukihiro
- ORCID
- Shimizu, Yukihiro
- Venue
- World Journal of Gastroenterology
- Publisher
- Baishideng Publishing Group Inc.
- Published
- 2018-11-14
- Volume
- 24
- Issue
- 42
- Pages
- 4750-4758
- ISSN
- 1007-9327 (ISSN-L)
- PMC
- PMC6235798
- OpenAlex
- W2900559388
- Cited by
- 40
- References
- 69
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 6 · 2023: 5 · 2022: 5 · 2021: 5 · 2020: 9 · 2019: 5
- FWCI
- 0.47
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by-nc
- Locations
- World Journal of Gastroenterology (publishedVersion, cc-by-nc)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- 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 › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Keywords
- gut microbiota, activities of daily living, older adults, Alzheimer's disease, osteoporosis, sarcopenia, atherosclerotic stroke, cardiovascular disease, type 2 diabetes, hepatic steatosis, colorectal cancer, breast cancer, hepatocellular carcinoma, probiotics, prebiotics, microbial metabolites, mucosal barrier, physical activity, diet
- MeSH terms
- Gastrointestinal Microbiome, Activities of Daily Living, Aged, Alzheimer Disease, Cardiovascular Diseases, Diabetes Mellitus, Type 2, Humans, Neoplasms, Osteoporosis, Probiotics, Stroke, Gastrointestinal Tract, Sarcopenia, Prebiotics, Dysbiosis
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