Cited by 333Gut microbiota and healthFrailty in Older AdultsProbiotics and Fermented Foods

The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.

Fecal Microbiota Composition and Frailty

Open access

van Tongeren, Sandra P., Slaets, Joris P. J., Harmsen, H. J. M., Welling, Gjalt W.·2005·Applied and Environmental Microbiology

DOI 10.1128/aem.71.10.6438-6442.2005PMC PMC1265947

Open this paper in CoChat — free account

Abstract

The relationship between fecal microbiota composition and frailty in the elderly was studied. Fecal samples from volunteers with high frailty scores showed a significant reduction in the number of lactobacilli (26-fold). At much higher population levels, both the Bacteroides/Prevotella(threefold) and the Faecalibacterium prausnitzii(fourfold) groups showed a significant reduction in percentage of total number of hybridizable bacteria in the elderly with high frailty scores. In contrast to this, the number of Enterobacteriaceae was significantly higher (sevenfold) in samples from very frail volunteers.

Integrity signals

Registry

Crossref · 10.1128/aem.71.10.6438-6442.2005

Cites

37 of 37 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

The text we found for this paper looks like another document, so its claims and self-check weren’t run. The registry and citation checks still apply.

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The text we found for this paper looks like another document, so the self-check wasn’t run.

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
Combination of 16S rRNA-targeted oligonucleotide probes with flow cytometry for analyzing mixed microbial populations
Amann, R., Binder, B. J., Olson, R. J., Chisholm, S. W., Devereux, R., & Stahl, D. A. (1990) · Applied and Environmental Microbiology · doi:10.1128/aem.56.6.1919-1925.1990 · Cited by 4,049
Gut flora in health and disease
Guarner, F., & Malagelada, J. (2003) · The Lancet · doi:10.1016/s0140-6736(03)12489-0 · Cited by 3,480
Direct analysis of genes encoding 16S rRNA from complex communities reveals many novel molecular species within the human gut
Suau, A., Bonnet, R., Sutren, M., Godon, J.-J., Gibson, G. R., Collins, M. D., & Doré, J. (1999) · Applied and Environmental Microbiology · doi:10.1128/aem.65.11.4799-4807.1999 · Cited by 1,490
Temperature Gradient Gel Electrophoresis Analysis of 16S rRNA from Human Fecal Samples Reveals Stable and Host-Specific Communities of Active Bacteria
Zoetendal, E. G., Akkermans, A. D. L., & de Vos, W. M. (1998) · Applied and Environmental Microbiology · doi:10.1128/aem.64.10.3854-3859.1998 · Cited by 1,360
Analysis of Intestinal Flora Development in Breast-Fed and Formula-Fed Infants by Using Molecular Identification and Detection Methods
Harmsen, H. J. M., Wildeboer-Veloo, A. C. M., Raangs, G. C., Wagendorp, A. A., Klijn, N., BINDELS, J. G., & Welling, G. W. (2000) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/00005176-200001000-00019 · Cited by 1,326
Self-citation
Application of a suite of 16S rRNA-specific oligonucleotide probes designed to investigate bacteria of the phylum cytophaga-flavobacter-bacteroides in the natural environment
Manz, W., Amann, R., Ludwig, W., Vancanneyt, M., & SCHLEIFER, K. H. (1996) · Microbiology · doi:10.1099/13500872-142-5-1097 · Cited by 1,176
Variations of Bacterial Populations in Human Feces Measured by Fluorescent In Situ Hybridization with Group-Specific 16S rRNA-Targeted Oligonucleotide Probes
Franks, A. H., Harmsen, H. J. M., Raangs, G. C., Jansen, G. J., Schut, F., & Welling, G. W. (1998) · Applied and Environmental Microbiology · doi:10.1128/aem.64.9.3336-3345.1998 · Cited by 1,056
Self-citation
Quantitative fluorescence in situ hybridization of Bifidobacterium spp. with genus-specific 16S rRNA-targeted probes and its application in fecal samples
Langendijk-Genevaux, P. S., Schut, F., Jansen, G. J., Raangs, G. C., Kamphuis, G. R., Wilkinson, M. H. F., & Welling, G. W. (1995) · Applied and Environmental Microbiology · doi:10.1128/aem.61.8.3069-3075.1995 · Cited by 974
Self-citation
Characterization of Bacterial Communities in Feces from Healthy Elderly Volunteers and Hospitalized Elderly Patients by Using Real-Time PCR and Effects of Antibiotic Treatment on the Fecal Microbiota
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 3×
“(3) characterized bacterial communities in feces from healthy elderly volunteers and hospitalized elderly patients by real-time PCR.”
Background

Show all 37 references

Research works printed but not linked: 2

Mitsuoka, T. 1992. Intestinal flora and ageing. Nutr. Rev.50:438-446.
Sullivan Å., R. Bennet, M. Viitanen, A.-C. Palmgren, and C. E. Nord. 2002. Influence of Lactobacillus F19 on intestinal microflora in children and elderly persons and impact on Helicobacter pylori infections. Microb. Ecol. Health Dis.3:17-21.

Sorted by citations

Items 201–300 of 332

The Kidney–Gut–Muscle Axis in End-Stage Renal Disease is Similarly Represented in Older Adults
Lustgarten, M. S. (2019) · Nutrients · doi:10.3390/nu12010106 · Cited by 17
The Intestinal Microbiota and Probiotics
Forssten, S. D., Lahtinen, S. J., & Ouwehand, A. C. (2011) · Springer eBooks · doi:10.1007/978-94-007-0386-5_2 · Cited by 16
Pharmacogenetic Guidelines and Decision Support Tools for Depression Treatment: Application to Late-Life
Chang, D. D., Eyre, H. A., Abbott, R. B., Coudreaut, M. F., Baune, B. T., Shaman, J. A., Lavretsky, H., Lenze, E. J., Merrill, D. A., Singh, A., et al. (2018) · Pharmacogenomics · doi:10.2217/pgs-2018-0099 · Cited by 16
Does exercise impact gut microbiota composition in men receiving androgen deprivation therapy for prostate cancer? A single-blinded, two-armed, randomised controlled trial
Newton, R. U., Christophersen, C. T., Fairman, C. M., Hart, N. H., Taaffe, D. R., Broadhurst, D., Devine, A., Chee, R., Tang, C., Spry, N. A., et al. (2019) · BMJ Open · doi:10.1136/bmjopen-2018-024872 · Cited by 16
The endocannabinoid system: a bridge between alzheimer’s disease and gut microbiota
Bisogno, T., Lauritano, A., & Piscitelli, F. (2021) · Life · doi:10.3390/life11090934 · Cited by 16
Exploring the Gut Microbiota–Muscle Axis in Duchenne Muscular Dystrophy
Mostosi, D., Molinaro, M., Saccone, S., Torrente, Y., Villa, C., & Farini, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25115589 · Cited by 16
Association of Serum Indoxyl Sulfate Levels with Skeletal Muscle Mass and Strength in Chronic Hemodialysis Patients: A 2-year Longitudinal Analysis
Lin, Y., Liu, C., Lai, Y., Wang, C., Kuo, C., Liou, H., & Hsu, B. (2020) · Calcified Tissue International · doi:10.1007/s00223-020-00719-x · Cited by 16
The microbiome links between aging and lupus
Katz-Agranov, N. S., & Zandman‐Goddard, G. (2021) · Autoimmunity Reviews · doi:10.1016/j.autrev.2021.102765 · Cited by 15
Research progress regarding the effect and mechanism of dietary phenolic acids for improving nonalcoholic fatty liver disease via gut microbiota
Ji, L., Deng, H., Xue, H., Wang, J., Hong, K., Gao, Y., Kang, X., Fan, G., Huang, W., Zhan, J., et al. (2023) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/1541-4337.13106 · Cited by 16
Characterization of Gut Microbiota Composition in Hemodialysis Patients With Normal Weight Obesity
Lin, T., Wu, P., Lin, Y., & Hung, S. (2020) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgaa166 · Cited by 15
Alterations in the diversity, composition and function of the gut microbiota in Uyghur individuals with sarcopenia
Zhang, Q., Li, X., Huang, T., Zhang, S., Teng, K., Rousitemu, N., Lan, T., & Wen, Y. (2024) · Experimental Gerontology · doi:10.1016/j.exger.2024.112376 · Cited by 14
Aging Gut Microbiome in Healthy and Unhealthy Aging
Yangyanqiu, W., Qu, Z., Chu, J., & Han, S. (2024) · Aging and Disease · doi:10.14336/ad.2024.0331 · Cited by 17
Understanding the impact of the gut microbiome on opioid use disorder: Pathways, mechanisms, and treatment insights
Kazemian, N., & Pakpour, S. (2024) · Microbial Biotechnology · doi:10.1111/1751-7915.70030 · Cited by 17
Correlating the Gut Microbiome to Health and Disease
Marques, T. M., Holster, S., Wall, R., König, J., Brummer, R. J., & de Vos, W. M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802304-4.00012-8 · Cited by 13
Probiotics for the young and the not so young
Candy, D. C. A., HEATH, S. J., Lewis, J., & Thomas, L. V. (2008) · International Journal of Dairy Technology · doi:10.1111/j.1471-0307.2008.00419.x · Cited by 14
Health benefits of probiotics for the elderly: a review
Baker, H. C., Tran, D. N., & Thomas, L. V. (2009) · Journal of Foodservice · doi:10.1111/j.1748-0159.2009.00147.x · Cited by 15
Antimicrobial Resistance Gene Prevalence in a Population of Patients with Advanced Dementia Is Related to Specific Pathobionts
Rowan-Nash, A. D., Rafael Araos, B., D’Agata, E. M. C., & Belenky, P. A. (2020) · iScience · doi:10.1016/j.isci.2020.100905 · Cited by 13
PQQ and quinoprotein research--the first decade.
Duine, J. A. (1989) · PubMed · Cited by 13
Gut microb-aging and its relevance to frailty aging
Cosquer, G. L., Vergnolle, N., & Motta, J. (2024) · Microbes and Infection · doi:10.1016/j.micinf.2024.105309 · Cited by 16
Highly conserved bifidobacteria in the human gut: Bifidobacterium longum subsp. longum as a potential modulator of elderly innate immunity
Longhi, G., Lugli, G. A., Bianchi, M. G., Rizzo, S. M., Tarracchini, C., Mancabelli, L., Vergna, L. M., Alessandri, G., Fontana, F., Taurino, G., et al. (2024) · Beneficial Microbes · doi:10.1163/18762891-bja00013 · Cited by 13
Evaluation of different culture media for detection and quantification of H. pylori in environmental and clinical samples
Hortelano, I., Moreno, Y., Vesga, F., & Ferrús, M. A. (2020) · International Microbiology · doi:10.1007/s10123-020-00135-z · Cited by 12
Lipocalin 2 Deficiency Restrains Aging-Related Reshaping of Gut Microbiota Structure and Metabolism
Qiu, X., Chen, C., & Chen, X. (2021) · Biomolecules · doi:10.3390/biom11091286 · Cited by 13
Targeting the gut to prevent and counteract metabolic disorders and pathologies during aging
Milenković, D., Capel, F., Combaret, L., Comte, B., Dardevet, D. P., Evrard, B., Guillet, C., Monfoulet, L., Pinel, A., Polakof, S., et al. (2022) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2022.2089870 · Cited by 14
Insights into the Gut Microbiome and Its Functional Pathways in Asthma Patients Through High-Throughput Sequencing
Huang, C., Yu, Y., Du, W., Liu, Y., Dai, R., Wang, P., Zhang, C., & Shi, G. (2021) · Future Microbiology · doi:10.2217/fmb-2020-0101 · Cited by 11
The Connection between Gut and Lung Microbiota, Mast Cells, Platelets and SARS-CoV-2 in the Elderly Patient
Traina, G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232314898 · Cited by 11
Fermentation of feruloyl and non-feruloyl xylooligosaccharides by mixed fecal cultures of human and cow: a comparative study in vitro
Muralikrishna, G., Schwarz, S., Dobleit, G., Fuhrmann, H., & Krueger, M. (2011) · European Food Research and Technology · doi:10.1007/s00217-010-1422-4 · Cited by 11
Evidence that the loss of colonic anti-microbial peptides may promote dysbiotic Gram-negative inflammaging-associated bacteria in aging mice
Forsyth, C. B., Shaikh, M. W., Engen, P. A., Preuss, F., Naqib, A. D., Palmen, B. A., Green, S. J., Zhang, L., Bogin, Z. R., Lawrence, K. M., et al. (2024) · Frontiers in Aging · doi:10.3389/fragi.2024.1352299 · Cited by 11
The Role of the Gut Microbiome in Orthopedic Surgery—a Narrative Review
Hiltzik, D. M., Goodwin, A. M., Kurapaty, S. S., Inglis, J. E., Pagadala, M. S., Edelstein, A. I., & Hsu, W. K. (2023) · Current Reviews in Musculoskeletal Medicine · doi:10.1007/s12178-023-09878-4 · Cited by 10
A Unique Gut Microbiome–Physical Function Axis Exists in Older People with HIV: An Exploratory Study
Dillon, S. M., Abdo, M., Wilson, M. P., Liu, J., Jankowski, C. M., Robertson, C. E., Tunçil, Y. E., Hamaker, B. R., Frank, D. N., MaWhinney, S., et al. (2021) · AIDS Research and Human Retroviruses · doi:10.1089/aid.2020.0283 · Cited by 11
Crohn's Disease of the Elderly
Hong, S. J., Galati, J. S., & Katz, S. (2022) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2021.12.014 · Cited by 10
Carbapenemase-producing Klebsiella pneumoniae in elderly frail patients admitted to medical wards
Nouvenne, A., Ticinesi, A., & Meschi, T. (2014) · Italian Journal of Medicine · doi:10.4081/itjm.2014.476 · Cited by 9
Intestinal Microbiota: First Barrier Against Gut-Affecting Pathogens
Calo‐Mata, P., Ageitos, J. M., Böhme, K., & Barros‐Velázquez, J. (2016) · Springer eBooks · doi:10.1007/978-3-319-28368-5_12 · Cited by 9
Associations Between Walking Speed and Gut Microbiome Composition in Older Men From the MrOS Study
Farsijani, S., Cauley, J. A., Cawthon, P. M., Langsetmo, L., ORWOLL, E. S., Kado, D. M., Kiel, D. P., & Newman, A. B. (2024) · The Journals of Gerontology Series A · doi:10.1093/gerona/glae030 · Cited by 11
Microbiota: A Key for Healthy Aging
Choi, Y. J., & Lee, D. H. (2016) · Annals of Geriatric Medicine and Research · doi:10.4235/agmr.2016.20.4.168 · Cited by 8
Colonic bacterial composition is sex-specific in aged CD-1 mice fed diets varying in fat quality
Unger, A. L., Eckstrom, K. M., Jetton, T. L., & Kraft, J. (2019) · PLoS ONE · doi:10.1371/journal.pone.0226635 · Cited by 9
A Comprehensive Review of the Diagnosis and Pharmacological Management of Crohn’s Disease in the Elderly Population
Kim, D., & Taleban, S. (2019) · Drugs & Aging · doi:10.1007/s40266-019-00672-x · Cited by 8
Exploring the causal relationship between gut microbiota and frailty: a two-sample mendelian randomization analysis
Bo, F., Teng, H., Shi, J., Luo, Z., Xu, Y., Pan, R., Xia, Y., Zhu, S., Zhang, Y., & Zhang, W. (2024) · Frontiers in Medicine · doi:10.3389/fmed.2024.1354037 · Cited by 7
Gut frailty: the core of reversing frailty
Pan, Y., Yang, J., Jiang, Y., Zhu, F., Tang, X. Y., Yuan, Y., Hu, G. M., Luo, D. L., Jiang, Y., & Dong, J. C. (2025) · Annals of Medicine · doi:10.1080/07853890.2025.2527955 · Cited by 8
Identification of the Microbiota in the Aging Process
Sarkar, A., & Pitchumoni, C. S. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804024-9.00004-5 · Cited by 8
Prebiotics: a nutritional concept gaining momentum in modern nutrition
Loo, J. V. (2005) · Food Science & Technology Bulletin Functional Foods · doi:10.1616/1476-2137.13932 · Cited by 7
Age-Dependent Serum Volatilomics of Milk and Yogurt Intake: A Randomized Crossover Study in Healthy Young and Older Men
Meng, H. Y., Kim, J., Fleuti, C., Fuchsmann, P., Polakof, S., Dardevet, D. P., Marmonier, C., Burton-Pimentel, K. J., Bütikofer, U., & Vergères, G. (2023) · Journal of Proteome Research · doi:10.1021/acs.jproteome.2c00674 · Cited by 6
The gut as a central hub for multi-organ crosstalk in aging
Zhang, X., Li, R., Gao, Y., Zhang, W., Ni, T., & Liu, Y. (2026) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-026-06129-w · Cited by 7
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/s12603-014-0513-5 · Cited by 7
Whole-Genome Sequencing Reveals Age-Specific Changes in the Human Blood Microbiota
Lee, E., Sung, J., Kim, H., & Kim, H. (2022) · Journal of Personalized Medicine · doi:10.3390/jpm12060939 · Cited by 6
Host-age prediction from fecal microbiome composition in laboratory micePreprint
Low, A., Soh, M., Miyake, S., & Seedorf, H. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.12.04.412734 · Cited by 6
Immune system and gut microbiota senescence in elderly IBD patients
Fantini, M. C., Onali, S., Gasbarrini, A., & Lopetuso, L. R. (2021) · Minerva Gastroenterology · doi:10.23736/s2724-5985.21.02934-x · Cited by 5
[Research of relationship between frailty and gut microbiota on middle-aged and the aged patients with diabetes].
Peng, X., Zhao, Y., Lin, T., Shu, X., Hou, L., Gao, L., Wang, H., Ge, N., & Yue, J. (2021) · PubMed Central · doi:10.7507/1001-5515.202101083 · Cited by 5
Next-Generation Probiotics
Kumari, M., & Kokkiligadda, A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822909-5.00004-6 · Cited by 5
Randomised, Placebo-Controlled Investigation of the Impact of Probiotic Consumption on Gut Microbiota Diversity and the Faecal Metabolome in Seniors
van Zanten, G. C., Madsen, A. L., Yde, C. C., Krych, Ł., Yeung, N., Saarinen, M., Kot, W., Jensen, H. M., Rasmussen, M. A., Ouwehand, A. C., et al. (2024) · Microorganisms · doi:10.3390/microorganisms12040796 · Cited by 6
Gut Microbiology – A Relatively Unexplored Domain
Brooks, S. P. J., Green-Johnson, J. M., Inglis, G. D., Uwiera, R. R. E., & Kalmokoff, M. L. (2011) · Elsevier eBooks · doi:10.1016/b978-0-08-088504-9.00303-2 · Cited by 5
The potential of probiotic fermented milk products in reducing risk of antibiotic‐associated diarrhoea and Clostridium difficile disease
Lewis, J., Thomas, L. V., & Weir, W. (2009) · International Journal of Dairy Technology · doi:10.1111/j.1471-0307.2009.00518.x · Cited by 5
Sarcopenia, frailty, and its implications in cirrhosis
Ilyas, F., & Satapathy, S. K. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-26711-6.00032-9 · Cited by 4
Genetically supported causality between gut microbiota and frailty: a two-sample Mendelian randomization study
Wang, Z., Han, S., Xiao, Y., Zhang, Y., Ge, Y., Liu, X., & Gao, J. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1324209 · Cited by 4
Age and sex-related variations in murine laryngeal microbiota
An, R., Venkatraman, A., Binns, J., Saric, C., Rey, F. E., & Thibeault, S. L. (2024) · PLoS ONE · doi:10.1371/journal.pone.0300672 · Cited by 4
The Intestinal Microbiota and Aging
O’Toole, P. W., & Brigidi, P. (2013) · World review of nutrition and dietetics · doi:10.1159/000345748 · Cited by 4
The Gut Microbiome and Men’s Sexual Health
Osman, M. M., El‐Khatib, F. M., Roberts, N. H., Huynh, L. M., & Yafi, F. A. (2019) · Current Sexual Health Reports · doi:10.1007/s11930-019-00230-x · Cited by 5
Comparison of Frailty and Chronological Age as Determinants of the Murine Gut Microbiota in an Alzheimer’s Disease Mouse Model
Kapphan, L. M., Nguyen, V. T. T., Heinrich, I., Tüscher, O., Passauer, P., Schwiertz, A., & Endres, K. (2023) · Microorganisms · doi:10.3390/microorganisms11122856 · Cited by 4
Gut Microbiota and Aging: Targets and Anti-aging Interventions
Singh, B., Catanzaro, R., Mal, G., Gautam, S., Mohania, He, F., Yadav, H., Bissi, L., & Marotta, F. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.62181-5 · Cited by 4
A Method for Comprehensive Proteomic Analysis of Human Faecal Samples to Investigate Gut Dysbiosis in Patients with Cystic Fibrosis
Debyser, G., Aerts, M., Hecke, P. V., Mesuere, B., Duytschaever, G., Dawyndt, P., Boeck, K. D., Vandamme, P. A. R., & Devreese, B. V. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-12298-0_6 · Cited by 5
Nutritional advice for community patients: insights from a panel discussion
Thomas, L. V., Jenkins, G., Belton, J., Clements, S., Jacob, C., Johnson, N., Joy, D., Low, J., Munson, E., & Sheppard, J. (2016) · British Journal of Community Nursing · doi:10.12968/bjcn.2016.21.3.130 · Cited by 4
Taxonomic and functional remodeling of the gut microbiota during aging and implications for microbiota-derived biomarkers
Tekin, B., & Gurbanov, R. (2026) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-026-05017-6 · Cited by 4
Recycling source-separated human faeces
Deka, A., Kataki, R., & Simha, P. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90627-2.00023-x · Cited by 3
Metabonomics and Gut Microbial Paradigm in Healthy Aging
Biagi, E., Candela, M., Martin, F., Collino, S., Franceschi, C., & Brigidi, P. (2014) · Molecular and integrative toxicology · doi:10.1007/978-1-4471-6539-2_9 · Cited by 3
Human Microbiome and Aging
Joshi, S., & Navinskey, M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805376-8.00006-x · Cited by 3
Connection Between Fiber, Colonic Microbiota, and Health Across the Human Life Cycle
Dreher, M. L. (2017) · Springer eBooks · doi:10.1007/978-3-319-50557-2_4 · Cited by 3
3-Hydroxy fatty acids in faeces of patients with Crohn's disease or ulcerative colitis as a non-invasive diagnostic approach
Cochetiere, M. F. D. L., Rougé, C., Szponar, B., Larsson, L., & Potel, G. (2007) · Microbial Ecology in Health and Disease · doi:10.1080/08910600601132615 · Cited by 3
Viability of bifidobacteria in yogurts containing oat beta-glucan and/or corn starch during cold storage
Rosburg, V. A. (2009) · doi:10.31274/etd-180810-640 · Cited by 3
Unveiling the Gut Microbiome’s Role in Obesity and Insulin Resistance
Kumar, R., Shukla, S. K., Gupta, A., & Vibhuti, A. (2025) · Springer eBooks · doi:10.1007/978-981-96-6246-3_8 · Cited by 2
Disaster Risk Management, Ventilated Improved Pit Latrines, and Sanitation Challenges in South Africa
Madikizela, P., Hoossein, S., Laubscher, R. K., Whittington-Jones, K. J., Ahmed, M., Mutingwende, N., Ristvej, J., & Tandlich, R. (2022) · Sustainability · doi:10.3390/su14116934 · Cited by 3
The New Antigenic Ecospace of the Globalized World and its Impact on the Immune System: The Battleground of Trade-off and Antagonistic Pleiotropy
Capri, M., Salvioli, S., Monti, D., Bucci, L., Garagnani, P., Ottaviani, E., & Franceschi, C. (2014) · Springer eBooks · doi:10.1007/978-94-017-8712-3_7 · Cited by 2
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
Modulating the human intestinal microbiome in healthy adults and elderly through dietary supplements
An, R. (2020) · doi:10.18174/531631 · Cited by 2
Clinical Phenotypes Associated with the Gut Microbiome in Older Japanese People with Care Needs in a Nursing Home
Inoue, R., Hosomi, K., Park, J., Sakaue, H., Yumioka, H., Kamitani, H., Kinugasa, Y., Harano, K., Syauki, A. Y., Doi, M., et al. (2024) · Nutrients · doi:10.3390/nu16223839 · Cited by 1
Lignan-enriched nutmeg extract changes gut microbiota associated with aging in C57BL/6 mice
Ahn, J.-S., Kim, J. U., Lee, J.-H., Ban, G.-T., Yoon, Y., Yoo, H.-S., Choi, J.-S., & Chung, H.-J. (2025) · Journal of Functional Foods · doi:10.1016/j.jff.2025.106966 · Cited by 2
The Human Intestinal Microbiota and Its Impact on Health
Rajilić-Stojanović, M. D., de Vos, W. M., & Zoetendal, E. G. (2014) · ASM Press eBooks · doi:10.1128/9781555815509.ch2 · Cited by 1
Compositional characteristics of the gut microbiome in patients with uremia
Wu, Z., Bian, M., Zhang, H., Wang, M., Wang, P., Shao, Y., Shen, L., & Zhu, G. (2024) · Indian Journal of Pathology and Microbiology · doi:10.4103/ijpm.ijpm_554_23 · Cited by 1
Liver aging
Felli, É., & Gracia‐Sancho, J. (2025) · Elsevier eBooks · doi:10.1016/b978-0-12-823524-9.00022-8 · Cited by 1
Gut microbiota mediates the relationship between smoking and fall risk: A 2-step Mendelian randomization study
Zhang, J., Yan, X., Zhang, B., Zhang, H., Miao, S., Du, Q., Zhang, Q., & Du, J. (2025) · Medicine · doi:10.1097/md.0000000000044723 · Cited by 1
The Microbiome in Aging
Neto, M. C., & O’Toole, P. W. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802304-4.00010-4 · Cited by 1
Fiber-Rich Dietary Patterns and Colonic Microbiota in Aging and Disease
Dreher, M. L. (2018) · Springer eBooks · doi:10.1007/978-3-319-59180-3_4 · Cited by 1
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
Probiotics and Innovation
Antoine, J., Faurie, J., Oozeer, R., Vlieg, J. V. H., Knol, J., Bachmann, H., & Dore, J. M. (2010) · doi:10.1002/9781444329384.ch20 · Cited by 1
Microbiota of the Human Gut
Ghoddusi, H. B., & Thomas, L. V. (2017) · Wiley eBooks · doi:10.1002/9781119214137.ch1 · Cited by 1
Prevalence of the Frailty Phenotype in community-dwelling population aged 50 and over in the survey of health, ageing and retirement in Europe
Cuénoud, P. (2007) · IRIS · Cited by 1
"Smurf Mice": revolutionising our understanding of age-related and end-of-life animal physiologyPreprint
Cansell, C., Goepp, V., Bain, F., Todd, N., Douard, V., Monnoye, M., Zane, F., Sanchez, C., Pietrancosta, N., Rovère, C., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.14.659669 · Cited by 1
Dietary effects on human fecal microbiota
Simões, C. (2013) · Työväentutkimus Vuosikirja
Ampicillin-resistant Enterococcus faecium : ecology, transmission dynamics and intervention strategies
de Regt, M. J. A. (2010) · Utrecht University Repository (Utrecht University)
Probiotics for the elderly
Forssten, S. D., Lahtinen, S. J., & Ouwehand, A. C. (2009) · Food Science & Technology Bulletin Functional Foods · doi:10.1616/1476-2137.15746
MOLECULAR CHARACTERIZATION OF THE HUMAN GUT MICROBIOTA
Tesi, T. D. (2010)
Impact du vieillissement sur le microbiote intestinal
Gérard, P. (2013) · Pratiques en nutrition · doi:10.1016/j.pranut.2013.06.005
Microbial ecology at the International Space Station
van Tongeren, S. P. (2011)
70th Anniversary Conference on 'From plough through practice to policy' Symposium 3: Obesity-related cancers The gut microbial metabolome: modulation of cancer risk in obese individuals
Russell, W. R., Duncan, S. H., & Flint, H. J. (2013)
Exercise and Dietary Factors Affecting the Microbiota: Current Knowledge and Future Perspectives
Marroquín, F. E. M. (2017) · Journal of Nutritional Health & Food Engineering · doi:10.15406/jnhfe.2017.06.00199
A Review on Bifidobacteria for Human Health
Song, M., Park, W. S., Yoo, J., & Ham, J.-S. (2017) · Journal of Dairy Science and Biotechnology · doi:10.22424/jmsb.2017.35.2.73
Urologic Applications of the Microbiota in Multiple Sclerosis
May, D. N., & Togami, J. M. (2018) · Current Bladder Dysfunction Reports · doi:10.1007/s11884-018-0461-8
Efeito da suplementação de uma substância simbiótica sobre a permeabilidade intestinal, a inflamação sistêmica, a cognição e sintomas depressivos em idosos da comunidade
Louzada, E. R. (2017) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.89.2017.tde-28112017-160051
Verdauung und Darmerkrankungen
Fegerl, S. P., Sartor, H., & Witasek, A. (2019) · Springer eBooks · doi:10.1007/978-3-662-58111-7_6
The Aging Gut Microbiota
Keebaugh, E. S., Williams, L. D., & Ja, W. W. (2019) · Springer eBooks · doi:10.1007/978-3-030-28737-5_12
Clinical Features of Inflammatory Bowel Disease (Ulcerative Colitis and Crohn’s Disease) in Geriatric Practice in St. Petersburg
Baranovsky, A. Y., Александровна, К. Э., Щукина, О. Б., Raikhelson, K. L., Palgova, L. K., Marchenko, N. V., Константиновна, П. М., Владимировна, П. Е., Kovyazina, V. P., & Segal, A. M. (2020) · Advances in Gerontology · doi:10.1134/s2079057020020034
Nutrition, microbiome, aging, and cancer
Brown, T., Ahmed, F., Riscuta, G., Xi, D., & Zillow, A. L. (2019) · Journal of Bacteriology & Mycology Open Access · doi:10.15406/jbmoa.2019.07.00244

Authors: van Tongeren, S. P., Slaets, J. P. J., Harmsen, H. J. M., & Welling, G. W.
Affiliations: Department of Medical Microbiology
University Medical Center Groningen (NL)
ORCID: Slaets, Joris P. J.
Harmsen, H. J. M.
Venue: Applied and Environmental Microbiology
Publisher: American Society for Microbiology
Published: 2005-10
Volume: 71
Issue: 10
Pages: 6438-6442
ISSN: 0099-2240 (ISSN-L)
1098-5336
DOI: 10.1128/aem.71.10.6438-6442.2005
PMC: PMC1265947
OpenAlex: W2129130754
Cited by: 333
References: 37
Citations by year: 2026: 6 · 2025: 14 · 2024: 21 · 2023: 15 · 2022: 28 · 2021: 39 · 2020: 24 · 2019: 26 · 2018: 28 · 2017: 22 · 2016: 18 · 2015: 15 · 2014: 16 · 2013: 9 · 2012: 6
FWCI: 1.76
Type: journal article
Language: en
Open access: green
europepmc.org
Licence: journals.asm.org/non-commercial-tdm-license (tdm)
Locations: Applied and Environmental Microbiology (publishedVersion)
Europe PMC (PubMed Central) (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
University of Groningen research database (University of Groningen / Centre for Information Technology) (publishedVersion, other-oa)
University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion, other-oa)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
Health Sciences › Medicine › Geriatrics and Gerontology › Frailty in Older Adults
Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
Keywords: fecal microbiota, frailty, older adults, lactobacilli, Bacteroides-Prevotella, Faecalibacterium prausnitzii, Enterobacteriaceae, gut microbiota, microbial diversity
MeSH terms: Aged, Aged, 80 and over, Bifidobacterium, Enterobacteriaceae, Feces, Humans, Lactobacillus, Colony Count, Microbial, Frail Elderly, Prevotella

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

Fecal Microbiota Composition and Frailty

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks