The DOI matches its Crossref record; 83 of the 83 references it cites were found in a registry or an index.
Gut microbiome alterations in Alzheimer’s disease
Open accessAbstract
Alzheimer’s disease (AD) is the most common form of dementia. However, the etiopathogenesis of this devastating disease is not fully understood. Recent studies in rodents suggest that alterations in the gut microbiome may contribute to amyloid deposition, yet the microbial communities associated with AD have not been characterized in humans. Towards this end, we characterized the bacterial taxonomic composition of fecal samples from participants with and without a diagnosis of dementia due to AD. Our analyses revealed that the gut microbiome of AD participants has decreased microbial diversity and is compositionally distinct from control age- and sex-matched individuals. We identified phylum- through genus-wide differences in bacterial abundance including decreased Firmicutes, increased Bacteroidetes, and decreased Bifidobacterium in the microbiome of AD participants. Furthermore, we observed correlations between levels of differentially abundant genera and cerebrospinal fluid (CSF) biomarkers of AD. These findings add AD to the growing list of diseases associated with gut microbial alterations, as well as suggest that gut bacterial communities may be a target for therapeutic intervention.
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
Figures



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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“A variety of genetic and environmental factors have been implicated in AD etiopathogenesis, including contributions from gut microbiota [13–15].”
From The gut microbiota-derived metabolite trimethylamine N-oxide is elevated in Alzheimer’s disease (2018) · cites this paper as [15]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Diseases of cognitive decline, such as Alzheimer's disease and vascular dementia, are associated with aberrant microbial compositions when compared with healthy controls (297).”
From Diet and the Microbiota–Gut–Brain Axis: Sowing the Seeds of Good Mental Health (2021) · cites this paper as [297]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“These include reductions in beneficial genera such as Lactobacillus and Bifidobacterium, alongside increases in pro-inflammatory taxa like Enterobacteriaceae64.”
From Artificial intelligence-driven multi-omics approaches in Alzheimer's disease: Progress, challenges, and future directions (2025) · cites this paper as [64]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Studies using 16S rRNA gene sequencing and shotgun metagenomic sequencing have consistently identified significant changes in the gut microbiota composition of individuals with AD.”
From Artificial intelligence-driven multi-omics approaches in Alzheimer's disease: Progress, challenges, and future directions (2025) · cites this paper as [64]
Experimental — accuracy not yet measuredIn the citing paper
“Human studies show associations between gut microbiota and neurodegenerative diseases148.”
From Microglia in neurodegeneration (2018) · cites this paper as [148]
In the citing paper
“Human studies comparing the composition of the GM of elderly participants suffering from cognitive impairment with healthy individuals indicate significant changes in GM composition. Specifically, there is an increase in pro-inflammatory taxa and a reduction in anti-inflammatory taxa (104–109).”
From Signalling cognition: The gut microbiota and hypothalamic-pituitary-adrenal axis (2023) · cites this paper as [105]
In the citing paper
“Within the Firmicutes, the families Ruminococcaceae, Turicibacteraceae, and Clostridiaceae were all less abundant in AD patient (160).”
From The gut-brain axis: how microbiota and host inflammasome influence brain physiology and pathology (2020) · cites this paper as [160]
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
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
Love, M. I., Huber, W., & Anders, S. (2014) · Genome Biology · doi:10.1186/s13059-014-0550-8 · Cited by 95,106
Schloss, P. D., Westcott, S. L., Ryabin, T., Hall, J. R., Hartmann, M., Hollister, E. B., Lesniewski, R. A., Oakley, B. B., Parks, D. H., Robinson, C. J., et al. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01541-09 · Cited by 19,549
McKhann, G. M., Knopman, D. S., Chertkow, H., Hyman, B. T., Jack, C. R., Kawas, C. H., Klunk, W. E., Koroshetz, W. J., Manly, J. J., Mayeux, R., et al. (2011) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2011.03.005 · Cited by 18,657
Metagenomic biomarker discovery and explanation
Segata, N., Izard, J., Waldron, L., Gevers, D., Miropolsky, L., Garrett, W. S., & Huttenhower, C. (2011) · Genome Biology · doi:10.1186/gb-2011-12-6-r60 · Cited by 16,192
Structure, function and diversity of the healthy human microbiome
The Human Microbiome Project Consortium (2012) · Nature · doi:10.1038/nature11234 · Cited by 11,726
Predictive functional profiling of microbial communities using 16S rRNA marker gene sequences
Langille, M. G. I., Zaneveld, J., Caporaso, J. G., McDonald, D., Knights, D., Reyes, J. A., Clemente, J. C., Burkepile, D. E., Vega Thurber, R. L., Knight, R., et al. (2013) · Nature Biotechnology · doi:10.1038/nbt.2676 · Cited by 9,116
A core gut microbiome in obese and lean twins
Turnbaugh, P. J., Hamady, M., Yatsunenko, T., Cantarel, B. L., Duncan, A., Ley, R. E., Sogin, M. L., Jones, W. J., Roe, B. A., Affourtit, J. P., et al. (2009) · Nature · doi:10.1038/nature07540 · Cited by 7,823
Kozich, J. J., Westcott, S. L., Baxter, N. T., Highlander, S. K., & Schloss, P. D. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.01043-13 · Cited by 7,246
Metabolic Endotoxemia Initiates Obesity and Insulin Resistance
Cani, P. D., Amar, J., Iglesias, M. A., Poggi, M., Knauf, C., Bastelica, D., Neyrinck, A. M., Fava, F., Tuohy, K. M., Chabo, C., et al. (2007) · Diabetes · doi:10.2337/db06-1491 · Cited by 6,638
Obesity alters gut microbial ecology
Ley, R. E., Bäckhed, F., Turnbaugh, P., Lozupone, C. A., Knight, R. D., & Gordon, J. I. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504978102 · Cited by 6,176
Cited by
Sorted by citations
Items 501–600 of 1,007
Inflammatory bowel disease: A potential pathogenic factor of Alzheimer's disease
Wang, D., Zhang, X., & Du, H. (2022) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2022.110610 · Cited by 52
Zhang, Y., Ding, N., Hao, X., Zhao, J., Zhao, Y., Li, Y., & Li, Z. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1018371 · Cited by 52
Nutritional metabolism and cerebral bioenergetics in Alzheimer's disease and related dementias
Yassine, H. N., Self, W. K., Kerman, B. E., Santoni, G., Shanmugam, N. K. N., Abdullah, L. I., Golden, L. R., Fonteh, A. N., Harrington, M. G., Gräff, J., et al. (2022) · Alzheimer s & Dementia · doi:10.1002/alz.12845 · Cited by 52
Update on the gut microbiome in health and diseases
Salvadori, M., & Rosso, G. (2024) · World Journal of Methodology · doi:10.5662/wjm.v14.i1.89196 · Cited by 52
Li, L., Yang, C., Jia, M., Wang, Y., Zhao, Y., Li, Q., Gong, J., He, Y., Xu, K., Liu, X., et al. (2024) · Food & Function · doi:10.1039/d4fo00886c · Cited by 52
Gut microbial metabolism in Alzheimer's disease and related dementias
Kang, J. W., Vemuganti, V., Kuehn, J. F., Ulland, T. K., Rey, F. E., & Bendlin, B. B. (2024) · Neurotherapeutics · doi:10.1016/j.neurot.2024.e00470 · Cited by 53
Self-citationKrueger, M. E., Boles, J. S., Simon, Z. D., Alvarez, S. D., McFarland, N. R., Okun, M. S., Zimmermann, E. M., Forsmark, C. E., & Tansey, M. G. (2025) · npj Parkinson s Disease · doi:10.1038/s41531-025-00894-4 · Cited by 52
Age-Related Differences in the Gut Microbiome of Rhesus Macaques
Adriansjach, J., Baum, S. T., Lefkowitz, E. J., Pol, W. J. V. D., Buford, T. W., & Colman, R. J. (2020) · The Journals of Gerontology Series A · doi:10.1093/gerona/glaa048 · Cited by 52
Ling, Y., Gu, Q., Zhang, J., Gong, T., Weng, X., Liu, J., & Sun, J. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-200315 · Cited by 52
Emerging Roles of Functional Bacterial Amyloids in Gene Regulation, Toxicity, and Immunomodulation
Salinas, N., Povolotsky, T. L., Landau, M., & Kolodkin‐Gal, I. (2020) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00062-20 · Cited by 52
Ruiz‐González, C., Román, P., Rueda‐Ruzafa, L., Rodríguez-Arrastia, M. J., & Cardona, D. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.110189 · Cited by 52
Gene targeting techniques for Huntington’s disease
Fields, E., Vaughan, E., Tripu, D. R., Lim, I., Shrout, K., Conway, J., Salib, N., Lee, Y., Dhamsania, A., Jacobsen, M., et al. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101385 · Cited by 53
Influence of the Microbiota-Gut-Brain Axis on Cognition in Alzheimer’s Disease
Escobar, Y.-N. H., O’Piela, D., Wold, L. E., & Mackos, A. R. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-215290 · Cited by 52
Jeong, Y., Jhun, J., Lee, S.-Y., Na, H. S., Choi, J., Cho, K.-H., Lee, S. Y., Lee, A. R., Park, S.-J., You, H. J., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.736196 · Cited by 51
Gut microbiota and its metabolites in Alzheimer’s disease: from pathogenesis to treatment
Zou, X., Zou, G., Zou, X., Wang, K., & Chen, Z. (2024) · PeerJ · doi:10.7717/peerj.17061 · Cited by 51
A digital twin of the infant microbiome to predict neurodevelopmental deficits
Sizemore, N., Oliphant, K., Zheng, R., Martin, C. R., Claud, E. C., & Chattopadhyay, I. (2024) · Science Advances · doi:10.1126/sciadv.adj0400 · Cited by 51
Exploring the gut-brain Axis: Potential therapeutic impact of Psychobiotics on mental health
Cocean, A.-M., & Vodnar, D. C. (2024) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2024.111073 · Cited by 52
Metagenomic analysis characterizes stage-specific gut microbiota in Alzheimer’s disease
Jia, L., Ke, Y., Zhao, S., Liu, J., Luo, X., Cao, J., Liu, Y., Guo, Q., Chen, W., Chen, F., et al. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-02973-7 · Cited by 52
Cilia, R., Piatti, M., Cereda, E., Bolliri, C., Caronni, S., Ferri, V., Cassani, E., Bonvegna, S., Ferrarese, C., Zecchinelli, A., et al. (2020) · Journal of Parkinson s Disease · doi:10.3233/jpd-202297 · Cited by 51
Dysbiosis and Alzheimer’s Disease: Cause or Treatment Opportunity?
Janeiro, M. H., Ramírez, M. J., & Solas, M. (2021) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-01024-9 · Cited by 51
Diet-Microbiota-Brain Axis in Alzheimer’s Disease
Kincaid, H. J., Nagpal, R., & Yadav, H. (2021) · Annals of Nutrition and Metabolism · doi:10.1159/000515700 · Cited by 51
Bacterial Extracellular DNA Promotes β-Amyloid Aggregation
Tetz, G. V., & Tetz, V. (2021) · Microorganisms · doi:10.3390/microorganisms9061301 · Cited by 50
Sun, P., Zhu, H., Li, X., Shi, W., Guo, Y., Du, X., Zhang, L., Su, L., & Qin, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911560 · Cited by 50
Bacterial extracellular vesicles – brain invaders? A systematic review
Kaisanlahti, A., Salmi, S., Kumpula, S., Amatya, S. B., Turunen, J., Tejesvi, M. V., Byts, N., Tapiainen, T., & Reunanen, J. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1227655 · Cited by 50
Kurhaluk, N., Kamiński, P., Bilski, R., Kołodziejska, R., Woźniak, A., & Ткаченко, Г. М. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26083658 · Cited by 50
Modification of the gut microbiome to combat neurodegeneration
Sasmita, A. O. (2019) · Reviews in the Neurosciences · doi:10.1515/revneuro-2019-0005 · Cited by 50
Healthy Gut, Healthy Brain: The Gut Microbiome in Neurodegenerative Disorders
Chandra, S., Alam, M. T., Dey, J., Sasidharan, B. C. P., Ray, U., Srivastava, A. K., Gandhi, S., & Tripathi, P. P. (2020) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026620666200413091101 · Cited by 50
gutMEGA: a database of the human gut MEtaGenome Atlas
Zhang, Q., Yu, K., Li, S., Zhang, X.-L., Zhao, Q., Zhao, X., Liu, Z., Cheng, H. L., Li, X., & Li, X. (2020) · Briefings in Bioinformatics · doi:10.1093/bib/bbaa082 · Cited by 50
Relationship between Wine Consumption, Diet and Microbiome Modulation in Alzheimer’s Disease
Moreno-Arribas, M. V., Bartolomé, B., Peñalvo, J. L., Pérez‐Matute, P., & Motilva, M. (2020) · Nutrients · doi:10.3390/nu12103082 · Cited by 50
González-Sanmiguel, J., Schuh, C. M. A. P., Muñoz-Montesino, C., Contreras‐Kallens, P., Aguayo, L. G., & Aguayo, S. D. (2020) · Cells · doi:10.3390/cells9112476 · Cited by 50
Brown, T., Sykes, D., & Allen, A. R. (2021) · Biomedicines · doi:10.3390/biomedicines9020189 · Cited by 51
Regulation of microglial physiology by the microbiota
Cook, J., & Prinz, M. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2125739 · Cited by 49
Association of perturbation of oral bacterial with incident of Alzheimer's disease: A pilot study
Moghadam, M. T., Amirmozafari, N., Mojtahedi, A., Bakhshayesh, B., Shariati, A., & Jazi, F. M. (2022) · Journal of Clinical Laboratory Analysis · doi:10.1002/jcla.24483 · Cited by 49
Du, Y., Li, X., An, Y., Song, Y., & Lu, Y. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.930626 · Cited by 49
Impact of Microbiome–Brain Communication on Neuroinflammation and Neurodegeneration
Stolzer, I., Scherer, E., Süß, P., Rothhammer, V., Winner, B., Neurath, M. F., & Günther, C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914925 · Cited by 49
Fecal microbiota transplantation: a novel strategy for treating Alzheimer’s disease
Xiang, W., Xiang, H., Wang, J., Jiang, Y., Pan, C., Ji, B.-J., & Zhang, A. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1281233 · Cited by 49
Microglia and gut microbiota: A double-edged sword in Alzheimer's disease
Bano, N., Khan, S., Ahamad, S., Kanshana, J. S., Dar, N. J., Khan, S. J., Nazir, A., & Bhat, S. A. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102515 · Cited by 50
Lista, S., Munafò, A., Caraci, F., Imbimbo, C., Emanuele, E., Minoretti, P., Pinto-Fraga, J., Merino-País, M., Crespo‐Escobar, P., López‐Ortiz, S., et al. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102659 · Cited by 50
Paley, E. L. (2019) · International Journal of Tryptophan Research · doi:10.1177/1178646919834550 · Cited by 49
Qiu, Y., Chen, X., Yan, X., Wang, J., Yu, G., Ma, W., Xiao, B., Quiñones, S., Tian, X., & Ren, X. (2020) · Environment International · doi:10.1016/j.envint.2020.105763 · Cited by 49
Pellegrini, C., Daniele, S., Antonioli, L., Benvenuti, L., D’Antongiovanni, V., Piccarducci, R., Pietrobono, D., Citi, V., Piragine, E., Flori, L., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103523 · Cited by 49
Guo, Y., Wang, L., Lu, J., Jiao, J., Yang, Y., Zhao, H., Zhang, L., & Zheng, H. Y. (2021) · Molecular Medicine Reports · doi:10.3892/mmr.2021.11931 · Cited by 49
Sajdel, E. M. (2021) · BioMed Research International · doi:10.1155/2021/7880448 · Cited by 49
The Potential Utility of Prebiotics to Modulate Alzheimer’s Disease: A Review of the Evidence
Kang, J. W., & Zivkovic, A. M. (2021) · Microorganisms · doi:10.3390/microorganisms9112310 · Cited by 49
Abbas‐Egbariya, H., Haberman, Y., Braun, T., Hadar, R., Denson, L. A., Gal‐Mor, O., & Amir, A. (2022) · Genome biology · doi:10.1186/s13059-022-02637-7 · Cited by 49
Shou, J., & Shaw, P. (2022) · Cells · doi:10.3390/cells11050796 · Cited by 48
Skowron, K., Budzyńska, A., Wiktorczyk-Kapischke, N., Chomacka, K., Grudlewska‐Buda, K., Wilk, M., Wałecka-Zacharska, E., Andrzejewska, M., & Gospodarek-Komkowska, E. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23147820 · Cited by 48
Zhou, Z., Hui, E. S. K., Kranz, G. S., Chang, J. R., de Luca, K. E., Pinto, S. M., Chan, W. W. Y., Yau, S., Chau, B. K. H., Samartzis, D., et al. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101767 · Cited by 48
Peng, Y., Dong, W., Chen, G., Mi, J., Lu, L., Xie, Z., Xu, W., Zhou, W., Sun, Y., Zeng, X., et al. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.2c06713 · Cited by 48
Biomaterials-based anti-inflammatory treatment strategies for Alzheimer’s disease
Chu, J., Zhang, W., Liu, Y., Gong, B., Ji, W., Yin, T., Gao, C., Liangwen, D., Hao, M., Chen, C., et al. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.374137 · Cited by 48
Microbiota-mediated metabolic perturbations in the gut and brain of mice after microplastic exposure
Lee, S.-H., Lin, W., & Cheng, T. (2023) · Chemosphere · doi:10.1016/j.chemosphere.2023.141026 · Cited by 48
Yassin, L. K., Skrabulyte-Barbulescu, J., Alshamsi, S. H., Saeed, S., Alkuwaiti, S. H., Almazrouei, S., Alnuaimi, A., BaniYas, S., Aldhaheri, D., Alderei, M., et al. (2025) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2025.1667448 · Cited by 48
The role of microbiota in tissue repair and regeneration
Shavandi, A., Saeedi, P., Gérard, P., Jalalvandi, E., Cannella, D., & Bekhit, A. E. A. (2019) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.3009 · Cited by 48
Bello-Medina, P. C., Hernández-Quiroz, F., Pérez-Morales, M., González-Franco, D. A., Cruz-Pauseno, G., Garcı́a-Mena, J., Díaz-Cintra, S. Y., & Pacheco‐López, G. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.595583 · Cited by 48
Altered gut microbiota in older adults with mild cognitive impairment: a case-control study
Fan, K.-C., Lin, C.-C., Liu, Y.-C., Chao, Y.-P., Lai, Y.-J., Chiu, Y.-L., & Chuang, Y.-F. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1162057 · Cited by 47
“Studies in AD have demonstrated a microbial composition that deviates significantly from that of cognitively normal controls (Vogt et al., 2017; Zhuang et al., 2018; Liu et al., 2019; Saji et al., 2019a,b; Guo et al., 2021).”
BackgroundLiu, F., Duan, M., Fu, H., Zhao, G., Han, Y., Lan, F., Ahmed, Z., Cao, G., Li, Z., Ma, D., et al. (2022) · Annals of Surgery · doi:10.1097/sla.0000000000005489 · Cited by 47
Abdolmaleky, H. M., & Zhou, J. (2023) · Nutrients · doi:10.3390/nu15153456 · Cited by 47
The dopaminergic system and Alzheimer’s disease
Zhang, Y., Liang, Y., & Gu, Y. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-00230 · Cited by 47
Microbiome-Mediated Upregulation of MicroRNA-146a in Sporadic Alzheimer’s Disease
Zhao, Y., & Lukiw, W. J. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00145 · Cited by 47
Implications of the Human Gut–Brain and Gut–Cancer Axes for Future Nanomedicine
Javed, I., Cui, X., Wang, X., Mortimer, M., Andrikopoulos, N. K., Li, Y., Davis, T. P., Zhao, Y., Ke, P. C., & Chen, C. (2020) · ACS Nano · doi:10.1021/acsnano.0c07258 · Cited by 47
Subgingival microbiota in a population with and without cognitive dysfunction
Holmer, J., Aho, V. T. E., Eriksdotter, M., Paulin, L. G., Pietiäinen, M., Auvinen, P., Schultzberg, M., Pussinen, P. J., & Buhlin, K. (2021) · Journal of Oral Microbiology · doi:10.1080/20002297.2020.1854552 · Cited by 47
Effect of a Vegan Diet on Alzheimer’s Disease
Katonová, A., Sheardová, K., Amlerová, J., Angelucci, F., & Hort, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232314924 · Cited by 46
Gut microbiome and Alzheimer’s disease: What we know and what remains to be explored
Kapoor, B., Biswas, P., Gulati, M., Rani, P., & Gupta, R. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102570 · Cited by 46
Yadav, H., Jaldhi, Bhardwaj, R., Anamika, A., Bakshi, A., Gupta, S., & Maurya, S. K. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.122022 · Cited by 47
Rosell-Díaz, M., Petit-Gay, A., Molas-Prat, C., Gallardo‐Nuell, L., Ramió‐Torrentà, L., Garre‐Olmo, J., Pérez‐Brocal, V., Moyá, A., Jové, M., Pamplona, R., et al. (2024) · Metabolism · doi:10.1016/j.metabol.2024.155941 · Cited by 46
Borgiani, G., Possidente, C., Fabbri, C., Oliva, V., Bloemendaal, M., Vásquez, A. A., Dinan, T. G., Vieta, E., Menchetti, M., Ronchi, D. D., et al. (2024) · International Clinical Psychopharmacology · doi:10.1097/yic.0000000000000533 · Cited by 46
Systemic inflammation as a central player in the initiation and development of Alzheimer’s disease
Bayraktaroğlu, I., Ortí-Casañ, N., Dam, D. V., Deyn, P. P. D., & Eisel, U. L. M. (2025) · Immunity & Ageing · doi:10.1186/s12979-025-00529-5 · Cited by 49
Polyphenols in the management of brain disorders: Modulation of the microbiota-gut-brain axis
Serra, D., Almeida, L. M., & Dinis, T. C. P. (2019) · Advances in food and nutrition research · doi:10.1016/bs.afnr.2019.08.001 · Cited by 46
Gut Microbiota and Neurologic Diseases and Injuries
Patterson, T. T., & Grandhi, R. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-2385-4_6 · Cited by 46
Cognitive-Behavioural Correlates of Dysbiosis: A Review
Luca, M., Chattipakorn, S. C., Sriwichaiin, S., & Luca, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21144834 · Cited by 46
Gut Microbiome and Mycobiome Alterations in an In Vivo Model of Alzheimer’s Disease
D’Argenio, V., Veneruso, I., Gong, C., Cecarini, V., Bonfili, L., & Eleuteri, A. M. (2022) · Genes · doi:10.3390/genes13091564 · Cited by 46
Sanguinetti, E., Guzzardi, M. A., Tripodi, M., Panetta, D., Selma-Royo, M., Zega, A., Telleschi, M., Collado, M. C., & Iozzo, P. (2019) · Scientific Reports · doi:10.1038/s41598-019-48090-8 · Cited by 45
Yousefi, B., Kokhaei, P., Mehranfar, F., Bahar, A., Abdolshahi, A., Emadi, A., & Eslami, M. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.10.046 · Cited by 45
Alzheimer’s Disease: A Systems View Provides a Unifying Explanation of Its Development
Grobler, C., van Tongeren, M., Gettemans, J., Kell, D. B., & Pretorius, E. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-220720 · Cited by 45
Chaudhari, D. S., Jain, S., Yata, V. K., Mishra, S. P., Kumar, A., Fraser, A., Kociolek, J., Dangiolo, M. B., Smith, A., Golden, A. G., et al. (2023) · GeroScience · doi:10.1007/s11357-023-00799-1 · Cited by 45
Age-Related Cognitive Decline, Focus on Microbiome: A Systematic Review and Meta-Analysis
Coradduzza, D., Sedda, S., Cruciani, S., Miglio, M. R. D., Ventura, C., Nivoli, A., & Maioli, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241813680 · Cited by 45
Influence of human gut microbiome on the healthy and the neurodegenerative aging
Borrego-Ruiz, A., & Borrego, J. J. (2024) · Experimental Gerontology · doi:10.1016/j.exger.2024.112497 · Cited by 43
Chilton, P. M., Ghare, S. S., Charpentier, B. T., Myers, S., Rao, A. V., Petrosino, J. F., Hoffman, K. L., Greenwell, J. C., Tyagi, N., Behera, J., et al. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2389319 · Cited by 45
Munir, M. U., Ali, S. A., Chung, K. H. K., Käkinen, A., Javed, I., & Davis, T. P. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2422468 · Cited by 45
Can oral health and oral‐derived biospecimens predict progression of dementia?
Orr, M. E., Reveles, K. R., Yeh, C., Young, E. H., & Han, X. (2019) · Oral Diseases · doi:10.1111/odi.13201 · Cited by 45
Role of Gut Microbiota in Combating Oxidative Stress
Dam, B., Misra, A., & Banerjee, S. (2019) · Springer eBooks · doi:10.1007/978-981-13-8763-0_4 · Cited by 47
Hang, Z., Lei, T., Zeng, Z., Cai, S., Bi, W., & Du, H. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.112343 · Cited by 45
Wan, J., Zhou, S., Mea, H. J., Guo, Y., Ku, H., & Urbina, B. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00480 · Cited by 45
Borsom, E. M., Conn, K. A., Keefe, C. R., Herman, C., Orsini, G. M., Hirsch, A. H., Avila, M. P., Testo, G., Jaramillo, S. A., Bolyen, E. K., et al. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.03458-22 · Cited by 45
Urinary metabolic phenotyping for Alzheimer’s disease
Kurbatova, N., Garg, M., Whiley, L., Chekmeneva, E., Jiménez, B., Gómez-Romero, M., Pearce, J., Kimhofer, T., D’Hondt, E., Soininen, H., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-78031-9 · Cited by 44
Dhami, M., Raj, K., & Singh, S. (2023) · Aging and Health Research · doi:10.1016/j.ahr.2023.100128 · Cited by 44
Gut-brain axis: gut dysbiosis and psychiatric disorders in Alzheimer’s and Parkinson’s disease
Denman, C. R., Park, S. M., & Jo, J. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1268419 · Cited by 45
Butyrate as a potential therapeutic agent for neurodegenerative disorders
Chakraborty, P., Gamage, H. K. A. H., & Laird, A. S. (2024) · Neurochemistry International · doi:10.1016/j.neuint.2024.105745 · Cited by 44
Prabha, S., Sajad, M., Hasan, G. M., Islam, A., Hassan, M. I., & Thakur, S. C. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102476 · Cited by 44
Gut Microbiota and Microbiota-Related Metabolites as Possible Biomarkers of Cognitive Aging
Ticinesi, A., Nouvenne, A., Tana, C., Prati, B., & Meschi, T. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-25650-0_8 · Cited by 45
Liu, Y., Du, T., Zhang, W., Lu, W., Peng, Z., Huang, S., Sun, X., Zhu, X., Chen, C., Qian, L., et al. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/8340192 · Cited by 44
Gut dysbiosis in stroke and its implications on Alzheimer’s disease‐like cognitive dysfunction
Cho, J., Park, Y. J., Gonzales‐Portillo, B., Saft, M., Cozene, B., Sadanandan, N., & Borlongan, C. V. (2021) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13613 · Cited by 44
Wang, G., Zhou, H., Luo, L., Qin, L., Yin, J., Yu, Z., Zhang, L., & Wan, Z. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.105010 · Cited by 44
la Fuente, M. D. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-201587 · Cited by 44
Gut microbial involvement in Alzheimer's disease pathogenesis
Zhang, Y., Geng, R., & Tu, Q. (2021) · Aging · doi:10.18632/aging.202994 · Cited by 44
Gut Microbiota: Critical Controller and Intervention Target in Brain Aging and Cognitive Impairment
Li, H., Ni, J., & Qing, H. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.671142 · Cited by 44
Cui, J., Xiao, S., Cao, Y., Zhang, Y., Yang, J., Zheng, L., Zhao, F., Liu, X., Liu, D., Zhou, Z., et al. (2024) · Environmental Science & Technology · doi:10.1021/acs.est.4c07427 · Cited by 43
Gut microbial metabolites and the brain–gut axis in Alzheimer’s disease: A review
Ji, X., Wang, J., Lan, T., Zhao, D., & Xu, P. (2025) · Biomolecules and Biomedicine · doi:10.17305/bb.2025.12921 · Cited by 43
Neurotoxicity of Micro- and Nanoplastics: A Comprehensive Review of Central Nervous System Impacts
Ma, Q., Lei, J., Pang, Y., Yu, S., & Zhang, T. (2025) · Environment & Health · doi:10.1021/envhealth.5c00087 · Cited by 43
The sex-specific interaction of the microbiome in neurodegenerative diseases
Cox, L. M., Abou‐El‐Hassan, H., Maghzi, A. H., Vincentini, J., & Weiner, H. L. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146385 · Cited by 44
Metadata
- Authors
- 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., Bendlin, B. B., & Rey, F. E.
- Affiliations
- University of Wisconsin–Madison (US)
- Sahlgrenska University Hospital (SE)
- Corresponding author
- Bendlin, Barbara B.
- Rey, Federico E.
- ORCID
- Venue
- Scientific Reports
- Published
- 2017-10-19
- Volume
- 7
- Issue
- 1
- Pages
- 13537-13537
- ISSN
- 2045-2322 (ISSN-L)
- PMC
- PMC5648830
- OpenAlex
- W2761210275
- Cited by
- 2,137
- References
- 83
- Citations by year
- 2026: 205 · 2025: 322 · 2024: 328 · 2023: 269 · 2022: 339 · 2021: 283 · 2020: 205 · 2019: 119 · 2018: 64 · 2017: 1
- FWCI
- 43.23
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Scientific Reports (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- Alzheimer's Association (R01 AG027161, R01 AG037639, R01 AG021155)
- Torsten Söderbergs Stiftelse
- Rush University
- Georgia Clinical and Translational Science Alliance (UL1TR000427)
- Royal Swedish Academy of Sciences
- Vetenskapsrådet
- National Institutes of Health (UL1TR000427, NIH P50, AG027161, AG037639, NIH P50 AG033514, AG033514)
- Institute for Clinical and Translational Research, University of Wisconsin, Madison (UL1TR000427)
- National Institute on Aging (RF1AG027161, R01AG037639, P50AG033514, R01AG021155, R01AG027161, R56AG037639)
- National Institute of General Medical Sciences (T32GM008692)
- National Center for Advancing Translational Sciences
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Keywords
- Alzheimer's disease, gut microbiota, dementia, fecal microbiota, microbial diversity, Firmicutes, Bacteroidetes, Bifidobacterium, cerebrospinal fluid biomarkers, amyloid deposition, gut-brain axis, therapeutic target
- MeSH terms
- Bacillota, Gastrointestinal Microbiome, Aged, Alzheimer Disease, Bifidobacterium, Feces, Female, Humans, Male, Biomarkers, Case-Control Studies, tau Proteins, Bacteroidetes
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