Role of gut microbiota and nutrients in amyloid formation and pathogenesis of Alzheimer disease

Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa

De Filippo, C., Cavalieri, D., Di Paola, M., Ramazzotti, M., Poullet, J. B., Massart, S., Collini, S., Pieraccini, G., & Lionetti, P. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005963107 · Cited by 5,579

Mind-altering microorganisms: the impact of the gut microbiota on brain and behaviour

Cryan, J. F., & Dinan, T. G. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3346 · Cited by 4,572

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease.

Strittmatter, W. J., Saunders, A. M., Schmechel, D., Pericak-Vance, M., Enghild, J., Salvesen, G. S., & Roses, A. D. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.5.1977 · Cited by 4,268

Gut microbiota composition correlates with diet and health in the elderly

Claesson, M. J., Jeffery, I. B., Conde, S., Power, S. E., O’Connor, E. M., Cusack, S., Harris, H. M. B., Coakley, M., Lakshminarayanan, B., O’Sullivan, O., et al. (2012) · Nature · doi:10.1038/nature11319 · Cited by 3,314

The gut-brain axis: interactions between enteric microbiota, central and enteric nervous systems.

(2015) · PubMed Central · Cited by 2,540

n−3 Polyunsaturated fatty acids, inflammation, and inflammatory diseases

Calder, P. C. (2006) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/83.6.1505s · Cited by 2,525

Changes in gut microbiota control inflammation in obese mice through a mechanism involving GLP-2-driven improvement of gut permeability

Cani, P. D., Possemiers, S., Van de Wiele, T., Guiot, Y., Everard, A., Rottier, O., Geurts, L., Naslain, D., Neyrinck, A., Lambert, D. M., et al. (2009) · Gut · doi:10.1136/gut.2008.165886 · Cited by 2,518

Short-chain fatty acids in control of body weight and insulin sensitivity

Canfora, E. E., Jocken, J. W., & Blaak, E. E. (2015) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2015.128 · Cited by 2,298

Artificial sweeteners induce glucose intolerance by altering the gut microbiota

Suez, J., Korem, T., Zeevi, D., Zilberman-Schapira, G., Thaiss, C. A., Maza, O., Israeli, D., Zmora, N., Gilad, S., Weinberger, A., et al. (2014) · Nature · doi:10.1038/nature13793 · Cited by 2,067

Diet Drives Convergence in Gut Microbiome Functions Across Mammalian Phylogeny and Within Humans

Muegge, B. D., Kuczynski, J., Knights, D., Clemente, J. C., González, A., Fontana, L., Henrissat, B., Knight, R., & Gordon, J. I. (2011) · Science · doi:10.1126/science.1198719 · Cited by 1,988

Deciphering the interdependent labyrinth between gut microbiota and the immune system

Saini, A., Dalal, P., & Sharma, D. (2022) · Letters in Applied Microbiology · doi:10.1111/lam.13775 · Cited by 18

Microbes in fructooligosaccharides production

Bhadra, S., Chettri, D., & Verma, A. K. (2022) · Bioresource Technology Reports · doi:10.1016/j.biteb.2022.101159 · Cited by 19

Simvastatin improves learning and memory impairment via gut-brain axis regulation in an ovariectomized/D-galactose Alzheimer's rat model

Zahedi, E., Sanaeierad, A., Nikbakhtzadeh, M., Roghani, M., & Zamani, E. (2023) · Behavioural Brain Research · doi:10.1016/j.bbr.2023.114611 · Cited by 16

Lactiplantibacillus plantarum X7022 Plays Roles on Aging Mice with Memory Impairment Induced by D-Galactose Through Restoring Neuronal Damage, Relieving Inflammation and Oxidative Stress

Yin, D., Zhao, L. X., Deng, S., Xie, Y., Ro, K.-S., Yang, Z., Du, L., Xie, J., & Wei, D. (2024) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-023-10208-w · Cited by 18

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

Regulation by Different Types of Chaperones of Amyloid Transformation of Proteins Involved in the Development of Neurodegenerative Diseases

Muronetz, V. I., Kudryavtseva, S. S., Leisi, E. V., Kurochkina, L. P., Barinova, K. V., & Schmalhausen, E. V. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052747 · Cited by 15

Mitochondria of intestinal epithelial cells in depression: Are they at a crossroads of gut-brain communication?

Wang, Y., Lai, H., Zhang, T., Wu, J., Tang, H., Liang, X., Ren, D., Huang, J., & Li, W. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105403 · Cited by 17

Alzheimer’s disease in elderly COVID-19 patients: potential mechanisms and preventive measures

Wang, H., Lü, J., Zhao, X., Qin, R., Song, K., Xu, Y. Q., Zhang, J., & Chen, Y. (2021) · Neurological Sciences · doi:10.1007/s10072-021-05616-1 · Cited by 15

Gut microbiome in neuropsychiatric disorders

Granados, D. M. M., Villasana‐Salazar, B., Coan, A. C., Rizzi, L., Balthazar, M. L. F., Godoi, A. B., do Canto, A. M., da Rosa, D. C., Silva, L. S., Tacla, R., et al. (2022) · Arquivos de Neuro-Psiquiatria · doi:10.1590/0004-282x-anp-2021-0052 · Cited by 17

Lactobacillales derived from traditional Xizang dairy products improve insomnia and restore neurotransmitter-metabolic profiles via gut microbiota in PCPA-induced mice

Li, P., Yang, L., Shao, X., Zou, Z., Shi, H., Sun, Y., Wu, X., Li, Z., Li, Y., & Li, Z. (2025) · Microbiological Research · doi:10.1016/j.micres.2025.128276 · Cited by 14

Exogenous Players in Mitochondria-Related CNS Disorders: Viral Pathogens and Unbalanced Microbiota in the Gut-Brain Axis

Righetto, I., Gasparotto, M., Casalino, L., Vacca, M., & Filippini, F. (2023) · Biomolecules · doi:10.3390/biom13010169 · Cited by 14

A Bioresponsive Genetically Encoded Antimicrobial Crystal for the Oral Treatment of Helicobacter Pylori Infection

Zhang, W., Yang, Z., Zheng, J., Fu, K., Wong, J. H., Ni, Y., Ng, T. B., Cho, C. H., Chan, M. K., & Lee, M. M. (2023) · Advanced Science · doi:10.1002/advs.202301724 · Cited by 15

Clostridium butyricum Alleviates DEHP Plasticizer-Induced Learning and Memory Impairment in Mice via Gut–Brain Axis

Wang, J., Qiu, F., Zhang, Z., Liu, Y., Zhou, Q., Dai, S., Xiang, S., & Wei, C. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c03533 · Cited by 15

Long Non-Coding RNAs and Alzheimer’s Disease: Towards Personalized Diagnosis

Mosquera-Heredia, M. I., Vidal, O. M., Morales, L. C., Silvera-Redondo, C. A., Barceló, E., Allegri, R., Arcos‐Burgos, M., Velez, J. I., & Garavito, P. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25147641 · Cited by 16

Gene-environment interactions determine risk for dementia: the influence of lifestyle on genetic risk for dementia

Patten, K. T., & Lein, P. J. (2019) · Annals of Translational Medicine · doi:10.21037/atm.2019.09.155 · Cited by 15

Characterization of Neoagarooligosaccharide Hydrolase BpGH117 from a Human Gut Bacterium Bacteroides plebeius

Jin, Y., Yu, S., Kim, D. H., Yun, E. J., & Kim, K. H. (2021) · Marine Drugs · doi:10.3390/md19050271 · Cited by 15

Synergistic alleviation effects of anchovy hydrolysates-catechin on scopolamine-induced mice memory deficits: the exploration of the potential relationship among gut-brain-axis

Zhao, T., Zhang, C., Zhong, S., Chen, Q., Liu, S., Jiao, W., Liu, W., Huang, L., Zhang, Y., & Zhang, Y. (2022) · Food & Function · doi:10.1039/d1fo02195h · Cited by 15

Bridging the Gap between Gut Microbiota and Alzheimer’s Disease: A Metaproteomic Approach for Biomarker Discovery in Transgenic Mice

Ayan, E. B., DeMirci, H., Serdar, M. A., Palermo, F., & Baykal, A. T. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612819 · Cited by 15

Inflammatory Mechanisms and Cascades Contributing to Neurocognitive Impairment in HIV/AIDS

Fernandes, N. C., & Pulliam, L. (2019) · Current topics in behavioral neurosciences · doi:10.1007/7854_2019_100 · Cited by 13

High intake of chicken and pork proteins aggravates high-fat-diet-induced inflammation and disorder of hippocampal glutamatergic system

Zhang, M., Song, S., Zhao, D., Shi, J., Xu, X., Zhou, G., & Li, C. (2020) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2020.108487 · Cited by 14

Double blind placebo-controlled trial for the prevention of ulcerative colitis relapses by β-fructan prebiotics: efficacy and metabolomic analysisPreprint

Valcheva, R. S., Armstrong, H., Kovic, O., Bording‐Jorgensen, M., Veniamin, S., Pérez-Muñoz, M. E., Haskey, N., Silva, M., Peerani, F., Wong, K., et al. (2022) · medRxiv · doi:10.1101/2022.01.16.22269376 · Cited by 16

Rheum tanguticum Alleviates Cognitive Impairment in APP/PS1 Mice by Regulating Drug-Responsive Bacteria and Their Corresponding Microbial Metabolites

Gao, D., Zhao, H., Yin, Z., Chen, H., Wang, Y., Luo, G., & Gao, X. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.766120 · Cited by 13

Oral Administration of Lactobacillus gasseri and Lacticaseibacillus rhamnosus Ameliorates Amyloid Beta (Aβ)-Induced Cognitive Impairment by Improving Synaptic Function Through Regulation of TLR4/Akt Pathway

Choi, H., Lee, H. L., Kim, I. Y., Ju, Y., Heo, Y. M., Na, H. R., Lee, J. Y., Choi, S., & Heo, H. J. (2025) · Antioxidants · doi:10.3390/antiox14020139 · Cited by 14

The Role of Probiotics in Modulating the Gut Microbiome in Alzheimer’s Disease: A Review

Dong, Y., Wu, X., Zhang, Y., Hu, A., Zhou, Q., Yue, X., Liu, Z., & Li, M. (2025) · Foods · doi:10.3390/foods14091531 · Cited by 15

Angiotensin (1–7) Expressing Probiotic as a Potential Treatment for Dementia

Hernandez, A. R., Banerjee, A., Carter, C. S., & Buford, T. W. (2021) · Frontiers in Aging · doi:10.3389/fragi.2021.629164 · Cited by 12

Therapeutic Potential of Microbiota Modulation in Alzheimer’s Disease: A Review of Preclinical Studies

Haziot, C. B., & Birak, K. S. (2023) · Journal of Alzheimer s Disease Reports · doi:10.3233/adr-220097 · Cited by 13

Salivary Aβ Secretion and Altered Oral Microbiome in Mouse Models of AD

Floden, A. M., Sohrabi, M., Nookala, S., Cao, J., & Combs, C. K. (2021) · Current Alzheimer Research · doi:10.2174/1567205018666210119151952 · Cited by 13

Exploration of acupuncture therapy in the treatment of mild cognitive impairment based on the brain-gut axis theory

Jin, Y., Hu, F., & Zhu, J. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.891411 · Cited by 12

Effects of common plastic products heat exposure on cognition: Mediated by gut microbiota

Hu, N., Pan, D., Yang, Y. H., Pu, L., He, X., Wang, H., Zhang, X., Du, Y., Yu, Z., He, S., et al. (2023) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2023.114758 · Cited by 12

Lactiplantibacillus plantarum-encapsulated microcapsules prepared from okra polysaccharides improved intestinal microbiota in Alzheimer’s disease mice

Hsiao, Y.-K., Lee, B., & Wu, S. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1305617 · Cited by 14

The influence of time-restricted eating/feeding on Alzheimer’s biomarkers and gut microbiota

Gasmi, M., Hardiany, N. S., van der Merwe, M., Martins, I. J., Sharma, A., & Williams‐Hooker, R. (2024) · Nutritional Neuroscience · doi:10.1080/1028415x.2024.2359868 · Cited by 14

Influence of Gut Microbiota on Behavior and Its Disturbances

Ignatova, V. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.85317 · Cited by 13

Research trend of microbiota-gut-brain axis in Alzheimer’s disease based on CiteSpace (2012–2021): A bibliometrics analysis of 608 articles

Li, Z., Ma, H., Wang, M., & Qian, Y. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1036120 · Cited by 11

Sweet, bloody consumption – what we eat and how it affects vascular ageing, the BBB and kidney health in CKD

Schwarz, A., Hernandez, L. N., Arefin, S., Sartirana, E., Witasp, A., Wernerson, A. M., Stenvinkel, P., & Kublickiene, K. R. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2341449 · Cited by 15

Microbiome Dysbiosis as a Driver of Neurodegeneration: Insights into Alzheimer’s and Parkinson’s Diseases

Jagodic, A., Kršek, A., Schleicher, L. M. S., & Batičić, L. (2025) · Gastrointestinal Disorders · doi:10.3390/gidisord7020028 · Cited by 11

Chronic administration of prebiotics and probiotics prevent pathophysiological hallmarks of Alzheimer’s disease in the cortex of APP/PS1 mice

Sarti, G., Traini, C., Magni, G., Attorre, S., Tognozzi, G., Calussi, E., Giovannini, M. G., Vannucchi, M. G., & Lana, D. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1596469 · Cited by 11

Endogenous Aβ and Exogenous Wheat Gluten Nanostructures: Understanding Peptide Self-Assembly in Disease

Herrera, M. G., Ciccone, L., Moleiro, L. H., Tonali, N., & Dodero, V. I. (2025) · ACS Nano · doi:10.1021/acsnano.5c01662 · Cited by 11

The gut microbiota-polyphenol interplay and its role in gut-organ axes: From mechanisms to functional outcomes

Tang, X., & Peng, X. (2025) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2025.105192 · Cited by 10

Relationship between Alzheimer’s Disease and the Human Microbiome

Fujii, Y., Khasnobish, A., & Morita, H. (2019) · Codon Publications eBooks · doi:10.15586/alzheimersdisease.2019.ch9 · Cited by 11

From-Toilet-to-Freezer: A Review on Requirements for an Automatic Protocol to Collect and Store Human Fecal Samples for Research Purposes

Widjaja, F., & Rietjens, I. M. C. M. (2023) · Biomedicines · doi:10.3390/biomedicines11102658 · Cited by 12

Extra-cranial factors in the development of Alzheimer’s disease

Eiser, A. R., & Fülöp, T. (2020) · Brain Research · doi:10.1016/j.brainres.2020.147076 · Cited by 10

Association of Dietary and Supplement Intake of Antioxidants with Risk of Dementia: A Meta-Analysis of Cohort Studies

Zhao, R., Han, X., Jiang, S., Zhao, W., Liu, J., Zhang, H., Mao, X., Zhang, M., Lei, L., & You, H. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-220909 · Cited by 11

ApoE Mimetic Peptides to Improve the Vicious Cycle of Malnutrition and Enteric Infections by Targeting the Intestinal and Blood-Brain Barriers

Oriá, R. B., Freitas, R. S., Roque, C. R., Nascimento, J. C. R., Silva, A. P., Malva, J. O., Guerrant, R. L., & Vitek, M. P. (2023) · Pharmaceutics · doi:10.3390/pharmaceutics15041086 · Cited by 11

Microbiota–Gut–Brain Axis: Mass-Spectrometry-Based Metabolomics in the Study of Microbiome Mediators—Stress Relationship

Interino, N., Vitagliano, R., D’Amico, F., Lodi, R., Porru, E., Turroni, S., & Fiori, J. (2025) · Biomolecules · doi:10.3390/biom15020243 · Cited by 10

Bridging traditional Chinese medicine and Alzheimer’s disease: the pivotal role of gut microbiota in multitarget therapeutic mechanisms

Wu, W., Meng, T., Han, L., Jin, F., Han, P., & Zhou, Y. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1630205 · Cited by 9

Unravelling the Alzheimer's pathogenesis: Molecular and cellular pathways to neurodegeneration and therapeutic targets

Chauhan, P., Wadhwa, K., & Singh, G. (2025) · Pathology - Research and Practice · doi:10.1016/j.prp.2025.156109 · Cited by 12

Intestinal inflammation induces glymphatic remodeling, priming early neurodegenerative signals in male mice

Ciampi, C., Fagiani, F., Murtaj, V., Comella, F., Torre, V., Filibian, M., Andolfo, A., Braccia, C., Opallo, N., Bottone, M. G., et al. (2025) · Alzheimer s & Dementia · doi:10.1002/alz.70640 · Cited by 10

Integrating the Gut Microbiome and Stress-Diathesis to Explore Post-Trauma Recovery: An Updated Model

Mittinty, M. M., Lee, J., Walton, D. M., El-Omar, E. M., & Elliott, J. M. (2022) · Pathogens · doi:10.3390/pathogens11070716 · Cited by 9

The potential role of the brain–gut axis in the development and progression of Alzheimer's disease

Zhou, G., Yin, Y., Huan, X.-Y., Zhuang, Y., Xu, S., Liu, J., Liu, S., & Duan, J. (2022) · Journal of Translational Internal Medicine · doi:10.2478/jtim-2022-0016 · Cited by 11

The effects of esketamine on the intestinal microenvironment and intestinal microbiota in mice

Zhang, Y., Ma, W., Lin, H., Gu, X., & Xie, H. (2023) · Human & Experimental Toxicology · doi:10.1177/09603271231211894 · Cited by 9

Perinatal Exposure to Phenols and Poly- and Perfluoroalkyl Substances and Gut Microbiota in One-Year-Old Children

Davias, A., Lyon-Caen, S., Rolland, M., Iszatt, N., Thomsen, C., Haug, L. S., Sakhi, A. K., Monot, C., Rayah, Y., Ilhan, Z. E., et al. (2024) · Environmental Science & Technology · doi:10.1021/acs.est.3c09927 · Cited by 11

Nutrients in Alzheimer’s Disease: The Interaction of Diet, Drugs and Disease

Liyanage, S. I., Vilekar, P., & Weaver, D. F. (2019) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/cjn.2018.353 · Cited by 11

Oligosaccharides from Morinda officinalis Slow the Progress of Aging Mice by Regulating the Key Microbiota-Metabolite Pairs

Yang, X., Chen, D., Chen, T., Zhao, J., Xiaocui, T., Guo, Y., Shuai, O., Deng, T., & Guoyan, H. (2019) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2019/9306834 · Cited by 10

Altered Gut Microbial Load and Immune Activation in a Drosophila Model of Human Tauopathy

Rydbom, J., Kohl, H., Hyde, V. R., & Lohr, K. M. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.731602 · Cited by 9

The gut microbiota in neurodegenerative diseases: revisiting possible therapeutic targets for cannabidiol

de Oliveira, B. S. A., Milanezi, D. S., Gonzaga, P. D. V., Detoni, F. R., & Soriano, R. N. (2022) · Heliyon · doi:10.1016/j.heliyon.2022.e12172 · Cited by 10

Sourdough bread as nutritional intervention tool for improvement of cognitive dysfunction in diabetic rats

Mohamed, D. A., Fouda, K. A., Mabrok, H. B., El-Shamarka, M. E.-S., & Hamed, I. M. (2024) · BMC Nutrition · doi:10.1186/s40795-024-00861-x · Cited by 8

Microbiota and Alzheimer’s disease: mechanistic insights from a multi-organ perspective

Liao, J., Mou, H., Luo, S., Shen, L., & Jiao, B. (2026) · Translational Neurodegeneration · doi:10.1186/s40035-026-00541-9 · Cited by 11

Amelioration of Serum Aβ Levels and Cognitive Impairment in APPPS1 Transgenic Mice Following Symbiotic Administration

Traini, C., Bulli, I., Sarti, G., Morecchiato, F., Coppi, M., Rossolini, G. M., Pilato, V. D., & Vannucchi, M. G. (2024) · Nutrients · doi:10.3390/nu16152381 · Cited by 10

A Neuroscience Primer for Integrating Geroscience With the Neurobiology of Aging

Hernandez, C. M., Hernandez, A. R., Hoffman, J. M., King, P. H., McMahon, L. L., Buford, T. W., Carter, C. S., Bizon, J. L., & Burke, S. N. (2021) · The Journals of Gerontology Series A · doi:10.1093/gerona/glab301 · Cited by 10

Medicinal Plant-based Functional Foods for the Management of Neurological HealthPreprint

Ahmed, M. N. (2020) · Preprints.org · doi:10.20944/preprints202006.0311.v1 · Cited by 8

The brain-gut axis: communication mechanisms and the role of the microbiome as a neuroprotective factor in the development of neurodegenerative diseases: A literature overview

Białoń, N., Górka, D. H. N. O. Z. D., & Górka, M. (2024) · AIMS neuroscience · doi:10.3934/neuroscience.2024019 · Cited by 8

Microbiota-Immune System Interactions in Human Neurological Disorders

Huang, Q., Fang, Y., Liao, D., & Xia, J. (2020) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527319666200726222138 · Cited by 7

Neuroprotection of macamide in a mouse model of Alzheimer’s disease involves Nrf2 signaling pathway and gut microbiota

Xia, N., Xu, L., Huang, M., Xu, D., Li, Y., Wu, H., Mei, Z., & Yu, Z. (2024) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2024.176638 · Cited by 7

The role of gut-derived short-chain fatty acids in Parkinson's disease

Saadh, M. J., Mustafa, A. N., Mustafa, M. A., Renuka Jyothi, S., Dabis, H. K., Prasad, G. V. S., Mohammad, I. J., Adnan, A., & Idan, A. H. (2024) · Neurogenetics · doi:10.1007/s10048-024-00779-3 · Cited by 9

Ginger Extract Improves Cognitive Dysfunction via Modulation of Gut Microbiota-Derived Short-Chain Fatty Acids in D-Galactose/Ovariectomy-Induced Alzheimer-Like Disease

Zahedi, E., Naseri, F. M., Zamani, E., Nikbakhtzadeh, M., Rastegar, T., Sanaeirad, A., & Sadr, S. S. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04583-w · Cited by 9

Plants as Biofactories for Phenolic Compounds

Avilés‐Gaxiola, S., Vázquez-Olivo, G., Cabanillas-Bojórquez, L. Á., Gutiérrez‐Grijalva, E. P., & Heredia, J. B. (2020) · Springer eBooks · doi:10.1007/978-981-15-4890-1_20 · Cited by 7

Intestinal microbiota and nutrients as determinants of nervous system function. Part I. Gastrointestinal microbiota

Skonieczna‐Żydecka, K., Łoniewski, I., Maciejewska, D., & Marlicz, W. M. (2017) · Aktualności Neurologiczne · doi:10.15557/an.2017.0020 · Cited by 7

Polysaccharides from Basella alba Protect Post-Mitotic Neurons against Cell Cycle Re-Entry and Apoptosis Induced by the Amyloid-Beta Peptide by Blocking Sonic Hedgehog Expression

Hou, B.-Y., Wu, M.-H., Hsu, H.-Y., Lin, Y., & Yang, D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25137316 · Cited by 6

Alterations and mechanistic insights of gut microbiota and its metabolites in type 2 diabetes mellitus and Alzheimer's disease

Xu, G., An, Y., Du, Y., Cao, Z., Zheng, J., Wang, J., Li, T., Lei, X. G., & Lu, Y. (2025) · iMetaOmics. · doi:10.1002/imo2.70020 · Cited by 7

The effects of probiotic supplementation on cerebral cognitive function: a systematic review

Widyadharma, I. P. E., Hendellyn, A., de Liyis, B. G., Putri, N. L. P. S. W., Indrayani, A. W., Darwinata, A. E., & Sujaya, I. N. (2024) · The Egyptian Journal of Neurology Psychiatry and Neurosurgery · doi:10.1186/s41983-024-00840-w · Cited by 6

The role of gut microbiota in the pathogenesis of neuropsychiatric and neurodegenerative diseases

Szewczyk, A., Witecka, A., & Kiersztan, A. (2019) · Postępy Higieny i Medycyny Doświadczalnej · doi:10.5604/01.3001.0013.7326 · Cited by 6

Interrelationship between the 5-lipoxygenase pathway and microbial dysbiosis in the progression of Alzheimer's disease

Mathis, S., Bodduluri, S. R., & Haribabu, B. (2021) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2021.158982 · Cited by 6

Nutrition Module design in Maintain Your Brain: an internet-based randomised controlled trial to prevent cognitive decline and dementia

Rangel, C. A., Noble, Y., Radd‐Vagenas, S., Mavros, Y., Flood, V. M., O’Leary, F., Brodaty, H., Sachdev, P. S., Heffernan, M., Valenzuela, M., et al. (2021) · British Journal Of Nutrition · doi:10.1017/s0007114521001859 · Cited by 7

Associations between pre- and post-natal exposure to phthalate and DINCH metabolites and gut microbiota in one-year old children

Davias, A., Lyon-Caen, S., Rolland, M., Iszatt, N., Thomsen, C., Sabaredzovic, A., Sakhi, A. K., Monot, C., Rayah, Y., Ilhan, Z. E., et al. (2024) · Environmental Pollution · doi:10.1016/j.envpol.2024.125204 · Cited by 5

Stool-derived extracellular vesicles increase inflammasome signaling and regulate the gut-brain axis after stroke in Alzheimer's disease transgenic mice

Kerr, N. A., Bramlett, H. M., Sanchez‐Molano, J., Higueras, A. F., Walters, W. M., Vaccari, J. P. D. R., Keane, R. W., & Dietrich, W. D. (2025) · Experimental Neurology · doi:10.1016/j.expneurol.2025.115269 · Cited by 5

Novel Nutraceutical Milk Compound in Alzheimer’s Prevention

Forsan, H. F., & Hasan, R. S. (2023) · Springer eBooks · doi:10.1007/978-981-19-3949-5_45-1 · Cited by 5

Gut microbiome signature of Viliuisk encephalomyelitis in Yakuts includes an increase in microbes linked to lean body mass and eating behaviour

Kuznetsova, V., Tyakht, A., Akhmadishina, L. V., Odintsova, V. Y., Klimenko, N. S., Kostryukova, E., Vakhitova, M. T., Grigoryeva, T. V., Malanin, S., Vladimirtsev, V. A., et al. (2020) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-020-01612-4 · Cited by 5

Advances in the study of the relationship between Alzheimer's disease and the gastrointestinal microbiome

Li, X., Qin, H., & Li, T. (2022) · Ibrain · doi:10.1002/ibra.12065 · Cited by 4

Exploration of acupuncture therapy in the treatment of MCI patients with the ApoE ε4 gene based on the brain-gut axis theory

Jin, Y., Chen, J., Chai, Q., Zhu, J., & Jin, X. (2023) · BMC Complementary Medicine and Therapies · doi:10.1186/s12906-023-04060-2 · Cited by 6

Microbiota-Gut-Brain Axis

Szablewski, L. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819265-8.00065-6 · Cited by 5

Dietary modulation of the gut microbiome as a supportive strategy in the treatment of amyotrophic lateral sclerosis – a narrative review

Kiecka, A., & Szczepanik, M. (2025) · Pharmacological Reports · doi:10.1007/s43440-025-00800-y · Cited by 5

A novel gentiopicroside derivative clears phosphorylation tau to improve memory of AD mice by targeting AMPK and increase of gut neuroprotective metabolites

Wang, Y., Cheng, C., Li, L., Chen, D., Wang, G., Ohno, H., Xiang, L., & Qi, J. (2026) · Phytomedicine · doi:10.1016/j.phymed.2026.157781 · Cited by 4

Gut microbiota and central nervous system's direct bidirectional regulation: The mechanisms of the gut–brain axis in irritable bowel syndrome

Zhai, J., Li, Y., Liu, J., & Dai, C. (2026) · Clinical and Translational Discovery · doi:10.1002/ctd2.70117 · Cited by 4

An Overview of Neurodegenerative Disorders

Mittal, P., & Agrawal, N. (2024) · Springer eBooks · doi:10.1007/978-981-97-4288-2_1 · Cited by 4

Resilience and charge-dependent fibrillation of functional amyloid: Interactions of Pseudomonas biofilm-associated FapB and FapC amyloids

Golan, N., Parizat, A., Tabachnikov, O., Barnea, E., Olsen, W. P., Otzen, D. E., & Landau, M. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.108096 · Cited by 4

Mind over Microbes: Investigating the Interplay between Lifestyle Factors, Gut Microbiota, and Brain Health

Bali, P., Lal, P., Sivapuram, M. S., Kutikuppala, L. V. S., Avti, P., Chanana, A., Kumar, S., & Anand, A. (2024) · Neuroepidemiology · doi:10.1159/000538416 · Cited by 4

Navigating the Role and Approach of Gut Microbiota in Addressing Alzheimer's Disease Pathogenesis

Jazuli, I., Jazeel, A., Selvaratnam, L., Alex, D., & Kumari, Y. (2024) · Progress In Microbes & Molecular Biology · doi:10.36877/pmmb.a0000454 · Cited by 5

A Review of the Relationship Between Gut Microbiota and Memory

Benmelouka, A. Y., Sherif, A., & Ebada, M. A. (2019) · Springer eBooks · doi:10.1007/978-981-13-9636-6_8 · Cited by 4

The Role of the human microbiome in neurodegenerative diseases: A Perspective

Mukherjea, N., Khandelwal, A., Saluja, R., & Kalra, N. (2025) · Current Genetics · doi:10.1007/s00294-025-01319-8 · Cited by 3

The Brain-Gut-Microbiome Axis Across the Life Continuum and the Role of Microbes in Maintaining the Balance of Health

Halverson, T., & Alagiakrishnan, K. (2025) · Journal of Integrative Neuroscience · doi:10.31083/jin36616 · Cited by 4

Neuroinflammation in Alzheimer’s Disease: The Role of Obesity, Gut Microbiota, and Therapeutic Potential of Omega-3 Fatty Acids and Neural Stem Cells

Morovati, A., Moussa, Y., Kalupahana, N. S., Zu, Y., Jun, H., Fokar, M., & Moustaïd‐Moussa, N. (2026) · Journal of Nutrition · doi:10.1016/j.tjnut.2026.101407 · Cited by 3

Treadmill exercise attenuates neuroinflammation in APP/PS1 mice via gut microbiota remodeling: Evidence from fecal microbiota transplantation

Yuan, S., Lin, L., Liu, J., Lin, Q., Wang, S., Wu, J., Xu, D., Liu, Y., Lee, J. Y., & Qiu, L. (2026) · Life Sciences · doi:10.1016/j.lfs.2026.124500 · Cited by 3

The complex of gut microbial metabolites and sex hormones in Alzheimer’s disease

Bahar, A., Khazaei, M., & Tahmasebi, H. (2026) · Seminars in Immunopathology · doi:10.1007/s00281-026-01076-x · Cited by 5

Lifestyles and Cognition

Agarwal, S. K. (2021) · Integrative Journal of Medical Sciences · doi:10.15342/ijms.2021.399 · Cited by 4

Metformin, Microbiota and Health

Paz, G. S., & Fernandes, J. (2022) · Journal of Exploratory Research in Pharmacology · doi:10.14218/jerp.2022.00032 · Cited by 3

Mendelian randomization and transcriptomic analysis reveal a positive cause-and-effect relationship between Alzheimer's disease and colorectal cancer

Du, W., Xia, X., Gou, Q., & Qiu, Y. (2024) · Translational Oncology · doi:10.1016/j.tranon.2024.102169 · Cited by 3

Behavioral Abnormalities of Gut Microbiota and Progression of Dementia

Zubair, M., Fatima, F., & Husain, F. M. (2022) · Springer eBooks · doi:10.1007/978-981-16-7606-2_11 · Cited by 3

Structural Insights into Curli CsgA Cross-β Fibril Architecture Inspired Repurposing of Anti-amyloid Compounds as Anti-biofilm AgentsPreprint

Perov, S., Lidor, O., Salinas, N., Golan, N., Tayeb-Fligelman, E., Deshmukh, M. G., Willbold, D., & Landau, M. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/493668 · Cited by 2

Decoding the Gut-Brain Axis in Alzheimer’s Disease: Emerging Perspectives

Singh, V., Yadav, A., Taj, T., Islam, A., Mantry, S., Debnath, B., Kumar, B., & Ashique, S. (2025) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/0118715273390442250805174841 · Cited by 2

Growing Tibetan Pigs Adapt to High-Fiber Diets by Enhancing Fiber Degradation Capacity

Lamu, Z., Hao, S., Li, B., Yang, S., Shang, Z., Shang, P., Liu, S., Lin, Y., & Tan, Z. (2025) · Veterinary Sciences · doi:10.3390/vetsci12101010 · Cited by 3

The Gut Microbiome and Alzheimer’s Disease: A Growing Relationship

Zerdan, M. B., Hebbo, E., Hijazi, A., Gemayel, M. E., Nasr, J., Nasr, D., Yaghi, M., Bouferraa, Y., & Nagarajan, A. (2022) · Current Alzheimer Research · doi:10.2174/1567205020666221227090125 · Cited by 22

Brain-Gut-Microbiota Axis in Alzheimer’s Disease

Kowalski, K., & Mulak, A. (2019) · Journal of Neurogastroenterology and Motility · doi:10.5056/jnm18087 · Cited by 826

Nutrition, gut microbiota, and alzheimer’s disease

Romanenko, M., Kholin, V., Koliada, A., & Vaiserman, A. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.712673 · Cited by 56

Exploring the effect of gut microbiome on Alzheimer's disease

Pourahmad, R., Saleki, K., Zare, M., Aram, C., Farsani, A. S., Banazadeh, M., & Tafakhori, A. (2024) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2024.101776 · Cited by 20

The Gut Microbiota and Alzheimer’s Disease

Jiang, C., Li, G., Huang, P., Liu, Z., & Zhao, B. (2017) · Journal of Alzheimer's Disease · doi:10.3233/jad-161141 · Cited by 852