The gut-bone axis: how bacterial metabolites bridge the distance

From Dietary Fiber to Host Physiology: Short-Chain Fatty Acids as Key Bacterial Metabolites

Koh, A., De Vadder, F., Kovatcheva-Datchary, P., & Bäckhed, F. (2016) · Cell · doi:10.1016/j.cell.2016.05.041 · Cited by 7,070

Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells

Furusawa, Y., Obata, Y., Fukuda, S., Endo, T. A., Nakato, G., Takahashi, D., Nakanishi, Y., Uetake, C., Kato, K., Kato, T., et al. (2013) · Nature · doi:10.1038/nature12721 · Cited by 5,549

Regulatory T Cells and Immune Tolerance

Sakaguchi, S., Yamaguchi, T., Nomura, T., & Ono, M. (2008) · Cell · doi:10.1016/j.cell.2008.05.009 · Cited by 5,475

The Microbial Metabolites, Short-Chain Fatty Acids, Regulate Colonic T reg Cell Homeostasis

Smith, P. M., Howitt, M. R., Panikov, N., Michaud, M., Gallini, C. A., Bohlooly-Y, M., Glickman, J. N., & Garrett, W. S. (2013) · Science · doi:10.1126/science.1241165 · Cited by 5,413

Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation

Arpaia, N., Campbell, C., Fan, X., Dikiy, S., van der Veeken, J., deRoos, P., Liu, H., Cross, J. R., Pfeffer, K., Coffer, P. J., et al. (2013) · Nature · doi:10.1038/nature12726 · Cited by 4,838

Formation of short chain fatty acids by the gut microbiota and their impact on human metabolism

Morrison, D. J., & Preston, T. (2016) · Gut Microbes · doi:10.1080/19490976.2015.1134082 · Cited by 3,781

Induction of Colonic Regulatory T Cells by Indigenous Clostridium Species

Atarashi, K., Tanoue, T., Shima, T., Imaoka, A., Kuwahara, T., Momose, Y., Cheng, G., Yamasaki, S., Saito, T., Ohba, Y., et al. (2011) · Science · doi:10.1126/science.1198469 · Cited by 3,752

The impact of the gut microbiota on human health: an integrative view

Clemente, J. C., Ursell, L. K., Parfrey, L. W., & Knight, R. (2012) · Cell · doi:10.1016/j.cell.2012.01.035 · Cited by 3,710

Microbiota Modulate Behavioral and Physiological Abnormalities Associated with Neurodevelopmental Disorders

Hsiao, E. Y., McBride, S. W., Hsien, S., Sharon, G., Hyde, E. R., McCue, T., Codelli, J. A., Chow, J., Reisman, S. E., Petrosino, J. F., et al. (2013) · Cell · doi:10.1016/j.cell.2013.11.024 · Cited by 3,283

Short chain fatty acids in human large intestine, portal, hepatic and venous blood

Cummings, J. H., Pomare, E. W., Branch, W. J., Naylor, C. P., & Macfarlane, G. T. (1987) · Gut · doi:10.1136/gut.28.10.1221 · Cited by 3,119

The relationship between osteopenia and vascular tone disorders in mature and elderly women

Bazhenova, D. A., Голованова, Е. Д., & Lyamets, L. L. (2025) · Vrach · doi:10.29296/25877305-2025-06-12 · Cited by 1

Mikrobiom, Ernährung und Rheuma

Heidt, C., & Kriegel, M. A. (2025) · rheuma plus · doi:10.1007/s12688-025-00861-0 · Cited by 1

Bifidobacterium treatment for chronic low back pain in patients with Modic changes: study protocol for a multicenter, randomized, placebo-controlled trial

Nian, S., Li, C., Li, N., Chen, F., Zhao, C., Zhang, G., Lu, S., & Chen, J. (2025) · Trials · doi:10.1186/s13063-025-09084-2 · Cited by 1

Benefits that Death Does Not Part: the Promise of Postbiotics for Bone Health

Ribeiro, J. L., Santos, T. A., & Anbinder, A. L. (2025) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-025-10768-z · Cited by 2

Exploring the alteration of gut microbiota in the rats with steroid-induce osteonecrosis of the femoral head

Huang, C., Zhao, Y., Qing, L., Tang, J., Min, C., & Wu, P. (2025) · BMC Microbiology · doi:10.1186/s12866-025-03897-6 · Cited by 2

Effects of flammulina velutipes stipe wastes on egg performance, cecum microbiota, intestinal barrier and serum immune response of laying hens

Wei, J., Jing, B., Diao, Z., Tsopmejio, I. S. N., Li, Z., Jin, Z., & Song, H. (2025) · BMC Veterinary Research · doi:10.1186/s12917-025-05198-6 · Cited by 1

Metabolic Optimization Before Orthobiologic Therapies (MOBOT): A Narrative Review

Fernandes, G. C. D. A. M., & Rodeo, S. A. (2026) · Sports Health A Multidisciplinary Approach · doi:10.1177/19417381251409133 · Cited by 1

Effect of a Synbiotic Combination of 2′-Fucosyllactose and Lactiplantibacillus plantarum Hi188 on Skeletal Growth and Gut Microbial Metabolism in Growing Mice

Kuang, J., Li, Y., Wu, L., Bian, X., Li, J., Shi, F., Li, X., Wang, X., Pang, J., & Li, J. (2026) · Nutrients · doi:10.3390/nu18071123 · Cited by 1

Microbiota-specific serum IgG links gut and joints through immune–endothelial crosstalk in arthritis

Schmid, E., Otterbein, N., Ariyeloye, S., Danzer, H., Frech, M., Naschberger, E., Muñoz‐Becerra, M., Sarter, K., Schett, G. A., Kastbom, A., et al. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1821367 · Cited by 1

The role of gut microbiota in osteoporosis: underlying mechanisms, clinical associations, and emerging biomaterials

Ha, P., Wang, Z., Huo, G., Sun, X., & Yu, K. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1828297 · Cited by 2

Gut–bone axis in rheumatoid arthritis: microbiota-driven barrier dysfunction, immune crosstalk, and therapeutic strategies

Hu, Z., Yan, J., Wang, X., & Liu, Z. (2026) · Antonie van Leeuwenhoek · doi:10.1007/s10482-026-02353-3 · Cited by 1

Paradigm Shift of Microbiota-gut-brain Axis During Aging: Potential Role of Probiotics to Improve Cognitive Decline

Dutta, S., Dutta, T. K., Nanda, P. K., Dhar, P., Das, A. K., & Bhunia, A. K. (2026) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-026-11136-1 · Cited by 2

Links between bone fractures and the gut microbiota

Ohlsson, C., Lawenius, L., Grahnemo, L., & Sjögren, K. (2026) · Nature Reviews Endocrinology · doi:10.1038/s41574-026-01286-1 · Cited by 2

Signaling Metabolites in the Gut Microbiota–Organ Axes

Beyoğlu, D., & Idle, J. R. (2026) · Cells · doi:10.3390/cells15171558 · Cited by 1

Unequivocal Dyad of Gut Microbiome and Osteo Integrity- Dynamic Cross-Talk and Implications in Osteoporosis Management

Soumyakrishnan, S., & SREEPRIYA, M. (2022) · International Journal of Life Science and Pharma Research · doi:10.22376/ijpbs/lpr.2022.12.4.p61-74 · Cited by 1

Understanding the Relationship between Bone-Remodeling T Cells and Microbiota in Breast Cancer Bone Metastases

Masset, M. E. G., Canto, F. B., & Monteiro, A. C. (2025) · IntechOpen eBooks · doi:10.5772/intechopen.1010215 · Cited by 1

Case Reports: Beneficial Roles of Aloe vera Juice-successive Ingestion to Children with Steroid-Sensitive Nephrotic Syndrome

Koizumi, K., Hasegawa, M., Mukaitani, A., & Yagi, A. (2020) · Journal of Gastroenterology and Hepatology Research · doi:10.17554/j.issn.2224-3992.2020.09.893 · Cited by 1

The Gut-Bone Axis: Role of Gut Microbiota in Osteoporosis

Ilesanmi-Oyelere, B. L. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819265-8.00071-1 · Cited by 2

Polímeros de frutose: importância para a nutrição e saúde humana

Figueiredo-Ribeiro, R. D. C. L., Pessoni, R. A. B., Itaya, N. M., & Fialho, M. B. (2022) · Evidência · doi:10.18593/eba.27168 · Cited by 1

Upaya Pencegahan dan Penanganan Low Back Pain Akibat Work From Home pada Pekerja di Surabaya

Rahmah, A. M., Ghaisani, A., Kusuma, A. F. F. D., Nareswari, A. B., Azizah, A. N., Mufidah, A. D., Rafif, F. A., Prawadi, J. F., Natsier, N. A., Santi, R. A., et al. (2023) · Jurnal Farmasi Komunitas · doi:10.20473/jfk.v10i1.32919 · Cited by 1

Bone and the microbiome

Pacifici, R., Lawenius, L., Sjögren, K., & Ohlsson, C. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-813073-5.00039-3

Altered Intestinal Microbiomes and Lipid Metabolism in Patients With Chronic Disorders of ConsciousnessPreprint

Luo, B., Yu, J., Cheng, Q., He, F., Meng, F., Yu, Y., Xu, C., Wen, X., Hong, L., Gao, J., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-824411/v1

THE EFFECTS OF AUTOMOBILE MOTOR WORKSHOP WASTE WATER ON SEEDLING GROWTH OF KIDNEY BEAN AND MUNG BEAN CROPS UNDER ABIOTIC STRESS

Yusra, Z. I. A., IQBAL, M. Z., & SHAFIQ, M. (2022) · Journal of Plant Development · doi:10.47743/jpd.2022.29.1.881

Microbiota and its relationship with Inflammatory Bowel Diseases: An overview

Al-Judaibi, A. A., Al-Hebshi, B. M., & Al-Judaibi, E. A. (2023) · Microbial Biosystems · doi:10.21608/mb.2023.211583.1072 · Cited by 1

BMI mediates the effects of gut microbes on bone mineral density in the "intestinal bone axis": an observational study versus a mediation Mendelian randomization studyPreprint

Xu, W., Zhang, F., Xu, Z., Li, X., Li, H., Zhang, W., Yu, G., & Shi, B. (2023) · Research Square · doi:10.21203/rs.3.rs-3143056/v1

Study on the trend of changes in the gut microbiota of rats with ovariectomy-induced postmenopausal osteoporosis and the effect of estrogen interventionPreprint

Lei, X.-D., Cheng, T., Xia, J.-Y., Dong, H., Hong, Y., Cheng, G., Wang, Y., & Chen, T. (2023) · Research Square · doi:10.21203/rs.3.rs-3291416/v1

Gut microbiota and spinal stenosis: a two-sample Mendelian randomization studyPreprint

Chen, D., Xu, W., Xiao, K.-Y., Que, Z.-Q., Feng, J., Sun, N.-K., Cai, D.-X., & Rui, G. (2023) · Research Square · doi:10.21203/rs.3.rs-3310641/v1

Association between gut microbiota and osteoporosis from 2012 to 2023: Bibliometric analysis and global trendsPreprint

Hou, W., Xiao, F., Tian, J., He, X., lu, S., Lin, K., Wei, T., He, M., & Wei, Q. (2023) · Research Square · doi:10.21203/rs.3.rs-3469687/v1

Gut microbiota and radiculopathy: a bidirectional two-sample Mendelian randomization studyPreprint

Wang, J., Chen, Y., Han, L., Lu, Y., Sun, J., Shi, J., & Sun, K. (2024) · Research Square · doi:10.21203/rs.3.rs-3863003/v1

Associations between gut microbiota and osteoporosis or osteopenia in Chinese Han youthPreprint

Lai, J., Gong, L., Liu, Y., Zhang, X., Liu, W., Han, M., Zhou, D., & Shi, S. (2024) · Research Square · doi:10.21203/rs.3.rs-4163732/v1

Bone equilibria and disruptions

van Bosse, H. J. P. (2024) · Journal of the Pediatric Orthopaedic Society of North America · doi:10.1016/j.jposna.2024.100059

Additional file 1 of Gut microbiota and intervertebral disc degeneration: a bidirectional two-sample Mendelian randomization study

Geng, Z., Wang, J., Chen, G., Liu, J., Lan, J., Zhang, Z., & Miao, J. (2023) · Figshare · doi:10.6084/m9.figshare.23949810

Morphological predictors of water-electrolyte disorders in patients with preventive ileostomy after rectal resection for cancer

Maksimkin, A. I., Bagatelia, Z. A., Kulushеv, V. M., Гордиенко, Е. Н., Lebedko, M. S., Anikina, S. S., & Shin, E.-K. (2024) · Pirogov Russian Journal of Surgery · doi:10.17116/hirurgia202404116

Oral-Gut Microbiome and Bone Health: Exploring Interplay

Ferrante, L. (2024) · Current Trends in Biomedical Engineering & Biosciences · doi:10.19080/ctbeb.2024.22.556088

Probiotic Therapies for Skeleton and Bone Health

Singh, B., Mal, G., Kalra, R. S., & Marotta, F. (2024) · Springer eBooks · doi:10.1007/978-3-031-65459-6_9

Gut Microbiota Mechanism of Fetal-Originated Disease

Wang, H., Lu, X., & Ma, C. (2024) · Springer eBooks · doi:10.1007/978-981-97-5730-5_6

Associations between adherence to plant-based diets and osteoporosis and visceral fat area in middle-aged adults: evidence of a large population-based study

Soleimani, D., Azizi, A., Darbandi, M., Sharifi, M., Najafi, F., Anvari, B., Pasdar, Y., & Miryan, M. (2025) · Journal of Diabetes & Metabolic Disorders · doi:10.1007/s40200-025-01601-z

Research Progress of Probiotics on Postoperative Recovery of Spinal and Paravertebral Muscles

柏, 徐. (2025) · Advances in Clinical Medicine · doi:10.12677/acm.2025.153892

Evaluation of causal links of gut microbiota and inflammatory cytokines with 10 fracture locations: A Mendelian randomization study

Ding, H., Zhao, X., Liu, G., & Wen, H. (2025) · Medicine · doi:10.1097/md.0000000000042353

Microbial Production of Dietary Short‐Chain Fatty Acids

Wallimann, A. (2025) · doi:10.1002/9781394241538.ch3

Intermittent fasting alleviates obesity-associated impairments in bone fracture healing: Exploring the role of gut microbiome

Hendesi, H., Godfrey, D. A., Ruble, A. F., Tran, A. M., Villani, D. A., Landgrave, S. H., Hasan, N. A., Adams, D. J., & Zuscik, M. J. (2025) · Bone Reports · doi:10.1016/j.bonr.2025.101876 · Cited by 1

Lack of genetic correlation and causal association between specific gut microbiota and osteoporosis

Chen, D., Zhu, T., Liu, C., Zhang, Y., Wu, Y., Xiong, Z., Sun, J., & Zhang, W. (2025) · Medicine · doi:10.1097/md.0000000000045031

Du besoin de revisiter l’ostéosarcopénie par l’apport du microbiote intestinal

Cailleaux, P. (2025) · Revue du Rhumatisme · doi:10.1016/j.rhum.2025.11.004

Additional file 1 of Melatonin alleviates titanium nanoparticles induced osteolysis via activation of butyrate/GPR109A signaling pathway

Wu, Y., He, F., Zhang, C., Zhang, Q., Xinlin, S., Zhu, X., Liu, A., Shi, W., Lin, W., Jin, Z., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14741113

Additional file 1 of 25-hydroxycholecalciferol reverses heat induced alterations in bone quality in finisher broilers associated with effects on intestinal integrity and inflammation

Zhang, H., Majdeddin, M., Gaublomme, D., Taminiau, B., Boone, M., Elewaut, D., Daube, G., Josipovic, I., Zhang, K., & Michiels, J. (2021) · Figshare · doi:10.6084/m9.figshare.16767679

Additional file 2 of Gut microbiota and intervertebral disc degeneration: a bidirectional two-sample Mendelian randomization study

Geng, Z., Wang, J., Chen, G., Liu, J., Lan, J., Zhang, Z., & Miao, J. (2023) · Figshare · doi:10.6084/m9.figshare.23949813

The gut musculoskeletal axis

Narulla, R. S., Diwan, A. D., & Smith, G. C. S. (2025) · Journal of Orthopaedic Reports · doi:10.1016/j.jorep.2025.100847

Perennial ryegrass improves bone quality in geese: insights from the gut-bone axis

Zulfiqar, Z., Asif, M. A., Zhaoyang, L., Sun, J., Zhu, X., Wang, Z., Sun, H., Cui, Y., Liu, B., & Shi, Y. (2025) · AMB Express · doi:10.1186/s13568-025-01996-1

Mikrobiom, Ernährung und Rheuma

Heidt, C., & Kriegel, M. A. (2026) · Rheuma Plus / Schweiz · doi:10.1007/s44332-026-00108-w

Eje intestino–sistema osteomioarticular: mecanismos fisiopatológicos y aplicaciones clínicas.

Cardenas, V. M., & Miranda, V. R. M. (2026) · Nutrición clínica y dietética hospitalaria/Nutrición clínica, dietética hospitalaria · doi:10.12873/454vmmartinez

Combined metabolomics and microbiota analysis reveals the therapeutic effect of indole-3-propionic acid on ovariectomy-induced osteoporosis

Liang, A., Gong, N., Li, S., Lv, W., & Ji, Y. (2026) · Scientific Reports · doi:10.1038/s41598-026-61654-9

Network pharmacology, molecular docking, and in vivo experiments reveal the effects of Polygonati Rhizoma on periodontitis

Ren, Q., Xiaolan, L., Wang, J., Qian, W., Fangzhou, L., Bin, Z., Pan, G., Li, Y., Menglin, S., Zhongjia, T., et al. (2026) · Scientific Reports · doi:10.1038/s41598-026-40597-1

Dysbiosis in the Gut‐Liver Axis Is Associated With Low Bone Mass During Murine Cholestasis

Hutchison, B., Fornsaglio, J. L., Case, R., IV, Cornuet, P. K., Qin, F., Ma, X., Nejak‐Bowen, K. N., & Carson, M. D. (2026) · The FASEB Journal · doi:10.1096/fj.202502976r

Dietary index for gut microbiota and its protective role against osteoporosis: Evidence from NHANES 2007 to 2018

Feng, R., Xu, S., Cui, Y., Wang, K., Yang, F., & Chen, Q. (2026) · Medicine · doi:10.1097/md.0000000000048045

The Regulatory Role of the Gut-Bone Axis in the Pathogenesis of Ankylosing Spondylitis and Its Clinical Translational Potential

章, 杰. (2026) · Journal of Clinical Personalized Medicine · doi:10.12677/jcpm.2026.52102

Intestinal Epithelial-like Cells Stimulated by a Functional Food Ingredient Promote Lysyl Oxidase (LOX) Expression in Osteoblast Precursor Cells via BMP-1 Secretion

Fujimoto, N., Suzuki, S., Yano, T., Sakata, S., Ito, Y., & Ishida, T. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27073156

Association of the Dietary Index for Gut Microbiota with site-specific Osteoporosis: Insights from machine learning applied to a national population

Zhou, L., Liu, J., Xu, H., Sun, G., 楼宇梁, & Wang, J. (2026) · Metabolism Open · doi:10.1016/j.metop.2026.100467

Defined Microbiota Modulates Host Metabolome and Skeletal Adaptation to Diet‐Induced Obesity

Scalise, M. C., Simon, M., Bernhardt, J., Trümpi, O., Hettich, T., Gaugler, S., Saulačić, N., Gantenbein, B., Zysset, P. K., & Balmer, M. L. (2026) · The FASEB Journal · doi:10.1096/fj.202600564rr

Bacterial Extracellular Vesicles in Aging: Mechanisms and Therapeutic Prospects

Tan, J., Zubair, M., Zhang, L. Y., Liu, L.-P., Li, K., Wang, Y., Yan, Y., & Xu, W. (2026) · International Journal of Nanomedicine · doi:10.2147/ijn.s597419

Roles of gut metabolites on bone mineralization and remodeling: impact of metabolic dysregulation on the gut-immune-bone axis

Basak, S., Hridayanka, K. S. N., & Duttaroy, A. K. (2026) · Frontiers in Endocrinology · doi:10.3389/fendo.2026.1774824

Ancient Ayurveda Meets Modern Science: The Role of Panchakarma in Modulating Gut-Organ Axes - A Narrative Review

Bhatia, B., Shamkuwar, M., & ., M. (2026) · Journal of Natural Remedies · doi:10.18311/jnr/2026/45718

Impact of unbalanced and alternative protein diets on the cecal bacteria and skeletal development: A comparative study in rats

Janssen, J. N., Kesy, K., Becker, G., Shitrit-Tovli, A., Altman, H., Sides, R., & Ornan, E. M. (2026) · Next research. · doi:10.1016/j.nexres.2026.101780

Ayurvedic Management of Post-hysterectomy Osteoporosis: A Case Report

pole, Y., & Nakanekar, A. V. (2026) · Cureus · doi:10.7759/cureus.108840

Nature's blueprint: Exopolysaccharides linking microbiome dynamics to advanced bone tissue engineering

Manikandan, C., K., A. D. V., Manivasagam, G., Pereira, A., Mano, J. F., Borges, J., Jaiswal, A. K., & Udduttula, A. (2026) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2026.125447

The Gut–Bone Axis: A Systematic Review on the Potential Intervention Pathways for Bone Health

Cantón-Cordeiro, T., Shimochi, S., Nakamura, M., & Puigbò, P. (2026) · Life · doi:10.3390/life16060909

The Gut–Musculoskeletal Axis: Reframing Orthopaedic Disease Through the Microbiome Lens

Banskota, B. (2026) · Nepal Orthopaedic Association Journal · doi:10.59173/noaj.20261202a

Osteoclast-regulatory biomaterials: Direct cellular intervention and indirect microenvironment modulation

Ji, J., 王俏镟, & Gao, C. (2026) · Biomaterials · doi:10.1016/j.biomaterials.2026.124371

Natto May Alleviate Retinoic Acid-Induced Osteoporosis by Activating Gut Microbiota–Bile Acid Axis and OPG/RANKL Signaling Pathway

Zhang, B., Sun, M., Liu, Y., Pan, T., Zhang, X., He, Y., Gan, X., Li, D., Miao, X., Luo, Z., et al. (2026) · Nutrients · doi:10.3390/nu18121927

Interplay between gut health, immunity, and bone development in broilers: role of feed additives

Arachchi, A. E., Do, A. D. T., & Alrubaye, A. A. K. (2026) · Poultry Science · doi:10.1016/j.psj.2026.107407

Multidimensional regulatory mechanisms and targeted intervention strategies of the gut-joint axis in metabolic osteoarthritis

Chai, R., Liu, J., Hu, L., & Zheng, P. (2026) · Translational research · doi:10.1016/j.trsl.2026.07.003

Gut Microbiome-Mediated Inter-Organ Crosstalk in Obesity and Aging

Mehta, O., & Ghosh, T. S. (2026) · Healthy ageing and longevity · doi:10.1007/978-3-032-24097-2_10

Plant-based macronutrients and micronutrients in combating osteoporosis: research insights and molecular pathways

Roy, M., Dutta, G., Das, A., Roy, S. S., Debnath, B., Jana, M., & Sugumaran, A. (2026) · RSC Advances · doi:10.1039/d6ra02084d

Panax quinquefolius-derived nanovesicles: a synergistic nanotherapy for postmenopausal osteoporosis via modulating gut microbiota, MYC-mediated inflammation, and Nrf2/HO-1 antioxidant pathway

Yin, Q., Gu, J., Bai, R., Zhao, K., Wang, Q. Q., Liu, Y., Liu, Y., & Li, H. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1836521

From cooperation to collapse: the diet-microbiota-host gene triad in disease and aging

Bhattacharjee, S., & Mukhopadhyay, A. (2026) · Frontiers in Microbiomes · doi:10.3389/frmbi.2026.1872481

Multiomics profiling of bone in the Dpp3-deficient mice unveils altered protein and lipid composition

Bevacqua, E., Violi, F., Granata, V., Bedin, F., Santillo, M., Menale, C., Mazziotti, G., & Sobacchi, C. (2026) · Journal of Endocrinological Investigation · doi:10.1007/s40618-026-02949-6

GUT MICROBIOTA SIGNATURES AND CLINICAL CORRELATES IN OSTEOPOROSIS: A RETROSPECTIVE CASE-CONTROL STUDY

WANG, Y., & Jiang, Y. (2026) · Journal of Mechanics in Medicine and Biology · doi:10.1142/s0219519426400920

Effects of Environmental Enrichment on Leg Health and Locomotor Traits of Broiler Chickens Fed Antibiotic or Multi‐Strain Probiotic Performance Enhancers

de Lima, L. A. B., dos Ouros, C. C., da Silva, M. E. R., da Silveira, E. D. S., da Silva, M. R. A., Burbarelli, M. F. D. C., Caldara, F. R., Komiyama, C. M., Nääs, I. D. A., & Garcia, R. G. (2026) · Animal Science Journal · doi:10.1111/asj.70233

Gut microbiota as master regulators: Mapping gut-organ axes that orchestrate systemic health

Han, B., Kang, M., Huang, W., Lan, Y., Tong, S., Liu, S., Chen, S., Wen, H., Li, Y., & Tang, D. (2026) · TransMed · doi:10.1016/j.tmed.2026.100042

Comparison of yogurt and ultra-high-temperature milk on serum osteocalcin and calcium levels in rats

Junilla, R., Primadhi, R. A., & Budi, M. N. S. (2026) · Journal of Advanced Pharmaceutical Technology amp Research · doi:10.4103/japtr.japtr_56_26

Impact of antibiotic-induced gut dysbiosis model on bone mineralization and biomechanical properties in post-weaning rats

SÜZER, B., Arıcan, İ., Yumuşak, E., Akkoç, A., & Yalçın, M. (2026) · Ankara Üniversitesi Veteriner Fakültesi Dergisi · doi:10.33988/auvfd.1910833

Effect of perioperative multistrain probiotics on the CT callus volume fraction at 12 weeks after surgery for closed tibial shaft fracture: a single-center randomized controlled study

Yongbiao, H., Zheng, X., Liao, C., Liu, G., & Li, M. (2026) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2026.1778557

The gut-organ axis: A 25-year bibliometric analysis of 10327 publications on global research landscape and future directions

Liu, S., Han, B., Kang, M., Huang, W., Li, Y., & Tang, D. (2026) · TransMed · doi:10.1016/j.tmed.2026.100044

The Gut Microbiome as a Mechanistic Link Between the Planetary Health Diet and Healthy Aging

Jarecsny, T., Ceglédi, A., Csípő, T., Fazekas‐Pongor, V., Mózes, N., Csík, B., Zábó, V., Lipécz, Á., Nyáry, D., & Fekete, M. (2026) · Nutrients · doi:10.3390/nu18172864

Gut microbiome–metabolome signatures of osteosarcopenia in fracture patients in China

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