Ketogenic diet modifies the gut microbiota in a murine model of autism spectrum disorder
Open accessAbstract
BACKGROUND: Gastrointestinal dysfunction and gut microbial composition disturbances have been widely reported in autism spectrum disorder (ASD). This study examines whether gut microbiome disturbances are present in the BTBR(T + tf/j) (BTBR) mouse model of ASD and if the ketogenic diet, a diet previously shown to elicit therapeutic benefit in this mouse model, is capable of altering the profile. FINDINGS: Juvenile male C57BL/6 (B6) and BTBR mice were fed a standard chow (CH, 13 % kcal fat) or ketogenic diet (KD, 75 % kcal fat) for 10-14 days. Following diets, fecal and cecal samples were collected for analysis. Main findings are as follows: (1) gut microbiota compositions of cecal and fecal samples were altered in BTBR compared to control mice, indicating that this model may be of utility in understanding gut-brain interactions in ASD; (2) KD consumption caused an anti-microbial-like effect by significantly decreasing total host bacterial abundance in cecal and fecal matter; (3) specific to BTBR animals, the KD counteracted the common ASD phenotype of a low Firmicutes to Bacteroidetes ratio in both sample types; and (4) the KD reversed elevated Akkermansia muciniphila content in the cecal and fecal matter of BTBR animals. CONCLUSIONS: Results indicate that consumption of a KD likely triggers reductions in total gut microbial counts and compositional remodeling in the BTBR mouse. These findings may explain, in part, the ability of a KD to mitigate some of the neurological symptoms associated with ASD in an animal model.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
BTBR mice were characterized by a gut microbiota profile different from that of controls.
“Additionally BTBR mice was characterized by a gut microbiota profile that was different from that of controls [110].”
From Autism, Gastrointestinal Symptoms and Modulation of Gut Microbiota by Nutritional Interventions (2019) · cites this paper as [110]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Changes of Intestinal Functions in Liver Cirrhosis
Fukui, H., & Wiest, R. (2016) · Inflammatory Intestinal Diseases · doi:10.1159/000444436 · Cited by 6,820 · see citing works
Gut microbiota in health and disease
Sekirov, I., Russell, S. L., Antunes, L. C. M., & Finlay, B. B. (2010) · Physiological Reviews · doi:10.1152/physrev.00045.2009 · Cited by 4,182 · see citing works
Role of the gut microbiota in immunity and inflammatory disease
Kamada, N., Seo, S.-U., Chen, G. Y., & Núñez, G. (2013) · Nature reviews. Immunology · doi:10.1038/nri3430 · Cited by 2,256 · see citing works
Microbiota-Generated Metabolites Promote Metabolic Benefits via Gut-Brain Neural Circuits
De Vadder, F., Kovatcheva-Datchary, P., Goncalves, D., Vinera, J., Zitoun, C., Duchampt, A., Bäckhed, F., & Mithieux, G. (2014) · Cell · doi:10.1016/j.cell.2013.12.016 · Cited by 2,200 · see citing works
Dietary emulsifiers impact the mouse gut microbiota promoting colitis and metabolic syndrome
Chassaing, B., Koren, O., Goodrich, J. K., Poole, A. C., Srinivasan, S., Ley, R. E., & Gewirtz, A. T. (2015) · Nature · doi:10.1038/nature14232 · Cited by 2,055 · see citing works
Stoddard, S. F., Smith, B. J., Hein, R., Roller, B. R. K., & Schmidt, T. M. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku1201 · Cited by 1,096 · see citing works
Nau, R., Sörgel, F., & Eiffert, H. (2010) · Clinical Microbiology Reviews · doi:10.1128/cmr.00007-10 · Cited by 1,031 · see citing works
Pyrosequencing study of fecal microflora of autistic and control children
Finegold, S. M., Dowd, S. E., Gontcharova, V., Liu, C., Henley, K. E., Wolcott, R. D., Youn, E., Summanen, P. H., Granpeesheh, D., Dixon, D., et al. (2010) · Anaerobe · doi:10.1016/j.anaerobe.2010.06.008 · Cited by 977 · see citing works
De Angelis, M., Piccolo, M., Vannini, L., Siragusa, S., De Giacomo, A., Serrazzanetti, D. I., Cristofori, F., Guerzoni, M. E., Gobbetti, M., & Francavilla, R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076993 · Cited by 887 · see citing works
Autism‐like behavioral phenotypes in BTBR T+tf/J mice
McFarlane, H. G., Kusek, G. K., Yang, M., Phoenix, J. L., Bolivar, V. J., & Crawley, J. N. (2008) · Genes, Brain and Behavior · doi:10.1111/j.1601-183x.2007.00330.x · Cited by 812 · see citing works
Parracho, H. M., Bingham, M. O., Gibson, G. R., & McCartney, A. L. (2005) · Journal of Medical Microbiology · doi:10.1099/jmm.0.46101-0 · Cited by 784 · see citing works
Short-Term Benefit From Oral Vancomycin Treatment of Regressive-Onset Autism
Sandler, R. H., Finegold, S. M., Bolte, E. R., Buchanan, C. P., Maxwell, A. P., Väisänen, M.-L., Nelson, M. N., & Wexler, H. M. (2000) · Journal of Child Neurology · doi:10.1177/088307380001500701 · Cited by 614 · see citing works
Interaction of dietary compounds, especially polyphenols, with the intestinal microbiota: a review
Duda-Chodak, A., Tarko, T., Satora, P., & Sroka, P. (2015) · European Journal of Nutrition · doi:10.1007/s00394-015-0852-y · Cited by 599 · see citing works
de Magistris, L., Familiari, V., Pascotto, A., Sapone, A., Frolli, A., Iardino, P., Carteni, M., De Rosa, M., Francavilla, R., Riegler, G., et al. (2010) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0b013e3181dcc4a5 · Cited by 546 · see citing works
Ganesh, B. P., Klopfleisch, R., Loh, G., & Blaut, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0074963 · Cited by 522 · see citing works
Altered gut microbiota and activity in a murine model of autism spectrum disorders
de Theije, C. G. M., Wopereis, H., Ramadan, M., van Eijndthoven, T., Lambert, J., Knol, J., Garssen, J., Kraneveld, A. D., & Oozeer, R. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2013.12.005 · Cited by 433 · see citing works
Mucins in the gastrointestinal tract in health and disease
Anthony, P. P. (2001) · Frontiers in bioscience · doi:10.2741/corfield · Cited by 343 · see citing works
Voices from within: gut microbes and the CNS
Forsythe, P., & Kunze, W. A. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1028-z · Cited by 336 · see citing works
Scattoni, M. L., Ricceri, L., & Crawley, J. N. (2010) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2010.00623.x · Cited by 336 · see citing works
Ketogenic diets, mitochondria, and neurological diseases
Gano, L. B., Patel, M., & Rho, J. M. (2014) · Journal of Lipid Research · doi:10.1194/jlr.r048975 · Cited by 279 · see citing works
Ismail, N. A., Ragab, S. H., ElBaky, A. A., Shoeib, A. R. S., Alhosary, Y., & Fekry, D. (2011) · Archives of Medical Science · doi:10.5114/aoms.2011.23418 · Cited by 268 · see citing works
The role of the gut microbiota in metabolic health
Janssen, A. W. F., & Kersten, S. (2015) · The FASEB Journal · doi:10.1096/fj.14-269514 · Cited by 199 · see citing works
Ketogenic Diet Improves Core Symptoms of Autism in BTBR Mice
Ruskin, D. N., Svedova, J., Cote, J. L., Sandau, U., Rho, J. M., Kawamura, M., Boison, D., & Masino, S. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065021 · Cited by 173 · see citing works
Bomhof, M. R., Saha, D. C., Reid, D. T., Paul, H. A., & Reimer, R. A. (2013) · Obesity · doi:10.1002/oby.20632 · Cited by 150 · see citing works
The BTBR T+tf/J mouse model for autism spectrum disorders–in search of biomarkers
Meyza, K. Z., Defensor, E. B., Jensen, A. L., Corley, M. J., Pearson, B. L., Pobbe, R. L. H., Bolivar, V. J., Blanchard, D. C., & Blanchard, R. J. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.07.021 · Cited by 147 · see citing works
Autism and nutrition: the role of the gut–brain axis
Sande, M. M. H. V. D., van Buul, V. J., & Brouns, F. J. P. H. (2014) · Nutrition Research Reviews · doi:10.1017/s0954422414000110 · Cited by 143 · see citing works
Mucins in the gastrointestinal tract in health and disease
Corfield, A. P. (2001) · Frontiers in bioscience · doi:10.2741/a684 · Cited by 135 · see citing works
Puberty Is Delayed in Male Growth Hormone Receptor Gene—Disrupted Mice
KEENE, D. E., Suescun, M. O., BOSTWICK, M. G., Chandrashekar, V., Bartke, A., & Kopchick, J. J. (2002) · Journal of Andrology · doi:10.1002/j.1939-4640.2002.tb02308.x · Cited by 75 · see citing works
Gastrointestinal Microbiota and Metabolite Biomarkers in Children With Autism Spectrum Disorders
Wang, L., Conlon, M. A., Christophersen, C. T., Sorich, M. J., & Angley, M. T. (2014) · Biomarkers in Medicine · doi:10.2217/bmm.14.12 · Cited by 72 · see citing works
Klein, M. S., Newell, C., Bomhof, M. R., Reimer, R. A., Hittel, D. S., Rho, J. M., Vogel, H. J., & Shearer, J. (2016) · Journal of Proteome Research · doi:10.1021/acs.jproteome.5b01025 · Cited by 51 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Cryan, J. F., O'Riordan, K. J., Cowan, C. S. M., Sandhu, K. V., Bastiaanssen, T. F. S., Boehme, M., Codagnone, M. G., Cussotto, S., Fulling, C., Golubeva, A. V., et al. (2019) · Physiological Reviews · doi:10.1152/physrev.00018.2018 · Cited by 5,286 · see citing works
The gut microbiome in neurological disorders
Cryan, J. F., O'Riordan, K. J., Sandhu, K., Peterson, V., & Dinan, T. G. (2020) · The Lancet Neurology · doi:10.1016/s1474-4422(19)30356-4 · Cited by 1,336 · see citing works
Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice
Sharon, G., Cruz, N. J., Kang, D.-W., Gandal, M. J., Wang, B., Kim, Y.-M., Zink, E. M., Casey, C. P., Taylor, B. C., Lane, C. J., et al. (2019) · Cell · doi:10.1016/j.cell.2019.05.004 · Cited by 1,182 · see citing works
The Gut Microbiota Mediates the Anti-Seizure Effects of the Ketogenic Diet
Olson, C. A., Vuong, H. E., Yano, J. M., Liang, Q. Y., Nusbaum, D. J., & Hsiao, E. Y. (2018) · Cell · doi:10.1016/j.cell.2018.04.027 · Cited by 1,057 · see citing works
Zheng, P., Zeng, B., Liu, M., Chen, J., Pan, J., Han, Y., Liu, Y., Cheng, K., Zhou, C., Wang, H., et al. (2019) · Science Advances · doi:10.1126/sciadv.aau8317 · Cited by 704 · see citing works
Effect of Diet and Dietary Components on the Composition of the Gut Microbiota
Beam, A., Clinger, E., & Hao, L. (2021) · Nutrients · doi:10.3390/nu13082795 · Cited by 576 · see citing works
The Gut Microbiota and Autism Spectrum Disorders
Li, Q., Han, Y., Dy, A. B. C., & Hagerman, R. J. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00120 · Cited by 462 · see citing works
Zhu, H., Bi, D., Zhang, Y., Kong, C., Du, J., Wu, X., Wei, Q., & Qin, H. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-021-00831-w · Cited by 412 · see citing works
Gubert, C., Kong, G., Renoir, T., & Hannan, A. J. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.104621 · Cited by 372 · see citing works
Golubeva, A. V., Joyce, S. A., Moloney, G., Burokas, A., Sherwin, E., Arboleya, S., Flynn, I., Khochanskiy, D., Moya-Pérez, A., Peterson, V., et al. (2017) · EBioMedicine · doi:10.1016/j.ebiom.2017.09.020 · Cited by 364 · see citing works
Recent developments in understanding the role of the gut microbiota in brain health and disease
Sherwin, E., Dinan, T. G., & Cryan, J. F. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13416 · Cited by 338 · see citing works
Ketogenic diet enhances neurovascular function with altered gut microbiome in young healthy mice
Ma, D., Wang, A. C., Parikh, I. J., Green, S. J., Hoffman, J. D., Chlipala, G. E., Murphy, M. P., Sokola, B. S., Bauer, B., Hartz, A. M. S., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-25190-5 · Cited by 300 · see citing works
Roles of Short-Chain Fatty Acids in Inflammatory Bowel Disease
Shin, Y., Han, S., Kwon, J., Ju, S., Choi, T., Kang, I., & Kim, S. S. (2023) · Nutrients · doi:10.3390/nu15204466 · Cited by 296 · see citing works
Altered gut microbiome composition in children with refractory epilepsy after ketogenic diet
Zhang, Y., Zhou, S., Zhou, Y., Yu, L., Zhang, L., & Wang, Y. (2018) · Epilepsy Research · doi:10.1016/j.eplepsyres.2018.06.015 · Cited by 269 · see citing works
Ketogenic Diet and Microbiota: Friends or Enemies?
Paoli, A., Mancin, L., Bianco, A., Thomas, E., Mota, J. F., & Piccini, F. (2019) · Genes · doi:10.3390/genes10070534 · Cited by 265 · see citing works
New insights into the mechanisms of the ketogenic diet
Boison, D. (2017) · Current Opinion in Neurology · doi:10.1097/wco.0000000000000432 · Cited by 256 · see citing works
Autism, Gastrointestinal Symptoms and Modulation of Gut Microbiota by Nutritional Interventions
Ristori, M. V., Quagliariello, A., Reddel, S., Ianiro, G., Vicari, S., Gasbarrini, A., & Putignani, L. (2019) · Nutrients · doi:10.3390/nu11112812 · Cited by 214 · see citing works
Zheng, P., Wu, J., Zhang, H., Perry, S. W., Yin, B., Tan, X., Chai, T., Liang, W., Huang, Y., Li, Y., et al. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0744-2 · Cited by 202 · see citing works
The Effects of Intermittent Fasting on Brain and Cognitive Function
Gudden, J., Vásquez, A. A., & Bloemendaal, M. (2021) · Nutrients · doi:10.3390/nu13093166 · Cited by 204 · see citing works
Barlow, J. T., Bogatyrev, S. R., & Ismagilov, R. F. (2020) · Nature Communications · doi:10.1038/s41467-020-16224-6 · Cited by 188 · see citing works
The BTBR mouse model of idiopathic autism – Current view on mechanisms
Meyza, K. Z., & Blanchard, D. C. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.12.037 · Cited by 189 · see citing works
Coretti, L., Cristiano, C., Florio, E., Scala, G., Lama, A., Keller, S., Cuomo, M., Russo, R., Pero, R., Paciello, O., et al. (2017) · Scientific Reports · doi:10.1038/srep45356 · Cited by 175 · see citing works
Lee, R. W. Y., Corley, M. J., Pang, A. P. S., Arakaki, G., Abbott, L., Nishimoto, M., Miyamoto, R. H., Lee, E., Yamamoto, S., Maunakea, A. K., et al. (2018) · Physiology & Behavior · doi:10.1016/j.physbeh.2018.02.006 · Cited by 165 · see citing works
Gut microbiota profiles in treatment-naïve children with attention deficit hyperactivity disorder
Jiang, H.-Y., Zhou, Y.-Y., Zhou, G.-L., Li, Y.-C., Yuan, J., Li, X.-H., & Ruan, B. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.03.036 · Cited by 164 · see citing works
Gut Microbiota in Colorectal Cancer: Biological Role and Therapeutic Opportunities
Pandey, H., Tang, D. W. T., Wong, S. H., & Lal, D. (2023) · Cancers · doi:10.3390/cancers15030866 · Cited by 165 · see citing works
Mitochondrial Dysfunction in Autism Spectrum Disorder: Unique Abnormalities and Targeted Treatments
Frye, R. E. (2020) · Seminars in Pediatric Neurology · doi:10.1016/j.spen.2020.100829 · Cited by 161 · see citing works
Impact of Different Types of Diet on Gut Microbiota Profiles and Cancer Prevention and Treatment
Klement, R. J., & Pazienza, V. (2019) · Medicina · doi:10.3390/medicina55040084 · Cited by 158 · see citing works
Metabolic Dysfunction Underlying Autism Spectrum Disorder and Potential Treatment Approaches
Cheng, N., Rho, J. M., & Masino, S. A. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00034 · Cited by 148 · see citing works
Nutritional interventions for autism spectrum disorder
Karhu, E., Zukerman, R. J., Eshraghi, R. S., Mittal, J., Deth, R. C., Castejon, A. M., Trivedi, M. S., Mittal, R., & Eshraghi, A. A. (2019) · Nutrition Reviews · doi:10.1093/nutrit/nuz092 · Cited by 145 · see citing works
Diet can impact microbiota composition in children with autism spectrum disorder
Berding, K., & Donovan, S. M. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00515 · Cited by 144 · see citing works
Autism Spectrum Disorder as a Brain-Gut-Microbiome Axis Disorder
Saurman, V. E., Margolis, K. G., & Luna, R. A. (2020) · Digestive Diseases and Sciences · doi:10.1007/s10620-020-06133-5 · Cited by 140 · see citing works
Żarnowska, I. (2020) · Nutrients · doi:10.3390/nu12092616 · Cited by 129 · see citing works
The Current Status of the Ketogenic Diet in Psychiatry
Bostock, E. C. S., Kirkby, K. C., & Taylor, B. V. M. (2017) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2017.00043 · Cited by 127 · see citing works
The Role of Nutrition and the Gut-Brain Axis in Psychiatry: A Review of the Literature
Mörkl, S., Wagner‐Skacel, J., Lahousen, T., Lackner, S., Holasek, S. J., Bengesser, S., Painold, A., Holl, A. K., & Reininghaus, E. Z. (2018) · Neuropsychobiology · doi:10.1159/000492834 · Cited by 129 · see citing works
Xu, Y., Jiang, C., Wu, J., Liu, P., Deng, X., Zhang, Y., Peng, B., & Zhu, Y. (2021) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13779 · Cited by 122 · see citing works
Current nutritional approaches in managing autism spectrum disorder: A review
Çekici, H., & Şanlıer, N. (2017) · Nutritional Neuroscience · doi:10.1080/1028415x.2017.1358481 · Cited by 119 · see citing works
García-Gutiérrez, E., Narbad, A., & Rodríguez, J. M. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.578666 · Cited by 115 · see citing works
Wang, D., Wu, J., Zhu, P., Xie, H., Lu, L., Bai, W., Pan, W., Shi, R., Ye, J., Xia, B., et al. (2022) · Food Research International · doi:10.1016/j.foodres.2022.111289 · Cited by 112 · see citing works
Microbiota-brain interactions: Moving toward mechanisms in model organisms
Nagpal, J. K., & Cryan, J. F. (2021) · Neuron · doi:10.1016/j.neuron.2021.09.036 · Cited by 107 · see citing works
Can we ‘seize’ the gut microbiota to treat epilepsy?
De Caro, C., Iannone, L. F., Citraro, R., Striano, P., De Sarro, G., Constanti, A., Cryan, J. F., & Russo, E. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.10.002 · Cited by 110 · see citing works
Jang, J., Kim, S. R., Lee, J. E., Lee, S.-Y., Son, H. J., Choe, W., Yoon, K., Kim, S. S., Yeo, E., & Kang, I. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms25010124 · Cited by 107 · see citing works
Reddel, S., Putignani, L., & Del Chierico, F. (2019) · Nutrients · doi:10.3390/nu11020373 · Cited by 104 · see citing works
Liu, F., Horton-Sparks, K., Hull, V. L., Li, R. W., & Martínez‐Cerdeño, V. (2018) · Molecular Autism · doi:10.1186/s13229-018-0251-3 · Cited by 104 · see citing works
Gut microbiota and Autism Spectrum Disorder: From pathogenesis to potential therapeutic perspectives
Mehra, A., Arora, G., Sahni, G., Kaur, M., Singh, H. B., Singh, B., & Kaur, S. (2022) · Journal of Traditional and Complementary Medicine · doi:10.1016/j.jtcme.2022.03.001 · Cited by 106 · see citing works
Akkermansia muciniphila in neuropsychiatric disorders: friend or foe?
Lei, W., Cheng, Y., Gao, J., Liu, X., Shao, L., Kong, Q., Zheng, N., Ling, Z., & Hu, W. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1224155 · Cited by 101 · see citing works
The gut microbiota–brain axis in neurological disorders
You, M., Chen, N., Yang, Y., Cheng, L., He, H., Cai, Y., Liu, Y., Liu, H., & Hong, G. (2024) · MedComm · doi:10.1002/mco2.656 · Cited by 107 · see citing works
Hung, L. Y., & Margolis, K. G. (2024) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-023-00857-1 · Cited by 96 · see citing works
Xu, R., Zhang, Y., Chen, S., Zeng, Y., Fu, X., Chen, T., Luo, S., & Zhang, X. (2022) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2022.2044286 · Cited by 95 · see citing works
The Expanding Role of Ketogenic Diets in Adult Neurological Disorders
McDonald, T. J. W., & Cervenka, M. C. (2018) · Brain Sciences · doi:10.3390/brainsci8080148 · Cited by 88 · see citing works
Ketogenic diet as a metabolic treatment for mental illness
Norwitz, N. G., Sethi, S., & Palmer, C. (2020) · Current Opinion in Endocrinology Diabetes and Obesity · doi:10.1097/med.0000000000000564 · Cited by 87 · see citing works
A Ketogenic Diet and the Treatment of Autism Spectrum Disorder
Li, Q., Liang, J., Fu, N., Han, Y., & Qin, J. (2021) · Frontiers in Pediatrics · doi:10.3389/fped.2021.650624 · Cited by 90 · see citing works
The Role of the Gut Microbiota on the Beneficial Effects of Ketogenic Diets
Attaye, I., van Oppenraaij, S. L., Warmbrunn, M. V., & Nieuwdorp, M. (2021) · Nutrients · doi:10.3390/nu14010191 · Cited by 85 · see citing works
Good or bad: gut bacteria in human health and diseases
Wang, H., Wei, C.-X., Lu, M., & Zhu, L. (2018) · Biotechnology & Biotechnological Equipment · doi:10.1080/13102818.2018.1481350 · Cited by 84 · see citing works
Citraro, R., Lembo, F., Caro, C. D., Tallarico, M., Coretti, L., Iannone, L. F., Leo, A., Palumbo, D., Cuomo, M., Buommino, E., et al. (2021) · Epilepsia · doi:10.1111/epi.16813 · Cited by 82 · see citing works
Potential Protective Mechanisms of Ketone Bodies in Migraine Prevention
Gross, E. C., Klement, R. J., Schoenen, J. E., D’Agostino, D. P., & Fischer, D. (2019) · Nutrients · doi:10.3390/nu11040811 · Cited by 76 · see citing works
He, Y., Wang, K., Su, N., Yuan, C., Zhang, N., Hu, X., Fu, Y., & Zhao, F. (2024) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.70099 · Cited by 73 · see citing works
Beta-Hydroxybutyrate: A Dual Function Molecular and Immunological Barrier Function Regulator
Qi, J., Gan, L., Fang, J. S., Zhang, J., Yu, X., Guo, H., Cai, D., Cui, H., Gou, L., Deng, J., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.805881 · Cited by 72 · see citing works
Keto microbiota: A powerful contributor to host disease recovery
Cabrera-Mulero, A., Tinahones, A., Bandera-Merchán, B., Moreno‐Indias, I., Macías‐González, M., & Tinahones, F. J. (2019) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-019-09518-8 · Cited by 70 · see citing works
Crosstalk between the Ketogenic Diet and Epilepsy: From the Perspective of Gut Microbiota
Fan, Y., Wang, H., Liu, X., Zhang, J., & Liu, G. (2019) · Mediators of Inflammation · doi:10.1155/2019/8373060 · Cited by 70 · see citing works
The Gut Microbiota and Oxidative Stress in Autism Spectrum Disorders (ASD)
Hu, T., Dong, Y., He, C., Zhao, M., & He, Q. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/8396708 · Cited by 71 · see citing works
Obesity, Gut Microbiota, and Metabolome: From Pathophysiology to Nutritional Interventions
Puljiz, Z., Kumrić, M., Vrdoljak, J., Martinović, D., Kurir, T. T., Krnic, M. O., Urlić, H., Puljiz, Ž., Žučko, J., Dumanić, P., et al. (2023) · Nutrients · doi:10.3390/nu15102236 · Cited by 72 · see citing works
Ketogenic Diet for the Treatment and Prevention of Dementia: A Review
Davis, J. J., Fournakis, N. A., & Ellison, J. M. (2020) · Journal of Geriatric Psychiatry and Neurology · doi:10.1177/0891988720901785 · Cited by 70 · see citing works
Lim, J.-M., Letchumanan, V., Tan, L. T., Hong, K., Wong, S. H., Mutalib, N. A., Lee, L., & Law, J. W. (2022) · Nutrients · doi:10.3390/nu14173566 · Cited by 72 · see citing works
Ketogenic therapy in neurodegenerative and psychiatric disorders: From mice to men
Kraeuter, A.-K., Phillips, R., & Sarnyai, Z. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.109913 · Cited by 66 · see citing works
Gut microbiota and neuropsychiatric disorders: Implications for neuroendocrine-immune regulation
Ge, T., Yao, X., Zhao, H., Yang, W., Zou, X., Peng, F., Li, B., & Cui, R. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105909 · Cited by 62 · see citing works
Alteration of Gut Microbiota: New Strategy for Treating Autism Spectrum Disorder
Liu, J., Gao, Z., Chuanqi, L., Liu, T., Gao, J., Cai, Y., & Fan, X. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.792490 · Cited by 62 · see citing works
Roussin, L., Prince, N., Perez‐Pardo, P., Kraneveld, A. D., Rabot, S., & Naudon, L. (2020) · Microorganisms · doi:10.3390/microorganisms8091369 · Cited by 64 · see citing works
Trudeau, M. S., Madden, R. F., Parnell, J. A., Gibbard, W. B., & Shearer, J. (2019) · Nutrients · doi:10.3390/nu11081783 · Cited by 59 · see citing works
Needham, B. D., Tang, W., & Wu, W. (2018) · Developmental Neurobiology · doi:10.1002/dneu.22581 · Cited by 59 · see citing works
Zheng, Y., Bek, M. K., Prince, N., Marzal, L. N. P., Garssen, J., Perez‐Pardo, P., & Kraneveld, A. D. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.738220 · Cited by 58 · see citing works
Rawat, K., Singh, N., Kumari, P., & Saha, L. (2020) · Reviews in the Neurosciences · doi:10.1515/revneuro-2020-0078 · Cited by 58 · see citing works
The impact of keto-adaptation on exercise performance and the role of metabolic-regulating cytokines
Sherrier, M. C., & Li, H. (2019) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/nqz145 · Cited by 56 · see citing works
Ketogenic diet, neuroprotection, and antiepileptogenesis
Murugan, M., & Boison, D. (2020) · Epilepsy Research · doi:10.1016/j.eplepsyres.2020.106444 · Cited by 56 · see citing works
Genetic Approaches Using Zebrafish to Study the Microbiota–Gut–Brain Axis in Neurological Disorders
Lee, J. G., Cho, H.-J., Jeong, Y.-M., & Lee, J.-S. (2021) · Cells · doi:10.3390/cells10030566 · Cited by 55 · see citing works
Multi-Omics Analysis Reveals Aberrant Gut-Metabolome-Immune Network in Schizophrenia
Fan, Y., Gao, Y., Ma, Q., Yang, Z., Zhao, B., He, X., Yang, J., Yan, B., Gao, F., Li, Q., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.812293 · Cited by 56 · see citing works
Clinical studies and anti‐inflammatory mechanisms of treatments
French, J. A., Koepp, M. J., Naegelin, Y., Vigevano, F., Auvin, S., Rho, J. M., Rosenberg, E. C., Devinsky, O., Olofsson, P. S., & Dichter, M. A. (2017) · Epilepsia · doi:10.1111/epi.13779 · Cited by 54 · see citing works
Molecular Mechanisms Underlying the Bioactive Properties of a Ketogenic Diet
Murakami, M., & Tognini, P. (2022) · Nutrients · doi:10.3390/nu14040782 · Cited by 54 · see citing works
Comparing the Gut Microbiome in Autism and Preclinical Models: A Systematic Review
Alamoudi, M. U. A., Hosie, S., Shindler, A. E., Wood, J. L., Franks, A. E., & Hill‐Yardin, E. L. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.905841 · Cited by 52 · see citing works
Yu, Y., Huang, J.-Y., Chen, X., Fu, J., Wang, X., Pu, L., Gu, C., & Cai, C. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.844117 · Cited by 47 · see citing works
Crawford, J. A., Liu, S., & Tao, F. (2022) · Neurobiology of Pain · doi:10.1016/j.ynpai.2022.100090 · Cited by 48 · see citing works
Ferraris, C., Meroni, E., Casiraghi, M. C., Tagliabue, A., GIORGIS, V. D., & Erba, D. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.613100 · Cited by 47 · see citing works
Gut microbiota and host genetics modulate the effect of diverse diet patterns on metabolic health
Huda, M. N., Salvador, A. C., Barrington, W. T., Gacasan, C. A., D’Souza, E. M., Ramirez, L. D., Threadgill, D. W., & Bennett, B. J. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.896348 · Cited by 46 · see citing works
Dietary interventions for autism spectrum disorder: New perspectives from the gut-brain axis
Doenyas, C. (2018) · Physiology & Behavior · doi:10.1016/j.physbeh.2018.07.014 · Cited by 46 · see citing works
Predictive ability of host genetics and rumen microbiome for subclinical ketosis
Gebreyesus, G., Difford, G. F., Buitenhuis, B., Lassen, J., Noel, S. J., Højberg, O., Plichta, D. R., Zhu, Z., Poulsen, N. A., Sundekilde, U. K., et al. (2020) · Journal of Dairy Science · doi:10.3168/jds.2019-17824 · Cited by 46 · see citing works
Depicting the composition of gut microbiota in children with tic disorders: an exploratory study
Xi, W., Gao, X., Zhao, H., Luo, X., Li, J., Tan, X., Wang, L., Zhao, J., Wang, J., Yang, G., et al. (2021) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.13409 · Cited by 48 · see citing works
Yue, S., Li, Z., Hu, F., & Picimbon, J. (2020) · Scientific Reports · doi:10.1038/s41598-020-75207-1 · Cited by 45 · see citing works
Larroya, A., Pantoja, J., Codoñer‐Franch, P., & Cénit, M. C. (2021) · Frontiers in Pediatrics · doi:10.3389/fped.2021.705859 · Cited by 46 · see citing works
Gut microbiome-mediated mechanisms in aging-related diseases: are probiotics ready for prime time?
Ren, J., Li, H., Zeng, G., Pang, B., Wang, Q., & Wei, J.-P. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1178596 · Cited by 44 · see citing works
Gut microbiota as a biomarker and modulator of anti-tumor immunotherapy outcomes
Yan, J., Yang, L., Ren, Q., Zhu, C., Du, H., Wang, Z., Qi, Y., Xian, X., & Chen, D. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1471273 · Cited by 47 · see citing works
The link between autism spectrum disorder and gut microbiota: A scoping review
Nitschke, A. S., Deonandan, R., & Konkle, A. T. M. (2020) · Autism · doi:10.1177/1362361320913364 · Cited by 45 · see citing works
Targeted gut microbiota manipulation attenuates seizures in a model of infantile spasms syndrome
Mu, C., Nikpoor, N., Tompkins, T. A., Choudhary, A., Wang, M., Marks, W. N., Rho, J. M., Scantlebury, M. H., & Shearer, J. (2022) · JCI Insight · doi:10.1172/jci.insight.158521 · Cited by 41 · see citing works
Facts and Hopes for Gut Microbiota Interventions in Cancer Immunotherapy
Davar, D., & Zarour, H. M. (2022) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-21-1129 · Cited by 40 · see citing works
Wei, N., Ju, M., Su, X., Zhang, Y., Huang, Y., Rao, X., Cui, L., Lin, Z., & Dong, Y. W. (2024) · Schizophrenia · doi:10.1038/s41537-024-00460-6 · Cited by 45 · see citing works
Exploring the mechanisms of action of the antidepressant effect of the ketogenic diet
Ricci, A. L., Idzikowski, M. A., Soares, C. N., & Brietzke, E. M. (2020) · Reviews in the Neurosciences · doi:10.1515/revneuro-2019-0073 · Cited by 42 · see citing works
Kraeuter, A.-K., Phillips, R., & Sarnyai, Z. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00799 · Cited by 43 · see citing works
Wang, H., Sun, Y., Xin, J., Zhang, T., Sun, N., Ni, X., Zeng, D., & Bai, Y. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01941 · Cited by 41 · see citing works
Qin, L., Ma, K., & Yan, Z. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01212-1 · Cited by 41 · see citing works
Mruk-Mazurkiewicz, H., Kulaszyńska, M., Czarnecka, W., Podkówka, A., Ekstedt, N., Zawodny, P., Wierzbicka-Woś, A., Marlicz, W. M., Skupin, B., Stachowska, E., et al. (2024) · Nutrients · doi:10.3390/nu16111695 · Cited by 41 · see citing works
The role of microbiota in autism spectrum disorders
Campion, D., Ponzo, P., Alessandria, C., Saracco, G. M., & Balzola, F. A. (2018) · Minerva Gastroenterologica e Dietologica · doi:10.23736/s1121-421x.18.02493-5 · Cited by 40 · see citing works
Altered Gut Microbiota in a Fragile X Syndrome Mouse Model
Altimiras, F., García, J. A., Palacios-García, I., Hurley, M. J., Deacon, R., González, B., & Cogram, P. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.653120 · Cited by 34 · see citing works
- Authors
- Newell, C., Bomhof, M. R., Reimer, R. A., Hittel, D. S., Rho, J. M., & Shearer, J.
- Affiliations
- University of Calgary (CA)
- Corresponding author
- Newell, Christopher
- Venue
- Molecular Autism
- Published
- 2016-09-01
- Volume
- 7
- Issue
- 1
- Pages
- 37-37
- ISSN
- 2040-2392 (ISSN-L)
- PMC
- PMC5009541
- OpenAlex
- W2509638174
- Cited by
- 272
- References
- 30
- Citations by year
- 2026: 13 · 2025: 30 · 2024: 23 · 2023: 31 · 2022: 41 · 2021: 33 · 2020: 40 · 2019: 29 · 2018: 20 · 2017: 10 · 2016: 2
- FWCI
- 10.56
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Molecular Autism (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion, cc-by)
- Funders
- Alberta Children's Hospital Foundation
- Canadian Institutes of Health Research
- MitoCanada
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
- Health Sciences › Medicine › Physiology › Diet and metabolism studies
- Keywords
- ketogenic diet, autism spectrum disorder, gut microbiota, gut-brain axis, Akkermansia muciniphila, Firmicutes/Bacteroidetes ratio, cecal microbiota, fecal microbiota, dietary fat, gastrointestinal dysfunction
- MeSH terms
- Autism Spectrum Disorder, Gastrointestinal Microbiome, Animals, Bacteria, Behavior, Animal, Cecum, Disease Models, Animal, Feces, Male, Mice, Inbred C57BL, Social Behavior, Mice, Diet, Ketogenic
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