Background The classic ketogenic diet (KD) is an normocaloric dietary protocol with a high intake of fats (85-90% of energy), which is used as a therapy for drug-resistant epilepsies and type 1 glucose transporter deficiency syndromes (GLUT1-DS). It is known that specific dietetic patterns can influence the composition of the intestinal microbiota; in particular, it was shown that KD is associated with various pro-inflammatory changes in the microbiota. Aim To verify the impact of KD on the intestinal microbiota, through the evaluation of: intestinal bacterial composition, markers of bacterial metabolism (short chain fatty acids, SCFA), toxicity of faecal water. Materials and Methods Faecal samples were collected in 12 patients with GLUT1-DS or drug-resistant epilepsy (KD) and in matched healthy subjects (CTR); additionally, in 7 patients samples were collected also before the dietary treatment. The bacterial composition was evaluated by analysis of Next Generation Sequencing and Real-Time PCR. SCFAs were measured by gas-chromatography. Toxicity of faecal water was assessed by Trypan Blue (cytotoxicity) and Comet Assay (genotoxicity). Results The microbiota composition of KD patients was significantly different than CTR, especially for a different Firmicutes /Bacteroidetes ratio. SCFA decreased significantly during a KD, as well as the level of genotoxicity of faecal water. Conclusions This study confirmed the impact of KD on the intestinal microbiota, highlighting the need for further research to avoid long-term adverse effects and optimize therapy.

Impact of the ketogenic diet on human gut / E. Meroni, C. Ferraris, A. Tagliabue, E. Borghi, F. Borgo, G. Bassanini, C. Ceccarani, M.C. Casiraghi, D. Erba. ((Intervento presentato al 39. convegno Congresso Nazionale della Società di Nutrizione tenutosi a Napoli nel 2018.

Impact of the ketogenic diet on human gut

E. Meroni;E. Borghi;F. Borgo;G. Bassanini;C. Ceccarani;M.C. Casiraghi;D. Erba
2018

Abstract

Background The classic ketogenic diet (KD) is an normocaloric dietary protocol with a high intake of fats (85-90% of energy), which is used as a therapy for drug-resistant epilepsies and type 1 glucose transporter deficiency syndromes (GLUT1-DS). It is known that specific dietetic patterns can influence the composition of the intestinal microbiota; in particular, it was shown that KD is associated with various pro-inflammatory changes in the microbiota. Aim To verify the impact of KD on the intestinal microbiota, through the evaluation of: intestinal bacterial composition, markers of bacterial metabolism (short chain fatty acids, SCFA), toxicity of faecal water. Materials and Methods Faecal samples were collected in 12 patients with GLUT1-DS or drug-resistant epilepsy (KD) and in matched healthy subjects (CTR); additionally, in 7 patients samples were collected also before the dietary treatment. The bacterial composition was evaluated by analysis of Next Generation Sequencing and Real-Time PCR. SCFAs were measured by gas-chromatography. Toxicity of faecal water was assessed by Trypan Blue (cytotoxicity) and Comet Assay (genotoxicity). Results The microbiota composition of KD patients was significantly different than CTR, especially for a different Firmicutes /Bacteroidetes ratio. SCFA decreased significantly during a KD, as well as the level of genotoxicity of faecal water. Conclusions This study confirmed the impact of KD on the intestinal microbiota, highlighting the need for further research to avoid long-term adverse effects and optimize therapy.
19-nov-2018
ketogenic diet; gut microbiota; gas-chromatography, cytotoxicity
Settore MED/07 - Microbiologia e Microbiologia Clinica
Settore BIO/09 - Fisiologia
Impact of the ketogenic diet on human gut / E. Meroni, C. Ferraris, A. Tagliabue, E. Borghi, F. Borgo, G. Bassanini, C. Ceccarani, M.C. Casiraghi, D. Erba. ((Intervento presentato al 39. convegno Congresso Nazionale della Società di Nutrizione tenutosi a Napoli nel 2018.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/673536
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