Short-term impact of a classical ketogenic diet on gut microbiota in GLUT1 Deficiency Syndrome: A 3-month prospective observational study
Articolo
Data di Pubblicazione:
2017
Abstract:
Background&aims: The classical ketogenic diet (KD) is a high-fat, very low-carbohydrate normocaloric
diet used for drug-resistant epilepsy and Glucose Transporter 1 Deficiency Syndrome (GLUT1 DS). In
animal models, high fat diet induces large alterations in microbiota producing deleterious effects on gut
health. We carried out a pilot study on patients treated with KD comparing their microbiota composition
before and after three months on the diet.
Methods: Six patients affected by GLUT1 DS were asked to collect fecal samples before and after three
months on the diet. RT e PCR analysis was performed in order to quantify Firmicutes, Bacteroidetes,
Bifidobacterium spp., Lactobacillus spp., Clostridium perfringens, Enterobacteriaceae, Clostridium cluster XIV,
Desulfovibrio spp. and Faecalibacterium prausnitzii.
Results: Compared with baseline, there were no statistically significant differences at 3 months in Firmicutes
and Bacteroidetes. However fecal microbial profiles revealed a statistically significant increase in
Desulfovibrio spp. (p ¼ 0.025), a bacterial group supposed to be involved in the exacerbation of the inflammatory
condition of the gut mucosa associated to the consumption of fats of animal origin.
Conclusions: A future prospective study on the changes in gut microbiota of all children with epilepsy
started on a KD is warranted. In patients with dysbiosis demonstrated by fecal samples, it my be
reasonable to consider an empiric trial of pre or probiotics to potentially restore the «ecological balance»
of intestinal microbiota.
diet used for drug-resistant epilepsy and Glucose Transporter 1 Deficiency Syndrome (GLUT1 DS). In
animal models, high fat diet induces large alterations in microbiota producing deleterious effects on gut
health. We carried out a pilot study on patients treated with KD comparing their microbiota composition
before and after three months on the diet.
Methods: Six patients affected by GLUT1 DS were asked to collect fecal samples before and after three
months on the diet. RT e PCR analysis was performed in order to quantify Firmicutes, Bacteroidetes,
Bifidobacterium spp., Lactobacillus spp., Clostridium perfringens, Enterobacteriaceae, Clostridium cluster XIV,
Desulfovibrio spp. and Faecalibacterium prausnitzii.
Results: Compared with baseline, there were no statistically significant differences at 3 months in Firmicutes
and Bacteroidetes. However fecal microbial profiles revealed a statistically significant increase in
Desulfovibrio spp. (p ¼ 0.025), a bacterial group supposed to be involved in the exacerbation of the inflammatory
condition of the gut mucosa associated to the consumption of fats of animal origin.
Conclusions: A future prospective study on the changes in gut microbiota of all children with epilepsy
started on a KD is warranted. In patients with dysbiosis demonstrated by fecal samples, it my be
reasonable to consider an empiric trial of pre or probiotics to potentially restore the «ecological balance»
of intestinal microbiota.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Glucose Transporter 1 Deficiency Syndrome; Ketogenic diet; Microbiota; Endocrinology, Diabetes and Metabolism; Nutrition and Dietetics
Elenco autori:
Tagliabue, Anna; Ferraris, Cinzia; Uggeri, Francesca; Trentani, Claudia; Bertoli, Simona; DE GIORGIS, Valentina; Veggiotti, Pierangelo; Elli, Marina
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