An Integrated Understanding of the Rapid Metabolic Benefits of a Carbohydrate-Restricted Diet on Hepatic Steatosis in Humans

A carbohydrate-restricted diet is a widely recommended intervention for non-alcoholic fatty liver disease (NAFLD), but a systematic perspective on the multiple benefits of this diet is lacking. Here, we performed a short-term intervention with an isocaloric low-carbohydrate diet with increased prote...

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Published inCell metabolism Vol. 27; no. 3; pp. 559 - 571.e5
Main Authors Mardinoglu, Adil, Wu, Hao, Bjornson, Elias, Zhang, Cheng, Hakkarainen, Antti, Räsänen, Sari M., Lee, Sunjae, Mancina, Rosellina M., Bergentall, Mattias, Pietiläinen, Kirsi H., Söderlund, Sanni, Matikainen, Niina, Ståhlman, Marcus, Bergh, Per-Olof, Adiels, Martin, Piening, Brian D., Granér, Marit, Lundbom, Nina, Williams, Kevin J., Romeo, Stefano, Nielsen, Jens, Snyder, Michael, Uhlén, Mathias, Bergström, Göran, Perkins, Rosie, Marschall, Hanns-Ulrich, Bäckhed, Fredrik, Taskinen, Marja-Riitta, Borén, Jan
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 06.03.2018
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Summary:A carbohydrate-restricted diet is a widely recommended intervention for non-alcoholic fatty liver disease (NAFLD), but a systematic perspective on the multiple benefits of this diet is lacking. Here, we performed a short-term intervention with an isocaloric low-carbohydrate diet with increased protein content in obese subjects with NAFLD and characterized the resulting alterations in metabolism and the gut microbiota using a multi-omics approach. We observed rapid and dramatic reductions of liver fat and other cardiometabolic risk factors paralleled by (1) marked decreases in hepatic de novo lipogenesis; (2) large increases in serum β-hydroxybutyrate concentrations, reflecting increased mitochondrial β-oxidation; and (3) rapid increases in folate-producing Streptococcus and serum folate concentrations. Liver transcriptomic analysis on biopsy samples from a second cohort revealed downregulation of the fatty acid synthesis pathway and upregulation of folate-mediated one-carbon metabolism and fatty acid oxidation pathways. Our results highlight the potential of exploring diet-microbiota interactions for treating NAFLD. [Display omitted] •A low-carbohydrate diet (LCD) improves liver fat metabolism in NAFLD patients•The LCD promotes rapid shifts in the gut microbiota composition of NAFLD patients•The LCD-induced microbial changes are associated with increased circulating folate•The LCD increases folate-dependent one-carbon metabolism gene expression in liver Mardinoglu et al. use multi-omics to investigate the effects of a carbohydrate-restricted diet in obese NAFLD patients. They show that the diet improves liver fat metabolism, promotes rapid shifts in the gut microbiota, increases circulating folate, and upregulates expression of genes involved in folate-dependent one-carbon metabolism in the liver.
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M.-R.T., H.-U.M., K.H.P., F.B., K.J.W., N.M., and S.S. were involved in study design. S.M.R., S.S., N.M., and M.G. were involved in clinical studies in the first cohort. A.H. and N.L. collected and analyzed the magnetic resonance data of the first cohort. H.-U.M. and G.B. were involved in clinical studies in the second cohort. A.M., C.Z., and S.L. performed the transcriptome pre-processing and integration with metabolomics data using GEM. E.B. performed the pre-processing of the inflammation markers. R.M.M. and S.R. performed genetic screening and helped with the metadata preparation. B.D.P., J.N., M. Snyder, M.A., and M.U. were involved in data analyses. H.W. conducted computational and statistical analyses as well as data visualization. M.B. assisted in metagenomic analysis. M. Ståhlman and P.-O.B. measured the fecal SCFA and folate and performed lipidomics analyses. H.W., R.P., and J.B. wrote the paper. Corresponding authors: F.B. is responsible for analyses related to the gut microbiome, and J.B. is responsible for all other parts of the study. All authors commented on the manuscript.
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ISSN:1550-4131
1932-7420
1932-7420
DOI:10.1016/j.cmet.2018.01.005