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

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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.

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          In Brief

          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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          Author and article information

          Journal
          101233170
          32527
          Cell Metab
          Cell Metab.
          Cell metabolism
          1550-4131
          1932-7420
          24 July 2019
          15 February 2018
          06 March 2018
          22 August 2019
          : 27
          : 3
          : 559-571.e5
          Affiliations
          [1 ]Sciencefor Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden
          [2 ]Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden
          [3 ]Department of Molecular and Clinical Medicine, University of Gothenburg, and Sahlgrenska University Hospital, Gothenburg, Sweden
          [4 ]HUS Medical Imaging Center, Radiology, Helsinki University Hospital, University of Helsinki, Helsinki, Finland
          [5 ]Research Programs Unit, Diabetes and Obesity, University of Helsinki and Department of Internal Medicine, Helsinki University Hospital, Helsinki, Finland
          [6 ]Endocrinology, Abdominal Center, Helsinki University Hospital, Helsinki, Finland
          [7 ]Department of Genetics, Stanford University, Stanford, CA 94305, USA
          [8 ]These authors contributed equally
          [9 ]Lead Contact
          Author notes

          AUTHOR CONTRIBUTIONS

          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.

          Article
          PMC6706084 PMC6706084 6706084 nihpa1038351
          10.1016/j.cmet.2018.01.005
          6706084
          29456073
          d0682c16-685b-4462-81bb-6bd266d46d13
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