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Volume 16 Issue 8, August 2019

Reviews on microbiota–gut–brain communication, acute pancreatitis and inherited biliary diseases, and commentaries on NAFLD, viral hepatitis and the small intestinal microbiome.

Mouse small bowel myenteric neurons, nerve fibres and muscularis macrophages that control motility, visualized by immunohistochemistry and provided by S. Huerta López and M. Avetisyan, Heuckeroth Group, Children’s Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, USA. Cover design: Laura Marshall.

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Research Highlights

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News & Views

  • Small intestinal bacterial overgrowth (SIBO) has been linked to common gastrointestinal symptoms; yet its precise definition remains elusive. A new study shows that, when it comes to symptom prediction in functional gastrointestinal disorders, high-throughput sequencing analysis of the microbiome and not jejunal aspiration and culture is the clear winner.

    • Eamonn M. M. Quigley
    News & Views
  • A new study shows that a real-world care pathway for patients with NAFLD in primary care can increase the detection of patients with clinically significant liver disease and decrease referrals for patients who could be managed in the community.

    • Patricia C. Valery
    • Elizabeth E. Powell
    News & Views
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Reviews

  • Short-chain fatty acids (SCFAs) are speculated to have a key role in microbiota–gut–brain crosstalk, but the pathways influencing psychological functioning have not been fully elucidated. This Review summarizes existing knowledge of how SCFAs might indirectly or directly mediate psychological processes.

    • Boushra Dalile
    • Lukas Van Oudenhove
    • Kristin Verbeke
    Review Article
  • The incidence of acute pancreatitis is increasing worldwide, and it is one of the most common gastrointestinal causes for hospital admission. In this Review, the authors provide a summary of advances in acute pancreatitis with an emphasis on pathophysiological mechanisms and clinical management.

    • Peter J. Lee
    • Georgios I. Papachristou
    Review Article
  • New knowledge has been steadily acquired in genetic and congenital cholangiopathies. Here, the authors discuss Alagille syndrome, polycystic liver diseases, fibropolycystic liver diseases and cystic fibrosis-related liver disease and the insights that these conditions provide into the mechanisms of acquired cholangiopathies.

    • Luca Fabris
    • Romina Fiorotto
    • Mario Strazzabosco
    Review Article
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