Evidence map›Paper›PMID 30229970›Full record

ArticleHepatology (Baltimore, Md.)2019

Fine-Tuning of Sirtuin 1 Expression Is Essential to Protect the Liver From Cholestatic Liver Disease.

Britt A Blokker, Monica Maijo, Marta Echeandia, Mikel Galduroz, Angela M Patterson, Anna Ten, Mark Philo, Rebecca Schungel, Virginia Gutierrez-de Juan, Emina Halilbasic and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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  4. Article
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  6. Article
  7. Involvement of SIRT1-mediated aging in liver diseases.Frontiers in cell and developmental biology · 2025
    Review
  8. Review
  9. Review
  10. Article
  11. Review
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  13. Article
  14. Role and Regulation of Hepatobiliary ATP-Binding Cassette Transporters during Chemical-Induced Liver Injury.Drug metabolism and disposition: the biological fate of chemicals · 2022
    Review
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  16. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors at 8 institutions in 4 countries.

Britt A BlokkerNorwich Medical School, University of East Anglia, Norwich, United Kingdom.
Monica MaijoGut Microbes and Health Institute Strategic Programme, Quadram Institute, Norwich, United Kingdom.
Marta EcheandiaGut Microbes and Health Institute Strategic Programme, Quadram Institute, Norwich, United Kingdom.
Mikel GaldurozGut Microbes and Health Institute Strategic Programme, Quadram Institute, Norwich, United Kingdom.
Angela M PattersonGut Microbes and Health Institute Strategic Programme, Quadram Institute, Norwich, United Kingdom.
Anna TenGut Microbes and Health Institute Strategic Programme, Quadram Institute, Norwich, United Kingdom.
Mark PhiloMetabolomics Unit, Quadram Institute, Norwich, United Kingdom.
Rebecca SchungelGut Microbes and Health Institute Strategic Programme, Quadram Institute, Norwich, United Kingdom.
Virginia Gutierrez-de JuanCIC bioGUNE, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Derio, Spain.
Emina HalilbasicHans Popper Laboratory of Molecular Hepatology, Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University Vienna, Vienna, Austria.
Claudia FuchsHans Popper Laboratory of Molecular Hepatology, Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University Vienna, Vienna, Austria.
Gwenaelle Le GallMetabolomics Unit, Quadram Institute, Norwich, United Kingdom.
Malgorzata MilkiewiczDepartment of Medical Biology, Pomeranian Medical University, Szczecin, Poland.
Piotr MilkiewiczLiver and Internal Medicine Unit, Department of General, Transplant and Liver Surgery, Medical University of Warsaw, Warsaw, Poland.
Jesus M BanalesDepartment of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute, Donostia University Hospital, University of the Basque Country (UPV/EHU), CIBERehd, Ikerbasque, Donostia, Spain.
Simon M RushbrookDepartment of Gastroenterology, Norfolk and Norwich University Hospital, Norwich, United Kingdom.
José M MatoCIC bioGUNE, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Derio, Spain.
Michael TraunerHans Popper Laboratory of Molecular Hepatology, Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University Vienna, Vienna, Austria.
Michael MüllerNorwich Medical School, University of East Anglia, Norwich, United Kingdom.
María Luz Martínez-ChantarCIC bioGUNE, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Derio, Spain.
Marta Varela-ReyCIC bioGUNE, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Derio, Spain.
Naiara BerazaGut Microbes and Health Institute Strategic Programme, Quadram Institute, Norwich, United Kingdom.
Quadram Institute · GBCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas · ESUniversity of East Anglia · GBBiogipuzkoa Health Research Institute · ESCIC bioGUNE · ESMedical University of Warsaw · PLNorfolk and Norwich University Hospital · GBPomeranian Medical University · PL

Funding

Asociación Española contra el CáncerBBVA FoundationBiotechnology and Biological Sciences Research Council BB/J004529/1Biotechnology and Biological Sciences Research Council BBS/E/F/00044509Biotechnology and Biological Sciences Research Council BBS/E/F/000PR10355Camara de Comercio de NavarraEITB Maratoia BIO15/CA/014Fondo Europeo de Desarrollo Regional CON14/00129Gobierno Vasco-Departamento de Salud 2013111114Ikerbaske foundation FIS PI12/00380Ikerbaske foundation FIS PI15/01132Instituto de Salud Carlos III FIS PI12/00380Instituto de Salud Carlos III FIS PI15/01132Instituto de Salud Carlos III PS12/00402Ministry of Economy and Competitiveness, Spain SAF2014-54658-RNRP Science Links Seed Corn Fund
6 · The paper itself

Abstract

Cholestasis comprises aetiologically heterogeneous conditions characterized by accumulation of bile acids in the liver that actively contribute to liver damage. Sirtuin 1 (SIRT1) regulates liver regeneration and bile acid metabolism by modulating farnesoid X receptor (FXR); we here investigate its role in cholestatic liver disease. We determined SIRT1 expression in livers from patients with cholestatic disease, in two experimental models of cholestasis, as well as in human and murine liver cells in response to bile acid loading. SIRT1-overexpressing (SIRT

Indexed as

AnimalsBile Acids and SaltsCase-Control StudiesCholestasisDisease Models, AnimalHepatocytesHumansMiceSirtuin 1Bile Acids and SaltsSIRT1 protein, humanSirt1 protein, mouseSirtuin 1

Identifiers

PMID30229970
PMCPMC6492079
OpenAlexW2891712242

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.