Evidence map›Paper›PMID 34095797›Full record

ArticleJHEP reports : innovation in hepatology2021

Hepatic bile acid transport increases in the postprandial state: A functional

Nikolaj W Ørntoft, Lars C Gormsen, Susanne Keiding, Ole L Munk, Peter Ott, Michael Sørensen

Open access · goldAbstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Bile acid metabolism in type 2 diabetes mellitus.Nature reviews. Endocrinology · 2025
    Review
  4. Article
  5. Article
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

6 authors at 1 institution in 1 country.

Nikolaj W ØrntoftDepartment of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.
Lars C GormsenDepartment of Nuclear Medicine & PET Centre, Aarhus University Hospital, Aarhus, Denmark.
Susanne KeidingDepartment of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.
Ole L MunkDepartment of Nuclear Medicine & PET Centre, Aarhus University Hospital, Aarhus, Denmark.
Peter OttDepartment of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.
Michael SørensenDepartment of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.
Aarhus University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsIt is not known how hepatic bile acids transport kinetics changes postprandially in the intact liver. We used positron emission tomography (PET)/computed tomography (CT) with the tracer [

methodsSix healthy human participants underwent dynamic liver

resultsIn the postprandial state, hepatic blood perfusion increased on average by 30% (

conclusionsThe rate constant for the transport of bile acids from hepatocytes into biliary canaliculi and the bile flow increased significantly in the postprandial state. This reduced the mean LAY SUMMARY: Bile acids are important for digestion of dietary lipids including vitamins. We examined how the secretion of bile acids by the liver into the intestines changes after a standard liquid meal. The transport of bile acids from liver cells into bile and bile flow was increased after the meal.

Indexed as

11C-CSar, [N-methyl-11C]cholylsarcosineBSEP, bile salt export pumpCT, computed tomographyFGF-19, fibroblast growth factor 19FXR, farnesoid X receptorHepatobiliary kineticsICG, indocyanine greenLiver physiologyliver-VOI, liver volume of interestNTCP, Na+ taurocholate co-transporting polypeptidePET, positron emission tomographyPositron emission tomography

Identifiers

PMID34095797
PMCPMC8165435
OpenAlexW3153611483

What OpenQuestion holds

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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.