Evidence mapPaperPMID 39377212Full record

Trial reportJournal of the American Heart Association2024

Ursodeoxycholic Acid for Trans Intestinal Cholesterol Excretion Stimulation: A Randomized Placebo Controlled Crossover Study.

Reindert F Oostveen, Yannick Kaiser, Merel L Hartgers, Emma C E Meessen, Aldo Grefhorst, G Kees Hovingh, Folkert Kuipers, Erik S G Stroes, Albert K Groen, Laurens F Reeskamp

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of the American Heart Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
field-weighted citation impact
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

4 citing papers in PubMed.

  1. Protective Effects ofJournal of microbiology and biotechnology · 2026
    Article
  2. Review
  3. Review
  4. 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

10 authors.

Reindert F OostveenDepartment of Vascular Medicine, Amsterdam Cardiovascular Sciences Amsterdam UMC, University of Amsterdam The Netherlands.ORCID 0000-0001-7182-2886
Yannick KaiserDepartment of Vascular Medicine, Amsterdam Cardiovascular Sciences Amsterdam UMC, University of Amsterdam The Netherlands.
Merel L HartgersDepartment of Vascular Medicine, Amsterdam Cardiovascular Sciences Amsterdam UMC, University of Amsterdam The Netherlands.
Emma C E MeessenDepartment of Endocrinology and Metabolism Amsterdam UMC, University of Amsterdam The Netherlands.
Aldo GrefhorstDepartment of Experimental Vascular Medicine Amsterdam UMC, University of Amsterdam The Netherlands.ORCID 0000-0003-1761-9494
G Kees HovinghDepartment of Vascular Medicine, Amsterdam Cardiovascular Sciences Amsterdam UMC, University of Amsterdam The Netherlands.ORCID 0000-0002-8145-1676
Folkert KuipersDepartment of Pediatrics University Medical Center Groningen, University of Groningen The Netherlands.ORCID 0000-0003-2518-737X
Erik S G StroesDepartment of Vascular Medicine, Amsterdam Cardiovascular Sciences Amsterdam UMC, University of Amsterdam The Netherlands.ORCID 0009-0000-7584-7677
Albert K GroenDepartment of Endocrinology and Metabolism Amsterdam UMC, University of Amsterdam The Netherlands.ORCID 0000-0002-9942-1854
Laurens F ReeskampDepartment of Vascular Medicine, Amsterdam Cardiovascular Sciences Amsterdam UMC, University of Amsterdam The Netherlands.ORCID 0000-0002-8043-951X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe trans intestinal cholesterol excretion (TICE) pathway is a potential therapeutic target to reduce plasma low-density lipoprotein (LDL) cholesterol levels. TICE encompasses the direct excretion of cholesterol by enterocytes into feces. In mice, TICE has been shown to be stimulated by a hydrophilic bile acid pool, resulting in increased fecal neutral sterol loss and reduced plasma cholesterol levels. We investigated whether treatment with a hydrophilic bile acid, ursodeoxycholic acid (UDCA), would increase fecal neutral sterols in humans as a proxy for TICE. METHODS AND

resultsWe performed a randomized, double-blind, placebo-controlled, cross-over trial in 20 male participants aged >18 years, with plasma LDL cholesterol levels ≥2.6 mmol/L. After a run-in period of ezetimibe 20 mg once daily for 3 weeks, patients were randomized to UDCA 600 mg or placebo orally once daily for 2 weeks. After a 3 week washout, patients underwent the alternate treatment. At baseline, mean (SD) age, body mass index, and plasma LDL cholesterol were 59±11.3 years, 26.4±3.1 kg/m

conclusionsUDCA in combination with ezetimibe increased plasma bile acid hydrophilicity in healthy subjects with LDL cholesterol levels >2.6 mmol/L but did not result in increased fecal neutral sterols or decreased LDL cholesterol. This suggests that TICE is not stimulated by an increase in the hydrophilicity of the bile acid pool in humans.

Indexed as

Cholesterol, LDLCross-Over StudiesFecesUrsodeoxycholic AcidAgedAnticholesteremic AgentsCholesterolDouble-Blind MethodEzetimibeHumansIntestinal EliminationMaleMiddle AgedTreatment OutcomeAnticholesteremic AgentsCholesterolCholesterol, LDLEzetimibeUrsodeoxycholic Acidezetimibelipidstrans intestinal cholesterol excretionursodeoxycholic acid

Identifiers

PMID39377212
PMCPMC11935591

What Socratic holds

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Registered trials

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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 Socratic graph.