Evidence map›Paper›PMID 37246815›Full record

Trial reportMovement disorders : official journal of the Movement Disorder Society2023

A Double-Blind, Randomized, Placebo-Controlled Trial of Ursodeoxycholic Acid (UDCA) in Parkinson's Disease.

Thomas Payne, Matthew Appleby, Ellen Buckley, Linda M A van Gelder, Benjamin H Mullish, Matilde Sassani, Mark J Dunning, Dena Hernandez, Sonja W Scholz, Alisdair McNeill and 9 more

Open access · hybridAbstract readRandomized Controlled TrialClinical Trial, Phase II
In one paragraph

Trial report in Movement disorders : official journal of the Movement Disorder Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
9.9field-weighted citation impact, top 1% 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

42 citing papers in PubMed, 48 citations in OpenAlex.

  1. Gut microbes · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Emerging Roles of Bile Acids in Neuroinflammation.International journal of molecular sciences · 2025
    Review
  19. Article
  20. 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

19 authors at 11 institutions in 4 countries.

Thomas PayneSheffield Institute for Translational Neuroscience, The University of Sheffield, Sheffield, UK.
Matthew ApplebyNIHR UCLH Clinical Research Facility-Leonard Wolfson Experimental Neurology Centre, National Hospital for Neurology & Neurosurgery, London, UK.
Ellen BuckleyDepartment of Mechanical Engineering and Insigneo Institute for In Silico Medicine, The University of Sheffield, Sheffield, UK.
Linda M A van GelderDepartment of Mechanical Engineering and Insigneo Institute for In Silico Medicine, The University of Sheffield, Sheffield, UK.
Benjamin H MullishDivision of Digestive Diseases, Department of Metabolism, Digestion and Reproduction, St Mary's Hospital Campus, Imperial College London, London, UK.ORCID 0000-0001-6300-3100
Matilde SassaniSheffield Institute for Translational Neuroscience, The University of Sheffield, Sheffield, UK.
Mark J DunningSheffield Institute for Translational Neuroscience, The University of Sheffield, Sheffield, UK.
Dena HernandezMolecular Genetics Section, Laboratory of Neurogenetics, Bethesda, Maryland, USA.
Sonja W ScholzNeurodegenerative Diseases Research Unit, Laboratory of Neurogenetics, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.ORCID 0000-0002-6623-0429
Alisdair McNeillSheffield Institute for Translational Neuroscience, The University of Sheffield, Sheffield, UK.
Vincenzo LibriNIHR UCLH Clinical Research Facility-Leonard Wolfson Experimental Neurology Centre, National Hospital for Neurology & Neurosurgery, London, UK.
Sarah MollNIHR Sheffield Biomedical Research Centre, Royal Hallamshire Hospital, Sheffield, UK.
Julian R MarchesiDivision of Digestive Diseases, Department of Metabolism, Digestion and Reproduction, St Mary's Hospital Campus, Imperial College London, London, UK.
Rosie TaylorStatistical Services Unit, The University of Sheffield, Sheffield, UK.
Li SuSheffield Institute for Translational Neuroscience, The University of Sheffield, Sheffield, UK.
Claudia MazzàDepartment of Mechanical Engineering and Insigneo Institute for In Silico Medicine, The University of Sheffield, Sheffield, UK.
Thomas M JenkinsSheffield Institute for Translational Neuroscience, The University of Sheffield, Sheffield, UK.
Thomas FoltynieDepartment of Clinical and Movement Neurosciences, Institute of Neurology, University College London, London, UK.ORCID 0000-0003-0752-1813
Oliver BandmannSheffield Institute for Translational Neuroscience, The University of Sheffield, Sheffield, UK.ORCID 0000-0003-3149-0252
University of Sheffield · GBInsigneo · GBNational Hospital for Neurology and Neurosurgery · GBSt Mary's Hospital · GBLaboratory of Molecular Genetics · PLNational Institutes of Health · USRoyal Hallamshire Hospital · GBRoyal Perth Hospital · AUStatistical Research (United States) · USUniversity College London · GBUniversity of Cambridge · GB

Funding

Genetic characterization of atypical parkinsonismZIANS003154 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI SCHOLZ, SONJA · 2016 to 2025
$15.4M
Department of Health CL-2019-21-002Intramural NIH HHS ZIA NS003154Medical Research Council MC_PC_12025
6 · The paper itself

Abstract

backgroundRescue of mitochondrial function is a promising neuroprotective strategy for Parkinson's disease (PD). Ursodeoxycholic acid (UDCA) has shown considerable promise as a mitochondrial rescue agent across a range of preclinical in vitro and in vivo models of PD.

objectivesTo investigate the safety and tolerability of high-dose UDCA in PD and determine midbrain target engagement.

methodsThe UP (UDCA in PD) study was a phase II, randomized, double-blind, placebo-controlled trial of UDCA (30 mg/kg daily, 2:1 randomization UDCA vs. placebo) in 30 participants with PD for 48 weeks. The primary outcome was safety and tolerability. Secondary outcomes included 31-phosphorus magnetic resonance spectroscopy (

resultsUDCA was safe and well tolerated, and only mild transient gastrointestinal adverse events were more frequent in the UDCA treatment group. Midbrain

conclusionsHigh-dose UDCA is safe and well tolerated in early PD. Larger trials are needed to further evaluate the disease-modifying effect of UDCA in PD. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Parkinson DiseaseDouble-Blind MethodHumansUrsodeoxycholic AcidUrsodeoxycholic Acid31P-MR spectroscopyneuroprotectionsupervised gait analysisUDCAursodeoxycholic acid

Identifiers

PMID37246815
PMCPMC10527073
OpenAlexW4378640215

What OpenQuestion holds

Textmetadata
LicenceTDM
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.