Evidence map›Paper›PMID 33214235›Full record

ReviewBMJ open gastroenterology2020

Androgenic anabolic steroid-induced liver injury: two case reports assessed for causality by the updated Roussel Uclaf Causality Assessment Method (RUCAM) score and a comprehensive review of the literature.

Robin Daniel Abeles, Matthew Foxton, Shahid Khan, Robert Goldin, Belinda Smith, Mark R Thursz, Suman Verma

Open access · goldAbstract readCase ReportsReview
In one paragraph

Review in BMJ open gastroenterology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Selective Androgen Receptor Modulators: An Emerging Liver Toxin.Journal of clinical and translational hepatology · 2023
    Review
  10. Review
  11. Anabolic androgenic steroid-induced liver injury: An update.World journal of gastroenterology · 2022
    Review
  12. Review
  13. Review
  14. Versatility of Anabolic Androgenic Steroid-Induced Hepatotoxicity.Journal of clinical and experimental hepatology
    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

7 authors at 2 institutions in 3 countries.

Robin Daniel AbelesDivison of Surgery and Cancer, Department of Digestive Diseases, St Mary's Hospital, Imperial College London, London, UK r.abeles@imperial.ac.uk.ORCID 0000-0002-1527-4456
Matthew FoxtonDepartment of Hepatology, Chelsea and Westminster Healthcare NHS Trust, London, UK.
Shahid KhanDivison of Surgery and Cancer, Department of Digestive Diseases, St Mary's Hospital, Imperial College London, London, UK.
Robert GoldinCentre for Pathology, St Mary's Hospital, Imperial College, London, UK.
Belinda SmithDivison of Surgery and Cancer, Department of Digestive Diseases, St Mary's Hospital, Imperial College London, London, UK.
Mark R ThurszDivison of Surgery and Cancer, Department of Digestive Diseases, St Mary's Hospital, Imperial College London, London, UK.
Suman VermaDepartment of Hepatology, Chelsea and Westminster Healthcare NHS Trust, London, UK.
St Mary's Hospital · GBChelsea and Westminster Hospital NHS Foundation Trust · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundAnabolic androgenic steroids (AAS) usage is widespread and increasing. AAS drug-induced liver injury (DILI) is recognised but its clinical course and management is poorly described. We report 2 cases of AAS DILI with associated renal dysfunction, managed successfully with oral corticosteroids.

methodsA comprehensive review identified 50 further cases to characterise the clinical and biochemical course. Causality grading was calculated using the updated Roussel Uclaf Causality Assessment Method (RUCAM) score. Data are presented as median values.

resultsThe most common AAS taken was methyldrostanolone. Patients commonly present with jaundice and pruritus but may exhibit other constitutional symptoms. Patients presented 56 days after starting, and bilirubin peaked 28 days after stopping, AAS. Causality assessment was 'unlikely' in 1 (2%), 'possible' in 31 (60%) and 'probable' in 20 (38%). Peak values were: bilirubin 705 μmol/L, alanine transaminase 125 U/L, aspartate transaminase 71 U/L, alkaline phosphatase 262 U/L, gamma-glutamyl transferase 52 U/L, international normalised ratio 1.1. Liver biopsies showed 'bland' canalicular cholestasis. 43% of patients developed kidney injury (peak creatinine 225 μmol/L). Therapies included antipruritics, ursodeoxycholic acid and corticosteroids. No patients died or required liver transplantation.

conclusionsPhysicians are likely to encounter AAS DILI. Causality assessment using the updated RUCAM should be performed but defining indications and proving efficacy for therapies remains challenging.

Indexed as

Chemical and Drug Induced Liver InjuryChemical and Drug Induced Liver Injury, ChronicJaundiceHumansTestosterone CongenersTestosterone Congenersacute hepatitisdrug induced hepatotoxicitydrug induced liver injuryliver biopsy

Identifiers

PMID33214235
PMCPMC7678230
OpenAlexW3106060388

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.