Drug‐induced liver injury from selective androgen receptor modulators, anabolic‐androgenic steroids and bodybuilding supplements in Australia

Author:

Nash Emily12,Nicoll Amanda3ORCID,Batt Nicholas3,George Jacob45ORCID,Perananthan Varan6ORCID,Prince David78,Wallace Michael910ORCID,Gow Paul11,Vaz Karl11,Chitturi Shivakumar12,Flores Joan Ericka12,Braund Alicia13,Bonnichsen Mark7,Riordan Stephen14,Humphris Jeremy15,Duong Tuan15,McKenzie Catriona16,Liu Ken12ORCID,Strasser Simone I.12ORCID

Affiliation:

1. AW Morrow Gastroenterology and Liver Centre Royal Prince Alfred Hospital Sydney New South Wales Australia

2. Sydney Medical School University of Sydney Sydney New South Wales Australia

3. Eastern Health Melbourne Victoria Australia

4. Storr Liver Centre Westmead Millennium Institute, Westmead Hospital Westmead New South Wales Australia

5. University of Sydney Sydney New South Wales Australia

6. Department of Gastroenterology and Hepatology Westmead Hospital Westmead New South Wales Australia

7. Department of Gastroenterology and Liver Liverpool Hospital Sydney New South Wales Australia

8. Faculty of Medicine University of New South Wales Sydney New South Wales Australia

9. Sir Charles Gairdner Hospital Perth Western Australia Australia

10. Medical School University of Western Australia Perth Western Australia Australia

11. Austin Health Melbourne Victoria Australia

12. The Canberra Hospital Canberra Australian Capital Territory Australia

13. Gold Coast University Hospital Gold Coast Queensland Australia

14. Prince of Wales Hospital Sydney New South Wales Australia

15. The Wollongong Hospital Wollongong New South Wales Australia

16. NSW Health Pathology Sydney New South Wales Australia

Abstract

SummaryBackgroundReports of DILI due to herbal and dietary supplements have been increasing over time.AimsTo characterise clinical, laboratory and histopathological phenotypes and outcomes of drug‐induced liver injury (DILI) due to anabolic‐androgenic steroids (AAS), selective androgen receptor modulators (SARMs), and bodybuilding supplements (BBS) in Australia.MethodsRetrospective case series. Patients presented to nine Australian tertiary hospitals, 2017–2023. DILI was defined biochemically and patients were included if their treating physician attributed DILI to preceding use of AAS, SARMs or BBS. Primary endpoint was time to normalisation of liver biochemistry. Secondary endpoints were hospitalisation for investigation or management of DILI, death attributable to liver injury, and liver transplantation.ResultsTwenty‐three cases of DILI were identified, involving 40 drugs: 18 AAS, 14 SARMs and eight BBS. Patients were predominantly male (22/23), with median age 30 years (IQR 26–42). Most were symptomatic (21/23). Median latency of onset was 58 days (IQR 28–112 days) from drug commencement. Most patients (17/23) were admitted to hospital. Based on updated Roussel Uclaf Causality Assessment Method, DILI was possible in 17/23, probable in 2/23 and unlikely in 4/23. Median time to normalisation of liver biochemistry was 175 days (IQR 70–292 days) from presentation. Three (3/23) were treated with corticosteroids, 14/23 were treated for itch, and one (1/23) underwent liver transplantation. There were no deaths.ConclusionsThe prognosis of DILI from AAS, SARMs and BBS is good although liver transplantation may rarely be required. A detailed drug history is important in uncovering DILI due to these supplements.

Publisher

Wiley

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Drug-induced Liver Injury in Latin America: 10-year Experience of the Latin American DILI (LATINDILI) Network;Clinical Gastroenterology and Hepatology;2024-07

2. Multiple drugs;Reactions Weekly;2024-04-20

3. Editorial: Muscles at the expense of liver injury. Is it worth it?;Alimentary Pharmacology & Therapeutics;2024-03-24

4. Anabolic steroid-associated liver injury;Clinical Liver Disease;2024-01

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