<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ahmad J</submitter><funding>NIDDK NIH HHS</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><pagination>e16242</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11790010</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>45(2)</volume><pubmed_abstract>&lt;h4>Background and aims&lt;/h4>Short courses of intravenous (iv) methylprednisolone (MP) can cause drug induced liver injury (DILI). The aim of this study was to assess the clinical features and HLA associations of MP-related DILI enrolled in the US DILI Network (DILIN).&lt;h4>Methods&lt;/h4>DILIN cases with MP as a suspected drug were reviewed. DILIN causality scoring was assigned on a 5-point scale (definite, highly likely, probable, possible, unlikely). All cases with MP causality scores of definite, highly likely or probable were analysed. HLA data from direct sequencing were analysed.&lt;h4>Results&lt;/h4>Eleven cases of definite, highly likely, or probable MP DILI were identified. The median age was 48 years; 73% were female; median latency to onset was 30 days; 55% were jaundiced; and all had hepatocellular injury with one patient requiring transplantation. Nine of the 11 cases were in patients with multiple sclerosis (MS). Liver biopsies in 7 cases revealed mild acute hepatitis with/without cholestasis. HLA data demonstrated that HLA-DRB1*15:01, the primary HLA class II allele associated with MS was over-represented. HLA-DQB1*06:02-HLA-DQA1*01:02 which is haplotypic with the HLA-DRB1*15 haplotype was more common in the MP DILI cases compared to other DILI controls (p = 0.03) and to DILI controls exposed to MP (p = 0.04).&lt;h4>Conclusion&lt;/h4>MP DILI is characterised by hepatocellular injury, short latency and generally rapid recovery. There was no independent HLA haplotype associated with MP DILI.</pubmed_abstract><journal>Liver international : official journal of the International Association for the Study of the Liver</journal><pubmed_title>Liver Injury due to Intravenous Methylprednisolone in the Drug-Induced Liver Injury Network.</pubmed_title><pmcid>PMC11790010</pmcid><funding_grant_id>U01 DK065201</funding_grant_id><funding_grant_id>U01 DK065211</funding_grant_id><funding_grant_id>U01 DK083020</funding_grant_id><funding_grant_id>U01 DK065184</funding_grant_id><funding_grant_id>U01 DK083027</funding_grant_id><funding_grant_id>U01 DK100928</funding_grant_id><funding_grant_id>U24 DK065176</funding_grant_id><pubmed_authors>Drug‐Induced Liver Injury Network</pubmed_authors><pubmed_authors>Hayashi PH</pubmed_authors><pubmed_authors>Hoofnagle JH</pubmed_authors><pubmed_authors>Phillips E</pubmed_authors><pubmed_authors>Barnhart HX</pubmed_authors><pubmed_authors>Fontana RJ</pubmed_authors><pubmed_authors>Ahmad J</pubmed_authors><pubmed_authors>Chalasani N</pubmed_authors><pubmed_authors>Dellinger A</pubmed_authors><pubmed_authors>Li YJ</pubmed_authors><pubmed_authors>Kleiner DE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Liver Injury due to Intravenous Methylprednisolone in the Drug-Induced Liver Injury Network.</name><description>&lt;h4>Background and aims&lt;/h4>Short courses of intravenous (iv) methylprednisolone (MP) can cause drug induced liver injury (DILI). The aim of this study was to assess the clinical features and HLA associations of MP-related DILI enrolled in the US DILI Network (DILIN).&lt;h4>Methods&lt;/h4>DILIN cases with MP as a suspected drug were reviewed. DILIN causality scoring was assigned on a 5-point scale (definite, highly likely, probable, possible, unlikely). All cases with MP causality scores of definite, highly likely or probable were analysed. HLA data from direct sequencing were analysed.&lt;h4>Results&lt;/h4>Eleven cases of definite, highly likely, or probable MP DILI were identified. The median age was 48 years; 73% were female; median latency to onset was 30 days; 55% were jaundiced; and all had hepatocellular injury with one patient requiring transplantation. Nine of the 11 cases were in patients with multiple sclerosis (MS). Liver biopsies in 7 cases revealed mild acute hepatitis with/without cholestasis. HLA data demonstrated that HLA-DRB1*15:01, the primary HLA class II allele associated with MS was over-represented. HLA-DQB1*06:02-HLA-DQA1*01:02 which is haplotypic with the HLA-DRB1*15 haplotype was more common in the MP DILI cases compared to other DILI controls (p = 0.03) and to DILI controls exposed to MP (p = 0.04).&lt;h4>Conclusion&lt;/h4>MP DILI is characterised by hepatocellular injury, short latency and generally rapid recovery. There was no independent HLA haplotype associated with MP DILI.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2026-06-16T07:24:34.288Z</modification><creation>2026-06-16T03:10:09.949Z</creation></dates><accession>S-EPMC11790010</accession><cross_references><pubmed>39803998</pubmed><doi>10.1111/liv.16242</doi></cross_references></HashMap>