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Susceptibility to Amoxicillin-Clavulanate-Induced Liver Injury Is Influenced by Multiple HLA Class I and II Alleles

Susceptibility to Amoxicillin-Clavulanate-Induced Liver Injury Is Influenced by Multiple HLA Class I and II Alleles

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Authors

  • M. Isabel Lucena
  • Mariam Molokhia
  • Yufeng Shen
  • Thomas J. Urban
  • Guruprasad P. Aithal
  • Raul J. Andrade
  • Christopher P. Day
  • Francisco Ruiz-Cabello
  • Peter T. Donaldson
  • Camilla Stephens
  • Munir Pirmohamed
  • Manuel Romero-Gomez
  • Jose Maria Navarro
  • Robert J. Fontana
  • Michael Miller
  • Max Groome
  • Emmanuelle Bondon-Guitton
  • Anita Conforti
  • Bruno H. C. Stricker
  • Alfonso Carvajal
  • And 12 others
  • Luisa Ibanez
  • Qun-Ying Yue
  • Michel Eichelbaum
  • Aris Floratos
  • Itsik Pe'er
  • Mark J. Daly
  • David B. Goldstein
  • John F. Dillon
  • Matthew R. Nelson
  • Paul B. Watkins
  • Ann K. Daly
  • Int SAEC, EUDRAGENE, Spanish DILI Registry, DILIGEN, DILIN

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Info

Original languageEnglish
Pages338-347
Number of pages10
JournalGastroenterology
Journal publication date2011
Volume141
Issue1
DOIs
StatePublished

Abstract

BACKGROUND & AIMS: Drug-induced liver injury (DILI), especially from antimicrobial agents, is an important cause of serious liver disease. Amoxicillin-clavulanate (AC) is a leading cause of idiosyncratic DILI, but little is understood about genetic susceptibility to this adverse reaction. METHODS: We performed a genome-wide association study using 822,927 single nucleotide polymorphism (SNP) markers from 201 White European and US cases of DILI following AC administration (AC-DILI) and 532 population controls, matched for genetic background. RESULTS: AC-DILI was associated with many loci in the major histocompatibility complex. The strongest effect was with an HLA class II SNP (rs9274407, P = 4.8 X 10(-14)), which correlated with rs3135388, a tag SNP of HLA-DRB1*1501-DQB1*0602 that was previously associated with AC-DILI. Conditioned on rs3135388, rs9274407 is still significant (P = 1.1 X 10(-4)). An independent association was observed in the class I region (rs2523822, P = 1.8 X 10(-10)), related to HLA-A*0201. The most significant class I and II SNPs showed statistical interaction (P = .0015). High-resolution HLA genotyping (177 cases and 219 controls) confirmed associations of HLA-A*0201 (P = 2 X 10(-6)) and HLA-DQB1*0602 (P = 5 X 10(-10)) and their interaction (P = .005). Additional, population-dependent effects were observed in HLA alleles with nominal significance. In an analysis of autoimmune- related genes, rs2476601 in the gene PTPN22 was associated (P = 1.3 X 10(-4)). CONCLUSIONS: Class I and II HLA genotypes affect susceptibility to AC-DILI, indicating the importance of the adaptive immune response in pathogenesis. The HLA genotypes identified will be useful in studies of the pathogenesis of AC-DILI but have limited utility as predictive or diagnostic biomarkers because of the low positive predictive values.

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