Frontiers in Pharmacology · 2019 · 26 citations · 21 references
Life SciencesGeneticsPharmacologyHuman GeneticsImmunogeneticsPharmacogeneticsGenotype-phenotype Association AnalysisHla TypingPharmacoepidemiologyPharmacogenetic TestingPharmacogenomic TestingPopulation PharmacogeneticsDrug Hypersensitivity ReactionsGenetic Risk MarkersHigh-resolution Hla TypingHla Genotype AssociationsHla Risk AllelesHla-associated Adverse Drug ReactionsHuman AncestryMolecular Hla Typing
Purpose HLA-B*15:02 is strongly associated with life-threatening severe skin hypersensitivity reactions in patients treated with carbamazepine and structurally-related medications. FDA-approved labeling recommends HLA-B*15:02 screening before carbamazepine therapy in patients of Asian ancestry. In this study, we aimed to a) identify a direct method for screening HLA-B*15:02, and b) evaluate prevalence in a large cohort of United States (US) patients. Methods Candidate genetic markers were identified by mining public data. Association was tested in 28,897 individuals by comparing SNP results with high-resolution HLA typing. Retrospective analysis of de-identified SNP and ethnicity data from 130,460 individuals was performed to evaluate the ethnic distribution of HLA-B*15:02 in the US. Results 28,897 US individuals showed 100% concordance between HLA-B*15:02 and the minor allele of rs144012689 (100% sensitivity/99.97% specificity). Retrospective analysis of 160 positive individuals (66 with physician-reported ethnicity) notably included 28 Asians (42%), 15 African Americans (22%), 11 Caucasians (17%), 2 Hispanics (3%), and 10 ‘Other’ (15%). Conclusions Screening US patients for HLA-B*15:02 without ethnicity-based preselection identifies more than twice the number of carriers at risk of carbamazepine-related adverse events than screening patients of Asian ancestry alone. Risk assessment based on ethnicity assumptions may not identify a large portion of at-risk patients in the ethnically-diverse US population.
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The International HapMap Project
Richard A. Gibbs, John W. Belmont, Paul Hardenbol et al. · Nature · 2003 · 6.2K citations · Full text
The IPD and IMGT/HLA database: allele variant databases
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Wen‐Hung Chung, Hong‐Shang Hong, Mo‐Song Hsih et al. · Nature · 2004 · 1.7K citations
Faviel F. González-Galarza, Louise Y.C. Takeshita, Eduardo José Melo dos Santos et al. · Nucleic Acids Research · 2014 · 759 citations · Full text
Life Sciences, Genetics, Immunology +17