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. 2021 Jan 12;11:573573. doi: 10.3389/fphar.2020.573573

TABLE 4.

HLA associations in SCAR and DILI with possible clinical implications.

Reference Reaction type Drug HLA Ethnicity Screening NPV (%) PPV (%) NNT
(Konvinse et al. (2019)) DRESS Vancomycin A*32:01 European ancestry (6.8%) Pre-emptive♣ 99.99 0.51 75
African American (4%)
Southeast Asian (<1.5%)
(Daly et al., (2009)) DILI Flucloxacillin B*57:01 European ancestry (5–8%) None 99.99 0.14 13,819
African American (2.5%)
African/Asia (<1%)
(Mallal et al. (2002)) AB HS Abacavir B*57:01 Caucasian (5–8%) HIV positive patients 100 55 13
(Hung et al. (2005)) SJS/TEN Allopurinol B*58:01 Han Chinese (9–11%) None 100 3 250
DRESS Caucasian (1–6%)
(Zhang et al. (2013)) SJS/TEN Carbamazepine B*15:02ψ Han Chinese (10–15%) Routine in southeast Asian countries 100 3 1,000
(Zhang et al. (2013)) DRESS Dapsone B*13:01 Papuans/Australian aborigines (28%) Leprosy patients in countries with increased prevalence 99.8 7.8 84
Chinese (2–20%)
Japanese (1.5%)
Indian (1–12%)

AB HS, abacavir hypersensitivity syndrome; DILI, drug-induced liver injury; DRESS, drug reaction with eosinophilia and systemic symptoms; HIV, human immunodeficiency virus; NNT, numbers needed to test (to prevent one case); NPV, negative predictive value; PPV, positive predictive value; SJS/TEN, SJS/TEN, Stevens-Johnson syndrome/toxic epidermal necrolysis. ♣ HLA-A*32:01 testing could have a role in determining the culprit drug (vancomycin) when multiple drugs are implicated in a delayed hypersensitivity reaction.ψ Other described alleles: HLA-B*15:21, HLA-B*15:11, and HLA-B*15:18.