alexa High sensitivity of human leukocyte antigen-b*5701 as a marker for immunologically confirmed abacavir hypersensitivity in white and black patients.
Pharmaceutical Sciences

Pharmaceutical Sciences

Journal of Pharmacogenomics & Pharmacoproteomics

Author(s): Saag M, Balu R, Phillips E, Brachman P, Martorell C,

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Abstract BACKGROUND: Although the human leukocyte antigen (HLA)-B*5701 is highly associated with a hypersensitivity reaction (HSR) to abacavir (ABC), variable sensitivities have been reported when clinical data alone have been used to define an ABC HSR. This study evaluated the sensitivity of detection of the HLA-B*5701 allele as a marker of ABC HSRs in both white and black patients, using skin patch testing to supplement clinical diagnosis. METHODS: White and black patients, identified through chart review, were classified as having received a diagnosis of an ABC HSR based on clinical findings only (a clinically suspected ABC HSR) or based on clinical findings and a positive skin patch test result (an immunologically confirmed [IC] ABC HSR). Control subjects were racially matched subjects who tolerated ABC for >/=12 weeks without experiencing an ABC HSR. Patients and control subjects were tested for the presence of HLA-B*5701. Sensitivity, specificity, and odds ratios for the detection of HLA-B*5701 as a marker for an ABC HSR were calculated for white and black participants. RESULTS: Forty-two (32.3\%) of 130 white patients and 5 (7.2\%) of 69 black patients who met the criteria for clinically suspected HSRs had IC HSRs. All 42 white patients with IC HSRs were HLA-B*5701 positive (sensitivity, 100\%; odds ratio, 1945; 95\% confidence interval, 110-34,352). Among all white patients with clinically suspected HSRs, sensitivity was 44\% (57 of 130 patients tested positive for HLA-B*5701); specificity among white control subjects was 96\%. Five of 5 black patients with IC HSRs were HLA-B*5701 positive (sensitivity, 100\%; odds ratio, 900; 95\% confidence interval, 38-21,045). Among black patients with clinically suspected HSRs, the sensitivity was 14\% (10 of 69 tested positive for HLA-B*5701); specificity among black control subjects was 99\%. CONCLUSIONS: Although IC ABC HSRs are uncommon in black persons, the 100\% sensitivity of HLA-B*5701 as a marker for IC ABC HSRs in both US white and black patients suggests similar implications of the association between HLA-B*5701 positivity and risk of ABC HSRs in both races. This article was published in Clin Infect Dis and referenced in Journal of Pharmacogenomics & Pharmacoproteomics

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