Abstract | AIM: To determine diagnostic accuracy of HLA-B*57:01 testing for prediction of abacavir-induced hypersensitivity and to quantify the clinical benefit of pretreatment screening through a meta-analytic review of published studies. METHODS: A comprehensive search was performed up to June 2013. The methodological quality of relevant studies was assessed by the QUADAS-2 tool. The pooled diagnostic estimates were calculated using a random effect model. RESULTS: Despite the presence of heterogeneity in sensitivity or specificity estimates, the pooled diagnostic odds ratio to detect abacavir-induced hypersensitivity on the basis of clinical criteria was 33.07 (95% CI: 22.33-48.97, I(2): 13.9%), while diagnostic odds ratio for detection of immunologically confirmed abacavir hypersensitivity was 1141 (95% CI: 409-3181, I(2): 0%). Pooled analysis of risk ratio showed that prospective HLA-B*57:01 testing significantly reduced the incidence of abacavir-induced hypersensitivity. CONCLUSION: This meta-analysis demonstrates an excellent diagnostic accuracy of HLA-B*57:01 testing to detect immunologically confirmed abacavir hypersensitivity and corroborates existing recommendations.
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Authors | Sarah Cargnin, Claudio Jommi, Pier Luigi Canonico, Armando A Genazzani, Salvatore Terrazzino |
Journal | Pharmacogenomics
(Pharmacogenomics)
Vol. 15
Issue 7
Pg. 963-76
(May 2014)
ISSN: 1744-8042 [Electronic] England |
PMID | 24956250
(Publication Type: Journal Article, Meta-Analysis, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anti-HIV Agents
- Dideoxynucleosides
- HLA-B Antigens
- HLA-B*57:01 antigen
- abacavir
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Topics |
- Anti-HIV Agents
(therapeutic use)
- Dideoxynucleosides
(adverse effects, therapeutic use)
- Drug Hypersensitivity
(genetics, pathology)
- Genetic Testing
- HIV Infections
(drug therapy, genetics)
- HLA-B Antigens
(genetics)
- Humans
- Pharmacogenetics
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