1. HLA-B*5801: utility and cost-effectiveness in the Asia-Pacific Region.
- Author
-
Yeo SI
- Subjects
- Asia, Australasia, Cost-Benefit Analysis, Drug Hypersensitivity Syndrome immunology, Drug Hypersensitivity Syndrome prevention & control, Genetic Predisposition to Disease, Humans, Patient Selection, Phenotype, Predictive Value of Tests, Risk Factors, Stevens-Johnson Syndrome immunology, Stevens-Johnson Syndrome prevention & control, Allopurinol adverse effects, Drug Hypersensitivity Syndrome genetics, Genetic Testing economics, Gout drug therapy, Gout Suppressants adverse effects, HLA-B Antigens genetics, Health Care Costs, Pharmacogenetics economics, Stevens-Johnson Syndrome genetics
- Abstract
Gout is a common condition which is mainly treated with the hypo-uricemic agent, allopurinol. Although allopurinol is generally a well-tolerated drug, there is a small risk of developing potentially fatal complications, such as allopurinol hypersensitivity syndrome. Recent advances in pharmacogenomics have made possible the identification of genes which confer susceptibility to specific drugs. A recent multi-national case-control study has reported allopurinol as the most common drug associated with Stevens-Johnson syndrome and toxic epidermal necrolysis. Several studies have established a strong association between the human leukocyte antigen (HLA)-B*5801 gene and development of Stevens-Johnson syndrome and toxic epidermal necrolysis. The allele frequency of HLA-B*5801 is highest in the South East Asian population.Since other hypo-uricemic agents are available, patients may wish to have HLA-B*5801 testing before being started on allopurinol. As the test for HLA-B*5801 is expensive, time-consuming and only available in selected laboratories, there is a need to evaluate the utility and cost-effectiveness of this test in our region., (© 2013 The Author International Journal of Rheumatic Diseases © 2013 Asia Pacific League of Associations for Rheumatology and Wiley Publishing Asia Pty Ltd.)
- Published
- 2013
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