[16] Thus far, there is no definite proven mechanism, but Sumkrua[15] and Hung[9] have individually made the observation that although HLA-B*5801 plays a central role in allopurinol-related SJS/TEN, it may not be the only factor required for the occurrence of these severe conditions. In addition, most studies have examined the association of allopurinol-related SJS/TEN with HLA-B*5801, so that the interpretation of findings from these studies may only be limited to SJS/TEN cases. However, it should

be noted that a number of studies have also reported the potential association of DRESS (drug rash with eosinophilia and systemic symptoms) and HLA-B*5801.[9, 17] The implication of the strong association of HLA-B*5801 with allopurinol hypersensitivity syndrome is more likely to be significant in populations with

a high prevalence Belinostat cost of HLA-B*5801. Hence, genotype testing may be of benefit to high-risk groups, for example Asians, before treatment with allopurinol. However, http://www.selleckchem.com/products/Lapatinib-Ditosylate.html this test is only available in selected laboratories (e.g. laboratories affiliated to transplant centers), is time-consuming with turnaround times around 3–4 weeks, and may be costly. Formal assessment of the cost-effectiveness of routine HLA-B*5801 testing is not available. Somkrua[18] studied the range of genotyping costs that would be cost-effective from the healthcare provider perspective and found that the most influential parameters were the cost of genotyping and SJS/TEN management. Pharmacogenetic screening seemed to be cost-effective if the cost fell in the range of 393–1085 THB (US$13–35). In their attempt to expedite the application of pharmacogenomic information to proper PLEK2 use of allopurinol in the clinical situation, Maekawa[19] and his group have developed a polymerase chain reaction-restriction fragment length polymorphism (PCR-RLP) assay which is based on their demonstration that several single nucleotide polymorphisms

(SNPs) around the HLA region on chromosome 6 were strongly linked with HLA-B*5801. They claim that their use of this surrogate biomarker for carriers of HLA-B*5801 is a robust and inexpensive assay for the screening of subjects prior to starting allopurinol treatment. On the other hand, Lee et al.[20] have commented that utilization of HLA-B*5801 alone as a population screening test even in a Southeast Asian population is not effective. They argue that although the negative predictive value and sensitivity of HLA-B*5801 in cases of allopurinol-induced SJS/TEN are very high, the positive predictive value (of the screening test) of developing allopurinol hypersensitivity is low because of the very low incidence of allopurinol hypersensitivity itself and the relatively high prevalence of HLA-B*5801 in the Southeast Asian population.