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Recommendations for HLA-B*15:02 and HLA-A*31:01 genetic testing to reduce the risk of carbamazepine-induced hypersensitivity reactions.

Authors :
Amstutz, Ursula
Shear, Neil H.
Rieder, Michael J.
Hwang, Soomi
Fung, Vincent
Nakamura, Hidefumi
Connolly, Mary B.
Ito, Shinya
Carleton, Bruce C.
Source :
Epilepsia (Series 4). Apr2014, Vol. 55 Issue 4, p496-506. 11p.
Publication Year :
2014

Abstract

Objective To systematically review evidence on genetic risk factors for carbamazepine ( CBZ)-induced hypersensitivity reactions ( HSRs) and provide practice recommendations addressing the key questions: (1) Should genetic testing for HLA-B*15:02 and HLA-A*31:01 be performed in patients with an indication for CBZ therapy to reduce the occurrence of CBZ-induced HSRs? (2) Are there subgroups of patients who may benefit more from genetic testing for HLA-B*15:02 or HLA-A*31:01 compared to others? (3) How should patients with an indication for CBZ therapy be managed based on their genetic test results? Methods A systematic literature search was performed for HLA-B*15:02 and HLA-A*31:01 and their association with CBZ-induced HSRs. Evidence was critically appraised and clinical practice recommendations were developed based on expert group consensus. Results Patients carrying HLA-B*15:02 are at strongly increased risk for CBZ-induced Stevens-Johnson syndrome/toxic epidermal necrolysis ( SJS/ TEN) in populations where HLA-B*15:02 is common, but not CBZ-induced hypersensitivity syndrome ( HSS) or maculopapular exanthema ( MPE). HLA-B*15:02-positive patients with CBZ- SJS/ TEN have been reported from Asian countries only, including China, Thailand, Malaysia, and India. HLA-B*15:02 is rare among Caucasians or Japanese; no HLA-B*15:02-positive patients with CBZ- SJS/ TEN have been reported so far in these groups. HLA-A*31:01-positive patients are at increased risk for CBZ-induced HSS and MPE, and possibly SJS/ TEN and acute generalized exanthematous pustulosis ( AGEP). This association has been shown in Caucasian, Japanese, Korean, Chinese, and patients of mixed origin; however, HLA-A*31:01 is common in most ethnic groups. Not all patients carrying either risk variant develop an HSR, resulting in a relatively low positive predictive value of the genetic tests. Significance This review provides the latest update on genetic markers for CBZ HSRs, clinical practice recommendations as a basis for informed decision making regarding the use of HLA-B*15:02 and HLA-A*31:01 genetic testing in patients with an indication for CBZ therapy, and identifies knowledge gaps to guide future research. A PowerPoint slide summarizing this article is available for download in the Supporting Information section . [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00139580
Volume :
55
Issue :
4
Database :
Academic Search Index
Journal :
Epilepsia (Series 4)
Publication Type :
Academic Journal
Accession number :
95682720
Full Text :
https://doi.org/10.1111/epi.12564