Publication:
Shared Genetic Risk Factors Across Carbamazepine-Induced Hypersensitivity Reactions.

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2019-07-03

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Nicoletti, Paola
Barrett, Sarah
McEvoy, Laurence
Daly, Ann K
Aithal, Guruprasad
Lucena, M Isabel
Andrade, Raul J
Wadelius, Mia
Hallberg, Pär
Stephens, Camilla

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Carbamazepine (CBZ) causes life-threating T-cell-mediated hypersensitivity reactions, including serious cutaneous adverse reactions (SCARs) and drug-induced liver injury (CBZ-DILI). In order to evaluate shared or phenotype-specific genetic predisposing factors for CBZ hypersensitivity reactions, we performed a meta-analysis of two genomewide association studies (GWAS) on a total of 43 well-phenotyped Northern and Southern European CBZ-SCAR cases and 10,701 population controls and a GWAS on 12 CBZ-DILI cases and 8,438 ethnically matched population controls. HLA-A*31:01 was identified as the strongest genetic predisposing factor for both CBZ-SCAR (odds ratio (OR) = 8.0; 95% CI 4.10-15.80; P = 1.2 × 10-9 ) and CBZ-DILI (OR = 7.3; 95% CI 2.47-23.67; P = 0.0004) in European populations. The association with HLA-A*31:01 in patients with SCAR was mainly driven by hypersensitivity syndrome (OR = 12.9; P = 2.1 × 10-9 ) rather than by Stevens-Johnson syndrome/toxic epidermal necrolysis cases, which showed an association with HLA-B*57:01. We also identified a novel risk locus mapping to ALK only for CBZ-SCAR cases, which needs replication in additional cohorts and functional evaluation.

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Adult
Anaplastic Lymphoma Kinase
Carbamazepine
Chemical and Drug Induced Liver Injury
Drug Hypersensitivity
Drug Hypersensitivity Syndrome
Europe
Female
Genetic Predisposition to Disease
Genome-Wide Association Study
HLA-A Antigens
HLA-B Antigens
Humans
Male
Phenotype
Risk Factors
Stevens-Johnson Syndrome

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