Association of cutaneous adverse drug reactions due to antiepileptic drugs with HLA alleles in a North Indian population

•North Indian subjects with cADRs to AEDs were studied for HLA associations.•HLA-A*31:01 and B*51:01 were associated with MPE due to CBZ and PHT; p = 0.01,0.002.•HLA-DRB1*07:01 was associated with CBZ-induced SJS/TEN; p = 0.01.•HLA-B *51:01 was associated with DRESS caused by PHT; p = 0.007.•HLA-B*1...

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Published inSeizure (London, England) Vol. 66; pp. 99 - 103
Main Authors Ihtisham, Kavish, Ramanujam, Bhargavi, Srivastava, Shivani, Mehra, Narinder Kumar, Kaur, Gurvinder, Khanna, Neena, Jain, Satish, Kumar, Sachin, Kaul, Bhavna, Samudrala, Raghavan, Tripathi, Manjari
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.03.2019
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Summary:•North Indian subjects with cADRs to AEDs were studied for HLA associations.•HLA-A*31:01 and B*51:01 were associated with MPE due to CBZ and PHT; p = 0.01,0.002.•HLA-DRB1*07:01 was associated with CBZ-induced SJS/TEN; p = 0.01.•HLA-B *51:01 was associated with DRESS caused by PHT; p = 0.007.•HLA-B*15:02 was not significantly associated with any AED-related cADR. Aromatic antiepileptic drugs (AEDs) are frequently implicated in cutaneous adverse drug reactions (cADRs), a few of which are associated with certain human leukocyte antigen (HLA) alleles in some populations. We aimed to find HLA-associations with AED-related cADRs among North Indians. North Indian subjects with cADR due to an AED, and those who were AED-tolerant were recruited as cases and controls, respectively. Genotyping for HLA-A, B and DRB1 were performed. Statistical analysis to compare carrier-rates and allele-frequencies between cases and controls (and healthy population, where necessary), was done for HLA-alleles occurring more than twice in either group. 120 cases {11 - Lamotrigine (LTG), 14 -Valproic acid (VPA), 8 -Levetiracetam (LEV), 35 -Carbamazepine (CBZ) and 52 - Phenytoin (PHT)}, and 250 controls were recruited. Presence of HLA-A*31:01 and HLA-B*51:01 were found to increase the risk of Maculopapular exanthema (MPE) due to CBZ and PHT (OR = 6.38; 95% CI: 1.46–27.75; OR = 4.60; 95% CI: 1.54–13.72, respectively). Among the severe cADRs, HLA-B*57:01(OR = 11.00 95% CI: 1.41–85.81) and HLA-DRB1*07:01 (OR = 7.25; 95% CI: 1.09–48.18) were noted to be significantly associated with CBZ-induced Stevens Johnson Syndrome (SJS)/Toxic Epidermal Necrolysis (TEN); HLA-B *51:01 was associated with drug reaction eosinophilia and systemic symptoms (DRESS) caused by PHT (OR = 6.90; 95% CI: 1.38–34.29). We found significant associations of some HLA alleles with specific cADRs to CBZ and PHT in North Indians, which may need to be tested before AED-initiation; only screening for HLA-B*15:02 may not help in this population.
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ISSN:1059-1311
1532-2688
1532-2688
DOI:10.1016/j.seizure.2019.02.011