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Common risk allele in aromatic antiepileptic-drug induced Stevens–Johnson syndrome and toxic epidermal necrolysis in Han Chinese

机译:芳香族抗癫痫药物诱发的史蒂文斯-约翰逊综合征和中毒性表皮坏死溶解的常见风险等位基因

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Aims: Compared with other categories of drugs, such as antibiotics and NSAIDs, antiepileptic therapies are associated with a high incidence of Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN). We previously reported that carbamazepine (CBZ)–SJS/TEN is strongly associated with the HLA-B*1502 in Han Chinese, which has been confirmed in other Southeast Asian countries where the allele is prevalent. Here, we extend the study of HLA susceptibility to three different antiepileptic drugs, phenytoin (PHT), lamotrigine (LTG) and oxcarbazepine (OXC), which have structure similarity to CBZ. Materials & methods: We carried out a case–control association study. We enrolled 26 PHT-, six LTG- and three OXC-induced SJS/TEN patients, 113 PHT-tolerant and 67 LTG-tolerant subjects who were on the drug, respectively, for more than 3 months without the adverse reactions, and 93 normal subjects from the general population. The HLA-A, B, C and DRB1 genotypes were determined. Results: We found that HLA-B*1502 was present in eight out of 26 (30.8%) PHT–SJS/TEN (OR: 5.1; 95% CI: 1.8–15.1; p = 0.0041), two out of six (33%) LTG–SJS (odds ratio [OR]: 5.1; 95% CI: 0.8–33.8; p = 0.1266) and three out of three (100%) OXC–SJS (OR: 80.7; 95% CI: 3.8–1714.4; p = 8.4 × 10-4) patients. In addition, HLA-B*1301, Cw*0801 and DRB1*1602 also showed an association with PHT–SJS/TEN (p = 0.0128–0.0281; OR: 3.0–4.3). Conclusion: Our results indicate that OXC, PHT and LTG, which possess an aromatic ring just as CBZ does, when causing SJS/TEN, share a common risk allele. Aromatic antiepileptic drugs causing SJS/TEN in HLA-B*1502 carriers may act on a similar pathogenetic mechanism, although other geneticongenetic factor(s) may also contribute to the pathomechanism of the disease. We suggest that aromatic antiepileptic drugs, including CBZ, OXC and PHT, should be avoided in the B*1502 carrier and caution should also be exercised for LTG.
机译:目的:与其他种类的药物(例如抗生素和非甾体抗炎药)相比,抗癫痫治疗与史蒂文斯-约翰逊综合征(SJS)和中毒性表皮坏死症(TEN)的高发病率有关。我们先前曾报道,卡马西平(CBZ)–SJS / TEN与汉族人的HLA-B * 1502密切相关,这在等位基因盛行的其他东南亚国家中也得到了证实。在这里,我们将对HLA敏感性的研究扩展到三种不同的抗癫痫药:苯妥英钠(PHT),拉莫三嗪(LTG)和奥卡西平(OXC),它们与CBZ具有相似的结构。材料和方法:我们进行了病例对照研究。我们招募了26名PHT,6名LTG和3名OXC诱导的SJS / TEN患者,分别接受药物治疗超过3个月且无不良反应的113名耐PHT和67名耐LTG的受试者,以及93名正常一般人群的主题。确定了HLA-A,B,C和DRB1基因型。结果:我们发现HLA-B * 1502在26种(30.8%)PHT-SJS / TEN(OR:5.1; 95%CI:1.8-15.1; p = 0.0041)中有8种,在6种中有2种(33 %)LTG-SJS(赔率[OR]:5.1; 95%CI:0.8-33.8; p = 0.1266)和三分之三(100%)OXC-SJS(OR:80.7; 95%CI:3.8-1714.4 ; p = 8.4×10 -4 )患者。此外,HLA-B * 1301,Cw * 0801和DRB1 * 1602也显示与PHT-SJS / TEN相关(p = 0.0128-0.0281; OR:3.0-4.3)。结论:我们的结果表明,与CBZ一样具有芳环的OXC,PHT和LTG在引起SJS / TEN时具有共同的风险等位基因。在HLA-B * 1502携带者中引起SJS / TEN的芳香抗癫痫药可能具有相似的致病机制,尽管其他遗传/非遗传因素也可能导致了该病的发病机制。我们建议在B * 1502载体中应避免使用芳族抗癫痫药,包括CBZ,OXC和PHT,并应谨慎对待LTG。

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