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Association of HLA class I and II gene polymorphisms with acetaminophen-related Stevens–Johnson syndrome with severe ocular complications in Japanese individuals

机译:HLA I和II类基因多态性与对乙酰氨基酚相关的Stevens-Johnson综合征与日本人严重眼部并发症的关系

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摘要

Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are acute-onset mucocutaneous diseases induced by infectious agents and/or inciting drugs. We have reported that the main causative drugs for SJS/TEN with severe ocular complications (SOC) were cold medicines, including multi-ingredient cold medications and nonsteroidal anti-inflammatory drugs (NSAIDs). Moreover, we also reported that acetaminophen is the most frequent causative drug in various cold medicines. In this study, we focused on acetaminophen-related SJS/TEN with SOC and analyzed HLA-class II (HLA-DRB1, DQB1) in addition to HLA-class I (HLA-A, B, C). We studied the histocompatibility antigen genes HLA-DRB1 and DQB1 in addition to HLA-A, B, and C in 80 Japanese patients with acetaminophen-related SJS/TEN with SOC. We performed polymerase chain reaction amplification followed by hybridization with sequence-specific oligonucleotide probes (PCR-SSO) using commercial bead-based typing kits. We also used genotyped data from 113 healthy volunteers for HLA-DRB1 and DQB1, and 639 healthy volunteers for HLA-A, B, and C. HLA-DRB1*08:03 and DRB1*12:02 were associated with acetaminophen-related SJS/TEN with SOC, although the results ceased to be significant when we corrected the p-value for the number of alleles detected. HLA-A*02:06 was strongly associated with acetaminophen-related SJS/TEN with SOC (carrier frequency: p = 4.7 × 10−12, Pc = 6.6 × 10−11, OR = 6.0; gene frequency: p = 8.0 × 10−13, Pc = 1.1 × 10−11, OR = 4.9). HLA-B*13:01 (carrier frequency: p = 2.0 × 10−3, Pc = 0.042, OR = 4.1; gene frequency: p = 2.2 × 10−3, Pc = 0.047, OR = 3.9), HLA-B*44:03 (carrier frequency: p = 2.1 × 10−3, Pc = 0.045, OR = 2.4) and HLA-C*14:03 (carrier frequency: p = 3.4 × 10−3, Pc = 0.045, OR = 2.3) were also significantly associated, while HLA-A*24:02 was inversely associated (gene frequency: p = 6.3 × 10−4, Pc = 8.8 × 10−3, OR = 0.5). Acetaminophen-related SJS/TEN with SOC was not associated with HLA-class II (HLA-DRB1, DQB1). However, for acetaminophen-related SJS/TEN with SOC, we found an association with HLA-B*13:01 and HLA- C*14:03 in addition to HLA-A*02:06 and HLA-B*44:03, which have been described previously.
机译:史蒂文斯-约翰逊综合症(SJS)和中毒性表皮坏死溶解症(TEN)是由感染因子和/或煽动性药物诱发的急性发作性皮肤粘膜疾病。我们已经报道,具有严重眼部并发症(SOC)的SJS / TEN的主要致病药物是感冒药,包括多成分感冒药和非甾体抗炎药(NSAIDs)。此外,我们还报道了对乙酰氨基酚是各种感冒药中最常见的致病药物。在这项研究中,我们重点研究了带有SOC的对乙酰氨基酚相关SJS / TEN,并分析了HLA-I类(HLA-A,B,C)之外的HLA-II类(HLA-DRB1,DQB1)。除了HLA-A,B和C,我们还研究了80名日本对乙酰氨基酚相关SJS / TEN SOC患者的组织相容性抗原基因HLA-DRB1和DQB1。我们进行了聚合酶链反应扩增,然后使用基于商业磁珠的打字试剂盒与序列特异性寡核苷酸探针(PCR-SSO)进行了杂交。我们还使用了来自113位HLA-DRB1和DQB1健康志愿者和639位HLA-A,B和C健康志愿者的基因分型数据。HLA-DRB1 * 08:03和DRB1 * 12:02与对乙酰氨基酚相关的SJS相关/ TEN与SOC,尽管当我们校正检测到的等位基因数量的p值时,结果不再很重要。 HLA-A * 02:06与对乙酰氨基酚相关的SJS / TEN具有SOC密切相关(载波频率:p = 4.7×10 -12 ,Pc = 6.6×10 -11 ,OR = 6.0;基因频率:p = 8.0×10 −13 ,Pc = 1.1×10 -11 ,OR = 4.9)。 HLA-B * 13:01(载波频率: p = 2.0×10 -3 ,Pc = 0.042,OR = 4.1;基因频率: p = 2.2×10 -3 ,Pc = 0.047,OR = 3.9),HLA-B * 44:03 (载波频率: p = 2.1×10 -3 ,Pc = 0.045,OR = 2.4)和 HLA-C * 14:03 (载波频率: p = 3.4×10 -3 ,Pc = 0.045,OR = 2.3)也显着相关,而 HLA-A * 24:02 则呈反相关(基因频率:< em> p = 6.3×10 −4 ,Pc = 8.8×10 -3 ,OR = 0.5)。对乙酰氨基酚相关的SJS / TEN与SOC无关 HLA II类(HLA-DRB1,DQB1)。但是,对于与对乙酰氨基酚有关的SJS / TEN与SOC,除了> HLA-B * 13:01 HLA-C * 14:03 em> HLA-A * 02:06 HLA-B * 44:03

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