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是泰国患者中导致严重皮肤不良反应的预测标志物。

Is a Predictive Marker of Dapsone-Induced Severe Cutaneous Adverse Reactions in Thai Patients.

机构信息

Division of Pharmacogenomics and Personalized Medicine, Department of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

Laboratory for Pharmacogenomics, Somdech Phra Debaratana Medical Center (SDMC), Ramathibodi Hospital, Bangkok, Thailand.

出版信息

Front Immunol. 2021 May 4;12:661135. doi: 10.3389/fimmu.2021.661135. eCollection 2021.

Abstract

allele has been identified as the genetic determinant of dapsone hypersensitivity syndrome (DHS) among leprosy and non-leprosy patients in several studies. Dapsone hydroxylamine (DDS-NHOH), an active metabolite of dapsone, has been believed to be responsible for DHS. However, studies have not highlighted the importance of other genetic polymorphisms in dapsone-induced severe cutaneous adverse reactions (SCAR). We investigated the association of alleles and cytochrome P450 (CYP) alleles with dapsone-induced SCAR in Thai non-leprosy patients. A prospective cohort study, 16 Thai patients of dapsone-induced SCARs (5 SJS-TEN and 11 DRESS) and 9 Taiwanese patients of dapsone-induced SCARs (2 SJS-TEN and 7 DRESS), 40 dapsone-tolerant controls, and 470 general Thai population were enrolled. class I and II alleles were genotyped using polymerase chain reaction-sequence specific oligonucleotides (PCR-SSOs). , , and genotypes were determined by the TaqMan real-time PCR assay. We performed computational analyses of dapsone and DDS-NHOH interacting with and alleles by the molecular docking approach. Among all the alleles, only allele was found to be significantly associated with dapsone-induced SCARs (OR = 39.00, 95% CI = 7.67-198.21, p = 5.3447 × 10), SJS-TEN (OR = 36.00, 95% CI = 3.19-405.89, p = 2.1657 × 10), and DRESS (OR = 40.50, 95% CI = 6.38-257.03, p = 1.0784 × 10) as compared to dapsone-tolerant controls. Also allele was strongly associated with dapsone-induced SCARs in Asians (OR = 36.00, 95% CI = 8.67-149.52, p = 2.8068 × 10) and Taiwanese (OR = 31.50, 95% CI = 4.80-206.56, p = 2.5519 × 10). Furthermore, dapsone and DDS-NHOH fit within the extra-deep sub pocket of the antigen-binding site of the allele and change the antigen-recognition site. However, there was no significant association between genetic polymorphism of cytochrome P450 (, , and ) and dapsone-induced SCARs (SJS-TEN and DRESS). The results of this study support the specific genotyping of the allele to avoid dapsone-induced SCARs including SJS-TEN and DRESS before initiating dapsone therapy in the Asian population.

摘要

等位基因已在几项研究中被确定为麻风病和非麻风病患者中氨苯砜过敏综合征(DHS)的遗传决定因素。二氨嘧啶羟胺(DDS-NHOH),一种二氨嘧啶的活性代谢物,被认为是 DHS 的罪魁祸首。然而,研究并未强调其他遗传多态性在二氨嘧啶引起的严重皮肤不良反应(SCAR)中的重要性。我们调查了等位基因和细胞色素 P450(CYP)等位基因与泰国非麻风病患者中二氨嘧啶诱导的 SCAR 的关联。一项前瞻性队列研究纳入了 16 名二氨嘧啶诱导的 SCAR 泰国患者(5 例 SJS-TEN 和 11 例 DRESS)和 9 名二氨嘧啶诱导的 SCAR 台湾患者(2 例 SJS-TEN 和 7 例 DRESS)、40 名二氨嘧啶耐受对照者和 470 名普通泰国人群。使用聚合酶链反应-序列特异性寡核苷酸(PCR-SSOs)对 I 类和 II 类等位基因进行基因分型。使用 TaqMan 实时 PCR 测定法确定 、 和 基因型。我们通过分子对接方法对二氨嘧啶和 DDS-NHOH 与 等位基因相互作用进行了计算分析。在所有的等位基因中,只有等位基因与二氨嘧啶诱导的 SCARs(OR = 39.00,95%CI = 7.67-198.21,p = 5.3447×10)、SJS-TEN(OR = 36.00,95%CI = 3.19-405.89,p = 2.1657×10)和 DRESS(OR = 40.50,95%CI = 6.38-257.03,p = 1.0784×10)显著相关,与二氨嘧啶耐受对照者相比。等位基因也与亚洲人(OR = 36.00,95%CI = 8.67-149.52,p = 2.8068×10)和台湾人(OR = 31.50,95%CI = 4.80-206.56,p = 2.5519×10)中二氨嘧啶诱导的 SCAR 密切相关。此外,二氨嘧啶和 DDS-NHOH 适合于 等位基因抗原结合位点的超深亚袋内,并改变抗原识别位点。然而,细胞色素 P450(、和)的遗传多态性与二氨嘧啶诱导的 SCAR(SJS-TEN 和 DRESS)之间没有显著关联。这项研究的结果支持在亚洲人群中开始二氨嘧啶治疗之前,针对特定的等位基因进行基因分型,以避免二氨嘧啶诱导的包括 SJS-TEN 和 DRESS 在内的 SCAR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8070/8130671/b538fb307d33/fimmu-12-661135-g001.jpg

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