HLA-A、-B和-C等位基因与韩国人碘造影剂诱发的超敏反应的相关性。

IF 1.1 Q4 PHARMACOLOGY & PHARMACY
Translational and Clinical Pharmacology Pub Date : 2021-06-01 Epub Date: 2021-06-15 DOI:10.12793/tcp.2021.29.e10
Eun-Young Kim, Seok Jin Choi, Jong-Lyul Ghim, Mi-Yeong Kim, Jung Eun Seol, Minkyung Oh, Chan Sun Park, Jae-Gook Shin
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引用次数: 1

摘要

药物超敏反应的常见原因是碘造影剂(ICM)。ICM诱导的超敏反应被认为是一种非免疫反应,但近年来免疫学机制的证据越来越多。因此,我们评估了HLA-A、-B和-C等位基因是否与ICM诱导的超敏反应有关。2008年至2012年间,共有126名患者在三级转诊医院的门诊接受了计算机断层造影研究。61名患者出现ICM诱导的超敏反应,其余65名患者为ICM耐受患者(对照组)。ICM诱导的超敏反应患者显示51例为立即型,7例为非立即型,3例为两种或混合型。使用基于PCR序列的分型方法进行HLA-A、-B和-C基因分型。使用了四种ICM:碘溴胺、碘己醇、碘必妥醇和碘克沙醇。在超敏患者中,最常用的ICM是碘溴胺。ICM诱导的即时超敏反应和对照组之间的HLA-B*58:01频率存在显著差异(比值比[OR],3.90;p=0.0200,95%置信区间[CI],1.16-13.07)。在碘溴胺诱导的立即超敏反应和对照组之间,HLA-B*38:02(OR,10.24;p=0.0145;95%CI,1.09-96.14)和HLA-B*58:01(OR,3.98;p=0.0348;95%CI:1.03-15.39)的频率存在统计学显著差异。ICM诱导的超敏反应的机制尚不清楚,但本研究显示,ICM诱导立即超敏反应与HLA-B*58:01等位基因以及碘溴胺诱导的立即超敏作用与HLA-B*38:02和HLA-B*58:00等位基因之间的相关性虽然较弱,但可作为风险预测因子。需要进一步的研究来验证更大样本中的相关性,并确定这些结果背后的功能机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Associations between HLA-A, -B, and -C alleles and iodinated contrast media-induced hypersensitivity in Koreans.

Associations between HLA-A, -B, and -C alleles and iodinated contrast media-induced hypersensitivity in Koreans.

Associations between HLA-A, -B, and -C alleles and iodinated contrast media-induced hypersensitivity in Koreans.

Associations between HLA-A, -B, and -C alleles and iodinated contrast media-induced hypersensitivity in Koreans.

A common cause of drug hypersensitivity reactions is iodinated contrast media (ICM). ICM-induced hypersensitivity had been considered to be a non-immunological reaction, but evidence for an immunological mechanism has increased recently. Thus, we evaluated whether HLA-A, -B, and -C alleles were associated with ICM-induced hypersensitivity. In total, 126 patients who underwent contrast-enhanced computed tomography studies through outpatient clinics at a tertiary referral hospital between 2008 and 2012 were assessed. Sixty-one patients experienced ICM-induced hypersensitivity and the remainder, 65, were ICM-tolerant patients (control). ICM-induced hypersensitivity patients showed 51 with immediate, 7 with non-immediate, 3 with both or mixed type. HLA-A, -B, and -C genotyping was performed using a PCR sequence-based typing method. Four kinds of ICM were used: iopromide, iohexol, iobitridol, and iodixanol. The most used ICM among the hypersensitivity patients was iopromide. Significant difference in the frequency of HLA-B*58:01 (odds ratios [OR], 3.90; p = 0.0200, 95% confidence interval [CI], 1.16-13.07) was observed between ICM-induced immediate hypersensitivity and control. There were statistically significant differences in the frequencies of the HLA-B*38:02 (OR, 10.24; p = 0.0145; 95% CI, 1.09-96.14) and HLA-B*58:01 (OR, 3.98; p = 0.0348; 95% CI, 1.03-15.39) between iopromide-induced immediate hypersensitivity and control. The mechanism of ICM-induced hypersensitivity remains unknown, but this study showed associations, although weak, with HLA-B*58:01 alleles for ICM-induced immediate hypersensitivity and HLA-B*38:02 and HLA-B*58:01 for iopromide-induced immediate hypersensitivity as risk predictors. Further studies are needed to validate the associations in larger samples and to identify the functional mechanism behind these results.

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来源期刊
Translational and Clinical Pharmacology
Translational and Clinical Pharmacology Medicine-Pharmacology (medical)
CiteScore
1.60
自引率
11.10%
发文量
17
期刊介绍: Translational and Clinical Pharmacology (Transl Clin Pharmacol, TCP) is the official journal of the Korean Society for Clinical Pharmacology and Therapeutics (KSCPT). TCP is an interdisciplinary journal devoted to the dissemination of knowledge relating to all aspects of translational and clinical pharmacology. The categories for publication include pharmacokinetics (PK) and drug disposition, drug metabolism, pharmacodynamics (PD), clinical trials and design issues, pharmacogenomics and pharmacogenetics, pharmacometrics, pharmacoepidemiology, pharmacovigilence, and human pharmacology. Studies involving animal models, pharmacological characterization, and clinical trials are appropriate for consideration.
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