Manson Lisanne E N, Swen Jesse J, Guchelaar Henk-Jan
Department of Clinical Pharmacy & Toxicology, Leiden University Medical Center, Leiden, Netherlands.
Leiden Network for Personalized Therapeutics, Leiden, Netherlands.
Front Pharmacol. 2020 Sep 23;11:567048. doi: 10.3389/fphar.2020.567048. eCollection 2020.
Certain HLA variants are associated with an increased risk of hypersensitivity reactions to specific drugs. Both the Clinical Pharmacogenetics Implementation Consortium (CPIC) and the Dutch Pharmacogenetics Working Group (DPWG) have issued actionable HLA gene - drug interaction guidelines but diagnostic test criteria remain largely unknown. We present an overview of the diagnostic test criteria of the actionable HLA - drug pairs.
A systematic literature search was conducted in PubMed, Embase, Web of Science and Cochrane Library. Original case-control and cohort studies were selected and sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and number needed to genotype (NNG) were calculated for the actionable HLA-drug pairs.
In general, the HLA tests show high specificity and NPV for predicting hypersensitivity reactions. The sensitivity of HLA tests shows a wide range, from 0-33% for HLA-B1502 testing to predict lamotrigine induced SJS/TEN up to 100% for HLA-B5701 to predict immunologically confirmed abacavir hypersensitivity syndrome (ABC-HSR). PPV is low for all tests except for HLA-B5701 and ABC-HSR which is approximately 50%. HLA-B5701 to predict ABC-HSR shows the lowest NNG followed by HLA-B5801 for allopurinol induced severe cutaneous adverse drug reactions and HLA-B1502 for carbamazepine induced SJS/TEN.
This is the first overview of diagnostic test criteria for actionable HLA-drug pairs. Studies researching HLA genes and hypersensitivity are scarce for some of the HLA-drug pairs in some populations and patient numbers in studies are small. Therefore, more research is necessary to calculate the diagnostic test criteria more accurately.
某些人类白细胞抗原(HLA)变体与特定药物过敏反应风险增加相关。临床药物基因组学实施联盟(CPIC)和荷兰药物基因组学工作组(DPWG)均已发布了可操作的HLA基因-药物相互作用指南,但诊断测试标准在很大程度上仍不明确。我们对可操作的HLA-药物对的诊断测试标准进行了概述。
在PubMed、Embase、科学网和考克兰图书馆进行了系统的文献检索。选择了原始的病例对照研究和队列研究,并计算了可操作的HLA-药物对的敏感性、特异性、阳性预测值(PPV)、阴性预测值(NPV)和基因分型所需数量(NNG)。
总体而言,HLA检测在预测过敏反应方面显示出高特异性和NPV。HLA检测的敏感性范围很广,从用于预测拉莫三嗪诱导的史蒂文斯-约翰逊综合征/中毒性表皮坏死松解症(SJS/TEN)的HLA-B1502检测的0-33%到用于预测经免疫确认的阿巴卡韦过敏综合征(ABC-HSR)的HLA-B5701检测的100%。除了用于预测ABC-HSR的HLA-B5701,其PPV约为50%外,所有检测的PPV均较低。用于预测ABC-HSR的HLA-B5701显示出最低的NNG,其次是用于预测别嘌醇诱导的严重皮肤药物不良反应的HLA-B5801和用于预测卡马西平诱导的SJS/TEN的HLA-B1502。
这是可操作的HLA-药物对诊断测试标准的首次概述。在某些人群中,针对某些HLA-药物对研究HLA基因与过敏反应的研究较少,且研究中的患者数量较少。因此,需要更多的研究来更准确地计算诊断测试标准。