首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Clinical and genetic risk factors of self-reported penicillin allergy.
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Clinical and genetic risk factors of self-reported penicillin allergy.

机译:自我报告的青霉素过敏的临床和遗传危险因素。

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BACKGROUND: Patients with self-reported penicillin allergy are frequently denied beta-lactam antibiotics. OBJECTIVE: To identify and correlate clinical and genetic risk factors of self-reported penicillin allergy. METHODS: We conducted a case-control study of adults recruited from allergists' offices. Cases had a history of urticaria, angioedema, wheeze, hypotension, vomiting, or anaphylaxis after a dose of penicillin. DNA from buccal swabs was genotyped for variants associated with candidate genes linked to immediate hypersensitivity (IL4, IL4R, and IL10) and penicillin metabolism (LACTB). Logistic regression was used to calculate the association between penicillin allergy and clinical and genetic factors. RESULTS: Seventeen allergists identified 76 adults. Complete data were available for 23 cases and 39 controls. Penicillin allergy was associated with a history of penicillin allergy in first-degree relatives (P = .002), a history of other adverse drug reactions (P = .008), and atopy (P = .039). However, in the multivariable analysis, only family history of penicillin allergy remained significant. IL4 single nucleotide polymorphisms (SNPs) rs11740584 (P = .012), rs10062446 (P = .021), and rs2070874 (P = .035) were associated and LACTB SNP rs2729835 (P = .058) was marginally associated with penicillin allergy. Adding rs11740584 or rs10062446 individually improved the clinical multivariable model (R(2) increased from 0.23 to 0.33). Haplotype analysis did not provide additional information to the SNP analysis. CONCLUSION: Self-reported penicillin allergy may be influenced by clinical and genetic factors such as IL4.
机译:背景:自我报告的青霉素过敏患者经常被拒绝使用β-内酰胺类抗生素。目的:鉴定和报告自我报告的青霉素过敏的临床和遗传危险因素。方法:我们对从过敏症办公室招募的成年人进行了病例对照研究。服用青霉素后,有荨麻疹,血管性水肿,喘息,低血压,呕吐或过敏反应的病史。对来自口腔拭子的DNA进行基因分型,确定与候选基因相关的变体,这些候选基因与立即超敏反应(IL4,IL4R和IL10)和青霉素代谢(LACTB)相关。 Logistic回归用于计算青霉素过敏与临床和遗传因素之间的关联。结果:十七位过敏者确定了76名成人。完整的数据可用于23例和39例对照。青霉素过敏与一级亲属的青霉素过敏史(P = .002),其他药物不良反应史(P = .008)和特应性(P = .039)有关。但是,在多变量分析中,仅青霉素过敏的家族史仍然很重要。 IL4单核苷酸多态性(SNP)rs11740584(P = .012),rs10062446(P = .021)和rs2070874(P = .035)相关联,而LACTB SNP rs2729835(P = .058)与青霉素过敏程度相关。单独添加rs11740584或rs10062446可改善临床多变量模型(R(2)从0.23增至0.33)。单倍型分析未提供SNP分析的其他信息。结论:自我报告的青霉素过敏可能受临床和遗传因素如IL4的影响。

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