Allopurinol pharmacogenetics: assessment of potential clinical usefulness

被引:1
|
作者
Zineh, Issam [1 ]
Mummaneni, Padmaja [1 ]
Lyndly, Jenna [2 ]
Amur, Shashi [1 ]
La Grenade, Lois A. [3 ]
Chang, Stephen H. [4 ]
Rogers, Hobart [1 ]
Pacanowski, Michael A. [1 ]
机构
[1] US FDA, Genom Grp, Off Clin Pharmacol, Off Translat Sci,Ctr Drug Evaluat & Res, Silver Spring, MD 20993 USA
[2] US FDA, Div Biostat 6, Off Biostat, Off Translat Sci,Ctr Drug Evaluat & Res, Silver Spring, MD 20993 USA
[3] US FDA, Div Pharmacovigilance, Off Surveillance & Epidemiol, Ctr Drug Evaluat & Res, Silver Spring, MD 20993 USA
[4] Off Surveillance & Epidemiol, Div Epidemiol, Silver Spring, MD USA
关键词
adverse reaction; allopurinol; HLA-B*5801; safety; SCAR; Stevens-Johnson syndrome; US FDA; STEVENS-JOHNSON-SYNDROME; TOXIC EPIDERMAL NECROLYSIS; HLA-B; HLA-B-ASTERISK-5801; MANAGEMENT; ALLELE; GOUT;
D O I
10.2217/PGS.11.131
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Use of pharmacogenetics to inform treatment decisions remains a priority for clinicians, patients and public health agencies. We previously developed a framework for systematically assessing whether pharmacogenetic test information would likely bring value to clinical decision-making and enjoy practical uptake. We applied this tool to allopurinol to determine potential usefulness of HLA genetic information in assessing risk for allopurinol-induced severe cutaneous adverse reactions. We quantified allopurinol use data and the magnitude of adverse event signals using US FDA databases, reviewed reported cases of allopurinol-associated severe cutaneous adverse reactions to assess whether clinical subtypes of patients could be identified, performed pooled analyses of associations between HLA variation and allopurinol-induced severe cutaneous adverse reactions and described considerations in clinical implementation of allopurinol pharmacogenetics.
引用
收藏
页码:1741 / 1749
页数:9
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