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临床有效性:组合药物基因组学比单基因表型能更好地预测抗抑郁药反应和医疗保健利用情况。

Clinical validity: Combinatorial pharmacogenomics predicts antidepressant responses and healthcare utilizations better than single gene phenotypes.

作者信息

Altar C A, Carhart J M, Allen J D, Hall-Flavin D K, Dechairo B M, Winner J G

机构信息

Assurex Health, Inc., Mason, OH, USA.

Mayo Clinic, Departments of Psychiatry and Psychology, Rochester, MN, USA.

出版信息

Pharmacogenomics J. 2015 Oct;15(5):443-51. doi: 10.1038/tpj.2014.85. Epub 2015 Feb 17.

Abstract

In four previous studies, a combinatorial multigene pharmacogenomic test (GeneSight) predicted those patients whose antidepressant treatment for major depressive disorder resulted in poorer efficacy and increased health-care resource utilizations. Here, we extended the analysis of clinical validity to the combined data from these studies. We also compared the outcome predictions of the combinatorial use of allelic variations in genes for four cytochrome P450 (CYP) enzymes (CYP2D6, CYP2C19, CYP2C9 and CYP1A2), the serotonin transporter (SLC6A4) and serotonin 2A receptor (HTR2A) with the outcome predictions for the very same subjects using traditional, single-gene analysis. Depression scores were measured at baseline and 8-10 weeks later for the 119 fully blinded subjects who received treatment as usual (TAU) with antidepressant standard of care, without the benefit of pharmacogenomic medication guidance. For another 96 TAU subjects, health-care utilizations were recorded in a 1-year, retrospective chart review. All subjects were genotyped after the clinical study period, and phenotype subgroups were created among those who had been prescribed a GeneSight panel medication that is a substrate for either CYP enzyme or serotonin effector protein. On the basis of medications prescribed for each subject at baseline, the combinatorial pharmacogenomic (CPGx™) GeneSight method categorized each subject into either a green ('use as directed'), yellow ('use with caution') or red category ('use with increased caution and with more frequent monitoring') phenotype, whereas the single-gene method categorized the same subjects with the traditional phenotype (for example, poor, intermediate, extensive or ultrarapid CYP metabolizer). The GeneSight combinatorial categorization approach discriminated and predicted poorer outcomes for red category patients prescribed medications metabolized by CYP2D6, CYP2C19 and CYP1A2 (P=0.0034, P=0.04 and P=0.03, respectively), whereas the single-gene phenotypes failed to discriminate patient outcomes. The GeneSight CPGx process also discriminated health-care utilization and disability claims for these same three CYP-defined medication subgroups. The CYP2C19 phenotype was the only single-gene approach to predict health-care outcomes. Multigenic combinatorial testing discriminates and predicts the poorer antidepressant outcomes and greater health-care utilizations by depressed subjects better than do phenotypes derived from single genes. This clinical validity is likely to contribute to the clinical utility reported for combinatorial pharmacogenomic decision support.

摘要

在之前的四项研究中,一种组合多基因药物基因组检测(基因视窗)预测了那些接受重度抑郁症抗抑郁治疗后疗效较差且医疗资源利用率增加的患者。在此,我们将临床有效性分析扩展至这些研究的合并数据。我们还比较了四种细胞色素P450(CYP)酶(CYP2D6、CYP2C19、CYP2C9和CYP1A2)、5-羟色胺转运体(SLC6A4)和5-羟色胺2A受体(HTR2A)基因中等位基因变异组合使用的结果预测与使用传统单基因分析对相同受试者的结果预测。对119名完全盲法的受试者在基线时以及8至10周后测量抑郁评分,这些受试者接受常规抗抑郁标准治疗(TAU),未受益于药物基因组学用药指导。对于另外96名TAU受试者,通过回顾性图表审查记录了1年的医疗资源利用情况。所有受试者在临床研究期后进行基因分型,并在那些被开具基因视窗面板药物(该药物是CYP酶或5-羟色胺效应蛋白的底物)的受试者中创建表型亚组。根据每位受试者在基线时开具的药物,组合药物基因组学(CPGx™)基因视窗方法将每位受试者分类为绿色(“按指示使用”)、黄色(“谨慎使用”)或红色类别(“更谨慎使用并增加监测频率”)表型,而单基因方法将相同受试者分类为传统表型(例如,CYP代谢缓慢型、中间型、广泛型或超快型)。基因视窗组合分类方法区分并预测了被开具由CYP2D6、CYP2C19和CYP1A介导代谢药物的红色类别患者的较差结果(分别为P = 0.0034、P = 0.04和P = 0.03),而单基因表型未能区分患者结果。基因视窗CPGx过程也区分了这三个由CYP定义的药物亚组的医疗资源利用和残疾索赔情况。CYP2C19表型是预测医疗结果的唯一单基因方法。多基因组合检测比单基因衍生的表型更好地区分并预测了抑郁症患者较差的抗抑郁结果和更高的医疗资源利用率。这种临床有效性可能有助于为组合药物基因组学决策支持所报告的临床实用性。

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