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先前遗传咨询和客观计算能力对准确解读药物遗传学检测报告的影响。

Impact of Previous Genetic Counseling and Objective Numeracy on Accurate Interpretation of a Pharmacogenetics Test Report.

机构信息

Division of Human Genetics, Department of Internal Medicine, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, USA.

Division of Genetic and Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio, USA.

出版信息

Public Health Genomics. 2021;24(1-2):26-32. doi: 10.1159/000512476. Epub 2021 Jan 14.

DOI:10.1159/000512476
PMID:33445171
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7920902/
Abstract

INTRODUCTION

Pharmacogenetic (PGx) testing can be useful for providing information about a patient's drug response by increasing drug efficacy and decreasing the incidence of adverse drug events. While PGx tests were previously only offered to patients under healthcare provider supervision, they are now available as direct to consumer (DTC) tests. This study aimed to assess how accurately individuals from the general population were able to interpret a sample PGx test report and if accuracy differed based on individuals' numeracy or prior genetic counseling (GC).

METHODS

We surveyed 293 individuals from the general population, ascertained through ResearchMatch. The survey included questions about PGx test interpretation, numeracy, and genetic literacy.

RESULTS

In our cohort, numeracy level impacted PGx result interpretation, with those of high numeracy performing statistically significantly better on both the table format and graphical format (p value = 0.002 and p value <0.001, respectively) and genetic knowledge questions (p value <0.001) than those with low/average numeracy. In addition, previous GC did not impact test interpretation or genetic knowledge, but the number of individuals with prior GC was small (n = 26).

DISCUSSION/CONCLUSION: We found that numeracy had a significant impact on correct interpretation of PGx test reports. Because many individuals in the USA have low numeracy levels, it is extremely important that patients do not make their own medication management decision based on the test results and that they consult with their physicians about their PGx testing. The importance of consultation and discussion with providers about results should be emphasized on the test report.

摘要

简介

药物遗传学(PGx)测试可通过提高药物疗效和降低不良药物事件的发生率,为患者的药物反应提供信息。虽然 PGx 测试以前仅在医疗服务提供者的监督下提供给患者,但现在可以作为直接面向消费者(DTC)的测试。本研究旨在评估一般人群中的个体对样本 PGx 测试报告的解释能力,以及准确性是否因个体的计算能力或先前的遗传咨询(GC)而异。

方法

我们通过 ResearchMatch 调查了 293 名普通人群中的个体。该调查包括有关 PGx 测试解释、计算能力和遗传知识的问题。

结果

在我们的队列中,计算能力水平影响 PGx 结果的解释,高计算能力者在表格格式和图形格式(p 值分别为 0.002 和 p 值 <0.001)以及遗传知识问题上的表现均具有统计学意义(p 值 <0.001)均优于低/平均计算能力者。此外,先前的 GC 并未影响测试解释或遗传知识,但具有先前 GC 的个体数量较少(n = 26)。

讨论/结论:我们发现计算能力对正确解释 PGx 测试报告有重大影响。由于美国许多人计算能力较低,因此患者切勿根据测试结果自行决定药物管理,并且他们应就其 PGx 测试咨询他们的医生,这一点非常重要。应在测试报告上强调与提供者就结果进行咨询和讨论的重要性。