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消费者直接获得个性化基因风险报告者中,α-1 抗胰蛋白酶缺乏症的流行率、自我报告的行为改变和医疗保健参与情况。

Prevalence of Alpha-1 Antitrypsin Deficiency, Self-Reported Behavior Change, and Health Care Engagement Among Direct-to-Consumer Recipients of a Personalized Genetic Risk Report.

机构信息

23andMe Inc., Sunnyvale, CA.

23andMe Inc., Sunnyvale, CA.

出版信息

Chest. 2022 Feb;161(2):373-381. doi: 10.1016/j.chest.2021.09.041. Epub 2021 Oct 14.

Abstract

BACKGROUND

Alpha-1 antitrypsin deficiency (AATD) is an autosomal co-dominant condition that predisposes to emphysema, cirrhosis, panniculitis, and vasculitis. Underrecognition has prompted efforts to enhance early detection and testing of at-risk individuals. Direct-to-consumer (DTC) genetic testing represents an additional method of detection.

RESEARCH QUESTION

The study addressed three questions: (1) Does a DTC testing service identify previously undetected individuals with AATD? (2) What was the interval between initial AATD-related symptoms and initial diagnosis of AATD in such individuals? and (3) What was the behavioral impact of learning about a new diagnosis of AATD through a DTC test?

STUDY DESIGN AND METHODS

In this cross-sectional study, 195,014 individuals responded to a survey within the 23andMe, Inc. research platform.

RESULTS

Among 195,014 study participants, the allele frequency for the PI∗S and PI∗Z AATD variants was 21.6% (6.5% for PI∗Z and 15.1% for PI∗S); 0.63% were PI∗ZZ, half of whom reported having a physician confirm the diagnosis. Approximately 27% of those with physician-diagnosed AATD reported first becoming aware of AATD through the DTC test. Among those newly aware participants, the diagnostic delay interval was 22.3 years. Participants frequently shared their DTC test results with health care providers (HCPs) and the reported impact of learning a diagnosis of AATD was high. For example, 51.1% of PI∗ZZ individuals shared their DTC result with an HCP. The OR for PI∗ZZ smokers to report smoking reduction as a result of receiving the DTC result was 1.7 (95% CI = 1.4-2.2) compared with those without a Z allele and for reduced alcohol consumption this was 4.0 (95% CI = 2.6-5.9).

INTERPRETATION

In this largest available report on DTC testing for AATD, this test, in combination with clinical follow-up, can help to identify previously undiagnosed AATD patients. Moreover, receipt of the DTC AATD report was associated with positive behavior change, especially among those with risk variants.

摘要

背景

α-1 抗胰蛋白酶缺乏症(AATD)是一种常染色体共显性疾病,易导致肺气肿、肝硬化、脂膜炎和血管炎。由于识别不足,人们努力加强对高危人群的早期检测和筛查。直接面向消费者(DTC)的基因检测是另一种检测方法。

研究问题

本研究解决了三个问题:(1)DTC 检测服务是否能发现以前未被发现的 AATD 个体?(2)这些个体中,从最初的 AATD 相关症状到最初诊断 AATD 的时间间隔是多少?(3)通过 DTC 检测得知新的 AATD 诊断后,行为会发生什么变化?

研究设计和方法

在这项横断面研究中,共有 195014 名参与者在 23andMe,Inc. 研究平台上回答了一份调查。

研究结果

在 195014 名研究参与者中,PI∗S 和 PI∗Z AATD 变异等位基因的频率为 21.6%(PI∗Z 为 6.5%,PI∗S 为 15.1%);0.63%为 PI∗ZZ,其中一半人报告有医生证实了这一诊断。大约 27%的有医生诊断 AATD 的人表示,他们是通过 DTC 检测首次得知 AATD。在这些新发现的参与者中,诊断延迟时间为 22.3 年。参与者经常与医疗保健提供者(HCP)分享他们的 DTC 检测结果,他们对学习 AATD 诊断的反应很高。例如,51.1%的 PI∗ZZ 个体与 HCP 分享了他们的 DTC 结果。与没有 Z 等位基因的个体相比,PI∗ZZ 吸烟者因收到 DTC 结果而减少吸烟的几率为 1.7(95%置信区间[CI]为 1.4-2.2),而减少饮酒的几率为 4.0(95% CI 为 2.6-5.9)。

解释

在这项关于 AATD 的 DTC 检测的最大可用报告中,该检测与临床随访相结合,可以帮助识别以前未被诊断的 AATD 患者。此外,收到 DTC AATD 报告与积极的行为改变相关,尤其是在那些具有风险变异的个体中。

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