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个人基因组检测对健康行为的影响:以吸烟为例。

Implications of Personal Genomic Testing for Health Behaviors: The Case of Smoking.

作者信息

Olfson Emily, Hartz Sarah, Carere Deanna Alexis, Green Robert C, Roberts J Scott, Bierut Laura J

机构信息

Child Study Center and Department of Psychiatry, Yale University School of Medicine, New Haven, CT.

Department of Psychiatry, Washington University School of Medicine, St Louis, MO.

出版信息

Nicotine Tob Res. 2016 Dec;18(12):2273-2277. doi: 10.1093/ntr/ntw168. Epub 2016 Jul 12.

Abstract

INTRODUCTION

Direct-to-consumer personal genomic testing has the potential to influence health behaviors, including smoking. Critics of this testing highlight limited evidence to support positive behavioral benefits and caution that genomic results may provide false reassurance, leading to unhealthy behaviors. This study investigates interest in genetic risks of smoking-related diseases and changes in smoking behaviors among genomic testing consumers.

METHODS

From 2012 to 2013, a longitudinal series of web surveys was conducted. A total of 1464 customers of 23andMe and Pathway Genomics completed a survey prior to viewing genomic test results, of which 1002 participants provided data on smoking behaviors 6 months after receiving results.

RESULTS

At baseline, 64% of participants were never smokers, 29% were former smokers, and 7% were current smokers. Most baseline current smokers were very interested in genetic risk results for lung cancer (65%) and heart disease (72%). For lung cancer, this interest was significantly greater than former (50% very interested) and never smokers (37% very interested) (p < .0001). Even though participants were interested in smoking-related disease genetic risks, 96% reported the same smoking status at baseline and 6-month follow-up. Importantly, only 1% (n = 13/916) of former and never smokers became current smokers at 6 months and 22% (n = 14/64) of current smokers reported quitting.

CONCLUSIONS

Overall, smokers show a high level of interest in genetic risks of smoking-related illnesses. The experience of receiving direct-to-consumer genomic health risks does not appear to have obvious harms related to smoking behaviors, with some potential benefits.

IMPLICATIONS

In the setting of ongoing controversy surrounding direct-to-consumer genomic testing, this study provides evidence that consumers are interested in genetic risk results of smoking-related diseases. Receiving genomic testing results does not lead to smoking initiation among never smokers or reinitiation among former smokers and may be associated with a higher quit rate among current smokers at 6-month follow-up than the general population. These findings ease concerns that direct-to-consumer genomic testing could lead to false reassurance and unhealthy behaviors related to smoking.

摘要

引言

直接面向消费者的个人基因组检测有可能影响健康行为,包括吸烟行为。这种检测的批评者强调,支持积极行为益处的证据有限,并警告说基因组结果可能会提供虚假的安慰,从而导致不健康行为。本研究调查了基因组检测消费者对吸烟相关疾病遗传风险的兴趣以及吸烟行为的变化。

方法

在2012年至2013年期间,进行了一系列纵向网络调查。23andMe和Pathway Genomics的1464名客户在查看基因组检测结果之前完成了一项调查,其中1002名参与者在收到结果6个月后提供了吸烟行为数据。

结果

在基线时,64%的参与者从不吸烟,29%是既往吸烟者,7%是当前吸烟者。大多数基线时的当前吸烟者对肺癌(65%)和心脏病(72%)的遗传风险结果非常感兴趣。对于肺癌,这种兴趣明显高于既往吸烟者(50%非常感兴趣)和从不吸烟者(37%非常感兴趣)(p <.0001)。尽管参与者对吸烟相关疾病的遗传风险感兴趣,但96%的人在基线和6个月随访时报告的吸烟状况相同。重要的是,在6个月时,只有1%(n = 13/916)的既往吸烟者和从不吸烟者成为当前吸烟者,22%(n = 14/64)的当前吸烟者报告戒烟。

结论

总体而言,吸烟者对吸烟相关疾病的遗传风险表现出高度兴趣。接受直接面向消费者的基因组健康风险的经历似乎与吸烟行为没有明显危害,还有一些潜在益处。

启示

在围绕直接面向消费者的基因组检测的持续争议背景下,本研究提供了证据表明消费者对吸烟相关疾病的遗传风险结果感兴趣。接受基因组检测结果不会导致从不吸烟者开始吸烟或既往吸烟者重新开始吸烟,并且在6个月随访时,当前吸烟者的戒烟率可能高于一般人群。这些发现缓解了人们对直接面向消费者的基因组检测可能导致虚假安慰和与吸烟相关的不健康行为的担忧。

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