• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

传达遗传风险信息。

Communicating genetic risk information.

作者信息

Marteau T M

机构信息

Psychology and Genetics Research Group, King's College, London, UK.

出版信息

Br Med Bull. 1999;55(2):414-28. doi: 10.1258/0007142991902466.

DOI:10.1258/0007142991902466
PMID:10723866
Abstract

It is envisaged that genetic information will be used, together with other types of information, to assess individuals' risks of developing a variety of common conditions. Such risk assessments will involve providing probabilistic information partly based upon results of genetic tests in order to facilitate behaviour change without causing excessive anxiety. The behaviours targeted for change are likely to include adherence to prescribed medication, alteration to diet, increasing levels of exercise and quitting smoking. This paper reviews research already conducted on perceptions of risk and genes, methods of facilitating behaviour change and reducing anxiety following various types of risk assessment. Although risk assessment and interventions to reduce risks have been conducted for over 20 years, very little rigorous research exists. For the investments in the new genetics to be realised, research is now needed both in how individuals respond to risk information that involves the use of genetic information and in how to facilitate and maintain behaviour change to reduce such risks.

摘要

据设想,基因信息将与其他类型的信息一起用于评估个体患各种常见疾病的风险。此类风险评估将涉及提供部分基于基因检测结果的概率性信息,以便在不引起过度焦虑的情况下促进行为改变。旨在改变的行为可能包括坚持按规定服药、改变饮食、增加运动量和戒烟。本文回顾了已开展的关于风险和基因认知、促进行为改变以及在进行各类风险评估后减轻焦虑的方法的研究。尽管风险评估和降低风险的干预措施已经实施了20多年,但严谨的研究却很少。为了实现对新遗传学的投资,现在需要开展研究,一方面研究个体如何应对涉及使用基因信息的风险信息,另一方面研究如何促进和维持行为改变以降低此类风险。

相似文献

1
Communicating genetic risk information.传达遗传风险信息。
Br Med Bull. 1999;55(2):414-28. doi: 10.1258/0007142991902466.
2
Can Communicating Personalised Disease Risk Promote Healthy Behaviour Change? A Systematic Review of Systematic Reviews.传达个性化疾病风险能否促进健康行为改变?系统评价的系统综述
Ann Behav Med. 2017 Oct;51(5):718-729. doi: 10.1007/s12160-017-9895-z.
3
Policy interventions implemented through sporting organisations for promoting healthy behaviour change.通过体育组织实施的促进健康行为改变的政策干预措施。
Cochrane Database Syst Rev. 2005 Apr 18(2):CD004809. doi: 10.1002/14651858.CD004809.pub2.
4
Visual feedback of individuals' medical imaging results for changing health behaviour.用于改变健康行为的个人医学影像结果的视觉反馈。
Cochrane Database Syst Rev. 2010 Jan 20(1):CD007434. doi: 10.1002/14651858.CD007434.pub2.
5
[Predictive genetic testing - change in paradigms for prevention and health care?].
Gesundheitswesen. 2002 Apr;64(4):224-9. doi: 10.1055/s-2002-25207.
6
The behavioral response to personalized genetic information: will genetic risk profiles motivate individuals and families to choose more healthful behaviors?对个性化基因信息的行为反应:基因风险概况是否会激励个人和家庭选择更健康的行为?
Annu Rev Public Health. 2010;31:89-103. doi: 10.1146/annurev.publhealth.012809.103532.
7
A Systematic Review of Genetic Testing and Lifestyle Behaviour Change: Are We Using High-Quality Genetic Interventions and Considering Behaviour Change Theory?基因检测与生活方式行为改变的系统评价:我们是否采用了高质量的遗传干预措施并考虑了行为改变理论?
Lifestyle Genom. 2018;11(1):49-63. doi: 10.1159/000488086. Epub 2018 Apr 10.
8
Self-regulation and the behavioural response to DNA risk information: a theoretical analysis and framework for future research.自我调节与对DNA风险信息的行为反应:一项理论分析及未来研究框架
Soc Sci Med. 2006 Mar;62(6):1360-8. doi: 10.1016/j.socscimed.2005.08.005. Epub 2005 Sep 12.
9
American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility.美国临床肿瘤学会政策声明更新:癌症易感性基因检测
J Clin Oncol. 2003 Jun 15;21(12):2397-406. doi: 10.1200/JCO.2003.03.189. Epub 2003 Apr 11.
10
Is pregnancy a teachable moment for diet and physical activity behaviour change? An interpretative phenomenological analysis of the experiences of women during their first pregnancy.怀孕是改变饮食和身体活动行为的契机吗?对女性首次怀孕经历的诠释现象学分析。
Br J Health Psychol. 2016 Nov;21(4):842-858. doi: 10.1111/bjhp.12200.

引用本文的文献

1
How eHealth use and cancer information-seeking influence older adults' acceptance of genetic testing: Mediating roles of PIGI and cancer worry.电子健康的使用和癌症信息寻求如何影响老年人对基因检测的接受度:PIGI和癌症担忧的中介作用。
Digit Health. 2025 Jan 31;11:20552076251317658. doi: 10.1177/20552076251317658. eCollection 2025 Jan-Dec.
2
How can we improve amniocentesis decision-making?我们如何改进羊膜穿刺术的决策制定?
Isr J Health Policy Res. 2016 Feb 5;5:4. doi: 10.1186/s13584-016-0060-0. eCollection 2016.
3
Review of Spinal Muscular Atrophy (SMA) for Prenatal and Pediatric Genetic Counselors.
面向产前和儿科遗传咨询师的脊髓性肌萎缩症(SMA)综述
J Genet Couns. 2016 Feb;25(1):32-43. doi: 10.1007/s10897-015-9859-z. Epub 2015 Aug 8.
4
The utilization and choices of aneuploidy screening in a midwestern population.中西部人群中非整倍体筛查的应用与选择
J Genet Couns. 2014 Oct;23(5):874-80. doi: 10.1007/s10897-014-9711-x. Epub 2014 Apr 29.
5
Genetic testing of children for predisposition to mood disorders: anticipating the clinical issues.对儿童进行情绪障碍易感性的基因检测:预见临床问题。
J Genet Couns. 2014 Aug;23(4):566-77. doi: 10.1007/s10897-014-9710-y. Epub 2014 Mar 22.
6
Communicating genetic risk information for common disorders in the era of genomic medicine.在基因组医学时代传播常见疾病的遗传风险信息。
Annu Rev Genomics Hum Genet. 2013;14:491-513. doi: 10.1146/annurev-genom-092010-110722.
7
Effect of communicating genetic and phenotypic risk for type 2 diabetes in combination with lifestyle advice on objectively measured physical activity: protocol of a randomised controlled trial.联合生活方式建议沟通 2 型糖尿病遗传和表型风险对客观测量身体活动的影响:一项随机对照试验方案。
BMC Public Health. 2012 Jun 18;12:444. doi: 10.1186/1471-2458-12-444.
8
Families' experience of oncogenetic counselling: accounts from a heterogeneous hereditary cancer risk population.家庭对肿瘤基因咨询的体验:来自异质性遗传性癌症风险人群的报告。
Fam Cancer. 2012 Jun;11(2):291-306. doi: 10.1007/s10689-012-9514-x.
9
Information related to prenatal genetic counseling: interpretation by adolescents, effects on risk perception and ethical implications.与产前遗传咨询相关的信息:青少年的解读、对风险认知的影响及伦理意义。
J Genet Couns. 2012 Aug;21(4):536-46. doi: 10.1007/s10897-011-9418-1. Epub 2011 Oct 25.
10
Interest in genetic testing for modest changes in breast cancer risk: implications for SNP testing.对乳腺癌风险适度变化的基因检测的关注:对单核苷酸多态性检测的影响。
Public Health Genomics. 2011;14(3):178-89. doi: 10.1159/000324703. Epub 2011 Apr 2.