• 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

Can genetic information change patient behavior to reduce Type 2 diabetes risk?

作者信息

Vassy Jason L

机构信息

Section of General Internal Medicine, VA Boston HealthCare System, MA, USA, and G2P Research Program, Division of General Internal Medicine & Primary Care, Department of Medicine, Brigham & Women's Hospital, MA, USA, and Department of Medicine, Harvard Medical School, 150 South Huntington Avenue, Building 9, Suite 425, Boston, MA 02130, USA, Tel.: +1 857 364 2561, ,

出版信息

Per Med. 2013 Jan 1;10(1). doi: 10.2217/pme.12.116.

DOI:10.2217/pme.12.116
PMID:24358047
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3864859/
Abstract
摘要

相似文献

1
Can genetic information change patient behavior to reduce Type 2 diabetes risk?基因信息能改变患者行为以降低2型糖尿病风险吗?
Per Med. 2013 Jan 1;10(1). doi: 10.2217/pme.12.116.
2
Perceived impact of diabetes genetic risk testing among patients at high phenotypic risk for type 2 diabetes.2 型糖尿病表型高危患者对糖尿病遗传风险检测的感知影响。
Diabetes Care. 2011 Mar;34(3):568-73. doi: 10.2337/dc10-1960. Epub 2011 Feb 1.
3
Patient beliefs and behaviors about genomic risk for type 2 diabetes: implications for prevention.患者对2型糖尿病基因组风险的认知与行为:对预防的启示
J Health Commun. 2015;20(6):728-35. doi: 10.1080/10810730.2015.1018563. Epub 2015 Apr 6.
4
Impact of literacy and numeracy on motivation for behavior change after diabetes genetic risk testing.文化程度和计算能力对糖尿病遗传风险检测后行为改变动机的影响。
Med Decis Making. 2012 Jul-Aug;32(4):606-15. doi: 10.1177/0272989X11431608. Epub 2012 Jan 12.
5
Effect of genetic testing for risk of type 2 diabetes mellitus on health behaviors and outcomes: study rationale, development and design.2 型糖尿病风险基因检测对健康行为和结果的影响:研究背景、方法和设计。
BMC Health Serv Res. 2012 Jan 18;12:16. doi: 10.1186/1472-6963-12-16.
6
From Individualized to Personalized Medicine in Diabetes: An Expert Overview.从糖尿病的个体化医疗到个性化医疗:专家概述
J Assoc Physicians India. 2019 Sep;67(9):78-82.
7
Path to Personalized Medicine for Type 2 Diabetes Mellitus: Reality and Hope.2型糖尿病个性化医疗之路:现实与希望
Acta Med Iran. 2017 Mar;55(3):166-174.
8
Lifestyle Advice Combined with Personalized Estimates of Genetic or Phenotypic Risk of Type 2 Diabetes, and Objectively Measured Physical Activity: A Randomized Controlled Trial.生活方式建议结合2型糖尿病遗传或表型风险的个性化评估以及客观测量的身体活动:一项随机对照试验。
PLoS Med. 2016 Nov 29;13(11):e1002185. doi: 10.1371/journal.pmed.1002185. eCollection 2016 Nov.
9
Personalized medicine and stroke prevention: where are we?个性化医疗与中风预防:我们目前的进展如何?
Vasc Health Risk Manag. 2015 Dec 2;11:601-11. doi: 10.2147/VHRM.S77571. eCollection 2015.
10
Obesity Genes, Personalized Medicine, and Public Health Policy.肥胖基因、个性化医疗与公共卫生政策
Curr Obes Rep. 2015 Sep;4(3):319-23. doi: 10.1007/s13679-015-0163-x.

引用本文的文献

1
Recent advances and perspectives in next generation sequencing application to the genetic research of type 2 diabetes.下一代测序技术在2型糖尿病基因研究中的最新进展与展望
World J Diabetes. 2019 Jul 15;10(7):376-395. doi: 10.4239/wjd.v10.i7.376.
2
A randomized trial Examining The Impact Of Communicating Genetic And Lifestyle Risks For Obesity.一项探讨肥胖的遗传和生活方式风险沟通影响的随机试验。
Obesity (Silver Spring). 2016 Dec;24(12):2481-2490. doi: 10.1002/oby.21661.
3
Common genetic risk for melanoma encourages preventive behavior change.黑色素瘤的常见遗传风险促使预防行为发生改变。
J Pers Med. 2015 Feb 17;5(1):36-49. doi: 10.3390/jpm5010036.
4
Validation of a proposed warfarin dosing algorithm based on the genetic make-up of Egyptian patients.验证一种基于埃及患者基因构成的华法林剂量算法。
Mol Diagn Ther. 2013 Dec;17(6):381-90. doi: 10.1007/s40291-013-0046-3.

本文引用的文献

1
Genotype prediction of adult type 2 diabetes from adolescence in a multiracial population.从多民族人群的青春期预测成年 2 型糖尿病的基因型。
Pediatrics. 2012 Nov;130(5):e1235-42. doi: 10.1542/peds.2012-1132. Epub 2012 Oct 15.
2
Personalized genetic risk counseling to motivate diabetes prevention: a randomized trial.个性化遗传风险咨询以促进糖尿病预防:一项随机试验。
Diabetes Care. 2013 Jan;36(1):13-9. doi: 10.2337/dc12-0884. Epub 2012 Aug 28.
3
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.大规模的关联分析为 2 型糖尿病的遗传结构和病理生理学提供了深入了解。
Nat Genet. 2012 Sep;44(9):981-90. doi: 10.1038/ng.2383. Epub 2012 Aug 12.
4
Effect of genetic testing for risk of type 2 diabetes mellitus on health behaviors and outcomes: study rationale, development and design.2 型糖尿病风险基因检测对健康行为和结果的影响:研究背景、方法和设计。
BMC Health Serv Res. 2012 Jan 18;12:16. doi: 10.1186/1472-6963-12-16.
5
Design of a randomized trial of diabetes genetic risk testing to motivate behavior change: the Genetic Counseling/lifestyle Change (GC/LC) Study for Diabetes Prevention.糖尿病遗传风险检测以促进行为改变的随机试验设计:预防糖尿病的遗传咨询/生活方式改变(GC/LC)研究。
Clin Trials. 2011 Oct;8(5):609-15. doi: 10.1177/1740774511414159.
6
Updated genetic score based on 34 confirmed type 2 diabetes Loci is associated with diabetes incidence and regression to normoglycemia in the diabetes prevention program.基于 34 个已确认的 2 型糖尿病基因座的更新遗传评分与糖尿病预防计划中的糖尿病发病率和血糖正常化的逆转相关。
Diabetes. 2011 Apr;60(4):1340-8. doi: 10.2337/db10-1119. Epub 2011 Mar 4.
7
Effect of direct-to-consumer genomewide profiling to assess disease risk.直接面向消费者的全基因组分析评估疾病风险的效果。
N Engl J Med. 2011 Feb 10;364(6):524-34. doi: 10.1056/NEJMoa1011893. Epub 2011 Jan 12.
8
Identifying primary care patients at risk for future diabetes and cardiovascular disease using electronic health records.利用电子健康记录识别未来患有糖尿病和心血管疾病风险的初级保健患者。
BMC Health Serv Res. 2009 Sep 22;9:170. doi: 10.1186/1472-6963-9-170.
9
The clinical application of genetic testing in type 2 diabetes: a patient and physician survey.基因检测在 2 型糖尿病中的临床应用:患者和医生调查。
Diabetologia. 2009 Nov;52(11):2299-2305. doi: 10.1007/s00125-009-1512-7. Epub 2009 Sep 2.
10
Genotype score in addition to common risk factors for prediction of type 2 diabetes.除常见风险因素外,基因型评分对2型糖尿病的预测作用
N Engl J Med. 2008 Nov 20;359(21):2208-19. doi: 10.1056/NEJMoa0804742.