• 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

“尽管你只是拼图中的一小块,但也是大局的一部分”——参与遗传性共济失调注册观察性研究的个体的动机和期望。

"It's being part of the big picture, even though you're a tiny jigsaw piece"-motivations and expectations of individuals participating in the Enroll-HD observational study.

作者信息

Davies E, Craufurd D, MacLeod R

机构信息

Division of Evolution and Genomic Sciences, School of Biological Science, University of Manchester, Manchester, UK.

Department of Clinical Genetics, Addenbrooke's Hospital, Hills Road, Cambridge, UK.

出版信息

J Community Genet. 2020 Oct;11(4):421-432. doi: 10.1007/s12687-020-00459-3. Epub 2020 Mar 10.

DOI:10.1007/s12687-020-00459-3
PMID:32157658
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7475145/
Abstract

Predictive test guidelines for Huntington's disease (HD) recommend individuals are offered opportunities to participate in research regardless of test outcome. Consistent with most HD centres of excellence, the Manchester Centre for Genomic Medicine (MCGM) invites eligible individuals to participate in the observational study, Enroll-HD. Limited research has been conducted to date on the views of research participants and the possible impact of participation. The aim of this qualitative study was to explore the experiences of ten individuals taking part in the Enroll-HD study following pre-symptomatic testing for HD. Half of the individuals had tested positive for the HD mutation and the other half had tested negative. Participants were generally motivated to take part in the study by both personal and altruistic reasons. Overall, they were very positive about participation in Enroll-HD. Valuable aspects included good relationships with the research/clinical team, increased understanding of the condition, an enhanced self-image and a shared experience with affected parents. Issues for improvement to encourage participation included access to study site and more regular communication about study progress. Participants, while generally optimistic about research progress, were realistic about challenges.

摘要

亨廷顿舞蹈症(HD)的预测性检测指南建议,无论检测结果如何,都应为个人提供参与研究的机会。与大多数卓越的HD中心一致,曼彻斯特基因组医学中心(MCGM)邀请符合条件的个人参与观察性研究“入组HD研究(Enroll-HD)”。迄今为止,针对研究参与者的观点以及参与可能产生的影响开展的研究有限。这项定性研究的目的是探索10名在进行HD症状前检测后参与“入组HD研究”的个人的经历。其中一半个体的HD突变检测呈阳性,另一半呈阴性。参与者参与研究的动机通常既有个人原因,也有利他原因。总体而言,他们对参与“入组HD研究”非常积极。有价值的方面包括与研究/临床团队的良好关系、对病情的进一步了解、自我形象的提升以及与患病父母的共同经历。为鼓励参与而有待改进的问题包括前往研究地点的便利性以及关于研究进展的更定期沟通。参与者虽然总体上对研究进展持乐观态度,但对挑战也很现实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e230/7475145/d83f4de076e3/12687_2020_459_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e230/7475145/9d5547a1191f/12687_2020_459_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e230/7475145/d83f4de076e3/12687_2020_459_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e230/7475145/9d5547a1191f/12687_2020_459_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e230/7475145/d83f4de076e3/12687_2020_459_Fig2_HTML.jpg

相似文献

1
"It's being part of the big picture, even though you're a tiny jigsaw piece"-motivations and expectations of individuals participating in the Enroll-HD observational study.“尽管你只是拼图中的一小块,但也是大局的一部分”——参与遗传性共济失调注册观察性研究的个体的动机和期望。
J Community Genet. 2020 Oct;11(4):421-432. doi: 10.1007/s12687-020-00459-3. Epub 2020 Mar 10.
2
Enroll-HD: An Integrated Clinical Research Platform and Worldwide Observational Study for Huntington's Disease.Enroll-HD:一个用于亨廷顿舞蹈症的综合临床研究平台及全球观察性研究。
Front Neurol. 2021 Aug 18;12:667420. doi: 10.3389/fneur.2021.667420. eCollection 2021.
3
Positive Attitudes and Therapeutic Misconception Around Hypothetical Clinical Trial Participation in the Huntington's Disease Community.亨廷顿舞蹈症群体中关于假设性临床试验参与的积极态度和治疗误解
J Huntingtons Dis. 2019;8(4):421-430. doi: 10.3233/JHD-190382.
4
Speech and language difficulties in Huntington's disease: A qualitative study of patients' and professional caregivers' experiences.亨廷顿舞蹈症患者的言语和语言障碍:一项关于患者及专业护理人员经历的定性研究
Int J Lang Commun Disord. 2021 Mar;56(2):330-345. doi: 10.1111/1460-6984.12604. Epub 2021 Feb 12.
5
Another Perspective on Huntington's Disease: Disease Burden in Family Members and Pre-Manifest HD When Compared to Genotype-Negative Participants from ENROLL-HD.亨廷顿舞蹈症的另一种视角:与ENROLL-HD研究中基因阴性参与者相比,患者家庭成员及症状前亨廷顿舞蹈症患者的疾病负担
Brain Sci. 2021 Dec 8;11(12):1621. doi: 10.3390/brainsci11121621.
6
Data Analytics from Enroll-HD, a Global Clinical Research Platform for Huntington's Disease.来自Enroll-HD的数据分析,一个用于亨廷顿舞蹈症的全球临床研究平台。
Mov Disord Clin Pract. 2016 Jun 22;4(2):212-224. doi: 10.1002/mdc3.12388. eCollection 2017 Mar-Apr.
7
Machine learning in Huntington's disease: exploring the Enroll-HD dataset for prognosis and driving capability prediction.亨廷顿病的机器学习:探索 Enroll-HD 数据集以进行预后和驾驶能力预测。
Orphanet J Rare Dis. 2023 Jul 27;18(1):218. doi: 10.1186/s13023-023-02785-4.
8
Genetic and Environmental Contributors to Neurodegeneration: An Exploration of the Effects of Alcohol on Clinical Features of Huntington's Disease Using the Enroll-HD Global Platform.遗传和环境因素对神经退行性变的影响:利用 Enroll-HD 全球平台探索酒精对亨廷顿病临床特征的影响。
Int J Environ Res Public Health. 2021 May 12;18(10):5113. doi: 10.3390/ijerph18105113.
9
Genetic Counselling and Narrative Practices: A Model of Support following a "Negative" Predictive Test for Huntington's Disease.遗传咨询与叙事实践:亨廷顿舞蹈症“阴性”预测性检测后的支持模式
J Huntingtons Dis. 2018;7(2):175-183. doi: 10.3233/JHD-170276.
10
Psychosocial impact on individuals who received negative test results from predictive testing for Huntington's disease: An exploratory qualitative study.
J Genet Couns. 2025 Apr;34(2):e1981. doi: 10.1002/jgc4.1981. Epub 2024 Oct 4.

引用本文的文献

1
Investigating people's attitudes towards participating in longitudinal health research: an intersectionality-informed perspective.调查人们对参与纵向健康研究的态度:一个交叉视角。
Int J Equity Health. 2023 Jan 31;22(1):23. doi: 10.1186/s12939-022-01807-0.
2
Perceptions about Research Participation among Individuals at Risk and Individuals with Premanifest Huntington's Disease: A Survey Conducted by the European Huntington Association.欧洲亨廷顿病协会对亨廷顿病风险个体和症状前个体参与研究的认知情况调查
J Pers Med. 2021 Aug 20;11(8):815. doi: 10.3390/jpm11080815.

本文引用的文献

1
Young People's Experiences of Participation in Clinical Trials: Reasons for Taking Part.年轻人参与临床试验的体验:参与原因。
Am J Bioeth. 2015;15(11):3-13. doi: 10.1080/15265161.2015.1088974.
2
Diagnostic genetic testing for Huntington's disease.亨廷顿舞蹈症的诊断性基因检测
Pract Neurol. 2015 Feb;15(1):80-4. doi: 10.1136/practneurol-2013-000790. Epub 2014 Aug 28.
3
The impact of participation in genetic research for families with cleft lip with and without cleft palate: a qualitative study.唇腭裂及单纯唇裂家庭参与基因研究的影响:一项定性研究
J Community Genet. 2014 Jul;5(3):249-56. doi: 10.1007/s12687-014-0183-3. Epub 2014 Feb 6.
4
Role and Influence of the Patient's Companion in Family Medicine Consultations: "The Patient's Perspective".患者陪伴者在家庭医学咨询中的角色与影响:“患者视角”
J Family Med Prim Care. 2013 Jul;2(3):283-7. doi: 10.4103/2249-4863.120767.
5
Motives for participating in a clinical research trial: a pilot study in Brazil.参与临床试验的动机:巴西的一项试点研究。
BMC Public Health. 2013 Jan 10;13:19. doi: 10.1186/1471-2458-13-19.
6
Appealing to altruism is not enough: motivators for participating in health services research.仅诉诸利他主义是不够的:参与卫生服务研究的动机
J Empir Res Hum Res Ethics. 2012 Jul;7(3):84-90. doi: 10.1525/jer.2012.7.3.84.
7
Parents' perspectives on participating in genetic research in autism.家长对参与自闭症基因研究的看法。
J Autism Dev Disord. 2013 Mar;43(3):556-68. doi: 10.1007/s10803-012-1592-y.
8
The incidence and prevalence of Huntington's disease: a systematic review and meta-analysis.亨廷顿病的发病率和患病率:系统评价和荟萃分析。
Mov Disord. 2012 Aug;27(9):1083-91. doi: 10.1002/mds.25075. Epub 2012 Jun 12.
9
Allele-selective inhibition of trinucleotide repeat genes.三核苷酸重复基因的等位基因选择性抑制。
Drug Discov Today. 2012 May;17(9-10):443-50. doi: 10.1016/j.drudis.2012.01.006. Epub 2012 Jan 18.
10
Assessing research participants' perceptions of their clinical research experiences.评估研究参与者对其临床研究经历的看法。
Clin Transl Sci. 2011 Dec;4(6):403-13. doi: 10.1111/j.1752-8062.2011.00349.x. Epub 2011 Nov 7.