Literature DB >> 15475669

Public experiences, knowledge and expectations about medical genetics and the use of genetic information.

Lidewij Henneman1, Danielle R M Timmermans, Gerrit van der Wal.   

Abstract

OBJECTIVE: The objectives of this study were (1) to explore public experiences, genetic knowledge, expectations of future medical genetic developments, and the attitudes towards the use of genetic information, and (2) to determine whether there are subject characteristics associated with these variables.
METHODS: Participants (n = 1,308, age > or = 25 years) of a Dutch consumer panel were sent a questionnaire, specifically designed for this study.
RESULTS: Response was 63% (817/1,308). A minority of respondents reported to know someone with a hereditary disease (34%) or to have used a genetic test (8%). Overall, 57% perceived a lack of genetic knowledge. In multivariate analyses, high self-rated knowledge, younger age, having heard of genetic testing, high educational level, female gender, having children living at home, being a health professional, and familiarity with genetic testing were positively associated with genetic knowledge. Future expectations of the consequences of developments in medical genetics varied between the subjects. The great majority expected great benefits for medical practice such as an increasing use of genetic aspects of disease for diagnosis or prevention. One fifth, mainly older people, anticipated a negative impact of genetic developments on society. The results also show that most people are reserved to share their genetic information with others, especially with regard to the wider public domain (e.g. industry and insurers) and employers. Remarkably, respondents were more willing to share their genetic information with scientific researchers (68%) than with their relatives (54%).
CONCLUSION: This study suggests that although one fifth anticipates negative consequences of genetic developments, the great majority has high expectations about the increasing use of genetics in prevention, diagnosis and treatment of diseases. In developing educational programmes about genetic innovations in medicine, policymakers will have to take into account pre-existing lay knowledge, views and expectations of different groups of citizens towards these developments. 2004 S. Karger AG, Basel.

Entities:  

Keywords:  Empirical Approach; Genetics and Reproduction

Mesh:

Year:  2004        PMID: 15475669     DOI: 10.1159/000080302

Source DB:  PubMed          Journal:  Community Genet        ISSN: 1422-2795


  54 in total

1.  Veterans' experience in using the online Surgeon General's family health history tool.

Authors:  Nedal Arar; Joann Seo; Hanna E Abboud; Michael Parchman; Polly Noel
Journal:  Per Med       Date:  2011-09-01       Impact factor: 2.512

2.  Knowledge, Attitudes, and Practice Regarding Genetic Testing and Genetic Counselors in Jordan: A Population-Based Survey.

Authors:  Mamoun Ahram; Majd Soubani; Lana Abu Salem; Haneen Saker; Muayyad Ahmad
Journal:  J Genet Couns       Date:  2015-04-08       Impact factor: 2.537

3.  Subjects' expectations in neuroimaging research.

Authors:  Matthew P Kirschen; Agnieszka Jaworska; Judy Illes
Journal:  J Magn Reson Imaging       Date:  2006-02       Impact factor: 4.813

Review 4.  Incidental findings from clinical genome-wide sequencing: a review.

Authors:  Z Lohn; S Adam; P H Birch; J M Friedman
Journal:  J Genet Couns       Date:  2013-05-26       Impact factor: 2.537

5.  Use and evaluation of an individually tailored website for counselees prior to breast cancer genetic counseling.

Authors:  Akke Albada; Margreet G E M Ausems; Roel Otten; Jozien M Bensing; Sandra van Dulmen
Journal:  J Cancer Educ       Date:  2011-12       Impact factor: 2.037

6.  What's at stake? Genetic information from the perspective of people with epilepsy and their family members.

Authors:  Sara Shostak; Dana Zarhin; Ruth Ottman
Journal:  Soc Sci Med       Date:  2011-07-23       Impact factor: 4.634

7.  A pre-visit tailored website enhances counselees' realistic expectations and knowledge and fulfils information needs for breast cancer genetic counselling.

Authors:  Akke Albada; Sandra van Dulmen; Dick Lindhout; Jozien M Bensing; Margreet G E M Ausems
Journal:  Fam Cancer       Date:  2012-03       Impact factor: 2.375

8.  Measuring genetic knowledge: a brief survey instrument for adolescents and adults.

Authors:  S M Fitzgerald-Butt; A Bodine; K M Fry; J Ash; A N Zaidi; V Garg; C A Gerhardt; K L McBride
Journal:  Clin Genet       Date:  2015-06-29       Impact factor: 4.438

9.  Cultural beliefs on disease causation in the Philippines: challenge and implications in genetic counseling.

Authors:  Peter James B Abad; Michael L Tan; Melissa Mae P Baluyot; Angela Q Villa; Gay Luz Talapian; Ma Elouisa Reyes; Riza Concordia Suarez; Aster Lynn D Sur; Vanessa Dyan R Aldemita; Carmencita David Padilla; Mercy Ygona Laurino
Journal:  J Community Genet       Date:  2014-07-16

10.  Public attitudes towards genetic testing revisited: comparing opinions between 2002 and 2010.

Authors:  Lidewij Henneman; Eric Vermeulen; Carla G van El; Liesbeth Claassen; Danielle R M Timmermans; Martina C Cornel
Journal:  Eur J Hum Genet       Date:  2012-12-19       Impact factor: 4.246

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.