Literature DB >> 28719815

Receptiveness to participation in genetic research: A pilot study comparing views of people with depression, diabetes, or no illness.

Laura Weiss Roberts1, Jane Paik Kim2.   

Abstract

BACKGROUND: Genetic research in human health relies on the participation of individuals with or at-risk for different types of diseases, including health conditions that may be stigmatized, such as mental illnesses. This preliminary study examines the differences in attitudes toward participation in genetic research among individuals with a psychiatric disorder, individuals with a physical disorder, and individuals with no known illness.
METHODS: Seventy-nine individuals with a history of diabetes or depression, or no known illness, underwent a simulated consent process for a hypothetical genetic research study. They were then surveyed about their willingness to participate in the hypothetical study and their attitudes about future and family participation in genetic research.
RESULTS: Participants with and without a history of depression ranked participating in genetic and medical research as very important and indicated that they were likely to participate in the hypothetical genetics study. Expressed willingness to participate was generally stable and consistent with future willingness. Individuals less strongly endorsed willingness to ask family members to participate in genetic research.
CONCLUSION: Individuals with and without a history of mental illness viewed genetic and medical research favorably and expressed willingness to participate in real-time and in the future. Informed consent processes ideally include an exploration of influences upon volunteers' enrollment decisions. Additional empirical study of influences upon genetic research participation is important to ensure that volunteers' rights are respected and that conditions that greatly affect the health of the public are not neglected scientifically.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Attitudes; Depression; Genetics; Informed consent; Research participation

Mesh:

Year:  2017        PMID: 28719815      PMCID: PMC5621512          DOI: 10.1016/j.jpsychires.2017.07.002

Source DB:  PubMed          Journal:  J Psychiatr Res        ISSN: 0022-3956            Impact factor:   4.791


  52 in total

Review 1.  Genetic testing in psychiatry: a review of attitudes and beliefs.

Authors:  Ryan E Lawrence; Paul S Appelbaum
Journal:  Psychiatry       Date:  2011       Impact factor: 2.458

2.  Human behavioral informatics in genetic studies of neuropsychiatric disease: multivariate profile-based analysis.

Authors:  Cinnamon S Bloss; Kelly M Schiabor; Nicholas J Schork
Journal:  Brain Res Bull       Date:  2010-04-28       Impact factor: 4.077

3.  Genetics in psychiatry: are the promises met?

Authors:  Brigitta Bondy
Journal:  World J Biol Psychiatry       Date:  2011-03       Impact factor: 4.132

4.  Bioethics principles, informed consent, and ethical care for special populations: curricular needs expressed by men and women physicians-in-training.

Authors:  Laura Weiss Roberts; Cynthia M A Geppert; Teddy D Warner; Katherine A Green Hammond; Leandrea Prosen Lamberton
Journal:  Psychosomatics       Date:  2005 Sep-Oct       Impact factor: 2.386

5.  Substance use disorder genetic research: investigators and participants grapple with the ethical issues.

Authors:  Marilyn E Coors; Kristen M Raymond
Journal:  Psychiatr Genet       Date:  2009-04       Impact factor: 2.458

6.  Whole-genome association studies for multigenic diseases: ethical dilemmas arising from commercialization--the case of genetic testing for autism.

Authors:  Bertrand R Jordan; Daniel Fu Chang Tsai
Journal:  J Med Ethics       Date:  2010-06-16       Impact factor: 2.903

7.  Informed consent and subject motivation to participate in a large, population-based genomics study: the Marshfield Clinic Personalized Medicine Research Project.

Authors:  Catherine A McCarty; Anuradha Nair; Diane M Austin; Philip F Giampietro
Journal:  Community Genet       Date:  2007

Review 8.  Ethical issues in psychiatric genetics research: points to consider.

Authors:  Barbara Bowles Biesecker; Holly Landrum Peay
Journal:  Psychopharmacology (Berl)       Date:  2003-09-10       Impact factor: 4.530

9.  Pilot study on patients' and spouses' attitudes toward potential genetic testing for bipolar disorder.

Authors:  C L Trippitelli; K R Jamison; M F Folstein; J J Bartko; J R DePaulo
Journal:  Am J Psychiatry       Date:  1998-07       Impact factor: 18.112

Review 10.  Genomewide association studies: history, rationale, and prospects for psychiatric disorders.

Authors:  Sven Cichon; Nick Craddock; Mark Daly; Stephen V Faraone; Pablo V Gejman; John Kelsoe; Thomas Lehner; Douglas F Levinson; Audra Moran; Pamela Sklar; Patrick F Sullivan
Journal:  Am J Psychiatry       Date:  2009-04-01       Impact factor: 18.112

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  6 in total

1.  Do human subject safeguards matter to potential participants in psychiatric genetic research?

Authors:  Laura Weiss Roberts; Jane Paik Kim; Tenzin Tsungmey; Laura B Dunn
Journal:  J Psychiatr Res       Date:  2019-06-08       Impact factor: 4.791

2.  Attitudes Regarding Enrollment in a Genetic Research Project: An Informed Consent Simulation Study Comparing Views of People With Depression, Diabetes, and Neither Condition.

Authors:  Jane Paik Kim; Katie Ryan; Laura Weiss Roberts
Journal:  J Empir Res Hum Res Ethics       Date:  2019-07-22       Impact factor: 1.742

3.  Attitudes and experiences regarding genetic research among persons of African descent.

Authors:  Denise M Scott; Veronica G Thomas; Jane Otado; Faun Rockcliffe; Omotomilade Olopoenia; Dietrich Johnson; Shawneequa Callier
Journal:  J Community Genet       Date:  2019-05-06

4.  Maternal Perceptions of Safeguards for Research Involving Children.

Authors:  Maryam Rostami; Jane Paik Kim; Laura Turner-Essel; Laura Weiss Roberts
Journal:  J Child Fam Stud       Date:  2021-08-07

5.  Views of the importance of psychiatric genetic research by potential volunteers from stakeholder groups.

Authors:  Laura Weiss Roberts; Tenzin Tsungmey; Jane Paik Kim; Melinda Hantke
Journal:  J Psychiatr Res       Date:  2018-09-19       Impact factor: 4.791

6.  Consent for Use of Genetic Data among US Hispanics/Latinos: Results from the Hispanic Community Health Study/ Study of Latinos.

Authors:  Sara Gonzalez; Garrett Strizich; Carmen R Isasi; Simin Hua; Betsy Comas; Tamar Sofer; Bharat Thyagarajan; Krista M Perreira; Gregory A Talavera; Martha L Daviglus; Sarah C Nelson; Aida L Giachello; Neil Schneiderman; Robert C Kaplan
Journal:  Ethn Dis       Date:  2021-10-21       Impact factor: 1.847

  6 in total

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