Literature DB >> 26499982

A qualitative analysis of the attitudes of Irish patients towards participation in genetic-based research.

T P McVeigh1,2, K J Sweeney3, M J Kerin4, D J Gallagher5,6.   

Abstract

BACKGROUND: Progress in diagnostic and therapeutic strategies in medicine is dependent upon high-quality biomedical research. Technological advances have facilitated improved understanding of disease aetiology, and rapidly emerging data promises further progress. Translating this potential into the clinic depends on patient participation in innovative clinical trials. We investigated attitudes to genetic research in Ireland, particularly with respect to commercial and financial implications.
METHODS: A multi-centre, cross-sectional survey study was performed. Consecutive out-patients attending four clinics were asked to complete paper-based questionnaires. The same questionnaire was publicly available in electronic format on www.surveymonkey.com for 72 h. Data were analysed using SPSS.
RESULTS: 351 questionnaires were completed (99 paper, 252 electronic). The majority of respondents were female (n = 288, 82 %), and highly educated, with 244 (70 %) attending college/university. Most participants supported genetic research (267, 76 %), more frequently for common diseases (274, 78 %) than rare disorders (204, 58 %, p < 0.001, χ 2). 103 (29 %) had participated in scientific research, and 57 (16 %) had donated material to a bio-bank. The majority (n = 213, 61 %) would not support research with potential financial/commercial gain. 106 (30 %) would decline to participate in research if researchers would benefit financially, compared to 49 (14 %) if the research was supported by a pharmaceutical company (p < 0.001, χ 2). Respondents would provide buccal samples (258, 74 %) more readily than tissue (225, 64 %) or blood (222, 63 %).
CONCLUSIONS: A high level of support for genetic research exists among the Irish population, but active participation is dependent upon a number of factors, notably, type of biological material required, frequency of the disease in question, and commercial interest of the researchers.

Entities:  

Keywords:  Biobank; Biological specimen; Biomedical research; Data protection; Genetic research

Mesh:

Year:  2015        PMID: 26499982     DOI: 10.1007/s11845-015-1373-7

Source DB:  PubMed          Journal:  Ir J Med Sci        ISSN: 0021-1265            Impact factor:   1.568


  21 in total

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2.  Recruitment experience in the first phase of the African American Hereditary Prostate Cancer (AAHPC) study.

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Journal:  Ann Epidemiol       Date:  2000-11       Impact factor: 3.797

3.  Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder.

Authors:  Cristina Sánchez-Mora; Josep A Ramos-Quiroga; Rosa Bosch; Montse Corrales; Iris Garcia-Martínez; Mariana Nogueira; Mireia Pagerols; Gloria Palomar; Vanesa Richarte; Raquel Vidal; Alejandro Arias-Vasquez; Mariona Bustamante; Joan Forns; Silke Gross-Lesch; Monica Guxens; Anke Hinney; Martine Hoogman; Christian Jacob; Kaya K Jacobsen; Cornelis C Kan; Lambertus Kiemeney; Sarah Kittel-Schneider; Marieke Klein; Marten Onnink; Olga Rivero; Tetyana Zayats; Jan Buitelaar; Stephen V Faraone; Barbara Franke; Jan Haavik; Stefan Johansson; Klaus-Peter Lesch; Andreas Reif; Jordi Sunyer; Mònica Bayés; Miguel Casas; Bru Cormand; Marta Ribasés
Journal:  Neuropsychopharmacology       Date:  2014-10-06       Impact factor: 7.853

4.  Attitudes of genetics professionals toward the return of incidental results from exome and whole-genome sequencing.

Authors:  Joon-Ho Yu; Tanya M Harrell; Seema M Jamal; Holly K Tabor; Michael J Bamshad
Journal:  Am J Hum Genet       Date:  2014-06-26       Impact factor: 11.025

Review 5.  Defining and managing incidental findings in genetic and genomic practice.

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Authors:  Isabella Fogh; Antonia Ratti; Cinzia Gellera; Kuang Lin; Cinzia Tiloca; Valentina Moskvina; Lucia Corrado; Gianni Sorarù; Cristina Cereda; Stefania Corti; Davide Gentilini; Daniela Calini; Barbara Castellotti; Letizia Mazzini; Giorgia Querin; Stella Gagliardi; Roberto Del Bo; Francesca L Conforti; Gabriele Siciliano; Maurizio Inghilleri; Francesco Saccà; Paolo Bongioanni; Silvana Penco; Massimo Corbo; Sandro Sorbi; Massimiliano Filosto; Alessandra Ferlini; Anna M Di Blasio; Stefano Signorini; Aleksey Shatunov; Ashley Jones; Pamela J Shaw; Karen E Morrison; Anne E Farmer; Philip Van Damme; Wim Robberecht; Adriano Chiò; Bryan J Traynor; Michael Sendtner; Judith Melki; Vincent Meininger; Orla Hardiman; Peter M Andersen; Nigel P Leigh; Jonathan D Glass; Daniel Overste; Frank P Diekstra; Jan H Veldink; Michael A van Es; Christopher E Shaw; Michael E Weale; Cathryn M Lewis; Julie Williams; Robert H Brown; John E Landers; Nicola Ticozzi; Mauro Ceroni; Elena Pegoraro; Giacomo P Comi; Sandra D'Alfonso; Leonard H van den Berg; Franco Taroni; Ammar Al-Chalabi; John Powell; Vincenzo Silani
Journal:  Hum Mol Genet       Date:  2013-11-20       Impact factor: 6.150

7.  Multi-stage genome-wide association study identifies new susceptibility locus for testicular germ cell tumour on chromosome 3q25.

Authors:  Kevin Litchfield; Razvan Sultana; Anthony Renwick; Darshna Dudakia; Sheila Seal; Emma Ramsay; Silvana Powell; Anna Elliott; Margaret Warren-Perry; Rosalind Eeles; Julian Peto; Zsofia Kote-Jarai; Kenneth Muir; Jeremie Nsengimana; Michael R Stratton; Douglas F Easton; D Timothy Bishop; Robert A Huddart; Nazneen Rahman; Clare Turnbull
Journal:  Hum Mol Genet       Date:  2014-10-03       Impact factor: 6.150

8.  ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's disease.

Authors:  Christopher W Medway; Samer Abdul-Hay; Tynickwa Mims; Li Ma; Gina Bisceglio; Fanggeng Zou; Shane Pankratz; Sigrid B Sando; Jan O Aasly; Maria Barcikowska; Joanna Siuda; Zbigniew K Wszolek; Owen A Ross; Minerva Carrasquillo; Dennis W Dickson; Neill Graff-Radford; Ronald C Petersen; Nilüfer Ertekin-Taner; Kevin Morgan; Guojun Bu; Steven G Younkin
Journal:  Mol Neurodegener       Date:  2014-03-10       Impact factor: 14.195

Review 9.  Mapping the incidentalome: estimating incidental findings generated through clinical pharmacogenomics testing.

Authors:  Matthew J Westbrook; M Frances Wright; Sara L Van Driest; Tracy L McGregor; Joshua C Denny; Rebecca L Zuvich; Ellen Wright Clayton; Kyle B Brothers
Journal:  Genet Med       Date:  2012-11-29       Impact factor: 8.822

10.  Sample size and statistical power calculation in genetic association studies.

Authors:  Eun Pyo Hong; Ji Wan Park
Journal:  Genomics Inform       Date:  2012-06-30
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Authors:  Danya F Vears; Joel T Minion; Stephanie J Roberts; James Cummings; Mavis Machirori; Mwenza Blell; Isabelle Budin-Ljøsne; Lorraine Cowley; Stephanie O M Dyke; Clara Gaff; Robert Green; Alison Hall; Amber L Johns; Bartha M Knoppers; Stephanie Mulrine; Christine Patch; Eva Winkler; Madeleine J Murtagh
Journal:  PLoS One       Date:  2021-11-08       Impact factor: 3.240

2.  A pilot study investigating feasibility of mainstreaming germline BRCA1 and BRCA2 testing in high-risk patients with breast and/or ovarian cancer in three tertiary Cancer Centres in Ireland.

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Journal:  Fam Cancer       Date:  2022-08-27       Impact factor: 2.446

3.  Perceptions of patients and medical oncologists toward biospecimen donation in the setting of abnormal breast imaging findings.

Authors:  Davinia S Seah; Nabihah Tayob; Jose Pablo Leone; Jiani Hu; Jun Yin; Melissa Hughes; Sarah M Scott; Ruth I Lederman; Elizabeth Frank; Jessica J Sohl; Zsofia K Stadler; Timothy K Erick; Jeffrey Peppercorn; Eric P Winer; Stuart G Silverman; Steven E Come; Nancy U Lin
Journal:  Breast Cancer Res Treat       Date:  2022-01-23       Impact factor: 4.872

  3 in total

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