Literature DB >> 22113136

Predictive genetic testing and beyond: a theory of engagement.

Marion McAllister1.   

Abstract

This article presents a tentative grounded theory, which can provide some explanation of variation in behaviour around predictive genetic testing (PGT) for Hereditary Non-Polyposis Colorectal Cancer (HNPCC), based on interviews with individuals (n = 55) from families with a clinical diagnosis of HNPCC, 12 of whom were followed through the PGT protocol. The theory is built around a core category of engagement, a newly constructed concept reflecting the degree of cognitive and emotional involvement with cancer risk in individuals from these families, and models the psychosocial process of engaging with cancer risk. The degree of engagement at the time of testing can explain variations in approaches and reactions to PGT. A series of social factors, many related to the experiences of family life, emerged as either facilitating or blocking the process of engaging with cancer risk; a series of psychological factors emerged as interacting in a recursive, dynamic manner with each other and with engagement status. The degree of engagement can change with the unfolding of time and events in family life. The theory of engagement (TE) provides an explanatory framework for understanding behaviour related to PGT for HNPCC, and can potentially be applied to research on risk perception in the social sciences more generally. In addition, the theory may have potential uses in the genetics clinic, in identifying individuals at risk of adverse reactions to PGT for cancer, thus enabling better targeting of genetic counselling resources.

Entities:  

Year:  2002        PMID: 22113136     DOI: 10.1177/1359105302007005628

Source DB:  PubMed          Journal:  J Health Psychol        ISSN: 1359-1053


  18 in total

1.  Predictive testing of eighteen year olds: counseling challenges.

Authors:  Clara L Gaff; Elly Lynch; Lesley Spencer
Journal:  J Genet Couns       Date:  2006-08       Impact factor: 2.537

Review 2.  Information processing in the context of genetic risk: implications for genetic-risk communication.

Authors:  Holly Etchegary; Colin Perrier
Journal:  J Genet Couns       Date:  2007-05-01       Impact factor: 2.537

3.  Choosing not to undergo predictive genetic testing for hereditary colorectal cancer syndromes: expanding our understanding of decliners and declining.

Authors:  Louise A Keogh; Heather Niven; Alison Rutstein; Louisa Flander; Clara Gaff; Mark Jenkins
Journal:  J Behav Med       Date:  2017-02-14

4.  Choosing not to know: accounts of non-engagement with pre-symptomatic testing for Machado-Joseph disease.

Authors:  Álvaro Mendes; Milena Paneque; Angus Clarke; Jorge Sequeiros
Journal:  Eur J Hum Genet       Date:  2018-12-20       Impact factor: 4.246

5.  "Awakening to" a new meaning of being at-risk for arrhythmogenic right ventricular cardiomyopathy: a grounded theory study.

Authors:  April Manuel; Fern Brunger
Journal:  J Community Genet       Date:  2015-01-27

6.  Family communication following BRCA1/2 genetic testing: a close look at the process.

Authors:  Darquise Lafrenière; Karine Bouchard; Béatrice Godard; Jacques Simard; Michel Dorval
Journal:  J Genet Couns       Date:  2012-12-16       Impact factor: 2.537

7.  Death anxiety and symbolic immortality in relatives at risk for familial amyloid polyneuropathy type I (FAP I, ATTR V30M).

Authors:  Paula I Santos; Eurico Figueiredo; Inês Gomes; Jorge Sequeiros
Journal:  J Genet Couns       Date:  2010-08-03       Impact factor: 2.537

8.  Discussions about predictive genetic testing for Lynch syndrome: the role of health professionals and families in decisions to decline.

Authors:  Anaita Kanga-Parabia; Clara Gaff; Louisa Flander; Mark Jenkins; Louise A Keogh
Journal:  Fam Cancer       Date:  2018-10       Impact factor: 2.375

9.  Engagement with genetic discrimination: concerns and experiences in the context of Huntington disease.

Authors:  Yvonne Bombard; Elizabeth Penziner; Oksana Suchowersky; Mark Guttman; Jane S Paulsen; Joan L Bottorff; Michael R Hayden
Journal:  Eur J Hum Genet       Date:  2007-10-24       Impact factor: 4.246

10.  Discovering the family history of Huntington disease (HD).

Authors:  Holly Etchegary
Journal:  J Genet Couns       Date:  2006-04       Impact factor: 2.537

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