Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/27183
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dc.contributor.authorYanes, Tatiane-
dc.contributor.authorMeiser, Bettina-
dc.contributor.authorKaur, Rajneesh-
dc.contributor.authorYoung, Mary-Anne-
dc.contributor.authorMitchell, Philip B-
dc.contributor.authorScheepers-Joynt, Maatje-
dc.contributor.authorMcInerny, Simone-
dc.contributor.authorTaylor, Shelby-
dc.contributor.authorBarlow-Stewart, Kristine-
dc.contributor.authorAntill, Yoland-
dc.contributor.authorSalmon, Lucinda-
dc.contributor.authorSmyth, Courtney-
dc.contributor.authorBetz-Stablein, Brigid-
dc.contributor.authorJames, Paul A-
dc.date2021-
dc.date.accessioned2021-08-09T05:49:23Z-
dc.date.available2021-08-09T05:49:23Z-
dc.date.issued2021-
dc.identifier.citationGenetics in medicine : official journal of the American College of Medical Genetics 2021; 23(12): 2316-2323en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/27183-
dc.description.abstractTo prospectively assess patient reported outcomes and risk management behavior of women choosing to receive (receivers) or decline (decliners) their breast cancer polygenic risk score (PRS). Women either unaffected or affected by breast cancer and from families with no identified pathogenic variant in a breast cancer risk gene were invited to receive their PRS. All participants completed a questionnaire at study enrollment. Receivers completed questionnaires at two weeks and 12 months after receiving their PRS, and decliners a second questionnaire at 12 months post study enrollment. Of the 208 participants, 165 (79%) received their PRS. Among receivers, there were no changes in anxiety or distress following testing. However, compared to women with a low PRS, those with a high PRS reported greater genetic testing-specific distress, perceived risk, decisional regret, and less genetic testing-positive response. At 12 months, breast screening and uptake of risk-reducing strategies were consistent with current Australian guidelines of breast cancer risk management. Reasons for declining PRS included being unable to attend the appointment in person and concerns over potential emotional response. The outcomes of the study provide insight into women's responses to receiving PRS and highlight the issues that need to be addressed in the associated model of genetic counseling.en
dc.language.isoeng-
dc.subjectBreast canceren
dc.titleBreast cancer polygenic risk scores: a 12-month prospective study of patient reported outcomes and risk management behavior.en
dc.typeJournal Articleen
dc.identifier.journaltitleGenetics in Medicine : Official Journal of the American College of Medical Geneticsen
dc.identifier.affiliationNorthern Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australiaen
dc.identifier.affiliationPrince of Wales Clinical School, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australiaen
dc.identifier.affiliationFamilial Cancer Clinic, Monash Medical Centre, Melbourne, VIC, Australiaen
dc.identifier.affiliationQIMR Berghofer Medical Research Institute, Cancer and Population studies, Brisbane, QLD, Australiaen
dc.identifier.affiliationSir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC, Australiaen
dc.identifier.affiliationThe University of Queensland Diamantina Institute, Dermatology Research Centre, University of Queensland, Brisbane, QLD, Australiaen
dc.identifier.affiliationSchool of Psychiatry, University of New South Wales, Sydney, NSW, Australiaen
dc.identifier.affiliationParkville Familial Cancer Centre, Peter MacCallum Cancer Centre and the Royal Melbourne Hospital, Melbourne, VIC, Australiaen
dc.identifier.affiliationKinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Sydney, NSW, Australiaen
dc.identifier.affiliationBlack Dog Institute, Prince of Wales Hospital, Sydney, NSW, Australiaen
dc.identifier.affiliationFamilial Cancer Clinic, Cabrini Health, Melbourne, VIC, Australiaen
dc.identifier.affiliationClinical Geneticsen
dc.identifier.doi10.1038/s41436-021-01288-6en
dc.type.contentTexten
dc.identifier.orcid0000-0002-3905-3025en
dc.identifier.pubmedid34341522-
local.name.researcherSalmon, Lucinda
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptClinical Genetics-
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