Please use this identifier to cite or link to this item:
https://ahro.austin.org.au/austinjspui/handle/1/22279
Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Yanes, Tatiane | - |
dc.contributor.author | Meiser, Bettina | - |
dc.contributor.author | Kaur, Rajneesh | - |
dc.contributor.author | Scheepers-Joynt, Maatje | - |
dc.contributor.author | McInerny, Simone | - |
dc.contributor.author | Taylor, Shelby | - |
dc.contributor.author | Barlow-Stewart, Kristine | - |
dc.contributor.author | Antill, Yoland | - |
dc.contributor.author | Salmon, Lucinda | - |
dc.contributor.author | Smyth, Courtney | - |
dc.contributor.author | Young, Mary-Anne | - |
dc.contributor.author | James, Paul A | - |
dc.date | 2019-12-25 | - |
dc.date.accessioned | 2019-12-18T04:02:52Z | - |
dc.date.available | 2019-12-18T04:02:52Z | - |
dc.date.issued | 2020-03 | - |
dc.identifier.citation | Clinical genetics 2020; 97(3): 492-501 | - |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/22279 | - |
dc.description.abstract | Polygenic risk scores (PRS) are increasingly being implemented to assess breast cancer risk. This study aimed to assess and determine factors associated with uptake of PRS among women at increased risk of breast cancer for whom genetic testing to date had been uninformative. Participants were recruited from the Variants in Practice study from which breast cancer PRS had been calculated. Four hundred women were notified by letter of the availability of their PRS and invited to complete a self-administered survey comprising several validated scales. Considering non-participants, uptake of PRS lies between 61.8% to 42.1%. Multivariate logistic regression identified that women were more likely to receive their PRS if they reported greater benefits (odds ratio [OR]=1.17, p=0.011) and fewer barriers to receiving their PRS (OR= 0.80, p=0.007), had completed higher level education (OR=3.32, p=0.004), and did not have daughters (0.29, p=0.006). Uptake of breast cancer PRS varies according to several testing- and patient-related factors. Knowledge of these factors will facilitate the implementation of polygenic testing in clinical practice and support informed decision making by patients. This article is protected by copyright. All rights reserved. | - |
dc.language.iso | eng | - |
dc.subject | Breast cancer | - |
dc.subject | polygenic risk | - |
dc.subject | psychosocial | - |
dc.subject | single nucleotide polymorphism | - |
dc.subject | uptake | - |
dc.title | Uptake of Polygenic Risk Information among Women at Increased Risk of Breast Cancer. | - |
dc.type | Journal Article | - |
dc.identifier.journaltitle | Clinical genetics | - |
dc.identifier.affiliation | Familial Cancer Clinic, Monash Medical Centre, Melbourne, Victoria, Australia | en |
dc.identifier.affiliation | Parkville Familial Cancer Centre, Peter MacCallum Cancer Centre and the Royal Melbourne Hospital, Melbourne, Victoria, Australia | en |
dc.identifier.affiliation | Department of Clinical Genetics, Austin Health, Heidelberg, Victoria, Australia | en |
dc.identifier.affiliation | Familial Cancer Clinic, Cabrini Health, Melbourne, Victoria, Australia | en |
dc.identifier.affiliation | Prince of Wales Clinical School, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia | en |
dc.identifier.affiliation | School of Psychiatry, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia | en |
dc.identifier.affiliation | Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Australia | en |
dc.identifier.affiliation | Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Sydney, Australia | en |
dc.identifier.affiliation | Northern Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia | en |
dc.identifier.doi | 10.1111/cge.13687 | - |
dc.identifier.orcid | 0000-0002-3905-3025 | - |
dc.identifier.pubmedid | 31833054 | - |
dc.type.austin | Journal Article | - |
local.name.researcher | Salmon, Lucinda | |
item.grantfulltext | none | - |
item.openairetype | Journal Article | - |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | Clinical Genetics | - |
Appears in Collections: | Journal articles |
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