Evidence map›Paper›PMID 31916645›Full record

ArticleJournal of genetic counseling2020

Exploring relatives' perceptions of participation, ethics, and communication in a patient-driven study for hereditary cancer variant reclassification.

Ginger J Tsai, Annie T Chen, Lauren T Garrett, Wylie Burke, Deborah J Bowen, Brian H Shirts

Open access · greenAbstract read
In one paragraph

Article in Journal of genetic counseling, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Ginger J TsaiDepartment of Laboratory Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0002-8417-5697
Annie T ChenDepartment of Biomedical Informatics and Medical Education, University of Washington, Seattle, WA, USA.
Lauren T GarrettDepartment of Laboratory Medicine, University of Washington, Seattle, WA, USA.
Wylie BurkeDepartment of Bioethics and Humanities, University of Washington, Seattle, WA, USA.
Deborah J BowenDepartment of Bioethics and Humanities, University of Washington, Seattle, WA, USA.
Brian H ShirtsDepartment of Laboratory Medicine, University of Washington, Seattle, WA, USA.
University of Washington · USUniversity of Washington Medical Center · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Scientific/Technical CoreP2CHD042828 · NICHD · UNIVERSITY OF WASHINGTON · PI SARA R. CURRAN · 2017 to 2026
$6.3M
Developing and Evaluating Patient Centered Tools for Clinical Classification of Variants of Uncertain SignificanceR21HG008513 · NHGRI · UNIVERSITY OF WASHINGTON · PI SHIRTS, BRIAN HANSON · 2015 to 2016
$386k
NCI NIH HHS P30 CA015704NHGRI NIH HHS R21 HG008513NICHD NIH HHS P2C HD042828
6 · The paper itself

Abstract

Effective communication of genetic information within families depends on several factors. Few studies explore intra-familial communication of variant of uncertain significance (VUS) results or active collaboration between family members to classify VUS. Our qualitative study aimed to describe the experiences of individuals asked by family members to participate in the FindMyVariant study, a patient-driven family study which aimed to reclassify a clinically identified familial VUS in a hereditary cancer gene. We collected feedback from 56 individuals from 21 different families through phone interviews and written correspondence, transcribed the interviews, and performed thematic analysis on all text. We describe themes from three main topics: participation, ethical considerations, and study impacts. Participation in the FindMyVariant study, defined as returning a sample for targeted genotyping, was motivated by convenience and a desire to help the family, oneself, and science. Relatives were generally responsive to invitations to participate in FindMyVariant from another family member. Those who declined to participate did so due to concerns about research program confidentiality rather than family dynamics. No major ethical issues arose in response to the patient-driven study structure, and no major changes in stress and anxiety, medical care, or behavior occurred. Participation in patient-driven familial VUS classification studies has a neutral or positive impact on family health communication. While it is important to design studies to minimize familial coercion, intra-familial confidentiality breaches, and misinterpretation of genetic results, these were not major concerns among relatives in this study. Clinicians and laboratories may consider encouraging familial communication about genetic variants using family members as liaisons.

Indexed as

CommunicationEthicsFamilyFemaleGenetic Predisposition to DiseaseGenetic TestingHumansMaleMotivationNeoplasmsPerceptionQualitative ResearchattitudesCommunicationfamilyfamily communicationfamily historyfamily studiesgenetic counselinggenetics communicationgenetic testinghealth behaviorhealth communicationpatient-drivenperceptionsqualitative researchqualitative studyrisk perceptionvariant classificationvariant of uncertain significance (VUS)

Identifiers

PMID31916645
PMCPMC7343600
OpenAlexW2999917506

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.