Evidence map›Paper›PMID 31199558›Full record

ArticleJournal of genetic counseling2019

Female family members lack understanding of indeterminate negative BRCA1/2 test results shared by probands.

Deborah O Himes, Deborah K Gibbons, Wendy C Birmingham, Renea L Beckstrand, Amanda Gammon, Anita Y Kinney, Margaret F Clayton

Abstract read
In one paragraph

Article in Journal of genetic counseling, 2019. 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
0.9field-weighted citation impact, top 22% 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, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Response to Carlson.Genetics in medicine : official journal of the American College of Medical Genetics · 2021
    Article
  4. Observational
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

7 authors at 3 institutions in 1 country.

Deborah O HimesCollege of Nursing, Brigham Young University, Provo, Utah.ORCID 0000-0002-0799-1228
Deborah K GibbonsCollege of Nursing, Brigham Young University, Provo, Utah.
Wendy C BirminghamDepartment of Psychology, Brigham Young University, Provo, Utah.
Renea L BeckstrandCollege of Nursing, Brigham Young University, Provo, Utah.
Amanda GammonDepartment of Genetic Counseling, Huntsman Cancer Institute, Salt Lake City, Utah.
Anita Y KinneyDepartment of Biostatistics and Epidemiology, School of Public Health, Rutgers, The State University of New Jersey, Piscataway, New Jersey.
Margaret F ClaytonCollege of Nursing, University of Utah, Salt Lake City, Utah.
Brigham Young University · USUniversity of Utah · USRutgers, The State University of New Jersey · US

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI KATHARINE S ULLMAN · 1986 to 2026
$72.6M
UNIVERSITY OF UTAH CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCE-UL1: BPCAUL1RR025764 · NCRR · UNIVERSITY OF UTAH · PI MCCLAIN, DONALD A. · 2008 to 2011
$19.4M
Comparative Modeling: Informing Breast Cancer Control Practice & PolicyU01CA152958 · NCI · GEORGETOWN UNIVERSITY · PI BERRY, DONALD A, DE KONING, HARRY J · 2010 to 2015
$7.6M
University of Utah Center for Clinical and Translational Science-UL1UL1TR000105 · NCATS · UNIVERSITY OF UTAH · PI MCCLAIN, DONALD A. · 2012 to 2013
$5.1M
Bridging Geographic Barriers: Remote Cancer Genetics Counseling for Rural WomenR01CA129142 · NCI · UNIVERSITY OF UTAH · PI KINNEY, ANITA Y. · 2009 to 2013
$2.9M
Optimizing Personalized Care Using Economic Studies of Genomic Testing: Supporting Patient-ProviderU01CA183081 · NCI · GEORGETOWN UNIVERSITY · PI LIEU, TRACY A, MANDELBLATT, JEANNE · 2013 to 2017
$2.6M
Cancer Control at the Intersection of Aging ResearchK05CA096940 · NCI · GEORGETOWN UNIVERSITY · PI MANDELBLATT, JEANNE · 2002 to 2011
$1.5M
NCATS NIH HHS UL1 TR000105NCI NIH HHS HHSN261201000026CNCI NIH HHS K05 CA096940NCI NIH HHS P30 CA042014NCI NIH HHS R01 CA129142NCI NIH HHS U01 CA152958NCI NIH HHS U01 CA183081NCRR NIH HHS UL1 RR025764NIH HHS 8UL1TR000105NIH HHS U01CA152958NIH HHS U01 CA183081
6 · The paper itself

Abstract

Genetic test results have important implications for close family members. Indeterminate negative results are the most common outcome of BRCA1/2 mutation testing. Little is known about family members' understanding of indeterminate negative BRCA1/2 test results. The purpose of this mixed-methods study was to investigate how daughters and sisters received and understood genetic test results as shared by their mothers or sisters. Participants included 81 women aged 40-74 with mothers or sisters previously diagnosed with breast cancer and who received indeterminate negative BRCA1/2 test results. Participants had never been diagnosed with breast cancer nor received their own genetic testing or counseling. This Institutional Review Board-approved study utilized semi-structured interviews and surveys. Descriptive coding with theme development was used during qualitative analysis. Participants reported low amounts of information shared with them. Most women described test results as negative and incorrectly interpreted the test to mean there was no genetic component to the pattern of cancer in their families. Only seven of 81 women accurately described test results consistent with the meaning of an indeterminate negative. Our findings demonstrate that indeterminate negative genetic test results are not well understood by family members. Lack of understanding may lead to an inability to effectively communicate results to primary care providers and missed opportunities for prevention, screening, and further genetic testing. Future research should evaluate acceptability and feasibility of providing family members letters they can share with their own primary care providers.

Indexed as

Genes, BRCA1Genes, BRCA2AdultAgedBreast NeoplasmsCommunicationCounselingFamilyFemaleGenetic CounselingGenetic Predisposition to DiseaseGenetic TestingHumansMiddle AgedNuclear FamilySiblingsBRCA1/2 genetic testingfamily communicationgenetic counselinggenetic risk communicationindeterminate negative test resultsprecision medicine

Identifiers

PMID31199558
PMCPMC7340114
OpenAlexW2953231853

What OpenQuestion holds

Textmetadata
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.