Evidence map›Paper›PMID 30817954›Full record

ArticlePreventive medicine2019

Genetic counseling, genetic testing, and risk perceptions for breast and colorectal cancer: Results from the 2015 National Health Interview Survey.

Erin Turbitt, Megan C Roberts, Jennifer M Taber, Erika A Waters, Timothy S McNeel, Barbara B Biesecker, William M P Klein

Open access · greenAbstract read
In one paragraph

Article in Preventive medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 17 citations in OpenAlex.

  1. Pooled it
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  6. Perceived Risk of Colorectal Cancer in Oman:Sultan Qaboos University medical journal · 2025
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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 7 institutions in 2 countries.

Erin TurbittNational Human Genome Research Institute, Bethesda, MD, United States of America; University of Technology Sydney, NSW, Australia. Electronic address: erin.turbitt@uts.edu.au.
Megan C RobertsNational Cancer Institute, Rockville, MD, United States of America.
Jennifer M TaberKent State University, Kent, OH, United States of America.
Erika A WatersWashington University School of Medicine in St. Louis, St Louis, MO, United States of America.
Timothy S McNeelInformation Management Services, Inc., Calverton, MD, United States of America.
Barbara B BieseckerResearch Triangle Institute, International, Washington, DC, United States of America.
William M P KleinNational Human Genome Research Institute, Bethesda, MD, United States of America; National Cancer Institute, Rockville, MD, United States of America.
Information Management Services · USKent State University · USNational Cancer Institute · USNational Human Genome Research Institute · USRTI International · USUniversity of Technology Sydney · AUWashington University in St. Louis · US

Funding

Interventions in Genetic CounselingZ01HG200317 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI BIESECKER, BARBARA BOWLES · 2004 to 2008
$1.7M
Intramural NIH HHS Z01 HG200317
6 · The paper itself

Abstract

We examined what proportion of the U.S. population with no personal cancer history reported receiving either genetic counseling or genetic testing for cancer risk, and also the association of these behaviors with cancer risk perceptions. We used data from the 2015 National Health Interview Survey. Objective relative risk scores for breast (women) and colorectal (men and women) cancer risk were generated for individuals without a personal history of cancer. Participants' risk perceptions were compared with their objective relative risk. Of 12,631 women, 1.2% reported receiving genetic counseling and 0.8% genetic testing for hereditary breast cancer risk. Of 15,085 men and women, 0.8% reported receiving genetic counseling and 0.3% genetic testing for hereditary colorectal cancer risk. Higher breast cancer risk perception was associated with genetic counseling (OR: 4.31, 95%CI: 2.56, 7.26) and testing (OR: 3.56, 95%CI: 1.80, 7.03). Similarly, higher perception of colorectal cancer risk was associated with genetic counseling (OR: 5.04, 95%CI: 2.57, 9.89) and testing (OR: 5.92, 95%CI: 2.40, 14.63). A higher proportion of individuals with colorectal cancer risk perceptions concordant with their objective risk (vs. discordant) had undergone genetic counseling or testing for colorectal cancer risk. Concordant risk perceptions for breast cancer were not associated with breast cancer genetic counseling or testing. Given frequent dialogue about implementing population level programs involving genetic services for cancer risk, policy makers and investigators should consider the role of risk perceptions in the effectiveness and design of such programs and potential strategies for addressing inaccuracies in risk perceptions.

Indexed as

Early Detection of CancerGenetic Predisposition to DiseaseAdultAgedAged, 80 and overBreast NeoplasmsColorectal NeoplasmsFemaleGenetic CounselingGenetic TestingHumansMaleMiddle AgedRisk AssessmentSocioeconomic FactorsSurveys and Questionnaires

Identifiers

PMID30817954
PMCPMC7321923
OpenAlexW2915397185

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.