Evidence map›Paper›PMID 36053286›Full record

Trial reportGenetics in medicine : official journal of the American College of Medical Genetics2022

Educational considerations based on medical student use of polygenic risk information and apparent race in a simulated consultation.

Brittany M Hollister, Emma M Schopp, Sydney H Telaak, Ashley J Buscetta, Alexander P Dolwick, Christopher J Fortney, Vence L Bonham, Susan Persky

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Genetics in medicine : official journal of the American College of Medical Genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 1 institution in 1 country.

Brittany M HollisterSocial and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD.
Emma M SchoppSocial and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD.
Sydney H TelaakSocial and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD.
Ashley J BuscettaSocial and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD.
Alexander P DolwickSocial and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD.
Christopher J FortneySocial and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD.
Vence L BonhamSocial and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD.
Susan PerskySocial and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD. Electronic address: perskys@mail.nih.gov.
National Human Genome Research Institute · US

Funding

Communication of genomic information in clinical, community, and digital contextsZIAHG200383 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI PERSKY, SUSAN · 2012 to 2025
$3.5M
Intramural NIH HHS ZIA HG200383
6 · The paper itself

Abstract

purposeTo craft evidence-based educational approaches related to polygenic risk score (PRS) implementation, it is crucial to forecast issues and biases that may arise when PRS are introduced in clinical care.

methodsMedical students (N = 84) were randomized to a simulated primary care encounter with a Black or White virtual reality-based patient and received either a direct-to-consumer-style PRS report for 5 common complex conditions or control information. The virtual patient inquired about 2 health concerns and her genetic report in the encounter. Data sources included participants' verbalizations in the simulation, care plan recommendations, and self-report outcomes.

resultsWhen medical students received PRSs, they rated the patient as less healthy and requiring more strict advice. Patterns suggest that PRSs influenced specific medical recommendations related to the patient's concerns, despite student reports that participants did not use it for that purpose. We observed complex patterns regarding the effect of patient race on recommendations and behaviors.

conclusionEducational approaches should consider potential unintentional influences of PRSs on decision-making and evaluate ways that they may be applied inconsistently across patients from different racial groups.

Indexed as

Students, MedicalFemaleHumansMultifactorial InheritanceRacial GroupsReferral and ConsultationRisk FactorsClinical simulationCommon diseaseHealth equityPolygenic risk scoresRace

Identifiers

PMID36053286
PMCPMC12927178
OpenAlexW4294281514

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.