Evidence map›Paper›PMID 42299739›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2026

Decision-making criteria in polygenic embryo screening: A survey of reproductive medicine physicians.

Rémy A Furrer, Aayushi Gandhi, Dorit Barlevy, Shai Carmi, Todd Lencz, Stacey Pereira, Gabriel Lázaro-Muñoz

Abstract read
In one paragraph

Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2026. 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
–field-weighted citation impact
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.

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

7 authors.

Rémy A FurrerDepartment of Neurosurgery, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA. Electronic address: rfurrer@mgh.harvard.edu.
Aayushi GandhiStanford University, Stanford, CA.
Dorit BarlevyCenter for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, TX.
Shai CarmiBraun School of Public Health and Community Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.
Todd LenczInstitute of Behavioral Science, The Feinstein Institutes for Medical Research, Northwell Health, Manhasset, NY; Departments of Psychiatry and Molecular Medicine, Zucker School of Medicine at Hofstra/Northwell, Hempstead, NY; Division of Research, Department of Psychiatry, The Zucker Hillside Hospital Division of Northwell Health, Glen Oaks, NY.
Stacey PereiraCenter for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, TX.
Gabriel Lázaro-MuñozDepartment of Neurosurgery, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA; Department of Psychiatry, Massachusetts General Hospital, Boston, MA.

Funding

Polygenic Embryo Screening: Towards Informed Decision-MakingR01HG011711 · NHGRI · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI CARMI, SHAI, LAZARO-MUNOZ, GABRIEL · 2021 to 2025
$6.2M
Comprehension and Perception of Genetic Influence: A Psychosocial Examination of Polygenic Risk ScoresK99HG014202 · NHGRI · MASSACHUSETTS GENERAL HOSPITAL · PI Remy Furrer · 2026 to 2026
$143k
NHGRI NIH HHS K99 HG014202NHGRI NIH HHS R01 HG011711
6 · The paper itself

Abstract

purposePolygenic embryo screening (PES) examines embryos for their genetic likelihood of developing complex conditions and traits. The commercialization of PES places reproductive endocrinologists and infertility specialists (REIs) as the primary decision-makers in its use, despite professional guidelines cautioning that PES is not ready for clinical use.

methodsThis survey examines how 152 US REIs perceive and approach potential clinical decision-making scenarios regarding the use of PES.

resultsREIs were more likely to offer PES for medical conditions (up to 62% for cancer) than for traits (eg, 0% for skin color, 10% for body mass index). When evaluating 11 potential criteria to assess condition severity, clinical burden (eg, high mortality [80%]) was rated significantly higher than contextual burden (eg, low lifestyle modifiability [28%]); however, 82% to 93% of respondents considered each criterion at least slightly important. In hypothetical scenarios where PES rankings conflicted with embryo ploidy or morphology, only 8% preferred PES over ploidy, and 30% preferred PES over morphology. Still, 47% supported patient choice in morphology-based cases, and 30% supported patient choice in ploidy-based cases.

conclusionThese findings indicate skepticism toward PES, while underscoring the nuanced, context-dependent factors that influence its potential use.

Indexed as

Genetic TestingMultifactorial InheritancePreimplantation DiagnosisReproductive MedicineClinical Decision-MakingDecision MakingFemaleHumansMalePhysiciansSurveys and QuestionnairesGenomicsPGTPGT-PPolygenic embryo screeningReproductive medicine

Identifiers

PMID42299739
PMCPMC13573636

What OpenQuestion holds

Textmetadata
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.