Evidence map›Paper›PMID 39462080›Full record

SynthesisEuropean journal of human genetics : EJHG2025

Defining ethical criteria to guide the expanded use of Noninvasive Prenatal Screening (NIPS): Lessons about severity from preimplantation genetic testing.

Hortense Gallois, Vardit Ravitsky, Marie-Christine Roy, Anne-Marie Laberge

Abstract readSystematic Review
In one paragraph

Synthesis in European journal of human genetics : EJHG, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Editorial: severity in a genomic age.European journal of human genetics : EJHG · 2025
    Article
  3. 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

4 authors.

Hortense GalloisSimon Fraser University, Vancouver, BC, Canada.
Vardit RavitskyBioethics, Department of Social and Preventive Medicine, School of Public Health, Université de Montréal, Montreal, QC, Canada.
Marie-Christine RoyBioethics, Department of Social and Preventive Medicine, School of Public Health, Université de Montréal, Montreal, QC, Canada.
Anne-Marie LabergeBioethics, Department of Social and Preventive Medicine, School of Public Health, Université de Montréal, Montreal, QC, Canada. anne-marie.laberge.med@ssss.gouv.qc.ca.ORCID 0000-0003-1213-8288

Funding

Fonds de Recherche du Québec - Santé (Fonds de la recherche en sante du Quebec) 299178Genome Canada (Génome Canada) 13527
6 · The paper itself

Abstract

We hypothesized that ethical criteria that guide the use of preimplantation genetic testing (PGT) could be used to inform policies about expanded use of non-invasive prenatal screening (NIPS). We used a systematic review of reasons approach to assess ethical criteria used to justify using (or not using) PGT for genetic conditions. Out of 1135 identified documents, we retained and analyzed 216 relevant documents. Results show a clear distinction in acceptability of PGT for medical vs. non-medical conditions. Criteria to decide on use of PGT for medical conditions are largely based on their severity, but there is no clear definition of "severity". Instead, characteristics of the condition that relate to severity are used as sub-criteria to assess severity. We found that characteristics that are used as sub-criteria for assessing severity include monogenic etiology, high penetrance, absence of treatment, early age of onset, shortened lifespan, and reduced quality of life. Consensus about the use of PGT is highest for conditions that meet most of these criteria. There is no consensus around the acceptability of using PGT to detect non-medical conditions. We propose that the same severity criteria could be used by policymakers to assess the acceptability of using other genetic tests in screening and practice, including for the use of NIPS for additional conditions as indications broaden.

Indexed as

Genetic TestingNoninvasive Prenatal TestingPreimplantation DiagnosisPrenatal DiagnosisFemaleHumansPregnancy

Identifiers

PMID39462080
PMCPMC11840150

What OpenQuestion holds

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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.