Aug 2026· Nature Human Behaviour· 0 citations· 29 references
Medicine
TL;DR
Public views on polygenic embryo testing are examined, suggesting variability in choices across specific traits and conditions, rather than a uniform distinction between medical conditions and non-medical traits.
Abstract
Some advances in reproductive technologies raise substantial ethical and psychological challenges, for example, the use of preimplantation genetic testing to select embryos based on non-medical traits. While studies have explored public willingness to use preimplantation genetic testing for medical or non-medical attributes, stated willingness may not reflect implantation decisions when such information is available. This large cross-national study examined public views on polygenic embryo testing. In a US sample (N = 1,467), participants were more willing to test for medical conditions (for example, heart disease) than non-medical traits (for example, antisocial behaviour or low intelligence), although over half supported testing for non-medical traits. In a forced-choice implantation task, participants used medical and non-medical information to a similar extent when making decisions. Similar patterns were observed in Chinese participants (N = 623). These findings suggest variability in choices across specific traits and conditions, rather than a uniform distinction between medical conditions and non-medical traits. The Stage 1 protocol for this Registered Report was accepted in principle on 7 October 2025. The protocol, as accepted by the journal, can be found at https://osf.io/vb9c2 .
How Japanese adults of reproductive age understand “seriousness” in genetic disease and how they view PGT-M in relation to concerns about eugenics are examined, revealing a substantial gap between policy, public reasoning, and reproductive preferences.
S. Takahashi, R. Iizuka, S. Ong et al.· European Journal of Human Ge...· 1 citation
This paper examines how promotional language surrounding PGT-P undermines informed reproductive decision-making and argues that portraying risk as certainty misrepresents scientific evidence and may emphasize narratives of genetic optimization.
Connie Anne Fierro· Journal of Obstetrics and Gy...· 0 citations
Applying a bioethics framework of autonomy, beneficence, nonmaleficence, nonmaleficence, and justice allows these issues to be examined, and current protections to be evaluated for the purpose of instituting change.
Ava Borgess· Journal of healthcare manage...· 0 citations
It is argued that testing for adult-onset diseases in the prenatal setting (in the absence of a positive family history) is neither justified nor desirable, based on considerations of equity, scope of practice, downstream burden on the health care system, and psychosocial repercussions.
Wayne W. Grody· Clinical obstetrics and gyne...· 0 citations
Huntington's disease (HD) families face complex decisions about predictive genetic testing and reproductive options, including preimplantation genetic testing (PGT), and particularly PGT for Monogenic Disorders (PGT‐M). We examined attitudes toward genetic testing and reproductive options across affected groups within...
Noit Inbar, A. Socher, Aya Bar David et al.· Journal of Genetic Counselin...· 0 citations
Critical gaps in public knowledge in genetics are highlighted, emphasizing the need for improved genetic education, including incorporating genetics into school curricula and launching targeted awareness campaigns to promote informed decision-making.
S. Mercier, F. Petit, M. Misrahi et al.· medRxiv· 0 citations
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