Index/ConceptGenetics & reproductionupdated Mon Nov 02 2026 08:00:00 GMT+0800 (Philippine Standard Time)
Polygenic Embryo Screening
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Polygenic Embryo Screening
Scoring IVF embryos for traits and diseases governed by many genes (PGT-P), using polygenic risk scores derived from genome-wide association studies, and choosing which embryo to implant on that basis. Offered commercially since ~2025 by Herasight, Nucleus and Orchid (US), at up to $50,000, covering disease risk and, controversially, height, IQ, longevity, hair and eye colour.
Where it sits among embryo tests
- PGT-A (aneuploidy / chromosome count): long established; claimed to cut miscarriage risk; the 2026 Lancet review of IVF add-ons found no effect on live-birth odds (IVF Add-ons).
- PGT-M (monogenic): single-gene disorders such as cystic fibrosis or Huntington's; near-deterministic, uncontroversial in most jurisdictions.
- PGT-P (polygenic): probabilistic risk estimates; the subject of this page.
What the evidence supports
- Modelled gains are real but small. Karavani et al. (Cell, 2019, doi 10.1016/j.cell.2019.10.033): choosing among ten viable embryos yields a median gain of ~2.9 cm height or ~3 IQ points (the Economist Leader cites the same study as 1–6 cm and 1–7 points). Gains "drop precipitously" below five embryos. Larger GWAS databases could roughly double the IQ gain.
- Demand exists. Survey in Science (2023): 43% of IVF participants would use polygenic screening to improve a child's odds of an elite university if safe and free; a third said the same for editing. ~Three-quarters of Americans would use it if already doing IVF; about a third support screening for non-disease traits.
- Market base is small but growing. US IVF births 100,000 in 2024 (2.8% of births); fertility VC $254m → $496m (2019–22); the fertility market ~$25–30bn/yr, with a bull case of $400–500bn if a full IVF course fell to ~$15,000.
What is contested
- Individual vs population prediction. Selection on polygenic scores works across many offspring (animal breeding) but is less reliable for one child (Kevin Mitchell, Trinity College Dublin). Herasight answers with sibling-based validation inside GWAS datasets.
- Company claims are unverified. Herasight: ten embryos from two type-2-diabetic parents → child's absolute risk down 12–20 points from a 40–60% baseline. Not independently checked in the reporting.
- Relative vs absolute risk. Large relative reductions can be tiny absolute ones, especially for rare diseases.
- Ancestry bias. Scores are more accurate for European-ancestry embryos because databases over-represent them.
- Pleiotropy. Selecting against one condition may raise another the provider does not score; some studies find most polygenic-disease correlations positive or insignificant, which would cap the downside.
- Range limit. Even for strongly heritable traits, parents choose within the spread of their own embryos; environment dominates many conditions (Dagan Wells, Oxford).
Regulation and ethics
- Illegal in Britain (selection on non-approved factors) and many jurisdictions; America has a de-facto ban on embryo editing since 2016 but not on screening.
- Nearly every genetics and reproductive-medicine society in the rich world says the technology is not consumer-ready.
- The Economist's position (Leader): don't ban; mandate disclosure of limits and independent scrutiny of tests. Objections it rejects: "unnatural" (applies to IVF too), rich-only (costs fall), eugenics (coercion vs parental choice).
- Industry framing: "If this is eugenics, then so is Hinge" (Delian Asparouhov, Founders Fund). All three startups employ genetic counsellors.
Open questions
- Will within-family predictive validity hold up in born children, not just models?
- How fast does the ancestry gap close, and who pays to collect the data?
- Does offering IQ and aesthetic scores, while describing customers as health-motivated, survive regulatory scrutiny once IVF is cheap enough for mass uptake?
Related
- Newborn Genome Sequencing — the post-birth counterpart; both are hostage to overestimated penetrance and risk-not-destiny communication.
- IVF Add-ons — the evidence record of the procedures sold alongside screening.
- Type 2 Diabetes Remission — the condition behind Herasight's flagship risk claim.
- Sources: In Praise of Designer-ish Babies (Economist), How Much Would You Pay for a Smarter Baby (Economist).
Research notes, not medical advice. Findings are reported with the population, dose and duration they were measured in; whether they transfer to you is a question for a clinician.