ArticleJournal of assisted reproduction and genetics2026
Should PGT-A be routinely utilized for advanced maternal age?
Article in Journal of assisted reproduction and 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.
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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.
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.
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Authors and funding
3 authors.
Funding
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Abstract
Preimplantation genetic testing for aneuploidy (PGT-A) is often presented to women of advanced maternal age as a logical safeguard against miscarriage and chromosomal abnormality. Yet intuitive rationale and biological plausibility do not establish net clinical benefit. PGT-A does not improve oocyte or embryo quality; it ranks embryos that already exist. The appropriate objective endpoint is therefore cumulative live birth from an initiated treatment strategy, not implantation after transfer of a selected euploid embryo. Randomized clinical trials, contemporary systematic reviews, meta-analyses, and professional guidance have not shown that routine PGT-A improves cumulative live birth rates in older women, while mosaicism, limitations of trophectoderm sampling, invasive biopsy, variability in laboratory protocols, freeze-thaw requirements, embryo exclusion, financial cost, and treatment delay can impose material harms. These concerns are amplified in older women with fewer transferable blastocysts. Sociocultural anxiety about disability and delayed childbearing, reinforced by commercial promotion, clinical normalization, and misleading risk communication, can further compromise autonomous choice. PGT-A may be utilized selectively for older women, especially when several blastocysts are available and patients prioritize avoiding an aneuploid transfer, but advanced maternal age alone should not convert an uncertain add-on into a routine clinical strategy.
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42867733What OpenQuestion holds
Registered trials
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.