Evidence map›Paper›PMID 41968946›Full record

ReviewCurrent opinion in obstetrics & gynecology2026

Reproductive outcomes of mosaic embryo transfers - rethinking the clinical relevance of contemporary mosaicism reporting in preimplantation genetic testing for aneuploidy.

Christian Simon Ottolini, Silvia Caroselli, Antonio Capalbo

Abstract readReview
In one paragraph

Review in Current opinion in obstetrics & gynecology, 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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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

3 authors.

Christian Simon OttoliniDepartment of Maternal and Fetal Medicine, UCL Institute for Women's Health, University College London, London, UK.
Silvia CaroselliDepartment of Experimental Medicine, Sapienza University of Rome, Rome.
Antonio CapalboDepartment of Psychological Health and Territorial Sciences, School of Medicine and Health Sciences, 'G. d'Annunzio' University of Chieti-Pescara, Chieti.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewNext-generation sequencing-based preimplantation genetic testing for aneuploidy (PGT-A) has enabled the detection of intermediate copy-number signals, leading to widespread clinical classification of embryos as chromosomally 'mosaic'. Mosaic embryo transfer (MET) is now routinely considered in assisted reproduction, yet the clinical relevance of mosaic classification remains uncertain. This review critically evaluates reproductive outcomes following MET in light of embryonic biology, technical constraints of PGT-A, and study design. RECENT

findingsAcross the body of evidence, embryos labelled as mosaic retain substantial reproductive potential, with largely reassuring outcomes once implantation occurs. Apparent differences in reproductive efficiency, particularly among high-level mosaic categories, are better explained by study design bias, diagnostic imprecision, and classification artefact than by a clear biological intolerance to mosaicism. When selection bias and post hoc stratification are minimised, mosaic classification contributes little independent information beyond established clinical and embryological factors. The persistent signal observed in a small subset of embryos is increasingly attributable to misclassified constitutional aneuploidy rather than by adverse effects of mitotic mosaicism. SUMMARY: These findings shift the conceptual framework away from mosaicism as a clinically actionable diagnosis and toward a model in which accurate identification of constitutional aneuploidy is the principal determinant of reproductive outcome.

Indexed as

AneuploidyEmbryo TransferGenetic TestingMosaicismPreimplantation DiagnosisFemaleHumansPregnancyPregnancy Outcomeconstitutional aneuploidymosaic embryo transferpreimplantation genetic testing for aneuploidyreproductive potential

Identifiers

PMID41968946
PMCPMC13117582

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