Evidence map›Paper›PMID 27045374›Full record

ArticleScientific reports2016

Developmental potential of clinically discarded human embryos and associated chromosomal analysis.

Guidong Yao, Jiawei Xu, Zhimin Xin, Wenbin Niu, Senlin Shi, Haixia Jin, Wenyan Song, Enyin Wang, Qingling Yang, Lei Chen and 1 more

Registry-linked trialAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07533630 (Efficacy of PGT-A Upgrade in Preimplantation Genetic Testing of Embryos), which is not on this map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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.

NCT07533630 not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Efficacy of PGT-A Upgrade in Preimplantation Genetic Testing of Embryos: An International Multicenter Prospective Clinical Study

TypeobservationalSponsorReproductive & Genetic Hospital of CITIC-XiangyaRan2026 to 2028Enrolled1,700ConditionsInfertility Assisted Reproductive TechnologyArmsPGT-A upgrade
3 · Its place in the literature

Who cites it

27 citing papers in PubMed.

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  20. Human germline genome editing.Nature cell biology · 2019
    Review
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

11 authors.

Guidong YaoCenter for Reproductive Medicine, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Jiawei XuCenter for Reproductive Medicine, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Zhimin XinCenter for Reproductive Medicine, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Wenbin NiuCenter for Reproductive Medicine, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Senlin ShiCenter for Reproductive Medicine, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Haixia JinCenter for Reproductive Medicine, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Wenyan SongCenter for Reproductive Medicine, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Enyin WangCenter for Reproductive Medicine, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Qingling YangCenter for Reproductive Medicine, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Lei ChenCenter for Reproductive Medicine, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Yingpu SunCenter for Reproductive Medicine, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clinically discarded human embryos, which are generated from both normal and abnormal fertilizations, have the potential of developing into blastocysts. A total of 1,649 discarded human embryos, including zygotes containing normal (2PN) and abnormal (0PN, 1PN, 3PN and ≥4PN) pronuclei and prematurely cleaved embryos (2Cell), were collected for in vitro culture to investigate their developmental potential and chromosomal constitution using an SNP array-based chromosomal analysis. We found that blastocyst formation rates were 63.8% (for 2Cell embryos), 22.6% (2PN), 16.7% (0PN), 11.2% (3PN) and 3.6% (1PN). SNP array-based chromosomal analysis of the resultant blastocysts revealed that the percentages of normal chromosomes were 55.2% (2Cell), 60.7% (2PN), 44.4% (0PN) and 47.4% (0PN). Compared with clinical preimplantation genetic diagnosis (PGD) data generated with clinically acceptable embryos, results of the SNP array-based chromosome analysis on blastocysts from clinically discarded embryos showed similar values for the frequency of abnormal chromosome occurrence, aberrant signal classification and chromosomal distribution. The present study is perhaps the first systematic analysis of the developmental potential of clinically discarded embryos and provides a basis for future studies.

Indexed as

Chromosome AberrationsBiopsyBlastocystCell NucleusChromosomesCumulus CellsEmbryo Culture TechniquesEmbryonic DevelopmentFemaleFertilizationHumansMaleOligonucleotide Array Sequence AnalysisOocytesPolymorphism, Single NucleotidePreimplantation Diagnosis

Identifiers

PMID27045374
PMCPMC4820740

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