Evidence map›Paper›PMID 37656381›Full record

ArticleJournal of assisted reproduction and genetics2023

Conventional IVF is feasible in preimplantation genetic testing for aneuploidy.

Shuoping Zhang, Pingyuan Xie, Fang Lan, Yaxin Yao, Shujuan Ma, Liang Hu, Yueqiu Tan, Bo Jiang, Anqi Wan, Dunmei Zhao and 3 more

Open access · greenAbstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
5.2field-weighted citation impact, top 5% of its field
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

8 citing papers in PubMed, 9 citations in OpenAlex.

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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

13 authors at 5 institutions in 1 country.

Shuoping Zhang *Clinical Research Center for Reproduction and Genetics in Hunan Province, Reproductive and Genetic Hospital of CITIC-Xiangya, No. 567, Tongzipo West Road, Yuelu District, Changsha, 410008, Hunan, China.ORCID http://orcid.org/0000-0002-6866-7675
Pingyuan Xie *Hospital of Hunan Guangxiu, Hunan Normal University School of Medicine, Changsha, China.
Fang LanHospital of Hunan Guangxiu, Hunan Normal University School of Medicine, Changsha, China.
Yaxin YaoDepartment of Clinical Research, Yikon Genomics Company, Ltd., 218 Xinghu Street, Unit 301, Building A3, BioBay, Suzhou Industrial Park, Suzhou, 215000, Jiangsu, China.
Shujuan MaClinical Research Center for Reproduction and Genetics in Hunan Province, Reproductive and Genetic Hospital of CITIC-Xiangya, No. 567, Tongzipo West Road, Yuelu District, Changsha, 410008, Hunan, China.
Liang HuClinical Research Center for Reproduction and Genetics in Hunan Province, Reproductive and Genetic Hospital of CITIC-Xiangya, No. 567, Tongzipo West Road, Yuelu District, Changsha, 410008, Hunan, China.
Yueqiu TanClinical Research Center for Reproduction and Genetics in Hunan Province, Reproductive and Genetic Hospital of CITIC-Xiangya, No. 567, Tongzipo West Road, Yuelu District, Changsha, 410008, Hunan, China.
Bo JiangNational Engineering and Research Center of Human Stem Cells, Changsha, China.
Anqi WanDepartment of Clinical Research, Yikon Genomics Company, Ltd., 218 Xinghu Street, Unit 301, Building A3, BioBay, Suzhou Industrial Park, Suzhou, 215000, Jiangsu, China.
Dunmei ZhaoDepartment of Clinical Research, Yikon Genomics Company, Ltd., 218 Xinghu Street, Unit 301, Building A3, BioBay, Suzhou Industrial Park, Suzhou, 215000, Jiangsu, China.
Fei GongClinical Research Center for Reproduction and Genetics in Hunan Province, Reproductive and Genetic Hospital of CITIC-Xiangya, No. 567, Tongzipo West Road, Yuelu District, Changsha, 410008, Hunan, China.
Sijia LuDepartment of Clinical Research, Yikon Genomics Company, Ltd., 218 Xinghu Street, Unit 301, Building A3, BioBay, Suzhou Industrial Park, Suzhou, 215000, Jiangsu, China. lusijia@yikongenomics.com.
Ge LinClinical Research Center for Reproduction and Genetics in Hunan Province, Reproductive and Genetic Hospital of CITIC-Xiangya, No. 567, Tongzipo West Road, Yuelu District, Changsha, 410008, Hunan, China. linggf@hotmail.com.
Central South University · CNHunan Normal University · CNReproductive & Genetic Hospital CITIC-Xiangya · CNLuye Pharma (China) · CNNational Engineering Research Center of Human Stem Cells · CN

Funding

Hunan Provincial Grant for Innovative Province Construction 2019SK4012
6 · The paper itself

Abstract

purposeTo investigate the feasibility of the application of conventional in vitro fertilization (cIVF) for couples undergoing preimplantation genetic testing for aneuploidies (PGT-A) with non-male factor infertility.

methodsTo evaluate the efficiency of sperm whole-genome amplification (WGA), spermatozoa were subjected to three WGA protocols: Picoplex, ChromInst, and multiple displacement amplification (MDA). In the clinical studies, 641 couples who underwent PGT-A treatment for frozen embryos between January 2016 and December 2021 were included to retrospectively compare the chromosomal and clinical outcomes of cIVF and intracytoplasmic sperm injection (ICSI). Twenty-six couples were prospectively recruited for cIVF and PGT-A treatment between April 2021 and April 2022; parental contamination was analyzed in biopsied samples; and 12 aneuploid embryos were donated to validate the PGT-A results.

resultsSperm DNA failed to amplify under Picoplex and ChromInst conditions but could be amplified using MDA. In frozen PGT-A cycles, no significant differences in the average rates of euploid, mosaic, and aneuploid embryos per cycle between the cIVF-PGT-A and ICSI-PGT-A groups were observed. The results of the prospective study that recruited couples for cIVF-PGT-A treatment showed no paternal contamination and one case of maternal contamination in 150 biopsied trophectoderm samples. Among the 12 donated embryos with whole-chromosome aneuploidy, 11 (91.7%) presented uniform chromosomal aberrations, which were in agreement with the original biopsy results.

conclusionsUnder the Picoplex and ChromInst WGA protocols, the risk of parental contamination in the cIVF-PGT-A cycles was low. Therefore, applying cIVF to couples with non-male factor infertility who are undergoing PGT-A is feasible.

Indexed as

InfertilitySemenAneuploidyFertilization in VitroGenetic TestingHumansMaleProspective StudiesRetrospective StudiesConventional IVFEmbryo ploidyParental contaminationPGT-A

Identifiers

PMID37656381
PMCPMC10504148
OpenAlexW4386347643

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.