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      Aneuploidy and sex concordance rate between cell‐free DNA analysis from spent culture media of preimplantation embryo and DNA from whole embryo with respect to different morphological grading

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          Abstract

          Purpose

          The aneuploidy and sex concordance between cell‐free DNA in spent culture media (SCM) and DNA from whole embryo with respect to different morphological grading were examined to evaluate the feasibility of non‐invasive preimplantation genetic testing for aneuploidy (niPGT‐A).

          Methods

          A total of 46 pairs of embryos and corresponding SCM were divided into two groups based on the morphological grade. DNA was extracted from 22 and 24 pairs of low‐ and high‐grade embryos, respectively, and respective SCM followed by chromosomal analysis using next‐generation sequencing. Aneuploidy study and sex determination were conducted for both groups, and concordance rates were calculated.

          Results

          For low‐grade embryos, 63.6% (14/22) were determined as aneuploidy by whole embryo analysis, and concordance rates were 54.5% (12/22) using niPGT‐A. On the contrary, for high‐grade embryos 41.7% (10/24) were determined as aneuploidy by whole embryo analysis, and concordance rates were 62.5% (15/24) using niPGT‐A. The concordance rates were not statistically different between the low‐grade and high‐grade embryo groups ( p = 0.804). For sex determination, concordance rates between whole embryo and SCM were 81.8% (18/22) and 87.5% (21/24) in low‐ and high‐grade groups, respectively.

          Conclusion

          Aneuploidy and sex evaluation by niPGT‐A may be feasible for both morphologically low‐ and high‐grade embryos.

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          Most cited references25

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          The Istanbul consensus workshop on embryo assessment: proceedings of an expert meeting.

          Many variations in oocyte and embryo grading make inter-laboratory comparisons extremely difficult. This paper reports the proceedings of an international consensus meeting on oocyte and embryo morphology assessment. Background presentations about current practice were given. The expert panel developed a set of consensus points to define the minimum criteria for oocyte and embryo morphology assessment. It is expected that the definition of common terminology and standardization of laboratory practice related to embryo morphology assessment will result in more effective comparisons of treatment outcomes. This document is intended to be referenced as a global consensus to allow standardized reporting of the minimum data set required for the accurate description of embryo development.
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            Correlation between standard blastocyst morphology, euploidy and implantation: an observational study in two centers involving 956 screened blastocysts.

            Does conventional blastocyst morphological evaluation correlate with euploidy (as assessed by comprehensive chromosome screening (CCS) of trophectoderm (TE) biopsies) and implantation potential?
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              • Record: found
              • Abstract: found
              • Article: not found

              Correlation between aneuploidy, standard morphology evaluation and morphokinetic development in 1730 biopsied blastocysts: a consecutive case series study.

              Are there correlations among human blastocyst ploidy status, standard morphology evaluation and time-lapse kinetics?
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                Author and article information

                Contributors
                soneharahiroki@gmail.com
                Journal
                Reprod Med Biol
                Reprod Med Biol
                10.1111/(ISSN)1447-0578
                RMB2
                Reproductive Medicine and Biology
                John Wiley and Sons Inc. (Hoboken )
                1445-5781
                1447-0578
                16 December 2022
                Jan-Dec 2022
                : 21
                : 1 ( doiID: 10.1111/rmb2.v21.1 )
                : e12493
                Affiliations
                [ 1 ] Kashiwanoha Genome Clinic Kashiwa Japan
                [ 2 ] Hara Medical Clinic Tokyo Japan
                [ 3 ] Department of Reproductive Medicine, Graduate School of Medicine Chiba University Chiba Japan
                [ 4 ] Kobanawa Clinic Omitama Japan
                [ 5 ] Department of Obstetrics and Gynecology, Faculty of Medicine University of Tsukuba Tsukuba Japan
                [ 6 ] Evolution and Reproductive Biology, Medical Mycology Research Center Chiba University Chiba Japan
                Author notes
                [*] [* ] Correspondence

                Hiroki Sonehara, Kashiwanoha Genome Clinic, Tokatsu Techno Plaza 606, Kashiwanoha 5‐4‐6, Kashiwa, Chiba, Japan.

                Email: soneharahiroki@ 123456gmail.com

                Author information
                https://orcid.org/0000-0002-5425-6621
                https://orcid.org/0000-0002-5545-0477
                https://orcid.org/0000-0001-9425-4367
                Article
                RMB212493 RMB-2022-0197.R1
                10.1002/rmb2.12493
                9756929
                02300575-1078-4641-9d00-5a6cab5305c6
                © 2022 The Authors. Reproductive Medicine and Biology published by John Wiley & Sons Australia, Ltd on behalf of Japan Society for Reproductive Medicine.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 19 October 2022
                : 11 August 2022
                : 01 December 2022
                Page count
                Figures: 0, Tables: 2, Pages: 7, Words: 4042
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                January/December 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.3 mode:remove_FC converted:16.12.2022

                aneuploidy,low‐grade embryos,next‐generation sequencing,sex determination,spent culture media

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