Thomas Tf Huang1, David H Huang2, Hyeong J Ahn3, Christina Arnett4, Christopher Tf Huang4. 1. Department of Obstetrics and Gynecology and Women's Health, John A. Burns School of Medicine, Honolulu Hawaii, USA; Pacific In Vitro Fertilization Institute, Honolulu Hawaii, USA. Electronic address: antonio.lamarca@unimore.it. 2. Pacific In Vitro Fertilization Institute, Honolulu Hawaii, USA. 3. Department of Complementary and Integrative Medicine, University of Hawaii John A. Burns School of Medicine, Honolulu Hawaii, USA. 4. Advanced Reproductive Center of Hawaii, Kapiolani Medical Center for Women and Children, Honolulu Hawaii, USA.
Abstract
RESEARCH QUESTION: How can the kinetics of human blastocyst expansion be used to evaluate an embryo's ploidy identified using preimplantation genetic testing for aneuploidy (PGT-A)? DESIGN: This was a retrospective observational study of 188 autologous blastocysts from 34 sequential treatment cycles using PGT-A and blastocyst biopsy. Using time-lapse imaging, blastocyst expansion was evaluated using a quantitative standardized expansion assay (qSEA). Trophectoderm cell division was examined in selected, unbiopsied embryos (n = 7) to evaluate the contribution of mitosis to the expansion rate. RESULTS: The averaged euploid blastocyst expansion rate was significantly (52.8%) faster than in aneuploid blastocysts (P = 0.0041). Scatterplots, representing 'expansion maps', revealed that both populations showed a similarly overlapping distribution of blastocyst formation times at 80-140 h from fertilization. Euploidy and aneuploidy were better distinguished in regions of higher and lower expansion, respectively, in expansion maps. Based upon the expansion slopes, rank-ordering of individual embryos within cohorts resulted in more than 90% euploid embryos in the first two ranks in patients less than 35 years of age. Additional detailed time-lapse image analysis provided evidence that rapid expansion was associated with robust, integrative cellular mitosis in trophectoderm cells. CONCLUSIONS: The kinetics of human blastocyst expansion are related to an embryo's ploidy. These preliminary observations describe a new quantitative, non-invasive approach to embryo assessment that may be useful to identify single blastocysts for transfer, particularly in younger patient groups. However, this approach may also be useful for euploid embryo selection after PGT-A. The results support the hypothesis that aneuploidy universally impairs general cellular processes, including cell division, in differentiated cells.
RESEARCH QUESTION: How can the kinetics of humanblastocyst expansion be used to evaluate an embryo's ploidy identified using preimplantation genetic testing for aneuploidy (PGT-A)? DESIGN: This was a retrospective observational study of 188 autologous blastocysts from 34 sequential treatment cycles using PGT-A and blastocyst biopsy. Using time-lapse imaging, blastocyst expansion was evaluated using a quantitative standardized expansion assay (qSEA). Trophectoderm cell division was examined in selected, unbiopsied embryos (n = 7) to evaluate the contribution of mitosis to the expansion rate. RESULTS: The averaged euploid blastocyst expansion rate was significantly (52.8%) faster than in aneuploid blastocysts (P = 0.0041). Scatterplots, representing 'expansion maps', revealed that both populations showed a similarly overlapping distribution of blastocyst formation times at 80-140 h from fertilization. Euploidy and aneuploidy were better distinguished in regions of higher and lower expansion, respectively, in expansion maps. Based upon the expansion slopes, rank-ordering of individual embryos within cohorts resulted in more than 90% euploid embryos in the first two ranks in patients less than 35 years of age. Additional detailed time-lapse image analysis provided evidence that rapid expansion was associated with robust, integrative cellular mitosis in trophectoderm cells. CONCLUSIONS: The kinetics of humanblastocyst expansion are related to an embryo's ploidy. These preliminary observations describe a new quantitative, non-invasive approach to embryo assessment that may be useful to identify single blastocysts for transfer, particularly in younger patient groups. However, this approach may also be useful for euploid embryo selection after PGT-A. The results support the hypothesis that aneuploidy universally impairs general cellular processes, including cell division, in differentiated cells.
Authors: T Hirakawa; M Goto; K Takahashi; T Iwasawa; A Fujishima; K Makino; H Shirasawa; W Sato; T Sato; Y Kumazawa; Y Terada Journal: Hum Reprod Date: 2022-06-30 Impact factor: 6.353
Authors: Eva S van Marion; Effrosyni A Chavli; Joop S E Laven; Régine P M Steegers-Theunissen; Maria P H Koster; Esther B Baart Journal: Reprod Biol Endocrinol Date: 2022-03-19 Impact factor: 5.211