Improving the maturation rate of human oocytes collected ex vivo during the cryopreservation of ovarian tissue

被引:41
|
作者
Nikiforov, Dmitry [1 ,2 ,3 ]
Cheng Junping [1 ,2 ,4 ]
Cadenas, Jesus [1 ,2 ]
Shukla, Vallari [5 ]
Blanshard, Robert [6 ,7 ]
Pors, Susanne Elisabeth [1 ,2 ]
Kristensen, Stine Gry [1 ,2 ]
Macklon, Kirsten Tryde [8 ]
Colmorn, Lotte [8 ]
Ernst, Erik [9 ,10 ]
Bay-Bjorn, Anne-Mette [9 ]
Ghezelayagh, Zeinab [1 ,2 ]
Wakimoto, Yu [1 ,2 ,11 ]
Grondahl, Marie Louise [12 ]
Hoffmann, Eva [5 ]
Andersen, Claus Yding [1 ,2 ]
机构
[1] Univ Copenhagen, Copenhagen Univ Hosp, Juliano Marie Ctr Women Children & Reprod, Lab Reprod Biol, DK-2100 Copenhagen, Denmark
[2] Univ Copenhagen, Fac Hlth & Med Sci, DK-2100 Copenhagen, Denmark
[3] Univ Teramo, I-64100 Teramo, Italy
[4] Peoples Hosp Guangxi Autonomous Reg, Nanning 530000, Peoples R China
[5] Univ Copenhagen, Fac Hlth Sci, Dept Cellular & Mol Med, DNRF Ctr Chromosome Stabil, DK-2200 Copenhagen, Denmark
[6] Illumina UK Ltd, Clin Genom Grp, Fulbourn, England
[7] Univ Sussex, Genome Damage & Stabil Ctr, Sch Life Sci, Brighton BN1 9RQ, E Sussex, England
[8] Copenhagen Univ Hosp, Rigshosp, Fertil Clin, DK-2100 Copenhagen, Denmark
[9] Aarhus Univ Hosp, Fertil Clin, DK-8200 Aarhus, Denmark
[10] Horsens Reg Hosp, Fertil Clin, DK-8700 Horsens, Denmark
[11] Hyogo Coll Med, Dept Obstet & Gynecol, Nishinomiya, Hyogo 6638501, Japan
[12] Herlev Gentofte Hosp, Fertil Clin, DK-2740 Herlev, Denmark
基金
欧洲研究理事会; 新加坡国家研究基金会;
关键词
Human immature oocytes; Fertility preservation; Ovarian cryopreservation; In vitro maturation; Oocyte diameter; IN-VITRO MATURATION; HUMAN IMMATURE OOCYTES; DEVELOPMENTAL COMPETENCE; ANTRAL FOLLICLES; MATURED OOCYTES; BOVINE OOCYTES; MEDULLA TISSUE; MIDKINE; VITRIFICATION; METHYLATION;
D O I
10.1007/s10815-020-01724-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose The aim of the present study was to improve the in vitro maturation (IVM) procedure using oocytes from surplus ovarian tissue after fertility preservation. Methods Twenty-five patients aged 17-37 years were included in the study. Maturation was compared between oocytes collected in HEPES-buffered medium or saline, and we determined whether transport on ice prior to oocyte collection affected maturation. Two different IVM media were used that were supplemented with and without recombinant human midkine. Mature oocytes were assessed for aneuploidy using next-generation sequencing (NGS). Results On average, 36 immature oocytes were collected from each patient (range 7-90, N = 895). Oocytes recovered from HEPES-buffered medium matured at a higher rate than oocytes recovered from saline (36% vs 26%, p < 0.01). Ovarian transportation on ice prior to the procedure negatively affected maturation compared with non-transported samples (42% vs 27%, p < 0.01). The addition of midkine improved maturation rate (34% vs 27%, p < 0.05). On average, 11 MII oocytes were obtained per patient (range 1-30). NGS of 53 MII oocytes and their first polar bodies indicated that 64% were euploid. Conclusions The study demonstrated unexpectedly high number of immature oocytes collected from surplus ovarian tissue without any stimulation. The overall MII rate was one in three, resulting in a total number of MII oocytes that was similar to the number obtained after ovarian stimulation. If these MII oocytes prove suitable for IVF, they will provide a substantial improvement in fertility preservation for patients and advance IVM as an interesting platform for further improvements in assisted reproduction.
引用
收藏
页码:891 / 904
页数:14
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