Broothaers Klaartje, Pascottini Osvaldo Bogado, Hedia Mohamed, Angel-Velez Daniel, De Coster Tine, Peere Sofie, Polfliet Ellen, Van den Branden Emma, Govaere Jan, Van Soom Ann, Smits Katrien
Department of Internal Medicine, Reproduction and Population Medicine, Ghent University, Merelbeke, Belgium.
Department of Internal Medicine, Reproduction and Population Medicine, Ghent University, Merelbeke, Belgium; School of Veterinary Medicine, University College Dublin, Belfield, Dublin, Ireland.
Theriogenology. 2025 Feb;233:64-69. doi: 10.1016/j.theriogenology.2024.11.019. Epub 2024 Nov 22.
Previous studies in the horse highlight the potential benefit of prolonged in vitro maturation (IVM) (34 h) compared to short IVM (24 h) with or without prior oocyte holding, but little is known about the optimal IVM duration within this interval. To determine the effect of oocyte holding and duration of IVM ranged between 28 and 34 h on nuclear maturation, cleavage, blastocyst formation, and pregnancy rates, a retrospective study was performed in an equine clinical OPU-ICSI setting. The study included data of 2114 aspirated oocytes from 201 OPU-ICSI sessions. Duration of IVM was divided in three different time windows using quartiles, with 465 oocytes (22.0 %) between 28 and 30 h (first quartile), 1078 oocytes (51.0 %) >30 and 31.7 h (second and third quartiles), and 571 oocytes (27.0 %) >31.7 and 34 h (fourth quartile). Using logistic regression models, the effect of duration of IVM with and without holding was tested on nuclear maturation, cleavage, blastocyst, and pregnancy rates. The three IVM intervals did not show differences in nuclear maturation (respectively 64.5 ± 0.48 %, 65.7 ± 0.47 %, and 67.3 ± 0.47 %), cleavage (respectively 59.7 ± 0.49 %, 58.5 ± 0.49 %, and 64.8 ± 0.48 %), blastocyst (respectively 17.5 ± 0.38 %, 19.0 ± 0.39 %, and 20.8 ± 0.41 %) nor pregnancy rates (respectively 65.4 ± 0.49 %, 70.3 ± 0.46 %, and 74.2 % ± 0.44) (P ≥ 0.38). Oocyte holding prior to IVM did not affect the results either (P ≥ 0.15). In conclusion, oocyte holding and IVM duration between 28 and 34h do not significantly affect outcomes, allowing flexibility in the planning of clinical OPU-ICSI in horses.
此前针对马的研究强调了与短时间体外成熟(24小时)相比,延长体外成熟时间(34小时)的潜在益处,无论是否进行过卵母细胞保存,但对于这一区间内的最佳体外成熟时长却知之甚少。为了确定卵母细胞保存以及28至34小时的体外成熟时长对核成熟、卵裂、囊胚形成及妊娠率的影响,在马的临床卵母细胞采集-卵胞浆内单精子注射(OPU-ICSI)环境下开展了一项回顾性研究。该研究纳入了来自201次OPU-ICSI操作的2114枚抽吸卵母细胞的数据。使用四分位数将体外成熟时长分为三个不同的时间窗口,28至30小时之间有465枚卵母细胞(22.0%)(第一四分位数),大于30至31.7小时有1078枚卵母细胞(51.0%)(第二和第三四分位数),大于31.7至34小时有571枚卵母细胞(27.0%)(第四四分位数)。使用逻辑回归模型,测试了有无保存情况下体外成熟时长对核成熟、卵裂、囊胚及妊娠率的影响。三个体外成熟区间在核成熟(分别为64.5±0.48%、65.7±0.47%和67.3±0.47%)、卵裂(分别为59.7±0.49%、58.5±0.49%和64.8±0.48%)、囊胚(分别为17.5±0.38%、19.0±0.39%和20.8±0.41%)及妊娠率(分别为65.4±0.49%、70.3±0.46%和74.2%±0.44)方面均未显示出差异(P≥0.38)。体外成熟前的卵母细胞保存也未影响结果(P≥0.15)。总之,卵母细胞保存及28至34小时的体外成熟时长不会显著影响结果,这使得马的临床OPU-ICSI计划具有灵活性。