采用孕激素刺激卵巢或 GnRH 拮抗剂方案治疗的不同年龄患者植入前非整倍体基因检测结果的比较

IF 3.7 2区 医学 Q1 OBSTETRICS & GYNECOLOGY
Lili Wan , Furui Chen , Dongsheng Xiong , Shiqi Chen , Jiexiu Chen , Juan Qin , Jesse Li-Ling , Taiqing Zhong , Xueyan Wang , Yan Gong
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Protocols were as follows: PPOS: &lt;35 years (<em>n</em> = 131; 137 cycles); ≥35 years (<em>n</em> = 72; 80 cycles); GnRH-a: &lt;35 years (<em>n</em> = 149; 152 cycles); ≥35 years (<em>n</em> = 66; 71 cycles).</p></div><div><h3>Results</h3><p>For cycles treated with PPOS in the older group, rates of euploid blastocyst per metaphase Ⅱ oocyte (15.48% versus 10.47%) and per biopsied blastocyst (54.94% versus 40.88%) were significantly higher than those treated with GnRH-a (<em>P</em> &lt; 0.05). The mosaic rate per biopsied blastocyst was significantly lower for cycles treated with PPOS than cycles treated with GnRH-a (8.64% versus 23.36%) (<em>P</em> &lt; 0.001). In the younger group, no significant difference was found between treatments (<em>P</em> &gt; 0.05). In older and younger groups, the drug to inhibit LH surge was cheaper for cycles treated with PPOS compared with GnRH-a (<em>P</em> &lt; 0.001). 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引用次数: 0

摘要

研究问题采用孕激素刺激卵巢(PPOS)或促性腺激素释放激素拮抗剂(GnRH-a)方案治疗的不同年龄患者的非整倍体状态是否存在差异? 设计对接受 PGT-A 治疗的患者(n = 418;440 个周期)进行登记,并根据女性年龄进行分组(<35 岁和≥35 岁)。治疗方案如下PPOS:35 岁(n = 131;137 个周期);≥35 岁(n = 72;80 个周期);GnRH-a:35 岁(n = 149;152 个周期);≥35 岁(n = 66;71 个周期)。结果 在使用 PPOS 的高龄组周期中,每个分裂期 Ⅱ 卵母细胞的高倍囊胚率(15.48% 对 10.47%)和每个活检囊胚的高倍囊胚率(54.94% 对 40.88%)明显高于使用 GnRH-a 的高龄组(P <0.05)。用 PPOS 治疗的周期中,每个活检囊胚的嵌合率(8.64% 对 23.36%)明显低于用 GnRH-a 治疗的周期(P < 0.001)。在年轻组中,不同治疗方法之间没有明显差异(P> 0.05)。在年长组和年轻组中,与 GnRH-a 相比,PPOS 治疗周期中抑制 LH 激增的药物更便宜(P < 0.001)。基于二项分布的广义估计方程显示,所有参与者的女性年龄与非整倍体率呈显著负相关(β -0.109,95% CI -0.183至-0.035,P = 0.004),而在高龄组中,GnRH-a方案(参考:PPOS)与非整倍体率呈显著负相关(β -0.126,95% CI -0.248至-0.004,P = 0.042)。多重逻辑回归表明,卵巢刺激方案与持续妊娠率无关(OR 0.652,95% CI 0.358 至 1.177;P = 0.14)。结论PPOS 适合于接受 PGT-A 的患者,尤其是高龄患者,因为 PPOS 方案可获得更高的非整倍体囊胚率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of aneuploidy for patients of different ages treated with progestin-primed ovarian stimulation or GnRH antagonist protocols

Research question

Does euploidy status differ among patients of different ages treated with progestin-primed ovarian stimulation (PPOS) or gonadotrophin releasing hormone antagonist (GnRH-a) protocols?

Design

Patients undergoing PGT-A (n = 418; 440 cycles) were enrolled and grouped according to female age (<35 years and ≥35 years). Protocols were as follows: PPOS: <35 years (n = 131; 137 cycles); ≥35 years (n = 72; 80 cycles); GnRH-a: <35 years (n = 149; 152 cycles); ≥35 years (n = 66; 71 cycles).

Results

For cycles treated with PPOS in the older group, rates of euploid blastocyst per metaphase Ⅱ oocyte (15.48% versus 10.47%) and per biopsied blastocyst (54.94% versus 40.88%) were significantly higher than those treated with GnRH-a (P < 0.05). The mosaic rate per biopsied blastocyst was significantly lower for cycles treated with PPOS than cycles treated with GnRH-a (8.64% versus 23.36%) (P < 0.001). In the younger group, no significant difference was found between treatments (P > 0.05). In older and younger groups, the drug to inhibit LH surge was cheaper for cycles treated with PPOS compared with GnRH-a (P < 0.001). Generalized estimation equations based on binomial distribution female age and euploidy rate was significantly negatively correlated for all participants (β –0.109, 95% CI –0.183 to –0.035, P = 0.004), and between GnRH-a protocol (reference: PPOS) and the euploidy rate in the older group (β –0.126, 95% CI –0.248 to –0.004, P = 0.042). Multiple logistic regression indicated that ovarian stimulation protocol was not associated with ongoing pregnancy rate (OR 0.652, 95% CI 0.358 to 1.177; P = 0.14).

Conclusions

PPOS is suitable for patients undergoing PGT-A, particularly older patients for the higher euploid blastocyst rate attained by PPOS protocol.

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来源期刊
Reproductive biomedicine online
Reproductive biomedicine online 医学-妇产科学
CiteScore
7.20
自引率
7.50%
发文量
391
审稿时长
50 days
期刊介绍: Reproductive BioMedicine Online covers the formation, growth and differentiation of the human embryo. It is intended to bring to public attention new research on biological and clinical research on human reproduction and the human embryo including relevant studies on animals. It is published by a group of scientists and clinicians working in these fields of study. Its audience comprises researchers, clinicians, practitioners, academics and patients. Context: The period of human embryonic growth covered is between the formation of the primordial germ cells in the fetus until mid-pregnancy. High quality research on lower animals is included if it helps to clarify the human situation. Studies progressing to birth and later are published if they have a direct bearing on events in the earlier stages of pregnancy.
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