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400038 重庆,陆军军医大学(第三军医大学)第一附属医院妇产科,生殖医学中心
[ 何畏,E-mail:anyhewei@163.com HE Wei, E-mail: anyhewei@163.com
收稿:2021-07-28,
修回:2021-11-12,
纸质出版:2022-03-15
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张争, 蒋承芳, 李玉艳, 等. 正常反应人群拮抗剂方案与激动剂长方案的临床特点及结局比较[J]. 陆军军医大学学报, 2022,44(5):484-488.
Zheng ZHANG, Chengfang JIANG, Yuyan LI, et al. Clinical features and outcomes of IVF-ET cycles between GnRH antagonist and GnRH agonist long protocol in normal responders: a comparison of 266 cases[J]. Journal of Army Medical University, 2022, 44(5): 484-488.
张争, 蒋承芳, 李玉艳, 等. 正常反应人群拮抗剂方案与激动剂长方案的临床特点及结局比较[J]. 陆军军医大学学报, 2022,44(5):484-488. DOI: 10.16016/j.2097-0927.202107177.
Zheng ZHANG, Chengfang JIANG, Yuyan LI, et al. Clinical features and outcomes of IVF-ET cycles between GnRH antagonist and GnRH agonist long protocol in normal responders: a comparison of 266 cases[J]. Journal of Army Medical University, 2022, 44(5): 484-488. DOI: 10.16016/j.2097-0927.202107177.
目的
2
分析比较体外授精-胚胎移植(
in vitro
fertilization-embryo transfer
IVF-ET)治疗中采用促性腺激素释放激素(gonadotrophin releasing hormone
GnRH)拮抗剂方案(简称拮抗剂方案)或激动剂长方案(简称长方案)的正常反应人群IVF-ET周期的临床特点及结局。
方法
2
收集2017年1月至2019年3月我中心接受IVF-ET治疗采用拮抗剂或长方案的卵巢正常反应患者的临床资料,根据新鲜周期的方案及是否移植分为3组,A组:拮抗剂未移植组(128例),B组:拮抗剂移植组(138例),C组:长方案移植组(720例);同时,进一步统计拮抗剂未移植组患者第1次冷冻胚胎移植(frozen embryo transfer,FET)转化日内膜厚度及临床结局,作为D组,比较拮抗剂方案与长方案在正常反应人群中应用的临床特点及结局。
结果
2
① A、B组使用促性腺激素(gonadotropin
Gn)时间及用量均<C组,其中Gn时间差异均有统计学意义(
P
<
0.05),Gn用量A组及C组间差异有统计学意义(
P
<
0.05);②A、B组绒毛膜促性腺激素(chorionic gonadotropin,HCG)日血清雌二醇(estradiol
E2)水平均低于C组(
P
<
0.05);HCG日内膜C组最厚,D组黄体转化日内膜均低于A、B、C 3组,其中A组与B组、C组及D组间的差异均有统计学意义(
P
<
0.05);③A、B组获卵数均<C组(
P
<
0.05),A、B组及C组间成熟卵(metaphase Ⅱ
MⅡ)卵率、正常受精率及优质胚胎率差异均无统计学意义(
P
>
0.05);④B、C、D 3组患者生化妊娠率、临床妊娠率差异均无统计学意义,B组患者着床率最低,流产率最高,与C组间差异有统计学意义(
P
<
0.05)。
结论
2
正常反应人群拮抗剂方案可获得与长方案相似的卵母细胞及胚胎,拮抗剂对子宫内膜容受性的负面影响可能会引起临床妊娠率低,流产率高。
Objective
2
To analyze and compare the clinical features and outcomes of
in vitro
fertilization-embryo transfer (IVF-ET) cycles in normal responders
using gonadotrophin (Gn) releasing hormone (GnRH) antagonist or GnRH agonist long protocol.
Methods
2
The clinical data of patients who received IVF treatment and had normal ovarian response to GnRH antagonist or GnRH agonist long protocol in our reproductive center from January 2017 to March 2019 were collected. According to the treatment protocol and the fresh embryo transplanted or not
these patients were divided into Group A (receiving GnRH antagonist
but no fresh embryo transplanted
n
=128)
Group B (GnRH antagonist
with fresh embryo transplanted
n
=138)
and Group C (GnRH agonist long protocol
with fresh embryo transplanted
n
=720). Besides
the frozen embryo transfer (FET) cycles of Group A were analyzed
and served as Group D. The thickness of endometrium on luteal conversion day and outcome of Group D were compared with those of Group B and Group C.
Results
2
① The duration and dosage of Gn were shorter and less in Group A and B than Group C
and statistical difference was seen in Gn duration (
P
<
0.05)
and in Gn dosage only between Group A and C (
P
<
0.05). ②On HCG day
the serum estradiol (E2) level were lower in Group A and B than Group C (
P
<
0.05)
the endometrium of Group C was the thickest
and the thickness of endometrium on luteal conversion day of Group D was lower than that on the HCG day of Group A
B and C
where the differences between Group A and B
and Group C and D were statistically significant (
P
<
0.05). ③ The number of oocytes obtained in Group A and B were less than that in Group C (
P
<
0.05)
but there were no statistical difference in metaphase Ⅱ (MⅡ) oocyte rate
normal fertilization rate and high-quality embryo rate among Group A
B and C. ④ Biochemical pregnancy rate and clinical pregnancy rate had no statistical differences among Group B
C
and D (
P
<
0.05). Group B had the lowest implantation rate but the highest miscarriage rate
and had obvious differences with Group C (
P
<
0.05).
Conclusion
2
GnRH antagonist protocol can obtain similar oocytes and embryos as the GnRH-a long protocol in normal response population. However
the antagonist may exert negative impact on endometrial receptivity and result in low pregnancy rate and high abortion rate.
LAMBALK C B, BANGA F R, HUIRNE J A, et al . GnRH antagonist versus long agonist protocols in IVF: a systematic review and meta-analysis accounting for patient type[J ] . Hum Reprod Update, 2017, 23(5): 560-579. DOI: 10.1093/humupd/dmx017.
李宣, 刘嘉茵, 陈文森, 等. 比较长方案与拮抗剂方案在正常反应人群中的应用[J]. 中华生殖与避孕杂志, 2018, 38(3): 219-223. DOI: 10.3760/cma.j.issn.2096-2916.2018.03.009.
LI X, LIU J Y, CHEN W S, et al . Comparison of the agonist protocol and antagonist protocol in normal responders[J ] . Reprod Contracept, 2018, 38(3): 219-223. DOI: 10.3760/cma.j.issn.2096-2916.2018.03.009.
YANG R, GUAN Y, PERROT V, et al . Comparison of the long-acting GnRH agonist follicular protocol with the GnRH antagonist protocol in women undergoing in vitro fertilization: a systematic review and meta-analysis[J ] . Adv Ther, 2021, 38(5): 2027-2037. DOI: 10.1007/s12325-020-01612-7.
WANG R, LIN S, WANG Y, et al . Comparisons of GnRH antagonist protocol versus GnRH agonist long protocol in patients with normal ovarian reserve: a systematic review and meta-analysis[J ] . PLoS One, 2017, 12(4): e0175985. DOI: 10.1371/journal.pone.0175985.
XU B F, ZHOU M J, WANG J W, et al . Increased AIF-1-mediated TNF-α expression during implantation phase in IVF cycles with GnRH antagonist protocol[J ] . Hum Reprod, 2018, 33(7): 1270-1280. DOI: 10.1093/humrep/dey119.
GENG Y D, XUN Y, HU S Q, et al . GnRH antagonist versus follicular-phase single-dose GnRH agonist protocol in patients of normal ovarian responses during controlled ovarian stimulation[J ] . Gynecol Endocrinol, 2019, 35(4): 309-313. DOI: 10.1080/09513590.2018.1528221.[LinkOut ]
EFTEKHAR M, DEHGHANI FIROUZABADI R, KARIMI H, et al . Outcome of cryopreserved-thawed embryo transfer in the GnRH agonist versus antagonist protocol[J ] . Iran J Reprod Med, 2012, 10(4): 297-302.
CHEN Q, YU F, LI Y, et al . Comparative proteomics reveal negative effects of gonadotropin-releasing hormone agonist and antagonist on human endometrium[J ] . Drug Des Devel Ther, 2019, 13: 1855-1863. DOI: 10.2147/dddt.s201871.
KARACAN M, ARVAS A, CEBI Z, et al . A "freeze-all" strategy or GNRH agonist trigger and concomitant HCG in high responders: a retrospective cohort study[J ] . Fertil Steril, 2015, 104(3): e327. DOI: 10.1016/j.fertnstert.2015.07.1022.
马黔红, 朱桂金, 孙赟, 等. 促性腺激素释放激素拮抗剂方案在辅助生殖领域中使用的专家共识[J]. 中华妇产科杂志, 2015, 50(11): 805-809.
MA Q H, ZHU G J, SUN Y. et al . Expert consensus on application of gonadotropin releasing hormone antagonist programmes in the field of assisted reproduction[J ] . Chin J Obstet Gynecol, 2015, 5 0(11): 805-809.
闫桂敏, 王炎秋, 纪亚忠. GnRH-A在不同卵巢功能患者超排中应用的研究进展[J]. 同济大学学报(医学版), 2017, 38(1): 128-132. DOI: 10.16118/j.1008-0392.2017.01.027.
YAN G M, WANG Y Q, JI Y Z. Application of gonadotropin-releasing hormone antagonist in controlled ovarian hyperstimulation for patients with different ovarian function[J]. J Tongji Univ Med Sci, 2017, 38(1): 128-132. DOI: 10.16118/j.1008-0392.2017.01.027.
WEISS J M, LUDWIG M, ORTMANN O, et al . GnRH antagonists in the treatment of infertility[J ] . Ann Med, 2003, 35(7): 512-522. DOI: 10.1080/07853890310001302.
OLIVENNES F, CUNHA-FILHO J S, FANCHIN R, et al . The use of GnRH antagonists in ovarian stimulation[J ] . Hum Reprod Update, 2002, 8(3): 279-290. DOI: 10.1093/humupd/8.3.279.
CHEN Q, YU F, LI Y, et al . Comparative proteomics reveal negative effects of gonadotropin-releasing hormone agonist and antagonist on human endometrium[J ] . Drug Des Devel Ther, 2019, 13: 1855-1863. DOI: 10.2147/dddt.s201871.
陈骞. 促性腺激素释放激素拮抗剂对人子宫内膜容受性的影响及其机制研究[D]. 上海: 上海交通大学, 2016.
CHEN Q. Effect of gonadotropin releasing hormone antagonist on human endometrial receptivity and its mechanism[D]. Shanghai: Shanghai Jiaotong University, 2016.
YOELI R, ASHKENAZI J, ORVIETO R, et al . Significance of increased endometrial thickness in assisted reproduction technology treatments[J ] . J Assist Reprod Genet, 2004, 21(8): 285-289. DOI: 10.1023/b:jarg.0000043701.22835.56.
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