Yanbo Du1
Lei Yan
Yan Sheng
Rong Tang- 1Reproductive Hospital Affiliated to Shandong University, Jinan, China
- 2School of Medicine, Shandong University, Jinan, China
- 3National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Key Laboratory of Reproductive Endocrinology, Shandong University, Ministry of Education, Jinan, China
- 4Shandong Provincial Hospital, Jinan, China
Purpose: The aim of this study was to investigate the effect of human chorionic gonadotropin (hCG) in hormone replacement (HT) regime for frozen thawed embryo transfer in women with endometriosis (EM).
Methods: We performed a retrospective, database-search, cohort study and included data on EM patients who underwent frozen embryo transfer (FET) between January 1, 2009 and August 31, 2018. According to the protocols for FET cycle, the patients were divided into two groups: control group (n = 296) and hCG group (n = 355). Clinical pregnancy rate, live birth rate, early abortion rate, late abortion rate, and ectopic pregnancy rate were compared between the two groups.
Results: There was a significant increase in clinical pregnancy rate in the hCG group (57.7 vs. 49%, p = 0.027) compared with the control group. The live birth rate in the hCG group (45.6 vs. 38.5%, p = 0.080) was also elevated, but this difference was not statistically significant.
Conclusion: hCG administration in HT regime for FET increases the pregnancy rate in women with EM.
Introduction
Endometriosis (EM) is a chronic gynecological disease characterized by lesions of endometrial-like tissue outside of the uterine cavity (1, 2). Almost 50% of women with EM experience infertility (3). EM affects the outcomes of assisted reproductive technology (ART). There are different factors involved in poor outcomes, including poor quality of oocyte and/or embryo, impaired receptivity of the endometrium, and implantation failure (4, 5). Clinically, there is little doubt that the endometrium of women with EM is less receptive to embryo implantation, and strong evidence suggests that endometrial changes are associated with decreased cycle fecundity (6). Endometrial biomarkers are differentially expressed in the endometrium of women with EM compared with normal women (7, 8). Seeking an effective approach to improve endometrial receptivity in EM is a complex clinical issue.
Frozen embryo transfer (FET) is recommended for EM in ART. Mohamed et al. suggested that the preparation of the endometrium for FET with gonadotropin-releasing-hormone (GnRH) agonists could improve the live birth rate in EM compared with FET (9). Recently, Xu et al. found that pregnancy rate, clinical pregnancy rate, and birth weight were improved in women with EM who underwent intrauterine injection of human chorionic gonadotropin (hCG) before FET (10). However, these methods are either time-consuming or inconvenient. Therefore, we retrospectively analyzed the data on FET in patients with EM to determine a more effective strategy for FET. The aim of our study was to investigate the effect of hCG injection in hormone replacement (HT) regime on FET outcomes among patients with EM.
Materials and Methods
Subjects
This retrospective, database-search, cohort study was conducted at the Reproductive Hospital Affiliated Shandong University, Shandong, China. This study was reviewed and approved by the research ethics committee of our institution. All included patients provided written informed consent for use of their data.
All patients who were diagnosed with laparoscopically confirmed EM and underwent FET in our hospital during a 9-year period (January 1, 2009 to August 31, 2018) were included in the study. However, the stage of EM was not clear, as the operation records were not provided. Patients older than 42 years at the onset of the cycle; with basal follicle stimulating hormone (FSH) level >12 U/L; and with uterine malformation, chromosomal abnormalities, hydrosalpinx, recurrent spontaneous abortion, and submucosal fibroid or intrauterine adhesions were all excluded from the study. Finally, data on 651 women diagnosed with EM-associated infertility were collected. According to whether hCG injection was included in the protocols, the patients were divided into two groups—control group (n = 296) and hCG group (n = 355).
Endometrial Preparation
Patients in the control group received HT regime for FET. Oral estradiol valerate (Progynova, Delpharm Lille) at a dose of 4–8 mg/day was initiated on day 2 or 3 of the menstrual cycle and commonly lasted for 10–14 days to promote endometrial proliferation. The dosage and duration of estrogen were increased until the endometrial thickness reached an appropriate state for embryo transfer (commonly, at least 8 mm), at which time vaginal progestin (200 mg/day Utrogestan, Besins Healthcare) and oral dydrogesterone (20 mg b.i.d Duphaston, Abbott) were added. Patients who received FET earlier than 2011 were treated with intramuscular injection of progesterone (Progesterone Injection, Zhejiang Xianju Pharmaceutical Co., Ltd) instead.
Embryo Transfer
According to the embryo morphology assessment by the Istanbul consensus workshop, blastocysts on day 5 with inner cell mass in the hatching stage and trophectoderm layer (grade 1–2) were considered good embryos. While, as cleavage stage embryos, high-quality embryos were scored by morphologic criteria (11). Only good embryos were frozen and prepared for transfer. One or two cleavage-stage embryos or blastocysts frozen early were thawed and transferred 3 or 5 days, respectively, after progesterone initiation. Women in the hCG group received 8,000 IU hCG (HCG; Livzon) by intramuscular injection before progestin administration; the HT regime was the same as the control group. If conception was confirmed, estrogen was continued until 7 weeks of gestation, and progestin supplementation was continued until 10 weeks of gestation.
Outcomes
The primary outcome was clinical pregnancy, which was defined as the detection of an intrauterine gestational sac by transvaginal ultrasonography after 3 weeks of FET. The secondary outcome was live birth, which was defined as the delivery of a viable neonate that was at least of 28 gestational weeks. The early abortion rate was defined as the percentage of miscarriage occurring earlier than 12 weeks, whereas the late abortion rate was the proportion of miscarriage occurring between 12 and 28 weeks. Preterm birth rate was defined as the percentage of birth before 34 weeks in women with live birth. The live birth rate was the proportion of women who birthed at least one living child.
Statistical Analysis
Continuous variables were represented as means and standard deviations; differences in variables were compared by means of Student's t-test. Categorical variables were described as frequencies and percentages, with the between-group difference tested by means of the chi-square test and Fisher's exact test when the number of events was <5. A two-sided p-value < 0.05 was considered to indicate statistical significance.
Results
Patients
The baseline characteristics were similar in the control and hCG groups (Table 1). There were no differences in terms of age, body mass index (BMI), basal endocrine hormone levels, number of oocytes retrieved in the fresh cycle, fertilization rate of oocytes, number of available embryos, and the percentage of patients with coexisting polycystic ovarian syndrome (PCOS) and adenomyosis between the two groups. However, the level of anti-Müllerian hormone (AMH) was lower in the hCG group than in the control group.
Table 1. Basal characteristics of participants.
Outcomes of FET
The concentration of estrogen and luteinizing hormone (LH), the number and stage of transferred embryos, and the proportion of patients with recurrent endometrioma did not differ significantly between the two groups, but the endometrium was thicker in the hCG group than in the control group. FET outcomes were improved in the hCG group. The pregnancy rate of the hCG group was significantly higher than that of the control group (57.7 vs. 49%, p = 0.027) (Table 2). The live birth rate of the hCG group (45.6 vs. 38.5%, p = 0.080) was also higher than that of the control group, but this difference was not statistically significant (Table 2). In addition, there was no significant difference in early abortion rate, late abortion rate, preterm birth rate, and ectopic pregnancy rate between the two groups (Table 2). In a multivariate logistic regression model, we analyzed various clinical factors of the patients, and we found that hCG treatment, the age of patients, and recurrent endometrioma with a diameter >3 cm were associated with the pregnancy rate of FET in EM patients (Table 3).
Table 2. Outcomes of frozen embryo transfer.
Table 3. Multivariable logistic regression analysis.
Discussion
In our retrospective analysis, we found that hCG injection could significantly improve pregnancy rate in EM patients who underwent FET. Further, live birth rate was also elevated in the hCG group; however, the difference was not statistically significant.
LH/hCG receptors are detected in the glandular epithelium cells of the human endometrium (12), and hCG has been shown to promote human endometrium stromal cell decidualization when used in combination with progesterone (13). Transcription of hCG was found in two-cell-stage embryos (14), and the specific interaction of blastocyst-derived hCG and the endometrial LH/hCG receptors is a fundamental component in the materno-fetal interface dialogue (15). It has recently been reported that intrauterine hCG could improve FET outcomes for EM patients (10). However, intramuscular injection of hCG, in HT regime in EM patients who underwent FET, has never been reported. We found that hCG intramuscular injection before FET in EM could also improve pregnancy rate, but have no effect on live birth rate. However, the administration of hCG was not beneficial for FET in human replacement cycles for non-EM patients. The main reason for this was assumed to be the distinctive characteristics of EM.
EM is known as an immune disorder and a progesterone-resistant condition, which leads to impaired endometrial receptivity and reduced fertility (16–19). The expression of endometrial biomarkers is altered in the eutopic endometrium of patients with EM compared with normal women.
Lessey et al. reported that endometrial integrins, which are known as cell-surface receptors for extracellular matrix proteins, play an important role in embryo implantation and are decreased in women with infertility and EM (20). Reduced integrin expression is also associated with poor in vitro fertilization (IVF) outcomes (21). In vivo, hCG could up-regulate integrinβ5 expression in stromal cells from ectopic lesions in EM (22). Other key molecules, such as HOXA10, are required for normal endometrial receptivity (23), and their expression is also reduced in EM. It has been reported that the expression of HOXA10 could be induced by hCG (24). Therefore, hCG injection may improve endometrial receptivity via regulating key molecules related to embryo implantation.
Moreover, hCG was also reported to regulate progesterone expression via the ERK1/2 pathway (25) and promote human endometrial stromal cell decidualization (13).
Furthermore, an aberrant subset of uterine Natural Killer (uNK) cells was found in the eutopic endometrium of women with EM-associated infertility (26). Immature uNK cell populations exist in infertile women with EM (27), and hCG has been reported as a regulator of uNK cell proliferation, mediated via the mannose receptor (CD206) (28). These findings likely suggest that hCG could improve endometrial receptivity via regulating immune cells in the eutopic endometrium of women with EM-associated infertility.
The main limitation of our study is that only patients with appropriate endometrial thickness and good quality embryos were included. Furthermore, owing to the retrospective design of our study, the stage of EM could not be provided based on the collected data. Further evidence is needed to validate and determine an optimum protocol with maximum beneficial outcomes.
In our research, the pregnancy rate significantly increased after hCG injection in women with EM; however, the difference in live birth rate was not statistically significant with respect to that of controls. This may be the result of insufficient time or dose of hCG that may be improved by replacing single hCG treatments with a repetitive administration scheme (29).
Data Availability Statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics Statement
The studies involving human participants were reviewed and approved by research ethics committee of Reproductive Hospital affiliate d to Shandong University. The patients/participants provided their written informed consent to participate in this study.
Author Contributions
RT designed the study. YD interpreted the data and drafted the article. LY revised the manuscript critically and accounted for all aspects of the work. MS and YS collected all the data. XL and ZF analyzed the data. All the authors contributed equally to this manuscript.
Funding
This study was funded by a grant from the National Nature Science Foundation of China (81571414).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We wish to thank the colleagues in our hospital—Qin Gao, Zengxiang Ma, Jingjing Jiang, Hong Liu, Shanshan Gao, Na Yu, and Qiaona Yuan—who offered assistance in this study. This manuscript has been released as a pre-print at Research Square (30).
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmed.2020.592921/full#supplementary-material
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Keywords: endometriosis, frozen embryo transfer, human chorionic gonadotropin, hormone replacement, assisted reproductive technology
Citation: Du Y, Yan L, Sun M, Sheng Y, Li X, Feng Z and Tang R (2020) Effect of Human Chorionic Gonadotropin Injection Before Frozen Embryo Transfer on Pregnancy Outcomes in Endometriosis-Associated Infertility. Front. Med. 7:592921. doi: 10.3389/fmed.2020.592921
Received: 08 August 2020; Accepted: 16 November 2020;
Published: 14 December 2020.
Edited by:
Zaleha Abdullah Mahdy, National University of Malaysia, MalaysiaReviewed by:
Xuefeng Lu, Shanghai Jiao Tong University, ChinaMuhammad Azrai Abu, UKM Medical Centre, Malaysia
Copyright © 2020 Du, Yan, Sun, Sheng, Li, Feng and Tang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Rong Tang, tangrong2293@163.com