Effects of letrozole combined with human menopausal gonadotrophin in ovarian stimulation for intrauterine insemination cycles.

Subjects and grouping We organized a retrospective study at Yijishan Hospital’s Reproductive Medicine Center, Wannan Medical College. All data in this article were retrieved and exported from our clinical database. The research was approved by the local ethics committee and meets ethical demands. The patients treated with IUI in our study were divided into those treated with or without OS. From January 2014 to December 2018, 658 couples underwent IUI treatment. The inclusion criteria were as follows: (I) couples have normal sexual life without contraception for more than one year without pregnancy, and the wife’s hysterosalpingography or laparoscopy results show unilateral or bilateral fallopian tube patency; (II) the husband performed semen analysis with a semen concentration exceeding 5 million per ml or with the total number of sperm progressive motility greater than 3 million. The exclusion criteria were as follows: (I) bilateral fallopian tube pathology; (II) ovulation failure after IUI by ultrasound; (III) a total sperm count after semen treatment of <5 million per mL or total number of sperm progressive motility less than 3 million. NC or OS IUI cycles Patients were treated with NC IUI during a regular menstrual cycle. OS was performed in patients with irregular menstruation, abnormal follicle development, or ovulation disorders. Two types of OS protocols (letrozole vs. letrozole + HMG) were applied in this study: for the letrozole protocol, letrozole (Hengrui, Jiangsu Province, China) was administered continuously on the 3rd to 5th day after progesterone-induced menstruation or NC menstruation. The dosage was 2.5–5.0 mg/day for 5 days. For the letrozole plus HMG protocol, the dosage of letrozole was 2.5–5.0 mg per day, and letrozole was administered orally for 5 days. From day 3 to day 5, 75 IU HMG (Livzon, Zhuhai, China) was administered. Depending on the ovarian response, HMG was used at different times. We used transvaginal sonography (TVS) to monitor follicular growth on the 8th to the 10th day of the patient’s cycle. Next, we monitored the follicles every 2 days according to the follicle numbers and sizes. When TVS indicated that there were follicles larger than or equal to 18 mm, we induced oocyte excretion by injection of 5,000–10,000 IU human chorionic gonadotropin (hCG) (Livzon, Zhuhai, China). If more than three dominant follicles were present, the couple was advised to cancel the cycle. Insemination procedure Artificial fertilization was scheduled from 36 to 40 hours after hCG injection. After abstinence from sexual activity for 3–7 days, semen was collected in the laboratory, and then washed with density gradient centrifugation and evaluated for count and motility of spermatozoa. The patient was fertilized in the artificial insemination room with a fertilization dose of 0.5 mL. After the operation, the patient lay supine for 30 minutes. Luteal phase support Beginning on the 2nd after insemination, progesterone support comprised 20 mg/d dydrogesterone (Duphaston, Abbott Biologicals, USA) in all patients. Serum hCG levels were measured on the 14th day after insemination to evaluate the occurrence of pregnancy. Ultrasonography was used 16–19 days after artificial fertilization to confirm pregnancy. Outcomes Ultrasonographic findings of an intrauterine pregnancy sac can be was considered clinical pregnancy. Ultrasound examination revealing 2 or more gestational sacs in the uterus indicated multiple pregnancies. Live birth is defined as a fetus born more than 28 weeks pregnant and has signs of normal life after birth. Statistical analysis SPSS18.0 (IBM Corporation, USA) was used for statistical analysis of the data. Measuring data are expressed as mean ± standard, and counting data are expressed as a ratio. The data were analyzed by variance analysis and a chi-square test. P<0.05 indicated statistical significance.

From January 2014 to December 2018, data from 658 couples participating in this research were collected. Among the cycles studied, there were 150 NCs, 207 letrozole stimulation cycles, and 648 letrozole + HMG cycles. The patients’ basic characteristics are displayed in Table 1. The duration of infertility, infertility type, etiology, serum level of estradiol (E2), and PRL were not significantly different between the three groups (P>0.05). The female age, body mass index (BMI), serum level of follicle-stimulating hormone (FSH), serum level of luteinizing hormone (LH), and antral follicle count (AFC) were significantly different between the groups (P<0.05). Full table After hCG injection, TVS was used to monitor follicles. The number of follicles with diameters greater than 18 mm was higher in the letrozole + HMG (1.21±0.56) and letrozole (1.14±0.48) groups than that in the NC group (0.85±0.36) (P<0.010). The percentage of women with mono-follicular growth was 100.0%, 58.9%, and 45.5% in NC, letrozole, and letrozole + HMG group, respectively (Table 2). Compared to the letrozole and NC groups, the growth rate for multiple follicles of the cycles in the letrozole + HMG group was higher. Endometrial thickness on the day of hCG injection in the letrozole + HMG group (8.8±2.1 mm) was significantly higher than that in the letrozole group (7.3±1.6 mm). The NC group’s endometrial thickness (9.6±2.2 mm) was significantly higher than that of the letrozole and letrozole + HMG groups (Table 2). Full table Table 3 shows our statistical follow-up. We compared different IUI treatments for OS. The clinical pregnancy rate was 9.0% after NC, 13.0% after letrozole, and 17.0% after letrozole + HMG. Regarding the clinical pregnancy rate, the letrozole group and NC group had a lower rate than the letrozole + HMG group, but the statistical results showed no significant difference (P=0.052). In terms of live birth rate, the NC group was the lowest (7.0%), and the letrozole + HMG group was the highest (14.0%). The letrozole + HMG group had the highest live birth rate among the three groups (P<0.05). Only one triplet pregnancy occurred after treatment with letrozole+HMG. Full table

In the IUI protocols, OS include CC, letrozole, HMG, urinary FSH (uFSH) or recombinant FSH (rFSH), and GnRH agonists (9-13). Letrozole is used only for OS or in combination with injectable gonadotropin as an adjuvant (14-16). One of the main advantages of letrozole alone is its ability to restore single follicular ovulation in anovulatory infertility, for example, in polycystic ovary syndrome (PCOS) (17). Franik et al. (9) concluded that compared to CC, letrozole could enhance the pregnancy rate and live birth rate of subfertile patients with anovulatory PCOS. OS with letrozole may increase the live birth rate compared with NC IUI without increasing the multiple pregnancy rate in an IUI protocol for unexplained or mild male-factor infertility (7). In ovulating women, letrozole combined with HMG can significantly improve the live birth rate (2). Letrozole can act through different mechanisms in the central and external periphery. Aromatase inhibition improves gonadotropin secretion by decreasing estrogen output from the pituitary and hypothalamus to postmenopausal levels and by transmitting estrogen-associated negative feedback. The peripheral effects of letrozole involve the resulting accumulation of androgens in ovarian follicles when letrozole prevents androgens from converting into estrogens. The accumulation of androgens to a certain extent can promote the expression of the FSH receptor, thereby improving the sensitivity of growth follicles to FSH (9), which may account for the benefits of the combination of HMG and letrozole in OS. Ovarian-stimulating drugs can stimulate the growth and simultaneous development of multiple follicles in the ovary and endometrium proliferation. A successful pregnancy is affected by implantation, which is a complex process that requires an interaction between the blastocyst and endometrium. Studies have shown that letrozole can activate the Wnt/β-catenin pathway, with more endometrial growth in patients with OS using letrozole compared with patients who use CC to stimulate the ovary (18). Letrozole has a good response to the endometrium of PCOS patients throughout the proliferative phase, which is associated with CC (19). The above studies show that letrozole can better increase the thickness of intima compared with CC, which may be the reason for increasing the clinical pregnancy rate.

In IUI, a protocol with letrozole combined with HMG for OS can significantly improve follicular development and increase endometrial thickness. Compared with the other two schemes, the letrozole + HMG protocol of OS in IUI can significantly increase the live birth rate, but not significantly increase the multiple pregnancy rate. Acknowledgments Funding: This project was supported by the Science Foundation of Wannan Medical College for Young Scholars (Grant No. WK2017F28). Footnote Conflicts of Interest: The authors have no conflicts of interest to declare. Ethical Statement: The authors are accountable for all aspects of the work, and the questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. The research was approved by the local ethics committee and meets ethical demands.

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