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Iranian Journal of Reproductive Medicine logoLink to Iranian Journal of Reproductive Medicine
. 2012 Nov;10(6):567–570.

Efficacy of the local endometrial injury in patients who had previous failed IVF-ICSI outcome

Mustafa Kara 1, Turgut Aydin 2, Nurettin Turktekin 2, Karacavus S 3
PMCID: PMC4169851  PMID: 25246928

Abstract

Background: The latest studies reported that local endometrial injury is a useful method to improve the success of IVF-ICSI outcome.

Objective: To assess whether local endometrial injury occurred by Pipelle in the spontaneous cycle could improve implantation rate, cleavage rate, and pregnancy outcome in the subsequent IVF-ICSI cycle in patients who had recurrent IVF failure.

Materials and Methods: An endometrial biopsy was performed on day 21st in 41 patients as intervention group in this retrospective cross-sectional study. The control group contained 42 women.

Results: Implantation rate was 22.5% and 10.5% in intervention and control group, respectively and this difference was found to be statistically significant (p=001). Pregnancy rate was 43.9% in the intervention group and this parameter was significantly lower in control group (21.4%) (p=0.03).

Conclusion: Local endometrial injury in the nontransfer cycle increases the implantation rate and pregnancy rate in the subsequent IVF-ICSI cycle in patients who had previous failed IVF-ICSI outcome.

Key Words: Local endometrial injury, In vitro fertilization, Embryo transfer, Pregnancy

Introduction

IVF-ICSI is performed widely in the world and implantation is essential as much as follicular development for a successful treatment. Especially, implantation is necessary for a successful pregnancy and requires a healthy blastocyst apposition and endometrial receptivity (1, 2).

Many cytokines (IL-6, IL-8, and TNFα), matrix metalloproteinases (MMP), and molecules characterizing early implantation have been discovered (3, 4). Barash et al reported that endometrial biopsy taken spontaneous cycle that preceded IVF improves the IVF-ICSI outcomes such as implantation rate, clinical pregnancy rate, and live birth rate (5). They claimed that the cause of implantation improvement was secondary modifications due to an injury-induced inflammatory reaction. Despite considerable advances in assisted reproductive techniques (ART), management of the patients who had recurrent IVF failure is still a challenge.

The aim of this study was to detect the efficacy of the endometrial biopsy performed in the nontransfer cycle proceeding the IVF-ICSI cycle.

Materials and methods

This is a retrospective cross-sectional study. The patient characteristics (basal hormone levels, duration of infertility, number of attempt, body mass index, antral follicle count, and age) were analyzed, retrospectively. The groups were homogen in terms of these parameters. Inclusion criteria were at least one previous failed IVF-ICSI cycle with a fresh embryo, having good response in the previous IVF cycle, and less than or equal to 37 years old.

The cases in which testicular sperm extraction (TESE) procedures were performed were not included the study. Spermogram values of the patients were in normal ranges. Male factor patients were excluded from the study. The patients whose body mass index were (BMI) >30 were not included into the study. Standard IVF-ICSI procedure was performed for all of the patients. The patients were randomized to two groups. All women were assessed with baseline day 3 follicle stimulating hormone (FSH), antral follicle count (AFC), estradiole (E2) level, and hysteroscopy (H/S) on the 21st day of the previous cycle. Day 21 of the cycle has been assessed by ultrasonography and estradiole (E2) level.

The patients in the study group underwent endometrial sampling once, with a biopsy catheter (Pipelle; Gynetics Medical Products, Hamont Achel, Belgium) on the 21st day of the nontransfer cycle. The Pipelle was moved up and down into the uterine cavity. All the women were given Indomethacine 25mg 30-60 minutes prior the procedure. Ciprofloxacin 500 mg was given twice daily for 7 days after the biopsy. Contraception was suggested to women in the nontransfer cycle.

In long protocol cases, pituitary was down-regulated with Leuprolide acetate (Lucrin ® daily 0.25 mg Abbott, USA). Lucrin was given for at least 10 day starting on the 21st day of the menstrual cycles. On the 2nd day of menstruation, transvaginal ultrasonography (TV USG) and serum E2 level were monitorized to show the suppression. Controlled ovarian stimulation (COS) was performed with FSH starting on cycle day 3. Highly purified-urinary FSH (Fostimon HP ® 75 IBSA, Switzerland) was administered. Average FSH starting dose was 450 iu and the dose was individually adjusted according to the previous treatment cycles, body mass index (BMI), and age.

Pituitary was down-regulated with Cetrorelix (Cetrotide® 0.25 Merck-Serono, Switzerland) in the antagonist protocol starting on the sixth or seventh day of the cycle according to the follicular growth (when the leading follicle reached to 13-14 mm) and E2 level (when the level exceeded 600-800 pg/ml). Cetrorelix was continued until the day of hCG. COS was performed with either r FSH or HP-u FSH starting on cycle day 3. Age, body mass index (BMI), and response to the former treatment were used to detect the beginning FSH dose. Average FSH starting dose was 225 IU.

Ovulation induction was monitorized by using E2 measurement and TV USG. Human chorionic gonadothropin (Pregnyl® 5000 IU × 2, Schering-Plough, USA) was administered when the dominant follicle reaches 17 mm. Oocytes were retrieved by TV USG- guided needle aspiration. IVF- ICSI was performed in all cases. Embryos were classified according to percentage of fragmentation and blastomere appearances as type I, II, III or IV on 1st, 3rd and 5th days. Up to two embryos were transferred into the uterine cavity on day 2, 3 or 5. Luteal phase was supported by progesterone administration (Crinone %8 vaginal gel ® Merck-Serono, Switzerland). Progesterone was given during 12 days after oocyte retrieval.

Progesteron support was maintained until the 12th gestational week in the pregnancy cases. Implantation failure was defined as the failure of embryo to achieve pregnancy. Fertilization rate was determined as the number of embryos ( >1 cell) divided by the total of oocytes. Cleavage rate was defined as total number of day-3 embryos by total number of fertilized oocytes. Implantation rate was defined as the percentage of embryos given and resulted with pregnancy. Clinical pregnancy was defined by the presence of a fetal sac at ultrasound examination six weeks after embryo transfer.

Statistical analysis

Statistical analysis was performed using SPSS 10.00 (SPSS Inc., Chicago). The Chi-square test was used for categorical variables and an independent sample t-test was used for continuous variables that were normally distributed. p-value<0.05 was considered significant.

Results

In total 83 patients were included into the study and only one cycle for each patient was used. Forty one patients were included into the local endometrial injury group, and 42 women were included into the control group. The patient characteristics of both groups were comparable (Table I). The characteristics of the patients were the same. The patients age, duration of infertility, basal FSH levels, basal E2 levels, BMI, AFC, and number of previous attempt were assessed but there was no statistical difference.

Table I.

Characteristics of the patients

Local injury group (n=41) Control group (n=42) p-value
Age 32.1 ± 5.51 30.1 ± 5.2 0.34
Duration of infertility (year) 7.9 ± 4.8 6.1 ± 3.6 0.09
Number of previous attempt 3.3 ± 1.8 2.5 ± 0.9 0.09
BMI (body mass index) 28.4 ± 5.5 27.2 ± 4.2 0.29
Basal FSH level (iu/l) 6.13 ± 1.2 6.63 ± 1.3 0.84
Basal E2 level (pg/ml) 39.4 ± 11.8 41.7 ± 13.6 0.42
AFC (antral follicle count) 9.9 ± 5.2 10.5 ± 5.6 0.66

Endometrial thickness on hCG day, number of 12-17mm follicles on hCG day and number of >18mm follicles on hCG day, size of dominant follicle, retrieved oocyte number, and transferred embryo number were compared (Table II). All of these parameters were similar and the differences were not statistically significant. The IVF-ICSI outcomes are shown in Table III. The implantation rate was significantly higher in the study group as compared with the controls (22.5% vs. 10.5%, p=0.01). The clinical pregnancy rate was more in the intervention group than control (43.9% vs. 21.4%), and this difference was found to be statistically significant, p=0.03.

Table II.

Comparison of the IVF-ICSI outcomes of the patients performed local injury or not

Local injury group (n=41) Control group (n=42) p-value
Indication
Unexplained 18 24 NM
Male factor 12 7 NM
Poor reserve 5 4 NM
Tubal factor 3 2 NM
Endometriosis 2 1 NM
Anovulation 1 4 NM
Protocol
Antagonist protocol 35 31 NM
Long protocol 6 11 NM
ET on hCG day (mm) 9.9 ± 1.6 10.6 ± 1.4 0.06
Fol. no. 12-17mm on hCG day 8.4 ± 2.5 9.6 ± 2.8 0.23
Fol. no. >18mm on hCG day 4.2 ± 1.1 5.9 ± 2.0 0.36
Dom. Fol. on hCG day (mm) 20.2 ± 1.4 18. ± 1.2 0.18
Retrieved oocyte no. 10.4 ± 6.3 11.2 ± 7.4 0.61
Transferred embryo no. 1.9 ± 0.5 2.0 ± 0.3 0.49

ET: Endometrial thickness.

NM: Not measured.

Table III.

Comparison of the IVF-ICSI outcomes in two groups

Local injury group (n=41) Control group (n=42) p-value
Fertilization rate n (%) 274/430 (63.7) 307/493 (62.2) 0.27
Implantation rate n (%) 18/80 (22.5) 9/85 (10.5) 0.01*
Cleavage rate n (%) 258/430 (60) 256/493 (51.9) 0.16
Clinical pregnancy rate n (%) 18/41 (43.9) 9/42 (21.4) 0.03*
*

p< 0.05.

Discussion

Loeb first reported that scratching the guinea-pig uterus during the progestational phase increased the decidualization of the endometrium (6). Decidua formation was simulated by suturing the uterine horn and intra-uterine injection of oil in rodents. These experimental animal studies shown that local injury of the endometrium increases successful implantation percentage (7, 8). Barash et al performed endometrial biopsies four times (on the days 8, 12, 21, and 26) during the spontaneous cycle in their prospective case-control study.

All of the 45 patients were good responder and the clinical pregnancy rate, implantation rate, and live birth rate were more than control patients (66.7% vs. 30.3%, 22.7% vs. 14.2%, 48.9% vs. 22.5%, respectively). The efficacy of the endometrial biopsy performed in the nontransfer cycle was confirmed by Raziel et al (9). They studied 60 women who had recurrent IVF failure. The Pipelle biopsy was performed twice. They reported a significant increase in the success of IVF-ICSI in the endometrial biopsy group. A more recent study was done by Zhou et al in 2008 (10). The endometrial biopsy procedure was performed during the cycle of treatment (on the day 10) unlike the other studies. The outcomes were found to be significantly better in the intervention group.

Zhou et al also investigated the gene expressions. They found some upregulated and downregulated genes. As a conclusion, they suggested that implantation improvement occurred as the result of injury-induced inflammatory reaction. Kalma et al reported that endometrial injury taken twice in the spontaneous cycle led to upregulation and downregulation in some genes. Endometrial injury was accepted as a causative factor for these gene modifications (11).

More recently, a randomized controlled study indicating the success of the local endometrial injury in the IVF-ICSI outcome was done by Narvekar et al. They utilized Pipelle to create endometrial injury in 100 women with recurrent implantation failure. Endometrial injury was done twice in the follicular and luteal phase of the nontransfer cycle. Finally, they reported that endometrial injury in the nontransfer cycle increased the percentage of clinical pregnancy, implantation rate, and live birth rate (12).

Despite the unbelievable improvements in ART, embryo implantation remains the rate-limiting step for the success of IVF. We aimed to demonstrate the efficacy of the endometrial injury performed in the spontaneous cycle that preceded the IVF-ICSI. The results of our study were similar with the previous publications. The limitation of our study was the restricted number of patients. Prospective and randomized trials are required to evaluate the influence of local endometrial injury in the IVF-ICSI cycles.

Acknowledgments

We are grateful to Seyhan Karacavus, (Resident of nuclear medicine) for helping us to evaluate the statistical data. There was no association between authors and any person or institution.

Conflict of interest

The authors declare that there is no financial support for this paper.

References

  • 1.Wang H, Dey SK. Roadmap to embryo implantation: clues from mouse models. Nat Rev Genet. 2006;7:185–199. doi: 10.1038/nrg1808. [DOI] [PubMed] [Google Scholar]
  • 2.Dekel N, Gnainsky Y, Granot I, Mor G. Inflammation and implantation. Am J Reprod Immunol. 2010;63:17–21. doi: 10.1111/j.1600-0897.2009.00792.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Koga K, Mor G. Expression and function of toll-like receptors at the maternal-fetal interface. Reprod Sci. 2008;15:231–242. doi: 10.1177/1933719108316391. [DOI] [PubMed] [Google Scholar]
  • 4.Minas V, Loutradis D, Makrigiannakis A. Factors controlling blastocyst implantation. Reprod Biomed Online. 2005;10:205–216. doi: 10.1016/s1472-6483(10)60942-x. [DOI] [PubMed] [Google Scholar]
  • 5.Barash A, Dekel N, Fieldust S, Segal I, Schechtman E, Granot I. Local injury to the endometrium doubles the incidence of successful pregnancies in patients undergoing in vitro fertilization. Fertil Steril. 2003;79:1317–1322. doi: 10.1016/s0015-0282(03)00345-5. [DOI] [PubMed] [Google Scholar]
  • 6.Loeb L. The experimental proof changes in the uterine decidua of guinea pig after mating. Copulation Zentralbl AlIg Pathol Pathol Anat. 1907;18:563–565. [Google Scholar]
  • 7.Turner CD. General Endocrinology. Philadelphia, Pennsylvania: Saunders, WB; 1976. Biological effects of the ovarian hormones; pp. 466–76. [Google Scholar]
  • 8.Saito S, Sasaki Y. Th1/Th2 balance at implantation stage. In: Mor G, editor. Immunology of Pregnancy. New York: 2006. pp. 37–48. [Google Scholar]
  • 9.Raziel A, Schachter M, Strassburger D, Bern O, Ron-El R, Friedler S. Favorable influence of local injury to the endometrium in intracytoplasmic sperm injection patients with high-order implantation failure. Fertil Steril. 2007;87:198–201. doi: 10.1016/j.fertnstert.2006.05.062. [DOI] [PubMed] [Google Scholar]
  • 10.Zhou L, Wang R, Huang HX, Zhong K. Local injury to the endometrium in controlled ovarian hyperstimulation cycles improves implantation rates. Fertil Steril. 2008;89:1166–1176. doi: 10.1016/j.fertnstert.2007.05.064. [DOI] [PubMed] [Google Scholar]
  • 11.Kalma Y, Granot I, Gnainsky Y, Or Y, Czemobilsky B, Dekel N, et al. Endometrial biopsy induced gene modulation: First evidence for the expression of bladder transmembranal uroplakin Ib in human endometrium. Fertil Steril. 2009;91:1042–1049. doi: 10.1016/j.fertnstert.2008.01.043. [DOI] [PubMed] [Google Scholar]
  • 12.Narvekar SA, Gupta N, Shetty N, Kottur A, Srinivas MS, Rao KA. Does local endometrial injury in the nontransfer cycle improve the IVF-ET outcome in the subsequent cycle in patients with previous unsuccessful IVF? A randomized controlled pilot study. J Hum Reprod Sci. 2010;3:15–19. doi: 10.4103/0974-1208.63116. [DOI] [PMC free article] [PubMed] [Google Scholar]

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