{"paper_id":"18b5a625-064c-45cb-97b5-eab4804e4e30","body_text":"The tendency to marry later is becoming a major cause of infertility in Japan. Assisted reproductive technology (ART) is widely used in infertility treatment; however, deciding on an appropriate regimen for poor‐responder patients who are preparing for assisted reproductive techniques is quite difficult. 1  The success of in vitro fertilization (IVF) largely depends on the number and quality of retrieved oocytes following controlled ovarian hyperstimulation (COH). A variety of protocols has been reported with varying degrees of success, ranging from the unstimulated cycle to COH using clomiphene, urinary and recombinant gonadotropins, adjunctive gonadotropin‐releasing hormone (GnRH) agonists and antagonists, bromocriptine, growth hormone, and growth hormone‐releasing hormone. Factors, such as the basal antral follicle count with scanning and an elevated basal serum follicle‐stimulating hormone (FSH) level greater than 15 IU/mL in the early follicular phase, have been used to define a “poor response” to ovarian stimulation. 1 ,  2  On the other hand, we have encountered cases in which no oocyte was recovered, regardless of the development of multiple mature follicles. Regardless, obtaining a scant number of oocytes from numerous mature follicles that have just appeared is a frustrating experience that is more commonly encountered. It remains unclear, however, which factors most affect the oocyte retrieval rate, thus defined as the number of retrieved oocytes/aspirated follicles × 100. The primary aim of this study was to assess which predictive factors contribute to a lower oocyte retrieval rate and which provide an accurate estimation of the number of retrieved oocytes in patients undertaking ART under COH.\n\nThree‐hundred‐and‐twenty‐nine patients who underwent COH under a GnRH agonist (short protocol) or GnRH antagonist for IVF between 2008 and 2012 at Osaka Medical College, Japan, were enrolled in this study. This was a retrospective cross‐sectional, case‐controlled study of the oocyte retrieval ratio in IVF or intracytoplasmic sperm injection cycles. The inclusion criteria for patients were as follows: (1) 34–47 years of age with regular menstrual cycles; (2) the absence of endocrine disease; and (3) the diagnosis of endometriotic cysts by transvaginal ultrasound and by magnetic resonance imaging, followed by laparoscopic surgery. The exclusion criteria for patients were as follows: (1) a FSH level suggestive of menopause; (2) the suspicion of malignant ovarian disease; and (3) oral contraceptive use within 3 months before surgery. No patient had taken preoperative hormonal treatment. The infertile patients were classified into five groups: advanced age (older than 35 years old), severe endometriosis, male infertility, tubal infertility, and unexplained infertility (Table  1 ). All the patients with severe endometriosis and tubal infertility undertook a laparoscopic bilateral endometriotic cystectomy for endometriotic cysts and a subsequent salpingectomy for ectopic pregnancy within 1 year of oocyte retrieval respectively. Unexplained infertility was confirmed following a standard infertility evaluation, including a semen analysis, assessment of ovulation, hysterosalpingogram, and hysteroscopy. Our Institutional Review Board approved this protocol (No. 66) and its consent form and informed consent was obtained from all the participants.\nPatients characteristic\nFSH, follicle‐stimulating hormone.\nUnder the GnRH antagonist protocol, the women who enrolled started IVF cycles using the GnRH antagonist and, on day 3 of the treatment cycle, controlled ovarian stimulation was started by the daily injection of human menopausal gonadotropin (hMG) (HMG Teizo, Tokyo, Japan) at a dose of 150–300 IU/d. A daily dose of 0.25 mg of a GnRH antagonist (Cetrotide) was initiated when the mean diameter of the leading follicle had reached 14–15 mm on transvaginal ultrasound.\nUnder the short protocol, 600 μg of GnRH agonist (Suprecur, Mochida, Tokyo, Japan) was started on day 1 and controlled ovarian stimulation was started by the daily injection of hMG (HMG Teizo, Asuka, Tokyo, Japan) at a dose of 150 IU/d up to 300 IU on day 3. In both protocols, 10 000 IU of human chorionic gonadotropin (Gonadotropin, Asuka, Tokyo, Japan) was administered intramuscularly when the leading follicles reached a diameter of greater than 18 mm and transvaginal oocyte retrieval was performed 35 hours later. The oocyte retrieval ratio (%) was calculated as follows: the total number of retrieved oocytes/the total number of basal antral follicles × 100. Hormone assays, follicle monitoring, oocyte retrieval, insemination, embryo culture, embryo transfers, and the confirmation of embryo quality were performed as previously reported. 3  Hormone assaying was performed at the time of oocyte retrieval and the basic values for luteinizing hormone and FSH were assayed at the time of the basal antral follicle count. The number of basal antral follicles was counted at day 2 before starting hMG/FSH administration. Pregnancy was confirmed by the identification of an intrauterine gestational sac during an ultrasound examination.\nThe statistical analysis was conducted with StatMate IV (ATMS Co., Ltd., Tokyo, Japan). Comparisons between the two non‐parametric groups were performed with the non‐parametric Mann‐Whitney  U  test, the parametric unpaired  t  test, or the chi‐square test. The Pearson's correlation coefficient was performed for the normally distributed data and differences were considered to be statistically significant at  P <.05. A stepwise multivariate regression analysis was performed in order to investigate the independent variables associated with a decline in the oocyte retrieval rate. All the parameters that significantly correlated with a decline in the oocyte retrieval rate were subsequently evaluated in the forward stepwise multivariate regression model.\nA stepwise multivariate logistic regression analysis also was performed in order to assess the factors that were associated with a decline in the oocyte retrieval rate. A  P ‐value of <.05 was considered as statistically significant.\n\nThe median age of the study group as a whole was 37.8 years (range 34‐47 years). The median serum basal FSH level was 10.5 mIU/mL (range 0.6‐30.2 mIU/mL). Advanced age was the most frequently identified cause of infertility (Table  1 ); moreover, the oocyte retrieval ratio correlated negatively with age (Figure  1 ).\nRelationship between the oocyte retrieval ratio and the patient's age\nThe mean age, serum basal FSH level, and total dose of hMG were significantly higher in the unsuccessfully retrieved cycles (URCs; a cycle in which no oocyte was retrieved) than in the successfully retrieved cycles (SRCs; a cycle in which more than one oocyte was retrieved) ( P <.05). The number of aspirated follicles in the URCs was significantly lower than that in the SRCs. As well, the ratio of women associated with severe endometriosis was significantly higher in the URCs than in the SRCs (Table  2 ). Table  3  reveals the clinical outcomes according to each infertility factor. The age and basal serum FSH level in cases of unexplained infertility were lower than for the other causes of infertility ( P <.05). The implantation rate in the advanced‐age patients and the pregnancy rate in the patients with severe endometriosis were lower than in relation to the other causes of infertility (Table  3 ). The oocyte retrieval ratio (%) in cases where at least one high‐quality embryo was retrieved was statistically higher than that in cases where a high‐quality embryo was not available (Figure  2 ). The univariate and multivariate logistic regressions showed that the oocyte retrieval rate was significantly associated with age and the presence of severe endometriosis (Figure  3 ).\nPatients characteristic\nFSH, follicle‐stimulating hormone; hMG, human menopausal gonadotropin. Values are presented as the mean±SD or %. Comparisons between the two non‐parametric groups were performed with the non‐parametric Mann‐Whitney  U  test or the parametric unpaired  t  test or chi‐square test.\nThe clinical outcomes according to each infertility factor\nFSH, follicle‐stimulating hormone.\nThe oocyte retrieval ratio (%) in cases where at least one high‐quality embryo was retrieved was statistically higher than that in cases where a high‐quality embryo was not available\nForest plot (univariate/multivariate logistic regression) indicating the association between the cause of infertility and the risk of oocyte retrieval failure among 329 treatment cycles.  CI , confidence interval\n\nIn many IVF cycles, in spite of the numerous developed follicles that are visualized at the time of ultrasound, a scant number of oocytes is often retrieved and thus leads to a poor pregnancy outcome. This study revealed that the oocyte retrieval rate declines significantly with age. There is an evident gradual decline in female fecundity with age, particularly noticeable in those who are older than 30 years, accelerating between the ages of 35 and 40, and reducing to almost zero by 45 years. 4 ,  5  There is also a decrease in the ovarian reserve with age, caused by the decreased number of oocytes and the concomitant increase in the rate of oocyte aneuploidy and subsequent reduced reproductive potential. 6  It was reported that women who were older than 40 years and who had not been pregnant with their own oocytes showed a significantly higher pregnancy rate by using donated oocytes from young women. 7  These data support the idea that a decline in female fecundity with age is largely attributed to oocyte quality.\nEndometriosis is still one of the most enigmatic of all gynecological diseases; however, recent epigenetic changes in the disease have gradually come under close investigation. 8 ,  9  Some studies suggest that infertility as a result of endometriosis is caused mainly by an impaired ovarian reserve and reduced ovarian response, as indicated by lower anti‐Müllerian hormone, higher FSH, and the aberrant expression of some proteins. 10 ,  11  Several retrospective studies have reported on poor responses to FSH/hMG in patients with endometriosis. 12 ,  13  In particular, the number of retrieved oocytes has been shown to decline in the ovary following a cystectomy for endometriotic cysts. 14  In this study, all the patients with severe endometriosis received a laparoscopic cystectomy and therefore the number of retrieved oocytes was lower in these women than in the patients with other causes of infertility. In order to prevent postoperative ovarian reserve impairment, such as that seen after the treatment of recurrent and bilateral endometriotic cysts, using plasma energy for the ablation of endometrial tissue has been recommended, thus causing minimal damage to the ovarian parenchyma. 15  Recently, it was reported that a combined technique, including the vaporization of cysts in close proximity to the hilus and a cystectomy for distant portions, can preserve the ovarian reserve. 16  Also recently, the potential contribution of inflammation to follicle burnout in cases of endometriotic cysts was reported 17  and the proactive management of endometriotic cysts, including conservative surgery in young women, has been suggested could prevent ovarian dysfunction. 18  Therefore, early detection and treatment should be considered in order to prevent future infertility.\nIn conclusion, although more studies are necessary, our study indicates that both severe endometriosis and advanced age are the highest risk factors that contribute to a lower oocyte retrieval rate in IVF.\n\nConflict of interest : The authors declare no conflict of interest.  Human rights statement and informed consent : All the procedures were followed in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1964 and its later amendments. Informed consent was obtained from all the patients to be included in the study.  Animal studies : This article does not contain any study with animals that was performed by any of the authors.","source_license":"CC0","license_restricted":false}