Reproductive Biology and Endocrinology Open Access Endometrial Thickness, Caucasian Ethnicity, and Age Predict Clinical Pregnancy following Fresh Blastocyst Embryo Transfer: a Retrospective Cohort

Background: In-vitro fertilization (IVF) with blastocyst as opposed to cleavage stage embryos has been advocated to improve success rates. Limited information exists on which to predict which patients undergoing blastocyst embryo transfer (BET) will achieve pregnancy. This study's objective was to evaluate the predictive value of patient and cycle characteristics for clinical pregnancy following fresh BET.


Background
Technical advances in assisted reproductive technologies (ART) have led to improving pregnancy rates with in-vitro fertilization (IVF). Traditionally following controlled ovarian hyperstimulation (COH) and oocyte retrieval, cleaving embryos have been transferred 2-3 days after fertilization; over the last decade, improvements in laboratory techniques and embryo culture media have allowed successful in vitro culture of embryos to the blastocyst stage. Blastocyst embryo transfer (BET) has been shown to correlate to higher live birth rates [1]. Higher success rates with BET may reflect an enhanced natural selection process that allows for biologically superior embryos to be transferred, rather than relying on morphological assessment of cleavage stage embryos [2]. Alternatively, improved pregnancy rates with BET may reflect a more synchronous environment between the blastocyst and the endometrium as blastocyst-endometrial interactions are an essential part of implantation [3]. Valbuena et al [4] have suggested that higher detrimental estradiol levels at the time of cleavage embryo transfer compared to the later timing of the blastocyst transfer, may also contribute to the differential pregnancy rates seen. Finally, it has been proposed that decreasing uterine contractility each day following oocyte retrieval may reduce embryo displacement inside the uterus and improve pregnancy success with blastocyst embryos [5].
A large body of retrospective data first suggested higher clinical pregnancy rates after BET. In one of the larger studies, Schwarzler et al. [6] showed clinical pregnancy rates of 44% after blastocyst and 28% after cleavage stage transfer. A prospective, randomized study of single embryo transfer showed high pregnancy rates (33% vs. 23%) after BET in patients with high embryo quality (6-8 cells, <25% fragmentation, and even-numbered blastomeres), proposed to be from natural selection of the best embryos [7]. Papanikolaou et al. [8] in a prospective randomized study showed both higher clinical pregnancy rate (58% vs. 41%) and lower pregnancy loss rate (14% vs. 20%) after single embryo transfer at the blastocyst versus cleavage stage, postulated to be due to lower rates of aneuploidy. A recent Cochrane meta-analysis including nine randomized control trials showed higher live birth rates in blastocyst cycles (OR 1.35, 95% CI 1.05 -1.74) with no difference in miscarriage or multiple pregnancy rates [1]. The authors suggest this may be due to either natural selection of the 'best embryo' or due to a difference in the interactions between the embryo and uterine environment.
Although these studies have suggested that it is primarily embryological characteristics (i.e. higher number of embryos at the 6-8 cell stage, high quality embryos) that predict the successful development of a blastocyst, a sys-tematic assessment of predictors of successful clinical outcome after BET cycles is lacking. Many articles have examined the ability of embryos to develop to the blastocyst stage and subsequently impact pregnancy rate. Almost none have reported on the ability to differentially predict pregnancy rates once a patient has already developed blastocysts [1]. In one of the larger studies, which examined single blastocyst transfer and where more than 95% of patients received a good quality blastocyst (thus providing a more controlled environment to adjust for embryo factors), no predictive factors were reported within the blastocyst group [8]. In one of the only studies which have reported predictive factors, Richter et al. demonstrated that age, embryo quality, and endometrial thickness were related to clinical pregnancy [9]. Our objective in this study was to identify patient and COH cycle characteristics that may impact on the probability of clinical pregnancy (CP) after fresh BET in our patient population.

Subjects
All IVF cycles between 2003 and 2007 at Montefiore's Institute for Reproductive Medicine and Health (MIRMH) were reviewed. Data were collected from patient charts, computerized ultrasound reports, completed patient intake questionnaires including information on racial and ethnic background, and detailed embryology records. Analyses were restricted to all fresh IVF cycles proceeding to BET (n = 114). IVF cycles utilizing donor oocytes and thawed BET cycles were excluded; ART cycles utilizing preimplantation genetic screening or diagnosis were included (n = 4). Early follicular phase (cycle days 1-3) serum levels of FSH reflected "ovarian reserve" status [10]; for those patients in whom prior FSH values were available, the highest available level was taken to reflect ovarian reserve for the individual.
Patient management was per routine clinical practice, and all patient stimulation protocols were reviewed and approved by a single clinical director. Ovulation suppression was achieved with either GnRH agonists or antagonists; COH was achieved with injectable gonadotropins and transvaginal ultrasound guided oocyte retrieval was performed 34 hours after hCG injection. Patients met criteria for hCG injection when 2 follicles (mean diameter) were >17 mm. All patients received luteal supplementation with intramuscular progesterone in oil. During the study period, there were no major changes in laboratory personnel or protocols. IVF (n = 48), intracytoplasmic sperm injection (ICSI)(n = 51), and Split cycles (partial IVF/partial ICSI) (n = 15) cycles were included. The decision to proceed to BET was based on the number and cleavage status of available embryos 2 days post insemination; patients with at least six four-cell embryos (<20% fragmentation) that continued to divide were taken to the blastocyst stage. Patients age >35 were additionally taken to blastocyst culture if they failed to achieve CP in a prior ART cycle using cleavage stage embryos (n = 19). Outcome of interest was CP, defined by the presence of an intrauterine gestational sac on trans-vaginal ultrasound. All other cycle outcomes (non-pregnant, biochemical, and ectopic pregnancies) were classified as negative pregnancy (NP).
The study was approved by the Institutional Review Board at Montefiore Medical Center, Bronx, New York. Given the retrospective nature of analyses, written informed consent was waived.

Statistical analysis
Distribution of continuous variables was assessed by Shapiro-Wilk test. Associations of CP with patient characteristics (age, body-mass index (BMI), FSH, ethnicity) and ART cycle parameters (serum E 2 levels on day of hCG, maximal cycle thickness of endometrial stripe-ES on day of hCG, number of eggs retrieved, number of mature (metaphase 2) eggs, number of fertilized embryos, available cleaving embryos on Day 2 and 3, number of blastocysts available, transferred, and cryopreserved) were evaluated using Student's T test (for data demonstrating Gaussian distribution) or the Mann-Whitney tests (for skewed data) as appropriate. Spearman's correlation analyses evaluated associations between the various patient and cycle parameters. Fertilization % (% of mature eggs fertilized) by fertilization method (IVF, ICSI, Split) was evaluated by ANOVA. Multivariable logistic regression models reporting odds ratios (OR) ± 95% confidence intervals were created to determine independent predictors of CP following BET as well as to examine the relationship between weight and Caucasian ethnicity. Additionally, the influence of fertilization method on CP was evaluated by chi-squared test (χ 2 ). Embryo quality was defined according to our standard assessment practices [11]. Embryo quality was categorized according to the criteria set forth by the Society for Assisted Reproductive Technology (SART) guidelines ('SART Bulletin, 5/7/07) which is currently used for reporting of all SART data. Embryos were assigned as "good" (4AA, 4AB, 4BA, 5AA, 5AB, 5BA, 3AA), "fair" (5AC, 5CA, 4AC, 4CA, 3AB, 3BA, 3BB, 3AC, 3CA, 3BC, 3CB, 3CC) or "poor" (all others). Additionally, a total embryo quality score was calculated by adding up the individual scores of all embryos transferred in a patient (good = 3, fair = 2, poor = 1). Receiver Operating Characteristic (ROC) analyses were used to determine the optimal thickness of ES for predicting CP following BET. A two tailed p <0.05 was considered statistically significant and p values are reported to the third decimal place. All analyses were performed used STATA SE v 8 (College Station, TX).

Results and discussion
CP was observed in 50% of the BET cycles. Table 1 describes patient and ART cycle characteristics according to cycle outcome. Continuous data are presented as mean ± standard deviation and categorical data are presented as percentage (%). Patients achieving CP compared to NP were significantly younger (32.4 ± 3.5 vs. 34.1 ± 4.1 years old, p = 0.019) but had comparable ovarian reserve status (as reflected by FSH level) and BMI values. The range of patient ages in our cohort was 24 to 43 years. Both groups received a similar number of blastocysts for embryo transfer and had comparable embryological parameters (Table  1). There were no differences in fertilization (%) (p = 0.251) or CP by fertilization method (p = 0.364). For the four cycles utilizing either pre-implantation genetic screening (n = 2, recurrent pregnancy loss) or diagnosis (n = 2, single gene disorders), the genetically normal embryos were either the only blastocysts that grew in culture or they were the best embryos morphologically.
Independent predictors of CP were determined by creating multivariable logistic regression models (Figure 1).  (Figure 2), area under the ROC curve was modest at 0.627, making the cutoff a poor overall indicator of successful CP (specificity of 47%). Of the 54 clinical pregnancies with known ES thickness, only 3 occurred in patients with an ES thickness <8 mm; the other 9 patients whose ES thickness was <8 mm did not achieve clinical pregnancy.
Finally, we examined the impact of primary etiology of infertility diagnoses on BET cycle outcome. There were no overall differences in contributory infertility etiologies by CP outcome (CP v NP; Fisher's Exact test, p = 0.366). Diagnoses included: male factor (n = 27), tubal factor (n = 28), ovulatory dysfunction (including diminished ovarian reserve; n = 24), unexplained infertility (n = 21), and other causes of infertility (endometriosis, recurrent pregnancy loss, neurofibromatosis, and uterine factors; n = 14). However, infertility diagnosis differed by ethnicity (Fisher's Exact Test, p < 0.001); Caucasians were less likely to have a diagnosis of tubal factor (15% v 66%, p < 0.001) and more likely to have a diagnosis of "other causes of infertility" (18% v 0%, p = 0.009, Fisher's Exact Test).

Conclusion
In this study, we have identified patient parameters that are predictive of success of fresh BET cycles. Even among this subset of "excellent prognosis" patients by virtue of  Receiver-operating characteristic analysis of thickness of ES demonstrates a 9.5 mm cutoff best predicts CP Figure 2 Receiver-operating characteristic analysis of thickness of ES demonstrates a 9.5 mm cutoff best predicts CP. , Indian (n = 12) Black (n = 9), Hispanic (n = 5), and unknown (n = 1) patients.
with increasing BMI [25][26][27]. However, uterine receptivity was unimpaired in women with increased BMI, when hormonal support and embryo quality were standardized [28,29]. Additionally, Bellver et al. [30] found CP to be unaffected by obesity in oocyte donor-recipient cycles but did see an association between obesity and spontaneous abortion. The existing data imply a link between BMI and oocyte/embryo characteristics that is more likely to account for the reduced clinical pregnancies seen in association with obesity. Interestingly, we found no overall correlation between polycystic ovarian syndrome (PCOS) and BMI (r = 0.024, p = 0.801); additionally PCOS was not correlated with being overweight (r = 0.047, p = 0.620), obese (r = 0.032, p = 0.741), or Caucasian (r = -0.010, p = 0.914). This reinforces that our patient population overall is overweight (mean BMI 25.2 kg/m 2 ); only 60/114 (53%) patients had a BMI < 25 kg/m 2 .
A longer duration of infertility prior to treatment may lower pregnancy rates even with BET [31]. Sharara et al. [32] previously found that African-American (compared to Caucasian) women had a significantly longer duration of infertility prior to seeking treatment and had a 3-fold lower odds of achieving pregnancy. Seifer et al. [33] again demonstrated that African-American women had a longer duration of infertility prior to seeking treatment and were underrepresented in IVF centers (5% of cycles) compared to their proportion of the general population of reproductive age women (8%). It is possible that an ethnic disparity in access to ART played a role in our findings. We believe it is especially important for future research to document and systematically study the impact of ethnicity on outcomes of fertility treatments.
Ethnic differences in the prevalence of common conditions associated with infertility may also have played a role in BET success. Ethnic variability in prevalence of both uterine leiomyoma [34] and endometriosis is previously described [35][36][37][38] Since the diagnosis of leiomyoma or endometriosis was only represented in our data if identified as the primary cause of infertility, it is not possible to determine whether these conditions varied by ethnicity and/or impacted BET success. The likelihood of a PCOS diagnosis was comparable between Caucasian (11%) and non-Caucasian (12%) patients, a finding common to other published data, [39] and did not seem to impact CP rates in our population.
We acknowledge certain limitations of our study which prevent us from making broader conclusions. The study was retrospective and included a relatively small sample of patients. Ethnicity and thickness of ES though statistically significant were closer to the upper limit of significance which most likely reflects the number of patients included in the study. Our patients were heterogeneous both in their underlying fertility diagnoses and by ethnicity. Therefore broader implications on noted relationships with ethnicity are limited. Both ethnicity and diagnosis impact pregnancy rates; not all diagnoses confer the same prognosis. Information on the duration of infertility is lacking in our patient population.
We herein have identified differences between patients following fresh BET; specifically, our data identify advancing age, endometrial thickness and patient's ethnicity as independent correlates to the success of BET cycle. These data are consistent with the previous finding that patients achieving clinical pregnancy after BET are younger with a thicker ES [9]. More data are needed to determine the exact way in which ethnicity impacts on success of ART following BET. While the past few years have allowed insights into embryo parameters that help identify patients who are likely to achieve embryo growth to the blastocyst stage, our present observations indicate specific host factors that contribute to the success of BET cycles.