Excerpt: High Fecundity Rates Following In-Vitro Fertilization and Embryo Transfer in Antiphospholipid Antibody Seropositive Women Treated with Heparin and Aspirin


Dr. William Matzner
William Matzner, MD, Simi Valley, California

Excerpt: High Fecundity Rates Following In-Vitro Fertilization and Embryo Transfer in Antiphospholipid Antibody Seropositive Women Treated with Heparin and Aspirin 

This is an excerpt of an article originally published in Human Reproduction and was co-authored by Dr. William Matzner.  The full article is available here. 

INTRODUCTION

One of the great endeavours facing reproductive medicine is to improve pregnancy rates following in-vitro fertilization (IVF) and embryo transfer. Patients undergo IVF and embryo transfer for infertility secondary to organic pelvic disease, ovarian dysfunction, male factor, and immunological and unexplained aetiologies. It has been well documented that fertilization rates by assisted reproductive technologies are high (Lopata et al., 1982), yet the North American national IVF/embryo transfer birth rate for the year ending December 1991 was only 15.2% per egg retrieval (Society for Assisted Reproductive Technology, 1993). Autoantibodies have been detected in humans and other animals who have failed to conceive despite repeated attempts at IVF/embryo transfer. One such study has implicated antibodies to negatively charged phospholipids in unsuccessful IVF/embryo transfer cycles (Fisch et al., 199l). An increased prevalence of antiphospholipid antibodies (APA) has also been demonstrated in patients diagnosed with pelvic endometriosis (Gleicher et al., 1987). This has led to speculation that autoimmune processes similar to those known to be associated with recurrent pregnancy wastage may compromise embryo implantation following IVF/embryo transfer. 

Several mechanisms have been proposed to explain how APA contribute to pregnancy wastage: platelet membrane and/ or endothelial cell wall damage may initiate the clotting cascade, and inhibition of prostacyclin and inability to activate protein C (an endogenous anticoagulant) may contribute to a hypercoagulable state (Harris et al., 1985). More recent work has demonstrated that several negatively charged APA, notably antiphosphoserine and antiphosphoethanolamine, interfere with the formation of syncytiotrophoblasts from cytotrophoblasts (Rote et al., 1992). This latter mechanism may also play a significant role in IVF/embryo transfer, as it emphasizes the function of phospholipids as adhesion molecules modulating the process of implantation. Interference with these adhesive properties may preclude implantation altogether or result in spontaneous abortions.

A study was undertaken to evaluate the effect of APA on women undergoing IVF/embryo transfer so as to determine (i) the prevalence of APA seropositivity in women with organic pelvic disease (i.e. post-surgical adhesions, endometriosis and/or pelvic inflammatory disease), compared to women whose infertility was not associated with tissuedamaging conditions (e.g. male factor and/or unexplained infertility), (ii) whether APA seropositivity adversely affects implantation and pregnancy rates with IVF/embryo transfer, and (iii) whether combined treatment with heparin and aspirin (H/A) improves ongoing clinical pregnancy rates in seropositive women who undergo IVF/embryo transfer.

MATERIALS AND METHODS

Patient population

We evaluated 429 women <40 years of age who underwent IVF/ embryo transfer at the Pacific Fertility Medical Centers in California, during the 30 month period commencing January 1, 1992 through June 30, 1994 in order to assess the relationship between APA seropositivity and the cause of infertility. The assessment of outcome following IVF/embryo transfer was confined to those cycles of treatment which immediately followed the diagnosis of APA status. Patients were divided into two groups: group 1 comprised 365 women with organic pelvic disease. Male factor infertility was absent in all cases. This group was further subdivided according to diagnosis as follows: group 1A comprised 79 women with endometriosis and of these, 52 (66%) women were APA seropositive; group 1B comprised 187 women who underwent IVF/embryo transfer for infertility due to pelvic inflammatory disease, and of these 85 (45%) women were APA seropositive; group 1C comprised 99 women who underwent IVF/embryo transfer for infertility due to abdominal/pelvic adhesions unassociated with prior pelvic inflammatory disease or endometriosis and 57 (58%) of these women were APA seropositive.

Group 2 comprised 64 women whose infertility was not associated with female pelvic pathology. The cause of infertility in this group was an ‘isolated male factor’ in 49 of these women and was ‘unexplained’ in 15 cases. Nine (14%) women in group 2 were APA seropositive.

The diagnosis of ‘isolated male factor infertility’ required the detection of < 10 x 106/ml motile spermatozoa on semen analysis in the absence of any identifiable female cause for infertility. Organic pelvic pathology was diagnosed or excluded by any combination of hysterosalpingography, laparoscopy and/or laparotomy. All women in the study had normal uterine cavities as observed at hysteroscopy. Women with thyroid dysfunction or hyperprolactinaemia were treated appropriately prior to commencing IVF/embryo transfer cycles.

Laboratory evaluation

All women were required to undergo serum follicle stimulating hormone (FSH) and oestradiol measurements (by radioimmunoassay) on the second or third day of a preceding menstrual cycle and were only included in this study if the FSH and oestradiol concentrations were < 15 mIU/ml and 40 pg/ml respectively. These women also underwent concomitant APA testing using an enzyme-linked immunosorbent assay for antibodies to six phospholipid epitopes (cardiolipin, phosphoserine, phosphoglycerol, phosphoethanolamine, phosphatidic acid and phosphoinositol), as previously described (Matzner et al, 1994). Cervical swabs and cultures were obtained tor Ureaplasma urealyticum as well as DNA probes for Chlamydia and Gonococcus. Male partners underwent semen evaluations which included sperm counts, motility, morphology and culture for pathogenic organisms. In addition, both women and men had sperm antibody serologies performed using the indirect immunobead test.

Treatment

Since women of a similar age with organic pelvic disease in the absence of male factor are expected to have comparable clinical pregnancy rates following IVF/embryo transfer attempts, evaluation of treatment with H/A was limited to patients in group 1. Antiphospholipid antibody seropositivity was defined by the detection of any concentration of APA in the IgG, IgM and/or IgA immunoglobulin fraction. There were 194 IVF/embryo transfer cycles performed on APA seropositive women. Of these, a total of 169 women received heparin sulphate [Lyphomed, Deerfield, Illinois, 60015; (5000 units s.c.)] twice daily, along with aspirin [Bayer, Division of Sterling Winthrop Inc, New York, NY 10016; (81mg)] orally once a day and there were 25 APA seropositive women who did not receive H/A. Treatment with H/A commenced with the initiation of ovarian stimulation on cycle day 2 to be continued through the 34th week of pregnancy. A luteal phase pituitary gland ‘down-regulation’ protocol using a gonadotrophin-releasing hormone agonist in conjunction with gonadotrophins was employed to achieve optimal ovarian stimulation as previously described (Feinman et al., 1993). Heparin was temporarily withheld after the morning administration on the day prior to oocyte retrieval and aspirin was withheld 2 days prior to this procedure (i.e. from the day of human chorionic gonadotrophin administration). Both heparin and aspirin therapy were reinitiated immediately following transvaginal ultrasound-guided oocyte retrieval. All patients undergoing H/ A therapy had normal activated partial prothrombin times, serum glutamic-oxalacetic transaminase and serum glutamic-pyruvic transaminase concentrations and normal red blood cell and platelet counts prior to initiating treatment. These tests were repeated at 2 week intervals for 2 months and thereafter at monthly intervals until termination of the medication regimen.

Endpoint

The endpoint was defined as either a viable pregnancy or delivery. The diagnosis of a viable pregnancy was based on sonographic confirmation of fetal cardiac activity.

Statistical methods

Comparisons of individual proportions in any two treatment groups were carried out using Fisher’s exact test. A collective test for treatment over several subgroups, such as groups 1A, 1B, and 1C in Table II, was made using the logarithmic regression model proposed by Cox (1972). The estimates and confidence limits obtained by this technique are computed from the complete data, and not simply from the marginal totals.

RESULTS

Table I illustrates that there was no evidence of systematic differences in the mean ages, ovarian stimulation protocols employed and the number of embryos transferred per IVF attempt among the group of women with organic pelvic pathology, male factor and unexplained infertility. There was, however, evidence that women in group l had a higher prevalence (P < 0.001) of APA seropositivity (53%) than women in group 2 (14%).

To determine whether APA seropositivity adversely affected IVF/ embryo transfer outcome, the pregnancy rates of untreated APA seropositive women were compared with those for APA seronegative women, following one IVF/embryo transfer cycle performed on group 1 patients, in the cycle that followed the diagnosis of the women’s APA status (see Table II). However, there was no firm statistical evidence of differential pregnancy rates. The ratio of pregnancy rates (APA- /APA+) was estimated as 1.66 with 95% confidence limits of 0.58 and 4.72, which embraced the ‘null hypothesis’ value of 1.0. The small number of untreated APA + women no doubt contributed to this failure to find evidence of an effect.

There was statistical evidence that the pregnancy rate in H/ A-treated APA seropositive women (49%) was significantly higher (P < 0.05) than for untreated APA seropositive women (16%). The logarithmic regression estimated the ratio of pregnancy rates (treated/untreated) as 3.02, with 95% confidence limits of 1.09 and 8.40); limits which do not embrace the ‘null hypothesis’ value of 1.0. The viable pregnancy rates per IVF/embryo transfer cycle, stratified by subgroups of organic pelvic pathology, are presented in Table II.

The pregnancy rate of the APA seropositive treatment group treated with heparin and aspirin (49%) was also significantly higher (P < 0.001) than that obtained from the APA seronegative group (27%). The ratio of pregnancy rates (APA + /APA-) was estimated as 1.79, with 95% confidence limits of 1.24 and 2.59, providing convincing evidence of the effect.

Rest of the article can be found at the link provided above. 

About William L. Matzner, M.D., PhD, FACP 

Dr. William Matzner works in the area of healthcare economics consulting at Healthcare Analytics, LLC, in California. He graduated Phi Beta Kappa from Stanford University. He received his M.D. with Honors from Baylor College of Medicine. In 1988, he was the Solomon Scholar for Resident Research at Cedar Sinai Medical Center. Dr. Matzner subsequently was awarded a PhD in Neuro Economics from Claremont Graduate University. He is board certified in Internal Medicine and Palliative Medicine. He has researched and published extensively on the issue of reproduction and immunology in medical literature. He has been in private practice since 1989, specializing in Reproductive Immunology and Internal medicine. 

Consulting Website: https://healthcareanalytics.biz
News: https://medicogazette.com/dr-william-matzner 
 
William Matzner, MD (Simi Valley, California), has been practicing medicine since 1989, Internal Medicine and Reproductive Immunology. M.D. with Honors from Baylor College of Medicine.

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