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Obstet Gynecol Sci > Volume 61(3); 2018 > Article
Hong, Kim, Moon, Kim, Jee, Lee, and Kim: Impact of presence of antiphospholipid antibodies on in vitro fertilization outcome

Abstract

Objective

To investigate prevalence of antiphospholipid antibody (APA) in Korean infertile women undergoing the first in vitro fertilization (IVF) treatment and to evaluate the influence of APA on the subsequent IVF outcomes.

Method

Two hundred nineteen infertile women who destined the first IVF were prospectively enrolled in 2 infertility centers. Male factor or uterine factor infertility and women with past or current endocrine or immunologic disorders were completely excluded. Plasma concentration of lupus anticoagulant was measured by clot-based method, and anticardiolipin antibody (IgG/IgM), and anti-β2-glycoprotein 1 antibody (IgG/IgM) was measured by enzyme-linked immunosorbent assay method before starting ovarian stimulation for IVF.

Results

APA was positive in 13 women (5.9%). Lupus anticoagulant was positive in 2 women (0.9%), anticardiolipin antibody was positive in 7 women (3.2%), and anti-β2-glycoprotein 1 antibody was positive in 4 women (1.8%). In 193 women entering embryo transfer, clinical characteristics and stimulation outcomes were comparable between APA-positive (n=12) and APA-negative group (n=181). The clinical pregnancy rate (66.7% vs. 45.9%), ongoing pregnancy rate (58.3% vs. 37.0%), and miscarriage rate (12.5% vs. 19.3%) were all similar between APA-positive and APA-negative group.

Conclusion

The prevalence of APA is low in Korean infertile women undergoing the first IVF cycle, and the presence of APA appears to neither decrease their first IVF success nor increase abortion rate.

Introduction

It has been proposed that antiphospholipid antibodies (APAs) may have some relationship with infertility and in vitro fertilization (IVF) outcomes [1].
From the literatures, the prevalence of positive APA ranged from 0% to 11.4% in healthy or fertile women, from 3.3% to 23.7% in unexplained infertility, and from 0% to 66% in women undergoing IVF [2,3,4,5,6,7,8,9,10,11,12,13]. From 54 Korean women undergoing IVF due to tubal factor, the prevalence of APA was 16.7% [14].
In women with IVF failure, the prevalence of positive APA ranged from 4.2% to 30.4%, but it was 0% in women conceived or delivered after IVF [1,10,12]. In women with 3 or more failed IVF, the prevalence ranged from 6.0% to 65.9%, in contrast, it ranged from 0% to 33% in women conceived within 2-3 IVF cycles [3,7,8]. Collectively, the prevalence of APA was higher in infertile women than fertile control and the presence of APA appears to be associated with IVF failure.
In 2008, American Society for Reproductive Medicine (ASRM) announced that there is no association between APA and pregnancy rate or live birth rate after IVF [15]. They identified 16 literatures in which the pregnancy rate or live birth rate after IVF treatment in APA-negative and APA-positive women were examined. The pooled clinical pregnancy rate and live birth rate were 57% and 46% in APA-positive group and 49.2% and 42.9% in APA-negative group, respectively. They concluded that assessment of APA is not recommended among couples undergoing IVF, and the therapy is not justified. A subsequent meta-analysis including 7 studies also showed that there is no significant association between APA and clinical pregnancy or live birth in patients underwent IVF [16].
However, in a recent retrospective study, APA positivity was associated with significantly lower pregnancy rate and higher abortion rate after IVF [17]. As far as we know, there has been only one report with regards impact of APA positivity on IVF outcomes in Korean infertile women; pregnancy rate was similar between APA-positive and APA-negative group in infertile women who underwent IVF in Korea, however, abortion rate was significantly higher in APA-positive group (62.5% vs. 20.0%) [14].
It would be very important whether APA-positive women have poorer IVF outcome. If this is true, immunotherapy should be considered in APA-positive women prior to IVF. As shown in Table 1, the majority of previous studies included women who underwent IVF irrespective of number of previous cycles or women with 2 or more failed IVF cycles. When an association of APA positivity with pregnancy results after IVF is directly assessed, women who underwent the first IVF cycle should be included.
Table 1

Literatures about in vitro fertilization (IVF) pregnancy outcomes in women with positive or negative for antiphospholipid antibodies

APA, antiphospholipid antibody, NA, not available; LA, Lupus anticoagulant; aCL, anticardiolipin antibody; ab2GPI, anti-b2 glycoprotein I antibody; aPS, anti-phosphatydilserine antibody.
a)P<0.05.
Author, year [reference number] Study group No. Positivity APA-positive vs. APA-negative
Pregnancy rate Live birth rate Miscarriage rate
El-Roeiy et al., 1987 [25] Women undergoing IVF 26 aCL 34.6% 10.0% vs. 37.5% 0% vs. 18.8% NA
aPS 26.9%
Gleicher et al., 1994 [26] Women undergoing IVF 105 27.6% 32.8% vs. 23.9% 26.3% vs. 15.8% NA
Sher et al., 1994 [12] Women undergoing IVF without habitual abortion 25 NA 16% vs. 27% NA NA
Nip et al., 1995 [10] Women with unexplained infertility 30 3.3% 33% vs. NA 30% vs. NA NA
Women with tubal factor infertility 50 22% vs. NA 20% vs. NA
Birdsall et al., 1996 [3] Women undergoing IVF 240 15.0% 38.9% vs. 36.1% 27.9% vs. 25.5% NA
Kutteh, 1997 [8] Women undergoing IVF 191 18.8% 35.3% vs. 39.7% NA NA
Kowalik et al., 1997 [27] Women undergoing IVF 525 14.9% 57.7% vs. 49.7% 46.2% vs. 43.8% 20.0% vs. 23.7%
Eldar-Geva et al., 1999 [23] Women with 2 or more failed IVF 56 37.0% 18.8-52.2% vs. 17.3-50% 6.3-25.4% vs. 9.9-27.7% NA
Chilcott et al., 2000 [6] Women undergoing IVF 380 aCL or LA 23.4% 15.7% vs. 19.6% 9.0% vs. 12.0% 75.0% vs. 62.8%
ab2GPI 3.3%
Hornstein et al., 2000 [16] Women undergoing IVF 2,053 34% 57% vs. 46% 49.2% vs. 42.9% NA
Buckingham et al., 2005 [4] Women undergoing IVF 99 aCL IgG 2%, IgM 2% 31.6% vs. 36.3% 15.8% vs. 23.8% NA
ab2GPI IgG 10%, IgM 4%
aPS IgG 4%, IgM 0%
Matsubayashi et al., 2006 [28] Women with 2 or more failed IVF 44 65.9% 29.4% vs. 33.3% NA NA
Sanmarco et al., 2007 [29] Women with 2 or more failed IVF 101 39.6% 42.7% vs. 41.9% 32.5% vs. 32.2% 5.0% vs. 6.5%
Lee et al., 2007 [14] Women undergoing IVF with tubal factor 54 LA 1.8% 20.5% vs. 17.6% 7.7% vs. 14.1%a) 62.5% vs. 20.0%a)
aCL 14.8%
Zhong et al., 2011 [17] Women undergoing IVF with tubal factor 76 NA 31.3% vs. 48.6%a) NA 32% vs. 15.1%a)
Paulmyer-Lacroix et al., 2014 [30] Women with 2 or more failed IVF 40 20% 50% vs. 53% 0% vs. 35.3% 25.0% vs. 52.9%
Here we assessed the prevalence of APA among Korean women who attempted the first IVF cycle and the influence of APA on clinical pregnancy, miscarriage, and ongoing pregnancy in a subsequent IVF cycle.

Materials and methods

This was a prospective observational study including 219 Korean infertile women undergoing their first IVF at the Seoul Maria Fertility Hospital, and the Seoul National University Bundang Hospital (March 2013 to November 2016). Committee approval was validated and informed consent was obtained from all patients before the study (IRB No. B-1302/190-003).
We included women aged 24-44 years who had female factor or unexplained infertility and destined to the first IVF cycle. The indications of IVF were unexplained (n=83), tubal (n=50), ovulatory (n=23), old age (n=18), decreased ovarian reserve (n=15) endometriosis (n=10), or multiple factors (n=20). During the study period, male factor infertility or uterine factor (uterine malformation, intrauterine adhesion) was completely excluded. Women with past or current thyroid disease, endocrine disorders (diabetes mellitus, hyperprolactinemia), immunologic disorders (rheumatoid arthritis, systemic lupus erythematosus), or current obesity (body mass index ≥30 kg/m2) were excluded.
Before starting ovarian stimulation for IVF, plasma concentration of lupus anticoagulant was measured by clot-based method, and anticardiolipin antibody (IgG/IgM) and anti-β2-glycoprotein 1 antibody (IgG/IgM) were measured by enzyme-linked immunosorbent assay method. Measurement of lupus anticoagulant consisted of screening and confirmative test; if the titer from initial screening was more than 51, a confirmative test was performed and lupus anticoagulant was considered as positive if the titer from confirmative test was 1.2 or more. Anticardiolipin antibody and anti-β2-glycoprotein 1 antibody were considered as positive if the titer was 20 phospholipid unit (PLU) or more.
Except 6 women with stimulation cancellation, 213 women underwent ovarian stimulation for IVF by using recombinant or urinary follicle-stimulating hormone with or without luteinizing hormone. Two types of pituitary suppression protocol were used: luteal long protocol of gonadotropin releasing hormone (GnRH) agonist (113 cycles) or flexible GnRH antagonist protocol (100 cycles). After 2 or more follicles had reached a diameter >18 mm, 250 μg of recombinant human chorionic gonadotropin (hCG; Ovidrel®; Merck-Serono, Darmstadt, Germany) was injected. The oocyte was retrieved 35 hours after the hCG injection. Fertilization was considered if 2 distinct pronuclei and a second polar body were visible. The quality of embryos was evaluated by morphological criteria based on the fragmentation degree and the regularity of blastomeres on day 3 after fertilization and classified as 4 grades (with grade A being the top embryo). We assessed blastocyst quality method presented by Gardner et al. [18]. Embryo transfer was performed day 2 to 5 after the oocyte collection. Luteal phase was supported either by daily progesterone injection or vaginal gel (Crinone®; Merck-Serono). Clinical pregnancy was confirmed by the presence of gestational sac(s) with visible fetal heartbeat(s). Ongoing pregnancy was defined if the pregnancy continued after 12 weeks of gestation, and clinical miscarriage was defined if the pregnancy terminated before 12 weeks of gestation.
The prevalence of APA was assessed in 219 women. The association between the presence of APA and pregnancy results was assessed in 193 women who attempted embryo transfer. Twenty-six women did not reach embryo transfer because of stimulation cancellation (n=6), cancellation of ovum pick up (n=1), no oocyte retrieved (n=1), failed fertilization (n=4), or freezing-all-embryo due to high-risk of ovarian hyperstimulation syndrome (OHSS) (n=14). All statistical analyses were performed using IBM SPSS ver. 19 (IBM Co., Armonk, NY, USA). The data were analyzed using the Mann-Whitney U test or Fisher's exact test as indicated. The results were considered significantly different when the P-value was <0.05.

Results

Among 219 women, APA was positive in 13 women (5.9%). Lupus anticoagulant (confirmative test) was positive in 2 women (0.9%). No woman had a positive anticardiolipin IgG antibody, but 7 women was positive for anticardiolipin IgM antibody (3.2%); low titer (20-29 PLU) in 4 women, moderate titer (30-79 PLU) in 2 women, and high titer (>80 PLU) in 1 woman. Anti-β2-glycoprotein 1 antibody was positive in 4 women (1.8%); IgG antibody was positive in 2 women and IgM antibody was positive in 2 women. No women are positive for 2 kinds of APA.
In 193 women entering embryo transfer, clinical pregnancy was noted in 91 women (clinical pregnancy rate per transfer: 47.2%) and twin rate was 27.5% (25/91). Chemical pregnancy occurred in 15 women and ectopic pregnancy occurred in one woman but these were excluded from the assessment of clinical pregnancy rate. Among 91 women with clinical pregnancy, clinical miscarriage occurred in 17 women (clinical miscarriage rate per clinical pregnancy: 18.7%). Sixteen miscarriages occurred among singleton pregnancy and 1 in twin pregnancy. Vanishing twin was observed in 3 women but these were not included into the miscarriage rate.
In 193 women entering embryo transfer, clinical characteristics and stimulation outcomes were comparable between APA-positive (n=12) and APA-negative group (n=181) (Table 2). The clinical pregnancy rate (66.7% vs. 45.9%) and ongoing pregnancy rate (58.3% vs. 37.0%) was similar between APA-positive and APA-negative group. Miscarriage rate was also similar between 2 groups (12.5% vs. 19.3%) (Table 3).
Table 2

Clinical characteristics and ovarian stimulation outcomes in women with antiphospholipid antibody (APA)-positive and -negative group

Data shown are median (95% confidence interval). Mann-Whitney U test, χ2 or Fisher's exact test.
NS, not significant; IVF, in vitro fertilization; DOR, diminished ovarian reserve; AMH, anti-Müllerian hormone; GnRH, gonadotropin releasing hormone.
Characteristics APA-positive group (n=12) APA-negative group (n=181) P
Age of women (yr) 34 (33-38) 35 (33-37) NS
Body mass index (kg/m2) 21.4 (19.5-23.5) 21.5 (20.1-23.6) NS
Parous 0 12 NS
Indications for IVF NS
Unexplained 2 75
Tubal 5 49
Ovulatory 0 6
Old age 2 17
DOR 2 19
Endometriosis 0 14
Multiple factors 1 16
Serum AMH level (ng/mL) 3.8 (2.1-8.1) 2.8 (1.4-5.2) NS
Titers of APA
Lupus anticoagulant - screening 39.3 (36.1-48.7) 37.3 (37.0-38.7) NS
Lupus anticoagulant - confirmative 1.5 (−1.7-4.6) 1.1 (0.1-1.2) NS
Anticardiolipin antibody IgG 4.0 (2.7-5.5) 3.0 (3.5-4.3) NS
Anticardiolipin antibody IgM 18.0 (6.0-43.4) 7.0 (7.0-8.3) 0.001
Anti-β2-glycoprotein 1 antibody IgG 0.1 (−3.9-19.1) 0.1 (0.1-0.5) NS
Anti-β2-glycoprotein 1 antibody IgM 1.1 (−1.7-13.3) 0.5 (0.9-1.5) NS
Pituitary suppression NS
GnRH agonist 6 101
GnRH antagonist 6 80
Dose of gonadotropin (ampule) 34 (22-42) 34 (27-44) NS
No. of retrieved oocytes 16 (8.5-22.0) 10 (7-14) 0.044
No. of retrieved mature oocytes 9.5 (4.5-14.5) 8 (5-11) NS
No. of fertilized oocytes 9 (5-13) 6 (4-10) NS
Triple pattern endometrium 4 77 NS
No. of transferred embryos
Overall 2 (2-2) 2 (2-2) NS
Day 2-4 transfer 2 (2-2) 2 (2-2) NS
Day 5 transfer 2 (2-2) 2 (2-2) NS
Table 3

Pregnancy outcomes in women with antiphospholipid antibody (APA)-positive and -negative group

Data shown are number (%). χ2 or Fisher's exact test.
NS, not significant.
Characteristics APA-positive group (n=12) APA-negative group (n=181) P
Clinical pregnancy
Overall 8/12 (66.7) 83/181 (45.9) NS
Day 2-4 transfer 7/11 (63.6) 76/166 (45.8) NS
Day 5 transfer 1/1 (100) 7/15 (46.7) NS
Ongoing pregnancy
Overall 7 (58.3) 67 (37.0) NS
Day 2-4 transfer 6/11 (54.5) 61/166 (36.7) NS
Day 5 transfer 1/1 (100) 6/15 (40.0) NS
Clinical miscarriage 1 (12.5) 16 (19.3) NS
In 2 women with positive lupus anticoagulant, one woman was pregnant and no miscarriage occurred (clinical pregnancy rate: 50%, ongoing pregnancy rate: 50%).
In 7 women with positive anticardiolipin IgM antibody, embryo transfer was cancelled in one woman because of high-risk of OHSS; among 6 women, 3 women were pregnant and one miscarriage occurred (clinical pregnancy rate: 50%, ongoing pregnancy rate: 33.3%).
All 4 women with positive for anti-β2-glycoprotein 1 antibody were pregnant and no miscarriage occurred (clinical pregnancy rate: 100%, ongoing pregnancy rate: 100%).

Discussion

In the present study, the prevalence of APA was 5.9% among Korean women destined to the first IVF cycle. This prevalence is quite low when considering the result from previous studies (Table 1). The prevalence of each APA was also low when comparing with the result from other reports.
The prevalence of positive lupus anticoagulant in infertile women has been reported to be highly variable ranged from 0% to 17.8% [1]. In our study, lupus anticoagulant was rarely positive (0.9%) among women destined to the first IVF cycle, as like in another report from Korea (1.8% among women undergoing IVF due to tubal factor) [14].
The prevalence of positive anticardiolipin antibody has been reported to be higher in infertile women (15-53%) compared with those in healthy women with normal fertility (1-3%) [3,17]. However, the prevalence of anticardiolipin antibody was rather low in our study (3.2%). This was contrast in another report from Korea, in which anticardiolipin antibody was positive in 14.8% among women undergoing IVF [19].
In women with unexplained infertility undergoing IVF, the prevalence of anti-β2-glycoprotein 1 antibody was 13.3% [20]. The prevalence of positive anti-β2-glycoprotein 1 antibody has been reported to be 9% in the IVF failure group, 16% in the recurrent miscarriage group, and 0% in fertile control group [21]. In our study, the prevalence of anti-β2-glycoprotein 1 antibody in women destined to the first IVF cycle was rather low (1.8%).
In the present study, clinical pregnancy rate and miscarriage rate were all similar between APA-positive and APA-negative group. These findings were consistent with most previous studies, as listed in Table 1. Thus, the screening of APA positivity appears to be unnecessary in couples who try first IVF cycle.
Currently, only 2 studies described a detrimental effect of APA on IVF outcomes. In one report from Korea, abortion rate after IVF was significantly higher in APA-positive group (62.5% vs. 20.0%), although pregnancy rate was similar between APA-positive and APA-negative group [14]. Zhong et al. [17] demonstrated a significantly lower pregnancy rate (31.3% vs. 48.6%) and higher pregnancy loss (32.0% vs. 15.1%) after IVF in anticardiolipin antibody positive women than anticardiolipin antibody negative women.
Detrimental impact of APA on miscarriage can be explained by attachment of APA to the surface phospholipids on trophoblasts. This action may cause direct cellular injury and inhibition of conversion from cytotrophoblast to syncytiotrophoblast [22]. Indirect damage on trophoblasts is also possible via formation of intravascular micro-thrombosis [3,23].
If APA-positive women have poorer IVF outcome, immunotherapy should be considered in APA-positive women prior to IVF. However, there is a controversy about this. A retrospective study was performed in 116 infertile women who are positive for anticardiolipin antibody; they were treated by methylprednisolone plus low-dose aspirin or not [24]. Pregnancy rate after IVF was 46.6% in treated group, 33.3% in untreated group, and 53.9% in antibody negative group. Although pregnancy rates were similar between treated and untreated group, pregnancy rate in untreated group was significantly lower than antibody negative group. However, this study included small sample size and was not a randomized study. In one small study performed in Korea, short term corticosteroid therapy has no impact on pregnancy rate after IVF [14]. Further well-designed prospective randomized studies should be conducted to verify the effectiveness of immunotherapy in APA-positive women.
Our study has several strengths and limitations. APA was measured in women scheduled for the first IVF cycle and the association of pregnancy results was prospectively analyzed. In a previous report, a higher prevalence of antiphospholipid antibodies was found in the repeated IVF failure group than control group [21], thus inclusion of women who received several IVF cycles would enhance the prevalence of antiphospholipid antibodies and this would mislead the real prevalence of APA positivity and the association between APA positivity and IVF pregnancy results.
In our study, male factor or uterine factor infertility was completely excluded. Severe form of male or uterine factor infertility would result in high miscarriage rate. In addition, we excluded women with past or current endocrine or immunologic disorders, because the presence of endocrine or immunologic disorders and treatment of those diseases could affect APA positivity.
Small sample size in APA-positive group might be a major limitation in our study. Before initiation of study, the sample size was calculated as 220 at 80% power and 5% significance level with the assumption of 20% prevalence of APA and 20% difference in pregnancy rate. However, the prevalence of APA was unexpectedly low; APA was positive in only 12 out of 193 women entering embryo transfer (6.2%). Thus, more women would be needed to assess the real association between APA positivity and IVF pregnancy results. Further adequately powered and large-scaled prospective study would be needed.
We measured only 3 APAs among various APAs and this could result in underestimation of real APA prevalence. However, it may be impractical to measure all the APA and APA not included in current classification criteria for antiphospholipid syndrome has little clinical significance [1].
In conclusion, the prevalence of APA is low in Korean infertile women undergoing the first IVF cycle and the presence of APA appears to neither decrease their first IVF success nor increase abortion rate. Thus, the screening of APA positivity appears to be unnecessary in women who try first IVF cycle.

Acknowledgements

This work was supported by grant (No. A120043) from the Korea Health Care Technology R&D Project, Ministry of Health and Welfare, Korea.

Notes

Conflict of interest: No potential conflict of interest relevant to this article was reported.

References

1. Chighizola C, de Jesus G. Antiphospholipid antibodies and infertility. Lupus 2014;23:1232-1238. PMID: 25228713.
crossref pmid
2. Azem F, Geva E, Amit A, Lerner-Geva L, Shwartz T, Ben-Yosef D, et al. High levels of anticardiolipin antibodies in patients with abnormal embryo morphology who attended an in vitro fertilization program. Am J Reprod Immunol 1998;39:161-163. PMID: 9526604.
crossref pmid
3. Birdsall M, Lockwood G, Ledger W, Johnson P, Chamley L. Antiphospholipid antibodies in women having in-vitro fertilization. Hum Reprod 1996;11:1185-1189. PMID: 8671420.
crossref pmid
4. Buckingham K, Stone P, Smith J, Chamley L. Antiphospholipid antibodies in serum and follicular fluid - is there a correlation with IVF implantation failure? Hum Reprod 2005;21:728-734. PMID: 16253967.
crossref pmid
5. Caccavo D, Pellegrino N, Lorusso F, Capotorto M, Vacca M, Vimercati A, et al. Anticardiolipin antibody levels in women undergoing first in vitro fertilization/embryo transfer. Hum Reprod 2007;22:2494-2500. PMID: 17609246.
crossref pmid
6. Chilcott IT, Margara R, Cohen H, Rai R, Skull J, Pickering W, et al. Pregnancy outcome is not affected by antiphospholipid antibody status in women referred for in vitro fertilization. Fertil Steril 2000;73:526-530. PMID: 10689007.
crossref pmid
7. Kaider BD, Price DE, Roussev RG, Coulam CB. Antiphospholipid antibody prevalence in patients with IVF failure. Am J Reprod Immunol 1996;35:388-393. PMID: 8739459.
crossref pmid
8. Kutteh WH. Antiphospholipid antibodies and reproduction. J Reprod Immunol 1997;35:151-171. PMID: 9421798.
crossref pmid
9. Martinelli I, Taioli E, Ragni G, Levi-Setti P, Passamonti SM, Battaglioli T, et al. Embryo implantation after assisted reproductive procedures and maternal thrombophilia. Haematologica 2003;88:789-793. PMID: 12857558.
crossref pmid
10. Nip M, Taylor P, Rutherford A, Hancock K. Autoantibodies and antisperm antibodies in sera and follicular fluids of infertile patients; relation to reproductive outcome after in-vitro fertilization. Hum Reprod 1995;10:2564-2569. PMID: 8567771.
crossref pmid
11. Radojcić L, Marjanović S, Vićovac L, Kataranovski M. Anticardiolipin antibodies in women with unexplained infertility. Physiol Res 2004;53:91-96. PMID: 14984319.
pmid
12. Sher G, Feinman M, Zouves C, Kuttner G, Maassarani G, Salem R, et al. High fecundity rates following in-vitro fertilization and embryo transfer in antiphospholipid antibody seropositive women treated with heparin and aspirin. Hum Reprod 1994;9:2278-2283. PMID: 7714144.
crossref pmid
13. Steinvil A, Raz R, Berliner S, Steinberg DM, Zeltser D, Levran D, et al. Association of common thrombophilias and antiphospholipid antibodies with success rate of in vitro fertilisation. Thromb Haemost 2012;108:1192-1197. PMID: 23052827.
crossref pmid
14. Lee SR, Park EJ, Kim SH, Chae H, Kim CH, Kang BM. Influence of antiphospholipid antibodies on pregnancy outcome in women undergoing in vitro fertilization and embryo transfer. Am J Reprod Immunol 2007;57:34-39. PMID: 17156189.
crossref pmid
15. Practice Committee of American Society for Reproductive Medicine. Anti-phospholipid antibodies do not affect IVF success. Fertil Steril 2008;90:S172-3. PMID: 19007620.
crossref pmid
16. Hornstein MD, Davis OK, Massey JB, Paulson RJ, Collins JA. Antiphospholipid antibodies and in vitro fertilization success: a meta-analysis. Fertil Steril 2000;73:330-333. PMID: 10685538.
crossref pmid
17. Zhong YP, Ying Y, Wu HT, Zhou CQ, Xu YW, Wang Q, et al. Impact of anticardiolipin antibody on the outcome of in vitro fertilization and embryo transfer. Am J Reprod Immunol 2011;66:504-509. PMID: 21762406.
crossref pmid
18. Gardner DK, Lane M, Stevens J, Schlenker T, Schoolcraft WB. Blastocyst score affects implantation and pregnancy outcome: towards a single blastocyst transfer. Fertil Steril 2000;73:1155-1158. PMID: 10856474.
crossref pmid
19. Lee KA, Koo JJ, Yoon TK, Do BR, Ko JJ, Cha KY. Immunosuppression by corticosteroid has no effect on the pregnancy rate in routine in-vitro fertilization/embryo transfer patients. Hum Reprod 1994;9:1832-1835. PMID: 7844211.
crossref pmid
20. Proietta M, Ferrero S, Del Porto F. Prevalence of antiphospholipid antibodies in patients with sterility undergoing ‘in vitro' fertilization. Lupus 2014;23:724-725. PMID: 24569392.
crossref pmid
21. Stern C, Chamley L, Hale L, Kloss M, Speirs A, Baker HG. Antibodies to beta2 glycoprotein I are associated with in vitro fertilization implantation failure as well as recurrent miscarriage: results of a prevalence study. Fertil Steril 1998;70:938-944. PMID: 9806580.
crossref pmid
22. Gleicher N, Harlow L, Zilberstein M. Regulatory effect of antiphospholipid antibodies on signal transduction: a possible model for autoantibody-induced reproductive failure. Am J Obstet Gynecol 1992;167:637-642. PMID: 1530016.
crossref pmid
23. Eldar-Geva T, Wood C, Lolatgis N, Rombauts L, Kovacs G, Fuscaldo J, et al. Cumulative pregnancy and live birth rates in women with antiphospholipid antibodies undergoing assisted reproduction. Hum Reprod 1999;14:1461-1466. PMID: 10357959.
crossref pmid
24. Ying Y, Zhong Yp, Zhou Cq, Xu Yw, Wang Q, Li J, et al. A retrospective study on IVF outcome in patients with anticardiolipin antibody: effects of methylprednisolone plus low-dose aspirin adjuvant treatment. J Reprod Immunol 2012;94:196-201. PMID: 22542909.
crossref pmid
25. El-roeiy A, Gleicher N, Friberg J, Confino E, Dudkiewicz A. Correlation between peripheral blood and follicular fluid autoantibodies and impact on in vitro fertilization. Obstet Gynecol 1987;70:163-170. PMID: 3601277.
crossref pmid
26. Gleicher N, Liu HC, Dudkiewicz A, Rosenwaks Z, Kaberlein G, Pratt D, et al. Autoantibody profiles and immunoglobulin levels as predictors of in vitro fertilization success. Am J Obstet Gynecol 1994;170:1145-1149. PMID: 8166199.
crossref pmid
27. Kowalik A, Vichnin M, Liu HC, Branch W, Berkeley AS. Midfollicular anticardiolipin and antiphosphatidylserine antibody titers do not correlate with in vitro fertilization outcome. Fertil Steril 1997;68:298-304. PMID: 9240260.
crossref pmid
28. Matsubayashi H, Sugi T, Arai T, Shida M, Kondo A, Suzuki T, et al. IgG-antiphospholipid antibodies in follicular fluid of IVF-ET patients are related to low fertilization rate of their oocytes. Am J Reprod Immunol 2006;55:341-348. PMID: 16635208.
crossref pmid
29. Sanmarco M, Bardin N, Camoin L, Beziane A. Antigenic profile, prevalence, and clinical significance of antiphospholipid antibodies in women referred for in vitro fertilization. Ann N Y Acad Sci 2007;1108:457-465. PMID: 17894010.
crossref pmid
30. Paulmyer-Lacroix O, Despierres L, Courbiere B, Bardin N. Antiphospholipid antibodies in women undergoing in vitro fertilization treatment: clinical value of IgA anti-β2glycoprotein I antibodies determination. Biomed Res Int 2014;2014:314704PMID: 24967354.
crossref pmid pmc


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