Reproduction   citetrack
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS  
Reproduction (2006) 131 817-822
DOI: 10.1530/rep.1.01060
Copyright © 2006 Society for Reproduction and Fertility
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zammiti, W.
Right arrow Articles by Mahjoub, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zammiti, W.
Right arrow Articles by Mahjoub, T.

RESEARCH

A case-control study on the association of idiopathic recurrent pregnancy loss with autoantibodies against ß2-glycoprotein I and annexin V

Walid Zammiti, Nabil Mtiraoui, Choumous Kallel, Eric Mercier1, Wassim Y Almawi2 and Touhami Mahjoub

Laboratory of Hematology, Faculty of Pharmacy, University of Monastir, Tunisia, 1 University of Montpellier, Montpellier, France, 2 Department of Medical Biochemistry, College of Medicine and Medical Sciences, Arabian Gulf University, P O Box 22979, Manama, Bahrain

Correspondence should be addressed to W Y Almawi; Email: wyalmawi{at}yahoo.co.uk


   Abstract
Top
 Abstract
Introduction
 Subjects and Methods
 Results
 Discussion
 Acknowledgements
 References
 
Whereas antiphospholipid antibodies (aPL) are associated with thrombotic events and recurrent spontaneous abortion (RSA), the contribution of anti-ß2 glycoprotein 1 (ß2GP1) and anti-annexin V antibodies as risk factors for RSA remain poorly understood. We investigated anti-ß2-GPI and anti-annexin V IgM and IgG antibodies as potential risk factors for RSA in 200 women with more than three consecutive idiopathic RSA, and 200 age-matched, healthy, parous women. Pearson’s chi squared test analysis showed that while anti-ß2-GPI IgG (P = 0.416) and IgM (P = 0.72) were comparable between patients and controls, elevated anti-annexin V IgG (P = 0.006), but not IgM (P = 0.084), was more pronounced in patients. Higher frequencies of elevated IgG-only (P = 0.005), but not IgM-only (P = 1.000; OR = 6.66), anti-annexin V antibodies were noted among patients. Multinomial regression analysis showed that body-mass index (overweight and obesity; P = 0.008), education status (P < 0.001) and anti-ß2-GPI IgM (P = 0.033), but not IgG (P = 0.723), were associated with early abortion, while anti-ß2-GPI IgG (P = 0.030) and anti-annexin V IgG (P = 0.004) were associated with late RSA. For combined early-late RSA, the only variable selected was education status (P < 0.001), and neither anti-annexin V nor anti-ß2-GPI IgM and IgG was associated with early-late RSA. Accordingly, anti-annexin V and anti-ß2-GPI should be regarded as independent risk markers of RSA.


   Introduction
Top
 Abstract
 Introduction
Subjects and Methods
 Results
 Discussion
 Acknowledgements
 References
 
Pregnancy loss after implantation is frequent (Wilcox et al. 1988, Chaouat et al. 1995), and idiopathic recurrent spontaneous abortion (RSA) is often seen in otherwise healthy women (Mahjoub et al. 2005, Quenby et al. 2005). While several mechanisms have been proposed for early RSA (Huang et al. 2005), the exact causes of late miscarriage remain poorly understood. Inherited thrombophilia, including point mutations in factor V (Leiden) and prothrombin (G20210A) genes (Mahjoub et al. 2005), and antiphospholipid (aPL) antibodies, including anticardiolipin (aCL) antibodies and lupus anticoagulant (LA) (Mtiraoui et al. 2005), constitute significant risk factors for late RSA (Gris et al. 1999, Norwitz et al. 2001), since women who are carriers of prothrombotic gene polymorphisms or aPL are predisposed to pregnancy failure due to placental thrombosis (Gris et al. 1999, Martinelli et al. 2002).

Insofar as they recognize many phospholipids, phospholipid-binding proteins, or both, aPL antibodies have been associated with a hypercoagulable state – antiphospholipid syndrome (APS) – which arises from platelet activation, impairment of the endothelial system and facilitation of blood coagulation (Mercanoglu et al. 2004), and have been implicated in pregnancy complications (Gris et al. 2003, Levine et al. 2002, Rand et al. 2005). The precise mechanism of aPL in precipitating fetal loss is unclear, and may include precipitation of a prothrombotic state in the uteroplacental vasculature (Matsubayashi et al. 2001). ß2-Glycoprotein I (ß2-GPI), a single-chain 50 kDa glycoprotein and a target of aPL (Galli et al. 1990), was found to be involved in RSA, as its reduced expression was reported in women with APS (Miyakis et al. 2004). Antibodies to ß2-GPI (anti-ß2-GPI) were described as prothrombotic in individuals with APS (Falcon et al. 1997), and were suggested to play a role in RSA, since they inhibit trophoblast proliferation (Norwitz et al. 2001), and enhance uteroplacental thrombosis and abnormal placentation (Gris et al. 2003).

In addition to ß2-GPI, annexin V is a potent anticoagulant that regulates exocytosis and syncytiotrophoblast membrane fusion (Arai et al. 2003), and has been implicated in RSA, as shown by findings that anti-annexin V antibodies induce thrombosis in human umbilical vein endothelial cells (HUVEC) (Arnold et al. 2001), and that their concentrations are reduced in isolated placenta from women with aPL-associated RSA (Gris et al. 1999, Matsubayashi et al. 2001). Antibodies against annexin V may interfere with syncytiotrophoblast function (Rand et al. 1994, 2005), resulting in altered expression of anionic lipids on the plasma membrane, and induction of apoptosis in HUVEC (Ailus et al. 1996). Others argue against involvement of anti-annexin V with RSA, since comparable prevalence rates of IgG (25% vs 23%) and IgM (27% vs 28%) anti-annexin V were seen in RSA vs control women respectively (Bizzaro et al. 2005).

We previously reported on the association of aCL antibodies and LA with idiopathic RSA, where elevated aCL antibody-only, positive LA only, or combined elevated aCL-positive LA were consistently higher in RSA patients (Mtiraoui et al. 2005). Since the exact role and clinical significance of anti-ß2-GPI and anti-annexin V IgG and IgM antibodies as risk factors for RSA are unclear, this study aimed to determine the prevalence of anti-annexin V and anti-ß2-GPI IgG and IgM antibodies in women with idiopathic RSA, and to evaluate their contribution with other confounding variables in RSA.


   Subjects and Methods
Top
 Abstract
 Introduction
 Subjects and Methods
Results
 Discussion
 Acknowledgements
 References
 
Study subjects
From 2002 to 2004, 200 women with three or more unexplained consecutive pregnancy losses 5–30 weeks post-gestation (mean age 28.6 ± 5.6 years), and attending the hospital maternity service of Sousse (Tunisia), were recruited (Table 1Go). Pregnancy losses were classified as early (5–10 weeks) and late (11–30 weeks). Exclusion criteria included induced abortions, infections, systemic disease, uterine structural abnormalities, and personal or family history of thrombosis. As control, 200 age-matched, healthy women with uncomplicated pregnancies (mean 28.2 ± 5.5 years) were recruited (Table 1Go). Patients and controls were asked to complete a questionnaire detailing demographic details, number and outcome of pregnancies, and RSA risk factors, and to sign an informed, consent form. The study was conducted after all institutional ethics requirements were met. Blood samples were obtained from study participants 8–12 weeks after the last pregnancy.


View this table:
[in this window]
[in a new window]
  		Table 1 Clinical characteristics of patients and controls.
 
Antibody measurements
Serum anti-ß2-GPI IgG and IgM levels were measured by quantitative ELISA, using the Zymutest kit according to the manufacturer’s instructions (Hyphen Biomed, Neuville-Sur-Oise, France). Results of <20 U/ml were interpreted as negative, while specimens with values of ≥20 U/ml were considered positive. Serum samples were also tested for anti-annexin V IgG and IgM by quantitative ELISA, using the Zymutest kit, according to manufacturer’s instructions (Hyphen Biomed). Results of <20 U/ml were interpreted as negative and results of ≥20 U/ml as positive.

Statistical analysis
First, we examined means and standard deviation of all biomarkers in case and control patients. Statistical analysis was performed on SPSS v. 11.5 statistics software (SPSS, Chicago, IL, USA). Data were expressed as percentages of the mean. The Mann–Whitney nonparametric U-test, regression multinomial logistic and Pearson’s chi-square test were used to assess intergroup significance. In addition, the odds ratios (OR) and 95% confidence intervals (CI) were calculated. Statistical significance was set at P < 0.05.


   Results
Top
 Abstract
 Introduction
 Subjects and Methods
 Results
Discussion
 Acknowledgements
 References
 
Patients and controls
The characteristics of patients and controls are summarized in Table 1Go. Both patients and controls had similar age (P = 0.434) and body-mass index (BMI; P = 0.360), and were from different parts of Tunisia (P = 0.531). While there was no significant difference between patients and controls in terms of alcohol consumption (P = 1.000) or smoking (P = 1.000), differences in terms of education background were noted among study participants (P < 0.001), exemplified by the higher proportion of patients having a university-level education, while controls generally had an intermediate level education.

Prevalence of anti-ß2-glycoprotein I (anti-ß2-GPI) IgG and IgM antibodies
The status of anti-ß2-GPI IgG and IgM, and that of anti-annexin V IgM and IgG antibodies were assessed. Anti-ß2-GPI IgG and IgM, and anti-annexin V IgM and IgG were categorized as normal or elevated according to a cutoff value of 20 U/ml. Anti-ß2-GPI IgG (P = 0.416) and IgM (P = 0.72) were comparable between patients and controls (Table 2Go). In contrast, elevated anti-annexin V IgG (P = 0.006), but not IgM (P = 0.084), was more pronounced in patients than control parous women (Table 2Go).


View this table:
[in this window]
[in a new window]
  		Table 2 Prevalence of anti-ß2-GPI and anti-annexin V IgG and IgM antibodies.
 
Analysis of anti-annexin V antibodies
In view of the association of anti-annexin V, but not anti-ß2-GPI antibodies with RSA, we tested the anti-annexin V IgM and IgG status (normal, elevated) in patients and controls. Higher frequencies of elevated IgG-only (P = 0.005), but not IgM-only (P = 1.000), were noted among patients (Table 3Go). Only one patient presented with elevated IgM-elevated IgG.


View this table:
[in this window]
[in a new window]
  		Table 3 Isotype distribution of anti-annexin V antibodies.
 
Risk factors for pregnancy loss
Predictors of early, late and early-late abortions were determined by performing three logistic regression analysis models with the dependent variable being early, late, and early-late RSA, and the independent potentially confounding variables being age, BMI, use of oral contraceptives, education, anti-annexin V IgM and IgG, and anti-ß2-GPI IgM and IgG (Table 4Go). The only variables that were selected by this technique for the first outcome (early RSA) were BMI of >25 (P = 0.008), education status (P < 0.001) and anti-ß2-GPI IgM (P = 0.033) (Table 4Go). For the second outcome (late RSA), it was anti-ß2-GPI IgG (P = 0.030) and anti-annexin V IgG (P = 0.004). For the third outcome (early-late), the only variable selected was education status (P < 0.001). Adjusting for the variables selected, anti-ß2-GPI IgM and IgG and anti-annexin V IgM and IgG were not associated with combined early-late RSA (Table 4Go).


View this table:
[in this window]
[in a new window]
  		Table 4 Regression analysis.
 

   Discussion
Top
 Abstract
 Introduction
 Subjects and Methods
 Results
 Discussion
Acknowledgements
 References
 
Autoimmune factors involving production of antibodies targeting phospholipids (cardiolipin and phosphatidylserine) or phospholipid-binding proteins (ß2GPI and annexin V) were previously described as risk factors for RSA (Martinelli et al. 2002, Gris et al. 2003, Rand et al. 2005). Unlike the well-documented involvement of aCL and LA, the role of anti-annexin V and anti-ß2-GPI antibodies in idiopathic RSA has yet to be established, although it is presumed that it involves precipitation of a prothrombotic state that favors altered placentation, poor fetal circulation and possibly induction of apoptosis (Arai et al. 2003, Rand et al. 2005).

Results from this study demonstrated that anti-annexin V, but not anti-ß2-GPI, antibodies were elevated in women with idiopathic RSA. Added to our previous finding on association of aCL and LA with RSA (Mtiraoui et al. 2005), these results indicate that the presence of these autoantibodies is closely related to RSA, via a mechanism which requires participation of immune and nonimmune factors in precipitating a prothrombotic state that favors fetal loss. Multivariate regression analysis demonstrated that anti-ß2-GPI IgM was associated with early RSA, while anti-annexin V IgG was a significant risk factor for (exclusively) late RSA. Neither anti-ß2-GPI nor annexin V IgG or IgM was associated with combined early-late RSA. Interestingly, university education was associated with early and early-late RSA. While the cause of this remains speculative, it is possible that sociocultural habits (Tan et al. 1995), together with career-related factors (Bocciolone et al. 1989, Tan et al. 1995), may have contributed to RSA in university-educated women, the majority of whom are working women.

Results on the role of anti-ß2-GPI in RSA are controversial, and some reports described an association of anti-ß2-GPI IgG with RSA (Lee et al. 1999, Gris et al. 2000), and others implicated IgM (Foratseiro et al. 1997), but not IgG (Lynch et al. 1999, Arnold et al. 2001) anti-ß2-GPI, as potential risk factor for idiopathic RSA, as also shown here. In our hands, the presence of anti-ß2-GPI IgM was associated with (exclusively) early RSA, while IgG was associated with (exclusively) late RSA, in apparent agreement with previous studies which also found no significant association of anti-ß2-GPI antibodies in women with three or more consecutive pregnancy losses (Lynch et al. 1999, Arnold et al. 2001), and in antiphospholipid-positive patients with obstetric complications (two or more spontaneous fetal losses) (Foratseiro et al. 1997). This may be explained by differences in assay sensitivity, and the low number of patients (21–44) included in some studies (Ailus et al. 1996, Foratseiro et al. 1997). Insofar as aCL antibodies target plasma proteins bound to anionic phospholipids, including ß2-GPI (Marai et al. 2005), it was suggested that the association of anti-ß2-GPI with RSA was dependent on aCL antibody status, since anti-ß2-GPI antibody was elevated in aCL-negative patients (Lee et al. 1999). This does not appear to be the case here, since comparable prevalence rates of anti-ß2-GPI were seen in patients and controls, irrespective of aCL isotype (P = 0.569) or status (P = 0.495).

In accordance with previous findings (Gris et al. 2000, 2003, Matsubayashi et al. 2001), anti-annexin V antibodies were significantly higher in RSA patients than in fertile women. Logistic regression analysis confirmed the association of anti-annexin V IgG in late RSA, which was reminiscent of the findings of the Nimes group that anti-annexin V IgG is an independent risk factor for unexplained RSA (Gris et al. 2000, 2003), and in apparent disagreement with other reports, which disputed such an association (Siaka et al. 1999, Arnold et al. 2001, Arai et al. 2003, Bizzaro et al. 2005). However, the small sample size (Siaka et al. 1999, Arnold et al. 2001), coupled with poor assay sensitivity (Siaka et al. 1999), and ethnic origin (Arai et al. 2003, Bizzaro et al. 2005) employed in the latter studies warrants scrutiny in evaluating their conclusion.

While RSA may be partly explained by placental thrombosis precipitated by endothelial cell activation and annexin V displacement, this does not account for all miscarriages, thus pointing to an antibody-directed mechanism. Accordingly, the presence of antibodies that bind trophoblast-associated ß2-GPI may interfere with trophoblast cell maturation, resulting in defective placentation. In addition, as annexin V acts as an inhibitor of lipid-dependent blood coagulation, antibodies against it may serve a procoagulant function. This was supported by the findings that administration of annexin V inhibited thrombus formation (Romisch et al. 1991) and fibrin accretion (Van Ryn-McKenna et al. 1993), and administration of anti-annexin V induced placental thrombosis, necrosis and fetal loss (Wang et al. 1999). Mechanistically, it was hypothesized that anti-annexin V antibodies can disrupt or compromise the antithrombotic shield, thereby contributing to reproductive failure. Furthermore, by inducing trophoblast apoptosis and significantly reducing trophoblast gonadotropin secretion, anti-annexin V antibody was found to induce defective placentation (Di Simone et al. 2001).

As with similar studies, a limitation of our study is that anti-annexin V and anti-ß2GPI antibodies were measured in the patients after event establishment (pregnancy failure), thereby raising the possibility that these antibodies were the consequence, and not necessarily the cause of RSA, as was also suggested elsewhere (Gris et al. 2003). This can be resolved only by a prospective study that monitors changes in pregnancy outcomes in antibody-positive versus antibody-negative patients.

In conclusion, our study proposes a role for anti-ß2GPI IgM (but not IgG) and anti-annexin V IgG antibodies in mediating exclusively early and late RSA respectively. This may serve as a diagnostic tool as part of the routine workup for women with idiopathic RSA, and also has therapeutic implications, evidenced by the utility of combining intravenous immunoglobulin in the standard therapy regimen, which allegedly resulted in excellent fetal and maternal outcome (Branch et al. 2000), in particular in cases of APS (Diejomaoh et al. 2002). However, the definitive utility of this treatment modality awaits the outcome of international randomized trials, which are currently in progress.


   Acknowledgements
Top
 Abstract
 Introduction
 Subjects and Methods
 Results
 Discussion
 Acknowledgements
References
 
The authors declare that there is no conflict of interest that would prejudice the impartiality of this scientific work.


   Footnotes
 
Received 1 December 2005
First decision 11 January 2006
Revised manuscript received 15 January 2006
Accepted 17 January 2006


   References
Top
 Abstract
 Introduction
 Subjects and Methods
 Results
 Discussion
 Acknowledgements
 References
 

Ailus K, Tulppala M, Palosuo T, Ylikorkala O & Vaarala O 1996 Antibodies to beta 2-glycoprotein I and prothrombin in habitual abortion. Fertility and Sterility 66 937–941.[ISI][Medline]

Arai T, Matsubayashi H, Sugi T, Kondo A, Shida M, Suzuki T, Izumi SI, McIntyre JA & Makino T 2003 Anti-annexin A5 antibodies in reproductive failures in relation to antiphospholipid antibodies and phosphatidylserine. American Journal of Reproduction and Immunology 50 202–208.[CrossRef]

Arnold J, Holmes Z, Pickering W, Farmer C, Regan L & Cohen H 2001 Anti-beta 2 glycoprotein 1 and anti-annexin V antibodies in women with recurrent miscarriage. British Journal of Haematology 113 911–914.[CrossRef][ISI][Medline]

Bizzaro N, Antico A, Musso M, Platzgummer S, Camogliano L, Tozzoli R & Villalta D 2005 A prospective study of 1038 pregnancies on the predictive value of anti-annexin V antibodies for fetal loss. Annals of the New York Academy of Sciences 1050 348–356.[Abstract/Free Full Text]

Bocciolone L, Parazzini F, Fedele L, Acaia B & Candiani GB 1989 Epidemiology of spontaneous abortion: a review of the literature. Annali di ostetricia, ginecologia, medicina perinatale 110 323–334.

Branch DW, Peaceman AM, Druzin M, Silver RK, El-Sayed Y, Silver RM, Esplin MS, Spinnato J & Harger J 2000 A multicenter, placebo-controlled pilot study of intravenous immune globulin treatment of antiphospholipid syndrome during pregnancy. The Pregnancy Loss Study Group. American Journal of Obstetrics and Gynecology 182 122–127.[CrossRef][ISI][Medline]

Chaouat G, Menu E, Delage G, Moreau JF, Khrishnan L, Hui L, Meliani AA, Martal J, Raghupathy R, Lelaidier C et al. 1995 Immuno-endocrine interactions in early pregnancy. Human Reproduction 10 (Suppl 2) 55–59.

Di Simone N, Castellani R, Caliandro D & Caruso A 2001 Monoclonal anti-annexin V antibody inhibits trophoblast gonadotropin secretion and induces syncytiotrophoblast apoptosis. Biology of Reproduction 65 1766–1770.[Abstract/Free Full Text]

Diejomaoh MF, Al-Azemi MM, Bandar A, Egbase PE, Jirous J, Al-Othman S, Bukhadour N & Al-Sweih N 2002 A favorable outcome of pregnancies in women with primary and secondary recurrent pregnancy loss associated with antiphospholipid syndrome. Archives in Gynecology and Obstetrics 266 61–66.[CrossRef]

Falcon CR, Martinuzzo ME, Forastiero RR, Cerrato GS & Carreras LO 1997 Pregnancy loss and autoantibodies against phospholipid-binding proteins. Obstetrics and Gynecology 89 975–980.[Abstract]

Forastiero RR, Martinuzzo ME, Cerrato GS, Kordich LC & Carreras LO 1997 Relationship of anti-beta2-glycoprotein I and anti-prothrombin antibodies to thrombosis and pregnancy loss in patients with antiphospholipid antibodies. Thrombosis and Haemostasis 78 1008–1014.[ISI][Medline]

Galli M, Comfurius P, Maassen C, Hemker HC, de Baets MH, van Breda-Vriesman PJ, Barbui T, Zwaal RF & Bevers EM 1990 Anticardiolipin antibodies (ACA) directed not to cardiolipin but to a plasma protein cofactor. Lancet 335 1544–1547.[CrossRef][ISI][Medline]

Gris JC, Quere I, Monpeyroux F, Mercier E, Ripart-Neveu S, Tailland ML, Hoffet M, Berlan J, Daures JP & Mares P 1999 Case-control study of the frequency of thrombophilic disorders in couples with late foetal loss and no thrombotic antecedent – the Nimes Obstetricians and Haematologists Study 5 (NOHA5). Thrombosis and Haemostasis 81 891–899.[ISI][Medline]

Gris JC, Quere I, Sanmarco M, Boutiere B, Mercier E, Amiral J, Hubert AM, Ripart-Neveu S, Hoffet M, Tailland ML et al. 2000 Antiphospholipid and antiprotein syndromes in non-thrombotic, non-autoimmune women with unexplained recurrent primary early foetal loss. The Nimes Obstetricians and Haematologists Study-NOHA. Thrombosis and Haemostasis 84 228–236.[ISI][Medline]

Gris JC, Perneger TV, Quere I, Mercier E, Fabbro-Peray P, Lavigne-Lissalde G, Hoffet M, Dechaud H, Boyer JC, Ripart-Neveu S et al. 2003 Antiphospholipid/antiprotein antibodies, hemostasis-related autoantibodies, and plasma homocysteine as risk factors for a first early pregnancy loss: a matched case-control study. Blood 102 3504–3513.[Abstract/Free Full Text]

Huang T, Owolabi T, Summers AM, Meier C & Wyatt PR 2005 The identification of risk of spontaneous fetal loss through second-trimester maternal serum screening. American Journal of Obstetrics and Gynecology 193 395–403.[CrossRef][ISI][Medline]

Lee RM, Emlen W, Scott JR, Branch DW & Silver RM 1999 Anti-beta2-glycoprotein I antibodies in women with recurrent spontaneous abortion, unexplained fetal death, and antiphospholipid syndrome. American Journal of Obstetrics and Gynecology 181 642–648.[CrossRef][ISI][Medline]

Levine JS, Branch DW & Rauch J 2002 The antiphospholipid syndrome. New England Journal of Medicine 346 752–763.[Free Full Text]

Lynch A, Byers T, Emlen W, Rynes D, Shetterly SM & Hamman RF 1999 Association of antibodies to beta2-glycoprotein 1 with pregnancy loss and pregnancy-induced hypertension: a prospective study in low-risk pregnancy. Obstetrics and Gynecology 93 193–198.[Abstract/Free Full Text]

Mahjoub T, Mtiraoui N, Tamim H, Hizem S, Finan RR, Nsiri B & Almawi WY 2005 Association between adverse pregnancy outcomes and maternal factor V G1691A (Leiden) and prothrombin G20210A genotypes in women with a history of recurrent idiopathic miscarriages. American Journal of Hematology 80 12–19.[CrossRef]

Marai I, Tincani A, Balestrieri G & Shoenfeld Y 2005 Anticardiolipin and anti-beta-2-glycoprotein I antibodies. Autoimmunity 38 33–38.[CrossRef][ISI][Medline]

Martinelli I, Taioli E, Cetin I & Mannucci PM 2002 Recurrent late fetal death in women with and without thrombophilia. Thrombosis and Haemostasis 87 358–359.[ISI][Medline]

Matsubayashi H, Arai T, Izumi S, Sugi T, McIntyre JA & Makino T 2001 Anti-annexin V antibodies in patients with early pregnancy loss or implantation failures. Fertility and Sterility 76 694–699.[CrossRef][ISI][Medline]

Mercanoglu F, Erdogan D, Oflaz H, Kucukkaya R, Selcukbiricik F, Gul A & Inanc M 2004 Impaired brachial endothelial function in patients with primary anti-phospholipid syndrome. International Journal of Clinical Practice 58 1003–1007.[CrossRef][ISI][Medline]

Miyakis S, Giannakopoulos B & Krilis SA 2004 Beta 2 glycoprotein I-function in health and disease. Thrombosis Research 114 335–346.[CrossRef][ISI][Medline]

Mtiraoui N, Borgi L, Hizem S, Nsiri B, Finan RR, Gris J-C, Almawi WY & Mahjoub T 2005 Prevalence of antiphospholipid antibodies, factor V G1691A (Leiden) and prothrombin G20210A mutations in early and late recurrent pregnancy loss. European Journal of Obstetrics, Gynecology, and Reproductive Biology 119 164–170.[CrossRef]

Norwitz ER, Schust DJ & Fisher SJ 2001 Implantation and the survival of early pregnancy. New England Journal of Medicine 345 1400–1408.[Free Full Text]

Quenby S, Farquharson RG, Dawood F, Hughes AM & Topping J 2005 Recurrent miscarriage and long-term thrombosis risk: a case-control study. Human Reproduction 20 1729–1732.[Abstract/Free Full Text]

Rand JH, Wu XX, Guller S, Gil J, Guha A, Scher J & Lockwood CJ 1994 Reduction of annexin-V (placental anticoagulant protein-I) on placental villi of women with antiphospholipid antibodies and recurrent spontaneous abortion. American Journal of Obstetrics and Gynecology 171 1566–1572.[ISI][Medline]

Rand J, Eerden PV, Wu XX & Chazotte C 2005 Defective annexin A5 crystallization: a mechanism for pregnancy losses in the antiphospholipid syndrome. Thrombosis Research 115 (Suppl 1) 77–81.

Romisch J, Seiffge D, Reiner G, Paques EP & Heimburger N 1991 In-vivo antithrombotic potency of placenta protein 4 (annexin V). Thrombosis Research 61 93–104.[ISI][Medline]

Siaka C, Lambert M, Caron C, Amiral J, Hachulla E, Hatron PY & Goudemand J 1999 Low prevalence of anti-annexin V antibodies in antiphospholipid syndrome with fetal loss. La Revue de medecine interne 20 762–765.

Tan NH, Yahya A & Adeeb N 1995 Sociobiological risk factors for spontaneous abortion in Malaysia. Journal of Obstetrics and Gynaecology 21 313–318.

Van Ryn-McKenna J, Merk H, Muller TH, Buchanan MR & Eisert WG 1993 The effects of heparin and annexin V on fibrin accretion after injury in the jugular veins of rabbits. Thrombosis and Haemostasis 69 227–230.[ISI][Medline]

Wang X, Campos B, Kaetzel MA & Dedman JR 1999 Annexin V is critical in the maintenance of murine placental integrity. American Journal of Obstetrics and Gynecology 180 1008–1016.[CrossRef][ISI][Medline]

Wilcox AJ, Weinberg CR, O’Connor JF, Baird DD, Schlatterer JP, Canfield RE, Armstrong EG & Nisula BC 1988 Incidence of early loss of pregnancy. New England Journal of Medicine 319 189–194.[Abstract]


This article has been cited by other articles:


Home page
 Mol Hum ReprodHome page
W. Zammiti, N. Mtiraoui, E. Cochery-Nouvellon, T. Mahjoub, W.Y. Almawi, and J.-C. Gris
Association of -592C/A, -819C/T and -1082A/G interleukin-10 promoter polymorphisms with idiopathic recurrent spontaneous abortion
Mol. Hum. Reprod., December 1, 2006; 12(12): 771 - 776.
[Abstract] [Full Text] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zammiti, W.
Right arrow Articles by Mahjoub, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zammiti, W.
Right arrow Articles by Mahjoub, T.

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS