Article Text


Lupus anticoagulant is the main predictor of adverse pregnancy outcomes in aPL-positive patients: validation of PROMISSE study results
  1. Cecile M Yelnik1,2,
  2. Carl A Laskin3,
  3. T Flint Porter4,
  4. D Ware Branch4,
  5. Jill P Buyon5,
  6. Marta M Guerra1,
  7. Michael D Lockshin1,
  8. Michelle Petri6,
  9. Joan T Merrill7,
  10. Lisa R Sammaritano1,
  11. Mimi Y Kim8 and
  12. Jane E Salmon1
  1. 1Department of Medicine, Hospital for Special Surgery, New York City, New York, USA
  2. 2Internal Medicine Department, University of Lille, UFR Médecine, Lille, France
  3. 3University of Toronto and LifeQuest Centre for Reproductive Medicine, Toronto, Canada
  4. 4Department of Obstetrics and Gynecology, University of Utah and Intermountain Healthcare, Salt Lake City, Utah, USA
  5. 5Department of Medicine, New York University School of Medicine, New York City, New York, USA
  6. 6Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
  7. 7Department of Medicine, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA
  8. 8Department of Epidemiology and Public Health, Albert Einstein College of Medicine, New York City, New York, USA
  1. Correspondence to Professor Jane E Salmon; salmonj{at}


Objective We previously reported that lupus anticoagulant (LAC) is the main predictor of poor pregnancy outcome in antiphospholipid antibody (aPL)-positive patients. We sought to confirm this finding in an independent group of patients who were subsequently recruited into the PROMISSE study.

Methods The PROMISSE study is a multicentre, prospective, observational study of pregnancy outcomes in women with aPL and/or systemic lupus erythematosus (SLE) that enrolled patients from 2003 to 2015. All consecutive, aPL-positive patients from the PROMISSE study who completed their pregnancy between April 2011 and January 2015 (after the previous PROMISSE report) are included in the current report. Patients were followed monthly until delivery, and aPL was tested at first, second and third trimesters of pregnancy and at 12 weeks post partum. Adverse pregnancy outcomes (APOs) were defined as fetal death after 12 weeks of gestation, neonatal death, delivery prior to 36 weeks of gestation due to pre-eclampsia or placental insufficiency or small-for-gestational age (birth weight <5th percentile).

Results Forty-four aPL-positive patients are included in this paper. Thirteen patients had APOs, which occurred in 80% of cases during the second trimester of pregnancy. LAC was present in 69% of patients with APOs compared with 27% of patients without APOs (p=0.01). No association was found between anticardiolipin antibodies (aCL) or anti-β2 glycoprotein I antibodies (aβ2GPI) IgG or IgM positivity and APOs. Definite antiphospholipid syndrome (history of thrombosis and/or pregnancy morbidity and aPL) was found in 92% of patients with any APOs compared with 45% of patients without APOs (p=0.004). Conversely, the frequency of SLE was not statistically different between those with and without APOs (30% vs 39%).

Conclusions Our findings, in an independent group of aPL-positive patients from the PROMISSE study, confirm that LAC, but not aCL and aβ2GPI, is predictive of poor pregnancy outcomes after 12 weeks of pregnancy.

Trial registration number NCT00198068.

  • Antiphospholipid Antibodies
  • Lupus Anticoagulant
  • Pregnancy
  • Antiphospholipid Syndrome
  • Systemic Lupus Erythematosus
  • Received October 2, 2015.
  • Revision received November 17, 2015.
  • Accepted November 23, 2015.

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See:

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Lupus anticoagulant (LAC), anticardiolipin antibodies (aCL) and anti-β2 glycoprotein I antibodies (aβ2GPI) are associated with thrombosis and are included in the international classification criteria for antiphospholipid syndrome (APS).1 These antiphospholipid antibodies (aPL) are also associated with obstetrical morbidity, such as recurrent early miscarriage, otherwise unexplained fetal death and preterm delivery for pre-eclampsia or placental insufficiency.2 However, the association between specific aPL and pregnancy complications has not been precisely defined, and results from published studies have varied.3 Also, the prognostic value of the three accepted aPL in the prediction of pregnancy outcome is not well established.

The PROMISSE study (Predictors of pRegnancy Outcome: bioMarkers In antiphospholipid antibody Syndrome and Systemic lupus Erythematosus), a prospective multicentre observational study of pregnancies in women with systemic lupus erythematosus (SLE) and/or aPL, was designed to identify clinical features, laboratory tests and biomarkers that could be used to predict adverse pregnancy outcomes (APOs) after the first trimester of pregnancy. The initial analysis of data from PROMISSE, published in 2012, reported that LAC, but not aCL or aβ2GPI, was a strong independent predictor of APO in aPL-positive patients.4 In this study, we aimed to validate the predictive value of different aPLs in an independent group of patients enrolled subsequent to those reported in our previous paper.

Patients and methods

Study population

All consecutive PROMISSE patients with aPL who finished their pregnancies between April 2011 and January 2015 are included; the previous study reported aPL-positive patients who delivered between September 2003 and March 2011.4 Inclusion and exclusion criteria are described elsewhere.4 ,5 Briefly, consecutive patients, aged 18–45 years, with singleton intrauterine pregnancy were enrolled before 18 weeks of gestation at six sites in North America and one in the UK.

Data collection and follow-up

The screening visit included medical history, physical examination and laboratory tests, including aPL. Patients were followed monthly during the pregnancy. Laboratory tests were repeated during the second (20–23 weeks of gestation) and third trimesters (32–35 weeks of gestation) of pregnancy and at 3 months post partum. The patients’ physicians made all treatment decisions.

aPL assays

aPL assays were performed in core laboratories as previously described and following the international guidelines for APS laboratory criteria.4 ,5 For LAC determination, three screening tests (dilute Russell's viper venom time (dRVVT), dilute prothrombin time (dPT) and LAC-sensitive test for activated partial thromboplastin time (aPTT)) with confirmation were performed. Our previous report4 included patients with low aPL titre, defined as being negative for LAC and having aCL or aβ2GPI titres <40 IU/mL. In the present study, only the presence of aCL and/or aβ2GPI titres IgG or IgM ≥40 GPL or MPL units, respectively, and/or LAC was considered positive, in accordance with Sapporo criteria.1

Adverse pregnancy outcomes assessment

APOs were determined as reported by the patients’ obstetrician and included in the medical record. In equivocal cases, obstetrical members of the PROMISSE team adjudicated causes of fetal demise. APOs in PROMISSE were defined as: fetal death after 12 weeks of gestation, neonatal death before hospital discharge due to complications of prematurity, preterm delivery before 36 weeks of gestation due to gestational hypertension, pre-eclampsia or placental insufficiency and small-for-gestational-age (SGA) neonate (birth weight, fifth percentile).4 ,5 Other aetiologies for APOs were not included in the analyses.

Statistical analysis

Data are expressed as number (percentage), mean (SD) or median (InterQuartile). The association of patient characteristics with APOs was evaluated using the Fisher's exact or Mann–Whitney tests. A two-tailed p<0.05 was considered statistically significant. Data were analysed using SPSS software package V.22.


Baseline characteristics of the study population

Forty-four new aPL-positive patients were enrolled in this study between April 2011 and January 2015 (table 1).

Table 1

Baseline characteristics of the study population

Thirteen patients had any APOs (table 2), which occurred primarily during the second trimester of pregnancy.

Table 2

Description of the 13 patients with adverse pregnancy outcomes

Analysis of clinical and demographic predictors of APOs

Age, race and ethnicity were similar in patients with and without APOs. Patients with APOs had higher body mass index (BMI) than patients without APOs (p=0.04). Clinical APS and history of thrombosis were significantly associated with APOs (p=0.004), whereas the diagnosis of SLE was not associated with APOs (table 1). The majority of the patients were treated with aspirin and/or low molecular weight heparin (n=42). Given that few patients were untreated, no differences in pregnancy outcomes were evident in patients receiving these therapies. All patients who had APOs received aspirin and/or heparin. Only two patients in this study did not receive antithrombotic prophylaxis; both were LAC negative and had successful pregnancies. The frequency of treatment with hydroxychloroquine was similar in those with and without APOs.

Analysis of laboratory variables predictive of APO

Among LAC-positive patients, 53% (9/17) had APOs, including 29% with fetal death, while in LAC-negative patients 17% (4/24) had APOs with no fetal deaths. LAC was present at screening in 69% of the APO group compared with 27% of the non-APOs group (p=0.01; table 1). Description of APOs according to the presence of LAC is shown in table 3.

Table 3

Adverse pregnancy outcomes among LAC-positive and LAC-negative patients

The subgroup of patients with both prior thrombosis and LAC positivity were at very high risk of APOs (occurring in 78% in those patients). There was no difference in the frequency of aCL IgG between patients with and without APOs (69% vs 55%, respectively, p=0.37). Moreover, LAC was also present in six of nine patients who were aCL IgG positive and had APOs. A similar result was found for aβ2GPI IgG (61% vs 50%, p=0.48), and LAC was present in five of eight patients who were aβ2GPI positive and had APOs. APOs occurred in five of the six patients who were positive for all three aPL tests. Of laboratory tests measured during the second trimester, when the majority of APOs occurred, LAC remained the only aPL associated with APOs.

Of note, five patients had pregnancy complications (two HELLP pre-eclampsia after 36 weeks of gestation and three SGA <10th percentile) that did not fulfil the PROMISSE study definition of APOs. Among those patients, four of five were LAC positive. When the definition of APOs is expanded to include these five patients yielding a total of 18 APO, the rate of APOs was significantly higher in LAC-positive patients compared with LAC-negative patients (76% vs 21%, p=0.01). The presence of other aPLs remained not significant.


In this report, we show that LAC was the only aPL associated with APOs after the first trimester, confirming the findings from our previous study in an independent group of aPL-positive patients.4 We also confirmed that clinical APS and history of thrombosis are strong risk factors for APOs.4

Despite the small sample size, the present study has strengths, including prospective design and multicentre recruitment of a precisely characterised, homogeneous study population with regard to aPL determinations. All aPL assays were performed in core laboratories and international classification criteria were strictly followed. We determined LAC to be present if any of three screening tests (dRVVT, dPT or aPTT) followed by confirming tests were abnormal, because any single positive test was not predictive of outcomes and no single test was superior.4 Hence, in clinical practice, excluding LAC with a single screening test may be insufficient, but this approach may be impractical. The main limitation was the inability to perform a multivariate analysis to adjust for potential confounders because of the small number of patients and APOs.

Our previous report described findings from a prospective cohort of 144 patients from PROMISSE.4 Differences in study design make comparison of our results with those published in other studies difficult. Consistent with our findings, Helgadottir et al6 reported that LAC, but not aβ2GPI nor aCL, was the only aPL associated with a history of fetal death after 26 weeks of gestation in a retrospective study, which included 105 cases compared with 262 controls with live births. Data prospectively and retrospectively collected on 247 patients with obstetrical APS from the European Registry of APS showed that LAC and triple aPL positivity, but not single aPL positivity, was associated with early and late obstetrical complications.7 Others have argued that LAC alone is not as significant a risk factor as is the presence of triple aPL positivity suggested to be the independent predictor of poor pregnancy outcomes.8 ,9 In contrast, our findings show that in two separate prospective cohorts, LAC positivity was sufficient to predict risk of APOs regardless of the association with aCL or aβ2GPI positivity.

Because medications were at the discretion of the treating physician, our study was not designed to evaluate treatment. Nonetheless, both of the current and our previous report did not show a beneficial effect of low molecular weight heparin. This result may reflect the bias of physicians to treat patients they consider at higher risk for APOs more intensely, or that low molecular weight heparin is not effective.10 ,11 Others reported, in a meta-analysis, no preventive effect of heparin against obstetrical complications. Of note, only asymptomatic aPL carriers (patients without any history of thrombosis or obstetrical morbidity) were included in this meta-analysis, whereas in our study only 40% were asymptomatic carriers.12


This study independently confirmed that LAC is the only aPL predictor of poor pregnancy outcomes after the first trimester of pregnancy in aPL-positive patients.

  • Received October 2, 2015.
  • Revision received November 17, 2015.
  • Accepted November 23, 2015.


View Abstract


  • Funding National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institutes of Health AR49772.

  • Competing interests None declared.

  • Ethics approval IRBs of the different institutions approved the study.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement Because the investigative team is still analysing the data for biomarkers and genetics, at this time we are not willing to make the protocol or data public except for what is currently published in

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