Predictors of Pregnancy Outcome in Systemic Lupus Erythematosus (SLE) and Antiphospholipid Syndrome (APS)
- Conditions
- Antiphospholipid SyndromeSystemic Lupus Erythematosus
- Registration Number
- NCT00198068
- Lead Sponsor
- Hospital for Special Surgery, New York
- Brief Summary
The PROMISSE Study is an observational study of 700 pregnant patients, enrolled at nine major clinical centers. The purpose of the study is 1) to determine whether certain proteins (called complement split products) that can injure healthy organs can be used to predict poor pregnancy outcome in patients with systemic lupus erythematosus (SLE) and anti-phospholipid syndrome (APS), and/or 2) to determine whether elevated levels of circulating antiangiogenic factors predict pregnancy complications in patients with aPL antibodies and/or SLE.
- Detailed Description
Thrombosis and pregnancy loss are common features of systemic lupus erythematosus (SLE), particularly in the presence of antiphospholipid (aPL) antibodies. The in vivo mechanisms by which aPL antibodies lead to vascular events and, specifically, to recurrent fetal loss are largely unknown. Studies in a mouse model of antiphospholipid antibody syndrome (APS) indicate that in vivo complement activation is necessary for fetal loss caused by aPL antibodies. This study represents an effort to translate these research observations on the potential role of complement activation in the pathogenesis of aPL antibody-mediated pregnancy loss to a clinically relevant human study.
In addition, studies in humans and mice have shown 1) that the balance of circulating angiogenic and antiangiogenic factors predicts preeclampsia and fetal growth restriction in healthy women, 2) circulating antiangiogenic factors cause endothelial dysfunction and abnormal placental development in animal models, and 3) complement activation leads to elevated levels of circulating antiangiogenic factors and complement inhibition prevents increased levels of antiangiogenic factors, placental dysfunction and fetal growth restriction in a mouse model of APS. This study will permit testing the hypothesis that, like in healthy women, the balance of circulating angiogenic and antiangiogenic factors predict complications in women with SLE and APS and to translate the findings in animal models into humans.
The PROMISSE Study is a prospective observational study that will follow 700 pregnant patients who will be grouped and analyzed according to the presence or absence of aPL antibodies and preexisting SLE. The patients are followed regularly during the course of the pregnancy, collecting medical and obstetrical information as well as serial blood specimens for complement and cytokine assays. The data obtained will be analyzed and used to identify mechanisms and predictors of poor fetal outcome. We expect that the insights provided through this study will suggest means to prevent, arrest or modify these conditions.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 700
-
Patient pregnant with live intrauterine pregnancy, as defined by positive test for elevated β-HCG, but ≤ 12 weeks by gestation (for subjects without aPL antibodies) and ≤18 weeks (for subjects with aPL antibodies)
-
Patient between the ages of 18-45 and able to give informed consent, or age < 18 years with parental consent
-
Hematocrit > 26%
-
For APL positive:
- aCL: IgG >= 40 GPL units; IgM >= 40 MPL units
- Positive LAC (RVVT, Kaolin, dilute TTI or PTT LA)
- Anti-β2GPI: IgG >= 40 GPL units; IgM >= 40 MPL units
-
For control subjects:
- At least one successful pregnancy
- No history of fetal death (death of conceptus ≥ 10 weeks' gestation)
- No more than 1 miscarriage < 10 weeks' gestation
- No history of positive aPL in local lab or positive aPL in core labs at screening
- Not currently a smoker
- No medical problems requiring chronic treatment
- Diabetes mellitus (Type I and Type II) antedating pregnancy
- Known or suspected hereditary complement deficiency (defined by CH50 = 0)
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Neonatal death Time of neonatal death Neonatal death prior to hospital discharge and due to complications of prematurity
Otherwise unexplained fetal death occurring after 12 weeks gestation End of pregnancy Fetal death occurring after 12 weeks' gestation and not explained by chromosomal abnormalities, anatomic malformations, or congenital infections.
Preterm delivery prior to 36 weeks' gestation End of pregnancy Indicated preterm delivery prior to 36 weeks' gestation because of gestational hypertension, preeclampsia-eclampsia or placental insufficiency
Small for gestational age (SGA) <5th %ile End of pregnancy Small for gestational age (SGA) \<5th %ile in the absence of anatomical or chromosomal abnormalities and/or delivery before 36 weeks because of intrauterine growth restriction (IUGR).
- Secondary Outcome Measures
Name Time Method Birth weight End of pregnancy Birth weight
Number of days neonate requires positive pressure ventilation Neonate discharge from hospital Number of days neonate requires positive pressure ventilation
Gestational age End of pregnancy Gestational age (weeks and days) at the end of pregnancy
Total number of days neonate is hospitalized Neonate discharge from hospital Total number of days neonate is hospitalized
Trial Locations
- Locations (10)
Northwestern University
🇺🇸Chicago, Illinois, United States
Johns Hopkins Hospital
🇺🇸Baltimore, Maryland, United States
NYU Langone Medical Center/Hospital for Joint Diseases
🇺🇸New York, New York, United States
Hospital for Special Surgery
🇺🇸New York, New York, United States
University of Chicago
🇺🇸Chicago, Illinois, United States
Columbia University Medical Center
🇺🇸New York, New York, United States
Oklahoma Medical Research Foundation
🇺🇸Oklahoma City, Oklahoma, United States
University of Utah Salt Lake City
🇺🇸Salt Lake City, Utah, United States
Mt. Sinai Hospital
🇨🇦Toronto, Ontario, Canada
Guy's & St Thomas' NHS Foundation Trust
🇬🇧London, United Kingdom