Systemic lupus erythematosus: strategies to improve pregnancy outcomes

Abstract

Systemic lupus erythematosus (SLE) is a chronic autoimmune inflammatory disease with a high prevalence in females of childbearing age. Thus, reproduction in SLE patients is a major concern for clinicians. In the past, SLE patients were advised to defer pregnancy because of poor pregnancy outcomes and fear of SLE flares during pregnancy. Investigations to date show that maternal and fetal risks are higher in females with SLE than in the general population. However, with appropriate management of the disease, sufferers may have a relatively uncomplicated pregnancy course. Factors such as appropriate preconception counseling and medication adjustment, strict disease control prior to pregnancy, intensive surveillance during and after pregnancy by both the obstetrician and rheumatologist, and appropriate interventions when necessary play a key role. This review describes the strategies to improve pregnancy outcomes in SLE patients at different time points in the reproduction cycle (preconception, during pregnancy, and postpartum period) and also details the neonatal concerns.

Keywords:

• systemic lupus erythematosus
• pregnancy outcomes
• lupus flare

Introduction

Systemic lupus erythematosus (SLE) is a chronic autoimmune inflammatory disease that can affect any organ of the body. The prevalence rate of SLE is 20–70 cases per 100,000 people, and it varies between ethnic groups.¹ In the US, females of African and Asian descent are two to three times more likely to be affected than those of European descent.² SLE affects females nine times more than males and occurs most frequently between the age of 20 years and 39 years.² This high predisposition of females of childbearing age makes reproduction a major concern for clinicians involved in the care of these patients. In the past, SLE patients were advised to defer pregnancy because of poor pregnancy outcomes and fear of flares during pregnancy. Investigations till date show that the maternal and fetal risks are higher for females with SLE than for the general population. However, the outcomes for SLE patients in general have now improved, and it has also been shown that with appropriate management of the disease, many SLE patients can have a relatively uncomplicated pregnancy course. This review describes the strategies to improve pregnancy outcomes for SLE patients at different time points in the reproduction cycle (preconception, during pregnancy, and postpartum period) and also details the neonatal concerns.

Preconception

Although SLE patients can theoretically develop ovarian failure due to autoimmune ovarian injury, altered hypothalamic–pituitary–ovarian axis, and diminished ovarian reserve,³ current evidence suggests that they are as fertile as the general population.⁴ The exception to this is when cytotoxic immunosuppressive agents are used for SLE treatment prior to conception. Cyclophosphamide is most toxic to ovarian function and can lead to permanent ovarian failure depending on the patient’s age, dose, and duration.⁵ It is known that initiation of treatment at older age and cumulative dose are risk factors for irreversible damage of ovarian function.^6,7 Anti-Müllerian hormone, secreted from growing ovarian follicles, is considered to be a reliable marker of ovarian reserve, and there are attempts to use this indicator to aid treatment for patients who wish to conceive.⁴ Fertility preservation options should be discussed with patients prior to treatment. If the patient has a history of pregnancy, obstetric outcomes should be carefully reviewed, including history of fetal growth restriction (FGR), pregnancy-induced hypertension and preeclampsia, miscarriage, preterm birth, and intrauterine fetal death.

Based on expert opinion, lupus patients with established organ damage may be advised to avoid pregnancy, including patients with severe pulmonary hypertension (estimated systolic pulmonary artery pressure >50 mmHg), advanced renal insufficiency (creatinine level >2.8 mg/dL), severe restrictive lung disease (forced vital capacity <1 L), heart failure, a history of severe preeclampsia or a severe lupus flare within the past 6 months, active lupus nephritis, or stroke.⁸

In order to improve pregnancy outcomes in SLE patients, pregnancy should be well planned. Disease activity at the time of conception is an indicator of maternal outcomes, and high activity leads to poor outcomes. Based on a multi-center analysis of 56 pregnancies of patients diagnosed with SLE before pregnancy, many agree that prognosis for both mother and child is best when SLE activity is in remission for at least 6 months before conception.^9,10 Compared with patients with clinically active SLE before conception, those in remission for at least 6 months before conception had a higher live birth rate (64% versus 88%), full-term delivery (64% versus 56%), and lower rate of exacerbation of SLE during pregnancy or postpartum (32% versus 28%).¹¹ In a retrospective analysis of 183 pregnancies in Korean females with SLE, based on a receiver operating characteristic curve for prediction of adverse pregnancy outcomes, Ko et al stated that a stable period of at least 4 months is essential in reducing pregnancy loss, premature birth, pregnancy-induced hypertension, and FGR.¹² An overview of the risk assessment in the SLE patients is summarized in Table 1.

Table 1 Preconception risk assessment for SLE patients

Contraindications of pregnancy^Citation6

History of severe preeclampsia despite aspirin and heparin use

Heart failure

Restrictive lung disease (FVC <1 L)

Renal insufficiency (Cr >2.8 mg/dL)

Severe pulmonary hypertension (sPAP >50 mmHg)

Suspend pregnancy until stable for 6 months

Active lupus nephritis

Recent SLE flare

High-risk patients

Active lupus nephritis or SLE flare within 6 months

APS

Anti-SS-A or SS-B antibodies

Low-risk patients

No history of severe organ damage

Quiescent disease at conception

Abbreviations: SLE, systemic lupus erythematosus; FVC, forced vital capacity; Cr, creatinine; sPAP, systolic pulmonary artery pressure; APS, antiphospholipid syndrome.

Contraception

Contraception options for SLE patients depends on current disease activity, presence of antiphospholipid (aPL) antibodies, age, reproductive history, and other factors such as patient’s preference and cultural values. Intrauterine device is a safe option, and no increased risk is reported for infection with combined use of immunosuppressive medication.¹² For stable patients with low disease activity and negative aPLs, estrogen–progestin contraception seems to be a safe option.¹³ However, patients on medications that might interact with estrogen-containing pills such as mycophenolate, corticosteroids, cyclosporine, and warfarin need to be evaluated for the risks and benefits of its use. For patients with a higher risk of thrombosis, progestin-only contraception may be an option. However, information on the risk of thromboembolism in SLE patients on progestin-only contraception is still not sufficient, and guidelines on its use are still controversial.¹⁴ Because of its low effectiveness, barrier methods such as condoms and diaphragms may be necessary as a second-line method when other options are contraindicated. Emergency contraception is indicated regardless of disease activity or aPL status, and patients should be well informed of the option.¹⁵

Medication

Discontinuation of medication before conception by the patient for fear of fetotoxicity is a frequently encountered problem in practice. Patients should be well informed that discontinuation of medication may activate SLE and lead to pregnancy complications.

When planning pregnancy, medication of the patient must be reviewed and adjusted to minimize its effect on the fetus while maintaining the current stable condition of the mother. Nonsteroidal anti-inflammatory drug is commonly prescribed to SLE patients and is generally safe during pregnancy, except in the third trimester, which may cause premature closure of ductus arteriosus. Low-dose aspirin, which is often used for the prevention of preeclampsia, is also considered safe. Antihypertensive medications such as nifedipine, methyldopa, and hydralazine are widely used during pregnancy.¹⁶ On the other hand, angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers are contraindicated throughout pregnancy because of their association with congenital anomalies and pregnancy complications.¹⁷ Hydroxychloroquine use is encouraged throughout pregnancy because of its safety profile and possible preventive effect against neonatal congenital heart block (described in the “Neonatal concerns” section). The effects of glucocorticoids include a possible increase in the incidence of oral cleft in the fetus, FGR, and premature rupture of membranes, although reports are conflicting.¹⁸

Among the immunosuppressive agents, cyclophosphamide, methotrexate, and mycophenolate are contraindicated during pregnancy because of their association with congenital anomalies.^19–21 Azathioprine is considered relatively safer than other immunosuppressive drugs, and many reports encourage transition for patients who wish to conceive.²² However, recently, concerns have been raised for late developmental delays in children who were exposed to azathioprine in utero.²³ Calcineurin inhibitors such as tacrolimus and cyclosporine also seem to be acceptable options.^24,25 The biological agents such as anti-TNF agents and rituximab administered by pregnant females with rheumatoid arthritis and inflammatory bowel disease do not seem to place the mother and fetus at risk at the time of conception and during the first trimester.²⁶ However, their use in the third trimester must be cautioned, as these agents readily cross the placenta and fatal infection has been reported after live vaccination in an exposed infant.²⁷

During pregnancy

Whether SLE activity is influenced by pregnancy has been a controversial subject for decades. It is generally considered that SLE flares are likely during pregnancy. However, some argue that SLE activity is worsened,^28,29 while others report that no change in disease activity is observed.³⁰ The mixed results are understandable, as the studies were mostly retrospective in design and patient history such as disease activity at the time of conception, previous history of disease, and medication profile were diverse. In addition, different definitions were given for disease flare and, as described below, lupus flare during pregnancy is often difficult to distinguish from preeclampsia. Recently, attention is less on whether flare is likely or not and is more on which specific population of patients needs special attention for exacerbation of SLE. Some argue that in patients with stable condition at the time of conception, disease activity is generally not worsened, and even if so, the flare is usually mild and seldom requires a change in the treatment.^9,11,31 A history of lupus nephritis and active disease at the time of conception are indicators of poor maternal outcomes.^32,33

On the other hand, the effects of the disease on pregnancy outcomes are clear. The incidence of complications, including preeclampsia, prematurity, FGR, and fetal loss, is higher in SLE patients than that in the general population. Preeclampsia is reported to occur in 7.5%–22%^34–38 of pregnant SLE patients, which is higher than ~3% in the general population.³⁹ It is not clear why these adverse outcomes are increased in SLE patients; lupus nephritis and aPL antibodies have been identified as risk factors. The direct effect on placental trophoblast and complement activation, as well as procoagulant effect of aPL, seems to play a role in the pathogenesis.^40,41 Premature delivery, either indicated or spontaneous, is observed in 12.1%–54% of patients.^{9,11,34–38,42–44} The incidence rate of fetal loss was reported as 3%–36%, which varies among studies.^{33,35,38,44,45} The incidence rate of these adverse outcomes is reported to substantially increase for females with a history of nephritis, positive aPL, and active disease at conception.^46,47 Lupus nephritis and antiphospholipid syndrome (APS) are discussed separately in the following sections.

Pregnant females with SLE should be closely monitored by both an experienced obstetrician and a rheumatologist. Neonatal care should be readily available considering the high rate of premature birth. Although no consensus has been reached on management strategies, recommendations have been made to achieve early detection of change in SLE activity, fetal compromise, and maternal complications.^48,49 The key points in management of pregnant SLE patients are described in Table 2.

Table 2 Key points in managing the pregnant SLE patients

	Observant	Timing	Monitoring details
Maternal monitoring	Obstetrician	First visit Repeated monthly until 20 weeks Every 2 weeks until 24 weeks Every week until delivery	History taking, physical examination, urine analysis (if dipstick is positive for protein, measure protein–creatinine ratio)
	Rheumatologist	First visit Repeat every month until postpartum	History taking, physical examination, complement, anti ds-DNA antibody, SS-A and SS-B antibodies, cardiolipin antibodies, lupus anticoagulant History taking, physical examination, complement
	Both	First visit Repeat every month until postpartum	CBC, chemistry (including uric acid, liver enzymes, creatinine) Protein–creatinine ratio
Fetal monitoring	Obstetrician	Starting at 16 weeks Starting at 24 weeks Repeated every week until delivery	Echocardiogram BPP, fetal growth, umbilical artery Doppler velocimetry
	Neonatologist	When signs of fetal compromise detected	Consultation for appropriate timing/mode of delivery
	Cardiologist	When signs of CHB or heart failure detected	Consultation for therapy and appropriate timing/mode of delivery

Abbreviations: SLE, systemic lupus erythematosus; CBC, complete blood count; BPP, biophysical profile; CHB, congenital heart block; dsDNA, double stranded DNA.

Lupus nephritis

Patients with a previous history of lupus nephritis or active lupus nephritis during pregnancy require careful monitoring during pregnancy, as they are associated with higher rates of maternal and fetal complications. In a cohort study of 166 pregnancies, first-trimester proteinuria, indicative of lupus nephritis, resulted in a 2.6-fold increase in pregnancy loss.⁴⁶ Renal involvement, defined as proteinuria in the absence of preeclampsia or dysmorphic hematuria and cellular casts in urine, was reported as a prognostic factor of FGR and/or preeclampsia in a retrospective study of 65 pregnancies.³⁸ As discussed earlier, in order to improve pregnancy outcome in this patient population, females with active lupus nephritis should be advised to postpone pregnancy until the disease is in remission for at least 6 months. Lupus nephritis in pregnancy should be dealt with caution, because it can possibly lead to irreversible renal injury.³³ In addition, it is often difficult to differentiate renal flare and preeclampsia, which can cause dilemma in the choice of treatment. Details on treatment are described as follows.

Treatment of SLE flare during pregnancy

The treatment of SLE flare during pregnancy is the same as that in nonpregnancy. The choice of medication and dose depends on the severity and the degree of organ involvement. However, special consideration is necessary for the possible harm it may do to the fetus. The risks and benefits of initiating treatment should be evaluated carefully. When indicated, the treatment should not be withheld due to pregnancy, as it may lead to serious morbidity and mortality.³²

Diagnosis of SLE exacerbation during pregnancy is challenging, as many physiological changes in normal pregnancy and obstetric complications may mimic SLE symptoms. For instance, mild thrombocytopenia, anemia, arthralgia, edema, mild dyspnea, and effusion of knees, which are all frequent observations during pregnancy, can be confused with early signs of flare.^48,50 Complement levels are also known to be slightly elevated during pregnancy.⁵¹ The C3 and C4 levels must be evaluated in caution, because even a sign of slight decrease in the normal range might indicate lupus flare.⁵⁰

In particular, renal flare and preeclampsia are difficult to differentiate, which share clinical features including hypertension, proteinuria, and thrombocytopenia. Moreover, the two conditions may coexist, further complicating management of the condition.^48,52–54 When preeclampsia is suspected as the culprit of the medical condition and termination of pregnancy is indicated, one should always keep in mind the possibility of coexisting lupus nephritis. When lupus nephritis is involved in the pathogenesis, the patient’s condition might worsen.⁵² Some key points to differentiate preeclampsia and renal flare are listed in Table 3. It is essential that obstetricians discuss each case individually with a rheumatologist.

Table 3 Key points to differentiate preeclampsia from lupus nephritis

	Preeclampsia	Lupus nephritis
Onset	After 20 weeks	Possible onset before 20 weeks
Hypertension	Present	May be present or absent
Urinary sediment	Negative	Positive
Uric acid	>4.9 mg/dL	<4.9 mg/dL^Citation90
Complement	No change	Decrease from baseline during pregnancy (could be within the normal range)
Anti-dsDNA	No change	Increased
Other signs of SLE activity	Absent	Present
Urinary calcium	<195 mg/24 hours	>195 mg/24 hours^Citation91

Abbreviations: dsDNA, double stranded DNA; SLE, systemic lupus erythematosus.

Antiphospholipid syndrome

APS is an autoimmune disorder characterized by the occurrence of venous and arterial thromboses, which may or may not coexist with other autoimmune diseases such as SLE. In a study of 1,000 patients with a diagnosis of APS, 36.2% were found to have SLE.⁵⁵ Its diagnosis consists of the presence of both specific autoantibodies and clinical manifestations.⁵⁶ One of the major clinical manifestations of APS is adverse obstetric outcomes such as 1) three or more consecutive spontaneous abortions before 10 weeks of gestation, 2) one or more unexplained fetal loss beyond 10 weeks of gestation, or 3) one or more premature births of a morphologically normal neonate before 34 weeks of gestation due to eclampsia or preeclampsia.⁵⁶ When APS is diagnosed together with SLE or other autoimmune diseases, the risk of adverse pregnancy outcomes is higher.⁵⁷ The treatment for APS includes prevention of adverse pregnancy outcomes by aspirin or aspirin in combination with heparin started empirically to prevent thrombosis.⁵⁸ However, studies from animal models suggest that inflammation also plays a key role in the pathogenesis of APS,^59,60 and the anti-inflammatory aspect of heparin might also be responsible for the effect on outcomes.^49,51 Management of APS during pregnancy depends on whether the patient has a history of thrombosis. For those with a history of thrombotic event, most experts recommend heparin use until 6 weeks postpartum. Although the effectiveness is not proven, it is common to use aspirin in combination with heparin. The optimal treatment for those without a history of thrombosis is not well studied.⁶¹ Randomized controlled trials have shown that the combination of aspirin and heparin is superior to aspirin alone in preventing pregnancy loss and that pregnancies that ended in live births had favorable outcomes^62,63 on the other hand there is a study that shows aspirin alone is equally effective in pregnancy loss.⁶⁴ These trials are of small scale, vary in therapeutic protocols, and, most importantly, exclude SLE patients. Some retrospective studies on the effectiveness of pharmacological treatment for APS patients include SLE patients, but their therapeutic regimens and diagnosis of APS are not consistent.^64–67 One systematic review based on two small trials concluded that a combination of heparin and aspirin reduced pregnancy loss by 54% in patients with a history of at least one pregnancy loss and positive aPL.⁶⁸ Well-designed trials are necessary to find the appropriate treatment for lupus patients with APS. Currently, expert opinion favors the use of aspirin during pregnancy and also anticoagulation with heparin postpartum to reduce the risks of thrombosis in APS patients.^69–71

Postpartum period

SLE flares can occur after termination of pregnancy, especially in patients with active disease at conception and during pregnancy.⁷² Of note, for those who have terminated pregnancy due to SLE flare or with coexisting preeclampsia, intensive monitoring for severe maternal postpregnancy exacerbations is needed.^52,73 The treatment for postpartum females with active SLE is similar to that for nonpregnant females. Many medications for aggressive therapy are not compatible with breastfeeding.¹⁸ Breastfeeding females must be informed of the risks and benefits of continuing lactation during treatment.

Neonatal concerns

Neonates born to mothers with SLE need to be monitored for neonatal lupus (NL). NL is believed to be caused by transplacental transfer of the autoantibodies anti-Ro/SSA and anti-RA/SSB to the newborn. The incidence rate of cardiac NL was reported as 1%–2% in mothers who are antibody positive and can increase to as high as 18% in mothers who had previously given birth to an affected child.^74,75 The major clinical manifestations of NL are rash and heart block. Cutaneous involvement is typically observed as multiple erythematous macules or plaques around the head and neck at birth to 20 weeks of age. The mean age of detection of the rash was 6 weeks.⁷⁶ It is usually self-limiting, disappearing as the circulating antibodies are removed, but some might have residual telangiectasia and hyperpigmentation in the affected area.⁷⁶ Cardiac manifestation of NL is more serious, with a reported mortality as high as 16%–17.5% and pacemaker implantation is required for ~70% of patients by the age of 10 years.^77,78

In order to improve outcomes in fetus/neonates diagnosed with heart block, close monitoring is necessary during pregnancy and after delivery, as a first- or second-degree heart block can potentially progress to a third-degree heart block, necessitating pacemaker implantation. Heart block is often diagnosed between 18 weeks and 24 weeks of gestation by using echocardiography, and a diagnosis of onset is rare after 30 weeks of pregnancy.^74,79 Thus, intensive fetal echocardiography during this period is essential for early diagnosis. In addition, prenatal fluorinated steroids can reverse a second-degree heart block,^79–81 although its efficacy is still controversial.⁷⁷ Intravenous immunoglobulin and plasmapheresis have also been considered as candidate agents to reverse the progression of heart block, but have not been proven as effective.^82,83

Hydroxychloroquine, originally an antimalarial medication, has been widely prescribed to patients with autoimmune disease, especially SLE patients.⁸⁴ It is believed to prevent tissue injury by interfering with Toll-like receptor activity.⁸⁵ In a recent retrospective study, this medication has been associated with a reduction in the incidence of cardiac NL in mothers who had previously given birth to an affected child.⁸⁶ A few other studies have indicated the possible therapeutic effect of hydroxychloroquine for congenital heart block.^87–89

Summary

With better treatment options and extensive clinical and molecular research, many SLE patients can have favorable pregnancy outcomes with careful management. Factors such as appropriate preconception counseling and medication adjustment, strict disease control prior to pregnancy, intensive surveillance during and after pregnancy by both the obstetrician and rheumatologist, and appropriate interventions when necessary play a key role.

Disclosure

The authors report no conflicts of interest in this work.