Fetal and Maternal Outcomes of Planned Pregnancy in Patients with Systemic Lupus Erythematosus: A Retrospective Multicenter Study.
Compared with the general population, patients with SLE are still at high risk of adverse pregnancy outcomes (APOs) . A number of studies have shown that patients with SLE are more likely to develop fetal complications, including fetal loss, preterm birth, and IUGR, compared to healthy women . However, recent studies have reported that fetal outcomes are relatively favorable if lupus is stable or mildly active . Moreover, the occurrence of disease flares increases during SLE pregnancies but decreases if pregnancy is delayed until disease is quiescent . Currently, patients with SLE were advised to consider pregnancy during periods of inactive or stable disease , the so-called "planned pregnancy." However, such researches usually enrolled a small number of candidates, and data is lacking in China.
Therefore, we performed a retrospective multicenter research in South China aimed at investigating the fetal and maternal outcomes, predictors of APOs, and pregnancy-associated disease flares in women with SLE who underwent planned pregnancy and close pregnancy monitoring by a multidisciplinary team.
2. Patients and Methods
2.1. Patient Population. A total of 243 patients with SLE who underwent planned pregnancy from three tertiary hospitals in Guangzhou from December 2011 to December 2016 were included (127 pregnancies in the First Affiliated Hospital of Sun Yat-sen University; 66 pregnancies in Guangzhou First People's Hospital, the Second Affiliated Hospital of South China University of Technology; and 50 pregnancies in the Third Affiliated Hospital of Guangzhou Medical University). Only one pregnancy for each patient was included. All patients fulfilled the 1997 ACR diagnostic criteria for SLE . Planned pregnancy was defined according to Chinese recommendations for perinatal management in women with SLE , as lupus patients who were allowed to conceive under the situation of (1) stable disease activity for at least six months; (2) dose of oral prednisone < 15 mg per day); (3) urine protein < 0.5 g/24 hours; (4) absence of major organ dysfunction; (5) discontinuation of immunosuppressants including cyclophosphamide, methotrexate, and mycophenolate mofetil for at least six months; and (6) for those who were taking leflunomide, wash-out therapy should be administered and leflunomide was withdrawn for at least six months.
2.2. Screening and Follow-Ups. All pregnant women with SLE in the Chinese tertiary hospitals were followed according to Chinese recommendations for perinatal care in high-risk women , namely, every four weeks up to the 28th week of gestation and every two weeks from the 28th week up to delivery. Patients who were not followed regularly or without complete records were excluded. Regular obstetric practice, blood pressure, fetal heartbeat, clinical symptoms of lupus, laboratory tests including complete blood count, routine urine test, blood biochemical test, 24-hour urine protein, complement C3 and C4, anti-dsDNA antibodies, anti-SSA antibodies, anti-SSB antibodies, antiphospholipid antibody (including anticardiolipin (aCL) antibody IgM, aCL antibody IgG, and anti-[beta]2GP1 antibody lupus anticoagulants (LAC)), and medical treatments were recorded. SLE activity was measured by the Systemic Lupus Erythematosus Pregnancy Disease Activity Index (SLEPDAI) at the first trimester, second trimester, and third trimester. The highest score was used in statistical analysis. Fetal Doppler sonography was performed every 4~8 weeks since the 16th week of gestation and every 2~4 weeks since the 28th week of gestation. Patients with positive antiphospholipid antibody were pretreated with aspirin. Patients with antiphospholipid antibody syndrome (APS) were pretreated with aspirin and low molecular heparin until delivery.
2.3. APOs. Fetal APOs include the following: (1) fetal loss, including spontaneous abortion (termination of pregnancy before the 20th week of gestation caused by natural factors), therapeutic abortion (artificial termination of pregnancy because of life-threatening progression of lupus or obstetric complications), stillbirth (intrauterine fetal demise after 20 weeks of gestation unexplained by chromosomal abnormalities, anatomic malformation, or congenital infection), and neonatal death referred to as the death of a live infant within 28 days after birth; (2) preterm birth (live birth before 37 weeks of gestation); (3) IUGR (birth weight below the 10th percentile of the Chinese population according to gestational week at delivery and fetal gender; and (4) fetal distress referred to as fetus hypoxia and acidosis, which could endanger the health of the fetus. Composite APOs were defined as the occurrence of any adverse outcomes including fetal loss, preterm birth, SGA babies, and fetal distress during gestation. Maternal APOs include the following: (1) disease flare was defined according to the International Consensus for disease flare in lupus , namely, new onset or worsening of specific and associated cutaneous manifestations of SLE; arthritis; one or more hemocytopenia not attributed to immunosuppressive drugs; neurological, cardiopulmonary, and renal manifestations; elevated serum creatinine in association with low-serum complement; and/or elevated titers of anti-dsDNA antibodies. Active lupus nephritis was defined according to the following: proteinuria > 0.5 g/24h, active urinary sediment (>3 red blood cells/high-power field (HPF), or >5 white blood cells/HPF, or cellular casts), or estimated creatinine clearance (CrCl) <60ml/min/1.73[m.sup.2] with active urinary sediment. Mild disease activity was defined as SLEPDAI score 5 to 9, moderate disease activity as SLEPDAI score 10 to 14, and severe disease activity as SLEPDAI score [greater than or equal to] 15. (2) Pregnancy-induced hypertension (PIH) was defined as hypertension during pregnancy, which included gestational hypertension, preeclampsia, and eclampsia. Hypertension was defined as systolic blood pressure > 140 mmHg and/or diastolic blood pressure > 90 mmHg in sitting position in at least two consecutive measurements during pregnancy. Preeclampsia was defined as a new onset of hypertension with or without proteinuria after the 20th week of gestation in a previously normotensive woman .
2.4. Statistical Analysis. Software SPSS 20.0 was used for data analysis. Quantitative variables were recorded as mean [+ or -] standard deviation and compared by Student's t-test. Categorical variables were described as frequency and percentage and compared by a chi-square test. Factors related to APOs at P < 0.10 in univariate analyses were entered into a multivariate logistic model. P < 0.05 was considered as statistically significant.
2.5. Ethics Statement. Since this is a retrospective study, patient's interest was not involved; therefore, no ethical approval was required. The Ethical Committees of the above three centers waived that the research could be done based on a record review without contacting the patients. A support letter was obtained from the medical director's office of the three hospitals for retrieving retrospective data from the database and records. All the information was kept confidential, and no individual identifiers were collected.
3.1. Demographic Data and History of Pregnancy. The average age at conception was 28.9 [+ or -] 3.9 years (20 to 38 years). Duration of SLE before pregnancy was 4.4 [+ or -] 4.3 years (1.5 to 21 years). Of the 243 patients, 146 patients became pregnant for the first time and 97 patients had prior history of pregnancy. Fifty-one patients had a history of adverse pregnancy, indicated abortion (n = 25), stillbirth (n = 3), premature delivery (n =17), IUGR (n = 5), fetal distress (n = 1), and PIH (n = 5). Five patients experienced adverse pregnancy twice.
3.2. Fetal Outcomes. One hundred and fifty-seven (64.6%) patients ended in delivery without APOs, and 86 (35.4%) patients had at least one episode of APOs. Fetal APOs were shown in Table 1. In total, 12 patients (4.9%) experienced fetal loss. Spontaneous abortion, stillbirth, and therapeutic abortion accounted for one (0.4%), six (2.5%), and five (2.1%) cases, respectively. Causes of therapeutic abortion included active lupus nephritis (n = 3), severe thrombocytopenia (n = 1), and anatomic malformation (n = 1). Live birth delivery was succeeded in 231 patients (95.1%), among which 177 patients (72.8%) had term births, 54 (22.2%) had preterm births, 36 (14.8%) had IUGR, and 27 (11.1%) had fetal distress. Average birth weight was 2713.7 [+ or -] 521.3 g (790.0~4150.0g). The average weights of preterm birth and term birth were 2198.5 [+ or -] 637.1 g (790.0~3200.0g) and 2868.8 [+ or -] 359.0 g (1940.0~4150.0g), respectively. Forty-two preterm infants (42/54, 77.8%) were delivered after the 34th week of gestation. Causes of preterm births included therapeutic preterm births (23/54, 42.6%), preterm premature rupture of membranes (PPROM) (19/54, 35.2%), and spontaneous preterm births (12/54, 22.2%). Preeclampsia (n = 14), lupus flares (n = 6), IUGR (n = 6), placenta previa (n = 3), and placental abruption (n = 2) were the main causes that led to therapeutic preterm births. All the preterm infants were viable.
3.3. Maternal Outcomes. Maternal APOs were presented in Table 1. Fifty-two disease flares (21.4%) occurred, among which 8 disease flares occurred during the first trimester, 15 during the second trimester, and 29 during the third trimester. Disease activity was mild in 45 (45/52, 86.5%) patients, moderate in 6 (6/52, 11.5%), and high in 1 (1/52, 1.9%). Disease flares were presented as active lupus nephritis (41/52, 78.8%), thrombocytopenia (10/52, 19.2%), skin/ mucosa lesions (9/52, 17.3%), leukopenia (6/52, 11.5%), arthritis (6/52, 11.5%), alopecia (2/52, 3.8%), hemolytic anemia (1/52, 1.9%), and pulmonary hypertension (1/52, 1.9%). All disease flares were promptly diagnosed and treated when necessary. Of the 52 flares, 20 were treated with an increase of oral prednisone, associated with three intravenous methylprednisolone pulses. Prednisone was prescribed 10 to 15 mg per day to patients with mild disease activity, 15 to 30 mg per day to patients with moderate disease activity, and over 30 mg per day to patients with high disease activity. In total, 27 patients (11.1%) took prednisone more than 10 mg per day. Increased azathioprine dose was prescribed to three patient, and introduction of azathioprine to seven cases. One patient with severe disease flares received therapeutic abortion and was treated with cyclophosphamide subsequently. Of these 52 pregnancies, 27 ended in preterm births, 16 in IUGR, 9 in fetal distress, and 11 in fetal loss. Causes for fetal loss in patients with disease flare included therapeutic abortion (n = 5, 9.6%), spontaneous abortion (n = 1, 1.9%), and stillbirth (n = 5, 9.6%).
In this study, PIH occurred in 29 cases, among which 3 were gestational hypertension and 26 were preeclampsia. No eclampsia occurred. Of the 29 patients, fetal loss occurred in 5 patients, preterm births in 20, IUGR in 13, and fetal distress in 10. Causes for fetal loss in patients with PIH included therapeutic abortion (n = 2, 6.9%) and stillbirth (n = 3, 10.3%). Neither the incidence of spontaneous loss nor the incidence of therapeutic abortion differed between patients with disease flares and those with PIH.
3.4. Risk Factors for Fetal APOs. Table 2 reveals a comparison of clinical events as well as laboratory parameters in patients with or without composite fetal APOs. Disease flares at any time, active lupus nephritis, thrombocytopenia, LAC positivity, aCL antibody positivity, and hypocomplementemia were more likely to occur in patients with APOs. Multivariate analysis revealed that disease flares and aCL antibody positivity were risk factors for composite fetal APOs (Table 3).
Univariate analysis for respective fetal APOs was shown in Table 4. Multivariate analysis revealed that disease flares and aCL antibody positivity were risk factors for fetal loss. Disease flares and PIH were responsible for preterm birth. PIH was also the independent predictor of IUGR and fetal distress.
3.5. Risk Factors for Maternal APOs. The rates of disease flares, active lupus nephritis, thrombocytopenia, leukopenia, LAC positivity, aCL antibody positivity, and hypocomplementemia were higher in mothers with PIH than those without (Table 5). Multivariate analysis revealed that disease flares, thrombocytopenia, and aCL antibody positivity were independent predictors of PIH.
Herein, we leveraged a retrospective multicenter study on planned pregnancy in women with SLE. All patients were in inactive or stable state prior to conception and followed by a multidisciplinary team of experts. In our research, two-thirds of the pregnancies ended in successful delivery without any fetal APOs and severe maternal disease flares occurred in only 0.4%. Our results showed that the rate of fetal loss was significantly decreased and the occurrence of moderate-to-severe disease flares was remarkably reduced in lupus patients who underwent planned pregnancy, although preterm births remained an important issue.
Our study showed that 4.9% of the pregnancies ended in fetal loss. In comparison, a meta-analysis by Smyth et al. including 37 studies with 1842 patients and 2751 pregnancies, whose disease activity was not strictly controlled prior to pregnancy, revealed that the rate of fetal loss was as high as 23.4% . Our previous research also indicated that 28.5% of pregnancies in the general lupus patients ended in fetal loss, which was significantly higher than that in women undergoing planned pregnancy. Two prospective studies evaluating fetal outcomes in lupus patients in a stable disease state reported approximate rates of fetal loss to our study, indicating 8.4% and 4.0%, respectively [3, 12]. All the three researches, ours included, suggested that planned pregnancy was beneficial for decreasing fetal loss. The above meta-analysis also revealed a higher preterm rate in women with SLE who did not undergo planned pregnancy (39.4%) . In our research, the rate of preterm birth (22.2%) exceeded that in the Chinese general population (6.2~7.2%) , comparable to the results from the multicenter prospective study by Clowse et al. mainly focusing on lupus patients with inactive or mild stable disease state (28.2%) . In our research, most preterm births occurred after the 34th week of gestation with favorable outcomes. No neonatal death occurred. Planned pregnancy, partially by decreasing the preterm rate, could improve the overall outcomes of infants in women with SLE. PPROM is considered as the primary cause for preterm birth in the general population, followed by therapeutic or spontaneous preterm . Different from the general population, in our research, therapeutic preterm was the primary cause for preterm birth. Preeclampsia and disease flares are the major causes that lead to therapeutic preterm. Therefore, disease evaluation and blood pressure monitoring is of great importance.
Major risk factors for APOs in SLE pregnancy have been investigated in multiple studies and generally fall into three categories: renal involvement, SLE disease activity, and presence of aPL antibodies . In our research, risk factors for fetal APOs included disease flares during pregnancy and aCL positivity, consistent with previous findings. Our results showed that fetal loss was strongly associated with both disease flares during pregnancy and the presence of aCL. It was reported that high disease activity increased the risk of fetal loss fourfold . In this study, an approximate 66.7% of pregnant patients who had fetal loss were aCL antibody-positive, compared to 9.1% in the group with live births. A previous report also pointed out that there was an increased risk in fetal loss in mothers with aCL antibodies . Our study indicated that disease flares during pregnancy and PIH were responsible for preterm births in patients with SLE, consistent with previous findings . A prospective research also demonstrated that a high SLEDAI score increased the possibility of preterm delivery . Increase in blood pressure is associated with preterm births  and low offspring birth weight  according to previous findings. In healthy pregnant women, hypertension increases the likelihood of placenta dysfunction, resulting in fetal intrauterine distress and fetal growth restriction [22,23]. A similar association was found in our research, showing that PIH contributed to an increased risk of IUGR and fetal distress. Overall, this data suggested that maintaining inactive disease during pregnancy, treating with positive aCL antibodies, and controlling blood pressure were important for successful pregnancy.
We observed mild-moderate flares in 21.0% of pregnancies and severe flares in 0.4%, a total of 21.4%. A multicenter prospective trial assessing maternal outcomes of pregnant women with slightly active or inactive lupus nephritis before pregnancy reported that mild-to-moderate disease flares occurred in 18.3% and severe flares in 1.4% of pregnancies, which were comparable to our findings . It suggested that lupus patients undergoing planned pregnancy experienced less severe disease flares with more favorable consequences. Therefore, early recognition and prompt treatment are necessary during pregnancy and could improve disease outcomes.
In our research, the rate of PIH (11.9%) was approximately twice over the general population in China (5.2%) . A retrospective study of 103 pregnancies in Chinese patients with SLE found higher frequencies of PIH (20.0%) in SLE women without planned pregnancy . The PROMISSE study also demonstrated that patients with inactive disease at conception had lower rates of PIH (11.2%). In our research, the independent risk factors for PIH included disease flares during pregnancy, thrombocytopenia, and aCL positivity. Active disease was the strongest predictor of preeclampsia, consistent with previous studies . A systematic review indicated that there is an association between aCL antibodies and severe preeclampsia .
In conclusion, our research showed that planned pregnancy improved fetal and maternal outcomes in lupus patients, presenting as lower rates of fetal loss, more favorable outcomes for preterm infants, and less severe disease flares during pregnancy. Our research reinforced the importance of planned pregnancy, which allowed women with SLE to conceive in a proper time monitored by multidisciplinary experts. Disease flares should be recognized and treated immediately in order to prevent severe complications. Blood pressure should be closely controlled during pregnancy.
An earlier version of this work has been presented as an abstract at the Annual European Congress of Rheumatology, 2018, according to the following link: https://ard.bmj.com/ content/annrheumdis/77/Suppl_2/1468.2.full.pdf.
Conflicts of Interest
The authors declare that they have no conflicts of interest.
Dongying Chen and Minxi Lao contributed equally to this work.
This project was supported by grants from the Guangdong Science and Technology Project (2016A020215043), Guangzhou Science and Technology Plan Project (201607010145), and the National Natural Science Foundation of China (81603435, 81601403).
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Dongying Chen, (1) Minxi Lao, (2) Jianyu Zhang, (3) Yanfeng Zhan, (4) Weinian Li, (5) Xiaoyan Cai (ID), (5) and Zhongping Zhan
(1) Department of Rheumatology, The First Affiliated Hospital of Sun Yat-sen University, No. 58, Zhongshan 2nd Road, Guangzhou 510080, China
(2) Department of Rheumatology and Department of Geriatrics, The First Affiliated Hospital of Sun Yat-sen University, No. 58, Zhongshan 2nd Road, Guangzhou 510080, China
(3) Department of Rheumatology, The Third Affiliated Hospital of Guangzhou Medical University, No. 63, Duobao Road, Guangzhou 510150, China
(4) Department of Obstetrics and Gynecology, The First Affiliated Hospital of Sun Yat-sen University, No. 58, Zhongshan 2nd Road, Guangzhou 510080, China
(5) Department of Rheumatology, Guangzhou First People's Hospital, The Second Affiliated Hospital of South China University of Technology, No. 1, Panfu Road, Guangzhou 510180, China
Correspondence should be addressed to Xiaoyan Cai; email@example.com and Zhongping Zhan; firstname.lastname@example.org
Received 22 November 2017; Accepted 11 July 2018; Published 3 September 2018
Academic Editor: Bogdan Kolarz
Table 1: Maternal and fetal outcomes in pregnant women with SLE. Fetal adverse events N % Preterm birth 54 22.2 Intrauterine growth retardation 36 14.8 Fetal distress 27 11.1 Fetal loss 12 4.9 Spontaneous abortion 1 0.4 Therapeutic abortion 5 2.1 Stillbirth 6 2.5 Neonatal death 0 0 Maternal adverse events Disease flares 52 21.4 In the first trimester 8 3.3 In the second trimester 15 6.2 In the third trimester 29 11.9 SLEPDAI max > 4 5~9 45 18.5 10~14 6 2.5 [greater than or equal to] 15 1 0.4 Pregnancy-induced hypertension 29 11.9 Gestational hypertension 3 1.2 Preeclampsia 26 10.7 Eclampsia 0 0 Table 2: Association of different characteristics during pregnancy with composite fetal APOs. Characteristics Total With fetal (n = 243) APOs (n = 86) Clinical manifestation at any time (n, %) Flare during pregnancy 52 (21.4) 40 (46.5) Active lupus nephritis 45 (18.5) 32 (37.2) Thrombocytopenia 23 (9.5) 14 (16.3) Leukopenia 7 (2.9) 4 (4.7) Skin rash 19 (7.8) 9 (10.5) Joint involvement 18 (7.4) 6 (7.0) Serological profile at any time (n, %) Anti-dsDNA antibody positivity 93 (38.3) 34 (39.5) Anti-Ro antibody positivity 50 (20.6) 19 (22.1) Anti-La antibody positivity 33 (13.6) 12 (14.0) LAC positivity 19 (7.8) 14 (16.3) aCL IgG positivity 25 (10.3) 21 (24.4) aCL IgM positivity 13 (5.3) 11 (12.8) Anti-beta2 GP1 positivity 21 (8.6) 7 (8.1) Hypoalbuminemia 66 (27.2) 29 (33.7) C3 < 80 mg/dL 40 (16.5) 24 (27.9) C4 < 15 mg/dL 51 (21.0) 29 (33.7) Characteristics Without fetal P value APOs (n = 157) Clinical manifestation at any time (n, %) Flare during pregnancy 12 (7.6) <0.001 Active lupus nephritis 13 (8.3) <0.001 Thrombocytopenia 9 (5.7) 0.01 Leukopenia 3 (1.9) 0.2 Skin rash 10 (6.4) 0.3 Joint involvement 12 (7.6) 0.9 Serological profile at any time (n, %) Anti-dsDNA antibody positivity 59 (37.6) 0.8 Anti-Ro antibody positivity 31 (19.8) 0.7 Anti-La antibody positivity 21 (13.4) 1.0 LAC positivity 5 (3.2) <0.001 aCL IgG positivity 4 (2.5) <0.001 aCL IgM positivity 2 (1.3) <0.001 Anti-beta2 GP1 positivity 14 (8.9) 0.8 Hypoalbuminemia 37 (23.6) 0.09 C3 < 80 mg/dL 16 (10.2) <0.001 C4 < 15 mg/dL 22 (14.0) <0.001 Table 3: Association of different characteristics during pregnancy with APOs: results of multivariate analysis. Characteristics P value OR OR 95% CI Fetal APOs Composite APOs Disease flares during pregnancy <0.001 8.1 3.8-17.2 Anticardiolipin antibody positivity <0.001 7.4 2.5-21.8 Fetal loss Disease flares during pregnancy 0.002 28.4 3.4-239.0 Anticardiolipin antibody positivity 0.004 7.8 1.9-31.4 Preterm birth Disease flares during pregnancy 0.002 3.5 1.6-7.7 PIH <0.001 6.0 2.3-15.8 IUGR PIH <0.001 6.7 2.9-15.8 Fetal distress PIH <0.001 6.1 2.5-15.2 Maternal APOs PIH Disease flares during pregnancy <0.001 12.2 4.4-33.3 Thrombocytopenia 0.04 4.0 1.1-14.8 aCL antibody positivity <0.001 7.5 2.5-22.4 Table 4: Univariate analysis of variables associated with different fetal adverse maternal outcomes. Characteristics Yes Fetal P loss No n 12 231 -- Disease flares during pregnancy 11(91.7) 41(17.7) <0.001 Active lupus nephritis 9(75.0) 36(15.6) <0.001 Thrombocytopenia 5(41.7) 18(7.8) 0.002 Leukopenia 2(16.7) 5(2.2) 0.04 PIH 5(41.7) 24(10.4) 0.007 Anti-dsDNA antibody positivity 5(41.7) 88(38.1) 0.8 Anti-Ro antibody positivity 8(66.7) 91(39.4) 0.07 Anti-La antibody positivity 2(16.7) 31(13.4) 0.7 LAC positivity 5(41.7) 14(6.1) 0.001 Anticardiolipin antibody positivity 8(66.7) 21(9.1) <0.001 Anti-beta2 GP1 positivity 2(16.7) 19(8.2) 0.3 Hypoalbuminemia 6(50.0) 60(26.0) 0.09 Hypocomplementemia 9(75.0) 47(20.3) <0.001 Hydroxychloroquine 9(75.0) 117(50.6) 0.1 Characteristics Yes Preterm P birth No n 54 189 -- Disease flares during pregnancy 27(50.0) 25(13.2) <0.001 Active lupus nephritis 23(42.6) 22(11.6) <0.001 Thrombocytopenia 8(14.8) 15(7.9) 0.1 Leukopenia 2(3.7) 5(2.6) 0.7 PIH 20(37.0) 9(4.8) <0.001 Anti-dsDNA antibody positivity 21(38.9) 72(38.1) 1.0 Anti-Ro antibody positivity 21(38.9) 78(41.3) 0.8 Anti-La antibody positivity 8(14.8) 25(13.2) 0.8 LAC positivity 8(14.8) 11(5.8) 0.03 Anticardiolipin antibody positivity 15(27.8) 14(7.4) <0.001 Anti-beta2 GP1 positivity 4(7.4) 17(9.0) 0.7 Hypoalbuminemia 17(31.5) 49(25.9) 0.4 Hypocomplementemia 17(31.5) 39(20.6) 0.1 Hydroxychloroquine 29(53.7) 97(51.3) 0.8 Characteristics Yes IUGR No P n 36 207 -- Disease flares during pregnancy 16(44.4) 36(17.4) <0.001 Active lupus nephritis 12(33.3) 33(15.9) 0.01 Thrombocytopenia 4(11.1) 19(9.2) 0.8 Leukopenia 0 7(3.4) 0.3 PIH 13(36.1) 16(7.7) <0.001 Anti-dsDNA antibody positivity 16(44.4) 77(37.2) 0.4 Anti-Ro antibody positivity 17(47.2) 82(39.6) 0.4 Anti-La antibody positivity 5(13.9) 28(13.5) 1.0 LAC positivity 4(11.1) 15(7.2) 0.4 Anticardiolipin antibody positivity 7(25.9) 22(10.2) 0.03 Anti-beta2 GP1 positivity 2(5.6) 19(9.2) 0.7 Hypoalbuminemia 7(19.4) 59(28.5) 0.3 Hypocomplementemia 10(27.8) 46(22.2) 0.3 Hydroxychloroquine 16(44.4) 46(22.2) 0.3 Characteristics Yes Fetal P distress No n 27 216 Disease flares during pregnancy 9(33.3) 43(19.9) 0.1 Active lupus nephritis 7(25.9) 38(17.6) 0.3 Thrombocytopenia 5(18.5) 18(8.3) 0.2 Leukopenia 1(3.7) 6(2.8) 0.6 PIH 10(37.0) 19(8.8) <0.001 Anti-dsDNA antibody positivity 9(33.3) 84(38.9) 0.6 Anti-Ro antibody positivity 16(59.3) 83(38.3) 0.04 Anti-La antibody positivity 3(11.1) 30(13.9) 0.7 LAC positivity 4(14.8) 15(6.9) 0.2 Anticardiolipin antibody positivity 9(25.0) 20(9.7) 0.02 Anti-beta2 GP1 positivity 2(7.4) 19(8.8) 0.8 Hypoalbuminemia 7(25.9) 59(27.3) 0.9 Hypocomplementemia 6(22.2) 50(23.1) 0.9 Hydroxychloroquine 11(40.7) 115(53.) 0.2 Table 5: Univariate analysis of variables associated with adverse maternal outcomes. PIH Characteristics Yes No P value (n = 29) (n = 214) Disease flares during pregnancy 22(75.9) 30(14.0) <0.001 Active lupus nephritis 18(62.1) 27(12.6) <0.001 Thrombocytopenia 9(31.0) 14(6.5) <0.001 Leukopenia 3(10.3) 4(1.9) 0.04 Anti-dsDNA antibody positivity 12(41.4) 81(37.9) 0.7 Anti-Ro antibody positivity 14(48.3) 85(39.7) 0.4 Anti-La antibody positivity 2(6.9) 31(14.5) 0.4 LAC positivity 7(24.1) 12(5.6) 0.003 Anticardiolipin antibody positivity 15(51.7) 14(6.5) <0.001 Anti-beta2 GP1 positivity 1(3.4) 20(9.3) 0.5 Hypoalbuminemia 11(37.9) 55(25.7) 0.2 Hypocomplementemia 14(48.3) 42(19.6) 0.001 Hydroxychloroquine 13(44.8) 113(52.8) 0.4
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|Title Annotation:||Research Article|
|Author:||Chen, Dongying; Lao, Minxi; Zhang, Jianyu; Zhan, Yanfeng; Li, Weinian; Cai, Xiaoyan; Zhan, Zhongping|
|Publication:||Journal of Immunology Research|
|Date:||Jan 1, 2018|
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