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Pregnancy outcomes and risk factors for preeclampsia in dichorionic twin pregnancies after in vitro fertilization: a five-year retrospective study

Abstract

Background

Both in vitro fertilization (IVF) and preeclampsia (PE) were associated with placental dysfunction. Although IVF can increase the incidence of PE, the pregnancy outcomes and risk factors for preeclampsia in dichorionic twin pregnancies conceived via IVF remain unclear. This study aimed to investigate the pregnancy outcomes and the risk factors for preeclampsia in dichorionic twin pregnancies conceived through IVF compared to those conceived after natural conception (NC).

Methods

This retrospective observational study enrolled 181 dichorionic twin pregnancy women with preeclampsia from 2016 to 2020. According to the mode of conception, they were allocated into IVF (n = 117) and NC groups (n = 64). The clinical characteristics of preeclampsia and pregnancy outcomes between the two groups were compared by using Student’s t test, chi-square test, and Fisher’s exact test, and logistic regression models were used to obtain adjusted odds ratios (aOR) with 95% confidence intervals (CI) for risk factors of early-onset preeclampsia.

Results

The incidence of early-onset PE and growth discordance in dichorionic twin pregnancies with PE is significantly higher in IVF-PE group than in NC group (78.60% vs 43.80%, P < 0.001, 11.10% vs 25.00%, P = 0.015). We found that IVF (aOR = 4.635, 95% CI: 2.130–10.084, P < 0.001) and growth discordance (aOR = 3.288; 95% CI: 1.090–9.749, P < 0.05) increased the incidence of early-onset PE.

Conclusions

In preeclamptic dichorionic twin pregnancies, IVF and growth discordance were associated with the increased incidence of early-onset PE. The underlying mechanism for the relationship between IVF and early-onset PE or growth discordance may be placental dysfunction.

Peer Review reports

Background

Preeclampsia (PE), characterized by new-onset maternal hypertension with end organ injury and proteinuria after 20 weeks of gestation, and was divided into early-onset (< 34 weeks) and late-onset preeclampsia (≥34 weeks) according to the time of onset PE [1, 2], especially early-onset preeclampsia has substantial contributions to severe obstetric adverse complications such as postpartum hemorrhage, fetal growth restriction, preterm birth and long-term cardiovascular disease (CVD) in the mothers [3, 4]. It affects approximately 3 to 5% of all pregnancies worldwide [1]. In China, PE accounted for 4.02–5.22% of all pregnancies, of which mild preeclampsia accounted for 15.13–17.00% and severe preeclampsia accounted for 36.30–39.96% [5, 6]. PE is the leading cause of maternal death in industrialized countries, and low-income countries may suffer from a higher burden of maternal death due to lack of access to adequate obstetric care [7, 8].

However, the etiology of this heterogeneous syndrome is not completely understood, although many risk factors for PE, such as advanced maternal age, multiple pregnancy, assisted reproductive technology, pregestational hypertension and diabetes have been identified [9]. There is accumulating evidence that variable degrees of placental malperfusion was the pathogenesis of pre-eclampsia [1, 4]. and in vitro fertilization (IVF) was also strongly associated with ischemic placental disease [10]. In view of the similar placental pathologic mechanisms, IVF has been proved as an independent risk factor for PE [9].

In recent years, with the extensive introduction and application of assisted reproductive technology mainly IVF, the incidence of twin pregnancy has risen sharply. Women who conceived twins through IVF had an increased risk of hypertensive disorders of pregnancy (HDP) and PE [11, 12]. A recent study analyzed the clinical characteristics and pregnancy outcomes of preeclampsia women with twins via IVF, and found no significant differences in rates of severe PE, early-onset PE, as well as mean systolic, or diastolic blood pressure compared to preeclamptic women conceiving twins naturally [13]. But it remained a challenge to obtain conclusive evidence because the sample size was small and their study did not calculate the risk ratio. Moreover, perinatal complications, for example, intrahepatic cholestasis of pregnancy (ICP) and growth discordance, the latter being unique in twin pregnancies, were associated with an increased risk for severe and early-onset PE [14, 15]. Hence, it is more scientific to evaluate the effect of IVF on PE or the early-onset PE when taking these variables into account.

The purpose of this study was to investigate differences in clinical manifestations and pregnancy outcomes in preeclampsia women with twins after IVF compared with natural conception, and further explore the association of IVF with early-onset preeclampsia and the potential risk factors for early-onset preeclampsia after adjustment for confounders.

Methods

Study design and subjects

This retrospective observational study enrolled all the women with twin pregnancies who were monitored prenatally and delivered in the Second Affiliated Hospital of Wenzhou Medical University, a maternal-fetal medicine center with 8000–10,000 births per year, between January 2016 and December 2020. Inclusion criteria were: dichorionic twin pregnancies with preeclampsia and nonsmoking Han Chinese. The exclusion criteria were: (1) preeclampsia in a previous pregnancy, patients complicated with diseases such as chronic hypertension or development of superimposed PE (PE in addition to baseline chronic hypertension), gestational hypertension, pregestational diabetes, kidney disease, autoimmune disease; (2) one fetus with intrauterine death or multifetal pregnancy reduction (MFPR); (3) fetal congenital anomalies and pregnancies resulting in miscarriage; (4) mono-chorionic twins; (5) pregnancies conceived by ovulation induction and intrauterine insemination. Participants in this study were divided into IVF group and the NC group according to the mode of conception.

Ethical statement

The study protocol was reviewed and approved by the medical ethics committee of The Second Affiliated Hospital of Wenzhou Medical University. Women were informed that their records could be used to evaluate medical practices and were allowed to opt out of the study.

Data collection

Data were obtained from medical records and was independently reviewed by an experienced obstetrician, including the mode of conception, demographic features, clinical characteristics of PE, laboratory values, obstetric complications and neonatal outcomes. The clinical indicators of PE included maximum systolic/ diastolic BP, the percentage of systolic BP (blood pressure) ≥ 180 mmHg or diastolic BP ≥ 120 mmHg, 24-hour urine protein, eclampsia, HELLP syndrome, early-onset PE and severe PE, as well as some specific symptoms of severe PE such as pleural effusion and (or) ascites, liver or (and) renal insufficiency, thrombocytopenia and cardiac failure. Maternal outcomes included mode of delivery, the gestational age at delivery, gestational diabetes mellitus (GDM), gestational hypothyroidism, ICP, postpartum hemorrhage (PPH), placental abruption and oligohydramnios. Neonatal outcomes included growth discordance in twins, intrauterine growth retardation, neonatal birth weight, very low birth weight and neonatal asphyxia.

Relative definitions

The definition of PE and eclampsia were based on the current criteria from ACOG (American College of Obstetrics and Gynecology) [9]. PE was subdivided into mild and severe PE according to the signs and symptoms of PE, and early-onset PE and late-onset PE based on onset time of PE [9]. Chorionicity and amnionicity were diagnosed by ultrasound between 7 and 14 weeks’ gestation and confirmed by postnatal placental pathology. Growth discordance between twins was defined as a twin birth weight difference ≥ 20% and calculated by the following equation (large fetal birth weight-small fetal birth weight) / large fetal birth weight × 100%) [16].

GDM was diagnosed by a 75 g oral glucose tolerance test according to International Association of Diabetes in Pregnancy Study Groups (IADPSG) criteria [17]. The diagnose of intrahepatic cholestasis of pregnancy (ICP) was established in presence pruritus and elevated bile acids [18]. Gestational hypothyroidism was diagnosed when TSH levels > 2.5mIU/L in the first trimester or 3.0mIU/L in the second and third trimester [19]. Additional information extracted in detail from the medical records is as follows: preterm birth (birth at < 37.0 week’s gestation) and very preterm birth (birth at < 34 week’s gestation), postpartum hemorrhage (PPH, blood loss more than 1000 ml in 24 hours by Caesarean section or > 500 ml via vaginal delivery), neonatal asphyxia (5-minute Apgar score < 7),, intrauterine growth restriction (IUGR) was diagnosed when only one fetus’s birthweight was below the 10th percentile according to the Chinese twin reference curve [20]. very low birth weight (birth weight < 1500 g), placental abruption (premature separation of a normally implanted placenta before birth).

Statistical analysis

Data analysis was performed using SPSS version 22.0 (SPSS, Statistical Package for the Social Sciences, IBM, NY, USA). The continuous data with normal distributions were presented as mean and standard deviation (SD), while categorical variables were expressed as numbers and percentages (%). Parametric t-tests, Chi-square tests and Fisher’s exact test were used to compare the demographic characteristics in dichorionic twins by IVF and those by NC according to the feature of variables. Logistic regressions were used to model the associations between early-onset PE and late-onset PE to identify potential risk factors. The odds ratio (OR) and 95% confidence interval (CI) after adjustment for potential confounders such as maternal age, body mass index (BMI) at delivery, gravidity, primipara, IVF, growth discordance and ICP were calculated. A 2-tailed P < 0.05 was considered statistically significant.

Results

During the study period from 2016 to 2020, 1922 women with twin pregnancies gave birth in our hospital. Of these, 963 (50.10%) conceived via IVF and 959 (49.90%) conceived via natural conception. The incidence of PE was higher in women who conceived twins after IVF compared with those conceived naturally (OR 1.733; 95%CI, 1.283–2.340). After exclusion of 20 women with monochorionic pregnancies, 181 twin pregnancies with PE remained and constituted the study group: 117 pregnancies resulted from IVF and 64 pregnancies from NC (Fig. 1).

Fig. 1
figure 1

Flowchart of participants in the study

Patient population

The maternal baseline characteristics were analyzed in Table 1.Women in the IVF-PE group were significantly older than those who conceived naturally (30.96 ± 3.88 vs 28.63 ± 3.45; P < 0.001). And the BMI at delivery was higher in IVF-PE group than NC-PE group (29.31 ± 3.69 vs 28.14 ± 3.15; P < 0.05). Also, we found higher rates of primipara, pregestational obesity and low-dose aspirin (LDA) use in IVF-PE group versus NC-PE group (P < 0.05). The groups did not differ significantly in gravidity, pregnancy weight gain, the percentage of advanced age and family history of preeclampsia.

Table 1 Maternal characteristics of IVF-PE and NC-PE group

Clinical characteristics, perinatal complications and outcomes were summarized in Table 2. Compared with preeclamptic dichorionic twin pregnancies after natural conception, the incidence of early-onset PE and growth discordance is significantly higher in women after IVF. Of course, the gestational weeks at diagnose of PE is earlier in IVF-PE group. Other clinical characteristics, including gestational weeks at delivery, hospitalization time, systolic BP, diastolic BP, urine protein, the rate of severe PE, HELLP syndrome, placental abruption and end-organ dysfunction were similar between two groups. No significant difference was found between IVF-PE and NC-PE groups regarding the rate of perinatal complications and outcomes (P > 0.05).

Table 2 Clinical characteristics and pregnancy outcome of IVF-PE and NC-PE group

Compared to naturally conceived pregnancies, the odds ratios of early-onset PE were significantly increased in the IVF group (OR 4.731; 95% CI:2.439–9.180, P < 0.001), with an adjusted odds ratio (aOR) of 4.635 (95% CI: 2.130–10.084, P < 0.001) after adjustments for confounding factors, including ICP and growth discordance. Moreover, the growth discordance appeared to be associated with an increased risk for early-onset PE (aOR = 3.288; 95% CI: 1.109–9.749, P < 0.05) after accounting for confounding factors (Table 3 and Fig. 2).

Table 3 Logistic regression analysis of risk factors for early-onset PE
Fig. 2
figure 2

Forest plot of risk factors for early-onset preeclampsia

Discussion

In this study, we found that PE was more common in dichorionic twin pregnancies via IVF than via natural conception. In addition, we observed a higher rate of early-onset PE and growth discordance in IVF-PE group than NC-PE group. Last but most importantly, in preeclamptic dichorionic twin pregnancies, IVF and growth discordance seem to increase the risk for early-onset PE after adjusting for various confounders.

Our finding that the rate of PE was higher in IVF twin pregnancies supported the previous studies [13, 21]. Although interest in this area is growing rapidly, it’s not clear whether IVF itself has an impact on the occurrence of PE. Several pathophysiological hypotheses have been proposed to explain the relationship between IVF and PE. One of the strongest possibilities is that the IVF process itself is associated with epigenetic changes and gene expression changes in fetal and maternal tissues, and that modifications of the maternal endometrium can cause trophoblast infiltration and placental dysfunction, triggering placental diseases in early pregnancy [22, 23]. These findings also were confirmed in some studies that IVF increase ischemic placental diseases [10].

One of the important evidences is that angiogenic factors produced by the placental tissue are involved in endothelial injury and vasoconstriction, leading to placental dysfunction, such as soluble fms-like tyrosine kinase-1 (sFlt-1) and soluble endoglin serum levels are significantly elevated in patients with early-onset preeclampsia (< 34 weeks) [24]. Furthermore, in the first trimester, serum concentrations of sFlt-1 were higher in twin pregnancies conceived by ART than in spontaneous twin pregnancies [25].

Another evidence was that patients with early-onset PE had higher of alpha fetoprotein (AFP) value at their second trimester biochemical screening [26], and the levels of AFP were significantly higher in IVF pregnancies versus natural conception pregnancies [23, 27]. Early-onset PE arises primarily due to defective placentation during the first few weeks of pregnancy [28]. Therefore, these evidences suggest that IVF itself may play a role in the increased incidence of early-onset PE.

The clinical manifestations of PE is highly variable among individuals. Our study found that twin pregnancies via IVFwere more likely to develop an early-onset PE and this risk remained after adjustment for confounders Interestingly, in spite of the increasing occurrence of early onset PE, the gestational age at delivery and the rate of preterm were not significantly different between IVF-PE group and NC-PE group. One potential explanation was that the enhanced awareness of antenatal care among the IVF pregnancies, as well as great attention from obstetricians, may play a protective role in these pregnancy outcomes.

Growth discordance, defined as a difference of 20% in the birth weights between twins, is a unique complication of multiple pregnancies. In dichorionic twins, each fetus has its own placenta and vascular anastomoses, and the growth curve is theoretically similar to that of a singleton fetus before 32 weeks [29]. But a large, prospective, multicenter study reported that the rate of the placental abnormalities in both birthweight discordance and small for gestational age were significant higher in dichorionic twins versus monochorionic twins [30]. IVF procedure is associated with placental abnormalities [31]. This may account for our findings that the proportion of growth discordance in dichorionic twin pregnancies was higher in the IVF-PE group, which is corroborate with previous data [32]. Another plausible explanation for this result is that IVF pregnancies appear to have a higher proportion of genetic dissimilarity and different genetic growth potentials, resulting in the discordant growth [33].

On the other hand, growth discordance is associated with a high risk for preeclampsia in dichorionic twin pregnancy [15, 34]. Sharing the same pathophysiologic mechanism may explain the interaction between preeclampsia and growth discordance.. Placental ischemia/hypoxia, which coexist either in preeclampsia or growth discordance women, appears to be responsible for this association [24]. This association is further supported by our findings that growth discordance is strongly associated with early-onset PE after adjusting for confounders.

Furthermore, common umbilical cord abnormalities, such as velamentous cord, may mediate the association between growth discordance and PE in twin pregnancies. Velamentous cord insertions, a major indicator of growth discordance, has been reported as a risk factor for PE [35]. In addition, advanced maternal age was associated with an increased incidence of severe growth discordance and PE [9, 36], which may be another risk factor. Based on these findings, we speculate that the relationship between growth inconsistency and PE may not be caused by a single cause, but by the coexistence of multiple factors.

PE and IVF share multiple risk factors such as advanced maternal age, nulliparity, and obesity, which were indeed significantly different between the IVF group and the spontaneous group in previous studies [12, 22]. Older mothers or obese women may be at risk for endothelial dysfunction, making them more susceptible to pre-eclampsia, and these women often conceive the baby via IVF.. Likewise, our data showed that in twin pregnancies with PE, IVF was associated with older maternal age, higher BMI at delivery, higher rates of primipara and pregestational obesity, and higher use of low-dose aspirin (LDA) compared with natural conception. But advanced maternal age, obesity and primipara were not risk factors for early-onset preeclampsia. The similar results were found in the previous studies [37, 38].

In addition, low-dose aspirin (LDA) can effectively reduce the incidence of severe PE [39]. The underlying mechanism is that LDA can improve spiral artery blood flow, promote trophoblast migration and subsequent spiral artery remodeling, thereby preventing placental defects. Nevertheless, once preeclampsia has developed, aspirin does not seem to change the course of the disease because the insufficient placenta has been formed [40]. National guidelines also recommend commencing aspirin as soon as possible after the end of early pregnancy to prevent preeclampsia [9]. However, our research indicated that despite higher aspirin use in the IVF-PE group, there was no difference in the incidence of severe PE compared to the NC-PE group. Aspirin use appeared to have no benefit in reducing the incidence of severe PE.It is difficult to explain. We proposed a hypotheses that preconception or early administration of low-dose aspirin may not ameliorate the placental dysfunction which is closely associated with the early-onset PE. In addition, it has also been proposed that the administration of low-dose aspirin at < 11 weeks’ gestation in high-risk women, including those pregnancies conceived via IVF, does not reduce the risk of preeclampsia, gestational hypertension and any hypertensive disorder of pregnancy [41]. It has been believed that IVF, at least in part, was responsible for increasing the incidence of severe preeclampsia [42, 43]. Further research is needed to clarify this mechanism.

The strengths of the present study is that we focused on the dichorionic twin pregnancies in order to reduce the confounding, as chorionicity was an independent risk factor for PE and early-onset PE [44], and we excluded the confounders such as pre-gestational diseases, immune system disorders, and intrauterine treatment. Futhermore, we assessed risk factors for early-onset preeclampsia, especially after adjusting for confounding variables such as baseline characteristics and pregnancy complications.

The limitations of our study is a single-center, retrospective and small sample size analysis, which limites the generalizability/power of findings. Large prospective trials and the long term follow up are needed to investigate the effect of IVF on the pregnancy outcomes and the risk factors of preeclampsia in dichorionic twin pregnancies.

Conclusions

Overall, in dichorionic twin pregnancies with pre-eclampsia, IVF increase the incidence of early-onset PE and act as an isolated risk factor. Furthermore, growth discordance appears to be associated with the higher incidence of early-onset PE. Placental abnormalities maybe responsible for this association. Of course, due to the co-existence of individual variability and confounding bias associated with pre-eclampsia, it warrants further investigation.

Availability of data and materials

The datasets used and/or analyzed during the study are available from the corresponding author upon reasonable request.

Abbreviations

IVF:

In vitro fertilization

PE:

Preeclampsia

NC:

Natural conception

aOR:

Adjusted odds ratios

CI:

Confidence intervals

CVD:

Cardiovascular disease

HDP:

Hypertensive disorders of pregnancy

ICP:

Intrahepatic cholestasis of pregnancy

MFPR:

Multifetal pregnancy reduction

BP:

Blood pressure

HELLP:

Hemolysis, elevated liver enzymes, and low platelet

GDM:

Gestational diabetes mellitus

PPH:

Postpartum hemorrhage

ACOG:

American College of Obstetrics and Gynecology

SPSS:

Statistical Package for the Social Sciences

SD:

Standard deviation

OR:

Odds ratios

BMI:

Body mass index

LDA:

Low-dose aspirin

sFlt-1:

Soluble fms-like tyrosine kinase-1

References

  1. Chappell LC, Cluver CA, Kingdom J, Tong S. Pre-eclampsia. Lancet. 2021;398(10297):341–54. https://doi.org/10.1016/s0140-6736(20)32335-7.

    Article  CAS  PubMed  Google Scholar 

  2. Tranquilli AL, Brown MA, Zeeman GG, Dekker G, Sibai BM. The definition of severe and early-onset preeclampsia. Statements from the International Society for the Study of hypertension in pregnancy (ISSHP). Pregnancy Hypertens. 2013;3(1):44–7. https://doi.org/10.1016/j.preghy.2012.11.001.

    Article  PubMed  Google Scholar 

  3. Kuklina EV, Ayala C, Callaghan WM. Hypertensive disorders and severe obstetric morbidity in the United States. Obstet Gynecol. 2009;113(6):1299–306. https://doi.org/10.1097/AOG.0b013e3181a45b25.

    Article  PubMed  Google Scholar 

  4. Rana S, Lemoine E, Granger JP, Karumanchi SA. Preeclampsia: pathophysiology, challenges, and perspectives. Circ Res. 2019;124(7):1094–112. https://doi.org/10.1161/circresaha.118.313276.

    Article  CAS  PubMed  Google Scholar 

  5. Yang Y, Ray IL, Zhu J, Zhang J, Reilly M. Preeclampsia prevalence, risk factors, and pregnancy outcomes in Sweden and China. JAMA Netw Open. 2021;4(5):e218401. https://doi.org/10.1001/jamanetworkopen.2021.8401.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Ye C, Ruan Y, Zou L, Li G, Li C, Chen Y, et al. The 2011 survey on hypertensive disorders of pregnancy (HDP) in China: prevalence, risk factors, complications, pregnancy and perinatal outcomes. PLoS One. 2014;9(6):e100180. https://doi.org/10.1371/journal.pone.0100180.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Hutcheon JA, Lisonkova S, Joseph KS. Epidemiology of pre-eclampsia and the other hypertensive disorders of pregnancy, Best. Pract Res Clin Obstet Gynaeco. 2011;25(4):391–403. https://doi.org/10.1016/j.bpobgyn.2011.01.006.

    Article  Google Scholar 

  8. Khan KS, Wojdyla D, Say L, Gülmezoglu A, Look P. WHO analysis of causes of maternal death: a systematic review. Lancet. 2006;367(9516):1066–74. https://doi.org/10.1016/S0140-6736(06)68397-9.

    Article  PubMed  Google Scholar 

  9. Gestational Hypertension and Preeclampsia. ACOG practice bulletin summary, number 222. Obstet Gynecol. 2020;135(6):1492–5. https://doi.org/10.1097/aog.0000000000003892.

    Article  Google Scholar 

  10. Johnson KM, Hacker MR, Thornton K, Young BC, Modest AM. Association between in vitro fertilization and ischemic placental disease by gestational age. Fertil Steril. 2020;114(3):579–86. https://doi.org/10.1016/j.fertnstert.2020.04.029.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Barda G, Gluck O, Mizrachi Y, Bar J. A comparison of maternal and perinatal outcome between in vitro fertilization and spontaneous dichorionic-diamniotic twin pregnancies. J Matern Fetal Neonatal Med. 2017;30(24):2974–7. https://doi.org/10.1080/14767058.2016.1270934.

    Article  PubMed  Google Scholar 

  12. Wang Y, Shi H, Chen L, Zheng D, Qiao J. Absolute risk of adverse obstetric outcomes among twin pregnancies after in vitro fertilization by maternal age. JAMA Netw Open. 2021;4(9):e2123634. https://doi.org/10.1001/jamanetworkopen.2021.23634.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Gui J, Ling ZH, Hou XJ, Fan YR, Xie KP, Shen R. In vitro fertilization is associated with the onset and progression of preeclampsia. Placenta. 2020;89:50–7. https://doi.org/10.1016/j.placenta.2019.09.011.

    Article  PubMed  Google Scholar 

  14. Mor M, Shmueli A, Krispin E, Bardin R, Sneh-Arbib O, Braun M, et al. Intrahepatic cholestasis of pregnancy as a risk factor for preeclampsia. Arch Gynecol Obstet. 2020;301(2):655–64. https://doi.org/10.1007/s00404-020-05456-y.

    Article  CAS  PubMed  Google Scholar 

  15. Qiao P, Zhao Y, Jiang X, Xu CL, Yang YY, Bao YR, et al. Impact of Growth Discordance in Twins on Preeclampsia: based on chorionicity. Am J Obstet Gynecol. 2020;223(4):572.e571–8. https://doi.org/10.1016/j.ajog.2020.03.024.

    Article  Google Scholar 

  16. Jahanfar S, Jacqueline JH, Jaafar SH, Abraha L, Noura M, Ross CR, et al. Ultrasound for diagnosis of birth weight discordance in twin pregnancies. Cochrane Database Syst Rev. 2021;3(3):CD012553. https://doi.org/10.1002/14651858.CD012553.pub2.

    Article  PubMed  Google Scholar 

  17. International association of diabetes and pregnancy study groups recommendations on the diagnosis and classification of hyperglycemia in pregnancy. Diabetes Care. 2010;33(3):676–82. https://doi.org/10.2337/dc09-1848.

  18. Wood AM, Livingston EG, Hughes BL, Kuller JA. Intrahepatic cholestasis of pregnancy: a review of diagnosis and management. Obstet Gynecol Surv. 2018;73(2):103–9. https://doi.org/10.1097/ogx.0000000000000524.

    Article  PubMed  Google Scholar 

  19. Stagnaro-Green A, Abalovich M, Alexander E, Azizi F, Mestman J, Negro R, et al. Guidelines of the American Thyroid Association for the diagnosis and management of thyroid disease during pregnancy and postpartum. Thyroid. 2011;21(10):1081–125. https://doi.org/10.1089/thy.2011.0087.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Dai L, Deng CF, Li YH, Yi L, Li XH, Mu Y, et al. Population-based birth weight reference percentiles for Chinese twins. Ann Med. 2017;49(6):470–8. https://doi.org/10.1080/07853890.2017.1294258.

    Article  PubMed  Google Scholar 

  21. Okby R, Harlev A, Sacks KN, Sergienko R, Sheiner E. Preeclampsia acts differently in in vitro fertilization versus spontaneous twins. Arch Gynecol Obstet. 2018;297(3):653–8. https://doi.org/10.1007/s00404-017-4635-y.

    Article  PubMed  Google Scholar 

  22. Senapati S, Wang F, Ord T, Coutifaris C, Feng R, Mainigi M. Superovulation alters the expression of endometrial genes critical to tissue remodeling and placentation. J Assist Reprod Genet. 2018;35(10):1799–808. https://doi.org/10.1007/s10815-018-1244-z.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Zhao L, Sun L, Zheng X, Liu J, Wang Y. Invitro fertilization and embryo transfer alter human placental function through trophoblasts in early pregnancy. Mol Med Rep. 2020;21(4):1897–909. https://doi.org/10.3892/mmr.2020.10971.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Tobinaga CM, Torloni MR, Gueuvoghlanian-Silva BY, Pendeloski K, Akita PA, Sass N, et al. Angiogenic factors and uterine Doppler velocimetry in early- and late-onset preeclampsia. Acta Obstet Gynecol Scand. 2014;93(5):469–76. https://doi.org/10.1111/aogs.12366.

    Article  CAS  PubMed  Google Scholar 

  25. Sánchez O, Llurba E, Marsal G, Domínguez C, Aulesa C, Sánchez-Durán MA, et al. First trimester serum angiogenic/anti-angiogenic status in twin pregnancies: relationship with assisted reproduction technology. Hum Reprod. 2012;27(2):358–65. https://doi.org/10.1093/humrep/der394.

    Article  CAS  PubMed  Google Scholar 

  26. Omer W, Yael Y, Tal W, Man EG, Tal BS. Preeclampsia: risk factors and neonatal outcomes associated with early- versus late-onset disease. J Matern Fetal Neonatal Med. 2018:1–11. https://doi.org/10.1080/14767058.2018.1500551.

  27. Maymon R, Shulman A. Serial first- and second-trimester Down's syndrome screening tests among IVF-versus naturally-conceived singletons. Hum Reprod. 2002;17(4):1081–5. https://doi.org/10.1093/humrep/17.4.1081 Update.

    Article  CAS  PubMed  Google Scholar 

  28. Burton GH, Redman CW, Roberts JM, Moffett A. Pre-eclampsia: pathophysiology and clinical implications. BMJ. 2019;366:l2381. https://doi.org/10.1136/bmj.l2381.

    Article  PubMed  Google Scholar 

  29. Loos RJF, Derom C, Derom R, Vlietinck R. Determinants of birthweight and intrauterine growth in liveborn twins. Paediatr Perinat Epidemiol. 2005;19(s1):15–22. https://doi.org/10.1111/j.1365-3016.2005.00611.x.

    Article  PubMed  Google Scholar 

  30. Kent EM, Breathnach FM, Gillan JE, Mcauliffe FM, Geary MP, Daly S, et al. Placental pathology, birthweight discordance, and growth restriction in twin pregnancy: results of the ESPRiT study. Am J Obstet Gynecol. 2012;207(3):220.e221–5. https://doi.org/10.1016/j.ajog.2012.06.022.

    Article  Google Scholar 

  31. Korb D, Seco TSA, Ray CL, Santulli P, Goffinet F, Deneux-Tharaux C. Increased risk of severe maternal morbidity in women with twin pregnancies resulting from oocyte donation. Hum Reprod. 2020;35(8):1922–32. https://doi.org/10.1093/humrep/deaa108.

    Article  PubMed  Google Scholar 

  32. Ben-Ami I, Sheena L, Svirsky R, Odeh M, Rosen H, Melcer Y, et al. The association of crown-rump length discrepancy with birthweight discordance in spontaneous versus assisted conception dichorionic twins. Prenat Diagn. 2014;34(8):748–52. https://doi.org/10.1002/pd.4359.

    Article  PubMed  Google Scholar 

  33. Anja P, Anne L, Steen R, Lone S, Jens LR, Gorm G, et al. Neonatal outcome in a Danish national cohort of 3438 IVF/ICSI and 10,362 non-IVF/ICSI twins born between 1995 and 2000. Hum Reprod Update. 2004;19(2):435–41. https://doi.org/10.1093/humrep/deh063.

    Article  Google Scholar 

  34. Lin D, Luo BC, Chen G, Fan D, Liu Z. The association of hypertensive disorders of pregnancy with small for gestational age and intertwin birthweight discordance. J Clin Hypertens (Greenwich). 2021;23(7):1354–62. https://doi.org/10.1111/jch.14257.

    Article  Google Scholar 

  35. Olaya-C M, Salcedo-Betancourt J, Galvis SH, Ortiz AM, Gutierrez S, et al. Umbilical cord and preeclampsia. J Neonatal Perinatal Med. 2016;9(1):49. https://doi.org/10.3233/NPM-16814108.

    Article  CAS  PubMed  Google Scholar 

  36. Azcorra H, Rodriguez L, Méndez N. The association between maternal and fetal factors with birth weight discordance in twins from Yucatan, Mexico. Ann Hum Biol. 2021;48(3):1–13. https://doi.org/10.1080/03014460.2021.1921847.

    Article  Google Scholar 

  37. Mbah AK, Kornosky JL, Kristensen S, August EM, Alio AP, Marty PJ, et al. Super-obesity and risk for early and late pre-eclampsia %J BJOG: an international journal of Obstetrics & Gynaecology. BJOG. 2010;117(8). https://doi.org/10.1111/j.1471-0528.2010.02593.x.

  38. Nguefack CT, Ako MA, Dzudie AT, Nana TN, Tolefack PN, Mboudou E. Comparison of materno-fetal predictors and short-term outcomes between early and late onset pre-eclampsia in the low-income setting of Douala, Cameroon. Int J Gynaecol Obstet. 2018;142(2):228–34. https://doi.org/10.1002/ijgo.12531.

    Article  PubMed  Google Scholar 

  39. Park F, Russo K, Williams P, Pelosi M, Puddephatt R, Walter M, et al. Prediction and prevention of early-onset pre-eclampsia: impact of aspirin after first-trimester screening. Ultrasound Obstet Gynecol. 2015;46(4):419–23. https://doi.org/10.1002/uog.14819.

    Article  CAS  PubMed  Google Scholar 

  40. Sibai BM, Caritis SN, Thom E, Klebanoff M, Mcnellis D, Rocco L, et al. Prevention of preeclampsia with low-dose aspirin in healthy, nulliparous pregnant women. The National Institute of Child Health and Human Development Network of Maternal-Fetal Medicine Units. N Engl J Med. 1993;46(17):1213–8. https://doi.org/10.1056/NEJM199310213291701.

    Article  Google Scholar 

  41. Chaemsaithong P, Cuenca-Gomez D, Plana MN, Gil MM, Poon LC. Does low-dose aspirin initiated before 11 weeks' gestation reduce the rate of preeclampsia? Am J Obstet Gynecol. 2020;222(5):437–50. https://doi.org/10.1016/j.ajog.2019.08.047.

    Article  CAS  PubMed  Google Scholar 

  42. Lynch A, McDuffie R, Murphy J, Faber K, Orleans M. Preeclampsia in multiple gestation: the role of assisted reproductive technologies. Obstet Gynecol. 2002;99(3):445–51. https://doi.org/10.1016/s0029-7844(01)01733-1.

    Article  PubMed  Google Scholar 

  43. Erez O, Vardi IS, Hallak M, Hershkovitz R, Dukler D, Mazor M. Preeclampsia in twin gestations: association with IVF treatments, parity and maternal age. J Matern Fetal Neonatal Med. 2006;19(3):141–6. https://doi.org/10.1080/14767050500246045.

    Article  PubMed  Google Scholar 

  44. Bartnik P, Kosinska-Kaczynska K, Kacperczyk J, Ananicz W, Szymusik I. Twin Chorionicity and the risk of hypertensive disorders: gestational hypertension and pre-eclampsia. Twin Res Hum Genet. 2016;19(4):377–82. https://doi.org/10.1017/thg.2016.17.

    Article  PubMed  Google Scholar 

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Acknowledgements

Thanks are due to Chengya Lin for assistance with data management.

Funding

This study did not receive any external funding.

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Contributions

Fen Dai was the principal investigator and drafted the manuscript and collected data.. Fen Dai and Shuangjia Pan contributed equally to this work. Ying Hua and Shuangjia Pan contributed to data analysis and manuscript revision. Yehui Lan, Hongying Tan, contributed to data management and manuscript revision. Jinman Li analyzed the data and revised the article. Ying Hua supervised the study. All authors have read and approved the final manuscript. All authors have contributed to the design of the study, drafting the paper and revising it critically for important intellectual content and approved it for publication.

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Correspondence to Ying Hua.

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The study protocol was reviewed and approved by the medical ethics committee of The Second Affiliated Hospital of Wenzhou Medical University (Approval No.2022-K-39-01). The requirement for written informed consent was waived by the medical ethics committee of The Second Affiliated Hospital of Wenzhou Medical University. All methods were performed in accordance with the relevant guidelines and regulations.

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Dai, F., Pan, S., Lan, Y. et al. Pregnancy outcomes and risk factors for preeclampsia in dichorionic twin pregnancies after in vitro fertilization: a five-year retrospective study. BMC Pregnancy Childbirth 22, 830 (2022). https://doi.org/10.1186/s12884-022-05184-y

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