Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

Maternal HBsAg carriers and pregnancy outcomes: a retrospective cohort analysis of 85,190 pregnancies

BMC Pregnancy and Childbirth volume 20, Article number: 724 (2020) Cite this article

A Correction to this article was published on 12 February 2021

This article has been updated

Abstract

Background

Nowadays, a positive HBV carrier status is common among pregnant women, especially in endemic areas (such as China), little is known about the impact of maternal HBV infection on the risk of adverse pregnancy outcomes. Pregnant women with HBV infection often develop obstetric complications, such as pregnancy-induced hypertension (PIH) syndrome, postpartum hemorrhage, and gestational diabetes mellitus (GDM), and their infants often exhibit neonatal complications.

Methods

This study undertook a retrospective cohort analysis to explore the association of HBV carrier status with adverse pregnancy outcomes. A cohort of 85,190 women including 9699 HBsAg-positive and 73,076 HBsAg-negative pregnancies was retrospectively analyzed.

Results

It’s found that HBsAg-positive pregnancies may result in higher risk of various maternal outcomes such as ICP (OR 3.4,95%CI 2.80 to 4.13), postpartum hemorrhage (OR 1.16,95%CI 1.00 to 1.34). Interestingly, there was a decreased risk of Preeclampsia (OR 0.91,95%CI 0.87 to 0.96), premature rupture of membrane (OR 0.91,95%CI 0.87 to 0.96) and gestational hypertension (OR 0.828,95%CI 0.701 to 0.978). And in vaginal delivery subgroup analysis, It’s found that the HBsAg-positive group had a higher risk of placental abruption (OR, 1.44; 95% CI, 1.16–1.79).

Conclusions

The present results suggest that compared with HBV positive pregnancies were more likely to be ICP and postpartum hemorrhage. HBV-positive pregnant women underwent vaginal delivery were more likely to have placental abruption and premature birth compared with HBV-negative women. Obstetricians should be aware of ICP, postpartum hemorrhage, placental abruption and premature birth in HBV-positive pregnant women.

Peer Review reports

Background

Chronic hepatitis B virus (HBV) infection is an important global health problem. Up to 600,000 of the 350–400 million carriers of HBV worldwide die annually of chronic hepatitis B (CHB)-related disease [1]. Women of childbearing age who are infected with HBV tend to be in the immune-tolerant or immune-active phases of chronic HBV infection and have high levels of viremia. The prevalence of HBV infection among these women may be as high as 0.4% in the USA [2] and 2–8% in China [3,4,5]. Most pregnant women with HBV infection are chronic carriers of the virus, which can be detected by the presence of the hepatitis B surface antigen (HBsAg) in serum.

Although a positive HBV carrier status is common among pregnant women, especially in endemic areas (such as China), little is known about the impact of maternal HBV infection on the risk of adverse pregnancy outcomes. Pregnant women with HBV infection often develop obstetric complications, such as pregnancy-induced hypertension (PIH) syndrome, postpartum hemorrhage, and gestational diabetes mellitus (GDM), and their infants often exhibit neonatal complications. A higher prevalence of preterm delivery in women with chronic HBV infection was reported in several epidemiological studies [6, 7]. intrahepatic cholestasis of pregnancy (ICP) is a pregnancy-specific liver disorder that typically commences in the late-second or third trimester and resolves within 48 h after delivery. Several studies have mentioned an association between ICP and hepatitis C virus (HCV) infection [8]. Locatelli et al. found that women with HCV antibody positivity had a significantly increased incidence of cholestasis compared with those without HCV antibodies (15.9% versus 0.8%, P < 0.001) [9]. HBV infection may affect trophoblast cells, which play an important role in placental development [10, 11]. Two recent studies reported an independent association between chronic HBV infection and GDM [12, 13], which is in disagreement with our results. Therefore, additional studies are required to elucidate this issue. Preeclampsia (which is characterized by multilevel maternal endothelial dysfunction) may be triggered by or result from an imbalance between angiogenic, antiangiogenic, and proangiogenic factors, e.g., vascular endothelial growth factor [8, 14]. Ahmed et al. reported that women who were seropositive for HBsAg had a higher risk of preeclampsia compared with women who were seronegative for HBsAg [15]. Conversely, KLB R et al. found no association between maternal HBV infection and preeclampsia [6, 16]. Lao et al. reported that the incidence of gestational diabetes was significantly increased in the HBsAg-positive group.

Moreover, the relationship between HBsAg-positive and adverse pregnancy outcomes remains controversial. Most published studies used data from countries where the prevalence of HBsAg positivity during pregnancy was low. Besides, the outcomes may not be applicable to higher risk countries and regions. Therefore, we performed this retrospective hospital-based cohort study to explore the association between HBV carrier status and adverse pregnancy outcomes.

Method

Patients and grouping

All women who were followed at the Fujian Provincial Maternity and Children’s Hospital, China, between July 2009 and December 2018 for singleton pregnancies carried to 24 completed weeks of gestation or beyond were included in this retrospective and consecutive cohort study. A total of 85,190 pregnant women were reviewed and screened, of these, 2415 subjects were excluded: due to unconscious or severely ill status, learning difficulties or serious mental illness, major fetal abnormality identified at the time that scanning. Finally, The cohort included 85,190 women: 9699 HBsAg-positive and 73,076 HBsAg-negative pregnancies. HBV infection was defined as HBsAg seropositivity. The study group consisted of all pregnancies with maternal HBV infection, as demonstrated by a positive HBsAg status on antenatal screening, while the control group consisted of the remainder of the obstetric population. The study was legally approved by the institutional ethics committee of Fujian Provincial Maternity and Children’s Hospital and conducted in accord with the guidelines of the Declaration of Helsinki, and the rights of all participants were protected. Fig. 1 shows a flow chart of study from total results to the final inclusion or exclusion. (Fig. 1).

Fig. 1
figure 1

Flow chart of study from total results to the final inclusion or exclusion

Full size image

Inclusion and exclusion criteria

The inclusion criteria of this trial were as follows: age ≥ 18 years, singleton pregnancy, and maternal HBV infection (as reflected by a positive HBsAg status on antenatal screening). The exclusion criteria were as follows: unconsciousness or a severely ill status, learning difficulties or serious mental illness, and major fetal abnormalities identified at the time of scanning but we were not excluded the subjects who were vaccinated with Hepatitis B vaccine so it can lead to HbsAg positive for approximately 14 days after the vaccine has been given.

Outcome measurements

We reviewed the records of 82,775 women who had delivered their infants during the study period and recorded the following parameters: pregnancy and delivery characteristics, including gestational age (years; determined from the fetal crown–rump length), gestational age (weeks), gravidity, parity, mode of delivery, neonatal weight, placental weight, and amount of bleeding; and pregnancy outcomes and maternal complications, including gestational hypertension, premature rupture of membranes, postpartum hemorrhage, GDM, intrahepatic cholestasis of pregnancy (ICP), placental abruption, premature birth, HELLP syndrome, abortion, and small-for-gestational-age fetal status.

The diagnostic criteria for GDM were based on the National Health and Family Planning Commission of the People’s Republic of China guidelines. When the 75 g OGTT results met or exceeded the following plasma glucose levels at the noted time-points, the women were diagnosed with GDM: 0 h, 5.1 mmol/L; 1 h, 10.0 mmol/L; and 2 h, 8.5 mmol/L. A 75 g OGTT was performed between the 24th and 28th weeks of gestation for all pregnant women who had not previously been diagnosed with diabetes. Hypertension in pregnancy was defined as a systolic blood pressure of at least 140 mmHg or a diastolic blood pressure of at least 90 mmHg. Using semi-quantitative urine dipsticks, proteinuria of at least 1+ in the presence of hypertension without evidence of urinary tract infection was considered significant. HDPs were classified as: gestational hypertension, chronic hypertension, pre-eclampsia superimposed on chronic hypertension, pre-eclampsia or eclampsia. The diagnosis of PPROM was confirmed by well-established clinical and/or biological diagnostic procedures: the visualization of amniotic fluid passing from the cervical canal and pooling in the vagina, a basic pH test of vaginal fluid, or arborization (ferning) of dried vaginal fluid identified under microscopic evaluation. ICP diagnosis was carried out based on new onset pruritus with a total bile acid level > 10 μmol/l without any additional liver diseases. Small-for-gestational age was defined as neonatal birthweight below the 10th percentile for gestational age. HELLP syndrome was specified by hemolysis (serum LDH > 600 IU/L; bilirubin > 1.2 mg/dL; presence of schistocytes in peripheral blood), elevated liver enzymes (serum ALT and/or AST > 70 IU/L) and thrombocytopenia (platelet count < 100,000/mm3). The diagnosis of placental abruption was based on clinical findings of abdominal pain, vaginal bleeding, uterine contractions, fetal distress and vital sign abnormalities. We excluded women with multiple gestation and gestational age less than 20 weeks.

Statistical analyses

SPSS 19.0 (SPSS Inc., Chicago, IL) was used to perform the statistical analyses. Continuous data (e.g. age and operating time) are presented as means  ±   standard deviation (SD) and were analyzed using an independent t-test or a nonparametric test (Kruskal–Wallis test). Dichotomous data (e.g. sex and age group) are presented as percentages and were compared between the two groups using the χ2 test or a nonparametric test (Fisher’s exact test). Significance was set at P   < 0 .05. In the outcome analyses, relative risks and absolute risk differences with 95% confidence intervals (95% CI) were calculated for dichotomous outcomes using Fisher’s exact test.

Results

Baseline characteristics

The patient and pregnancy characteristics are presented in Table 1. Women with singleton pregnancies underwent routine examinations at their hospital. The patient characteristics included: maternal age; cigarette smoking during pregnancy; history of chronic hypertension or diabetes mellitus; family history of PE (Preeclampsia) in the mother of the patient; obstetric history, including parity (parous or nulliparous in the case of presence/absence of previous deliveries at or after 24 weeks of gestation, respectively); previous pregnancy with PE; gestational age at delivery; and the baby’s birthweight. There were no differences in mean maternal age or gestational age between the study group and control group. In contrast, significant differences were found for gravidity (the proportion of nulliparous women was higher in the control group (34.26% versus 38.42%)). However, no significant differences in parity, mode of delivery, and birth weight were found between the two groups. The routes of HBV transmission include sexual contact, parenteral drug use with shared paraphernalia, tattoos, piercings, acupuncture, and needlestick injuries in the health-care setting. In countries where HBV is endemic, most infections are acquired through perinatal exposure.

Table 1 Baseline characteristics of the included patientsa
Full size table

Maternal HBV-positive

Table 2 shows that HBV-positive during pregnancy increased the risk of some maternal outcomes, including ICP (OR, 3.4; 95% CI, 2.80–4.13), and postpartum hemorrhage (OR, 1.16; 95% CI, 1.00–1.34). Interestingly, a decreased risk of preeclampsia (OR, 0.91; 95% CI, 0.87–0.96), premature rupture of membranes (OR, 0.91; 95% CI, 0.87–0.96), and gestational hypertension (OR, 0.828; 95% CI, 0.701–0.978) was observed in this group. There were no significant differences between the two groups regarding placental abruption (OR, 1.17; 95% CI, 0.98–1.4), preterm labor (OR, 1.17; 95% CI, 0.98–1.40), small-for-gestational-age status (OR, 0.93; 95% CI, 0.84–1.04), GDM (OR, 0.8; 95% CI, 0.67–0.96), and HELLP syndrome (OR, 0.78; 95% CI, 0.31–1.97).

Table 2 The association between HBV positive pregnancies and outcomes
Full size table

The association between HBV positive pregnancies and pregnancy outcomes of vaginal delivery

As shown in Table 3, the HBsAg-positive group had a higher risk of postpartum hemorrhage (OR, 1.19; 95% CI, 1.01–1.39), ICP (OR, 3.73; 95% CI, 2.84–4.90), placental abruption (OR, 1.44; 95% CI, 1.16–1.79), and premature birth (OR, 1.44; 95% CI, 1.16–1.79). A significant difference in ICP was also detected between the two groups. The incidence of premature rupture of membranes was significantly lower in HBV carriers (OR, 0.88; 95% CI, 0.83–0.93), suggesting that infection with HBV protects against this outcome. However, small-for-gestational-age status (OR, 1.12; 95% CI, 0.98–1.28), gestational hypertension (OR, 0.83; 95% CI, 0.67–1.04), HELLP syndrome (OR, 1.27; 95% CI, 0.15–10.57), and gestational diabetes (OR, 1.07; 95% CI, 0.99–1.14) were not significantly different between the two groups.

Table 3 Gestational complications in Vaginal delivery
Full size table

The association between HBV positive pregnancies and pregnancy outcomes by cesarean section

The results pertaining to the group of women who underwent cesarean section are listed in Table 4. Similar to that observed for the vaginal delivery group, the incidence of ICP in the HBsAg-positive group was higher than that in the HBsAg-negative group (OR, 3.06; 95% CI, 2.31–4.04). In contrast, the risk of the small-for-gestational-age outcome was significantly different, and the incidence of cesarean section was higher in the HBsAg-positive group compared with the HBsAg-negative group (OR, 0.68; 95% CI, 0.56–0.82). Moreover, there were no significant differences in premature rupture of membranes (OR, 0.91; 95% CI, 0.82–1.01), gestational hypertension (OR, 0.82; 95% CI, 0.64–1.05), HELLP syndrome (OR, 0.70; 95% CI, 0.25–1.95), GDM (OR, 1.03; 95% CI, 0.94–1.14), placental abruption (OR, 0.78; 95% CI, 0.56–1.08), preterm labor (OR, 0.91; 95% CI, 0.82–1.01), and postpartum hemorrhage (OR, 1.08; 95% CI, 0.77–1.50) between the groups.

Table 4 Gestational complications in Cesarean section
Full size table

Discussion

Our study revealed an association between chronic HBV infection and an increased risk of placental abruption, preterm labor, ICP, GDM, SGA and postpartum hemorrhage. Moreover, we detected a decreased risk of premature rupture of membranes in women who underwent vaginal delivery, and of PIH regardless of delivery mode. However, no significant differences were observed between the group with chronic HBV infection and the control group regarding the prevalence of GDM, HELLP, and small-for-gestational-age status.

A higher prevalence of preterm delivery in women with chronic HBV infection was reported in several epidemiological studies [6, 7], which is consistent with our results. Inflammation is one of the most common risk factors for preterm labor [17, 18]. Therefore, it is plausible to hypothesize that low-grade inflammation induced by chronic HBV infection is partially responsible for the increased risk of preterm labor observed in these studies. Local and systemic inflammation caused by HBV infection may play an independent etiological role in preterm birth. According to previous studies, a large proportion of preterm births are caused by overproduction of proinflammatory cytokines [19]. The liver is a critical organ for human health, especially because it regulates inflammation by controlling local and systemic inflammatory responses via different molecular mechanisms [20]. However, chronic HBV infection can cause liver dysfunction, thus affecting inflammatory regulation. Another explanation for the association between maternal HBV infection and preterm birth is the accumulation of viral DNA in the placenta and in the trophoblast cells that initiate the placental inflammatory response, which is a known contributor to preterm birth [21]. Therefore, further research is needed to elucidate the mechanism underlying the association between preterm birth and HBV infection.

ICP is a pregnancy-specific liver disorder that typically commences in the late-second or third trimester and resolves within 48 h after delivery. We found that pregnant women with HBsAg positivity exhibited an increased risk of ICP compared with pregnant women who were HBsAg negative (0.46% versus 1.54%, P < 0.05). Therefore, HBV infection may also be related to an increased incidence of ICP, but further research of the underlying mechanism is warranted. Elevated estrogen levels are a possible cause of ICP. Because the liver is the main organ for estrogen metabolism, the dysregulation of liver function due to HBV infection may lead to metabolic disorders of estrogen. This is a possible cause of HBV-infection-induced ICP. Moreover, the risk of postpartum hemorrhage was increased in the HBV-infected group compared with the control group, which is a plausible outcome if liver function is affected.

We noticed that chronic HBV infection was associated with an increased risk of placental abruption. HBV infection may affect trophoblast cells, which play an important role in placental development [10, 11]. The HBV X protein may contribute to the migration and invasion of some types of cancer cells [22, 23]. Thus, it is plausible to hypothesize that the trophoblast migration and invasive capacity is also increased in women with chronic HBV infection. Moreover, subclinical inflammation caused by chronic HBV infection may induce trophoblast dysfunction. A recent publication demonstrated that inflammation decreases extravillontation and the associated placental trophoblast invasion [24], thus contributing to placental complications. This process causes abnormal implantation and impaired spiral artery remodeling, which are involved in the pathogenesis of placenta previa and placental abruption [11, 25]. Although Huang et al. reported no significant association between chronic HBV infection and an increased risk of placental abruption [26], our findings imply that chronic HBV infection increases the risk of this complication.

Two recent studies reported an independent association between chronic HBV infection and GDM [12, 13], which is in disagreement with our results. Lao et al. reported that the incidence of gestational diabetes was significantly increased in the HBsAg-positive group. Multiple logistic regression analysis revealed an independent association between HBsAg carrier status and GDM (relative risk, 3.51; 95% CI, 1.83–6.73) [27]. Liver plays a key role in regulating glucose homeostasis. Liver damage from the hepatitis B virus might cause a glycometabolic disorder [28], Therefore, additional studies are required to elucidate this issue.

Although the mechanism underlying the association between maternal HBV infection and the incidence of PIH is unclear, the latter is most likely related to an altered maternal immune response to the fetal allograft, toward increased immunotolerance, leading to a reduced incidence of PIH and PE. A multicenter study performed by Reddick et al. showed that maternal HBV infection was not associated with PE [6]. Another multicenter study carried out in Florida and a cohort study performed in Liuyang in rural China also reported an absence of significant associations between HBV infection and PIH [16, 29]. However, the authors of a case–control study that was carried out in Iran and included 450 HBV carriers and 450 controls reported an increased risk of PIH in women with HBV infection (OR, 54.2; 95% CI, 2.2–8.1) [30]. In contrast, Lao et al. found that maternal HBV infection reduced the risk of PIH (OR, 50.79; 95% CI, 0.66–0.95) and PE (OR, 50.71; 95% CI, 0.56–0.91) [4]. Here, maternal HBV infection reduced the risk of PIH (HbsAg-positive group: 3.05%; HBsAg-negative group: 3.73%). The inconsistency of these results may be explained by a selection bias caused by the research methods and the size of the cohorts used in each study.

Interestingly, there was a significant difference between the HBV-infected and the normal groups regarding mode of delivery. Here, a decreased risk of premature rupture of fetal membranes was observed in HBV-infected women compared with the normal group, whereas a previous report describes opposite findings [31]. These results suggest that HBV-infected pregnant women may maintain a good self-management level and obtain additional help from their physicians and families.

Preeclampsia (which is characterized by multilevel maternal endothelial dysfunction) may be triggered by or result from an imbalance between angiogenic, antiangiogenic, and proangiogenic factors, e.g., vascular endothelial growth factor [8, 14]. Moreover, significant associations/correlations between HBV, insulin resistance, obesity, and renal injury/proteinuria have been reported [32,33,34]. Lao et al. reported that the incidence of gestational diabetes was significantly increased in the HBsAg-positive group. Multiple logistic regression analysis revealed an independent association between HBsAg carrier status and GDM (relative risk, 3.51; 95% CI, 1.83–6.73) [27]. Cui et al. showed that the proportion of miscarriages was significantly higher among HBV carriers compared with controls (9.36% versus 5.70%; P < 0.001), which suggests that maternal HBV carrier status is an independent risk factor for miscarriage and that careful surveillance of these women is necessary [35]. Chronic HBV infection is a major cause of liver dysfunction (e.g., it increases serum aminotransferase and bilirubin levels). However, preterm birth was more common in women with abnormal alanine aminotransferase (ALT), aspartate aminotransferase (AST), glutamyl transpeptidase (GGT), or total bilirubin. Xun Zhuang et al. showed that the incidences of ICP, preeclampsia/eclampsia, and HELLP syndrome were 1.37, 3.14, and 0.02%, respectively [36].

A large-scale population-based cohort study showed that pre-pregnancy HBV infection may be associated with an increased risk of preterm delivery. Here, women who were HBsAg positive and HBeAg negative had a 26% higher risk of preterm birth, and women who were both HBsAg and HBeAg positive had a 20% higher risk of preterm birth than did women who were not infected with HBV. In addition, women who were HBsAg positive and HBeAg negative exhibited an 18% higher risk of early preterm birth, and women who were both HBsAg and HBeAg positive had a 34% higher risk of early preterm birth compared with women without HBV infection. Maternal pre-pregnancy HBV infection is independently associated with a higher risk of preterm birth and early preterm birth [37]. Moreover, three review articles reported a significantly increased risk of preterm birth among HBV carriers [35, 38, 39]. Safir et al. found that the presence of the HBsAg in pregnant women poses an additional risk for the pregnancy [6, 12, 21, 40, 41]; in contrast, Pastorek et al. stated that there is no significant difference between HBV-infected and non-infected pregnant women [5, 42].

It’s found that HBV-positive pregnant women underwent vaginal delivery were more likely to have placental abruption and premature birth compared with HBV-negative women in our study. Placental abruption, classically defined as a premature separation of the placenta before delivery, is one of the leading causes of vaginal bleeding in the second half of pregnancy. It’s proposed that changes in the population and function of immunocytes at the maternal-fetal interface can be part of the mechanism of disease of obstetrical disorders, such as placental abruption [43], and whether HBV would affect the population and function of immunocytes at the maternal-fetal interface was unclear, perhaps this was the reason why HBV-positive pregnant women underwent vaginal delivery were more likely to have placental abruption.

This study had several limitations. First, we collected very few data regarding viral load in the HBV carriers included in the analyses. Second, we did not examine HBV activity (e.g., `16yt55g4erwq32156rt2HBV DNA), which might affect pregnancy outcomes. Moreover, the presence of HBeAg in serum indicates active viral replication in hepatocytes; thus, it is a surrogate marker of HBV DNA [44]. Therefore, we were unable to conclude on the presence/absence of significant correlations between higher viral loads at the time of pregnancy and adverse outcomes. Third, potential confounders that might affect pregnancy outcomes were not included in this study. For example, cigarette smoking, and alcohol and caffeine consumption may be risk factors for miscarriage. In fact, in Chinese cultural tradition, women are discouraged from drinking alcohol and smoking cigarettes, and most people drink tea rather than coffee. Another limitation of this study was its single-center design: the study was carried out in a tertiary maternal and child health hospital; however, this hospital serves nearly half of the city’s population and guarantees good patient representativeness. Finally, this study lacked information regarding hepatitis B e-antigen status and liver function, further research should focus on the effect of hepatitis B e-antigen status on pregnancy outcomes.

Conclusion

The present results suggest that compared with HBV positive pregnancies were more likely to be ICP and postpartum hemorrhage. HBV-positive pregnant women underwent vaginal delivery were more likely to have placental abruption abruption and premature birth compared with HBV-negative women. Obstetricians should be aware of ICP, postpartum hemorrhage, placental abruption and premature birth in HBV-positive pregnant women..

Availability of data and materials

The datasets used and analysed during the current study are available from the corresponding author on reasonable request.

Change history

Abbreviations

HBV:

Chronic hepatitis B viral

CHB:

Chronic hepatitis B.

HBsAg:

1. hepatitis B surface antigen

MTCT:

Mother-to-child transmission

PIH:

Pregnancy-induced hypertension syndrome

GDM:

Gestational diabetes

ICP:

Intrahepatic cholestasis of pregnancy

SD:

Standard deviation

References

  1. Maynard JE. Hepatitis B: global importance and need for control. Vaccine. 1990;8(Suppl):S18–20 discussion S21–13.

    PubMed  Google Scholar 

  2. Sorrell MF, Belongia EA, Costa J, Gareen IF, Grem JL, Inadomi JM, et al. National Institutes of Health consensus development conference statement: management of hepatitis B. Hepatology. 2009;49(5 Suppl):S4–s12.

    PubMed  Google Scholar 

  3. Huang Y, Li L, Sun X, Lu M, Liu H, Tang G, et al. Screening of pregnant women for hepatitis B virus surface antigen (HBsAg) and subsequent management, Qiandongnan prefecture, Guizhou, China, 2010. Vaccine. 2013;31(Suppl 9):J62–5.

    PubMed  Google Scholar 

  4. Lao TT, Sahota DS, Law LW, Cheng YK, Leung TY. Age-specific prevalence of hepatitis B virus infection in young pregnant women, Hong Kong special administrative region of China. Bull World Health Organ. 2014;92(11):782–9.

    PubMed  PubMed Central  Google Scholar 

  5. Wong S, Chan LY, Yu V, Ho L. Hepatitis B carrier and perinatal outcome in singleton pregnancy. Am J Perinatol. 1999;16(9):485–8.

    CAS  PubMed  Google Scholar 

  6. Reddick KL, Jhaveri R, Gandhi M, James AH, Swamy GK. Pregnancy outcomes associated with viral hepatitis. J Viral Hepat. 2011;18(7):e394–8.

    CAS  PubMed  Google Scholar 

  7. Lu Y, Chen Y, Xiao X, Liang X, Li J, Huang S, et al. Impact of maternal hepatitis B surface antigen carrier status on preterm delivery in southern China. Nan Fang Yi Ke Da Xue Xue Bao. 2012; 32;(9):1369–72.

  8. Levine RJ, Maynard SE, Qian C, Lim KH, England LJ, Yu KF, et al. Circulating angiogenic factors and the risk of preeclampsia. N Engl J Med. 2004;350(7):672–83.

    CAS  PubMed  Google Scholar 

  9. Locatelli A, Roncaglia N, Arreghini A, Bellini P, Vergani P, Ghidini A. Hepatitis C virus infection is associated with a higher incidence of cholestasis of pregnancy. Br J Obstet Gynaecol. 1999;106(5):498–500.

    CAS  PubMed  Google Scholar 

  10. Zhao Y, Koga K, Osuga Y, Nagai M, Izumi G, Takamura M, et al. Thrombin enhances soluble Fms-like tyrosine kinase 1 expression in trophoblasts; possible involvement in the pathogenesis of preeclampsia. Fertil Steril. 2012;98(4):917–21.

    CAS  PubMed  Google Scholar 

  11. Li P, Guo W, Du L, Zhao J, Wang Y, Liu L, et al. microRNA-29b contributes to pre-eclampsia through its effects on apoptosis, invasion and angiogenesis of trophoblast cells. Clin Sci (Lond). 2013;124(1):27–40.

    CAS  Google Scholar 

  12. Tse KY, Ho LF, Lao T. The impact of maternal HBsAg carrier status on pregnancy outcomes: a case-control study. J Hepatol. 2005;43(5):771–5.

    CAS  PubMed  Google Scholar 

  13. Lao TT, Chan BC, Leung WC, Ho LF, Tse KY. Maternal hepatitis B infection and gestational diabetes mellitus. J Hepatol. 2007;47(1):46–50.

    CAS  PubMed  Google Scholar 

  14. Hirokoshi K, Maeshima Y, Kobayashi K, Matsuura E, Sugiyama H, Yamasaki Y, et al. Increase of serum angiopoietin-2 during pregnancy is suppressed in women with preeclampsia. Am J Hypertens. 2005;18(9 Pt 1):1181–8.

    CAS  PubMed  Google Scholar 

  15. Ahmed MA, Sharif ME, Rayis DA, Nasr AM, Adam I. Hepatitis B infection and preeclampsia among pregnant Sudanese women. Virol J. 2018;15(1):20.

    PubMed  PubMed Central  Google Scholar 

  16. Connell LE, Salihu HM, Salemi JL, August EM, Weldeselasse H, Mbah AK. Maternal hepatitis B and hepatitis C carrier status and perinatal outcomes. Liver Int. 2011;31(8):1163–70.

    PubMed  Google Scholar 

  17. Petraglia F, Arcuri F, de Ziegler D, Chapron C. Inflammation: a link between endometriosis and preterm birth. Fertil Steril. 2012;98(1):36–40.

    PubMed  Google Scholar 

  18. Vrachnis N, Vitoratos N, Iliodromiti Z, Sifakis S, Deligeoroglou E, Creatsas G. Intrauterine inflammation and preterm delivery. Ann N Y Acad Sci. 2010;1205:118–22.

    CAS  PubMed  Google Scholar 

  19. Wei SQ, Fraser W, Luo ZC. Inflammatory cytokines and spontaneous preterm birth in asymptomatic women: a systematic review. Obstet Gynecol. 2010;116(2 Pt 1):393–401.

    PubMed  Google Scholar 

  20. Marra F, Tacke F. Roles for chemokines in liver disease. Gastroenterology. 2014;147(3):577–594.e571.

    CAS  PubMed  Google Scholar 

  21. Sirilert S, Traisrisilp K, Sirivatanapa P, Tongsong T. Pregnancy outcomes among chronic carriers of hepatitis B virus. Int J Gynaecol Obstet. 2014;126(2):106–10.

    PubMed  Google Scholar 

  22. Jin Y, Gao H, Chen H, Wang J, Chen M, Li G, et al. Identification and impact of hepatitis B virus DNA and antigens in pancreatic cancer tissues and adjacent non-cancerous tissues. Cancer Lett. 2013;335(2):447–54.

    CAS  PubMed  Google Scholar 

  23. Liu Y, Tong Z, Li T, Chen Q, Zhuo L, Li W, et al. Hepatitis B virus X protein stabilizes amplified in breast cancer 1 protein and cooperates with it to promote human hepatocellular carcinoma cell invasiveness. Hepatology. 2012;56(3):1015–24.

    CAS  PubMed  Google Scholar 

  24. Anton L, Brown AG, Parry S, Elovitz MA. Lipopolysaccharide induces cytokine production and decreases extravillous trophoblast invasion through a mitogen-activated protein kinase-mediated pathway: possible mechanisms of first trimester placental dysfunction. Hum Reprod. 2012;27(1):61–72.

    CAS  PubMed  Google Scholar 

  25. Brosens I, Pijnenborg R, Vercruysse L, Romero R. The "great obstetrical syndromes" are associated with disorders of deep placentation. Am J Obstet Gynecol. 2011;204(3):193–201.

    PubMed  Google Scholar 

  26. Huang QT, Chen JH, Zhong M, Xu YY, Cai CX, Wei SS, et al. The risk of placental abruption and placenta previa in pregnant women with chronic hepatitis B viral infection: a systematic review and meta-analysis. Placenta. 2014;35(8):539–45.

    CAS  PubMed  Google Scholar 

  27. Lao TT, Tse KY, Chan LY, Tam KF, Ho LF. HBsAg carrier status and the association between gestational diabetes with increased serum ferritin concentration in Chinese women. Diabetes Care. 2003;26(11):3011–6.

    PubMed  Google Scholar 

  28. Raddatz D, Ramadori G. Carbohydrate metabolism and the liver: actual aspects from physiology and disease. Z Gastroenterol. 2007;45:51–62. https://doi.org/10.1055/s-2006-927394 [PubMed].

    Article  CAS  PubMed  Google Scholar 

  29. Huang X, Tan H, Li X, Zhou S, Wen SW, Luo M. Maternal chronic HBV infection would not increase the risk of pregnancy-induced hypertension--results from pregnancy cohort in Liuyang rural China. PLoS One. 2014;9(12):e114248.

    PubMed  PubMed Central  Google Scholar 

  30. Salehgargari S, Hantoushzadeh S, Zendehdel N, et al. The Association of Maternal HBsAg Carrier Status and Perinatal Outcome[J]. Hepatitis Monthly. 2009;9(3):180-4.

  31. Hu Y, Ding YL, Yu L. The impact of intrahepatic cholestasis of pregnancy with hepatitis B virus infection on perinatal outcomes. Ther Clin Risk Manag. 2014;10:381–5.

    PubMed  PubMed Central  Google Scholar 

  32. Joo EJ, Chang Y, Yeom JS, Lee YG, Ryu S. Hepatitis B infection is associated with an increased incidence of thrombocytopenia in healthy adults without cirrhosis. J Viral Hepat. 2017;24(3):253–8.

    CAS  PubMed  Google Scholar 

  33. Chien CH, Chen LW, Lin CL, Chang SW, Shyu YC, Chen KF, et al. Unawareness of hepatitis B virus infection confers on higher rate of metabolic syndrome: a community-based study. Sci Rep. 2017;7(1):9869.

    PubMed  PubMed Central  Google Scholar 

  34. Shah AS, Amarapurkar DN. Spectrum of hepatitis B and renal involvement. Liver Int. 2018;38(1):23–32.

    PubMed  Google Scholar 

  35. Cui AM, Cheng XY, Shao JG, Li HB, Wang XL, Shen Y, et al. Maternal hepatitis B virus carrier status and pregnancy outcomes: a prospective cohort study. BMC Pregnancy Childbirth. 2016;16:87.

    PubMed  PubMed Central  Google Scholar 

  36. Zhuang X, Cui AM, Wang Q, Cheng XY, Shen Y, Cai WH, et al. Liver dysfunction during pregnancy and its Association of with Preterm Birth in China: a prospective cohort study. EBioMedicine. 2017;26:152–6.

    PubMed  PubMed Central  Google Scholar 

  37. Liu J, Zhang S, Liu M, Wang Q, Shen H, Zhang Y. Maternal pre-pregnancy infection with hepatitis B virus and the risk of preterm birth: a population-based cohort study. The lancet. Glob Health. 2017;5(6):e624–32.

    Google Scholar 

  38. Huang QT, Wei SS, Zhong M, Hang LL, Xu YY, Cai GX, et al. Chronic hepatitis B infection and risk of preterm labor: a meta-analysis of observational studies. J Clin Virol. 2014;61(1):3–8.

    PubMed  Google Scholar 

  39. Ma X, Sun D, Li C, Ying J, Yan Y. Chronic hepatitis B virus infection and preterm labor (birth) in pregnant women-an updated systematic review and meta-analysis. J Med Virol. 2018;90(1):93–100.

    PubMed  Google Scholar 

  40. Safir A, Levy A, Sikuler E, Sheiner E. Maternal hepatitis B virus or hepatitis C virus carrier status as an independent risk factor for adverse perinatal outcome. Liver Int. 2010;30(5):765–70.

    PubMed  Google Scholar 

  41. Elefsiniotis I, Tsoumakas K, Vezali E, Glynou I, Drakoulis N, Saroglou G. Spontaneous preterm birth in women with chronic hepatitis B virus infection. Int J Gynaecol Obst. 2010;110(3):241–4.

    Google Scholar 

  42. Pastorek JG 2nd, Miller JM Jr, Summers PR. The effect of hepatitis B antigenemia on pregnancy outcome. Am J Obstet Gynecol. 1988;158(3 Pt 1):486–9.

    PubMed  Google Scholar 

  43. Romero R, Kusanovic JP, Chaiworapongsa T, et al. Placental bed disorders in preterm labor, preterm PROM, spontaneous abortion and abruptio placentae [J]. Best Pract Res Clin Obstet Gynaecol. 2011;25(3):313–27.

    PubMed  PubMed Central  Google Scholar 

  44. Yang HI, Lu SN, Liaw YF. Hepatitis B e antigen and the risk of hepatocellular carcinoma. N.Engl. J. Med. 2002;347(3):168–74.

    CAS  Google Scholar 

Download references

Acknowledgments

Not applicable.

Funding

This research was funded by Fujian medical innovation project (2017-CX-11), Fujian Science and Technology Project (number 2018Y0005) and Key Clinical Specialty Discipline Construction of Fujian,P.R.C ([2015] no. 593).

Author information

Author notes

  1. Yulong Zhang and Jiacheng Chen contributed equally to this work.

Authors and Affiliations

  1. Department of Obstetrics and Gynecology, Fujian Provincial Maternity and Children’s Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, 350001, Fujian, China

    Yulong Zhang, Jiacheng Chen, Tingting Liao, Siwen Chen, Jianying Yan & Xiaoqian Lin

Authors
  1. Yulong Zhang
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Jiacheng Chen
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Tingting Liao
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Siwen Chen
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Jianying Yan
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Xiaoqian Lin
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

All authors contributed to manuscript editing and read and approved the final manuscript. YLZ and JY Y contributed to the study design. The analysis was made by YLZ in discussion and with the assistance of JCC and TTL. JCC, TTL, XQL and SWL drafted the manuscript.

Corresponding author

Correspondence to Jianying Yan.

Ethics declarations

Ethics approval and consent to participate

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional research committee and the data used in oue research acquired administrative permissions, the study was legally approved by the institutional ethics committee of Fujian Provincial Maternity and Children’s Hospital and conducted in accord with the guidelines of the Declaration of Helsinki, and the rights of all participants were protected.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

The original online version of this article was revised: the authors reported an error in Tables 1-3 headers and equal contribution statement.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Zhang, Y., Chen, J., Liao, T. et al. Maternal HBsAg carriers and pregnancy outcomes: a retrospective cohort analysis of 85,190 pregnancies. BMC Pregnancy Childbirth 20, 724 (2020). https://doi.org/10.1186/s12884-020-03257-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12884-020-03257-4

Keywords

BMC Pregnancy and Childbirth

ISSN: 1471-2393

Contact us