Abstract
To elucidate the impact of a hepatitis B (HB) vaccination program on the prevalence of HB surface antigen (HBsAg) and HB envelope antigen (HBeAg) as well as the success rate of HBeAg clearance among parturients, we collected data on parturients who gave birth between 2000 and 2010, and recorded the HB status postpartum of those with positive HBeAg before birth. A total of 8696 parturients were enrolled, of whom 113 with prenatal positive HBeAg were invited back. The prevalence of HBsAg decreased over the study period, particularly in the vaccinated cohort, while there was no change in the prevalence of HBeAg. Foreign parturients had a higher HBeAg-positive rate and delayed HBeAg clearance, and those with a higher body mass index (>24 kg/m2) had earlier HBeAg clearance (51.9% vs. 23.9%, p = 0.005). Only 30% of the subjects who were positive for HBeAg before birth became negative 5 years after delivery. In conclusion, the downward trend in HB infection with more significance among vaccinated parturients reflects effective prevention and the impact of universal HB immunization. Nonetheless, aggressive follow-up is necessary for parturients who are persistently positive for HBeAg postpartum, as well as developing different public health policies for foreign parturients from endemic areas.
Introduction
There are almost 360 million chronic carriers of hepatitis B (HB) virus (HBV) worldwide, with a higher prevalence in Asian countries1. In Taiwan, HBV infection is an important public health issue due to its association with hepatocellular carcinoma (HCC), the second leading cause of cancer death of Taiwan, and chronic liver disease2. Moreover, HBsAg-positive parous women have been reported to have a significantly high mortality rate due to both liver and non-liver-related causes3.
A high prevalence of HB envelope antigen (HBeAg) among pregnant women positive for HB surface antigen (HBsAg) has been reported to result in a high incidence of HBV infection in newborns through mother-to-infant transmission4. In July 1984, Taiwan launched a nationwide HB vaccination program for infants born to HBV carrier mothers, primarily to interrupt vertical transmission. Two years later, the vaccination program extended the coverage to all newborns, and also gave hepatitis B immune globulin (HBIG) injections to the newborns of HBeAg-positive mothers within 24 hours after birth. Thus Taiwan was the first country to introduce an HB vaccination program in the world5. The program as then further extended to cover all preschool children in 1987, primary-school children in 1988, and middle-school children in 1989, resulting in a high national coverage rate in the targeted cohort of 92.8% by 20026.
Early HBeAg seroconversion in the immune clearance phase has been shown to indicate a favorable outcome in the natural course of chronic HBV infection. In contrast, late HBeAg clearance has been associated with the progression of chronic hepatitis and a poor long-term outcome such as liver cirrhosis and HCC7–9. Previous studies have reported a decrease in the prevalence of HBeAg among pregnant women in Taiwan during the 1990s10, 11; however, trends in those vaccinated after the introduction of the vaccination program have yet to be reported. Since the vaccinated cohort are now of child-bearing age, we aimed to investigate the effect of the universal HBV vaccination program in Taiwan on this cohort, including the trend of HBeAg prevalence during the 2000s. Moreover, during the past decade an increasing number of foreign spouses have immigrated to Taiwan, mostly from China and other Southeast Asian countries with a high prevalence of HBV infection12, 13. Therefore, we also aimed to investigate the status of HBV infection among Taiwanese pregnant women and those from other Asian countries in order to explore the potential impact of foreign immigration on public health in Taiwan.
We conducted this large-scale 10-year retrospective analysis to explore the trends of the prevalence of HBsAg and HBeAg in pregnant women, and also a follow-up study for the mothers who were HBeAg-positive to evaluate the rate of postpartum HBeAg seroconversion as well as the associated factors. We hope the results can provide data on the impact of the universal hepatitis B vaccination program in Taiwan, and also provide a reference to improve the efficacy of such programs.
Results
Retrospective study
From January 2001 to April 2010, we recruited 8696 pregnant women including 8258 Taiwanese women and 438 foreign spouses from China and other Southeast Asian countries. We excluded 426 (4.9%) who had no data on birth date (Table 1). The prevalence rate of positive HBsAg decreased in each year over the 10-year study period (p < 0.001). By stratifying the mothers by birth date into four groups under different coverage strategies of HBV vaccination as before June 1979, July 1979 to June 1984 (5 years before universal immunization to newborns born to HBeAg-positive mothers), July 1984 to June 1986, and after July 1986 (nationwide vaccination to all newborns), the HBsAg-positive rates were 15.9%, 12.4%, 7.8%, and 2.6%, respectively (p = 0.001). The subjects born after the universal vaccination program had been implemented (July 1986) had a much lower seropositive rate than those born before the program had been launched (June 1984) (p < 0.001). However, the carrier rate had already started to decrease in the women born 5 years before the introduction of the HB vaccination program (July 1979 to June 1984). With regards to nationality, we did not find any statistical difference in the HBsAg carrier rate between Taiwanese and other Asian women (14.5% vs. 12.6%, p = 0.249).
Table 1.
Factors | Number of subjects | Number HBsAg(+) | Percentage HBsAg(+) | P1 | P2 | |
---|---|---|---|---|---|---|
Total | 8696 | 1256 | 14.4% | |||
Calendar year of HBsAg test | 2000 | 928 | 147 | 15.8 | 0.001 | 0.001 |
2001 | 1561 | 256 | 16.4 | |||
2002 | 1558 | 206 | 13.2 | |||
2003 | 597 | 112 | 18.8 | |||
2004 | 403 | 59 | 14.6 | |||
2005 | 513 | 64 | 12.5 | |||
2006 | 628 | 94 | 15.0 | |||
2007 | 718 | 103 | 14.3 | |||
2008 | 707 | 75 | 10.6 | |||
2009 | 729 | 97 | 13.3 | |||
2010 | 354 | 43 | 12.1 | |||
Birthday | Before June 1979 | 6905 | 1099 | 15.9 | <0.001 | <0.001 |
July, 1979 to June 1984 | 1186 | 147 | 12.4 | |||
July, 1984 to June 1986 | 103 | 8 | 7.8 | |||
After July, 1986** | 76 | 2 | 2.6 | |||
Nationality | Native | 8258 | 1201 | 14.5 | 0.249 | |
Other Asian countries | 438 | 55 | 12.6 |
*P1. Pearson’s chi-square test; P2. chi-square test for a linear trend.
**Stratifying their birth of dates into four groups based on the time when the HBV vaccination program was launched in Taiwan.
A total of 263 HBeAg-positive mothers with 353 deliveries were identified from 1256 HBsAg-positive mothers with 1595 deliveries. No trend was identified in the positive rates of HBeAg during the 2000s (Table 2). Even so, the positive rates of HBeAg did decline with age, from 42.0% in women aged less than 25 years to 9.9% in those aged 35 years or older (p < 0.001). Neither the number of pregnancies nor parity were significantly associated with the positive rate of HBeAg. Moreover, women born in Taiwan had a significant lower HBeAg-positive rate than those from other Asian countries (21.3% vs. 40.6%, p < 0.001). In multiple logistic regression analysis, age and nationality were still independently associated with HBeAg-positive rate (Table 3). Compared to the women aged 35 years or older, those parturients aged <25, 25–29 and 30–34 years had higher positive HBeAg rate with odds ratios (ORs) (95% confidence intervals (CIs)) of 5.97 (3.52–10.13), 3.49 (2.30–5.31), and 2.18 (1.44–3.32), respectively. The OR of a positive HBeAg rate was 1.74 (1.03–2.92) for the women from other Asian countries compared to Taiwanese women (p = 0.037).
Table 2.
Factors | Number HBsAg(+)a n = 1595 | Number HBeAg(+)b n = 353 | Percentage HBeAg(+) 22.1% | P1 | P2 | |
---|---|---|---|---|---|---|
Calendar year of delivery | 2001 | 232 | 62 | 26.7 | 0.647 | 0.249 |
2002 | 258 | 56 | 21.7 | |||
2003 | 190 | 35 | 18.4 | |||
2004 | 78 | 22 | 28.2 | |||
2005 | 113 | 24 | 21.2 | |||
2006 | 167 | 38 | 22.8 | |||
2007 | 150 | 32 | 21.3 | |||
2008 | 144 | 30 | 20.8 | |||
2009 | 149 | 32 | 21.5 | |||
2010 | 114 | 22 | 19.3 | |||
Age (years) | <25 | 119 | 50 | 42.0 | <0.001 | <0.001 |
25–29 | 512 | 145 | 28.3 | |||
30–34 | 652 | 127 | 19.5 | |||
≥35 | 312 | 31 | 9.9 | |||
Number of pregnancies | 1 | 348 | 78 | 22.4 | 0.386 | 0.391 |
2 | 655 | 132 | 20.2 | |||
3 | 382 | 94 | 24.6 | |||
>3 | 210 | 49 | 23.3 | |||
Parity | 1 | 510 | 111 | 21.8 | 0.613 | 0.398 |
2 | 823 | 179 | 21.7 | |||
3 | 219 | 50 | 22.8 | |||
>3 | 43 | 13 | 30.2 | |||
Nationality | Native | 1526 | 325 | 21.3 | <0.001 | |
Foreign | 69 | 28 | 40.6 |
*P1. Pearson’s chi-square test; P2. chi-square test for linear trend.
aNumber of deliveries from 1256 HBsAg-positive mothers.
bNumber of deliveries from 263 HBeAg-positive mothers.
Table 3.
Factor | Comparison | OR (95% C.I.) | P value |
---|---|---|---|
Age (years) | <25 vs. >=35 | 5.97 (3.52–10.13) | <0.001 |
25–29 vs. >=35 | 3.49 (2.30–5.31) | <0.001 | |
30–34 vs. >=35 | 2.18 (1.44–3.32) | <0.001 | |
Nationality | Other Southeast Asian countries vs. Taiwanese | 1.74 (1.03–2.92) | 0.037 |
Follow-up study
A total of 133 women of the 263 HBeAg-positive mothers responded to our request to return for a postpartum follow-up study. After excluding 14 subjects who had received antiviral therapy, the remaining 119 were recruited for analysis. The mean age of these mothers at follow-up was 35.2 ± 4.7 years, and the mean duration from the first diagnosis of being HBeAg-positive during pregnancy to returning for the follow-up study was 5.1 ± 3.2 years. Thirty-six (30.3%) of the women tested negative for serum HBeAg with HBV DNA levels less than 2000 IU/ml, and were regarded as having successful HBeAg clearance. In addition, among those mothers who were persistently positive for HBeAg, 86.7% had an HBV DNA level higher than 2000 IU/ml (not shown in the tables). In univariate analysis comparing factors related to HBeAg clearance, body mass index (BMI), fatty liver and nationality had a trend of association with successful HBeAg clearance (Table 4). Furthermore, in multiple logistic regression analysis for these associated factors, only BMI was statistically significant, showing a delayed HBeAg clearance in the women with a BMI < 24 kg/m2 (OR 3.43, CI 1.40–3.38, p = 0.007).
Table 4.
Variable | Comparison | HBeAg clearance | P value | |
---|---|---|---|---|
Failureb n = 83 (69.7%) | Successc n = 36 (30.3%) | |||
Duration | Years | 4.8 ± 3.2 | 5.8 ± 2.9 | 0.101 |
Age | Years | 34.7 ± 4.8 | 36.4 ± 4.2 | 0.070 |
Nationality | Foreign | 7 (100) | 0 (0) | 0.100 |
Native | 76 (67.9) | 36 (32.1) | ||
Number of parity | 1 | 27 (71.1) | 11 (28.9) | 0.928 |
2 | 43 (68.3) | 20 (31.7) | ||
≥3 | 13 (72.2) | 5 (27.8) | ||
BMI | ≤24 kg/m2 | 70 (76.1) | 22 (23.9) | 0.005 |
>24 kg/m2 | 13 (48.1) | 14 (51.9) | ||
Fatty liver | N | 48 (77.4) | 14 (22.6) | 0.057 |
Y | 35 (61.4) | 22 (38.6) | ||
HBV | B | 59 (72.8) | 22 (27.2) | 0.177 |
genotypea | C | 22 (88.0) | 3 (12.0) |
aSubjects with detectable HBV DNA were included.
bHBeAg(+) or HBeAg(−) but HBV DNA > 2000 IU/ml.
cHBeAg(−) and HBV DNA < 2000 IU/ml.
Discussion
In this study, we found that the prevalence of HBsAg had already begun to decrease in the women born as early as 5 years before the introduction of the national HB vaccination program in Taiwan, and there was an even more dramatic decrease in the vaccinated cohort. We also found that the HBeAg-positive rate in the HBsAg-positive parturients was consistently around 22% over the study period, with a decrease in the rate with age. Foreign parturients seemed to have a higher HBeAg-positive rate as well as delayed HBeAg clearance compared to Taiwanese parturients. Furthermore, the women with a BMI < 24 kg/m2 also had delayed HBeAg clearance compared to those with a BMI > 24 kg/m2. Among the women positive for HBeAg identified during the prenatal period, about 30% were negative for serum HBeAg with HBV DNA levels <2000 IU/ml. However, the HBeAg-positive rate among the HBsAg-positive mothers with a mean age of 35 years as still as high as 69.7% even 5 years after delivery.
In July 1984, Taiwan launched a mass nationwide hepatitis B vaccination program for infants born to HBsAg-positive mothers. Two years later, the program was extended to cover all newborns as well as to give HBIG injections to the newborns with HBeAg-positive mothers14, 15. In the current study, the overall prevalence rate of HBsAg in the pregnant women over the past 10 years was 10.6–18.8%, with a decreasing trend in each calendar year. There was an abrupt decrease in the number of parturients in 2003, as the hospital was isolated due to a nosocomial outbreak of severe acute respiratory syndrome (SARS)16. We found a dramatic decrease in the HBsAg-positive rate to 2.6% in the vaccinated parturients, suggesting that the universal immunization program was successful in reducing the rate of perinatal infection. Interestingly, we also noted a decrease in the prevalence rate of HBsAg among the group born before the universal vaccination program was launched, suggesting the protective impact of the additional vaccination since 1987 on pre-school and middle school children. Similar results were also reported by a systematic review reporting the prevalence of HBV infection in two time periods (1990 and 2005)17. Moreover, owing to efforts on primary strategies to reduce or eliminate the risk of HBV transmission from nosocomial exposure (e.g. screening for safe blood and blood products for transfusion, use of disposable syringes and needles and universal precautions), the risk of hepatitis B infection as well as super-infections with hepatitis D virus among HBV carriers has dramatically decreased, which also had a protective impact on the unvaccinated cohort18, 19.
Lu et al. and Lin et al. reported a decrease in the HBeAg-positive rate by year in the 1990s among HBsAg-positive mothers10, 11, and a systematic literature review conducted to estimate age- and region-specific HBeAg prevalence rates for females in the Asia Pacific region also showed a remarkable decrease in HBeAg prevalence from 1990 to 2005, and this was even more pronounced among those aged <9 years20. In the current study, the HBeAg-positive rate further declined to 22% in the early 2000s, but remained stationary thereafter. The decrease in positive HBeAg rate in the 1990s may be explained by marked improvements in the living environment and economy in Taiwan, while these improvements may not have been as pronounced in the 2000s.
HBeAg clearance has been reported to be both a critical serological endpoint for patients with chronic hepatitis B and also an important consideration when choosing the treatment to achieve this goal21. The reported factors associated with early HBeAg clearance include age, parity, HBV genotype, pretreatment low serum HBV DNA level, molecular virological factors as well as the degree of both biochemical and histologic activity22–25. Lin et al. reported that the positive HBeAg rate in Taiwanese parturients from 1985 and 1990 decreased from 49.4% in those aged 21–25 years to 20% in those aged >35 years11. Lu et al. also reported a similar decline with advanced age in the 1990s10. In the current study, the HBeAg-positive rate among the HBsAg-positive mothers still declined with increasing age in the past 10 years, and it is encouraging that the prevalence was much lower than in the equivalent group in the 1990s.
Several studies have reported that immigrants from endemic areas with a higher HBV prevalence and later implementation of vaccination programs can be a challenge for public health policies of the countries to which they move26–28. We found that the foreign parturients had higher HBeAg prevalence and delayed HBeAg clearance rates compared to the Taiwanese mothers. Despite World Health Organization (WHO) recommendations that HBV vaccines should have been incorporated into routine childhood immunization programs by 1997, and that the primary strategy to control HBV infection is universal infant immunization, some countries have not been able to afford to implement such measures as early as recommended29, 30. Chu et al. reported a change in the epidemiology of hepatitis B related to migration by comparing six northern and north-western European countries31. Their results showed evident differences in the HBsAg prevalence rate between the migrants and general population, which the authors concluded was because most of the migrants acquired the infection in early childhood in their country of birth. In Taiwan, most foreign mothers come from China and Vietnam. China launched a nationwide HBV vaccination program in 200232, and Vietnam’s National Expanded Program on Immunization (NEPI) introduced hepatitis B vaccines in 1997. However, a number of infant deaths in 2006 were linked to the HBV vaccine in Vietnam, hence its coverage rate was only 20% by 200833. This may explain why we found higher HBeAg prevalence and delayed HBeAg clearance rates in the foreign parturients than in those born in Taiwan. This issue cannot be ignored, and different strategies should be considered for HBV infection surveillance in the migrant population34.
Although nationality, BMI, fatty liver and HBV genotypes were all associated with HBeAg clearance, BMI was the only statistically significant factor in this study. Although the impact of BMI on the natural history of chronic hepatitis B infection still remains unclear, several studies have demonstrated an inverse relationship between BMI and metabolic syndrome and HBsAg serum clearance35–37. Chiang et al. reported a relationship between extreme obesity or central obesity and a low prevalence of high HBV viral load in patients seropositive for HBeAg38. Larger longitudinal studies are required to further clarify the association and mechanism between obesity and the natural course of HBV infection.
Genotypes B and C are the predominant HBV strains in far-eastern Asian countries. Genotype C has been associated with more severe liver disease and delayed spontaneous HBeAg seroconversion than genotype B in both adults and children in Taiwan39, 40. The HBV DNA of the HBeAg-positive mothers was checked during the follow-up study, however not all parturients in Taiwan undergo routine HBV DNA testing before delivery. Therefore, we could not analyze those with postpartum successful HBeAg clearance and undetectable HBV DNA, which may be a limitation of this study.
In conclusion, the downward trend in HB infection among parturients, and particularly in the vaccinated cohort, reflects effective horizontal prevention as well as the impact of the universal HB immunization program. It is worth noting that among the parturients who were positive for HBeAg before birth, up to 70% did not achieve serum HBeAg clearance even 5 years after delivery. Therefore, aggressive follow-up for these parturients and also developing different public health policies for foreign parturients from endemic areas to prevent subsequent complications caused by persistent chronic HBV infection are necessary.
Methods
All experiments were performed in accordance with the relevant guidelines and regulations, and informed consent was obtained from all participants for the chart review and to use blood samples to check hepatitis B status. This study was approved by the Institutional Review Board of Chang Gung Memorial Hospital (CGMH), Taiwan, and it was also funded by a grant from CGMH (CMRPG8A0031) and the Ministry of Science and Technology of Taiwan (NMRPG8F0261).
Retrospective study
All parturients who delivered between January 2001 and April 2010 at the Department of Obstetrics of CGMH in southern Taiwan were recruited. Serum HBsAg and HBeAg were tested routinely at the prenatal clinic in all parturients at a gestational age between 28 to 32 weeks. Therefore, some of the parturients who delivered in early 2001 may have been tested for HBV at the end of 2000. We retrospectively obtained data including date of birth, nationality, parity, date of delivery, and the results of HBsAg and HBeAg tests during pregnancy from their medical records. In order to compare the HBsAg and HBeAg positive rates over time and according to four different coverage strategies of HB vaccination (before June 1979, from July 1979 to June 1984 (5 years before universal immunization was given to infants born to HBeAg-positive mothers), July 1984 to June 1986, and after July 1986 (when nationwide vaccination was given to all newborns), we performed analysis stratified by age, parity, date of birth, and relevant time periods.
Follow-up study
In April 2011, we invited 263 mothers confirmed to be HBeAg-positive during pregnancy from 2001 to 2010 to return to check their hepatitis status. All of the women provided informed consent, and all provided blood samples to measure the level of HBeAg, titer of HBV DNA and genotype of the HBV. HBeAg was analyzed using a microparticle enzyme immunoassay (AxSYM, Abbott GmbH & Co. KG, Wiesbaden, Germany), and HBV DNA was detected by real-time PCR (TaqMan HBV analyte-specific reagent, ASR; Roche Molecular Systems, Inc., Branchburg, NJ). HBV genotypes were determined using a restriction fragment length polymorphism on the surface gene (between nucleotide positions 256 and 796), which was amplified by PCR using nested primers as described in our previous study41. Women negative for HBeAg who were previously HBeAg-positive were defined as having HBeAg clearance42. We defined the subjects who were negative HBeAg and an HBV DNA level <2000 IU/ml as the “success” group, and we excluded those who had received antiviral therapy for HB.
Statistical analysis
Continuous and categorical data were presented as mean, standard deviation, and percentage. Comparisons between groups and linear trends between variables were analyzed using the chi-square test and chi-square test for trends, respectively. In univariate analysis, Fisher’s exact test was also used to examine group differences for categorical variables. Independent factors possibly associated with HBeAg prevalence and clearance were analyzed using multiple logistic regression models. A p value of <0.05 was considered to be statistically significant.
Acknowledgements
We thank the Biostatistics Center, Kaohsiung Chang Gung Memorial Hospital for assistance with the statistical analysis in this study. The study was funded by Chang Gung Memorial Hospital in Taiwan (grant number CMRPG8A0031 to Dr. Chen-Hsuan Wu) and the Ministry of Science and Technology of Taiwan (grant number NMRPG8F0261 to Dr. Chen-Hsuan Wu).
Author Contributions
S.L. designed the study and C.W. collected data, analyzed data and wrote the manuscript. T.H., F.K., C.C. and C.T. gave technical support and conceptual advice. All authors reviewed the manuscript.
Competing Interests
The authors declare that they have no competing interests.
Footnotes
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Merican I, et al. Chronic hepatitis B virus infection in Asian countries. J Gastroenterol Hepatol. 2000;15:1356–1361. doi: 10.1046/j.1440-1746.2000.0150121356.x. [DOI] [PubMed] [Google Scholar]
- 2.Lu SN, et al. Secular trends and geographic variations of hepatitis B virus and hepatitis C virus-associated hepatocellular carcinoma in Taiwan. Int J Cancer. 2006;119:1946–1952. doi: 10.1002/ijc.22045. [DOI] [PubMed] [Google Scholar]
- 3.Fwu CW, et al. Mortality after chronic hepatitis B virus infection: a linkage study involving 2 million parous women from Taiwan. J Infect Dis. 2010;201:1016–1023. doi: 10.1086/651231. [DOI] [PubMed] [Google Scholar]
- 4.Chang MH, Chen DS, Hsu HC, Hsu HY, Lee CY. Maternal transmission of hepatitis B virus in childhood hepatocellular carcinoma. Cancer. 1989;64:2377–2380. doi: 10.1002/1097-0142(19891201)64:11<2377::AID-CNCR2820641130>3.0.CO;2-8. [DOI] [PubMed] [Google Scholar]
- 5.Chen DS, et al. A mass vaccination program in Taiwan against hepatitis B virus infection in infants of hepatitis B surface antigen-carrier mothers. Jama. 1987;257:2597–2603. doi: 10.1001/jama.1987.03390190075023. [DOI] [PubMed] [Google Scholar]
- 6.Huang K, Lin S. Nationwide vaccination: a success story in Taiwan. Vaccine. 2000;18(Suppl 1):S35–38. doi: 10.1016/S0264-410X(99)00460-0. [DOI] [PubMed] [Google Scholar]
- 7.Chen YC, Chu CM, Liaw YF. Age-specific prognosis following spontaneous hepatitis B e antigen seroconversion in chronic hepatitis B. Hepatology. 2010;51:435–444. doi: 10.1002/hep.23348. [DOI] [PubMed] [Google Scholar]
- 8.Hsu YS, et al. Long-term outcome after spontaneous HBeAg seroconversion in patients with chronic hepatitis B. Hepatology. 2002;35:1522–1527. doi: 10.1053/jhep.2002.33638. [DOI] [PubMed] [Google Scholar]
- 9.Geier, A., Gartung, C. & Dietrich, C. G. Hepatitis B e Antigen and the Risk of Hepatocellular Carcinoma. N Engl J Med347, 1721–1722, author reply 1721–1722, 10.1056/nejm200211213472119 (2002). [DOI] [PubMed]
- 10.Lu SN, Liu JH, Wang JH, Lu CC. Secular trends of HBeAg prevalence among HBsAg-positive delivery mothers in a hepatitis B endemic area. J Trop Pediatr. 2000;46:121–123. doi: 10.1093/tropej/46.2.121. [DOI] [PubMed] [Google Scholar]
- 11.Lin HH, Kao JH, Chang TC, Hsu HY, Chen DS. Secular trend of age-specific prevalence of hepatitis B surface and e antigenemia in pregnant women in Taiwan. Journal of medical virology. 2003;69:466–470. doi: 10.1002/jmv.10332. [DOI] [PubMed] [Google Scholar]
- 12.Caruana SR, et al. Knowledge about hepatitis and previous exposure to hepatitis viruses in immigrants and refugees from the Mekong Region. Aust N Z J Public Health. 2005;29:64–68. doi: 10.1111/j.1467-842X.2005.tb00751.x. [DOI] [PubMed] [Google Scholar]
- 13.Wingate MS, Alexander GR. The healthy migrant theory: variations in pregnancy outcomes among US-born migrants. Soc Sci Med. 2006;62:491–498. doi: 10.1016/j.socscimed.2005.06.015. [DOI] [PubMed] [Google Scholar]
- 14.Beasley RP, et al. Prevention of perinatally transmitted hepatitis B virus infections with hepatitis B immune globulin and hepatitis B vaccine. Lancet. 1983;2:1099–1102. doi: 10.1016/S0140-6736(83)90624-4. [DOI] [PubMed] [Google Scholar]
- 15.Hsu HM, et al. Efficacy of a mass hepatitis B vaccination program in Taiwan. Studies on 3464 infants of hepatitis B surface antigen-carrier mothers. Jama. 1988;260:2231–2235. doi: 10.1001/jama.1988.03410150079034. [DOI] [PubMed] [Google Scholar]
- 16.Liu JW, et al. Epidemiologic study and containment of a nosocomial outbreak of severe acute respiratory syndrome in a medical center in Kaohsiung, Taiwan. Infect Control Hosp Epidemiol. 2006;27:466–472. doi: 10.1086/504501. [DOI] [PubMed] [Google Scholar]
- 17.Ott JJ, Stevens GA, Groeger J, Wiersma ST. Global epidemiology of hepatitis B virus infection: new estimates of age-specific HBsAg seroprevalence and endemicity. Vaccine. 2012;30:2212–2219. doi: 10.1016/j.vaccine.2011.12.116. [DOI] [PubMed] [Google Scholar]
- 18.Van Herck K, Vorsters A, Van Damme P. Prevention of viral hepatitis (B and C) reassessed. Best Pract Res Clin Gastroenterol. 2008;22:1009–1029. doi: 10.1016/j.bpg.2008.11.008. [DOI] [PubMed] [Google Scholar]
- 19.Huo TI, et al. Decreasing hepatitis D virus infection in Taiwan: an analysis of contributory factors. J Gastroenterol Hepatol. 1997;12:747–751. doi: 10.1111/j.1440-1746.1997.tb00364.x. [DOI] [PubMed] [Google Scholar]
- 20.Ott JJ, Stevens GA, Wiersma ST. The risk of perinatal hepatitis B virus transmission: hepatitis B e antigen (HBeAg) prevalence estimates for all world regions. BMC Infect Dis. 2012;12:131. doi: 10.1186/1471-2334-12-131. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Liaw YF, Lau GK, Kao JH, Gane E. Hepatitis B e antigen seroconversion: a critical event in chronic hepatitis B virus infection. Dig Dis Sci. 2010;55:2727–2734. doi: 10.1007/s10620-010-1179-4. [DOI] [PubMed] [Google Scholar]
- 22.Liaw YF, et al. Age-specific prevalence and significance of hepatitis B e antigen and antibody in chronic hepatitis B virus infection in Taiwan: a comparison among asymptomatic carriers, chronic hepatitis, liver cirrhosis, and hepatocellular carcinoma. Journal of medical virology. 1984;13:385–391. doi: 10.1002/jmv.1890130410. [DOI] [PubMed] [Google Scholar]
- 23.Kao JH, Chen PJ, Lai MY, Chen DS. Hepatitis B virus genotypes and spontaneous hepatitis B e antigen seroconversion in Taiwanese hepatitis B carriers. Journal of medical virology. 2004;72:363–369. doi: 10.1002/jmv.10534. [DOI] [PubMed] [Google Scholar]
- 24.Liaw YF. Current therapeutic trends in therapy for chronic viral hepatitis. J Gastroenterol Hepatol. 1997;12:S346–353. doi: 10.1111/j.1440-1746.1997.tb00520.x. [DOI] [PubMed] [Google Scholar]
- 25.Kao JH, Chen PJ, Lai MY, Chen DS. Basal core promoter mutations of hepatitis B virus increase the risk of hepatocellular carcinoma in hepatitis B carriers. Gastroenterology. 2003;124:327–334. doi: 10.1053/gast.2003.50053. [DOI] [PubMed] [Google Scholar]
- 26.Kawsar M, Goh BT. Hepatitis B virus infection among Chinese residents in the United Kingdom. Sex Transm Infect. 2002;78:166–168. doi: 10.1136/sti.78.3.166. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Denis F, et al. Screening of pregnant women for hepatitis B markers in a French Provincial University Hospital (Limoges) during 15 years. Eur J Epidemiol. 2004;19:973–978. doi: 10.1007/s10654-004-5755-9. [DOI] [PubMed] [Google Scholar]
- 28.Lin CC, et al. Hepatitis B virus infection among pregnant women in Taiwan: comparison between women born in Taiwan and other southeast countries. BMC Public Health. 2008;8:49. doi: 10.1186/1471-2458-8-49. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Clements CJ, et al. Progress in the control of hepatitis B infection in the Western Pacific Region. Vaccine. 2006;24:1975–1982. doi: 10.1016/j.vaccine.2005.11.035. [DOI] [PubMed] [Google Scholar]
- 30.Rani M, Yang B, Nesbit R. Hepatitis B control by 2012 in the WHO Western Pacific Region: rationale and implications. Bull World Health Organ. 2009;87:707–713. doi: 10.2471/BLT.08.059220. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Chu JJ, et al. Changing epidemiology of hepatitis B and migration–a comparison of six Northern and North-Western European countries. Eur J Public Health. 2013;23:642–647. doi: 10.1093/eurpub/cks067. [DOI] [PubMed] [Google Scholar]
- 32.Sun Z, Ming L, Zhu X, Lu J. Prevention and control of hepatitis B in China. Journal of medical virology. 2002;67:447–450. doi: 10.1002/jmv.10094. [DOI] [PubMed] [Google Scholar]
- 33.Progress towards measles elimination -South-East Asia Region, 2003–2013. Releve epidemiologique hebdomadaire90, 297–305 (2015). [PubMed]
- 34.Chu CM, Hung SJ, Lin J, Tai DI, Liaw YF. Natural history of hepatitis B e antigen to antibody seroconversion in patients with normal serum aminotransferase levels. Am J Med. 2004;116:829–834. doi: 10.1016/j.amjmed.2003.12.040. [DOI] [PubMed] [Google Scholar]
- 35.Hsu CS, et al. Impact of hepatitis B virus infection on metabolic profiles and modifying factors. J Viral Hepat. 2012;19:e48–57. doi: 10.1111/j.1365-2893.2011.01535.x. [DOI] [PubMed] [Google Scholar]
- 36.Jan CF, et al. A population-based study investigating the association between metabolic syndrome and hepatitis B/C infection (Keelung Community-based Integrated Screening study No. 10) Int J Obes (Lond) 2006;30:794–799. doi: 10.1038/sj.ijo.0803204. [DOI] [PubMed] [Google Scholar]
- 37.Chu CM, Lin DY, Liaw YF. Does increased body mass index with hepatic steatosis contribute to seroclearance of hepatitis B virus (HBV) surface antigen in chronic HBV infection? Int J Obes (Lond) 2007;31:871–875. doi: 10.1038/sj.ijo.0803479. [DOI] [PubMed] [Google Scholar]
- 38.Chiang CH, et al. Association between obesity, hypertriglyceridemia and low hepatitis B viral load. Int J Obes (Lond) 2013;37:410–415. doi: 10.1038/ijo.2012.63. [DOI] [PubMed] [Google Scholar]
- 39.Kao JH, Chen PJ, Lai MY, Chen DS. Hepatitis B genotypes correlate with clinical outcomes in patients with chronic hepatitis B. Gastroenterology. 2000;118:554–559. doi: 10.1016/S0016-5085(00)70261-7. [DOI] [PubMed] [Google Scholar]
- 40.Ni YH, et al. Clinical relevance of hepatitis B virus genotype in children with chronic infection and hepatocellular carcinoma. Gastroenterology. 2004;127:1733–1738. doi: 10.1053/j.gastro.2004.09.048. [DOI] [PubMed] [Google Scholar]
- 41.Lee CM, et al. Prevalence and clinical implications of hepatitis B virus genotypes in southern Taiwan. Scandinavian journal of gastroenterology. 2003;38:95–101. doi: 10.1080/00365520310000500. [DOI] [PubMed] [Google Scholar]
- 42.Sarin SK, et al. Asian-Pacific clinical practice guidelines on the management of hepatitis B: a 2015 update. Hepatology international. 2016;10:1–98. doi: 10.1007/s12072-015-9675-4. [DOI] [PMC free article] [PubMed] [Google Scholar]